U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS
Allylprodine (Ro 2-7113) is an opioid analgesic. It is stereoselective, with one isomer being much more active. Allylprodine is included in Schedule I of the US Controlled Substances Act 1970 as a Narcotic with ACSCN 9602 and a 2014 annual aggregate manufacturing quota of 2 grammes.

Approval Year

PubMed

PubMed

TitleDatePubMed
Analgesic activity and toxicity of Ro 2-7113.
1957 Jan 1
Stereochemical studies on medicinal agents. 19. X-ray crystal structures of two (+/-)-allylprodine diastereomers. The role of the allyl group in conferring high stereoselectivity and potency at analgetic receptors.
1976 Jan
Conformation of 2,9-dimethyl-3'-hydroxy-5-phenyl-6,7-genzomorphan and its relation to other analgetics and enkephalin.
1978 Jul
Allylprodine analogues as receptor probes. Evidence that phenolic and nonphenolic ligands interact with different subsites on identical opioid receptors.
1981 Jul
Patents
Substance Class Mixture
Created
by admin
on Fri Dec 15 16:05:44 GMT 2023
Edited
by admin
on Fri Dec 15 16:05:44 GMT 2023
Record UNII
4343OEZ18O
Record Status Validated (UNII)
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Name Type Language
ALLYLPRODINE
INN   MI  
INN  
Official Name English
3-ALLYL-1-METHYL-4-PHENYL-4-PROPIONYLOXYPIPERIDINE
Common Name English
ACSCN-9602
Code English
ALPERIDINE
Common Name English
allylprodine [INN]
Common Name English
DEA NO. 9602
Code English
NIH-7440
Code English
IDS-NA-007
Code English
ALLYLPRODINE [MI]
Common Name English
RO 2-7113
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C241
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
DEA NO. 9602
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
Code System Code Type Description
INN
891
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
PRIMARY
EPA CompTox
DTXSID80865210
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
PRIMARY
ChEMBL
CHEMBL2103995
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
PRIMARY
MERCK INDEX
m1557
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C72102
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
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DRUG BANK
DB01542
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
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PUBCHEM
32938
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
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FDA UNII
4343OEZ18O
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
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WIKIPEDIA
ALLYLPRODINE
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
PRIMARY
CAS
25384-17-2
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
PRIMARY
EVMPD
SUB05340MIG
Created by admin on Fri Dec 15 16:05:44 GMT 2023 , Edited by admin on Fri Dec 15 16:05:44 GMT 2023
PRIMARY
All of the following components must be present:
Related Record Type Details
SALT/SOLVATE -> PARENT
APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)
Related Record Type Details
ACTIVE MOIETY
Definition References