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

Details

Stereochemistry ABSOLUTE
Molecular Formula C19H20N4O2
Molecular Weight 336.3877
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VAROGLUTAMSTAT

SMILES

CCCOC1=CC=C(C=C1)[C@H]2CNC(=O)N2C3=CC4=C(NC=N4)C=C3

InChI

InChIKey=XHIKZWOEFZENIX-GOSISDBHSA-N
InChI=1S/C19H20N4O2/c1-2-9-25-15-6-3-13(4-7-15)18-11-20-19(24)23(18)14-5-8-16-17(10-14)22-12-21-16/h3-8,10,12,18H,2,9,11H2,1H3,(H,20,24)(H,21,22)/t18-/m1/s1

HIDE SMILES / InChI

Molecular Formula C19H20N4O2
Molecular Weight 336.3877
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:54:29 GMT 2023
Edited
by admin
on Sat Dec 16 16:54:29 GMT 2023
Record UNII
E3DSH8LL4L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VAROGLUTAMSTAT
INN  
Official Name English
(5S)-1-(1H-BENZIMIDAZOL-5-YL)-5-(4- PROPOXYPHENYL)IMIDAZOLIDIN-2-ONE
Systematic Name English
2-IMIDAZOLIDINONE, 1-(1H-BENZIMIDAZOL-6-YL)-5-(4-PROPOXYPHENYL)-, (5S)-
Systematic Name English
varoglutamstat [INN]
Common Name English
PQ-912
Code English
PQ912
Code English
(S)-1-(1H-BENZIMIDAZOL-5-YL)-5-(4-PROPOXYPHENYL)IMIDAZOLIDIN-2-ONE
Systematic Name English
Code System Code Type Description
PUBCHEM
51030870
Created by admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
PRIMARY
FDA UNII
E3DSH8LL4L
Created by admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
PRIMARY
NCI_THESAURUS
C179133
Created by admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
PRIMARY
SMS_ID
300000006000
Created by admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
PRIMARY
CAS
1276021-65-8
Created by admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
PRIMARY
CLINICAL_TRIALS.GOV
NCT03919162
Created by admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
PRIMARY
INN
11664
Created by admin on Sat Dec 16 16:54:30 GMT 2023 , Edited by admin on Sat Dec 16 16:54:30 GMT 2023
PRIMARY INN
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Inhibit conversion of N-terminal Q to pE. formation of pE was prevented by inhibiting isoQC, CCL2 was more prone to N-terminal degradation, which resulted in less functional CCL2 activity. This had the net effect of decreasing monocyte infiltration in vivo, resulting in decreased lung inflammation,
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IN-VITRO
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