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

Details

Stereochemistry ABSOLUTE
Molecular Formula C15H29N3O5
Molecular Weight 331.4079
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MARIMASTAT

SMILES

CNC(=O)[C@@H](NC(=O)[C@H](CC(C)C)[C@H](O)C(=O)NO)C(C)(C)C

InChI

InChIKey=OCSMOTCMPXTDND-OUAUKWLOSA-N
InChI=1S/C15H29N3O5/c1-8(2)7-9(10(19)13(21)18-23)12(20)17-11(14(22)16-6)15(3,4)5/h8-11,19,23H,7H2,1-6H3,(H,16,22)(H,17,20)(H,18,21)/t9-,10+,11-/m1/s1

HIDE SMILES / InChI

Molecular Formula C15H29N3O5
Molecular Weight 331.4079
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:52:58 UTC 2023
Edited
by admin
on Fri Dec 15 15:52:58 UTC 2023
Record UNII
D5EQV23TDS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MARIMASTAT
INN   MART.   MI   USAN   WHO-DD  
INN   USAN  
Official Name English
KB-R 8898
Code English
GI-5712
Code English
GI5712
Code English
TA2516
Code English
MARIMASTAT [MART.]
Common Name English
MARIMASTAT [USAN]
Common Name English
NSC-719333
Code English
TA-2516
Code English
MARIMASTAT [MI]
Common Name English
BB2516
Code English
BUTANEDIAMIDE, N(SUP 4)-(2,2-DIMETHYL-1-((METHYLAMINO)CARBONYL)PROPYL)-N1,2-DIHYDROXY-3-(2-METHYLPROPYL)-, (2S-(N4(R*),2R*,3S*))-
Common Name English
marimastat [INN]
Common Name English
(2S,3R)-3-[[(1S)-2,2-Dimethyl-1-(methylcarbamoyl)propyl]carbamoyl]-2-hydroxy-5-methylhexanohydroxamic acid
Systematic Name English
BB-2516
Code English
Marimastat [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1970
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
Code System Code Type Description
PUBCHEM
119031
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
EPA CompTox
DTXSID20165524
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
NSC
719333
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
ChEMBL
CHEMBL279785
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
MERCK INDEX
m7088
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY Merck Index
CHEBI
50662
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
MESH
C100342
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
CAS
154039-60-8
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
DRUG BANK
DB00786
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
NCI_THESAURUS
C1652
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
USAN
HH-42
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
SMS_ID
100000079297
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
INN
7480
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
WIKIPEDIA
MARIMASTAT
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
FDA UNII
D5EQV23TDS
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
EVMPD
SUB12420MIG
Created by admin on Fri Dec 15 15:52:58 UTC 2023 , Edited by admin on Fri Dec 15 15:52:58 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY