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Details

Stereochemistry ACHIRAL
Molecular Formula C21H20N2O5
Molecular Weight 380.3939
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VARESPLADIB

SMILES

CCC1=C(C(=O)C(N)=O)C2=C(OCC(O)=O)C=CC=C2N1CC3=CC=CC=C3

InChI

InChIKey=BHLXTPHDSZUFHR-UHFFFAOYSA-N
InChI=1S/C21H20N2O5/c1-2-14-19(20(26)21(22)27)18-15(9-6-10-16(18)28-12-17(24)25)23(14)11-13-7-4-3-5-8-13/h3-10H,2,11-12H2,1H3,(H2,22,27)(H,24,25)

HIDE SMILES / InChI

Molecular Formula C21H20N2O5
Molecular Weight 380.3939
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/10027849

Varespladib (LY315920; A-001) is a potent and selective inhibitor of IIa, V, and X isoforms of human non-pancreatic secretory phospholipase A2 with nM IC50. The molecule acts as an anti-inflammatory agent by disrupting the first step of the arachidonic acid pathway of inflammation. Varespladib methyl is being developed by Anthera Pharmaceuticals Inc for the potential treatment of coronary artery disease, acute coronary syndrome and inflammation. Varespladib methyl is a prodrug that is rapidly metabolized to varespladib, and both compounds are able to potently inhibit the enzymes of the human secretory phospholipase groups. Phase II clinical trials of varespladib methyl in patients with coronary artery disease, rheumatoid arthritis, asthma and ulcerative colitis revealed that the drug was well tolerated. Varespladib methyl did not demonstrate a good efficacy profile in patients with rheumatoid arthritis, asthma and ulcerative colitis; whereas in patients with coronary artery disease, varespladib methyl consistently reduced LDL-cholesterol levels, (elevated LDL-cholesterol levels are a marker of increased cardiovascular risk). Varespladib methyl could represent a novel therapy for the treatment of cardiovascular disease, although the efficacy, safety profile and advantages of this drug compared with existing therapeutic options would need to be established in upcoming phase III trials.

Approval Year

Doses

Doses

DosePopulationAdverse events​
500 mg 1 times / day multiple, oral
Studied dose
Dose: 500 mg, 1 times / day
Route: oral
Route: multiple
Dose: 500 mg, 1 times / day
Sources:
unhealthy
n = 2572
Health Status: unhealthy
Condition: Acute Coronary Syndrome
Sex: M+F
Food Status: UNKNOWN
Population Size: 2572
Sources:
Disc. AE: aspartate transaminase elevations, aspartate transaminase elevations...
AEs leading to
discontinuation/dose reduction:
aspartate transaminase elevations (1.5%)
aspartate transaminase elevations (1.5%)
Sources:
AEs

AEs

AESignificanceDosePopulation
aspartate transaminase elevations 1.5%
Disc. AE
500 mg 1 times / day multiple, oral
Studied dose
Dose: 500 mg, 1 times / day
Route: oral
Route: multiple
Dose: 500 mg, 1 times / day
Sources:
unhealthy
n = 2572
Health Status: unhealthy
Condition: Acute Coronary Syndrome
Sex: M+F
Food Status: UNKNOWN
Population Size: 2572
Sources:
aspartate transaminase elevations 1.5%
Disc. AE
500 mg 1 times / day multiple, oral
Studied dose
Dose: 500 mg, 1 times / day
Route: oral
Route: multiple
Dose: 500 mg, 1 times / day
Sources:
unhealthy
n = 2572
Health Status: unhealthy
Condition: Acute Coronary Syndrome
Sex: M+F
Food Status: UNKNOWN
Population Size: 2572
Sources:
PubMed

PubMed

TitleDatePubMed
An update on inhibitors of human 14 kDa Type II s-PLA2 in development.
2001 Feb
Regioselective synthesis of 4- and 7-alkoxyindoles from 2,3-dihalophenols: application to the preparation of indole inhibitors of phospholipase A2.
2007 Jul 6
Patents

Sample Use Guides

Unknown
Route of Administration: Oral
LY315920 (VARESPLADIB) (10 μM) significantly inhibits all-trans-retinoic acid (RA) -induced membrane-associated mucin MUC16 expression by 100% at 24 hours and 99% at 48 hours.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:26:33 GMT 2023
Edited
by admin
on Fri Dec 15 16:26:33 GMT 2023
Record UNII
2Q3P98DATH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VARESPLADIB
INN   MI   USAN  
INN   USAN  
Official Name English
VARESPLADIB [USAN]
Common Name English
ACETIC ACID, ((3-(AMINOOXOACETYL)-2-ETHYL-1-(PHENYLMETHYL)-1H-INDOL-4-YL)OXY)-
Common Name English
LY-315920
Code English
((3-(AMINO(OXO)ACETYL)-1-BENZYL-2-ETHYL-1H-INDOL-4-YL)OXY)ACETIC ACID
Systematic Name English
Varespladib [WHO-DD]
Common Name English
varespladib [INN]
Common Name English
VARESPLADIB [MI]
Common Name English
LY315920
Code English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
FDA ORPHAN DRUG 677919
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID50169378
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
ChEMBL
CHEMBL148674
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
DRUG BANK
DB11909
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
MERCK INDEX
m11396
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY Merck Index
FDA UNII
2Q3P98DATH
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
PUBCHEM
155815
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
NCI_THESAURUS
C152832
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
WIKIPEDIA
VARESPLADIB
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
INN
8243
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
USAN
UU-55
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
CAS
172732-68-2
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
EVMPD
SUB25685
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
SMS_ID
100000091706
Created by admin on Fri Dec 15 16:26:33 GMT 2023 , Edited by admin on Fri Dec 15 16:26:33 GMT 2023
PRIMARY
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