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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H18FN3O2S
Molecular Weight 323.386
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RIPASUDIL

SMILES

C[C@H]1CNCCCN1S(=O)(=O)C2=CC=CC3=C2C(F)=CN=C3

InChI

InChIKey=QSKQVZWVLOIIEV-NSHDSACASA-N
InChI=1S/C15H18FN3O2S/c1-11-8-17-6-3-7-19(11)22(20,21)14-5-2-4-12-9-18-10-13(16)15(12)14/h2,4-5,9-11,17H,3,6-8H2,1H3/t11-/m0/s1

HIDE SMILES / InChI
Molecular Formula C15H18FN3O2S
Molecular Weight 323.386
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 Sat Dec 16 10:42:42 UTC 2023
Edited
by admin
on Sat Dec 16 10:42:42 UTC 2023
Record UNII
11978226XX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RIPASUDIL
INN   WHO-DD  
INN  
Official Name English
1H-1,4-DIAZEPINE, 1-((4-FLUORO-5-ISOQUINOLINYL)SULFONYL)HEXAHYDRO-2-METHYL-, (2S)-
Systematic Name English
ripasudil [INN]
Common Name English
ISOQUINOLINE, 4-FLUORO-5-(((2S)-HEXAHYDRO-2-METHYL-1H-1,4-DIAZEPIN-1-YL)SULFONYL)-
Systematic Name English
Ripasudil [WHO-DD]
Common Name English
RIPASUDIL [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1404
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
NCI_THESAURUS C29705
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
Code System Code Type Description
FDA UNII
11978226XX
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
CAS
223645-67-8
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
EVMPD
SUB185276
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
NCI_THESAURUS
C152226
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
SMS_ID
100000171185
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
DRUG BANK
DB13165
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
DRUG CENTRAL
4938
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
MERCK INDEX
m11878
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
EPA CompTox
DTXSID001025609
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
WIKIPEDIA
Ripasudil
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
PUBCHEM
9863672
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
INN
9691
Created by admin on Sat Dec 16 10:42:42 UTC 2023 , Edited by admin on Sat Dec 16 10:42:42 UTC 2023
PRIMARY
Related Record Type Details
Structure of RIPASUDIL HYDROCHLORIDE DIHYDRATE
SALT/SOLVATE -> PARENT
RHO-ASSOCIATED PROTEIN KINASE 2
TARGET -> INHIBITOR
RHO-ASSOCIATED PROTEIN KINASE 1
TARGET -> INHIBITOR
Related Record Type Details
Structure of RIPASUDIL
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