6-hydroxy-3-oxo-5H-phenazine-1-carboxylic acid

Details

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Internal ID 63b557d3-e764-4cb8-b2cb-6bea7ec0054c
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name 6-hydroxy-3-oxo-5H-phenazine-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H8N2O4/c16-6-4-7(13(18)19)11-9(5-6)15-12-8(14-11)2-1-3-10(12)17/h1-5,15,17H,(H,18,19)
InChI Key GWSIQHUBLBTSBD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8N2O4
Molecular Weight 256.21 g/mol
Exact Mass 256.04840674 g/mol
Topological Polar Surface Area (TPSA) 99.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.43
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-hydroxy-3-oxo-5H-phenazine-1-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9586 95.86%
Caco-2 - 0.8670 86.70%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7564 75.64%
OATP2B1 inhibitior - 0.7091 70.91%
OATP1B1 inhibitior + 0.9557 95.57%
OATP1B3 inhibitior + 0.9632 96.32%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6406 64.06%
P-glycoprotein inhibitior - 0.9577 95.77%
P-glycoprotein substrate - 0.9243 92.43%
CYP3A4 substrate - 0.6321 63.21%
CYP2C9 substrate - 0.6091 60.91%
CYP2D6 substrate - 0.9019 90.19%
CYP3A4 inhibition - 0.9717 97.17%
CYP2C9 inhibition - 0.8883 88.83%
CYP2C19 inhibition - 0.9285 92.85%
CYP2D6 inhibition - 0.9116 91.16%
CYP1A2 inhibition - 0.7071 70.71%
CYP2C8 inhibition + 0.5133 51.33%
CYP inhibitory promiscuity - 0.9794 97.94%
UGT catelyzed - 0.5638 56.38%
Carcinogenicity (binary) - 0.9057 90.57%
Carcinogenicity (trinary) Non-required 0.7254 72.54%
Eye corrosion - 0.9936 99.36%
Eye irritation + 0.7780 77.80%
Skin irritation - 0.7569 75.69%
Skin corrosion - 0.9674 96.74%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9364 93.64%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.9044 90.44%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.4774 47.74%
Acute Oral Toxicity (c) III 0.6683 66.83%
Estrogen receptor binding + 0.5666 56.66%
Androgen receptor binding + 0.7545 75.45%
Thyroid receptor binding - 0.5148 51.48%
Glucocorticoid receptor binding + 0.8135 81.35%
Aromatase binding + 0.7161 71.61%
PPAR gamma + 0.8884 88.84%
Honey bee toxicity - 0.9703 97.03%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity - 0.5607 56.07%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4040 P28482 MAP kinase ERK2 95.47% 83.82%
CHEMBL2581 P07339 Cathepsin D 94.07% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.42% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.93% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.88% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.59% 99.15%
CHEMBL1937 Q92769 Histone deacetylase 2 89.99% 94.75%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.91% 81.11%
CHEMBL2535 P11166 Glucose transporter 87.46% 98.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.29% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.58% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.13% 94.00%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 86.00% 87.67%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.73% 91.71%
CHEMBL213 P08588 Beta-1 adrenergic receptor 83.06% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.92% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.75% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.57% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 80.95% 97.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.24% 94.42%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 125262
LOTUS LTS0001311
wikiData Q82886249