GB1304074A - - Google Patents
Info
- Publication number
- GB1304074A GB1304074A GB2129570A GB2129570A GB1304074A GB 1304074 A GB1304074 A GB 1304074A GB 2129570 A GB2129570 A GB 2129570A GB 2129570 A GB2129570 A GB 2129570A GB 1304074 A GB1304074 A GB 1304074A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phe
- met
- trp
- asp
- gly
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 108010069205 aspartyl-phenylalanine Proteins 0.000 abstract 7
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 7
- 108010068265 aspartyltyrosine Proteins 0.000 abstract 5
- XMBSYZWANAQXEV-UHFFFAOYSA-N N-alpha-L-glutamyl-L-phenylalanine Natural products OC(=O)CCC(N)C(=O)NC(C(O)=O)CC1=CC=CC=C1 XMBSYZWANAQXEV-UHFFFAOYSA-N 0.000 abstract 4
- 108010008671 glycyl-tryptophyl-methionine Proteins 0.000 abstract 3
- -1 α-aminobutyryl Chemical group 0.000 abstract 3
- WXYGVKADAIJGHB-ZDUSSCGKSA-N (2s)-3-(1h-indol-2-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid Chemical compound C1=CC=C2NC(C[C@H](NC(=O)OC(C)(C)C)C(O)=O)=CC2=C1 WXYGVKADAIJGHB-ZDUSSCGKSA-N 0.000 abstract 2
- MDXGYYOJGPFFJL-QMMMGPOBSA-N N(alpha)-t-butoxycarbonyl-L-leucine Chemical compound CC(C)C[C@@H](C(O)=O)NC(=O)OC(C)(C)C MDXGYYOJGPFFJL-QMMMGPOBSA-N 0.000 abstract 2
- AJHCSUXXECOXOY-UHFFFAOYSA-N N-glycyl-L-tryptophan Natural products C1=CC=C2C(CC(NC(=O)CN)C(O)=O)=CNC2=C1 AJHCSUXXECOXOY-UHFFFAOYSA-N 0.000 abstract 2
- 125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 abstract 2
- 108010011559 alanylphenylalanine Proteins 0.000 abstract 2
- 108010070783 alanyltyrosine Proteins 0.000 abstract 2
- 108010073383 cholecystokinin hexapeptide Proteins 0.000 abstract 2
- 108010054346 cholecystokinin pentapeptide Proteins 0.000 abstract 2
- 108010050848 glycylleucine Proteins 0.000 abstract 2
- 108090000765 processed proteins & peptides Proteins 0.000 abstract 2
- VAMUDINSUBSTNS-AAEUAGOBSA-N (2s)-2-[[(2s)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]amino]-3-phenylpropanoic acid Chemical compound CC(C)(C)OC(=O)N[C@@H](C)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 VAMUDINSUBSTNS-AAEUAGOBSA-N 0.000 abstract 1
- VNEOHNUYPRAJMX-AMEOFWRWSA-N (3s)-3-[[(2s)-2-[[(2s)-2-amino-3-(1h-indol-3-yl)propanoyl]amino]-4-methylpentanoyl]amino]-4-[[(2s)-1-(butoxycarbonylamino)-1-oxo-3-phenylpropan-2-yl]amino]-4-oxobutanoic acid Chemical compound C([C@@H](C(=O)NC(=O)OCCCC)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC=1C2=CC=CC=C2NC=1)C1=CC=CC=C1 VNEOHNUYPRAJMX-AMEOFWRWSA-N 0.000 abstract 1
- KPAUJSXYKQJSSO-UWVGGRQHSA-N (3s)-4-[[(2s)-1-amino-1-oxo-3-phenylpropan-2-yl]amino]-3-azaniumyl-4-oxobutanoate Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(N)=O)CC1=CC=CC=C1 KPAUJSXYKQJSSO-UWVGGRQHSA-N 0.000 abstract 1
- 125000000349 (Z)-3-carboxyprop-2-enoyl group Chemical group O=C([*])/C([H])=C([H])\C(O[H])=O 0.000 abstract 1
- OBSIQMZKFXFYLV-UHFFFAOYSA-N 2-amino-3-phenylpropanamide Chemical compound NC(=O)C(N)CC1=CC=CC=C1 OBSIQMZKFXFYLV-UHFFFAOYSA-N 0.000 abstract 1
- 101100505161 Caenorhabditis elegans mel-32 gene Proteins 0.000 abstract 1
- VJMAITQRABEEKP-UHFFFAOYSA-N [6-(phenylmethoxymethyl)-1,4-dioxan-2-yl]methyl acetate Chemical compound O1C(COC(=O)C)COCC1COCC1=CC=CC=C1 VJMAITQRABEEKP-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 108700041425 butyloxycarbonyl-tryptophyl-leucyl-aspartyl-phenylalaninamide Proteins 0.000 abstract 1
- 125000000291 glutamic acid group Chemical group N[C@@H](CCC(O)=O)C(=O)* 0.000 abstract 1
- 108010084389 glycyltryptophan Proteins 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000001909 leucine group Chemical group [H]N(*)C(C(*)=O)C([H])([H])C(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
- 108010005942 methionylglycine Proteins 0.000 abstract 1
- 102000004196 processed proteins & peptides Human genes 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- QIQCZROILFZKAT-UHFFFAOYSA-N tetracarbon dioxide Chemical group O=C=C=C=C=O QIQCZROILFZKAT-UHFFFAOYSA-N 0.000 abstract 1
- 108010080629 tryptophan-leucine Proteins 0.000 abstract 1
Classifications
-
- 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
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/081—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing O or S as heteroatoms, e.g. Cys, Ser
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/595—Gastrins; Cholecystokinins [CCK]
-
- 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)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Gastroenterology & Hepatology (AREA)
- Zoology (AREA)
- Toxicology (AREA)
- Endocrinology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US82836869A | 1969-05-27 | 1969-05-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1304074A true GB1304074A (enrdf_load_stackoverflow) | 1973-01-24 |
Family
ID=25251606
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2129570A Expired GB1304074A (enrdf_load_stackoverflow) | 1969-05-27 | 1970-05-04 |
Country Status (6)
| Country | Link |
|---|---|
| BR (1) | BR6915336D0 (enrdf_load_stackoverflow) |
| CA (1) | CA919658A (enrdf_load_stackoverflow) |
| CH (1) | CH515893A (enrdf_load_stackoverflow) |
| DE (1) | DE2022623A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2051561B1 (enrdf_load_stackoverflow) |
| GB (1) | GB1304074A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2751026A1 (de) | 1976-11-29 | 1978-06-01 | Akad Wissenschaften Ddr | Verfahren zur herstellung von peptiden, die tyrosinsulfat enthalten |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0019115B1 (de) * | 1979-04-30 | 1983-01-12 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Pankreozymin-Cholezystokinin aktive Peptide, Verfahren zu ihrer Herstellung und sie enthaltende Arzneimittel |
| DK489683A (da) * | 1982-10-27 | 1984-04-28 | Amano Pharma Co Ltd | Fremgangsmaade til fremstilling af peptider |
| ES2069272T3 (es) * | 1989-11-27 | 1995-05-01 | Fisons Corp | Hexapeptidos con grupos esteres sulfato. |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3472832A (en) * | 1966-08-09 | 1969-10-14 | Farmaceutici Italia | Peptides related to caerulein |
-
1969
- 1969-12-19 BR BR21533669A patent/BR6915336D0/pt unknown
-
1970
- 1970-04-30 CA CA081527A patent/CA919658A/en not_active Expired
- 1970-05-04 GB GB2129570A patent/GB1304074A/en not_active Expired
- 1970-05-08 DE DE19702022623 patent/DE2022623A1/de active Pending
- 1970-05-26 FR FR7019205A patent/FR2051561B1/fr not_active Expired
- 1970-05-27 CH CH789870A patent/CH515893A/fr not_active IP Right Cessation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2751026A1 (de) | 1976-11-29 | 1978-06-01 | Akad Wissenschaften Ddr | Verfahren zur herstellung von peptiden, die tyrosinsulfat enthalten |
Also Published As
| Publication number | Publication date |
|---|---|
| BR6915336D0 (pt) | 1973-03-13 |
| CH515893A (fr) | 1971-11-30 |
| DE2022623A1 (de) | 1970-12-03 |
| FR2051561B1 (enrdf_load_stackoverflow) | 1974-08-30 |
| FR2051561A1 (enrdf_load_stackoverflow) | 1971-04-09 |
| CA919658A (en) | 1973-01-23 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |