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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H24N4O6
Molecular Weight 452.4599
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MERIMEPODIB

SMILES

COC1=C(C=CC(NC(=O)NC2=CC=CC(CNC(=O)O[C@H]3CCOC3)=C2)=C1)C4=CN=CO4

InChI

InChIKey=JBPUGFODGPKTDW-SFHVURJKSA-N
InChI=1S/C23H24N4O6/c1-30-20-10-17(5-6-19(20)21-12-24-14-32-21)27-22(28)26-16-4-2-3-15(9-16)11-25-23(29)33-18-7-8-31-13-18/h2-6,9-10,12,14,18H,7-8,11,13H2,1H3,(H,25,29)(H2,26,27,28)/t18-/m0/s1

HIDE SMILES / InChI
Molecular Formula C23H24N4O6
Molecular Weight 452.4599
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:30:06 UTC 2023
Edited
by admin
on Fri Dec 15 16:30:06 UTC 2023
Record UNII
2ZL2BA06FU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MERIMEPODIB
INN   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
MERIMEPODIB [USAN]
Common Name English
VX-497
Code English
CARBAMIC ACID, ((3-((((3-METHOXY-4-(5-OXAZOLYL)PHENYL)AMINO)CARBONYL)AMINO)PHENYL)METHYL)-, (3S)-TETRAHYDRO-3-FURANYL ESTER
Common Name English
(S)-TETRAHYDRO-3-FURYL (M-(3-(3-METHOXY-4-(5-OXAZOLYL)PHENYL)UREIDO)BENZYL)CARBAMATE
Systematic Name English
Merimepodib [WHO-DD]
Common Name English
VI-21,497
Code English
merimepodib [INN]
Common Name English
VI-21497
Code English
MERIMEPODIB [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C281
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
NCI_THESAURUS C2087
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C66097
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
MERCK INDEX
m7238
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY Merck Index
USAN
MM-03
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
WIKIPEDIA
Merimepodib
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
ChEMBL
CHEMBL304087
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
EPA CompTox
DTXSID70173639
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
CAS
198821-22-6
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
FDA UNII
2ZL2BA06FU
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
EVMPD
SUB34886
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
SMS_ID
100000128133
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
DRUG BANK
DB04862
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
PUBCHEM
153241
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
INN
8123
Created by admin on Fri Dec 15 16:30:06 UTC 2023 , Edited by admin on Fri Dec 15 16:30:06 UTC 2023
PRIMARY
Related Record Type Details
ZIKA VIRUS
TARGET ORGANISM->INHIBITOR
HEPATITIS C VIRUS
TARGET ORGANISM->INHIBITOR
Related Record Type Details
Structure of MERIMEPODIB
ACTIVE MOIETY
NIH
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