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Details

Stereochemistry ACHIRAL
Molecular Formula C21H19N2O5.Na
Molecular Weight 402.3757
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VARESPLADIB SODIUM

SMILES

[Na+].CCC1=C(C(=O)C(N)=O)C2=C(C=CC=C2OCC([O-])=O)N1CC3=CC=CC=C3

InChI

InChIKey=XZZUHXILQXLTGV-UHFFFAOYSA-M
InChI=1S/C21H20N2O5.Na/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);/q;+1/p-1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C21H19N2O5
Molecular Weight 379.386
Charge -1
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

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.028 µM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
163.6 ng/mL
50 mg single, oral
dose: 50 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
VARESPLADIB plasma
Homo sapiens
population: HEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
755.3 ng × h/mL
50 mg single, oral
dose: 50 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
VARESPLADIB plasma
Homo sapiens
population: HEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
5 h
single, intravenous
VARESPLADIB unknown
Homo sapiens
population: HEALTHY
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
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
Health Status: unhealthy
Sex: M+F
Food Status: UNKNOWN
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
Health Status: unhealthy
Sex: M+F
Food Status: UNKNOWN
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
Health Status: unhealthy
Sex: M+F
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
Regioselective synthesis of 4- and 7-alkoxyindoles from 2,3-dihalophenols: application to the preparation of indole inhibitors of phospholipase A2.
2007-07-06
An update on inhibitors of human 14 kDa Type II s-PLA2 in development.
2001-02
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 Mon Mar 31 18:22:17 GMT 2025
Edited
by admin
on Mon Mar 31 18:22:17 GMT 2025
Record UNII
F6M52CDT0W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LY315920-NA
Preferred Name English
VARESPLADIB SODIUM
USAN  
USAN  
Official Name English
Sodium [[3-(aminooxoacetyl)-1-benzyl-2-ethyl-1H-indol-4-yl]oxy]acetate
Systematic Name English
VARESPLADIB SODIUM [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Mon Mar 31 18:22:17 GMT 2025 , Edited by admin on Mon Mar 31 18:22:17 GMT 2025
FDA ORPHAN DRUG 240107
Created by admin on Mon Mar 31 18:22:17 GMT 2025 , Edited by admin on Mon Mar 31 18:22:17 GMT 2025
Code System Code Type Description
SMS_ID
300000044509
Created by admin on Mon Mar 31 18:22:17 GMT 2025 , Edited by admin on Mon Mar 31 18:22:17 GMT 2025
PRIMARY
ChEMBL
CHEMBL148674
Created by admin on Mon Mar 31 18:22:17 GMT 2025 , Edited by admin on Mon Mar 31 18:22:17 GMT 2025
PRIMARY
NCI_THESAURUS
C73040
Created by admin on Mon Mar 31 18:22:17 GMT 2025 , Edited by admin on Mon Mar 31 18:22:17 GMT 2025
PRIMARY
USAN
NN-32
Created by admin on Mon Mar 31 18:22:17 GMT 2025 , Edited by admin on Mon Mar 31 18:22:17 GMT 2025
PRIMARY
CAS
172733-42-5
Created by admin on Mon Mar 31 18:22:17 GMT 2025 , Edited by admin on Mon Mar 31 18:22:17 GMT 2025
PRIMARY
FDA UNII
F6M52CDT0W
Created by admin on Mon Mar 31 18:22:17 GMT 2025 , Edited by admin on Mon Mar 31 18:22:17 GMT 2025
PRIMARY
DRUG BANK
DBSALT002103
Created by admin on Mon Mar 31 18:22:17 GMT 2025 , Edited by admin on Mon Mar 31 18:22:17 GMT 2025
PRIMARY
EPA CompTox
DTXSID10169379
Created by admin on Mon Mar 31 18:22:17 GMT 2025 , Edited by admin on Mon Mar 31 18:22:17 GMT 2025
PRIMARY
PUBCHEM
23674730
Created by admin on Mon Mar 31 18:22:17 GMT 2025 , Edited by admin on Mon Mar 31 18:22:17 GMT 2025
PRIMARY
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