KR840003235A - N-아실펩티드 화합물의 제조방법 - Google Patents
N-아실펩티드 화합물의 제조방법 Download PDFInfo
- Publication number
- KR840003235A KR840003235A KR1019830000017A KR830000017A KR840003235A KR 840003235 A KR840003235 A KR 840003235A KR 1019830000017 A KR1019830000017 A KR 1019830000017A KR 830000017 A KR830000017 A KR 830000017A KR 840003235 A KR840003235 A KR 840003235A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- compound
- salt
- formula
- carboxy
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims 17
- 108090000765 processed proteins & peptides Proteins 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims 18
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 16
- 150000003839 salts Chemical class 0.000 claims 16
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- 125000003277 amino group Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000006239 protecting group Chemical group 0.000 claims 2
- 125000004423 acyloxy group Chemical group 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 238000006114 decarboxylation reaction Methods 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/12—Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06104—Dipeptides with the first amino acid being acidic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/06034—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms
- C07K5/06052—Val-amino acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06078—Dipeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06086—Dipeptides with the first amino acid being basic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (5)
- 일반식(Ⅱ)의 화합물 또는 카복시그룹에서 그것의 반용성유도체 또는 그의 염을 일반식(Ⅲ)의 화합물 또는 아미노그룹에서 그것의 반용성유도체 또는 그의 염과 반응시키거나, 일반식(Ⅱa)의 화합물 또는 카복시그룹에서 그것의 반응성유도체 또는 그의 염을 일반식(Ⅲa)의 화합물 또는 아이노그룹에서 그것의 반응성유도체 또는 그의 염과 반응시키거나, 일반식(Ia)의 화합물 또는 카복시그룹에서 그것의 반응성유도체 또는 그의 염의 R4a및 /또는 R5a및 /또는 R6a및/또는 (R3a,R4a,R5a,R6a는 후술함)에서 카복시그룹을 에스테르화시켜 일반식(Ib)의 화합물 또는 그의 염을 제조하거나, 일반식(Ib)의 화합물 또는 그의 염의 R3b및 /또는 R4b및/또는 R5b및 /또는 R6b(R3b,R4b,R5b및 R5c는 후술함)에서 에스테르화된 카복시그룹을 탈에스테르화시켜 일반식(Ia)의 화합물 또는 그의 염을 제조하거나, 일반식(Ic)의 화합물 또는 그의 염의 R3c및 /또는 R4c및 /또는 R5c(R3c,R4c및 R|5c는 후술함)에서 아미노보호그룹을 제거시켜 일반식(Id)의 화합물 또는 그의 염을 제조하거나, 일반식(Ⅱ)의 화합물 또는 카복시그룹에서 그것의 반응성유도체 또는 그의 염을 일반식(Ⅲ)'의 화합물 또는 아미노그룹에서 그것의 반응성유도체 또는 그의 염과 반응시켜 일반식(Ic)의 화합물 또는 그의 염을 제조하고생성된 화합물 또는 그의 염의 아미노 보호그룹을 제거시켜 일반식(Id)의 화합물 또는 그의 염을 제조함을 특징으로 하여 일반식(Ⅰ)의 화합물 또는 그것의 약제학적으로 허용할 수 있는 염을 제조하는 방법.
-
-
- 상기식에서 R¹은 수소, 알카노일옥시 또는 알케노일옥시이며, R²는 알킬 또는 알케닐이며, R³및 R⁴각각은 수소, 저급알킬, 히드록시(저급)알킬, 아르(저급)알킬, 에스테르화된 카복시(저급)알킬, 카복시(저급)알킬, 보호된 아미노(저급)알킬 또는 아미노(저급)알킬이고, R5 는 수소, 히드록시(저급)알킬, 보호된(저급)알킬, 아미노(저급)알킬, 카복시(저급)알킬 또는 에스테르화된 카복시(저급)알킬이며, R6는 카복시, 에스테르화된 카복시 또는 설포(저급)알킬이고, A¹,A²및 A³각각은 결합선(bond)이거나 저급알킬렌이며, m 및 n은 각각 0 또는 1의 정수이고,R3a,R4a,R5a 및 R6a 각각은 R3a,R4a및 R5a중의 적어도 하나가 카복시 (저급)알킬이고 및 /또는 R6a가 카복시이라는 조건으로 R3,R4,R5및 R6에서 정의된 바와 같으며,R3b,R4b,R5b및 R6b각각은 R3b,R4b및 R5b중의 적어도 하나가 에스테르화된 카복시(저급)알킬이고 및/또는 R6b가 에스테르화된 카복시이라는 조건으로 R3,R4,R5및 R6에서 정의된 바와 같고 R3c,R4c및R5c중의 적어도 하나가 보호된 아미노(저급)알킬이라는 조건으로 R3,R4및 R5에서 정의된 바와 같으며, R3b ,R 4d및 R5d각각은 R3d,R4d및 R5중의 적어도 하나가 아미노(저급)알킬이라는 조건으로 R3,R4및 R5에서 정의된 바와 같다.
- 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8200212 | 1982-01-05 | ||
GB8200212 | 1982-01-05 | ||
GB8215910 | 1982-06-01 | ||
GB8215910 | 1982-06-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR840003235A true KR840003235A (ko) | 1984-08-20 |
Family
ID=26281659
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019830000017A KR840003235A (ko) | 1982-01-05 | 1983-01-05 | N-아실펩티드 화합물의 제조방법 |
Country Status (11)
Country | Link |
---|---|
US (1) | US4643990A (ko) |
EP (1) | EP0085255B1 (ko) |
KR (1) | KR840003235A (ko) |
AT (1) | ATE22087T1 (ko) |
AU (1) | AU9173582A (ko) |
DE (1) | DE3273256D1 (ko) |
DK (1) | DK579682A (ko) |
ES (1) | ES518771A0 (ko) |
FI (1) | FI824453L (ko) |
GR (1) | GR77060B (ko) |
NO (1) | NO830011L (ko) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU560285B2 (en) * | 1982-07-19 | 1987-04-02 | Imperial Chemical Industries Plc | Heterocyclyl carbonyl sulphonamides |
EP0136879A3 (en) * | 1983-09-30 | 1987-01-07 | Yamanouchi Pharmaceutical Co., Ltd. | Fatty acid derivatives and processes of producing them |
DE3423582A1 (de) * | 1984-06-27 | 1986-01-09 | Bayer Ag, 5090 Leverkusen | Substituierte 5-acylamino-1-phenylpyrazole |
DE3700173A1 (de) * | 1987-01-05 | 1988-07-14 | Hoechst Ag | Verfahren zur herstellung von lipophilen aminosaeurederivaten sowie lipophile aminosaeurederivate |
FR2611205B1 (fr) * | 1987-02-20 | 1990-03-02 | Serbio | Dipeptides, procede de preparation et utilisation dans le dosage de proteases |
US5464825A (en) * | 1991-03-14 | 1995-11-07 | Cornell Research Foundation, Inc. | Raising glutathione equivalent levels using N-acyl glutathione monoesters |
EP0697882A4 (en) * | 1993-05-03 | 1999-04-07 | Cornell Res Foundation Inc | USE OF GLUTATHION DIESTERS |
US5627210A (en) * | 1995-02-06 | 1997-05-06 | Chiron Corporation | Branched combinatorial libraries |
WO2001035982A1 (fr) * | 1999-11-12 | 2001-05-25 | Fujimoto Brothers Co., Ltd. | Compositions medicinales anti-inflammatoires |
WO2005053727A2 (en) * | 2003-11-29 | 2005-06-16 | Sangstat Medical Corporation | Pharmaceutical compositions for bioactive peptide agents |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL279057A (ko) * | 1900-01-01 | |||
NL109134C (ko) * | 1900-01-01 | |||
FR2907E (fr) * | 1903-03-09 | 1904-07-12 | Brunet Loiseau Freres Soc | Interrupteur-vibreur pour bobine d'induction, en vue de l'allumage des moteurs |
FR4629E (fr) * | 1904-04-21 | 1905-09-02 | Jean Victorin Poplawski | Générateur de vapeur à mèche |
FR7648E (fr) * | 1906-02-26 | 1907-09-17 | Georges Clesse | Dispositif de changement de vitesse et de renversement de marche pour voitures automobiles |
NL299197A (ko) * | 1957-07-11 | |||
JPS4211925Y1 (ko) * | 1966-02-09 | 1967-07-05 | ||
DE1593858A1 (de) * | 1967-03-02 | 1970-10-29 | Hoechst Ag | Verfahren zur Herstellung tyrosinhaltiger Peptide und deren Derivaten |
JPS468685Y1 (ko) * | 1967-08-02 | 1971-03-27 | ||
JPS46164Y1 (ko) * | 1967-09-05 | 1971-01-07 | ||
US3893992A (en) * | 1970-11-19 | 1975-07-08 | Rohm & Haas | N-acylated peptides of amino aromatic sulfonic acids and their derivatives |
FR2340983A1 (fr) * | 1976-02-10 | 1977-09-09 | Ugine Kuhlmann | Activateurs pour percomposes |
LU78804A1 (de) * | 1977-12-30 | 1979-07-20 | Byk Gulden Lomberg Chem Fab | N-substituierte w-aminoalkanoyl-w-aminoalkansaeuren,ihre verwendung und verfahren zu ihrer herstellung sowie diese verbindungen enthaltende arzneimittel |
US4205069A (en) * | 1978-09-29 | 1980-05-27 | American Home Products Corporation | Dipeptide narcotic antagonists |
EP0011283B1 (en) * | 1978-11-14 | 1982-07-28 | Fujisawa Pharmaceutical Co., Ltd. | New lactyl tetrapeptide, processes for preparation thereof and pharmaceutical compositions containing it |
US4311640A (en) * | 1978-11-14 | 1982-01-19 | Fujisawa Pharmaceutical Co., Ltd. | Peptide, process for preparation thereof and use thereof |
FR2460288A1 (fr) * | 1979-06-29 | 1981-01-23 | Rhone Poulenc Ind | Nouveaux dipeptides, leur preparation et les medicaments qui les contiennent |
US4436726A (en) * | 1980-12-15 | 1984-03-13 | Fujisawa Pharmaceutical Co., Ltd. | N-Acylpeptide compound, processes for the preparation thereof and the pharmaceutical compositions |
-
1982
- 1982-12-21 AU AU91735/82A patent/AU9173582A/en not_active Abandoned
- 1982-12-22 GR GR70144A patent/GR77060B/el unknown
- 1982-12-23 DE DE8282306928T patent/DE3273256D1/de not_active Expired
- 1982-12-23 US US06/452,827 patent/US4643990A/en not_active Expired - Fee Related
- 1982-12-23 AT AT82306928T patent/ATE22087T1/de active
- 1982-12-23 EP EP82306928A patent/EP0085255B1/en not_active Expired
- 1982-12-27 FI FI824453A patent/FI824453L/fi not_active Application Discontinuation
- 1982-12-30 DK DK579682A patent/DK579682A/da not_active Application Discontinuation
-
1983
- 1983-01-04 ES ES518771A patent/ES518771A0/es active Granted
- 1983-01-04 NO NO830011A patent/NO830011L/no unknown
- 1983-01-05 KR KR1019830000017A patent/KR840003235A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
EP0085255A2 (en) | 1983-08-10 |
ES8500892A1 (es) | 1984-03-01 |
AU9173582A (en) | 1983-07-14 |
US4643990A (en) | 1987-02-17 |
ES518771A0 (es) | 1984-03-01 |
DK579682A (da) | 1983-07-06 |
FI824453L (fi) | 1983-07-06 |
FI824453A0 (fi) | 1982-12-27 |
ATE22087T1 (de) | 1986-09-15 |
NO830011L (no) | 1983-07-06 |
EP0085255A3 (en) | 1984-08-01 |
EP0085255B1 (en) | 1986-09-10 |
DE3273256D1 (en) | 1986-10-16 |
GR77060B (ko) | 1984-09-05 |
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WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |