TREA

Anthelmintic composition and the use thereof

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Information

  • Patent Grant
  • 4468390
  • Patent Number
    4,468,390
  • Date Filed
    Monday, February 22, 1982
    43 years ago
  • Date Issued
    Tuesday, August 28, 1984
    40 years ago
Information
Abstract
The combined administration of:(a) one or more macrolide anthelmintic agents selected from the group consisting of B-41 series antibiotics, C-076 series antibiotics and 22,23-dihydro C-076 derivatives; and(b) one or more anthelmintic agents selected from the group consisting of benzimidazole, salicylamide and isoquinoline compounds,has been bound to exhibit enhanced anthelmintic activity as compared with the additive use of the individual compounds.
Description

BACKGROUND TO THE INVENTION
The present invention relates to an anthelmintic composition comprising a mixture of a macrolide antibiotic selected from those of the B-41, C-076 and 22,23-dihydro C-076 series (all of which are known to have anthelmintic activity) with certain other known anthelmintic agents, whereby the anthelmintic activity of the composition is synergistically enhanced.
The compounds referred to herein as "B-41 series antibiotics," "C-076 series antibiotics" and "22,23-dihydro C-076 series antibiotics" are a group of macrolide antibiotics which, despite their different nomenclatures (arising from their different methods of production by various microorganisms), have very closely related molecular structures and activities.
The B-41 series antibiotics were originally isolated from a culture broth of Streptomyces B-41-146 strain (deposited with the Fermentation Research Institute, Agency of Industrial Science and Technology, Ministry of International Trade and Industry, Japan, whence it is available under the Accession No. 1438).
Since the original discovery of the B-41 series compounds, described in British patent specification No. 1,390,336, wherein nine compounds were characterized, a number of other compounds from the same series have been isolated from a culture broth of the same microorganism. As disclosed in this British patent specification, these compounds may be prepared by cultivating a microorganism of the genus Streptomyces, preferably Streptomyces B-41-146 strain, in a suitable culture medium for a period of from 5 to 10 days at about 28.degree. C. under aerobic conditions, after which the culture broth is filtered through diatomaceous earth, the cake obtained is extracted with methanol and then with hexane to given an oily substance and finally the substance is fractionated by column chromatography through silica gel.
The B-41 series compounds thus include compounds having the following formulae (I) or (II), in which the groups represented by R.sup.1 -R.sup.6 are as defined in Tables 1 and 2. ##STR1##
TABLE 1______________________________________B-41 R.sup.1 R.sup.2 R.sup.3 R.sup.4 R.sup.5______________________________________.alpha..sub.1 (A.sub.3) H H CH.sub.3 CH.sub.3 OH.alpha..sub.2 (B.sub.2) H H CH.sub.3 CH.sub.3 OCH.sub.3.alpha..sub.3 (A.sub.4) H H C.sub.2 H.sub.5 CH.sub.3 OH.alpha..sub.4 (B.sub.3) H H C.sub.2 H.sub.5 CH.sub.3 OCH.sub.3 (D) H H i-C.sub.3 H.sub.7 CH.sub.3 OH (G) H H i-C.sub.3 H.sub.7 CH.sub.3 OCH.sub.3.alpha..sub.5 (A.sub.2) OH MH CH.sub.3 CH.sub.3 OH.alpha..sub.6 (B.sub.1) OH MH CH.sub.3 CH.sub.3 OCH.sub.3.alpha..sub.7 OH MH C.sub.2 H.sub.5 CH.sub.3 OH.alpha..sub.8 OH MH C.sub.2 H.sub.5 CH.sub.3 OCH.sub.3.alpha..sub.9 (C.sub.1) H H CH.sub.3 PC OH.alpha..sub.10 (C.sub.2) H H C.sub.2 H.sub.5 PC OH (F) H H i-C.sub.3 H.sub.7 PC OH______________________________________
In this Table, the following abbreviations are used:
iC.sub.3 H.sub.7 --means an isopropyl group;
MH--means a 2-methylhexanoyloxy group of formula ##STR2## and PC--means a 2-pyrrolylcarbonyloxymethyl group of formula ##STR3##
TABLE 2______________________________________B-41 R.sup.3 R.sup.6______________________________________.beta..sub.1 (A.sub.1) CH.sub.3 CH.sub.2 OH.beta..sub.2 (A.sub.5) C.sub.2 H.sub.5 CH.sub.2 OH (E) i-C.sub.3 H.sub.7 CH.sub.2 OH______________________________________
Of the compounds shown above, those identified as A.sub.1, A.sub.2, A.sub.3, A.sub.4, A.sub.5, B.sub.1, B.sub.2, B.sub.3, C.sub.1 and C.sub.2 are described in British patent specification No. 1,390,336. Those compounds identified by .alpha. or .beta. are described in The Journal of Antibiotics, 29(3), 76-14 to 76-16 and 29(6), 76-35 to 76-42 and the use of these compounds as anthelmintic agents is described in European Patent Publication No. 2916. Compound B-41D is described in British patent specification No. 2,056,986.
Compounds B-41E and B-41F are described in Japanese Patent Application No. 153,141/80 and Compound B-41G is described in Japanese patent application No. 7091/81.
All of these compounds were obtained from a culture broth of the microorganism Streptomyces strain B-41-146 in the form of an amorphous powder. The properties of Compounds B-41E, B-41F and B-41G are given below.
Compound B-41D
Molecular Weight: 556
Ultraviolet Absorption Spectrum: 237 m.mu., 243 m.mu..
Infrared Absorption Spectrum: 3450, 1710 cm.sup.-1.
Nuclear Magnetic Resonance Spectrum .delta.ppm:
1.52 (singlet, 14--CH.sub.3);
1.86 (broad singlet, 4--CH.sub.3);
3.94 (doublet, J=6.2 Hz, 6--H);
4.63 (singlet, 26--CH.sub.2);
4.91 (broad triplet, J=8 Hz).
Thin layer chromatography, R.sub.f value: 0.4.
Compound B-41E
Molecular Weight: 572
Ultraviolet Absorption Spectrum: 241 m.mu..
Infrared Absorption Spectrum: 3475, 1710 cm.sup.-1.
Nuclear Magnetic Resonance Spectrum .delta.ppm:
1.59 (singlet, 14--CH.sub.3);
1.81 (broad singlet, 4--CH.sub.3);
3.06 (singlet, 5--OCH.sub.3);
4.12 (doubled doublet, J=4.5 and 12 Hz, 26--CH.sub.2);
4.30 (doubled doublet, J=6 and 12 Hz, 26--CH.sub.2);
4.87 (broad triplet, J=7 Hz, 15--CH.dbd.);
6.23 (doubled doublet, J=11 and 12 Hz, 10--CH.dbd.);
6.43 (doublet, J=11 Hz, 9--CH.dbd.).
Thin layer chromatography, R.sub.f value: 0.61
Compound B-41F
Molecular Weight: 665
Ultraviolet Absorption Spectrum: 245 m.mu., 253 m.mu..
Infrared Absorption Spectrum: 3320, 1730, 1710 cm.sup.-1.
Nuclear Magnetic Resonance Spectrum .delta.ppm:
1.48 (singlet, 4--CH.sub.3);
3.91 (doublet, J=6 Hz, 6--H);
4.60 (singlet, 26--CH.sub.2);
6.1-6.3 (1H, multiplet);
6.8-7.0 (2H, multiplet).
Thin layer chromatography, R.sub.f value: 0.27.
Compound B-41G
Molecular Weight: 570
Ultraviolet Absorption Spectrum: 237 m.mu., 244 m.mu..
Infrared Absorption Spectrum: 3475, 1715 cm.sup.-1.
Nuclear Magnetic Resonance Spectrum .delta.ppm:
1.50 (singlet, 14--CH.sub.3);
1.79 (broad singlet, 4--CH.sub.3);
3.44 (singlet, 5--OCH.sub.3);
4.59 (singlet, 26--CH.sub.2);
4.89 (broad triplet, J=8 Hz, 15--H).
Thin layer chromatography, R.sub.f value: 0.86.
In the above, the infrared absorption spectra were measured in a Nujol-trade mark-mull, the nuclear magnetic resonance spectrum was measured in CDCl.sub.3 at a frequency of 100 MHz and the thin layer chromatography was measured on Kieselgel 60 F.sub.254, using a 18:42 by volume mixture of dioxan and carbon tetrachloride as the developing solvent.
The C-076 series compounds may be obtained from a C-076 producing strain of Streptomyces avermitilis (such as that deposited under the Accession No. NRRL8165 at the Agricultural Research Service, Northern Regional Research Laboratory, Peoria, Ill., U.S.A.). The use of these compounds as anthelmintic agents is described in Antimicrobial Agents and Chemotherapy 15, (3), 361-367 (1979). The 22,23-dihydro C-076 compounds and their preparation are described in European patent publication No. 1689.
The C-076 series and 22,23-dihydro C-076 series compounds include those represented by formula (III): ##STR4## R.sup.1 -R.sup.5 are defined in the following Table 3 and the dotted line between the 22- and 23- positions either represents a single bond or a double bond. Where the dotted line represents a double bond, there are no substituents at the positions indicated by R.sup.1 and R.sup.2.
TABLE 3______________________________________C-076 R.sup.1 R.sup.2 R.sup.3 R.sup.5______________________________________A.sub.1a double bond sec-C.sub.4 H.sub.9 OCH.sub.3A.sub.1b double bond i-C.sub.3 H.sub.7 OCH.sub.3A.sub.2a H OH sec-C.sub.4 H.sub.9 OCH.sub.3A.sub.2b H OH i-C.sub.3 H.sub.7 OCH.sub.3B.sub.1a double bond sec-C.sub.4 H.sub.9 OHB.sub.1b double bond i-C.sub.3 H.sub.7 OHB.sub.2a H OH sec-C.sub.4 H.sub.9 OHB.sub.2b H OH i-C.sub.3 H.sub.7 OHDihydro A.sub.1a H H sec-C.sub.4 H.sub.9 OCH.sub.3Dihydro A.sub.1b H H i-C.sub.3 H.sub.7 OCH.sub.3Dihydro B.sub.1a H H sec-C.sub.4 H.sub.9 OHDihydro B.sub.1b H H i-C.sub.3 H.sub.7 OH______________________________________
Various benzimidazole compounds (for example Albendazole), salicylamide compounds (e.g., Niclosamide) and isoquinoline compounds (e.g. Praziquantel) are also known to have anthelmintic activity.
However, even the most valuable of therapeutic compounds is rarely free from side effects and, whilst these may not normally be serious, there is, naturally, a desire to reduce them. Clearly, if the anthelmintic activity of the known compounds could be increased without correspondingly increasing the intensity of the side effects, this would be a valuable contribution to the art.
BRIEF SUMMARY OF INVENTION
We have now surprisingly discovered that the joint use of one or more of the B-41 series antibiotics, the C-076 series antibiotics or the 22,23-dihydro C-076 series antibiotics with one or more other anthelmintic agents selected from benzimidazole, salicylamide and isoquinoline compounds substantially enhances anthelmintic activity synergistically, without a corresponding increase in the intensity of side effects. As a result, it is possible to reduce substantially the dose of the anthelmintic agent and thus reduce side effects, such as intoxication.
Accordingly, in one aspect, the invention provides a composition comprising:
(a) one or more anthelmintic agents selected from the group consisting of the B-41 series antibiotics, the C-076 series antibiotics and the 22,23-dihydro C-076 series antibiotics; and
(b) one or more other anthelmintic agents selected from the group consisting of benzimidazole, salicylamide and isoquinoline compounds.
The invention also provides a method of treating a human or other animal infested with helminths, which comprises administering to that human or other animal: (a) one or more anthelmintic agents selected from the group consisting of B-41 series antibiotics, C-076 series antibiotics and 22,23-dihydro C-076 series antibiotics; and
(b) one or more other anthelmintic agents selected from the group consisting of benzimidazole, salicylamide and isoquinoline compounds.
DETAILED DESCRIPTION OF INVENTION
Examples of suitable benzimidazole series anthelmintic agents which may be used in the composition and method of the present invention include, for example:
2-(Methoxycarbonylamino)benzimidazole;
5-Butyl-2-(methoxycarbonylamino)benzimidazole;
5-Propoxy-2-(methoxycarbonylamino)benzimidazole;
5-Ethoxy-2-(ethoxycarbonylamino)benzimidazole;
5-Propylthio-2-(methoxycarbonylamino)benzimidazole;
5-Phenylthio-2-(methoxycarbonylamino)benzimidazole;
5-Phenylsulphinyl-2-(methoxycarbonylamino)benzimidazole;
5-(2,4-Dichlorophenoxy)-6-chloro-2-methylthiobenzimidazole;
6-Chloro-5-(2,3-dichlorophenoxy)-2-methylthiobenzimidazole;
2-(4-Thiazolyl)benzimidazole; and
5-Isopropoxycarbonylamino-2-(4-thiazolyl)benzimidazole.
Suitable salicylamide series anthelmintic agents which may be used in the composition and method of the present invention include, for example:
5-Chloro-N-(2-chloro-4-nitrophenyl)salicylamide;
3,5-Diiodo-N-(3-chloro-4-p-chlorophenoxyphenyl)-salicylamide;
3,5-Diiodo-N-[5-chloro-2-methyl-4-(.alpha.-cyano-4-chlorobenzyl)phenyl]salicylamide;
3,5,6-Trichloro-N-(3,5-dichloro-2-hydroxyphenyl)-salicylamide;
2-Acetoxy-3,5-diiodo-N-(p-chlorophenyl)benzamide; and
2-Acetoxy-3-bromo-5-chloro-N-(p-bromophenyl)-thiobenzamide.
Suitable isoquinoline series anthelmintic agents, which may be used in the composition and method of the present invention include, for example, 1-isomers of:
2-Cyclohexylcarbonyl-4-oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline; and
2-Benzoyl-4-oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline.
These isoquinoline compounds may be represented by the formula (IV): ##STR5## in which R represents a cyclohexyl or phenyl group, respectively.
Particularly preferred are combinations of B-41D, C-076 B.sub.1a, C-076 B.sub.1b, 22,23-dihydro C-076 B.sub.1a or 22,23-dihydro C-076 B.sub.1b, with one or more of the abovementioned benzimidazole, salicylamide or isoquinoline series compounds.
The anthelmintic compositions of the invention are useful as parasiticides for the treatment of human beings and other animals. They are particularly useful for the treatment of diseases in livestock, poultry and pet animals (such as pigs, sheep, goats, cows, horses, dogs, cats and chickens) caused by the group of parasites known as the Nematoda, especially those of genera:
Haemonchus;
Trichostrongylus;
Ostertagia;
Nematodirus;
Cooperia;
Ascaris;
Bunostomum;
Oesophagostomum;
Chabertia;
Trichuris;
Strongylus;
Trichonema;
Dictyocaulus;
Capillaria;
Heterakis;
Toxocara;
Ascaridia;
Oxyuris;
Ancylostoma;
Uncinaria;
Toxascaris; and
Parascaris.
Some of the parasites of the genera Nematodirus, Cooperia and Oesophagostomum attack the intestines, whereas parasites of the genera Haemonchus and Ostertagia attack the stomach and parasites of the genus Dictyocaulus are found in the lungs. Parasites of the families Filariidae or Setariidae are found in the heart, the blood vessels and tissues and organs such as the subcutaneous tissues and lymphatic vessels.
The compositions of the invention may also be used for the treatment of diseases caused by, for example, the following Cestoidea:
Taenia saginata;
Hymenolepis diminuta;
Hymenolepis nana;
Moniezia benedeni;
Diphyllobothrium latum;
Diphyllobothrium erinacei;
Echinococcus glanulosus; and
Echinococcus multilocularis,
and caused by the following Trematoda;
Fasciola hepatica;
Fasciola gigantica;
Paragonimus westermanii;
Fasciolopsis buski;
Eurytrema pancreaticum;
Eurytrema coelomaticum;
Clonorchis sinensis;
Schistosoma japonicum;
Schistosoma haematobium; and
Schistosoma mansoni.
The anthelmintic compositions of the invention may be administered orally. One suitable oral formulation is as a drink, in which case the composition may be formulated as an aqueous solution, as a solution in another suitable non-toxic solvent or as a suspension or dispersion incorporating a suspension aid and a wetting agent (such as bentonite) or other constituents.
The composition of the invention may also be administered as a solid, suitably in unit dosage form, for example as a capsule, pill or tablet containing a predetermined amount of the active ingredients. These formulations can be prepared by homogeneously mixing the active ingredients with one or more other finely pulverized materials, generally diluents, filling agents, disintegrators and/or binding agents (e.g. starch, lactose, talc, magnesium stearate or vegetable gum). The weight and content of the active ingredients in such unit dosage forms may vary widely, depending upon the type of animal to be treated, the degree of infection, the kind of parasite and the body weight of the animal.
The anthelmintic compositions of the invention may also be administered to animals by uniformly dispersing them in their feed or they may be used a top dressing or in the form of pellets.
The active ingredients may also be dissolved or dispersed in a liquid carrier and administered parenterally to animals by injection into the proventriculus, the muscles, the lungs or under the skin. For parenteral administration, the carrier used is preferably a vegetable oil, such as peanut oil or cottonseed oil.
Topical administration of the compositions of the invention is also possible, in which case the active ingredients are preferably mixed with a suitable carrier (such as dimethyl sulphoxide or a hydrocarbon solvent). The resulting formulation can be directly applied to the outer skin of the animals, e.g. by spraying.
The optimum amount of the active ingredients of the composition of the invention desired to achieve best results will vary depending upon the kind of animal to be treated, the type of parasitic infection and the degree of infection. However, in general, we have found that good results are achieved by using from 0.01 to 100 mg, preferably from 0.1 to 50 mg, of the B-41, C-076 or 22,23-dihydro C-076 series antibiotics and from 0.5 to 200 mg, preferably from 1to 30 mg, of the benzimidazole, salicylamide or isoquinoline compound, per kg body weight for oral administration.





The enhanced activities of the compositions of the invention are illustrated by the following Examples.
EXAMPLE 1
The test animals used in this Example were goats (two per test group) parasitized by Haemonchus contortus, Ostertagia ostertagi and Fasciola species.
Each goat was given a single gelatin capsule containing the amount of B-41D and/or Albendazole [i.e. 5-propylthio-2-(methoxycarbonylamino)benzimidazole] shown in Table 4. The number of eggs per gram of faeces (E.P.G.) before and after administration was determined. 14 days after administration, the goats were sacrificed and the number of living parasites was determined. These results are also shown in Table 4.
The names of the parasites are abbreviated in the Table as follows:
H.c=Haemonchus contortus
O.o=Ostertagia ostertagi
F.sp.=Fasciola species
TABLE 4__________________________________________________________________________Anthelmintic efficacy in goats by single andjoint use of B-41D with Albendazole againstHaemonchus contortus, Ostertagia osteragi andFasciola sp. E.P.G. of H.c and O.o E.P.G. of F.sp. Number of living after after parasites atCompound and amount before administr. before administr. autopsy Reduction rate (%)(mg/kg) administr. 7 days 14 days administr. 14 days H.c O.o F.sp. H.c O.o F.sp.__________________________________________________________________________B-41D 0.2 3200 0 0 450 990 0 0 21 100 100 32.0 4400 0 0 880 620 0 0 13B-41D 0.05 3400 0 100 1320 940 78 455 19 68.2 70.5 34.0 2000 0 80 480 860 51 431 14B-41D + 0.05 + 4300 0 0 920 0 0 0 0 100 100 100Albendazole 2.5 600 0 0 810 0 0 0 0B-41D + 0.05 + 3800 0 0 1100 0 0 0 0 100 100 100Albendazole 5 2900 0 0 540 0 0 0 0Albendazole 5 3300 0 0 760 20 0 0 8 100 100 72.0 900 0 0 320 10 0 0 6None 2100 4210 3600 1800 1980 162 1022 27 3700 3100 2800 1710 1220 244 1982 23__________________________________________________________________________
EXAMPLE 2
The animals used in this Example were dogs (two per test group) parasitized by Toxocara canis (T.c), Ancylostoma caninum (A.c) and Dipylidium caninum (D.c). Each dog was given a single gelatin capsule containing the prescribed amounts of B-41D and/or Niclosamide [i.e. 5-chloro-N-(2-chloro-4-nitrophenyl)salicylamide], as shown in Table 5. The E.P.G. and the number of parasites excreted before and after administration were determined. The dogs were sacrificed 7 days after administration and the number of living parasites was determined. It was confirmed that Dipylidium caninum excreted its segments in the faeces before administration of the drugs.
The results are shown in Table 5.
TABLE 5__________________________________________________________________________Anthelmintic efficacy in dogs by singe and jointuse of B-41D with Niclosamide against Toxocaracanis, Ancylostoma caninum and Dipylidium caninum E.P.G. Number of Number of living before after excreted parasites parasites atCompound and amount administr. administr. (7 days) (for 7 days) autopsy Reduction rate (%)(mg/kg) T.c A.c T.c A.c T.c A.c T.c A.c D.c T.c A.c D.c__________________________________________________________________________B-41D 0.1 13400 1400 0 0 24 13 0 0 16 100 100 23.2 600 900 0 0 9 8 0 0 27B-41D 0.025 2100 750 0 30 7 9 3 3 11 67.8 71.4 23.2 8400 1100 0 100 12 11 6 5 32B-41D + 0.025+ 2600 500 0 0 13 10 0 0 0 100 100 100Niclosamide 75 600 450 0 0 4 16 0 0 0B-41D + 0.025+ 1800 350 0 0 8 6 0 0 0 100 100 100Niclosamide 150 1500 1450 0 0 9 23 0 0 0Niclosamide 150 3200 2100 2600 1200 0 1 6 14 8 13.0 31.0 73.2 4100 800 3100 450 0 0 14 6 7None 2400 2300 1800 3400 0 0 8 21 37 2100 850 3400 1600 0 0 15 8 19__________________________________________________________________________
EXAMPLE 3
The test animals used in this Example were dogs (two per test group) parasitized by Trichuris vulpis (T.v) and Dipylidium caninum (D.c). Each dog was given a single gelatin capsule containing the prescribed amount of B-41D and/or Praziquantel (i.e. 1-2-cyclohexylcarbonyl-4-oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2.1-a]isoquinoline). The E.P.G. and number of parasites before and after administration were determined. The dogs were sacrificed 7 days after administration and the number of living parasites was also determined. It was confirmed that Dipylidium caninum excreted its segments in the faeces before administration of the drugs.
The results are shown in Table 6.
TABLE 6__________________________________________________________________________Anthelmintic efficacy in dogs by single andjoint use of B-41D with Praziquantel againstTrichuris vulpis and Dipylidium caninum Number of living E.P.G. of T.v. Number of excreted parasites at Reduction rateCompound and amount before after parasites autopsy (%)(mg/kg) administr. administr. (7 days) (for 7 days) T.v. D.c. T.v. D.c.__________________________________________________________________________B-41D 0.1 800 0 68 0 17 100 16.6 100 0 18 0 28B-41D 0.05 1600 300 181 58 9 75.1 22.2 900 200 88 31 33B-41D + 0.05 + 300 0 0 0 0 100 100Praziquantel 2.5 1400 0 0 0 0B-41D + 0.05 + 500 0 0 0 0 100 100Praziquantel 5 200 0 0 0 0Praziquantel 5 700 300 0 142 6 -- 77.7 600 800 0 263 6None 1100 600 0 165 32 700 400 0 97 22__________________________________________________________________________
From the above results, it is apparent that B-41D, when used alone is ineffective against Trematoda (such as the liver fluke) but, when used together with Albendazole, the combination shows more activity than does Albendazole alone.
Niclosamide alone is ineffective against such Nematoda as Toxocara canis and Ancylostoma caninum whilst B-41D alone is ineffective against Dipylidium caninum, but the combination of the two compounds shows more activity against all of these parasites than do the respective active compounds when used alone.
Praziquantel alone is ineffective against such Nematodae as Trichuris vulpis but, when it is used jointly with B-41D, the combination shows greater activity than B-41D against both Nematoda and Cestoida
Moreover, the compounds, when used jointly, are effective in much smaller doses than are the compounds when used alone, thus strongly suggesting the presence of synergism.
Claims
  • 1. An anthelmintic composition comprising:
  • (a) an effective amount of one or more macrolide anthelmintic agents selected from the group consisting of B-41 series antibiotics, C-076 series antibiotics and 22,23-dihydro C-076 series compounds; and
  • (b) an effective amount of one or more anthelmintic agents selected from the group consisting of benzimidazole, salicylamide and isoquinoline compounds.
  • 2. The composition as claimed in claim 1, wherein said macrolide anthelmintic agent (a) is B-41D.
  • 3. The composition as claimed in claim 1, wherein the macrolide anthelmintic agent (a) is C-076 B.sub.1a, C-076 B.sub.1b, 22,23-dihydro C-076 B.sub.1a or 22,23-dihydro C-076 B.sub.1b.
  • 4. The composition as claimed in claim 1, wherein the benzimidazole, salicylamide and isoquinoline compounds are selected from the group consisting of;
  • 2-(Methoxycarbonylamino)benzimidazole;
  • 5-Butyl-2-(methoxycarbonylamino)benzimidazole;
  • 5-Propoxy-2-(methoxycarbonylamino)benzimidazole;
  • 5-Ethoxy-2-(ethoxycarbonylamino)benzimidazole;
  • 5-Propylthio-2-(methoxycarbonylamino)benzimidazole;
  • 5-Phenylthio-2-(methoxycarbonylamino)benzimidazole;
  • 5-Phenylsulphinyl-2-(methoxycarbonylamino)benzimidazole;
  • 5-(2,4-Dichlorophenoxy)-6-chloro-2-methylthiobenzimidazole;
  • 6-Chloro-5-(2,3-dichlorophenoxy)-2-methylthiobenzimidazole;
  • 2-(4-Thiazolyl)benzimidazole;
  • 5-Isopropoxycarbonylamino-2-(4-thiazolyl)benzimidazole;
  • 5-Chloro-N-(2-chloro-4-nitrophenyl)salicylamide;
  • 3,5-Diiodo-N-(3-chloro-4-p-chlorophenoxyphenyl)-salicylamide;
  • 3,5-Diiodo-N-[5-chloro-2-methyl-4-(.alpha.-cyano-4-chlorobenzyl)phenyl]salicylamide;
  • 3,5,6-Trichloro-N-(3,5-dichloro-2-hydroxyphenyl)-salicylamide;
  • 2-Acetoxy-3,5-diiodo-N-(p-chlorophenyl)benzamide;
  • 2-Acetoxy-3-bromo-5-chloro-N-(p-bromophenyl)-thiobenzamide;
  • 2-Cyclohexylcarbonyl-4-oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline; and
  • 2-Benzoyl-4-oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline.
  • 5. The composition as claimed in claim 1, wherein B-41 series antibiotics is B-41D and the benzimidazole, salicylamide and isoquinoline compounds are selected from the group consisting of;
  • 2-(Methoxycarbonylamino)benzimidazole;
  • 5-Butyl-2-(methoxycarbonylamino)benzimidazole;
  • 5-Propoxy-2-(methoxycarbonylamino)benzimidazole;
  • 5-Ethoxy-2-(ethoxycarbonylamino)benzimidazole;
  • 5-Propylthio-2-(methoxycarbonylamino)benzimidazole;
  • 5-Phenylthio-2-(methoxycarbonylamino)benzimidazole;
  • 5-Phenylsulphinyl-2-(methoxycarbonylamino)benzimidazole;
  • 5-(2,4-Dichlorophenoxy)-6-chloro-2-methylthiobenzimidazole;
  • 6-Chloro-5-(2,3-dichlorophenoxy)-2-methylthiobenzimidazole;
  • 2-(4-Thiazolyl)benzimidazole;
  • 5-Isopropoxycarbonylamino-2-(4-thiazolyl)benzimidazole;
  • 5-Chloro-N-(2-chloro-4-nitrophenyl)salicylamide;
  • 3,5-Diiodo-N-(3-chloro-4-p-chlorophenoxyphenyl)-salicylamide;
  • 3,5-Diiodo-N-[5-chloro-2-methyl-4-(.alpha.-cyano-4-chlorobenzyl)phenyl]salicylamide;
  • 3,5,6-Trichloro-N-(3,5-dichloro-2-hydroxyphenyl)-salicylamide;
  • 2-Acetoxy-3,5-diiodo-N-(p-chlorophenyl)benzamide;
  • 2-Acetoxy-3-bromo-5-chloro-N-(p-bromophenyl)-thiobenzamide;
  • 2-Cyclohexylcarbonyl-4-oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline; and
  • 2-Benzoyl-4-oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline.
  • 6. The composition as claimed in claim 1, comprising B-41D and 5-propylthio-2-(methoxycarbonylamino)benzimidazole.
  • 7. The composition as claimed in claim 1, comprising B-41D and 5-chloro-N-(2-chloro-4-nitrophenyl)salicylamide.
  • 8. The composition as claimed in claim 1, comprising B-41D and 1-2-cyclohexylcarbonyl-4-oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline.
  • 9. A method of treating a human or other animal infested with helminths, which comprises administering:
  • (a) an effective amount of one or more macrolide anthelmintic agents selected from the group consisting of B-41 series antibiotics, C-076 series antibiotics and 22,23-dihydro C-076 series compounds; and
  • (b) an effective amount of one or more anthelmintic agents selected from the group consisting of benzimidazole, salicylamide and isoquinoline compounds.
  • 10. The method as claimed in claim 7, wherein said macrolide anthelmintic agent (a) is B-41D.
  • 11. The method as claimed in claim 7, wherein the macrolide anthelmintic agent (a) is C-076 B.sub.1a, C-076 B.sub.1b, 22,23-dihydro C-076 B.sub.1a or 22,23-dihydro C-076 B.sub.1b.
  • 12. The method as claimed in claim 7, wherein there is administered B-41D and 5-propylthio-2-(methoxycarbonylamino)benzimidazole.
  • 13. The method as claimed in claim 7, wherein there is administered B-41D and 5-chloro-N-(2-chloro-4-nitrophenyl)salicylamide.
  • 14. The method as claimed in claim 7, wherein there is administered B-41D and 1-2-cyclohexylcarbonyl-4-oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinoline.
Priority Claims (1)
Number Date Country Kind
56-25058 Feb 1981 JPX
US Referenced Citations (1)
Number Name Date Kind
4144352 Putter Mar 1979
Non-Patent Literature Citations (3)
Entry
Campbell et al.-Chem. Abst., vol. 91(1979), p. 32780z.
Takiguchi et al.-Chem. Abst., vol. 95(1981), p. 22942x.
Chabala et al.-Chem. Abst., vol. 93(1980), p. 160,951j.