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Details

Stereochemistry ACHIRAL
Molecular Formula C13H19NOS
Molecular Weight 237.361
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SIB-1553A

SMILES

CN1CCCC1CCSC2=CC=C(O)C=C2

InChI

InChIKey=NVZGJSVPOOILDI-UHFFFAOYSA-N
InChI=1S/C13H19NOS/c1-14-9-2-3-11(14)8-10-16-13-6-4-12(15)5-7-13/h4-7,11,15H,2-3,8-10H2,1H3

HIDE SMILES / InChI

Molecular Formula C13H19NOS
Molecular Weight 237.361
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
SIB-1553A, (+/-)-4-[[2-(1-methyl-2-pyrrolidinyl)ethyl]thio]phenol hydrochloride, a subtype-selective ligand for nicotinic acetylcholine receptors with putative cognitive-enhancing properties: effects on working and reference memory performances in aged rodents and nonhuman primates.
2001 Oct
Effects of (+/-)-4-[[2-(1-methyl-2-pyrrolidinyl)ethyl]thio]phenol hydrochloride (SIB-1553A), a selective ligand for nicotinic acetylcholine receptors, in tests of visual attention and distractibility in rats and monkeys.
2002 Apr
Strain-dependent effects of cognitive enhancers in the mouse.
2008 Apr
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 01:32:23 UTC 2023
Edited
by admin
on Sat Dec 16 01:32:23 UTC 2023
Record UNII
TF4A9P6T8R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SIB-1553A
Common Name English
SIB 1553A
Code English
PHENOL, 4-((2-(1-METHYL-2-PYRROLIDINYL)ETHYL)THIO)-
Systematic Name English
4-(2-(1-METHYLPYRROLIDIN-2-YL)ETHYLSULFANYL)PHENOL
Systematic Name English
Code System Code Type Description
FDA UNII
TF4A9P6T8R
Created by admin on Sat Dec 16 01:32:23 UTC 2023 , Edited by admin on Sat Dec 16 01:32:23 UTC 2023
PRIMARY
EPA CompTox
DTXSID70940803
Created by admin on Sat Dec 16 01:32:23 UTC 2023 , Edited by admin on Sat Dec 16 01:32:23 UTC 2023
PRIMARY
PUBCHEM
5310968
Created by admin on Sat Dec 16 01:32:23 UTC 2023 , Edited by admin on Sat Dec 16 01:32:23 UTC 2023
PRIMARY
WIKIPEDIA
SIB-1553A
Created by admin on Sat Dec 16 01:32:23 UTC 2023 , Edited by admin on Sat Dec 16 01:32:23 UTC 2023
PRIMARY
CAS
191611-76-4
Created by admin on Sat Dec 16 01:32:23 UTC 2023 , Edited by admin on Sat Dec 16 01:32:23 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY