Set of Geldanamycin Derivatives and Their Preparation Methods

Abstract

A set of geldanamycin derivatives and their preparation methods. Pharmaceutical compositions comprising the said compounds as an active ingredient which are used as antivirus and antitumor agents. The said derivatives are used in the manufacture of heat shock protein 90 (Hsp 90) inhibiting agents which have the utility as antivirus and antitumor agents.

Description

TECHNICAL FIELD

The invention relates to a series of structurally modified derivatives of geldanamycin, the preparation methods of the said compounds, their applications in anti-virus and anti-tumor, and pharmaceutical composition of the said compounds.

BACKGROUND

Geldanamycin is a benzoquinone ansamycin antibiotic generated by fermentation of Streptomyces hygroscopicus. Its molecule composes of a benzoquinone structure and a planar macrocyclic ansamycin bridge. The target of geldanamycin is heat shock protein 90 (Hsp90), it deactivates Hsp90 specifically to inhibit tumor growth or virus replication. Through interfering normal functioning of Hsp90, geldanamycin holds back the activation of the substrate protein of Hsp90, induces interdiction of cell cycle and inhibits virus replication, thereby exerting anti-virus and anti-tumor effects. The unique mechanism of geldanamycin makes itself with broad anti-virus and anti-tumor spectra, it suffers no cross resistance of the subjects with other medicines and its subjects are difficult to generate resistance against it. Geldanamycin is an excellent lead compound for new anti-virus and anti-tumor drugs using cytokine as their targets.

With the study of Hsp90 inhibitor screening as the main object, the Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences carried out a series of studies on geldanamycin, it possesses a patent on the usage of geldanamycin as a anti-virus infection drug (ZL97100523), studied in depth the anti-virus activity and mechanism of geldanamycin, as well as its application development (Li Yuhuan, Tao Pei-Heng et al: Antimicrobial Agents and Chemotherapy, 48(3): 867-872; 2004). On the basis of synthesis and study on the anti-virus effect of geldanamycin 17-Nucleoside derivatives (CN1817866A), the applicant of this invention has further synthesized a series of new 17-modified as well as 17- and 19-simultaneously modified derivatives of geldanamycin, and has tested the anti-virus activities of the compounds. Up to now, no published reports on said modified derivatives of geldanamycin and their anti-virus activities have been seen in the literature in China as well as abroad.

A main object of this invention is to obtain new types of Hsp90 inhibitor with weaker toxicities through introduction of various substitutes in 17- and/or 19-positions of geldanamycin molecules, while they retain or strengthen the original anti-virus activity of geldanamycin. The achievements studied out these new types of Hsp90 inhibitor with weaker toxicities and higher efficiencies can lay a foundation for further studies and developments on anti-virus and anti-tumor medicines with Hsp90 as target.

SUMMARY OF THE INVENTION

This invention provides a series of structurally modified derivatives of geldanamycin, whose structures are shown in Formula (I):

wherein:R₁ is a substituent which has a linkage moiety on its one end consisting of linear or branched, saturated or unsaturated chain containing 3 to 20 carbon atoms and containing or not containing ether, ester or amide bonds in said chain, and the other end of the substituent is an alicyclic or aromatic cyclic group which may optionally be substituted by hydrocarbyl, halogen, hydroxyl, carboxyl, nitrile group, amino, sulfonic or phosphoric acid group or esters or salts thereof;R₂ is H or a same substituent as R₁ or a different substituent from R₁;

X is NH, O or S; or X—R₂ is H.

The preparation of Formula (I) compounds can be realized by using the following general method. The amine containing substituent R₁ is synthesized or purchased, and is allowed to react with geldanamycin in a haloalkane, alcoholic or polar aprotic solvent (N,N-dimethylformamide, dimethylsulfoxide, ethyl acetate, acetonitrile, or acetone) and under alkaline condition (triethylamine, pyridine, N, N-dimethylpyridine, potassium carbonate, sodium carbonate, or calcium hydroxide) to obtain 17-mono substituted compound (I, X—R₂ is H). The 17-, 19-bisubstituted compounds are prepared by reacting 17-monosubstituted compounds used as material with R₂XH under the similar condition to obtain target 17-, 19-bisubstituted compounds (I, both R₁ and X—R₂ are not H).

When the other side of R₁ is 3,4-di-hydroxyl-methylated caffeic acid moiety, the preparation of Formula (I) compounds can be realized according to the following route: firstly, caffeic acid reacts with a methyalting reagent (dimethyl sulfate, methyl methanesulfonate, methyl iodide, dimethyl carbonate) under alkaline condition to obtain 3,4-di-hydroxyl-methylated caffeic acid. The latter is reacted with acyl chlorinating reagent to obtain the acyl chloride, which reacts subsequently with mono N-tert-butoxycarbonyl-ethylenediamine

to obtain (2-tert-butoxycarbonylamino) ethyl-3,4-di-hydroxyl-methylated caffeoyl amide. After removal of tert-Butyl protective group, (2-amino)ethyl-3,4-di-hydroxyl-methylated caffeoylamide is obtained. The latter is subsequently reacted with geldanamycin using the method similar to the aforementioned to produce geldanamycin derivative containing di-hydroxyl-methylated caffeoylamide moiety in the 17-position of the compound.

When the other side of R₁ is a cytidine moiety, the preparation of the compounds of Formula (I) structure is as follows: cytidine is reacted with 2,2-dimethoxypropane under acidic condition to obtain 2′,3′-isopropylidene cytidine. Under the effect of a dehydrating reagent (DCC, TBU), the product condensates with γ-tert-Butoxycarbonylamino butyric acid to obtain esterification product of the acid with 2′,3′-isopropylidene cytidine. After removal of the BOC protective group by alcoholysis under acidic catalysis, cytidine γ-aminobutyrate hydrochloride is obtained. Finally, geldanamycin derivative with 17-cytidine moiety is produced by reacting cytidine γ-aminobutyrate hydrochloride with geldanamycin using the method similar to the aforementioned.

When the other side of R₁ is a niacinamido moiety, the preparation of the compound of Formula (I) structure is as follows: the nicotinoyl chloride produced by reacting nicotinic acid with acyl chlorination reagent (dichlorosulfoxide) is reacted with 2-(N-tert-butyloxycarbonyl)ethanediamine to obtain 2-(tert-butoxycarbonylamino) ethyl niacinamide. After removal of the protective group under acidic catalysis, (2-amino) ethyl niacinamide is obtained, which is finally reacted with geldanamycin to produce geldanamycin derivatives with 17-niacinamido moiety using the method similar to the aforementioned.

When the other side of R₁ is a phosphonate moiety, the preparation of the compound of Formula (I) structure is as follows: Phthalimide potassium salt is reacted with p-tolyl sulfonyloxoalkyl phosphonate diethyl ester in a polar aprotic solvent, to produce N-alkylphosphonate diethyl ester-phthalimide, which further reacts with hydrazine hydrate to produce aminoalkyl phosphonate diethyl ester. Finally, geldanamycin derivative with 17-phosphonate moiety is produced by reacting aminoalkyl phosphonate diethyl ester with geldanamycin using the method similar to the aforementioned.

All compounds comprised in this invention can be prepared according to aforementioned reaction route and method (Table 1).

Compounds having the structure of Formula (I) are tested for their anti-HBV, anti-HIV and anti-HSV activities. Based upon the mechanism of geldanamycin effect on Hsp90, geldanamycin has simultaneously anti-tumor activity.

This invention also provides the pharmaceutical compositions containing said compounds with therapeutically effective amount as the active components and one or more pharmacologically acceptable carriers.

The compounds and compositions provided by this invention can be used to prepare anti-virus and anti-tumor medicines.

Various formulations of the medicinal compositions provided by this invention can be prepared according to the conventional production methods in the realm of pharmacy, for example, mixing of an active ingredient with one or more kinds of carriers, and subsequently prepare the formulations needed.

The medicinal compositions prepared herein are preferably those containing 0.1%-99.5% weight ratio of the active ingredients, the most preferably weight ratio of the active ingredients are in the range of 0.5%-99.5%.

THE EFFECT OF THIS INVENTION

According to the aforementioned reaction routes and methods, a series of new derivatives of geldanamycin described herein can be obtained steadily and reproducibly. The result of tests on the biological activities and pharmacologies showed that the said derivatives has broad-spectrum anti-virus activities, especially showed relatively stronger inhibition effect against HIV-1 and HBV viruses. What is more, the compounds described herein also showed relatively strong inhibition activities against HSV. The structures of the said compounds and their activities measured are shown in Table 1.

TABLE 1
Structures and Anti-virus Activities of the Compounds in This Invention
						Activity of	Activity of
						HIV	HBV
No. of			Molecular			inhibition	inhibition
compound	characteristics	MW	formula	R1	R2	IC50, μg/ml	IC50, μg/ml
GM-APML	purple solid	658.78	C34H50N4O9		H	<0.01	0.064
GM-AEPD	purple solid	656.81	C35H52N4O8		H	<0.01	0.08
GM-ABPD	purple solid	718.88	C40H54N4O8		H	<0.03	0.32
GM-AMPP	purple solid	642.78	C34H50N4O8		H	0.06	8.0
GM-MTA	purple solid	681.86	C38H55N3O8		H	0.04	0.32
GM-GP	purple solid	695.74	C33H50N3O11P		H	1.36	3.24
GM-129	purple solid	653.77	C34H47N5O8		H	1.92	0.32
GM-208	purple solid	728.85	C36H48N4O10S		H	>0.82
GM-217	purple solid	679.76	C36H45N3O10		H	0.16
GM-221	purple solid	655.8	C34H45N3O8S		H	0.06
GM-223	purple solid	643.77	C34H49N3O9		H	0.10
GM-226	purple solid	670.79	C35H50N4O9		H	>0.14	1.6
GM-228	purple solid	656.81	C35H52N4O8		H	0.009	0/01
GM-206S	purple solid	656.81	C35H52N4O8		H	0.01	0.064
GM-210R	purple solid	656.81	C35H52N4O8		H	0.01	0.064
GM-413	purple solid	778.89	C41H54N4O11		H	0.48	0.32
GM-418	purple solid	693.79	C36H47N5O9		H	0.37	0.08
GM-CY	purple solid	856.92	C41H56N6O14		H	0.02	0.032
THFM(R)-GM	purple solid	629.74	C33H47N3O9		H	0.05	0.01
THFM(S)-GM	purple solid	629.74	C33H47N3O9		H	0.06	0.032
THFM-GM	purple solid	629.74	C33H47N3O9		H	0.14	0.01
THFM-GM2	purple solid	728.87	C38H56N4O10			0.24	0.064
THFM-II	purple solid	728.87	C38H56N4O10			>22.2	0.013
THFM + 2	purple solid	728.87	C38H56N4O10			0.18	0.10
GM-W1	purple solid	636.74	C34H44N4O8		H	36.7	0.69
GM-W2	purple solid	651.75	C34H45N5O8		H	19.6	8.0
GM-W3	purple solid	667.68	C31H46N3O11P		H	1.89	1.32
GM-W4	purple solid	654.71	C33H42N4O10		H	0.33	3.2
GM-W5	purple solid	653.74	C30H43N3O11S		H	10.26	6.4
GM-W6	purple solid	633.73	C32H47N3O10		H	1.47	1.32
GM-W7	purple solid	617.73	C32H47N3O9		H	9.89	8.0
GM-W8	purple solid	665.77	C36H47N3O9		H	1.22	1.32
GM-W9	purple solid	665.77	C36H47N3O9		H	2.46	3.2
GM-W10	purple solid	664.79	C36H48N4O8		H	40.71	6.4
GM-W11	purple solid	628.76	C33H48N4O8		H	3.87	8.0
GM-W12	purple solid	633.73	C32H47N3O10		H	0.46	3.2
GM-W13	purple solid	584.66	C30H40N4O8		H	0.65	0.64
GM-W14	purple solid	617.73	C32H47N3O9		H	3.91	0.32
GM-W15	purple solid	617.73	C32H47N3O9		H	1.47	0.01
GM-W16	purple solid	631.76	C33H49N3O9		H	0.43	0.064
GM-W17	purple solid	669.74	C30H43N3O12S		H	23.47	10.3
GM-W18	purple solid	650.76	C35H46N4O8		H	33.41	50.4
GM-W19	purple solid	636.74	C34H44N4O8		H	28.90	3.4
GM-W20	purple solid	636.74	C34H44N4O8		H	26.42	6.89
GM-W21	purple solid	661.78	C37H47N3O8		H	58.97	10.4
GM-W22	purple solid	642.78	C34H50N4O8		H	1.37	3.2
GM-W23	purple solid	642.78	C34H50N4O8		H	0.46	0.32
GM-W24	purple solid	601.69	C30H43N5O8		H	0.11	0.01
GM-W25	purple solid	633.73	C32H47N3O10		H	0.43	0.32
GM-W26	purple solid	632.74	C32H48N4O9		H	0.21	0.64
GM-W27	purple solid	746.93	C42H58N4O8		H	13.81	3.9
GM-W28	purple solid	645.74	C33H47N3O10		H	0.21	0.10
GM-W29	purple solid	631.71	C32H45N3O10		H	0.67	6.4
GM-W30	purple solid	706.87	C39H54N4O8		H	10.89	5.6
GM-W31	purple solid	631.76	C33H49N3O9		H	0.32	0.32
GM-W32	purple solid	650.76	C35H46N4O8		H	0.48	6.4
GM-W33	purple solid	658.78	C34H50N4O9		H	0.23	3.2
GM-W34	purple solid	658.78	C34H50N4O9		H	0.57	0.17
GM-W35	purple solid	643.77	C33H49N5O8		H	3.48	4.36
GM-W36	purple solid	665.77	C36H47N3O9		H	0.29	0.02
GM-W37	purple solid	628.76	C33H48N4O8		H	1.43	1.32
GM-W38	purple solid	705.84	C35H51N5O8		H	1.59	0.64
GM-W39	purple solid	603.7	C31H45N3O9		H	0.22	0.32
GM-W40	purple solid	603.7	C31H45N3O9		H	0.32	0.01
GM-W41	purple solid	603.7	C31H45N3O9		H	0.17	0.32
GM-W42	purple solid	589.68	C30H43N3O9		H	0.091	0.01
GM-W43	purple solid	690.82	C35H54N4O10		H	0.87	0.64
GM-W44	purple solid	711.84	C41H49N3O8		H	>60	>100
GM-W45	purple solid	692.84	C38H52N4O8		H	<1.67	0.32
GM-W46	purple solid	672.81	C35H52N4O9		H	1.32	1.49
GM-W47	purple solid	684.86	C37H56N4O8		H	1.84	3.87
GM-W48	purple solid	614.73	C32H46N4O8		H	3.79	0.64
GM-W49	purple solid	614.73	C32H46N4O8		H	5.41	3.2
GM-W50	purple solid	641.77	C33H43N3O8S		H	1.57	0.64
GM-W51	purple solid	657.8	C34H51N5O8		H	3.48	6.4
GM-W52	purple solid	642.78	C34H50N4O8		H	0.65	0.32
GM-W53	purple solid	641.71	C33H43N3O10		H	0.37	0.46
GM-W54	purple solid	777.9	C45H51N3O9		H	>60	>100
GM-W55	purple solid	707.85	C39H53N3O9		H	15.46	3.2
GM-W56	purple solid	615.71	C32H45N3O9		H	0.14	0.064
GM-W57	purple solid	651.75	C34H45N5O8		H	13.76	8.0
GM-W58	purple solid	631.76	C33H49N3O9		H	1.39	0.64
GM-W59	purple solid	741.87	C42H51N3O9		H	>60	32
GM-W60	purple solid	653.66	C30H44N3O11P		H	0.13	1.32
GM-W61	purple solid	639.63	C29H42N3O11P		H	0.42	0.64
GM-W62	purple solid	709.76	C34H52N3O11P		H	1.76	0.89
GM-W63	purple solid	647.76	C33H49N3O10		H	1.37	3.2
GM-W64	purple solid	673.8	C34H51N5O9		H	3.75	8.6
GM-W65	purple solid	657.79	C35H51N3O9		H	6.81	3.1
GM-W66	purple solid	657.79	C35H51N3O9		H	7.32	3.2
GM-W67	purple solid	657.79	C35H51N3O9		H	4.51	0.64
GM-W68	purple solid	630.73	C32H46N4O9		H	10.46	4.6
GM-W69	purple solid	698.89	C38H58N4O8		H	22.23	10.8
GM-W70	purple solid	679.8	C37H49N3O9		H	24.0	10.8
GM-W71	purple solid	693.83	C38H51N3O9		H	13.21	6.4
GM-W72	purple solid	628.76	C33H48N4O8		H	6.45	3.2
GM-W73	purple solid	619.7	C31H45N3O10		H	0.26	1.43
GM-W74	purple solid	619.7	C31H45N3O10		H	0.47	8.9
GM-W75	purple solid	672.81	C35H52N4O9		H	1.21	0.1
GM-W76	purple solid	656.81	C35H52N4O8		H	0.24	0.01
GM-W77	purple solid	612.67	C30H40N6O8		H	8.97	7.36
GM-W78	purple solid	687.82	C36H53N3O10		H	1.24	0.64
GM-W79	purple solid	801.96	C42H63N3O12		H	1.47	3.2
GM-W80	purple solid	700.82	C36H52N4O10		H	0.97	1.1
GM-W81	purple solid	734.66	C36H45Cl2N3O9		H	2.46	2.3
GM-W82	purple solid	697.81	C37H51N3O10		H	4.87	1.2
GM-W83	purple solid	654.71	C33H42N4O10		H,	3.56	3.2
GM-W84	purple solid	904.18	C52H77N3O10		H	1.24	0.8
GM-W85	purple solid	836.06	C47H69N3O10		H	0.78	0.01
GM-W86	purple solid	663.82	C33H49N3O9S		H	0.22	0.64
GM-W87	purple solid	679.8	C37H49N3O9		H	0.39	0.064
GM-W88	purple solid	639.74	C34H45N3O9		H	0.24	0.08
GM-W89	purple solid	702.84	C39H50N4O8		H	1.68	2.36
GM-W90	purple solid		C38H48N4O8		H	1.23	0.93

EXAMPLES

The technicians in this art are expected to understand this invention more comprehensively by the following examples, however, none of which are intended to limit the scope of the invention.

Example 1

Preparation of 17-(2′-(1″-oxa-4″-azacyclohexyl-1″-)ethylamino)-17-demethoxy geldanamycin (GM-APML)

50 mg geldanamycin (89.29 μmol) is added into 5 mL CHCl₃ and 0.5 ml methanol. The mixture is stirred until geldanamycin dissolved to result in an orange solution. 21 mg (164 μmol) 4-(2-aminoethyl)-1-oxa-4-azacyclohexane is subsequently added. After reacting at room temperature for 4 days, the solvent in resultant is evaporated to dryness to obtain dark purple solid. The solid residue is dissolved into 10 mL ethyl acetate and the resulted solution is washed successively with deionized water, saturated NaHCO₃ solution, 1 mol/LHCl solution and saturated NaCl solution. The organic phase is added with anhydrate Na₂SO₄ and is dried overnight. The Na₂SO₄ is then filtered out and the organic phase is concentrated under reduced pressure. The concentrated solution is then chromatographically separated using a silica gel column, 46.2 mg GM-APML is then obtained (yield 61.2%).

¹H-NMR (400 MHz, CDCl₃) δ(ppm): 0.9-1.0 (m, 6H, C10-CH3, C14-CH3), 1.28-1.38 (m, 2H, C13-H2), 1.5 (m, 1H, C14-H), 1.64 (m, 2H, C15-H2), 1.78 (s, 3H, C8-CH3), 2.03 (s, 3H, C2-CH3), 2.5 (br, 4H, C17-NH—CH2-CH2-N—), 2.6-2.7 (br, 4H, C17-N—CH2-CH2-O), 2.7-2.8 (m, 1H, C10-H), 3.23 (s, 3H, C12-OCH3), 3.36 (s, 3H, C6-OCH3), 3.44 (d, 1H, J=9.2 Hz, C12-H), 3.5 (br, 1H, C17-NH), 3.58 (d, 1H, J=9.2 Hz, C11-H), 3.64-3.8 (m, 4H, C17 O—(CH2-CH2)-N—), 4.31 (d, 1H, J=10.0 Hz, C6-H), 4.4 (br, 1H, C11-OH), 4.84 (br, 2H, —N H2), 5.19 (s, 1H, C7-H), 5.83 (t, 1H, J=10.4, C5-H) 5.86 (d, 1H, J=9.6, C9-H), 6.58 (t, 1H, J=11.2 Hz, C4-H), 6.96 (d, 1H, J=11.6 Hz, C3-H), 7.15 (br, 1H, C20-NH—CO), 9.19 (s, 1H, C19-H)

Example 2

Preparation of 17-(2′-(1″-azacyclohexyl-1″-)ethylamino)-17-demethoxy geldanamycin(GM-AEPD)

GM-AEPD can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is 2-(1′-azacyclohexyl)ethylamine.

1H-NMR (400 MHz, CDCl₃) δ(ppm): 0.82 (1H, m, C14-H), 0.94-1.0 (m, 6H, C10-CH3, C14-CH3), 1.24-1.3 (m, 4H, C13-H2, C15-H2), 1.4-1.5 (m, 2H, C17-N(CH2-CH2)₂CH2)), 1.6 (br, 4H, C17-N(CH2-CH2)₂CH2), 1.76 (br, 1H, C10-H), 1.78 (s, 3H, C8-CH3), 2.03 (s, 3H, C2-CH3), 2.3-2.4 (br, 4H, C17-N—(CH2-CH2)₂CH2), 2.6-2.8 (m, 4H, C17-NH—CH 2-CH2-N), 3.24 (s, 3H, C12-OCH3), 3.38 (s, 3H, C6-OCH3), 3.44 (d, 1H, J=9.2 Hz, C12-H), 3.58 (d, 1H, J=9.2 Hz, C11-H), 3.7 (br, 1H, C17-NH—), 4.31 (d, 1H, J=10.0 Hz, C6-H), 4.5 (br, 1H, C11-OH), 4.80 (br, 2H, —CO—NH2), 5.20 (s, 1H, C7-H), 5.83 (t, 1H, J=10.4, C5-H) 5.94 (d, 1H, J=9.6, C9-H), 6.59 (t, 1H, J=11.6 Hz, C4-H), 6.96 (d, 1H, J=11.6 Hz, C3-H), 7.22 (br, 1H, C20-NH—), 9.19 (s, 1H, C19-H)

Example 3

Preparation of 17-(4′-benzyl-4′-azacyclohexyl amino)-17-demethoxy geldanamycin(GM-ABPD)

GM-ABPD can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is 4′-benzyl-4′-azacyclohexyl amine.

¹H-NMR (400 MHz, CDCl₃) δ(ppm): 0.94-1.0 (dd, 6H, C10-CH3, C14-CH3), 1.5-1.6 (m, 4H, C17-NH—CH(CH2-CH2)₂N—), 1.64 (d, 2H, C15-H2), 1.7 (m, 2H, C13-H2), 1.8 (s, 3H, C8-CH3), 1.9 (s, 2H, C17-NH—CH—(CH2-CH2)₂—N—CH2-Ph), 2.03 (s, 3H, C2-CH3), 2.1-2.2 (m, 2H, C17-NH—CH—(CH2-CH2)₂—N—CH2-Ph), 2.7-2.8 (m, 3H, C14-CH, C17-NH—CH—(CH2-CH2)₂—N—CH2-Ph), 2.87 (br, 1H, C17-NH—CH(CH2-CH2)₂N—), 3.26 (s, 3H, C12-OCH3), 3.38 (s, 3H, C6-OCH3), 3.4 (d, 1H, J=9.2 Hz, C12-H), 3.58 (d, 1H, J=9.2 Hz, C11-H), 3.6 (s, 1H, C10-H), 3.9 (br, 1H, C17-NH—), 4.2 (br, 1H, C11-OH), 4.3 (d, 1H, J=10.0 Hz, C6-H), 4.78 (br, 2H, —CO—NH2), 5.17 (s, 1H, C7-H), 5.8-5.9 (m, 2H, C5-H, C9-H), 6.27 (br, 1H, C20-NH—CO), 6.5 (t, 1H, J=11.2 Hz, C4-H), 6.9 (d, 1H, J=11.6 Hz, C3-H), 7.34 (br, 5H, C17-Ph), 9.13 (s, 1H, C19-H)

Example 4

Preparation of 17-(tetrahydropiperazin-4′-yl-methylmino)-17-demethoxy geldanamycin(GM-AMPP)

GM-AMPP can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is tetrahydropiperazin-4′-yl-methylmine. ¹H-NMR (400 MHz, DMSO) δ(ppm): 0.6 (d, 3H, C10-CH3), 0.8 (m, 3H, C14-CH3), 0.82-1.08 (m, 5H, C17-N—(CH2-CH2)₂—CH—CH2-NH2), 1.24 (m, 2H, C13-H2), 1.5 (m, 1H, C14-H), 1.58 (s, 3H, C8-CH3), 1.60 (d, 2H, C15-H2), 1.8 (s, 3H, C2-CH3), 2.3 (br, 2H, C17-N—(CH2-CH2)₂—CH—CH2-NH2), 2.4-2.5 (br, 4H, C17-N—(CH2-CH2)₂—), 2.8 (m, 1H, C10-H), 3.18 (br, 6H, C6-OCH3, C12-OCH), 3.28 (d, 1H, J=8.8 Hz, C12-H), 3.38 (d, 1H, J=8.8 Hz, C11-H), 4.36 (t, 1H, C11-OH) 4.82 (d, 1H, J=6.8 Hz, C6-H), 4.82 (br, 2H, —NH2), 5.2 (s, 1H, C7-H), 5.22 (d, 1H, J=10.0, C9-H), 5.4 (t, 1H, J=10.4, C5-H), 6.4 (br, 2H, C17-CH2-NH2), 6.55 (t, 1H, J=11.2 Hz, C4-H), 6.99 (br, 1H, C20-NH—CO), 7.1 (s, 1H, C19-H), 7.12 (d, 1H, J=11.0 Hz, C3-H), 7.4, 7.7 (s,s, 2H, —CO—NH2)

Example 5

Preparation of 17-(myrtanylamino)-17-demethoxy geldanamycin (GM-MTA)

GM-MTA can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is myrtanylamine.

¹H-NMR (400 MHz, CDCl₃) δ(ppm): 0.87 (d, 3H, C14-CH3), 0.95 (d, 3H, C10-CH3), 1.02 (s, 3H, MTA-9′CH3), 1.24 (s, 3H, MTA-10′CH3), 1.5-1.6 (m, 3H, MTA-5′CH2,2′-CH), 1.72 (m, 1H, C14-CH), 1.80 (s, 3H, C8-CH3), 1.8-2.0 (m, 6H, MTA-3′CH2, 7′CH2, C15-CH2), 2.02 (s, 3H, C2-CH3), 2.32 (m, 1H, C17-6′CH), 2.42 (m, 2H, C13-CH2), 2.65 (d, 1H, C10-CH), 2.74 (m, 1H, C17-4′CH), 3.374 (s, 3H, C12-OCH3), 3.370 (s, 3H, C6-OCH3), 3.6-3.4 (m, 4H, C11-H, C12-H, C17-NH—CH2-), 4.3 (d, 2H, J=10 Hz, C6-H), 4.37 (br, 1H, C11-OH), 4.76 (br, 2H, C1-CO—NH2), 5.20 (s, 1H, C7-H), 5.857 (t, 1H, J=11.2 Hz, C5-H), 5.904 (d, 1H, J=10 Hz, C9-H), 6.38 (br, 1H, C20-NH—CO), 6.58 (t, 1H, J=11.4 Hz, C4-H), 6.97 (d, 1H, J=11.6 Hz, C3-H), 9.19 (s, 1H, C19-H)

Example 6

Preparation of 17-diethyloxy phosphoryl methylene amino-17-demethoxy geldanamycin (GM-AP)

1.1 g (3.4 mmol) p-benzylsulfonyl methylene phosphonate diethyl ester is dissolved into 15 ml DMF. 0.9 g (4.8 mmol) Phthalimide potassium salt is added into the resulted solution and mixed under stirring. The mixture is heated to make temperature gradually to 90° C. The material disappears after reacting for 2 h, then make the resultant return to room temperature. The solvent in the resultant is evaporated to dryness under reduced pressure. The residue is separated chromatographically using a silica gel column to obtain 500 mg yellow solid product aminomethylene phosphonate diethyl ester-phthalimide.

200 mg (0.7 mmol) of the product obtained from the previous procedure is dissolved in 15 ml ethanol, is added with 0.1 ml (2 mmol) hydrazine hydrate and is allowed to react for 4 h at room temperature. The resultant is evaporated to dryness under reduced pressure, then ethyl acetate is added into the residue, mixed and filtered out the solid. The filtrate is then separated using a silica gel column to obtain 80 mg of colorless oily product aminomethylene phosphonate diethyl ester.

The product aminomethylene phosphonate diethyl ester is subsequently reacted with geldanamycin to obtain the product GM-AP according to the procedure similar to that used in Example 1.

¹H-NMR (300 MHz, CDCl₃) δ(ppm): 0.94-1.04 (dd, 6H, C10-CH3, C14-CH3), 1.36 (dt, 6H, —PO(OCH2CH3)₂), 1.6-1.8 (br, 1H, C17-NH—CH2-), 1.8 (d, 6H, C8-CH3, C2-CH3), 2.03 (br, 3H, C13-H2, C14-H), 2.18 (s, C10-H—), 2.35 (m, 1H, C9-H), 2.7 (m, 2H, C15-CH2), 3.28 (s, 3H, C12-OCH3), 3.36 (s, 3H, C6-OCH3), 3.43 (d, 1H, J=9.2 Hz, C12-H), 3.58 (d, 1 H, J=9.2 Hz, C11-H), 3.9-4.0 (dd, 2H, C17-NH—CH2-P), 4.15-4.2 (five, 4H, —PO(OCH2C H3)₂), 4.3 (d, 1H, J=10.0 Hz, C6-H), 4.78 (br, 2H, —CO—NH2), 5.27 (s, 1H, C7-H), 5.8 (d, 1H, C5-H), 5.9 (d, 1H, C9-H), 6.3 (br, 1H, C20-NH—CO), 6.6 (t, 1H, J=11.2 Hz, C4-H), 6.9 (d, 1H, J=11.6 Hz, C3-H), 9.07 (s, 1H, C19-H)

Example 7

Preparation of 17-(3′-(1″-imidazolyl)propylamino)-17-demethoxy geldanamycin(ZJH061129)

ZJH061129 can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is N-(3-aminopropyl) imidazole. ZJH061129 can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is N-(3-aminopropyl) imidazole.

¹H-NMR (400M, CDCl₃) δ(ppm): 0.87 (d, 3H, J=6.5 Hz, CH₃); 0.99 (d, 3H, J=7.0 Hz, CH₃); 1.64-1.72 (m, 3H, CH, CH₂); 1.79 (s, 3H, CH₃); 2.02 (s, 3H, CH₃); 2.11-2.22 (m, 3H, imidazole NCHa, CH₂); 2.62-2.65 (m, 1H, OCH); 2.72-2.75 (m, 1H, CH); 3.27 (s, 3H, OCH₃); 3.35 (s, 3H, OCH₃); 3.42-3.43 (m, IH, OCH); 3.48-3.54 (m, 3H, imidazole NCHb, NCH₂); 4.04-4.14 (m, 2H, CH₂); 4.28-4.31 (m, 1H, OCH); 5.18 (s, 1H, OCH); 5.84-5.88 (m, 2H, 2×═CH); 6.19-6.21 (m, 1H, Ar—H); 6.55-6.60 (m, 1H, ═CH); 6.92-6.95 (m, 1H, ═CH); 7.11 (s, 1H, Ar—H); 7.51 (s, 1H, Ar—H); 9.12 (s, 1H, Ar—H).

MS(ESI): m/z=654 (M+1).

Example 8

Preparation of 17-(4″-aminosulfonyl)phenylethylamino-17-demethoxy geldanamycin(ZJH061208)

ZJH061208 can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is 4-aminoethyl benzenesulfonamide.

¹H-NMR (400 M, CDCl₃) δ(ppm): 0.94 (d, 3H, C₁₄—CH₃); 1.00 (d, 3H, C₁₀—CH₃); 1.24-1.31 (m, 2H, C₁₃—H₂); 1.79 (s, 3H, C₈—CH₃); 2.02 (s, 3H, C₂—CH₃); 2.31-2.37 (m, 1H, C₁₀—H); 2.66-2.69 (m, 1H, C₁₁—H); 2.72-2.75 (m, 1H, C₁₄—CH); 3.03-3.06 (m, 2H, C₂₄—CH₂); 3.27 (s, 3H, C₁₂—OCH₃); 3.36 (s, 3H, C₆—OCH₃); 3.43-3.58 (m, 2H, C₁₅—CH₂); 3.76-3.86 (m, 2H, C₂₅—CH₂); 4.11-4.13 (m, 1H, C₁₂—CH); 4.31 (d, 1H, C₆—CH); 5.19 (s, 1H, C₇—CH); 5.84-5.89 (m, 2H, C₅—CH, C₉—CH); 6.55-6.61 (m, 1H, C₄—CH); 6.95 (d, 1H, C₃—CH); 7.38 (d, 2H, C₂₇—CH, C₃₁—CH); 7.91 (d, 2H, C₂₈—CH, C₃₀—CH); 9.14 (s, 1H, C₁₉—CH).

MS(ESI):m/z=767.0 (M+K), 751.0 (M+Na).

Example 9

Preparation of 17-(3′,4′-(Methylenedioxy)benzylamino)-17-demethoxygeldanamycin(ZJH061217)

ZJH061217 can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is 3,4-(Methylenedioxy)benzylamine (piperonylamine).

¹H-NMR (400 M, CDCl₃) δ(ppm): 0.99-1.03 (m, 6H, 2CH₃); 1.80 (s, 3H, CH₃); 2.03 (s, 3H, CH₃); 2.41-2.47 (m, 1H); 2.68 (d, 1H); 2.73-2.77 (m, 1H); 2.88 (br, 1H); 2.95 (br, 1H); 3.27 (s, 3H, OCH₃); 3.37 (s, 3H, OCH₃); 3.44-3.60 (m, 2H, CH₂); 4.18 (br, 1H, OH); 4.31 (d, 1H, J=10 Hz); 4.48-4.68 (m, 2H, CH₂); 4.79 (br, 2H, NH₂); 5.19 (s, 1H); 5.84-5.93 (m, 2H, 2CH); 5.99 (d, 2H); 6.36 (br, 1H); 6.58 (t, 1H, J=11.5 Hz); 6.73-6.82 (m, 3H, 3CH); 6.96 (d, 1H, J=12 Hz); 7.30 (s, 1H); 8.02 (br, 1H); 9.16 (s, 1H).

MS(ESI):m/z=718.2 (M+K), 702.2 (M+Na), 679.2 (M⁺).

Example 10

Preparation of 17-(2′-thienylethylamino)-17-demethoxy geldanamycin (ZJH061221)

ZJH061221 can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is 2-aminoethyl thiophene.

¹H-NMR (400 M, CDCl₃) δ(ppm): 0.95-1.00 (m, 6H, 2CH₃); 1.79 (s, 3H, CH₃); 2.02 (s, 3H, CH₃); 2.35-2.41 (m, 1H); 2.68-2.76 (m, 2H, 2CH); 2.95 (s, 2H); 3.16-3.20 (t, 2H, CH₂); 3.26 (s, 3H, OCH₃); 3.36 (s, 3H, OCH₃); 3.43-3.58 (m, 2H, CH₂); 3.76-3.84 (m, 2H, CH₂); 4.30 (d, 1H, J=10 Hz); 4.84 (br, 2H, NH₂); 5.18 (s, 1H); 5.83-5.90 (m, 2H, 2CH); 6.36 (br, 1H, NH); 6.57 (t, 1H, J=11.5 Hz); 6.90-6.98 (m, 3H, 3CH); 7.21 (d, 1H, J=Hz); 7.61 (d, 1H, J=15.5 Hz); 8.01 (br, 1H, OH); 9.14 (s, 1H).

MS(ESI):m/z=678.2 (M+Na), 656.2 (M+H), 624.2 (M−33, −OCH₃).

Example 11

Preparation of 17-(trans-4′-hydroxyl cyclohexylamino)-17-demethoxy geldanamycin(ZJH061223)

ZJH061223 can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is trans-4-amino cyclohexanol.

¹H-NMR (400 M, CDCl₃) δ(ppm): 0.97-1.01 (m, 6H, 2CH₃); 1.38-1.57 (m, 2H, 2CH); 1.77 (m, 1H, CH); 1.80 (s, 5H, CH₃+2CH); 2.00 (m, 2H, 2CH); 2.03 (s, 3H, CH₃); 2.09-2.11 (d, 2H, 2CH); 2.16-2.22 (m, 1H); 2.72-2.77 (m, 2H, 2CH); 3.27 (s, 3H, OCH₃); 3.38 (s, 3H, OCH₃); 3.45-3.60 (m, 2H, CH₂); 3.72 (m, 2H, CH₂); 3.88 (m, 1H); 4.31 (d, 1H, J=10 Hz); 4.74 (br, 2H, NH₂); 5.19 (s, 1H); 5.84-5.92 (m, 2H, 2CH); 6.25 (br, 1H, NH); 6.58 (t, 1H, J=11.5 Hz); 6.94-7.00 (m, 1H); 7.28 (s, 1H); 9.17 (s, 1H).

MS(ESI):m/z=667.3 (M+Na), 644.3 (M⁺).

Example 12

Preparation of 17-(3′-(2″-pyrrolidonyl) propylamino)-17-demethoxy geldanamycin(ZJH061226)

ZJH061226 can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is N-(3′-aminopropyl)-2-pyrrolidone.

¹H-NMR (400 M, CDCl₃) δ(ppm): 0.98-1.00 (m, 6H, 2CH₃); 1.25 (s, 1H); 1.80 (s, 3H, CH₃); 1.83-1.88 (m, 2H, CH₂); 2.02 (s, 3H, CH₃); 2.07 (t, 2H, CH₂, J=Hz); 2.31-2.38 (m, 1H); 2.42 (t, 2H, CH₂, J=Hz); 2.66 (d, 1H); 2.72-2.76 (m, 1H); 3.26 (s, 3H, OCH₃); 3.36 (s, 3H, OCH₃); 3.37-3.46 (m, 5H, 2CH₂+CH); 3.54-3.58 (m, 3H, CH2+CH); 4.30 (d, 1H, J=Hz); 4.80 (br, 2H, NH₂); 5.18 (s, 1H); 5.83-5.92 (m, 2H, 2CH); 6.55-6.61 (t, 1H, J=Hz); 6.72 (br, 1H, NH); 6.95 (d, 1H, J=Hz); 7.24 (s, 1H); 7.26 (s, 1H); 9.15 (s, 1H);

Example 13

Preparation of 17-(2″-(N-ethyl pyrrolidinyl)-methylamino)-17-demethoxy geldanamycin(ZJH061228)

ZJH061228 can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is 2-aminomethyl-1-ethylpyrrole.

¹H-NMR (400 M, CDCl₃) δ(ppm): 0.96-1.01 (m, 3H, CH₃); 1.09-1.14 (s, 3H, CH₃); 1.54 (s, 3H, CH₃); 1.50-1.52 (m, 2H, CH₂); 1.70-1.82 (m, 2H, CH₂); 1.81 (s, 3H, CH3); 1.90-2.00 (m, 1H, CH); 2.03 (s, 3H, CH₃); 2.21-2.29 (m, 2H, CH₂); 2.35-2.46 (m, 1H, CH); 2.65-2.80 (m, 3H, NCH₂, NCH); 3.27 (s, 3H, OCH₃); 3.37 (s, 3H, OCH₃); 3.41-3.76 (m, 4H, 2×NCH₂); 4.32 (d, 1H, J=10 Hz, OCH); 4.51-4.20 (m, 1H, OCH); 4.20-4.35 (br); 5.19 (s, 1H, OCH); 5.83-5.94 (m, 2H, Ar—CH₂); 6.59 (t, 1H, J=11.2 Hz, ═CH); 6.96 (d, 1H, J=11.2 Hz, ═CH); 7.16-7.21 (m, 1H, ═CH); 7.26-7.32 (m, 1H, ═CH); 9.21-9.22 (s, s, 1H, Ar—H).

MS(ESI):m/z=657 (M+1).

Example 14

Preparation of 17-(2″S-2″-(N-ethylpyrrolidinyl)-methylamino)-17-demethoxy geldanamycin(ZJH071206S)

ZJH071206S can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is (S)-2-aminomethyl-1-ethylpyrrole.

¹H-NMR (400 M, CDCl₃) δ(ppm): 0.82-0.89 (m, 3H, CH₃); 0.95-1.00 (m, 3H, CH₃); 1.08-1.14 (m, 3H, CH₃); 1.25-1.30 (m, H,); 1.80 (s, 3H, CH₃); 2.02 (s, 3H, CH₃); 2.35-2.41 (m, 1H); 2.68-2.76 (m, 2H, 2CH); 2.95 (s, 2H); 3.16-3.20 (t, 2H, CH₂); 3.26 (s, 3H, OCH₃); 3.36 (s, 3H, OCH₃); 3.43-3.58 (m, 2H, CH₂); 3.76-3.84 (m, 2H, CH₂); 4.30 (d, 1H, J=10 Hz); 4.84 (br, 2H, NH₂); 5.18 (s, 1H); 5.83-5.90 (m, 2H, 2CH); 6.36 (br, 1H, NH); 6.57 (t, 1H, J=11.5 Hz); 6.90-6.98 (m, 3H, 3CH); 7.21 (d, 1H, J=Hz); 7.61 (d, 1H; J=15.5 Hz); 8.01 (br, 1H, OH); 9.14 (s, 1H).

MS (ESI):m/z=678.2 (M+Na), 656.2 (M+H), 624.2 (M-33, —OCH₃).

Example 15

Preparation of 17-(2″R-2″-(N-ethylpyrrolidinyl)-methylamino)-17-demethoxy geldanamycin(ZJH071210R)

ZJH071210R can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is (R)-2-aminomethyl-1-ethylpyrrole.

¹H-NMR (600 M, CDCl₃) δ(ppm): 0.83-0.89 (m, 6H, 2CH₃); 1.00 ( ) 1.80 (s, 3H, CH₃); 2.02 (s; 3H, CH₃); 2.35-2.41 (m, 1H); 2.68-2.76 (m, 2H, 2CH); 2.95 (s, 2H); 3.16-3.20 (t, 2H, CH₂); 3.26 (s, 3H, OCH₃); 3.36 (s, 3H, OCH₃); 3.43-3.58 (m, 2H, CH₂); 3.76-3.84 (m, 2H, CH₂); 4.30 (d, 1H, J=10 Hz); 4.84 (br, 2H, NH₂); 5.18 (s, 1H); 5.83-5.90 (m, 2H, 2CH); 6.36 (br, 1H, NH); 6.57 (t, 1H, J=11.5 Hz); 6.90-6.98 (m, 3H, 3CH); 7.21 (d, 1H, J=Hz); 7.61 (d, 1H, J=15.5 Hz); 8.01 (br, 1H, OH); 9.14 (s, 1H).

MS (ESI):m/z=678.2 (M+Na), 656.2 (M+H), 624.2 (M×33, ×OCH₃).

Example 16

Preparation of 17-(2′-(3″,4″-dimethylcaffeoyl amido)ethylamino)-17-demethoxy geldanamycin(ZJH070413)

1.8 g (0.01 mol) caffeic acid is added into 15 mL purified water and the resulted solution is adjusted to pH 13 using 30% NaOH to dissolve completely caffeic acid. 6 g dimethyl sulfate (0.05 mol) is added into the solution which is reacted at room temperature for 10 h with stirring and adjusting pH to higher than 10 at intervals, then adjusting pH to 3 using 2N HCl. After filtering the resultant, the solid is washed with water until the water filtered out reaches a pH of 6-7. The solid is dried to obtain 3,4-dimethyl caffeic acid.

5.25 g ethylenediamine is added into a 250 mL three necked flask, then 30 mL 1,4-dioxane is added and stirred. To the flask the solution of 2.45 g di-tert-butyl carbonate in 30 mL 1,4-dioxane is added dropwise at room temperature and under nitrogen protection. After reacting for 2 h, the resultant is evaporated to dryness under reduced pressure. 50 mL purified water is added into the residues under stirring and white solid precipitate can be seen. The precipitates are filtered and washed with water. The filtrate is extracted 3 times with 50 mL methylene chloride. The extractants are pooled and dried on anhydrous sodium sulfate, then filtered. The filtrate is evaporated to dryness to obtain colorless oily liquid. The product is separated chromatographically with a silica gel column to obtain mono-N-tert-butyloxycarbonylethylenediamine.

0.208 g (0.001 mol) 3,4-dimethyl caffeic acid is added into 3 mL dichlorosulfoxide and the mixture is reacted at 50° C. for 4 h. The resultant is evaporated into dryness under reduced pressure using an aspirator pump. 5 mL methylene dichloride is subsequently added to the residues and, the mixture is stirred. The solution of 0.160 g mono-N-tert-butyloxycarbonyldiamino ethane in 4 mL pyridine is added to the mixture and the resulted mixture is allowed to react for 3 h at room temperature. The resultant is filtered and the filtrate is washed successively with saturated NaHCO₃ solution and water. Then it is dried on anhydrous sodium sulfate and subsequently filtered. The filtrate is evaporated to dryness and separated chromatographically using a silica gel column to obtain (2-tert-butoxycarbonylamino)ethyl-3,4-dimethyl caffeoylamide.

2 mL methanol is added into 3-necked flask placed in an ice bath and 1 mL acetyl chloride is added dropwise into it. The mixture is subsequently stirred to react at room temperature for 30 min. The methanol solution of 0.263 g (0.75 mmol) (2-tert-butoxycarbonyl amino)ethyl-3,4-dimethyl caffeoylamide is added dropwise into the resultant and the resulted mixture is allowed to react completely at room temperature for 3 h, The resultant is filtered and washed with methanol. The filtrate is evaporated to dryness under reduced pressure and is added with petroleum ether to precipitate yellow solid. The latter is filtered out and washed successively with ethyl acetate and chloroform. The resulted solid is dried over heat to obtain (2-amino)ethyl-3,4-di-hydroxyl-methylated caffeoyl amide hydrochloride.

50 mg (89.29 μmol) geldanamycin is added into 5 mL CHCl₃ and 0.5 mL methanol and the mixture is stirred until the geldanamycin dissolved to form an orange solution. 75 mg (260 μmol) of the N-aminoethyl-3,4-dimethylated caffeoylamide hydrochloride produced with the previous procedure and 0.5 mL triethylamine are added into the solution. The mixture is allowed to react for 3 days at room temperature and the solvent in it is evaporated to dryness to obtain purple solid. The product is separated chromatographically using a silica gel column to obtain 55.2 mg 17-(2′-(3″,4″-dimethylated caffeoylamido) ethylamino)-17-de-methoxy geldanamycin (ZJH070413) (79.4%).

¹H-NMR (500 M, CDCl₃) δ(ppm): 0.98 (m, 6H, 2CH₃); 1.80 (s, 3H, CH₃); 2.02 (s, 3H, CH₃); 2.37-2.42 (m, 1H); 2.65 (d, 1H); 2.72-2.76 (m, 1H); 3.07-3.12 (m, 2H, CH₂); 3.26 (s, 3H, OCH₃); 3.35 (s, 3H, OCH₃); 3.57-3.58 (m, 2H, CH₂); 3.71-3.85 (m, 2H, CH₂); 3.90 (s, 6H, 2CH₃); 4.25 (br, 1H, OH); 4.30 (d, 1H, J=10 Hz); 4.80 (br, 1H, NH); 5.18 (s, 1H); 5.84-5.90 (m, 2H, 2CH); 6.15-6.17 (m, 1H); 6.30 (d, 1H, J=15.5 Hz); 6.57 (t, 1H, J=11.5 Hz); 6.83-6.84 (m, 1H); 6.86 (d, 1H, J=8 Hz); 6.94 (d, 1H, J=12 Hz); 7.02 (s, 1H); 7.08 (d, 1H, J=8 Hz); 7.24 (s, 1H); 7.61 (d, 1H, J=15.5 Hz); 9.13 (s, 1H); 12.00 (br, 4H, CONH).

Example 17

Preparation of 17-(2′-nicotinamidoethylamino)-17-demethoxy geldanamycin(ZJH070418)

Mono-N-tert-butoxycarbonyldiamino ethane can be prepared according to the procedure provided in Example 16.

1.85 g (0.015 mol) nicotinic acid is added into 5 mL methylene chloride under stirring and it is not dissolved. 4.4 mL (0.06 mol) dichlorosulfoxide is added into the mixture and the resulted mixture is allowed to react for 4 h at 50° C. under nitrogen protection and with refluxing in a oil bath. Then the oil bath is removed and the resultant is filtered. The solid residue is washed with methylene chloride to obtain nicotinoyl chloride as white acicular crystals.

2.4 g mono-N-tert-butoxycarbonyldiamino ethane (0.015 mol) is added into 2 ml methylene chloride and 2 mL tetrahydrofuran. With stirring, 5 mL triethylamine and the solid nicotinoyl chloride obtained in the previous procedure are successively added. The mixture is allowed to react completely at room temperature for 3 h. Then the resultant is filtered and subsequently washed with methylene chloride to obtain a viscous liquid. The product is separate chromatographically using a silica gel column to obtain (2-tert-butoxycarbonylamino)ethyl nicotinylamide.

4 ml anhydrous methanol is added into 3-necked flask placed in an ice bath, then 2 mL acetyl chloride is added dropwise. The mixture is allowed to react subsequently at room temperature for 30 min. 0.53 g (2 mmol) (2-tert-butoxycarbonylamino)ethyl nicotinylamide solution in methanol is added into the resultant and the resulted mixture is allowed to react completely at room temperature for 30 min. After filtering and washing the resultant with ethyl acetate, the white solid obtained is (2-amino) ethyl nicotinylamide.

50 mg geldanamycin (89.29 μmmol) is added into 5 mL CHCl₃ and 0.5 mL methanol, then geldanamycin is dissolved with stirring to make the orange reactive solution. 44 mg (2-amino)ethyl nicotinylamide (153 μmol) obtained from the previous procedure and 0.5 ml triethylaime is added into said reactive solution. The resulted mixture is allowed to react at room temperature for 2 days, then the resultant solution is evaporated to dryness to obtain purple solid. The product is separated is chromatographically using a silica gel column to obtain 58.3 mg (94.2%) of 17-(2′-nicotinylamioethylamino)-17-demethoxy geldanamycin (ZJH070418).

¹H-NMR (500 M, CDCl₃) δ(ppm): 0.98-0.99 (m, 6H, 2CH₃); 1.80 (s, 3H, CH₃); 2.02 (s, 3H, CH₃); 2.42-2.46 (m, 1H); 2.65 (d, 1H); 2.72-2.76 (m, 1H); 3.09-3.12 (m, 2H, CH₂); 3.27 (s, 3H, OCH₃); 3.35 (s, 3H, OCH₃); 3.42-3.57 (m, 2H, CH₂); 3.79-3.93 (m, 4H, 2CH₂); 4.30 (d, 1H, J=10 Hz); 4.80 (br, 2H, NH₂); 5.17 (s, 1H); 5.30 (br, 1H); 5.84-5.90 (m, 2H, 2CH); 6.57 (t, 1H, J=11.5 Hz); 6.93-6.95 (d, H, CH); 7.21 (s, 1H); 7.53 (s, 1H); 8.44 (d, 1H, J=15.5 Hz); 8.76 (s, 1H); 9.13 (s, 1H); 9.34 (s, 1H); 11.89 (br, 3H, 3NH).

Example 18

Preparation of 17-(4′-((5″-(4′″-amino-2′″-oxopyrimidine-1′″-(2H)-yl)-3″,4″-dihydroxyl-tetrahydrofuran-2″yl)methoxyl)-4′-oxobutylamino)-17-de methoxy geldanamycin(GM-CY)

The primary amino group of the γ-aminobutyric acid is protected with Boc₂O to obtain γ-tert-butoxycarbonylamino butyric acid according to the literature (Zhao Zhizhong et al. Protecting Groups in Organic Chemistry, Science Press, 1984: 41-49).

0.476 g p-toluenesulfonic acid (2.5 mmol) is added into 10 mL acetone. After dissolution of the solid, 1.5 mL 2,2-dimethoxy propane (12 mmol) and 0.486 g cytidine (2 mmol) are further added into the solution. The mixture is allowed to react with stirring at room temperature for 1.5 h. The reaction produce is large amount of white solid, which is filtered out and dried over heat to obtain 2′,3′-isopropylidenecytidine p-toluenesulfonate, which is reserved for further synthesis.

0.457 g γ-tert-butoxycarbonylaminobutyric acid (2.25 mmol) is added into 5 mL CHCl₃. After dissolving, 0.6 g dicyclohexylcarbodiimide (DCC) (2.91 mmol) is added into the solution with stirring at room temperature to appear white precipitates in the solution. After reacting for 4 h, the white precipitates are filter out and the collected filtrate containing γ-butoxycarbonylaminobutyric anhydride is reserved for further synthesis.

Isopropylidenecytidine p-toluenesulfonate is placed into a 100 mL round-bottom flask. 15 mL methylene chloride and 1 mL triethylamine are added into the flask, then the mixture is stirred until the solid dissolved. The filtrate from the previous synthesis is transferred into the flask. The resulted mixture is reacted under nitrogen protection for 30 h with stirring, then the insoluble materials are filtered out. The resultant filtrate is condensed under reduced pressure with a vacuum oil pump to obtain yellowish viscous liquid, which is separated chromatographically with a silica gel column to obtain esterification product of 2′,3′-isopropylidenecytidine with γ-butoxycarbonylaminobutyric acid.

4 ml anhydrous methanol is added into a three-necked flask, cooled in an ice bath and 2 mL acetyl chloride is added dropwise into the flask. The mixture is allowed to react for 30 min after completion of the dropping. Methanol solution of 50 mg to (0.107 mmol) the esterification product of 2′,3′-isopropylidenecytidine with γ-butoxycarbonylaminobutyric acid is added into the flask and is allowed to react completely for 30 min at room temperature. The resultant is filtered and the solid is washed with ethyl acetate to obtain white solid cytidine γ-amino butyrate hydrochloride.

50 mg geldanamycin (89.29 μmmol) is added into 5 mL CHCl₃ and methanol 0.5 ml, then the mixture is stirred until geldanamycin dissolved and the color of the liquid turns orange. 80.2 mg cytidine γ-amino butyrate hydrochloride (200 μmol) is added into the orange liquid and the resulted mixture is allowed to react for 3 days at room temperature. The solvent in resultant is evaporated to dryness to obtain dark purple solid. The solid residue is dissolved into 10 mL ethyl acetate and is washed successively with deionized water, saturated NaHCO₃ solution, 1 mol/L HCl solution and saturated NaCl solution. The organic phase is dried overnight on anhydrous Na₂SO₄. Then the anhydrous Na₂SO₄ is filtered out and the organic phase is concentrated under reduced pressure. The product is separated chromatographically using a silica gel column to obtain 17-(4′-((5″-(4′″-amino-2′″-oxopyrimidine-1′″-(2H)-yl)-3″,4″-dihydroxyl-tetrahydrofuran-2″-yl)methoxy)-4′-oxobutylamino)-17-demethoxy geldanamycin.

¹H-NMR (400 M, CDCl₃) δ(ppm): 0.94-1.00 (m, 6H, 2CH₃); 1.24-1.30 (m, 2H, CH₂); 1.64-1.67 (m, 2H, CH₂); 1.80 (s, 3H, CH₃); 2.02 (s, 3H, CH₃); 2.38 (t, 2H, CH₂); 2.41-2.47 (m, 1H); 2.66-2.75 (m, 1H); 2.72-2.76 (m, 1H); 2.98 (t, 2H, CH₂); 3.27 (s, 3H, OCH₃); 3.37 (s, 3H, OCH₃); 3.42-3.59 (m, 3H, CH+CH₂); 3.62-3.66 (m, 1H); 3.78-3.81 (m, 1H); 3.89-3.94 (m, 2H, CH₂); 4.08-4.11 (m, 1H); 4.31 (d, 1H); 4.81 (br, 2H, NH₂); 4.95 (br, 1H, OH); 5.19 (s, 1H); 5.26 (br, 1H, OH); 5.69 (d, 1H); 5.75 (d, 1H); 5.84-5.90 (m, 2H, 2CH); 6.55-6.61 (m, 1H); 6.93-6.95 (d, 1H); 7.11 (br, 2H, NH₂); 7.28 (s, 1H); 7.82 (d, 1H); 9.14 (br, 1H, NH).

MS(ESI):m/z=857.3 (M⁺), 880.3 (M+Na).

Example 19

Preparation of 2′R-17-tetrahydrofurfurylamino-17-demethoxy geldanamycin(THFM(R)-GM)

THFM(R)-GM can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is (R)-tetrahydrofurfurylamine.

¹H-NMR (400 M, CDCl₃) δ(ppm): 0.9-1.0 (m, 6H, 2CH₃); 1.25 (s, 2H, CH₂); 1.4-1.5 (m, 1H); 1.61-1.65 (m, 2H, CH₂); 1.70-1.74 (m, 2H, CH₂); 1.799 (s, 3H, CH₃); 1.93-1.98 (m, 2H, CH₂); 2.025 (s, 3H, CH₃); 2.36-2.39 (m, 1H); 2.66-2.75 (m, 2H, CH₂); 3.268 (s, 3H, OCH₃); 3.362 (s, 3H, OCH₃); 3.42-3.49 (m, 1H); 3.56-3.62 (m, 1H); 3.79-3.95 (m, 2H, CH₂); 4.08-4.11 (m, 1H); 4.311 (d, 1H); 4.806 (br, 2H, NH₂); 5.190 (s, 1H); 5.857 (t, 1H); 5.904 (d, 1H); 6.583 (t, 1H); 6.955 (d, 1H); 7.276 (s, 1H); 9.167 (br, 1H, NH).

MS(FAB):m/z=631 (M+1).

Example 20

Preparation of 2′S-17-tetrahydrofurfurylamino-17-demethoxy geldanamycin (THFM(S)-GM)

THFM(S)-GM can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is (S)-tetrahydrofurfurylamine.

The retention time of THFM(S)-GM differs minutely from THFM(R)-GM in the HPLC grams, the ¹H-NMR spectra of both compounds are essentially same.

¹H-NMR (400 M, CDCl₃) δ(ppm): 0.94-1.00 (m, 6H, 2CH₃); 1.25 (s, 2H, CH₂); 1.30-1.32 (m, 1H); 1.61-1.64 (m, 2H, CH₂); 1.73-1.75 (m, 2H, CH₂); 1.80 (s, 3H, CH₃); 1.93-2.00 (m, 2H, CH₂); 2.03 (s, 3H, CH₃); 2.31-2.37 (m, 1H); 2.67-2.75 (m, 2H, CH₂); 3.27 (s, 3H, OCH₃); 3.36 (s, 3H, OCH₃); 3.43-3.49 (m, 1H); 3.58-3.62 (m, 1H); 3.79-3.96 (m, 2H, CH₂); 4.08-4.11 (m, 1H); 4.31 (d, 1H); 4.81 (br, 2H, NH₂); 5.19 (s, 1H); 5.86 (t, 1H); 5.91 (d, 1H); 6.55-6.60 (m, 1H); 6.95 (d, 1H); 7.28 (s, 1H); 9.14 (br, 1H, NH).

MS (FAB):m/z=631 (M+1).

Example 21

Preparation of 17-tetrahydrofurfurylamino-17-demethoxy geldanamycin (THFM-GM)

THFM-GM can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is tetrahydrofurfurylamine.

¹H-NMR (400 M, CDCl₃) δ(ppm): 0.90-1.01 (m, 6H, C₁₀—CH₃, C₁₄—CH₃); 1.25 (s, 2H, C₁₃—H₂); 1.4-1.5 (m, 1H, C₁₄—H); 1.61-1.65 (m, 2H, THMF-CH₂—CH₂—CH₂—); 1.70-1.74 (m, 2H, C₁₅—H₂); 1.79 (s, 3H, C₈—CH₃); 1.93-1.98 (m, 2H, THMF-CH₂—CH₂—CH—); 2.02 (s, 3H, C₂—CH₃); 2.36-2.39 (m, 1H, C₁₀—H); 2.66-2.75 (m, 2H, C₁₇—NH—CH₂—); 3.26 (s, 3H, C₁₂—OCH₃); 3.36 (s, 3H, C₆—OCH₃); 3.42-3.49 (m, 1H, C₁₂—H); 3.56-3.62 (m, 1H, C₁₁—H); 3.79-3.95 (m, 2H, THMF-CH₂—CH—O); 4.08-4.11 (m, 1H, C₁₇—NH—CH₂—CH—); 4.31 (d, J=10 Hz, 1H, C₆—H);

4.80 (br, OH, NH); 5.19 (s, 1H, C₇—H); 5.85 (t, J=11.2 Hz, 1H, C₅—H); 5.90 (d, J=10 Hz, 1H, C₉—H); 6.58 (t, J=11.4 Hz, 1H, C₄—H); 6.95 (d, J=11.6 Hz, 1H, C₃—H); 7.27 (s, 1H, C₁₉—H); 9.16 (s, 1H, CH). MS(FAB):m/z=654 (M+Na).

Example 22

Preparation of 17,19-di-(R)-tetrahydrofurfuryl amino-17-demethoxy geldanamycin(THFM-II)

THFM-II can be obtained according to the procedure similar to that used in Example 1 when the side chain reactant is (R)-tetrahydrofurfurylamine. In this case the amount of the side chain compound fed is increased five fold and the reaction time elongated to 10 h.

¹H-NMR (400 M, CD₃COD) δ(ppm): 0.73 (d, 3H, J=6.4 Hz, CH₃); 1.02 (d, 3H, J=6.8 Hz, CH₃); 1.46-1.65 (m, 2H, CH₂); 1.60 (s, 3H, CH₃); 1.81-2.04 (m, 5H, CH, 2CH₂); 1.91 (s, 3H, CH₃); 2.28-2.46 (m, 2H, CH₂); 2.56-2.66 (m, 2H, CH₂); 3.08-3.17 (m, 1H, CH); 3.23 (s, 3H, OCH₃); 3.29 (s, 3H, OCH₃); 3.44-3.88 (m, 11H, 3OCH, 2OCH₂, 2NCH₂); 4.00-4.09 (m, 2H, CH₂); 4.34-4.38 (dd, 1H, J₁=10 Hz, J₂=7.0 Hz, OCH); 4.88 (d, 1H, J=4.8 Hz, OCH); 5.27 (s, 1H, OCH); 5.29 (d, 1H, J=10 Hz, ═CH); 5.49 (t, 1H, J=10 Hz, ═CH); 6.57 (t, 1H, J=12 Hz, ═CH); 7.27 (d, 1H, J=12 Hz, ═CH).

MS(+Q1):m/z=753 (M⁺+Na), 731 (M⁺+1).

Example 23

Preparation of 17,19-di-(S)-tetrahydrofurfuryl amino-17-demethoxy geldanamycin (THFM+2)

The product THFM+2 can be synthesized according to the procedure similar to that used in Example 1 when the side chain reactant is (S)-tetrahydrofurfurylamine. In this case the amount of the side chain compound fed is increased five fold and the reaction time elongated to 10 h.

¹H-NMR (400 M, CD₃COD) δ(ppm): 0.73 (d, 3H, J=6.4 Hz, CH₃); 0.92 (d, 3H, CH₃); 1.45-1.59 (m, 2H, CH₂); 1.60 (s, 3H, CH₃); 1.83-2.02 (m, 5H, CH, 2CH₂); 1.90 (s, 3H, CH₃); 2.29-2.46 (m, 2H, CH₂); 2.56-2.65 (m, 2H, CH₂); 3.07-3.12 (m, 1H, CH); 3.24 (s, 3H, OCH₃); 3.29 (s, 3H, OCH₃); 3.47-3.85 (m, 11H, 3OCH, 2OCH₂, 2NCH₂); 4.00-4.08 (m, 2H, CH₂); 4.34-4.38 (dd, 1H, J₁=10 Hz, J₂=7.0 Hz, OCH); 4.88 (d, 1H, J=4.8 Hz, OCH); 5.26 (s, 1H, OCH); 5.29 (d, 1H, J=10 Hz, ═CH); 5.47 (t, 1H, J=10 Hz, ═CH); 6.58 (t, 1H, J=12 Hz, ═CH); 7.24 (d, 1H, J=12 Hz, ═CH).

MS(+Q1):m/z=753 (M+Na), 731 (M+1).

Example 24

Test Procedure for Herpes Simplex Virus Activity (VR733 Strain)

0.1 ml 0.25% trypsin solution and 5 ml 0.02% EDTA solution are added into a culture flask confluent with VERO cells. The culture is digested 20-25 min at 37° C. and the digestion liquid is discarded. Then the cells are dispersed with adding culture medium and passage at a ratio of 1:3. The cells reach confluence after 3 days of culture. The culture is prepared into a concentration of 200,000-300,000 cells/mL and is inoculated into 96 well culture plate in 0.1 ml each well. The cells are cultured at 37° C. under 5% CO₂ condition for 24 h. Tests are carried out when the cells grow into a mono layer.

Cell culture with a concentration of 200,000-300,000 VERO cells/mL is inoculated into 96 well culture plate in 0.1 ml each well. The cells are cultured at 37° C. and under 5% CO₂ condition for 24 h, then the culture medium is discarded. Appropriate amount of HSV-1 is added into the culture plate and the virus is allowed to absorb for 1 h, then the virus liquid is discarded. The reagents to be tested (i.e target compounds of this invention) are added into the culture plate, wherein a series of concentrations of the reagent to be tested is added into culture plate in 2 wells per one concentration. The cells are cultured at 37° C. in 5% CO₂ and the pathological changes of the cells are observed after culturing for 48 h. It is calculated that the median effective concentration of the test reagent to inhibit ½ virus according to the following equation:

${\mathrm{IC}}_{50}=\mathrm{Anti}\log \left(A+\frac{50-A}{B-A}\times C\right)$ $A=\log \left(\mathrm{pathological}\mathrm{changes}<50\%\mathrm{concentration}\mathrm{of}\mathrm{the}\mathrm{reagent}\right)$ $B=\log \left(\mathrm{pathological}\mathrm{changes}>50\%\mathrm{concentration}\mathrm{of}\mathrm{the}\mathrm{reagent}\right)$ $C=\log \left(\mathrm{dilution}\mathrm{factor}\right)$

The calculated IC₅₀ values according to the test results are shown in Table 1.

Example 26

Test Procedure for Anti-HBV Activity

Using cell culture method, the preparation of the cells to be tested (100,000 cell's/mL) is inoculated into cell culture plate in 100 μl each well and the cells are cultured 24 h at 37° C. in 5% CO₂. Tests are carried out when the cells grow into a monolayer. The target compounds as well as the controls are prepared into a series of solutions of appropriate concentrations using the culture medium and are added into 96 well culture plate respectively in 4 wells per one concentration. Then the reagent solution in each well is changed into the fresh reagent solution with the same concentration every 4 days. A cell control without reagent treatment is simultaneously is set up. The observation index is based upon the pathological changes of the cells by observing the degrees of the pathological changes of the cells under microscope every 8 days. The test procedure for testing the inhibition of HBV activity of the drug is as follows: the tested cells at a concentration of 100,000/mL are inoculated into 96 well culture plate, in 100 μl each well and are cultured at 37° C. in 5% CO₂ for 24 h, then the reagent solutions are added into the well. Cell control without drug treatment is simultaneously is set up. The reagent solution or control medium in each well is changed into the fresh reagent solution or fresh medium respectively every 4 days. After cytolysis of the cells, HBV DNA is extracted from the cell lysis solution according to the molecular cloning technical procedure. The spots of different samples are hybridized and the A values of different hybridized spots are measured using autoradiograghic technique. The HBV DNA contents in the cell control as well as in the drug treated samples are calculated using the regression equations obtained from the standard curves to obtain half effective concentration values, the results are shown in Table 1.

Example 27

Test Procedure of Anti HIV-1 Activity

8 reagent solutions of different diluted concentrations and positive control solutions are added into cell cultures in 96 well plate respectively. The sample of each diluted solutions is made duplicately and a control cell sample is also is set up. 100 μl of cell sample at a concentration of 2×10⁵cells/ml is inoculated into the wells containing reagent in the plate. The cells samples are cultured in a saturated humidity culture chamber (at a 5% CO₂ atmosphere) at 37° C. The pathological changes of cells are observed daily. The contents of HIV-1 P24 antigen in the cell cultures are measured at 4 days after addition of the reagents according to the procedure provided by the HIV-1 P24 antigen test kit, the half effective concentrations (IC₅₀) of the reagents are calculated, the results are shown in Table 1.

Claims

1. A series of geldanamycin derivatives whose structure is shown in Formula (I):

2. A method for preparing the geldanamycin derivatives defined in claim 1, wherein the amine containing R1 substituent is allowed to react with geldanamycin in a haloalkane, alcoholic or polar aprotic solvent and under alkaline condition to obtain 17-mono-substituted compound (Formula I, wherein X—R2 is H); then the resulting 17-mono-substituted compound is allowed to react with R2XH under similar conditions to obtain 17,19-disubstituted compounds (Formula I, both R1 and X—R2 are not H).

3. The method of claim 2, wherein said solvent is selected from a group consisting of N,N-dimethylformamide, dimethylsulfoxide, ethyl acetate, acetonitrile and acetone.

4. The method of claim 2, wherein the alkaline condition is realized by using triethylamine, pyridine, N,N-dimethylpridine, potassium carbonate, sodium carbonate or calcium hydroxide.

5. A method for preparing the geldanamycin derivatives defined in claim 1, wherein, when R1 is a substituent containing a structure of 3,4-di-hydroxyl-methylated caffeic acid, the method is as follows, caffeic acid is firstly reacted with methylating reagent under alkaline condition to obtain 3,4-di-hydroxyl-methylated caffeic acid, which reacts subsequently with acyl chlorinating reagent to obtain the corresponding acyl chloride, which further reacts with mono N-tert-butoxycarbonylethyldiamine to obtain (2-tert-butoxycarbonylamino)ethyl-3,4-di-hydroxyl-methylated caffeoylmide, after removal of tert-butyl protecting group to obtain (2-amino)ethyl-3,4-di-hydroxyl-methylated caffeoylamide, which further reacts with geldanamycin according to the method of claim 2 to obtain geldanamycin derivative containing di-hydroxyl-methylated caffeoylamido structure linked to the 17-site.

6. The method of claim 5, wherein the methylating reagent is selected from a group consisting of dimethyl sulfate, methyl methanesulfonate, methyl iodide and dimethyl carbonate.

7. A method for preparing the geldanamycin derivatives defined in claim 1, wherein, when R1 is a substituent containing a structure of cytidine, the method is as follows, cytidine reacts with 2,2-dimethoxylpropane under acidic condition to obtain 2′,3′-isopropylidene cytidine, which condensates with γ-tert-Butoxycarbonylamino butyric acid under the effect of dehydrating reagent DCC or TBU to obtain esterification product of said acid with 2′,3′-isopropylidene cytidine, from which removes the BOC protective group by alcoholysis under acidic catalysis to obtain cytidine γ-aminobutyrate hydrochloride, which reacts with geldanamycin according to the method of claim 2 to obtain geldanamycin derivative containing cytidine structure linked to the 17-site.

8. A method for preparing the geldanamycin derivatives defined in claim 1, wherein, when R1 is a substituent containing a structure of niacinamide structure, the method is as follows, nicotinic acid reacts with acyl chlorinating reagent dichlorosulfoxide to obtain nicotinoyl chloride, which reacts with 2-(N-tert-butyloxycarbonyl)ethanediamine to obtain 2-(tert-butoxycarbonylamino) ethyl niacinamide, from which the BOC protective group is removed by alcoholysis under acidic catalysis to obtain (2-amino)ethyl nicotinoylamide, which reacts finally with geldanamycin according to the method of claim 2 to obtain geldanamycin derivative containing nicotinoylamide structure linked to the 17-site.

9. A method for preparing the geldanamycin derivatives defined in claim 1, wherein, when R1 is a substituent containing a phosphonate group, the method is as follows, p-tolyl sulfonyloxoalkyl phosphonate diethyl ester reacts with phthalimide potassium salt in a polar aprotic solvent to produce N-alkylphosphonate diethyl ester-phthalimide, which reacts with hydrazine hydrate to produce aminoalkyl phosphonate diethyl ester, which reacts with geldanamycin according to the method of claim 2 to obtain geldanamycin derivative containing a phosphonate group linked to the 17-site.

10. The pharmaceutical compositions of the compounds shown in Formula (I) of claim 1, wherein said compositions consists of said compounds with therapeutically effective amount as the active components and one or more pharmacologically acceptable carriers.

11. The use of the compounds defined in claim 1 for preparing anti-virus and anti-tumor medicines.

12. The use of the compositions defined in claim 10 for preparing anti-virus and anti-tumor medicines.