CA1064420A - Antiprotozoal agent for animals - Google Patents

Antiprotozoal agent for animals

Info

Publication number: CA1064420A
Authority: CA; Canada
Prior art keywords: antibiotic; salt; cultivation; medium; benzene
Prior art date: 1975-07-22
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

CA257,348A

Other languages

English (en)

French (fr)

Inventor

Masayuki Oshima

Kimihiko Abe

Noboru Ishizaki

Eiji Ohara

Masahiro Kato

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Daiichi Pharmaceutical Co Ltd

Original Assignee

Daiichi Pharmaceutical Co Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1975-07-22

Filing date

1976-07-20

Publication date

1979-10-16

1976-07-20 Application filed by Daiichi Pharmaceutical Co Ltd filed Critical Daiichi Pharmaceutical Co Ltd

1979-10-16 Application granted granted Critical

1979-10-16 Publication of CA1064420A publication Critical patent/CA1064420A/en

Status Expired legal-status Critical Current

Links

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150000001298 alcohols Chemical class 0.000 description 1
PNNNRSAQSRJVSB-BXKVDMCESA-N aldehydo-L-rhamnose Chemical compound C[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)C=O PNNNRSAQSRJVSB-BXKVDMCESA-N 0.000 description 1
HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 description 1
NGFMICBWJRZIBI-UHFFFAOYSA-N alpha-salicin Natural products OC1C(O)C(O)C(CO)OC1OC1=CC=CC=C1CO NGFMICBWJRZIBI-UHFFFAOYSA-N 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
RJGDLRCDCYRQOQ-UHFFFAOYSA-N anthrone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3CC2=C1 RJGDLRCDCYRQOQ-UHFFFAOYSA-N 0.000 description 1
230000001165 anti-coccidial effect Effects 0.000 description 1
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LFYJSSARVMHQJB-QIXNEVBVSA-N bakuchiol Chemical compound CC(C)=CCC[C@@](C)(C=C)\C=C\C1=CC=C(O)C=C1 LFYJSSARVMHQJB-QIXNEVBVSA-N 0.000 description 1
SLUNEGLMXGHOLY-UHFFFAOYSA-N benzene;hexane Chemical compound CCCCCC.C1=CC=CC=C1 SLUNEGLMXGHOLY-UHFFFAOYSA-N 0.000 description 1
125000005605 benzo group Chemical group 0.000 description 1
DAMJCWMGELCIMI-UHFFFAOYSA-N benzyl n-(2-oxopyrrolidin-3-yl)carbamate Chemical compound C=1C=CC=CC=1COC(=O)NC1CCNC1=O DAMJCWMGELCIMI-UHFFFAOYSA-N 0.000 description 1
GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
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230000037396 body weight Effects 0.000 description 1
239000002775 capsule Substances 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
238000002512 chemotherapy Methods 0.000 description 1
230000015271 coagulation Effects 0.000 description 1
238000005345 coagulation Methods 0.000 description 1
239000003224 coccidiostatic agent Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000011161 development Methods 0.000 description 1
230000029087 digestion Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000004467 fishmeal Substances 0.000 description 1
239000004052 folic acid antagonist Substances 0.000 description 1
239000012634 fragment Substances 0.000 description 1
FBPFZTCFMRRESA-GUCUJZIJSA-N galactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-GUCUJZIJSA-N 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
229930195712 glutamate Natural products 0.000 description 1
238000004896 high resolution mass spectrometry Methods 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
238000001802 infusion Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000002347 injection Methods 0.000 description 1
229910017053 inorganic salt Inorganic materials 0.000 description 1
239000002198 insoluble material Substances 0.000 description 1
230000000968 intestinal effect Effects 0.000 description 1
210000000936 intestine Anatomy 0.000 description 1
JYJIGFIDKWBXDU-MNNPPOADSA-N inulin Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@]1(OC[C@]2(OC[C@]3(OC[C@]4(OC[C@]5(OC[C@]6(OC[C@]7(OC[C@]8(OC[C@]9(OC[C@]%10(OC[C@]%11(OC[C@]%12(OC[C@]%13(OC[C@]%14(OC[C@]%15(OC[C@]%16(OC[C@]%17(OC[C@]%18(OC[C@]%19(OC[C@]%20(OC[C@]%21(OC[C@]%22(OC[C@]%23(OC[C@]%24(OC[C@]%25(OC[C@]%26(OC[C@]%27(OC[C@]%28(OC[C@]%29(OC[C@]%30(OC[C@]%31(OC[C@]%32(OC[C@]%33(OC[C@]%34(OC[C@]%35(OC[C@]%36(O[C@@H]%37[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O%37)O)[C@H]([C@H](O)[C@@H](CO)O%36)O)[C@H]([C@H](O)[C@@H](CO)O%35)O)[C@H]([C@H](O)[C@@H](CO)O%34)O)[C@H]([C@H](O)[C@@H](CO)O%33)O)[C@H]([C@H](O)[C@@H](CO)O%32)O)[C@H]([C@H](O)[C@@H](CO)O%31)O)[C@H]([C@H](O)[C@@H](CO)O%30)O)[C@H]([C@H](O)[C@@H](CO)O%29)O)[C@H]([C@H](O)[C@@H](CO)O%28)O)[C@H]([C@H](O)[C@@H](CO)O%27)O)[C@H]([C@H](O)[C@@H](CO)O%26)O)[C@H]([C@H](O)[C@@H](CO)O%25)O)[C@H]([C@H](O)[C@@H](CO)O%24)O)[C@H]([C@H](O)[C@@H](CO)O%23)O)[C@H]([C@H](O)[C@@H](CO)O%22)O)[C@H]([C@H](O)[C@@H](CO)O%21)O)[C@H]([C@H](O)[C@@H](CO)O%20)O)[C@H]([C@H](O)[C@@H](CO)O%19)O)[C@H]([C@H](O)[C@@H](CO)O%18)O)[C@H]([C@H](O)[C@@H](CO)O%17)O)[C@H]([C@H](O)[C@@H](CO)O%16)O)[C@H]([C@H](O)[C@@H](CO)O%15)O)[C@H]([C@H](O)[C@@H](CO)O%14)O)[C@H]([C@H](O)[C@@H](CO)O%13)O)[C@H]([C@H](O)[C@@H](CO)O%12)O)[C@H]([C@H](O)[C@@H](CO)O%11)O)[C@H]([C@H](O)[C@@H](CO)O%10)O)[C@H]([C@H](O)[C@@H](CO)O9)O)[C@H]([C@H](O)[C@@H](CO)O8)O)[C@H]([C@H](O)[C@@H](CO)O7)O)[C@H]([C@H](O)[C@@H](CO)O6)O)[C@H]([C@H](O)[C@@H](CO)O5)O)[C@H]([C@H](O)[C@@H](CO)O4)O)[C@H]([C@H](O)[C@@H](CO)O3)O)[C@H]([C@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 JYJIGFIDKWBXDU-MNNPPOADSA-N 0.000 description 1
229940029339 inulin Drugs 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000008101 lactose Substances 0.000 description 1
ORUIBWPALBXDOA-UHFFFAOYSA-L magnesium fluoride Chemical compound [F-].[F-].[Mg+2] ORUIBWPALBXDOA-UHFFFAOYSA-L 0.000 description 1
229960002160 maltose Drugs 0.000 description 1
235000010355 mannitol Nutrition 0.000 description 1
238000004949 mass spectrometry Methods 0.000 description 1
235000012054 meals Nutrition 0.000 description 1
235000013372 meat Nutrition 0.000 description 1
239000000155 melt Substances 0.000 description 1
239000000401 methanolic extract Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000002906 microbiologic effect Effects 0.000 description 1
239000012046 mixed solvent Substances 0.000 description 1
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
210000004400 mucous membrane Anatomy 0.000 description 1
239000013642 negative control Substances 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
FEMOMIGRRWSMCU-UHFFFAOYSA-N ninhydrin Chemical compound C1=CC=C2C(=O)C(O)(O)C(=O)C2=C1 FEMOMIGRRWSMCU-UHFFFAOYSA-N 0.000 description 1
239000006916 nutrient agar Substances 0.000 description 1
NRNCYVBFPDDJNE-UHFFFAOYSA-N pemoline Chemical compound O1C(N)=NC(=O)C1C1=CC=CC=C1 NRNCYVBFPDDJNE-UHFFFAOYSA-N 0.000 description 1
235000019319 peptone Nutrition 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
230000002265 prevention Effects 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
MUPFEKGTMRGPLJ-ZQSKZDJDSA-N raffinose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)O)O1 MUPFEKGTMRGPLJ-ZQSKZDJDSA-N 0.000 description 1
238000011160 research Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
NGFMICBWJRZIBI-UJPOAAIJSA-N salicin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC=CC=C1CO NGFMICBWJRZIBI-UJPOAAIJSA-N 0.000 description 1
229940120668 salicin Drugs 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
238000010898 silica gel chromatography Methods 0.000 description 1
229910001961 silver nitrate Inorganic materials 0.000 description 1
RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
229960002920 sorbitol Drugs 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229940031000 streptococcus pneumoniae Drugs 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000003826 tablet Substances 0.000 description 1
OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
235000013343 vitamin Nutrition 0.000 description 1
239000011782 vitamin Substances 0.000 description 1
229940088594 vitamin Drugs 0.000 description 1
229930003231 vitamin Natural products 0.000 description 1
150000003722 vitamin derivatives Chemical class 0.000 description 1
235000015099 wheat brans Nutrition 0.000 description 1

Classifications

- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

Preparation Of Compounds By Using Micro-Organisms (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Micro-Organisms Or Cultivation Processes Thereof (AREA)

CA257,348A 1975-07-22 1976-07-20 Antiprotozoal agent for animals Expired CA1064420A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP50089536		1975-07-22

Publications (1)

Publication Number	Publication Date
CA1064420A true CA1064420A (en)	1979-10-16

Family

ID=13973525

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA257,348A Expired CA1064420A (en)	1975-07-22	1976-07-20	Antiprotozoal agent for animals

Country Status (10)

Country	Link
AR (1)	AR209976A1 (de)
AT (1)	AT349139B (de)
BG (1)	BG28270A3 (de)
CA (1)	CA1064420A (de)
ES (1)	ES450428A1 (de)
IT (1)	IT1062633B (de)
MX (1)	MX5831E (de)
NZ (1)	NZ181531A (de)
PH (1)	PH14840A (de)
ZA (1)	ZA764157B (de)

1976
- 1976-07-13 ZA ZA764157A patent/ZA764157B/xx unknown
- 1976-07-19 PH PH18699A patent/PH14840A/en unknown
- 1976-07-20 CA CA257,348A patent/CA1064420A/en not_active Expired
- 1976-07-20 BG BG033789A patent/BG28270A3/xx unknown
- 1976-07-21 IT IT5053376A patent/IT1062633B/it active
- 1976-07-21 NZ NZ181531A patent/NZ181531A/xx unknown
- 1976-07-21 MX MX761790U patent/MX5831E/es unknown
- 1976-07-22 AR AR264045A patent/AR209976A1/es active
- 1976-07-22 AT AT538776A patent/AT349139B/de not_active IP Right Cessation
- 1976-07-22 ES ES450428A patent/ES450428A1/es not_active Expired

Also Published As

Publication number	Publication date
PH14840A (en)	1981-12-16
AR209976A1 (es)	1977-06-15
AT349139B (de)	1979-03-26
IT1062633B (it)	1984-10-20
AU1610576A (en)	1977-06-16
ES450428A1 (es)	1977-08-16
ZA764157B (en)	1977-06-29
MX5831E (es)	1984-07-31
BG28270A3 (en)	1980-03-25
NZ181531A (en)	1978-04-28
ATA538776A (de)	1978-08-15

Publication	Publication Date	Title
NL192989C (nl)	1998-07-03	Antibioticum, werkwijze voor de bereiding en farmaceutisch preparaat dat dit antibioticum bevat.
US5278052A (en)	1994-01-11	Process for the simultaneous production of benanomicins A and B
CA1041448A (en)	1978-10-31	Antibiotic a-28086 complex from streptomyces aureofaciens
US5510372A (en)	1996-04-23	Antiparasitic macrolide antiobiotics
US4141907A (en)	1979-02-27	Deoxynarasin antibiotics
CA2021894C (en)	1996-09-17	Antiparasitic agent
DE3880845T2 (de)	1993-08-26	Durch fermentation hergestellte antibiotika.
US4174404A (en)	1979-11-13	Deoxynarasin antibiotics
Tsukiura et al.	1980	Bu-2313, a new antibiotic complex active against anaerobes I. production, isolation and properties of Bu-2313 A and B
US4085224A (en)	1978-04-18	Method of increasing feed utilization
US4478831A (en)	1984-10-23	Antibiotics, pharmaceutical compositions and method of use
CA1064420A (en)	1979-10-16	Antiprotozoal agent for animals
US4226879A (en)	1980-10-07	Antibiotic composition
US4110436A (en)	1978-08-29	Antibiotic a-28086 factor d and process for production thereof
US4110435A (en)	1978-08-29	Antibiotic a-28086 factor d and process for production thereof
EP0085859B1 (de)	1986-04-09	Antibiotische Verbindung AM-2604-A und deren Herstellungsverfahren
US5695984A (en)	1997-12-09	Process for the preparation of antibiotics 10381B
US4440751A (en)	1984-04-03	Broad spectrum antibiotic complex produced by a novel micromonospora
US4232006A (en)	1980-11-04	Antibiotic W-10 complex, antibiotic 20561 and antibiotic 20562 as antifungal agents
US4137224A (en)	1979-01-30	Process for the preparation of antibiotic W-10 complex and for the isolation of antibiotic 20561 and antibiotic 20562 therefrom
US3991183A (en)	1976-11-09	Antibiotic produced by a species of micromonospora
US4204039A (en)	1980-05-20	Process for producing deoxynarasin antibiotics
US4536397A (en)	1985-08-20	Antibiotics, neoviridogriseins, and their method of production
US4230799A (en)	1980-10-28	Process for the preparation of antibiotic W-10 complex and for the isolation of Antibiotic 20561 and Antibiotic 20562 therefrom
CA1041930A (en)	1978-11-07	Antibiotic a-28086 complex from streptomyces aureofaciens