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
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
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 |
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/19697278Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/10027849
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19697278
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.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL3474 Sources: https://www.ncbi.nlm.nih.gov/pubmed/19697278 |
0.028 µM [IC50] | ||
Target ID: CHEMBL4342 Sources: https://www.ncbi.nlm.nih.gov/pubmed/19697278 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
Doses
Dose | Population | Adverse 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%) Sources: aspartate transaminase elevations (1.5%) |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
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: |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19697278
Unknown
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16249480
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
Edited
Fri Dec 15 16:13:19 GMT 2023
by
admin
on
Fri Dec 15 16:13:19 GMT 2023
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Record UNII |
F6M52CDT0W
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Record Status |
Validated (UNII)
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Record Version |
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Official Name | English | ||
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Code | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C257
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FDA ORPHAN DRUG |
240107
Created by
admin on Fri Dec 15 16:13:19 GMT 2023 , Edited by admin on Fri Dec 15 16:13:19 GMT 2023
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Code System | Code | Type | Description | ||
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300000044509
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CHEMBL148674
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C73040
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NN-32
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172733-42-5
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F6M52CDT0W
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DBSALT002103
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DTXSID10169379
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23674730
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PRIMARY |
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PARENT -> SALT/SOLVATE |
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ACTIVE MOIETY |