Biologically active peptides
US4350627A · kind A · utility
Assignee
Inventors
Key dates
| Filing date | Dec 3, 1980 |
| Grant date | Sep 21, 1982 |
| Priority date | — |
| Expiry date | Dec 3, 2000 |
Classification
- Technology area (CPC Y)Emerging Cross-Sectional Technologies
- CPC primaryY02P20/55
- WIPO fieldPharmaceuticals
- WIPO sectorChemistry
Abstract
There is disclosed biologically active peptides of the formula ##STR1## where X is a hydrogen atom, an N-terminus protecting group (any of an acyl-type protecting group, an aromatic urethane-type protecting group, an alkyl-type protecting group, or an alkyl urethane type protecting group), or a residue of a natural L-amino acid or a dipeptide formed of two natural L-amino acids, wherein the free amino group may be replaced by any of the foregoing N-terminus protecting groups; PA0 Y is a hydrogen atom or a protecting group for the phenolic hydroxyl group of tyrosine; PA0 A is a D-amino acid residue with a lower (thio) alkyl side chain; PA0 B is a neutral L-amino acid residue, a glycine residue, or an N-methyl amino acid residue; PA0 C is a direct bond or an amino acid or di-or tripeptide residue; and PA0 W is OH, OR, NH.sub.2, NHR, N(R).sub.2, NH-NH.sub.2, where R is an alkyl, cycloalkyl or aralkyl group of 1 to 7 carbon atoms or NHNHR' where R' is a hydrogen atom, linear or branched alkyl, cycloalkyl; alkenyl, a linear or branched or cyclic aliphatic urethane-type group, an aromatic urethane-type group normally used in polypeptide chemistry, a residue of an .alpha.-amino; .alpha.-i…
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.