5-(carboxymethyl)-10H-phenazine-1-carboxylic acid

Details

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Internal ID 5c1cd5b6-1342-4981-ba8c-954ed14e818c
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name 5-(carboxymethyl)-10H-phenazine-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12N2O4/c18-13(19)8-17-11-6-2-1-5-10(11)16-14-9(15(20)21)4-3-7-12(14)17/h1-7,16H,8H2,(H,18,19)(H,20,21)
InChI Key VBAHMOBEQLBTBK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12N2O4
Molecular Weight 284.27 g/mol
Exact Mass 284.07970687 g/mol
Topological Polar Surface Area (TPSA) 89.90 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(carboxymethyl)-10H-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 - 0.7128 71.28%
Caco-2 - 0.5660 56.60%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6438 64.38%
OATP2B1 inhibitior - 0.8620 86.20%
OATP1B1 inhibitior + 0.9491 94.91%
OATP1B3 inhibitior + 0.9368 93.68%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9317 93.17%
BSEP inhibitior - 0.5244 52.44%
P-glycoprotein inhibitior - 0.9508 95.08%
P-glycoprotein substrate - 0.9108 91.08%
CYP3A4 substrate - 0.6574 65.74%
CYP2C9 substrate - 0.5818 58.18%
CYP2D6 substrate - 0.9130 91.30%
CYP3A4 inhibition - 0.9538 95.38%
CYP2C9 inhibition - 0.8812 88.12%
CYP2C19 inhibition - 0.9447 94.47%
CYP2D6 inhibition - 0.9207 92.07%
CYP1A2 inhibition - 0.8735 87.35%
CYP2C8 inhibition - 0.9083 90.83%
CYP inhibitory promiscuity - 0.9266 92.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6144 61.44%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.7828 78.28%
Skin irritation - 0.7671 76.71%
Skin corrosion - 0.9619 96.19%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8990 89.90%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.9097 90.97%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.6417 64.17%
Acute Oral Toxicity (c) III 0.6666 66.66%
Estrogen receptor binding + 0.6447 64.47%
Androgen receptor binding + 0.6648 66.48%
Thyroid receptor binding - 0.6009 60.09%
Glucocorticoid receptor binding + 0.9069 90.69%
Aromatase binding + 0.6523 65.23%
PPAR gamma + 0.9135 91.35%
Honey bee toxicity - 0.9688 96.88%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity + 0.6442 64.42%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.11% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 95.81% 94.62%
CHEMBL2581 P07339 Cathepsin D 94.35% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.20% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 88.85% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.64% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.92% 86.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.92% 93.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.94% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.07% 99.23%

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 101960265
LOTUS LTS0163040
wikiData Q77279748