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Details

Stereochemistry RACEMIC
Molecular Formula C21H30N4O3S
Molecular Weight 418.553
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLIBUTIMINE

SMILES

CCCC(=O)NCCC1=CC=C(C=C1)S(=O)(=O)N2CCN(C3CCC=CC3)C2=N

InChI

InChIKey=NFGPIRVQFCRUFC-UHFFFAOYSA-N
InChI=1S/C21H30N4O3S/c1-2-6-20(26)23-14-13-17-9-11-19(12-10-17)29(27,28)25-16-15-24(21(25)22)18-7-4-3-5-8-18/h3-4,9-12,18,22H,2,5-8,13-16H2,1H3,(H,23,26)

HIDE SMILES / InChI

Molecular Formula C21H30N4O3S
Molecular Weight 418.553
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:57:22 GMT 2023
Edited
by admin
on Fri Dec 15 16:57:22 GMT 2023
Record UNII
NZB6U6187J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLIBUTIMINE
INN  
INN  
Official Name English
GP 51084
Code English
N-(P-((3-(3-CYCLOHEXEN-1-YL)-2-IMINO-1-IMIDAZOLIDINYL)SULFONYL)PHENETHYL)BUTYRAMIDE
Common Name English
glibutimine [INN]
Common Name English
GP-51084
Code English
Classification Tree Code System Code
NCI_THESAURUS C29701
Created by admin on Fri Dec 15 16:57:22 GMT 2023 , Edited by admin on Fri Dec 15 16:57:22 GMT 2023
Code System Code Type Description
EVMPD
SUB07918MIG
Created by admin on Fri Dec 15 16:57:22 GMT 2023 , Edited by admin on Fri Dec 15 16:57:22 GMT 2023
PRIMARY
CAS
25859-76-1
Created by admin on Fri Dec 15 16:57:22 GMT 2023 , Edited by admin on Fri Dec 15 16:57:22 GMT 2023
PRIMARY
PUBCHEM
219107
Created by admin on Fri Dec 15 16:57:22 GMT 2023 , Edited by admin on Fri Dec 15 16:57:22 GMT 2023
PRIMARY
SMS_ID
100000084219
Created by admin on Fri Dec 15 16:57:22 GMT 2023 , Edited by admin on Fri Dec 15 16:57:22 GMT 2023
PRIMARY
INN
3550
Created by admin on Fri Dec 15 16:57:22 GMT 2023 , Edited by admin on Fri Dec 15 16:57:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID80865255
Created by admin on Fri Dec 15 16:57:22 GMT 2023 , Edited by admin on Fri Dec 15 16:57:22 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104717
Created by admin on Fri Dec 15 16:57:22 GMT 2023 , Edited by admin on Fri Dec 15 16:57:22 GMT 2023
PRIMARY
FDA UNII
NZB6U6187J
Created by admin on Fri Dec 15 16:57:22 GMT 2023 , Edited by admin on Fri Dec 15 16:57:22 GMT 2023
PRIMARY
NCI_THESAURUS
C83730
Created by admin on Fri Dec 15 16:57:22 GMT 2023 , Edited by admin on Fri Dec 15 16:57:22 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY