KR840005741A - 제암 및 면역자극 작용을 갖는 물질의 제조방법 - Google Patents
제암 및 면역자극 작용을 갖는 물질의 제조방법 Download PDFInfo
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- KR840005741A KR840005741A KR1019830003811A KR830003811A KR840005741A KR 840005741 A KR840005741 A KR 840005741A KR 1019830003811 A KR1019830003811 A KR 1019830003811A KR 830003811 A KR830003811 A KR 830003811A KR 840005741 A KR840005741 A KR 840005741A
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- organic solvent
- hydrophilic organic
- extract
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- fuzobacterium
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- C12P1/00—Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes
- C12P1/02—Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes by using fungi
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- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/66—Microorganisms or materials therefrom
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- C12P1/00—Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1도는 본 발명에 사용되는 퓨조박테리움 뉴클레아툼(Fusobacterium nucleatum) TF-031(기탁기관 : 한국과학기술원, 기탁일 : 1982. 3. 19, 기탁번호 : 820319-01815호)의 형태를 제시하는 현미경 사진이고,
제2도는 후술하는 바의 실시예 1에서 수득되는 TF-500의 적외선 흡수 스펙트럼이며,
제3도는 전술한 물질의 자외선 흡수 스펙트럼이고,
제4도는 후술하는 바의 실시예 2에서 수득되는 TF-500의 적외선 흡수 스펙트럼이며,
제5도는 전술한 물질의 자외선 흡수 스펙트럼이고,
제6도는 후술하는 바의 실시예 3에서 수득되는 TF-500의 적외선 흡수 스펙트럼이며,
제7도는 전술한 물질의 자외선 흡수 스펙트럼이고,
제8도는 후술하는 바의 실시예 4에서 수득되는 TF-500의 적외선 흡수 스펙트럼이며,
제9도는 전술한 물질의 자외선 흡수 스펙트럼을 나타낸다.
Claims (16)
- 퓨조박테리움(Fusobacterium)속의 미생물을 디알킬 설폭사이드로 추출 처리하고 이 추출물로부터
- (a) 회백-연 갈색 불말로
- (b) 제암 및 면역자극 작용을 가지며
- (c) 수용성이나 메탄올, 에탄올, 아세톤, 벤젠, 클로로포름, 에틸 아세테이트 및 디에틸에테르에는 불용성이고, (d) 명확한 융점은 없으며, 약 180℃에서 분해되기 시작하고, 약 195℃에서 현저하게 분해되며, (d) KBr법으로 얻어진 적외선 흡수 스펙트럼에서 3500 내지 3200,2920,2850,1660 내지 1600,1580 내지 1520,1460 내지 1400,1380 내지 1360,1120내지 1100,1080 내지 1000,970 및 840 및 840cm-1. 근접부에서 흡수대가 있고, (f) pH7.0의 수용액에 대한 자외선 흡수스펙트럼에서는 흡수단에서 강한 흡수가 나타나며, 246내지 280nm근처에서 흡수피이크가 나타나고, (g) 몰리쉬반응(Molish reaction), 페놀-황산 반응, 안트론-황산반응, 인돌-염산 반응 및 로리-폴린 반응(Lowry-Folin's reaction)에는 양성이나, 닌히드린 반응에는 음성이며, (h) 원소분석치가 C : 38내지 47%, H : 5 내지 7%, N : 1내지 4%이고, (i) 페놀황산법으로 측정한 바의 당함량이 포도당으로서 약 12내지 30% (중량)이며, 로리-폴린법으로 측정한 바의 단백질 함량이 소혈청 알부민으로서 약 10%(중량)이하인 물질을 수집함을 특징으로 하여, 전술한 바의 특성을 갖는 제암물질 TF-500 또는 그의 염을 제조하는 방법.
- 제1항에 있어서, 퓨조박테리움 속의 미생물을 디알킬 서록사이드로 추출 처리하고, 생성된 추출물에 친수성 유기용매를 가하여, 생성된 침전을 제단백 처리한 후, 초여과 처리하는 방법.
- 제2항에 있어서, 디알킬 설폭사이드가 디메틸 설폭사이드인 방법.
- 제2항 또는 3항에 있어서, 친수성 유기용매가 아세톤인 방법.
- 제2항 내지 4항중 어느 하나에 있어서, 제단백 처리를 단백분해 효소로 효소처리하는 방법.
- 제5항에 있어서, 단백분해 효소가 프로나아제(pronase)인 방법.
- 제1항에 있어서, 퓨조박테리움 속의 미생물을 디알킬 설폭사이드로 추출 처리하고, 생성된 추출물에 친수성 유기 용매를 가하여 수득한 침전을 초여과하는 방법.
- 제7항에 있어서, 디알킬설폭사이드가 디메틸 설폭사이드인 방법.
- 제7항 또는 8항에 있어서, 친수성 유기용매가 아세톤인 방법.
- 제2항 내지 9항중 어느하나에 있어서, 초여과 처리를 명목 분자량이 50,000 내지 200,000인 초여과기로 수행하는 방법.
- 제1항 내지 10항중 어느 하나에 있어서, 퓨조박테리움 속의 미생물이 퓨조박테리움 뉴클레아툼(Fusobacterium nucleatum)인 방법.
- 제1항에 있어서, 퓨조박테리움 뉴클레아튬의 미생물을 디알킬 설폭사이드로 추출 처리하고, 산성 조건하에서 생성된 추출물에 친수성 유기용매를 추출물의 5배이상(용적/용적)가하여 생성된 침전을 프로나아제로 제단백 처리하고, 알코올 농도가 30내지 80%(용적)되도록 알코올을 가하여 생성된 침전을 수집하고 초여과한 후, 박막 여과기로 여과한 다음, 여액을 동결 건조시켜 제암물질을 수득하는 방법.
- ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57142439A JPS5931715A (ja) | 1982-08-17 | 1982-08-17 | 制癌性物質tf−500の製造法 |
JP142439 | 1982-08-17 | ||
JP142439/82 | 1982-08-17 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR840005741A true KR840005741A (ko) | 1984-11-15 |
KR860001213B1 KR860001213B1 (ko) | 1986-08-27 |
Family
ID=15315335
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019830003811A KR860001213B1 (ko) | 1982-08-17 | 1983-08-16 | 제암 및 면역자극 작용을 갖는 물질의 제조방법 |
Country Status (22)
Country | Link |
---|---|
US (1) | US4547462A (ko) |
JP (1) | JPS5931715A (ko) |
KR (1) | KR860001213B1 (ko) |
AT (1) | AT389525B (ko) |
AU (1) | AU556770B2 (ko) |
BE (1) | BE897549A (ko) |
CA (1) | CA1202585A (ko) |
CH (1) | CH659256A5 (ko) |
DD (1) | DD212401A5 (ko) |
DE (1) | DE3329255C2 (ko) |
DK (1) | DK374283A (ko) |
ES (1) | ES524977A0 (ko) |
FI (1) | FI79140C (ko) |
FR (1) | FR2531863B1 (ko) |
GB (1) | GB2126893B (ko) |
IT (1) | IT1168209B (ko) |
NL (1) | NL8302880A (ko) |
NO (1) | NO159452C (ko) |
NZ (1) | NZ205295A (ko) |
PT (1) | PT77207B (ko) |
SE (1) | SE456014B (ko) |
ZA (1) | ZA836021B (ko) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU572529B2 (en) * | 1983-08-01 | 1988-05-12 | Furukawa, Keiichiro | Spf-100 and process for the preparation thereof |
JPH0383097A (ja) * | 1989-08-28 | 1991-04-09 | Toshiba Corp | 縦スクロール用アドレス発生装置 |
US5215756A (en) * | 1989-12-22 | 1993-06-01 | Gole Dilip J | Preparation of pharmaceutical and other matrix systems by solid-state dissolution |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1245037B (de) * | 1965-08-21 | 1967-07-20 | Schering Ag | Verfahren zur Herstellung von antigen-wirksamen Polysacchariden und Lipopolysacchariden |
JPS53130496A (en) * | 1977-04-15 | 1978-11-14 | Japan Synthetic Rubber Co Ltd | Preparation of polysaccharides |
US4477437A (en) * | 1981-02-19 | 1984-10-16 | Toyama Chemical Co., Ltd. | Substances having carcinostatic and immunostimulating activity |
DE3205074A1 (de) * | 1981-02-19 | 1982-12-16 | Toyama Chemical Co. Ltd., Tokyo | Neue carcinostatische und immunostimulierende substanzen, verfahren zur herstellung derselben und carcinostatische mittel mit einem gehalt derselben |
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1982
- 1982-08-17 JP JP57142439A patent/JPS5931715A/ja active Granted
-
1983
- 1983-08-10 AU AU17848/83A patent/AU556770B2/en not_active Ceased
- 1983-08-12 DE DE3329255A patent/DE3329255C2/de not_active Expired
- 1983-08-12 CA CA000434476A patent/CA1202585A/en not_active Expired
- 1983-08-12 IT IT48851/83A patent/IT1168209B/it active
- 1983-08-15 FI FI832929A patent/FI79140C/fi not_active IP Right Cessation
- 1983-08-15 GB GB08321918A patent/GB2126893B/en not_active Expired
- 1983-08-16 CH CH4453/83A patent/CH659256A5/de not_active IP Right Cessation
- 1983-08-16 NO NO832938A patent/NO159452C/no unknown
- 1983-08-16 DK DK374283A patent/DK374283A/da not_active Application Discontinuation
- 1983-08-16 NL NL8302880A patent/NL8302880A/nl not_active Application Discontinuation
- 1983-08-16 US US06/523,438 patent/US4547462A/en not_active Expired - Fee Related
- 1983-08-16 DD DD83253996A patent/DD212401A5/de not_active IP Right Cessation
- 1983-08-16 AT AT0293783A patent/AT389525B/de not_active IP Right Cessation
- 1983-08-16 KR KR1019830003811A patent/KR860001213B1/ko not_active IP Right Cessation
- 1983-08-16 PT PT77207A patent/PT77207B/pt not_active IP Right Cessation
- 1983-08-16 NZ NZ205295A patent/NZ205295A/en unknown
- 1983-08-16 ZA ZA836021A patent/ZA836021B/xx unknown
- 1983-08-16 ES ES524977A patent/ES524977A0/es active Granted
- 1983-08-16 SE SE8304435A patent/SE456014B/sv not_active IP Right Cessation
- 1983-08-17 BE BE0/211367A patent/BE897549A/fr not_active IP Right Cessation
- 1983-08-17 FR FR8313363A patent/FR2531863B1/fr not_active Expired
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