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

Details

Stereochemistry ABSOLUTE
Molecular Formula C21H21FN2O4S
Molecular Weight 416.466
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RAMATROBAN

SMILES

OC(=O)CCN1C2=C(C[C@@H](CC2)NS(=O)(=O)C3=CC=C(F)C=C3)C4=C1C=CC=C4

InChI

InChIKey=LDXDSHIEDAPSSA-OAHLLOKOSA-N
InChI=1S/C21H21FN2O4S/c22-14-5-8-16(9-6-14)29(27,28)23-15-7-10-20-18(13-15)17-3-1-2-4-19(17)24(20)12-11-21(25)26/h1-6,8-9,15,23H,7,10-13H2,(H,25,26)/t15-/m1/s1

HIDE SMILES / InChI

Molecular Formula C21H21FN2O4S
Molecular Weight 416.466
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 17:49:56 UTC 2023
Edited
by admin
on Sat Dec 16 17:49:56 UTC 2023
Record UNII
P1ALI72U6C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RAMATROBAN
INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
RAMATROBAN [JAN]
Common Name English
EN-137774
Code English
BAYNAS
Brand Name English
RAMATROBAN [MART.]
Common Name English
(+)-(3R)-3-(P-FLUOROBENZENESULFONAMIDO)-1,2,3,4-TETRAHYDROCARBAZOLE-9-PROPIONIC ACID
Systematic Name English
(3R)-3-(((4-FLUOROPHENYL)SULFONYL)AMINO)-1,2,3,4-TETRAHYDRO-9H-CARBAZOLE-9-PROPANOIC ACID
Systematic Name English
RAMATROBAN [MI]
Common Name English
9H-CARBAZOLE-9-PROPANOIC ACID, 3-(((4-FLUOROPHENYL)SULFONYL)AMINO)-1,2,3,4-TETRAHYDRO-, (3R)-
Systematic Name English
ramatroban [INN]
Common Name English
Ramatroban [WHO-DD]
Common Name English
BAY-U-3405
Code English
Classification Tree Code System Code
NCI_THESAURUS C1327
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
Code System Code Type Description
INN
7273
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
EVMPD
SUB10245MIG
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
MESH
C063119
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
FDA UNII
P1ALI72U6C
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
WIKIPEDIA
Ramatroban
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
DRUG BANK
DB13036
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
ChEMBL
CHEMBL361812
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
DRUG CENTRAL
2354
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
MERCK INDEX
m9488
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
EPA CompTox
DTXSID1046685
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
NCI_THESAURUS
C76400
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
SMS_ID
100000080311
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
CAS
116649-85-5
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
PUBCHEM
123879
Created by admin on Sat Dec 16 17:49:57 UTC 2023 , Edited by admin on Sat Dec 16 17:49:57 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY