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

Details

Stereochemistry ABSOLUTE
Molecular Formula C25H32N4O7S
Molecular Weight 532.609
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OPROZOMIB

SMILES

COC[C@H](NC(=O)[C@H](COC)NC(=O)C1=CN=C(C)S1)C(=O)N[C@@H](CC2=CC=CC=C2)C(=O)[C@@]3(C)CO3

InChI

InChIKey=SWZXEVABPLUDIO-WSZYKNRRSA-N
InChI=1S/C25H32N4O7S/c1-15-26-11-20(37-15)24(33)29-19(13-35-4)23(32)28-18(12-34-3)22(31)27-17(21(30)25(2)14-36-25)10-16-8-6-5-7-9-16/h5-9,11,17-19H,10,12-14H2,1-4H3,(H,27,31)(H,28,32)(H,29,33)/t17-,18-,19-,25+/m0/s1

HIDE SMILES / InChI

Molecular Formula C25H32N4O7S
Molecular Weight 532.609
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 01:30:38 UTC 2023
Edited
by admin
on Sat Dec 16 01:30:38 UTC 2023
Record UNII
MZ37792Y8J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OPROZOMIB
INN   USAN   WHO-DD  
INN   USAN  
Official Name English
O-METHYL-N-((2-METHYLTHIAZOL-5-YL)CARBONYL)-L-SERYL-O-METHYL-N-((1S)-1-BENZYL-2-((2R)- 2-METHYLOXIRAN-2-YL)-2-OXOETHYL)-L-SERINAMIDE
Systematic Name English
ONX-0912
Code English
oprozomib [INN]
Common Name English
PR-047
Common Name English
ONX 0912
Code English
OPROZOMIB [USAN]
Common Name English
Oprozomib [WHO-DD]
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 449614
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
FDA ORPHAN DRUG 443614
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
NCI_THESAURUS C2160
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
Code System Code Type Description
EVMPD
SUB126055
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
PUBCHEM
25067547
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
FDA UNII
MZ37792Y8J
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
CAS
935888-69-0
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
EPA CompTox
DTXSID201025950
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
USAN
YY-148
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
NCI_THESAURUS
C91388
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
WIKIPEDIA
Oprozomib
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
INN
9597
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
DRUG BANK
DB11991
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
SMS_ID
100000151658
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
ChEMBL
CHEMBL2103884
Created by admin on Sat Dec 16 01:30:38 UTC 2023 , Edited by admin on Sat Dec 16 01:30:38 UTC 2023
PRIMARY
Related Record Type Details
METABOLIC ENZYME -> SUBSTRATE
TARGET -> INHIBITOR
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ACTIVE MOIETY