CARMANTADINE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C14H21NO2
Molecular Weight	235.322
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CARMANTADINE

Structure Search

SMILES

OC(=O)C1CCN1C23CC4CC(CC(C4)C2)C3

InChI

InChIKey=VPBLOJFGPORKQA-UHFFFAOYSA-N

InChI=1S/C14H21NO2/c16-13(17)12-1-2-15(12)14-6-9-3-10(7-14)5-11(4-9)8-14/h9-12H,1-8H2,(H,16,17)

HIDE SMILES / InChI

Description
Sources: https://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=0&ND=3&adjacent=true&locale=en_EP&FT=D&date=19720518&CC=DE&NR=2156499A1&KC=A1 | http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=3917840.PN.&OS=PN/3917840&RS=PN/3917840

Adamantyl is adamantly derivative patented by pharmaceutical company Scherico Ltd. as spasmolytic for treatment spasms associated with Parkinson's disease.

Originator

Approval Year

Patents

Patents

Name

Type

Language

CARMANTADINE

Official Name

English

SCH-15427

Code

English

2-AZETIDINECARBOXYLIC ACID, 1-TRICYCLO(3.3.1.1(SUP 3,7))DEC-1-YL-

Common Name

English

CARMANTADINE [USAN]

Common Name

English

SCH 15427

Code

English

1-(1-Adamantyl)-2-azetidinecarboxylic acid

Systematic Name

English

carmantadine [INN]

Common Name

English

NSC-172618

Code

English

Classification Tree Code System Code

NCI_THESAURUS

C38149

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

Code System Code Type Description

EVMPD

SUB06632MIG

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

PRIMARY

SMS_ID

100000084615

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

PRIMARY

NCI_THESAURUS

C96720

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

PRIMARY

FDA UNII

6EK3N87MMH

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

PRIMARY

CAS

38081-67-3

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

PRIMARY

NSC

172618

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

PRIMARY

ECHA (EC/EINECS)

253-774-9

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

PRIMARY

PUBCHEM

37906

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

PRIMARY

ChEMBL

CHEMBL2106463

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

PRIMARY

EPA CompTox

DTXSID00865898

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

PRIMARY

INN

3523

Created by admin on Sat Dec 16 17:15:53 GMT 2023 , Edited by admin on Sat Dec 16 17:15:53 GMT 2023

PRIMARY

ACTIVE MOIETY


					6EK3N87MMH