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Details

Stereochemistry RACEMIC
Molecular Formula C19H29NO
Molecular Weight 287.4397
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROCYCLIDINE

SMILES

OC(CCN1CCCC1)(C2CCCCC2)C3=CC=CC=C3

InChI

InChIKey=WYDUSKDSKCASEF-UHFFFAOYSA-N
InChI=1S/C19H29NO/c21-19(17-9-3-1-4-10-17,18-11-5-2-6-12-18)13-16-20-14-7-8-15-20/h1,3-4,9-10,18,21H,2,5-8,11-16H2

HIDE SMILES / InChI
Molecular Formula C19H29NO
Molecular Weight 287.4397
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:04:35 UTC 2023
Edited
by admin
on Fri Dec 15 15:04:35 UTC 2023
Record UNII
C6QE1Q1TKR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROCYCLIDINE
HSDB   INN   MI   VANDF   WHO-DD  
INN  
Official Name English
VAGOSIN
Brand Name English
LERGINE
Brand Name English
(±)-PROCYCLIDINE
Common Name English
PROCYCLIDINE [VANDF]
Common Name English
ELORINE
Brand Name English
NSC-169103
Code English
Procyclidine [WHO-DD]
Common Name English
PROCYCLIDINE [MI]
Common Name English
1-CYCLOHEXYL-1-PHENYL-3-(1-PYRROLIDINYL)-1-PROPANOL
Systematic Name English
TRICOLOID
Brand Name English
KEMADRINE
Brand Name English
PROCYCLIDINE [HSDB]
Common Name English
procyclidine [INN]
Common Name English
Classification Tree Code System Code
WHO-VATC QN04AA04
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
NDF-RT N0000175370
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
NCI_THESAURUS C29704
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
WHO-ATC N04AA04
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
NDF-RT N0000175574
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
Code System Code Type Description
WIKIPEDIA
PROCYCLIDINE
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
DRUG CENTRAL
2276
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
NCI_THESAURUS
C73270
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
ECHA (EC/EINECS)
201-023-0
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
NSC
169103
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
MERCK INDEX
m9151
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY Merck Index
PUBCHEM
4919
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
MESH
D011352
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
INN
224
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
RXCUI
8718
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY RxNorm
SMS_ID
100000081116
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
ChEMBL
CHEMBL86715
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
CAS
56172-67-9
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
SUPERSEDED
CAS
107661-03-0
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
SUPERSEDED
CAS
77-37-2
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
FDA UNII
C6QE1Q1TKR
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
EPA CompTox
DTXSID2023515
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
CHEBI
8448
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
HSDB
7678
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
EVMPD
SUB10064MIG
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
IUPHAR
7280
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
DRUG BANK
DB00387
Created by admin on Fri Dec 15 15:04:35 UTC 2023 , Edited by admin on Fri Dec 15 15:04:35 UTC 2023
PRIMARY
Related Record Type Details
Structure of PROCYCLIDINE HYDROCHLORIDE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of PROCYCLIDINE
ACTIVE MOIETY
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