Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H8N2O3 |
| Molecular Weight | 240.2142 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CNC2=C(C=CC3=CC=CN=C23)C1=O
InChI
InChIKey=XZZHOJONZJQARN-UHFFFAOYSA-N
InChI=1S/C13H8N2O3/c16-12-8-4-3-7-2-1-5-14-10(7)11(8)15-6-9(12)13(17)18/h1-6H,(H,15,16)(H,17,18)
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: P16924 Gene ID: NA Gene Symbol: P4HA1 Target Organism: Gallus gallus (Chicken) Sources: https://www.ncbi.nlm.nih.gov/pubmed/11139398 |
3.6 µM [IC50] |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Drug-induced regeneration in adult mice. | 2015-06-03 |
|
| Prolyl-4-hydroxylase α subunit 2 promotes breast cancer progression and metastasis by regulating collagen deposition. | 2014-01-02 |
|
| Transient inhibition of connective tissue infiltration and collagen deposition into porous poly(lactic-co-glycolic acid) discs. | 2013-12 |
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Preferred Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
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DTXSID90332701
Created by
admin on Wed Apr 02 05:22:03 GMT 2025 , Edited by admin on Wed Apr 02 05:22:03 GMT 2025
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459803
Created by
admin on Wed Apr 02 05:22:03 GMT 2025 , Edited by admin on Wed Apr 02 05:22:03 GMT 2025
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K73A9XJ8TU
Created by
admin on Wed Apr 02 05:22:03 GMT 2025 , Edited by admin on Wed Apr 02 05:22:03 GMT 2025
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PRIMARY |
SUBSTANCE RECORD