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序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
201 Chain terpene compound JP18171089 1989-07-14 JPH0348633A 1991-03-01 TAKAYANAGI HISAO; KITANO YASUNORI; MORINAKA YASUHIRO
NEW MATERIAL:The compound of formula [R is CO 2R 1 (R 1 is 1-4C alkyl or phenyl), hydroxymethyl, formyl or C(CN)HOR 2 (R 2 is H, trimethylsilyl or 1- ethoxyethyl); X is halogen or OSO 2R 3 (R 3 is (substituted) 1-4C alkyl or phenyl); the double bonds 8, 12 among the double bonds 2, 4, 8, 12 take type-E steric configuration and the double bonds 2, 4 take type-(Z, E), (E, E), (Z, Z) or (E, Z) configuration]. EXAMPLE: 14-Chloro-2-(1-methylethyl)-5,9,13-trimethyl 2,4,1,12-tetradecatetraenoic acid ethyl ester. USE: An intermediate for the total synthesis of an antitumor agent sarcophytol A. PREPARATION: The compound of formula wherein R is CO 2R 1 can be produced e.g. by halogenating a 14-hydroxy-2-(1-methylethyl)-5,9,13-trimethyl 2,4,8,12- tetradecatetraenoic acid ester. COPYRIGHT: (C)1991,JPO&Japio
202 스트랩토키나제와 스트렙토도르나제를 생산하는 미생물 및 이를 이용한 스트렙토키나제 및 스트렙토도르나제의 제조방법 KR1019940020022 1994-08-13 KR1019960007770A 1996-03-22 최덕호; 배신규; 최미영; 이상훈; 조연덕
203 STREPTOSPIROLE DERIVATIVES PCT/EP2009/005155 2009-07-16 WO2010012381A1 2010-02-04 WINK, Joachim; GERLITZ, Martin; OLIVAN, Hélène; KURZ, Michael

The invention relates to streptospirole derivatives of the general formula (I), wherein R1, R2, R3, X1, X2, Y1 and Y2 are as defined herein, a process for the preparation of said compounds by fermenting the microorganism Streptomyces sp. ST 108140 (DSM 19369) and optionally derivatizing the compounds produced by said microorganism, a pharmaceutical composition comprising at least one compound of the formula (I), and the use of a compound of the formula (I) for the preparation of a medicament for the treatment and/or prophylaxis of bacterial infections.

204 Reduction of streptomycins US33475953 1953-02-02 US2790792A 1957-04-30 ARTHUR KAPLAN MURRAY
205 Streptomycin extraction US63462245 1945-12-12 US2701795A 1955-02-08 WICK ARNE N; VANDER BROOK MILTON J
206 Cloning vectors for use in Streptomyces EP82305471.3 1982-10-14 EP0077649A2 1983-04-27 Fayerman, Jeffrey Tobin; Mabe, James Albert; Nakatsukasa, Walter Mitsuo; Richardson, Mark Alan

The present invention discloses selectable recombinant DNA cloning vectors comprising:

  • a) a functional origin of replication containing restriction fragment of plasmid pEL103, and
  • b) one or more DNA segments that convey resistance to at least one antibiotic when transformed into a sensitive host cell, said host cell being susceptible to transformation, cell division, and culture, for use in Streptomyces and related organisms.

207 Streptomycin and dihydrostreptomycin salts US64796357 1957-03-25 US2945784A 1960-07-19 WEITNAUER GUSTAVO A
208 Streptomycin purification US70918658 1958-01-16 US2921063A 1960-01-12 HEUSER LEON J
209 Crystallization of streptomycins US18648750 1950-09-23 US2633464A 1953-03-31 HEUSER LEON J
210 Streptomycin purification US17393450 1950-07-14 US2578840A 1951-12-18 RHODEHAMEL JR HARLEY W; FORTUNE WILLIAM B
211 Streptomycin preparation US6491148 1948-12-11 US2565402A 1951-08-21 SOLOMONS ISAIAH A
212 Production of streptomycin US2313648 1948-04-24 US2538943A 1951-01-23 EVERETT MCDANIEL LLOYD; DAVID HENDLIN
213 STREPTOSPIROLE DERIVATIVES EP09777218.0 2009-07-16 EP2321322B1 2012-12-19 WINK, Joachim; GERLITZ, Martin; OLIVAN, Hélène; KURZ, Michael; DUFOUR-SCHROIF, Cosima
214 Preparation of straight-chain polybenzyl JP2494178 1978-03-07 JPS54118500A 1979-09-13 TOYOSHIMA ISAMU; ARATA KAZUSHI
PURPOSE: To obtain a straight-chain polybenzyl by polycondensation of a hagenated benzyl in the presence of an iron oxide prepared through thermal decomposition of ferrous sulfate as a catalyst. CONSTITUTION: An ferric oxide prepared by thermal decomposition of ferrous or ferric sulfide is used as a catalyst in polycondensation of a halogenated benzyl. In the preparation of the catalyst, ferrous sulfate is heated in an atmosphere of air or nitrogen under a reduced or an atmospheric pressure at 250W750°C for 30 minutesW4 hours; ferric sulfate, at 550W750°C, and thermally decomposed into ferric oxide which is used as the catalyst to give a straight-chain polybenzyl free from branches. The catalyst has specificity. Ferric oxide prepared by heating ferric hydroxide has no effect, ferric oxide from nickel or cobalt sulfate which is a homologue compound of iron is inert. COPYRIGHT: (C)1979,JPO&Japio
215 지방산전이효소를 이용한 신규의 스트렙토마이신 생성균주의 생산 KR1019970004094 1997-02-12 KR1019980067794A 1998-10-15 서주원; 김종우
본 발명은 지방산 전이효소 유전자를 이용하여 살균력이 개선된 신규한 구조의 스트렙토마이신 유사물질을 제공하며, 종래의 스트렙토마이신 등 아미노글리코사이드계 항생물질에 대하여 내성을 갖는 균주를 살균할 수 있는 재조합 플라스미드백터pKTC로 형질전환시킨 신규한 숙주세포 Streptomyces griseus DW 1011를 제공한다.
216 二氫鏈黴素之製造 TW001816 1956-11-09 TW001266U 1960-05-01 HIROICHI YAMAMOTO 等12人; KAZUO TANABE; KOITI NAKAZAWA; MOTOO SHIBATA
217 Process for producing streptovaricin C EP92309457.7 1992-10-16 EP0538050A3 1994-05-04 Inoue, Kaname; Murofushi, Kanji; Yamazaki, Motohide; Armentrout, Richard W.

Disclosed is a method for selecting a mutant strain belonging to the genus Streptomyces which is a hyperproducer of Streptovaricin C by subjecting a natural strain of Streptomyces spectabilis to conditions so as to isolate streptovaricin resistant organism. Such organisms are subjected to mutagenesis and cultured. The strain producing the smallest pellet or having the deepest color is a streptovaricin hyperproducer.

218 POLYMER-LINKED PSEUDOMONAS EXOTOXIN IMMUNOTOXIN PCT/US2005045177 2005-12-14 WO2006065867A3 2007-07-19 FILPULA DAVID RAY; YANG KAREN; BASU AMARTYA; PASTAN IRA H
The present invention relates to polymer conjugates of SS 1 P, and methods of making and using the same.
219 POLYMER-LINKED PSEUDOMONAS EXOTOXIN IMMUNOTOXIN PCT/US2005/045177 2005-12-14 WO2006065867A2 2006-06-22 FILPULA, David, Ray; YANG, Karen; BASU, Amartya; PASTAN, Ira, H.

The present invention relates to polymer conjugates of SS 1 P, and methods of making and using the same.

220 PRODUCTION OPEN-CHAINED SOPHOROLIPIDS PCT/US2006/007399 2006-03-01 WO2006094112A2 2006-09-08 ASHBY, Richard, D.; SOLAIMAN, Daniel, K., Y.; FOGLIA, Thomas, A.; HAAS, Michael, J.

Methods for the production of open-chained sophoro lipids, involving cultivating a yeast capable of producing open-chained sophoro lipids in a culture medium containing fatty acid alkyl esters, and glycerol or carbohydrates (e.g., glucose) or mixtures thereof; wherein at least about 60% of the sophorolipids produced are open-chained sophoro lipids.

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