http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-1804894-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8b9036c33bbe3f4ea428655b76200f7c |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K15-28 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K15-28 |
| filingDate | 1968-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ecda3a149e471566a2a18bd0265b964 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1b7bbf3562347c1ed3c28d4410adb5f |
| publicationDate | 1969-08-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | DE-1804894-A1 |
| titleOfInvention | gamma-alkylthiolysines and processes for their preparation |
| abstract | Cpds. of formula (I) H2N-CH2-CH2- -CH2- -COOH (I) R = lower alkyl Antioxidants; accelerators of healing of wounds and burns; antitumour agents. The specification gives details of tests showing the antitumour activity (compared with mitomycin C) and antioxidant activity of (I). (II) H2N-CH2-CH2- -CH2- -COOH + R-SH (I) (II) can be obtd. by passing Cl2 gas into a strongly acidic soln. of lysine under the action of light. (II) may be used in the form of an acid salt and R-SH may be used in the form of an alkali or alkaline earth salt. The reaction is pref. carried out in a solvent at 20-120 deg.C. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5364881-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5663364-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5476871-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5424447-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5464858-A |
| priorityDate | 1967-10-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 51.