2,3-Dimethoxy-1-phenazinecarboxylic acid methyl ester

Details

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Internal ID 9f9badc3-0816-4e70-9001-adafd4acb832
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name methyl 2,3-dimethoxyphenazine-1-carboxylate
SMILES (Canonical) COC1=CC2=NC3=CC=CC=C3N=C2C(=C1OC)C(=O)OC
SMILES (Isomeric) COC1=CC2=NC3=CC=CC=C3N=C2C(=C1OC)C(=O)OC
InChI InChI=1S/C16H14N2O4/c1-20-12-8-11-14(13(15(12)21-2)16(19)22-3)18-10-7-5-4-6-9(10)17-11/h4-8H,1-3H3
InChI Key YTVYJJMELVOPAB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14N2O4
Molecular Weight 298.29 g/mol
Exact Mass 298.09535693 g/mol
Topological Polar Surface Area (TPSA) 70.50 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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2,3-Dimethoxy-1-phenazinecarboxylic acid methyl ester

2D Structure

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2D Structure of 2,3-Dimethoxy-1-phenazinecarboxylic acid methyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9837 98.37%
Caco-2 + 0.8081 80.81%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.6828 68.28%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.9593 95.93%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6447 64.47%
P-glycoprotein inhibitior - 0.6825 68.25%
P-glycoprotein substrate - 0.8800 88.00%
CYP3A4 substrate + 0.5239 52.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8253 82.53%
CYP3A4 inhibition - 0.7838 78.38%
CYP2C9 inhibition - 0.9791 97.91%
CYP2C19 inhibition - 0.7020 70.20%
CYP2D6 inhibition - 0.9167 91.67%
CYP1A2 inhibition + 0.7907 79.07%
CYP2C8 inhibition + 0.8421 84.21%
CYP inhibitory promiscuity + 0.5386 53.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5050 50.50%
Eye corrosion - 0.9895 98.95%
Eye irritation + 0.7009 70.09%
Skin irritation - 0.8380 83.80%
Skin corrosion - 0.9767 97.67%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4392 43.92%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.7177 71.77%
skin sensitisation - 0.9352 93.52%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.6286 62.86%
Acute Oral Toxicity (c) II 0.3939 39.39%
Estrogen receptor binding + 0.7200 72.00%
Androgen receptor binding + 0.6999 69.99%
Thyroid receptor binding + 0.7117 71.17%
Glucocorticoid receptor binding + 0.8367 83.67%
Aromatase binding + 0.7532 75.32%
PPAR gamma + 0.5789 57.89%
Honey bee toxicity - 0.9539 95.39%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.6482 64.82%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.39% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.30% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.22% 86.33%
CHEMBL2535 P11166 Glucose transporter 91.28% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 90.63% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.96% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.58% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.03% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.46% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.71% 85.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.41% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.02% 95.56%
CHEMBL2581 P07339 Cathepsin D 80.10% 98.95%

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 21856883
NPASS NPC29128