KR920021573A - 6-0-알킬엘사마이신 a 유도체의 제조 - Google Patents
6-0-알킬엘사마이신 a 유도체의 제조 Download PDFInfo
- Publication number
- KR920021573A KR920021573A KR1019920009159A KR920009159A KR920021573A KR 920021573 A KR920021573 A KR 920021573A KR 1019920009159 A KR1019920009159 A KR 1019920009159A KR 920009159 A KR920009159 A KR 920009159A KR 920021573 A KR920021573 A KR 920021573A
- Authority
- KR
- South Korea
- Prior art keywords
- elsamycin
- isopropylidene
- butoxycarbonyl
- alkyl
- compound
- Prior art date
Links
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 claims 15
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 10
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 6
- 150000001350 alkyl halides Chemical class 0.000 claims 5
- 229910000027 potassium carbonate Inorganic materials 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 claims 3
- -1 3-phthalimidopropyl Chemical group 0.000 claims 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims 3
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 claims 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims 2
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 102000001742 Tumor Suppressor Proteins Human genes 0.000 claims 1
- 108010040002 Tumor Suppressor Proteins Proteins 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 238000007069 methylation reaction Methods 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 230000000144 pharmacologic effect Effects 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (22)
- 다음 일반식의 화합물.상기식에서 R은 C1-C10알킬 치환되거나 미치환된 아미노알킬이다.
- 다음 일반식의 화합물.상기식에서 R은 C1-C10알킬 치환되거나 미치환된 아미노알킬이다.
- 제1항에 있어서, 6-0-메틸엘사마이신 A; 6-0-n-프로필엘사마이신 A; 6-0-이소프로필엘사마이신 A; 6-0-n-부틸엘사마이신 A; 6-0-n-헥실엘사마이신 A; 6-0-n-에틸엘사마이신 A; 6-0-n-데실엘사마이신 A; 6-0-n-(3-프탈이미도프로필)엘사마이신 A; 또는 6-0-(3-마이노프로필)엘사마이신 A인 화합물.
- 제2항에 있어서, 3',4'-0-이소프로필리덴-6-0-메틸엘사마이신 A; 6-0-에틸-3'-4'-0-이소프로필리덴엘사마이신 A; 6-0-n-헥실-3',4'-0-이소프로필리덴엘사마이신 A; 6-0-n-데실-3',4'-0-이소프로필리덴엘사마이신 A; 3',4'-0-이소프로필리덴-6-0-(3-프탈이미도프로필)엘사마이신 a; 또는 6-0-(3-아미노프로필)-3',4'-이소프로필리덴엘사마이신 A인 화합물.
- 2"-N-t-부톡시카르보닐-6-0-메틸엘사마이신 A.
- 2"-N-t-부톡시카르보닐-6-0-n-프로필엘사마이신 A.
- 2"-N-t-부톡시카르보닐-6-0-이소프로필엘사마이신 A.
- 2"-N-t-부톡시카르보닐-6-0-n-부틸엘사마이신 A.
- 2"-N-t-부톡시카르보닐-6-0-n-헥실엘사마이신 A.
- 2"-N-t-부톡시카르보닐-3',4' 0-이소프로필리덴-6-0-메틸엘사마이신 A.
- 2"-N-t-부톡시카르보닐-6-0-에틸-3',4'-0-이소프로필리덴엘사마이신 A.
- 2"-N-t-부톡시카르보닐-6-0-n-헥실-3',4'-0-이소프로필리덴엘사마이신 A.
- 2"-N-t-부톡시카르보닐-6-0-n-데실-3',4'-0-이소프로필리덴엘사마이신 A.
- 2"-N-t-부톡시카르보닐-3,4-이소프로필리덴-6-0-(3-프탈이미도프로필)엘사마이신 A.
- 2"-N-t-부톡시카르보닐-엘사마이신 A를 디메틸술폭시드내 요오드화 칼륨 및/또는 칼륨 카르보네이트 존재하에 알킬할라이드로서 처리하여 상응하는 6-0-알킬유도체를 제공한다음, 트리플루오로초산으로 처리하는 것으로 이루어진 제1 또는 3항의 화합물의 제조방법.
- 2"-N-t-부톡시카르보닐-3',4'-0-이소프로필리덴엘사마이신 A를 필요하다면 요오드화 칼륨 및/또는 칼륨 카르보네이트 존재하에 알킬 할라이드로서 처리하여 상응하는 6-0-알킬 유도체를 제공한다음, 트리플루오로초산으로 처리하는 것으로 이루어진 제1 또는 3항의 화합물의 제조방법.
- 2"-N-t-부톡시카르보닐-3',4'-0-이소프로필리덴엘사마이신 A를 디메틸술폭시드내 요오드화 칼륨 및/또는 칼륨 카르보네이트 존재하에 알킬 할라이드로서 처리하여 상응하는 6-0-알킬 유도체를 제공한다음, 상온에서 아세톤내 톨루엔술폰산으로 처리하는 것으로 이루어진 제2 또는 4항의 화합물의 제조방법.
- 엘사마이신 A의 디아조메탄과 0-메틸화반응으로 이루어진 6-0-메틸 엘사마이신 A의 제조방법.
- 2"-N-t-부톡시카르보닐-3',4'-0-이소프로필리덴엘사마이신 A를 디메틸술폭시드내 요오드화 칼륨 및 칼륨 카르보네이트 존재하에 알킬 할라이드로서 처리하여 상응하는 6-0-알킬 유도체를 제공한다음, 상온에서 아세톤내 톨루엔술폰산으로 처리하고, 히드라진 히드레이트로서 처리하는 것으로 이루어진 6-0-(3-아미노프로필)-3',4'-이소프로필리덴엘사마이신 A의 제조방법.
- 2"-N-t-부톡시카르보닐-3',4'-0-이소프로필리덴엘사마이신 A를 필요하다면 디메틸술폭시드내 요오드화 칼륨 및/또는 칼륨 카보네이트 존재하에 알킬 할라이드로서 처리하여 상응하는 6-0-알킬 유도체를 제공한다음, 상온에서 아세톤내 톨루엔술폰산으로 처리하고, 히드라진 히드레이트로서 처리하는 것을 이루어진 6-0-(3-아미노프로필)-엘사마이신 A의 제조방법.
- 한가지 또는 그이상의 약리적 담체 또는 희석제와 결합하여 활성성분으로서 제1-14항중 어느 한항의 화합물로 이루어진 약제 배합물.
- 포유류 숙주에 제1-14항중 어느 한항의 화합물의 종양억제 유효 투여량을 투여하는 것으로 이루어진 종양의 치료방법.※ 참고사항:최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US70750491A | 1991-05-30 | 1991-05-30 | |
US07/707,504 | 1991-05-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR920021573A true KR920021573A (ko) | 1992-12-18 |
Family
ID=24841970
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019920009159A KR920021573A (ko) | 1991-05-30 | 1992-05-28 | 6-0-알킬엘사마이신 a 유도체의 제조 |
Country Status (14)
Country | Link |
---|---|
EP (1) | EP0516157A1 (ko) |
JP (1) | JPH05148292A (ko) |
KR (1) | KR920021573A (ko) |
AU (1) | AU655024B2 (ko) |
CA (1) | CA2069716A1 (ko) |
CS (1) | CS158892A3 (ko) |
FI (1) | FI922443L (ko) |
HU (1) | HU210499B (ko) |
IE (1) | IE921764A1 (ko) |
IL (1) | IL101998A0 (ko) |
MX (1) | MX9202571A (ko) |
OA (1) | OA09753A (ko) |
TW (1) | TW218879B (ko) |
ZA (1) | ZA923816B (ko) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6703384B2 (en) | 1998-09-23 | 2004-03-09 | Research Development Foundation | Tocopherols, tocotrienols, other chroman and side chain derivatives and uses thereof |
KR20100014080A (ko) * | 2007-05-24 | 2010-02-10 | 스펙트럼 파마슈티컬즈 인크 | 약학적 제형에 적절한 안정한 고체 엘스아미트루신 염 |
JP5701387B2 (ja) * | 2010-08-27 | 2015-04-15 | ハンジョウ ベンシェン ファーマシューティカル シーオー., エルティーディー.Hangzhou Bensheng Pharmaceutical Co., Ltd. | ベルバミンのジカルボキシミド誘導体、その調製方法及び使用 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4518589A (en) * | 1983-10-03 | 1985-05-21 | Bristol-Myers Company | BBM-2478 Antibiotic complex |
EP0219852B1 (en) * | 1985-10-23 | 1992-02-05 | Ishihara Sangyo Kaisha, Ltd. | Chartreusin derivatives, salts thereof, antitumorous compositions containing the same, and processes for producing the same |
-
1992
- 1992-05-25 ZA ZA923816A patent/ZA923816B/xx unknown
- 1992-05-25 HU HU9201732A patent/HU210499B/hu not_active IP Right Cessation
- 1992-05-26 IL IL101998A patent/IL101998A0/xx unknown
- 1992-05-26 CS CS921588A patent/CS158892A3/cs unknown
- 1992-05-27 CA CA002069716A patent/CA2069716A1/en not_active Abandoned
- 1992-05-27 FI FI922443A patent/FI922443L/fi unknown
- 1992-05-27 TW TW081104187A patent/TW218879B/zh active
- 1992-05-27 OA OA60215A patent/OA09753A/en unknown
- 1992-05-28 KR KR1019920009159A patent/KR920021573A/ko not_active Application Discontinuation
- 1992-05-29 JP JP4138935A patent/JPH05148292A/ja active Pending
- 1992-05-29 EP EP92109112A patent/EP0516157A1/en not_active Withdrawn
- 1992-05-29 AU AU17241/92A patent/AU655024B2/en not_active Expired - Fee Related
- 1992-05-29 MX MX9202571A patent/MX9202571A/es unknown
- 1992-07-01 IE IE176492A patent/IE921764A1/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
IE921764A1 (en) | 1992-12-02 |
CA2069716A1 (en) | 1992-12-01 |
EP0516157A1 (en) | 1992-12-02 |
HUT61774A (en) | 1993-03-01 |
CS158892A3 (en) | 1992-12-16 |
FI922443A0 (fi) | 1992-05-27 |
MX9202571A (es) | 1992-10-01 |
FI922443L (fi) | 1992-12-01 |
ZA923816B (en) | 1993-11-25 |
TW218879B (ko) | 1994-01-11 |
AU655024B2 (en) | 1994-12-01 |
JPH05148292A (ja) | 1993-06-15 |
HU210499B (en) | 1995-04-28 |
AU1724192A (en) | 1992-12-03 |
IL101998A0 (en) | 1992-12-30 |
HU9201732D0 (en) | 1992-08-28 |
OA09753A (en) | 1993-11-30 |
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Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19920528 |
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