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
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
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
Title | Date | PubMed |
---|---|---|
Randomized, double-blind phase II trial of Lexipafant, a platelet-activating factor antagonist, in human acute pancreatitis. | 1995 Oct |
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What's new in the management of acute pancreatitis? | 2001 Apr |
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Effects of lexipafant (BB-882), a platelet activating factor receptor antagonist, on liver damage due to bile duct ligation in rats. | 2006 Apr-Jun |
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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
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10430432
250 mg twice a day for 6 weeks
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:57:30 GMT 2023
by
admin
on
Fri Dec 15 15:57:30 GMT 2023
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Record UNII |
H14917M9YW
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Record Status |
Validated (UNII)
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Record Version |
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-
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9804204
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DTXSID701318348
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139133-26-9
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7099
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C103289
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GG-53
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m6797
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SUB08498MIG
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H14917M9YW
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C170120
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