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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H30N4O4S
Molecular Weight 458.574
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEXIPAFANT

SMILES

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

InChI

InChIKey=AQRXDPFOYJSPMP-QFIPXVFZSA-N
InChI=1S/C23H30N4O4S/c1-6-31-23(28)22(13-16(2)3)26(5)32(29,30)19-9-7-18(8-10-19)15-27-17(4)25-20-14-24-12-11-21(20)27/h7-12,14,16,22H,6,13,15H2,1-5H3/t22-/m0/s1

HIDE SMILES / InChI

Molecular Formula C23H30N4O4S
Molecular Weight 458.574
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Lexipafant is a platelet-activating factor (PAF) antagonist. It was hypothesized that the substance could beneficially affect the cognitive performance of HIV infected people. Lexipafant was as tolerable as placebo. At week 6 and week 10 after baseline evaluations, the lexipafant group showed trends toward improvement on the Rey Auditory Verbal Learning test as well as the timed gait test. A phase IIa placebo-controlled study reported that lexipafant was not effective in patients with severe ulcerative colitis receiving corticosteroids. Two lexipafant treated patient had adverse events: severe influenza-like symptoms in one and hypotension with iliac artery thrombosis in one. The clinical trials of lexipafant in the treatment of acute pancreatitis were undertaken with considerable optimism. There was a significant reduction in the incidence of organ failure and in total organ failure score at the end of medication (72 h).

Approval Year

PubMed

PubMed

TitleDatePubMed
Randomized, double-blind phase II trial of Lexipafant, a platelet-activating factor antagonist, in human acute pancreatitis.
1995 Oct
What's new in the management of acute pancreatitis?
2001 Apr
Effects of lexipafant (BB-882), a platelet activating factor receptor antagonist, on liver damage due to bile duct ligation in rats.
2006 Apr-Jun
Existence of hepatitis C virus NS5B variants naturally resistant to non-nucleoside, but not to nucleoside, polymerase inhibitors among untreated patients.
2008 Jun
Pharmacological interventions for acute pancreatitis.
2017 Apr 21

Sample Use Guides

250 mg twice a day for 6 weeks
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:57:30 GMT 2023
Edited
by admin
on Fri Dec 15 15:57:30 GMT 2023
Record UNII
H14917M9YW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEXIPAFANT
INN   MART.   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
DO6
Code English
DO-6
Code English
LEXIPAFANT [MI]
Common Name English
lexipafant [INN]
Common Name English
LEXIPAFANT [MART.]
Common Name English
BB-882
Code English
Lexipafant [WHO-DD]
Common Name English
LEXIPAFANT [USAN]
Common Name English
Code System Code Type Description
PUBCHEM
9804204
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID701318348
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY
CAS
139133-26-9
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY
INN
7099
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY
MESH
C103289
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY
USAN
GG-53
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY
MERCK INDEX
m6797
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY Merck Index
EVMPD
SUB08498MIG
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY
FDA UNII
H14917M9YW
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY
SMS_ID
100000082306
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY
ChEMBL
CHEMBL322832
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY
NCI_THESAURUS
C170120
Created by admin on Fri Dec 15 15:57:30 GMT 2023 , Edited by admin on Fri Dec 15 15:57:30 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY