Phenazine-1-carboxylic acid

Details

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Internal ID e765b37f-ae30-48b7-9421-ea5d3f1f1efa
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name phenazine-1-carboxylic acid
SMILES (Canonical) C1=CC=C2C(=C1)N=C3C=CC=C(C3=N2)C(=O)O
SMILES (Isomeric) C1=CC=C2C(=C1)N=C3C=CC=C(C3=N2)C(=O)O
InChI InChI=1S/C13H8N2O2/c16-13(17)8-4-3-7-11-12(8)15-10-6-2-1-5-9(10)14-11/h1-7H,(H,16,17)
InChI Key JGCSKOVQDXEQHI-UHFFFAOYSA-N
Popularity 747 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8N2O2
Molecular Weight 224.21 g/mol
Exact Mass 224.058577502 g/mol
Topological Polar Surface Area (TPSA) 63.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.48
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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2538-68-3
1-Phenazinecarboxylic acid
Phenazinecarboxylic acid
Tubermycin B
1-Carboxylic acid phenazine
1-carboxyphenazine
EMR 211 [Russian]
NRRL B-1482 [Russian]
NRRL B-1576 [Russian]
102646-59-3
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 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 + 0.9954 99.54%
Caco-2 - 0.5384 53.84%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.7024 70.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9793 97.93%
OATP1B3 inhibitior + 0.9589 95.89%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.9354 93.54%
P-glycoprotein substrate - 0.9819 98.19%
CYP3A4 substrate - 0.7947 79.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9038 90.38%
CYP3A4 inhibition - 0.9248 92.48%
CYP2C9 inhibition - 0.9539 95.39%
CYP2C19 inhibition - 0.9529 95.29%
CYP2D6 inhibition - 0.9573 95.73%
CYP1A2 inhibition - 0.5537 55.37%
CYP2C8 inhibition - 0.6545 65.45%
CYP inhibitory promiscuity - 0.9765 97.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8857 88.57%
Carcinogenicity (trinary) Non-required 0.7740 77.40%
Eye corrosion - 0.9892 98.92%
Eye irritation + 0.7322 73.22%
Skin irritation + 0.6818 68.18%
Skin corrosion - 0.9608 96.08%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8921 89.21%
Micronuclear + 0.5100 51.00%
Hepatotoxicity + 0.7428 74.28%
skin sensitisation - 0.8505 85.05%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.7409 74.09%
Acute Oral Toxicity (c) III 0.5612 56.12%
Estrogen receptor binding + 0.8579 85.79%
Androgen receptor binding + 0.6109 61.09%
Thyroid receptor binding + 0.7156 71.56%
Glucocorticoid receptor binding + 0.9340 93.40%
Aromatase binding + 0.9195 91.95%
PPAR gamma + 0.9211 92.11%
Honey bee toxicity - 0.9690 96.90%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.6424 64.24%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3577 P00352 Aldehyde dehydrogenase 1A1 28183.8 nM
Potency
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.15% 99.23%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 92.30% 81.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.01% 95.56%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 88.42% 87.67%
CHEMBL2581 P07339 Cathepsin D 87.89% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.10% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.76% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 82.19% 94.73%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 81.13% 96.47%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.87% 94.62%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Aglaia tomentosa
Backhousia citriodora
Capraria biflora
Centipeda minima
Mentha suaveolens subsp. timija
Senecio macrocephalus
Upuna borneensis

Cross-Links

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PubChem 95069
NPASS NPC219848
ChEMBL CHEMBL463686
LOTUS LTS0104136
wikiData Q27131864