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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
Pharmacological interventions for acute pancreatitis.
2017-04-21
NF-κB in acute pancreatitis: Mechanisms and therapeutic potential.
2016-02-16
Pharmacological perioperative brain neuroprotection: a qualitative review of randomized clinical trials.
2013-06
Pharmacotherapy for acute pancreatitis.
2009-12
Existence of hepatitis C virus NS5B variants naturally resistant to non-nucleoside, but not to nucleoside, polymerase inhibitors among untreated patients.
2008-06
[Practical guidelines for management of severe acute pancreatitis with integrated Chinese traditional and Western medicine (Draft)].
2007-08
Effects of lexipafant (BB-882), a platelet activating factor receptor antagonist, on liver damage due to bile duct ligation in rats.
2006-08-26
Lexipafant and acute pancreatitis: a critical appraisal of the clinical trials.
2002
What's new in the management of acute pancreatitis?
2001-04
Acute pancreatitis: an overview of emerging pharmacotherapy.
1998-11
Randomized, double-blind phase II trial of Lexipafant, a platelet-activating factor antagonist, in human acute pancreatitis.
1995-10
Some wrong-way chemical changes during antihypertensive treatment: comparison of indapamide and related agents.
1983-07

Sample Use Guides

250 mg twice a day for 6 weeks
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:14:34 GMT 2025
Edited
by admin
on Mon Mar 31 18:14:34 GMT 2025
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
BB-882
Preferred Name English
DO6
Code English
DO-6
Code English
LEXIPAFANT [MI]
Common Name English
lexipafant [INN]
Common Name English
LEXIPAFANT [MART.]
Common Name English
Lexipafant [WHO-DD]
Common Name English
LEXIPAFANT [USAN]
Common Name English
Code System Code Type Description
PUBCHEM
9804204
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID701318348
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY
CAS
139133-26-9
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY
INN
7099
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY
MESH
C103289
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY
USAN
GG-53
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY
MERCK INDEX
m6797
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY Merck Index
EVMPD
SUB08498MIG
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY
FDA UNII
H14917M9YW
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY
SMS_ID
100000082306
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY
ChEMBL
CHEMBL322832
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY
NCI_THESAURUS
C170120
Created by admin on Mon Mar 31 18:14:34 GMT 2025 , Edited by admin on Mon Mar 31 18:14:34 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY