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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
Structure of 4-oxo-1H-1,10-phenanthroline-3-carboxylic acid

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)

HIDE SMILES / InChI

Molecular Formula C13H8N2O3
Molecular Weight 240.2142
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P16924
Gene ID: NA
Gene Symbol: P4HA1
Target Organism: Gallus gallus (Chicken)
3.6 µM [IC50]
PubMed

PubMed

TitleDatePubMed
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
Substance Class Chemical
Created
by admin
on Wed Apr 02 05:22:03 GMT 2025
Edited
by admin
on Wed Apr 02 05:22:03 GMT 2025
Record UNII
K73A9XJ8TU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-oxo-1H-1,10-phenanthroline-3-carboxylic acid
Systematic Name English
1,10-Phenanthroline-3-carboxylic acid, 1,4-dihydro-4-oxo-
Preferred Name English
1,4-Dihydro-4-oxo-[1,10]phenanthroline-3-carboxylic acid
Systematic Name English
Code System Code Type Description
EPA CompTox
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
PRIMARY
PUBCHEM
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
PRIMARY
FDA UNII
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
PRIMARY