KR830007518A - 약리적 활성 펩티드의 제조방법 - Google Patents
약리적 활성 펩티드의 제조방법 Download PDFInfo
- Publication number
- KR830007518A KR830007518A KR1019810003971A KR810003971A KR830007518A KR 830007518 A KR830007518 A KR 830007518A KR 1019810003971 A KR1019810003971 A KR 1019810003971A KR 810003971 A KR810003971 A KR 810003971A KR 830007518 A KR830007518 A KR 830007518A
- Authority
- KR
- South Korea
- Prior art keywords
- alanyl
- methyl
- tyrosyl
- ethyl
- glycyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 9
- 108090000765 processed proteins & peptides Proteins 0.000 title 1
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims 18
- -1 2-fluoromethyl Chemical group 0.000 claims 7
- 238000004519 manufacturing process Methods 0.000 claims 6
- NHTGHBARYWONDQ-JTQLQIEISA-N L-α-methyl-Tyrosine Chemical compound OC(=O)[C@](N)(C)CC1=CC=C(O)C=C1 NHTGHBARYWONDQ-JTQLQIEISA-N 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- UXUOYMBRDYAQAR-QMMMGPOBSA-N (2S)-2-(bromoamino)-3-phenylpropanamide Chemical compound BrN[C@@H](CC1=CC=CC=C1)C(=O)N UXUOYMBRDYAQAR-QMMMGPOBSA-N 0.000 claims 2
- XCKUCSJNPYTMAE-QMMMGPOBSA-N (2s)-2-(chloroamino)-3-phenylpropanoic acid Chemical compound OC(=O)[C@@H](NCl)CC1=CC=CC=C1 XCKUCSJNPYTMAE-QMMMGPOBSA-N 0.000 claims 2
- HUOYGRNYKOUAFE-QMMMGPOBSA-N (2s)-2-(iodoamino)-3-phenylpropanoic acid Chemical compound OC(=O)[C@@H](NI)CC1=CC=CC=C1 HUOYGRNYKOUAFE-QMMMGPOBSA-N 0.000 claims 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 2
- ULBLZIPFWGIOJF-QMMMGPOBSA-N (2s)-2-(bromoamino)-3-phenylpropanoic acid Chemical compound OC(=O)[C@@H](NBr)CC1=CC=CC=C1 ULBLZIPFWGIOJF-QMMMGPOBSA-N 0.000 claims 1
- PYRTVXRJEYPGJX-VIFPVBQESA-N (2s)-2-(methylamino)-3-phenylpropanamide Chemical compound CN[C@H](C(N)=O)CC1=CC=CC=C1 PYRTVXRJEYPGJX-VIFPVBQESA-N 0.000 claims 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 1
- 150000008574 D-amino acids Chemical group 0.000 claims 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 230000000903 blocking effect Effects 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000006351 ethylthiomethyl group Chemical group [H]C([H])([H])C([H])([H])SC([H])([H])* 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 231100000252 nontoxic Toxicity 0.000 claims 1
- 230000003000 nontoxic effect Effects 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 claims 1
- 210000003708 urethra Anatomy 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/06—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
-
- 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
- C07K5/10—Tetrapeptides
- C07K5/1027—Tetrapeptides containing heteroatoms different from O, S, or N
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
-
- 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
- C07K5/10—Tetrapeptides
- C07K5/1002—Tetrapeptides with the first amino acid being neutral
- C07K5/1016—Tetrapeptides with the first amino acid being neutral and aromatic or cycloaliphatic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Analytical Chemistry (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/198,900 US4322340A (en) | 1980-10-20 | 1980-10-20 | Pharmacologically active peptides |
US198,900 | 1980-10-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR830007518A true KR830007518A (ko) | 1983-10-21 |
Family
ID=22735344
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019810003971A KR830007518A (ko) | 1980-10-20 | 1981-10-20 | 약리적 활성 펩티드의 제조방법 |
Country Status (27)
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE16495T1 (de) * | 1981-06-22 | 1985-11-15 | Ici Plc | Peptide und pseudopeptide, die zwei substituenten am n-terminus aufweisen. |
US4448717A (en) * | 1982-11-12 | 1984-05-15 | Eli Lilly And Company | Pharmacologically active peptides |
US4473497A (en) * | 1983-03-07 | 1984-09-25 | Eli Lilly And Company | Pharmacologically active peptides |
DK134784A (da) * | 1983-03-07 | 1984-09-08 | Lilly Co Eli | Farmakologisk virksomme tripeptid-derivater og fremgangsmaade til fremstilling deraf |
US4510082A (en) * | 1983-03-07 | 1985-04-09 | Eli Lilly And Company | Pharmacologically active peptides |
US4495178A (en) * | 1983-10-06 | 1985-01-22 | G. D. Searle & Co. | Enkephalin analogs |
JPH0449298A (ja) * | 1990-06-19 | 1992-02-18 | Univ New York State | 新規なエンケファリン誘導体および鎮痛剤 |
US5209930A (en) * | 1990-12-10 | 1993-05-11 | Rohm And Haas Company | Preparation and use of n-iodopropargyl oxycarbonyl amino acid esters and derivatives as antimicrobial agents |
US5952465A (en) * | 1993-04-23 | 1999-09-14 | Virginia Commonwealth University | Polypeptides that include conformation-constraining groups which flank a protein-protein interaction site |
US5928896A (en) * | 1993-04-23 | 1999-07-27 | Virginia Commonwealth University | Polypeptides that include conformation-constraining groups which flank a protein--protein interaction site |
CA2161108A1 (en) * | 1993-04-23 | 1994-11-10 | Herbert J. Evans | Polypeptides that include conformation-constraining groups which flank a protein-protein interaction site |
US5965698A (en) * | 1993-04-23 | 1999-10-12 | Virginia Commonwealth University | Polypeptides that include conformation-constraining groups which flank a protein--protein interaction site |
US6258550B1 (en) | 1993-04-23 | 2001-07-10 | Virginia Commonwealth University | Polypeptides that include conformation-constraining groups which flank a protein-protein interaction site |
US6084066A (en) * | 1993-10-29 | 2000-07-04 | Virginia Commonwealth University | Polypetides that include conformation-constraining groups which flank a protein-protein interaction site |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1577115A (en) * | 1976-07-27 | 1980-10-22 | Reckitt & Colmann Prod Ltd | Container closure units |
CH619686A5 (en) * | 1976-02-02 | 1980-10-15 | Sandoz Ag | Process for the preparation of novel peptides or peptide derivatives |
DK28377A (da) * | 1976-02-02 | 1977-08-03 | Sandoz Ag | Fremgangsmade til fremstilling af polypeptidderivater |
US4264491A (en) * | 1977-10-03 | 1981-04-28 | Eli Lilly And Company | Analgesic compounds |
US4265808A (en) * | 1979-12-17 | 1981-05-05 | Eli Lilly And Company | Pharmacologically active peptides |
-
1980
- 1980-10-20 US US06/198,900 patent/US4322340A/en not_active Expired - Lifetime
-
1981
- 1981-10-13 ZA ZA817063A patent/ZA817063B/xx unknown
- 1981-10-13 PH PH26344A patent/PH17006A/en unknown
- 1981-10-13 GR GR66269A patent/GR75342B/el unknown
- 1981-10-13 NZ NZ198628A patent/NZ198628A/en unknown
- 1981-10-13 CA CA000387762A patent/CA1187871A/en not_active Expired
- 1981-10-14 RO RO105558A patent/RO83301B/ro unknown
- 1981-10-14 FI FI813198A patent/FI813198L/fi not_active Application Discontinuation
- 1981-10-16 ES ES506316A patent/ES506316A0/es active Granted
- 1981-10-16 BG BG053871A patent/BG36928A3/xx unknown
- 1981-10-16 HU HU812999A patent/HU185320B/hu unknown
- 1981-10-16 IE IE2442/81A patent/IE52186B1/en unknown
- 1981-10-19 YU YU02490/81A patent/YU249081A/xx unknown
- 1981-10-19 IL IL64083A patent/IL64083A/xx unknown
- 1981-10-19 AR AR287129A patent/AR230046A1/es active
- 1981-10-19 DD DD81234209A patent/DD200798A5/de unknown
- 1981-10-19 SU SU813345906A patent/SU1082319A3/ru active
- 1981-10-19 PL PL1981233498A patent/PL131155B1/pl unknown
- 1981-10-19 GB GB8131402A patent/GB2085893B/en not_active Expired
- 1981-10-19 DE DE8181304859T patent/DE3162823D1/de not_active Expired
- 1981-10-19 DK DK461481A patent/DK461481A/da not_active Application Discontinuation
- 1981-10-19 AT AT81304859T patent/ATE6777T1/de not_active IP Right Cessation
- 1981-10-19 AU AU76574/81A patent/AU547221B2/en not_active Expired - Fee Related
- 1981-10-19 EP EP81304859A patent/EP0050502B1/en not_active Expired
- 1981-10-19 PT PT73839A patent/PT73839B/pt unknown
- 1981-10-20 JP JP56169398A patent/JPS57108052A/ja active Pending
- 1981-10-20 KR KR1019810003971A patent/KR830007518A/ko unknown
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