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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H22N2O3
Molecular Weight 338.4003
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of NOLASIBAN

SMILES

CO\N=C1\C[C@@H](CO)N(C1)C(=O)C2=CC=C(C=C2)C3=C(C)C=CC=C3

InChI

InChIKey=OLUJSZLBWZWGJT-HGBKYHTQSA-N
InChI=1S/C20H22N2O3/c1-14-5-3-4-6-19(14)15-7-9-16(10-8-15)20(24)22-12-17(21-25-2)11-18(22)13-23/h3-10,18,23H,11-13H2,1-2H3/b21-17-/t18-/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H22N2O3
Molecular Weight 338.4003
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 1
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 17:27:01 UTC 2023
Edited
by admin
on Fri Dec 15 17:27:01 UTC 2023
Record UNII
3765U8A1EC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NOLASIBAN
INN   WHO-DD  
INN  
Official Name English
nolasiban [INN]
Common Name English
Nolasiban [WHO-DD]
Common Name English
OBE-001
Code English
OBE001
Code English
((2S,4Z)-2-(HYDROXYMETHYL)-4-(METHOXYIMINO)PYRROLIDIN-1-YL)(2'-METHYL(1,1'-BIPHENYL)-4-YL)METHANONE
Systematic Name English
3-PYRROLIDINONE, 5-(HYDROXYMETHYL)-1-((2'-METHYL(1,1'-BIPHENYL)-4-YL)CARBONYL)-, 3-(O-METHYLOXIME), (3Z,5S)-
Systematic Name English
ERLOSIBAN
Common Name English
Code System Code Type Description
SMS_ID
100000176871
Created by admin on Fri Dec 15 17:27:01 UTC 2023 , Edited by admin on Fri Dec 15 17:27:01 UTC 2023
PRIMARY
INN
10026
Created by admin on Fri Dec 15 17:27:01 UTC 2023 , Edited by admin on Fri Dec 15 17:27:01 UTC 2023
PRIMARY
FDA UNII
3765U8A1EC
Created by admin on Fri Dec 15 17:27:01 UTC 2023 , Edited by admin on Fri Dec 15 17:27:01 UTC 2023
PRIMARY
PUBCHEM
52947354
Created by admin on Fri Dec 15 17:27:01 UTC 2023 , Edited by admin on Fri Dec 15 17:27:01 UTC 2023
PRIMARY
NCI_THESAURUS
C166647
Created by admin on Fri Dec 15 17:27:01 UTC 2023 , Edited by admin on Fri Dec 15 17:27:01 UTC 2023
PRIMARY
CAS
1477482-19-1
Created by admin on Fri Dec 15 17:27:01 UTC 2023 , Edited by admin on Fri Dec 15 17:27:01 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
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ACTIVE MOIETY