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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H32N4O3S
Molecular Weight 444.59
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NUPAFANT

SMILES

CCOC[C@H](CC(C)C)N(C)S(=O)(=O)C1=CC=C(CN2C(C)=NC3=C2C=CN=C3)C=C1

InChI

InChIKey=GFUNPHNHBVCVHW-FQEVSTJZSA-N
InChI=1S/C23H32N4O3S/c1-6-30-16-20(13-17(2)3)26(5)31(28,29)21-9-7-19(8-10-21)15-27-18(4)25-22-14-24-12-11-23(22)27/h7-12,14,17,20H,6,13,15-16H2,1-5H3/t20-/m0/s1

HIDE SMILES / InChI

Molecular Formula C23H32N4O3S
Molecular Weight 444.59
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Nupafant (BB-960) is a potent platelet activating factor antagonist that is active both orally and intravenously. Nupafant was in phase I clinical trials in the UK for the treatment of ischemia-reperfusion injury, however this compound has since been suspended.

Approval Year

PubMed

PubMed

TitleDatePubMed
Nupafant, a PAF-antagonist prototype for suppression of ventricular fibrillation without liability for QT prolongation?
2006 Oct

Sample Use Guides

Global (whole-heart) delivery of 10 uM nupafant, reduced the incidence of ischaemia-induced VF and widened QT interval without affecting coronary flow. Importantly, lower concentrations (0.1 and 1 uM) had no effect on VF, yet widened QT almost identically to 10 uM nupafant.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:39:16 UTC 2023
Edited
by admin
on Fri Dec 15 16:39:16 UTC 2023
Record UNII
02NKI0ARRJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NUPAFANT
INN  
INN  
Official Name English
N-((S)-1-(ETHOXYMETHYL)-3-METHYLBUTYL)-N-METHYL-.ALPHA.-(2-METHYL-1H-IMIDAZO(4,5-C)PYRIDIN-1-YL)-P-TOLUENESULFONAMIDE
Common Name English
BENZENESULFONAMIDE, N-((1S)-1-(ETHOXYMETHYL)-3-METHYLBUTYL)-N-METHYL-4-((2-METHYL-1H-IMIDAZO(4,5-C)PYRIDIN-1-YL)METHYL)-
Systematic Name English
nupafant [INN]
Common Name English
BB-960
Code English
Classification Tree Code System Code
NCI_THESAURUS C1327
Created by admin on Fri Dec 15 16:39:16 UTC 2023 , Edited by admin on Fri Dec 15 16:39:16 UTC 2023
Code System Code Type Description
PUBCHEM
9846324
Created by admin on Fri Dec 15 16:39:16 UTC 2023 , Edited by admin on Fri Dec 15 16:39:16 UTC 2023
PRIMARY
EVMPD
SUB09391MIG
Created by admin on Fri Dec 15 16:39:16 UTC 2023 , Edited by admin on Fri Dec 15 16:39:16 UTC 2023
PRIMARY
INN
7206
Created by admin on Fri Dec 15 16:39:16 UTC 2023 , Edited by admin on Fri Dec 15 16:39:16 UTC 2023
PRIMARY
MESH
C515030
Created by admin on Fri Dec 15 16:39:16 UTC 2023 , Edited by admin on Fri Dec 15 16:39:16 UTC 2023
PRIMARY
ChEMBL
CHEMBL2104467
Created by admin on Fri Dec 15 16:39:16 UTC 2023 , Edited by admin on Fri Dec 15 16:39:16 UTC 2023
PRIMARY
FDA UNII
02NKI0ARRJ
Created by admin on Fri Dec 15 16:39:16 UTC 2023 , Edited by admin on Fri Dec 15 16:39:16 UTC 2023
PRIMARY
EPA CompTox
DTXSID20160933
Created by admin on Fri Dec 15 16:39:16 UTC 2023 , Edited by admin on Fri Dec 15 16:39:16 UTC 2023
PRIMARY
NCI_THESAURUS
C81564
Created by admin on Fri Dec 15 16:39:16 UTC 2023 , Edited by admin on Fri Dec 15 16:39:16 UTC 2023
PRIMARY
SMS_ID
100000083608
Created by admin on Fri Dec 15 16:39:16 UTC 2023 , Edited by admin on Fri Dec 15 16:39:16 UTC 2023
PRIMARY
CAS
139133-27-0
Created by admin on Fri Dec 15 16:39:16 UTC 2023 , Edited by admin on Fri Dec 15 16:39:16 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY