U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C20H23N3O2
Molecular Weight 337.4155
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENSERINE

SMILES

[H][C@]12N(C)CC[C@@]1(C)C3=C(C=CC(OC(=O)NC4=CC=CC=C4)=C3)N2C

InChI

InChIKey=PBHFNBQPZCRWQP-QUCCMNQESA-N
InChI=1S/C20H23N3O2/c1-20-11-12-22(2)18(20)23(3)17-10-9-15(13-16(17)20)25-19(24)21-14-7-5-4-6-8-14/h4-10,13,18H,11-12H2,1-3H3,(H,21,24)/t18-,20+/m1/s1

HIDE SMILES / InChI

Molecular Formula C20H23N3O2
Molecular Weight 337.4155
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
The cholinesterase inhibitor, phenserine, improves Morris water maze performance of scopolamine-treated rats.
2005 Jan 21
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:34:18 GMT 2023
Edited
by admin
on Sat Dec 16 09:34:18 GMT 2023
Record UNII
SUE285UG3S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENSERINE
MI  
Common Name English
PHENSERINE [MI]
Common Name English
BUNTANETAP, (-)-
Common Name English
PYRROLO(2,3-B)INDOL-5-OL, 1,2,3,3A,8,8A-HEXAHYDRO-1,3A,8-TRIMETHYL-, 5-(N-PHENYLCARBAMATE), (3AS,8AR)-
Common Name English
(-)-ESEROLINE PHENYLCARBAMATE
Common Name English
(-)-PHENSERINE
Common Name English
Code System Code Type Description
WIKIPEDIA
Phenserine
Created by admin on Sat Dec 16 09:34:19 GMT 2023 , Edited by admin on Sat Dec 16 09:34:19 GMT 2023
PRIMARY
PUBCHEM
192706
Created by admin on Sat Dec 16 09:34:19 GMT 2023 , Edited by admin on Sat Dec 16 09:34:19 GMT 2023
PRIMARY
MERCK INDEX
m8642
Created by admin on Sat Dec 16 09:34:19 GMT 2023 , Edited by admin on Sat Dec 16 09:34:19 GMT 2023
PRIMARY Merck Index
DRUG BANK
DB04892
Created by admin on Sat Dec 16 09:34:19 GMT 2023 , Edited by admin on Sat Dec 16 09:34:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID00906018
Created by admin on Sat Dec 16 09:34:19 GMT 2023 , Edited by admin on Sat Dec 16 09:34:19 GMT 2023
PRIMARY
FDA UNII
SUE285UG3S
Created by admin on Sat Dec 16 09:34:19 GMT 2023 , Edited by admin on Sat Dec 16 09:34:19 GMT 2023
PRIMARY
CAS
101246-66-6
Created by admin on Sat Dec 16 09:34:19 GMT 2023 , Edited by admin on Sat Dec 16 09:34:19 GMT 2023
PRIMARY