2,6-Dimethoxy-1-phenazinecarboxylic acid methyl ester

Details

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Internal ID a77e19c8-acb4-4328-830d-42721b4fafbd
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name methyl 2,6-dimethoxyphenazine-1-carboxylate
SMILES (Canonical) COC1=C(C2=NC3=C(C(=CC=C3)OC)N=C2C=C1)C(=O)OC
SMILES (Isomeric) COC1=C(C2=NC3=C(C(=CC=C3)OC)N=C2C=C1)C(=O)OC
InChI InChI=1S/C16H14N2O4/c1-20-11-8-7-10-15(13(11)16(19)22-3)18-9-5-4-6-12(21-2)14(9)17-10/h4-8H,1-3H3
InChI Key AXQRRUDMDZOPGI-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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There are no found synonyms.

2D Structure

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2D Structure of 2,6-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 + 0.9868 98.68%
Caco-2 + 0.7834 78.34%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7424 74.24%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9585 95.85%
OATP1B3 inhibitior + 0.9622 96.22%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7102 71.02%
P-glycoprotein inhibitior - 0.5827 58.27%
P-glycoprotein substrate - 0.8890 88.90%
CYP3A4 substrate + 0.5219 52.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8253 82.53%
CYP3A4 inhibition - 0.7005 70.05%
CYP2C9 inhibition - 0.9502 95.02%
CYP2C19 inhibition - 0.6816 68.16%
CYP2D6 inhibition - 0.9511 95.11%
CYP1A2 inhibition + 0.8135 81.35%
CYP2C8 inhibition + 0.6416 64.16%
CYP inhibitory promiscuity + 0.6074 60.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9426 94.26%
Carcinogenicity (trinary) Non-required 0.5887 58.87%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.6187 61.87%
Skin irritation - 0.8568 85.68%
Skin corrosion - 0.9777 97.77%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4664 46.64%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.6784 67.84%
skin sensitisation - 0.9452 94.52%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.6949 69.49%
Acute Oral Toxicity (c) III 0.5021 50.21%
Estrogen receptor binding + 0.8841 88.41%
Androgen receptor binding + 0.7519 75.19%
Thyroid receptor binding + 0.8186 81.86%
Glucocorticoid receptor binding + 0.8919 89.19%
Aromatase binding + 0.8465 84.65%
PPAR gamma + 0.7267 72.67%
Honey bee toxicity - 0.9676 96.76%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.3695 36.95%

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
CHEMBL1255126 O15151 Protein Mdm4 94.19% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.83% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.64% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.54% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.52% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.83% 99.23%
CHEMBL2535 P11166 Glucose transporter 88.84% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.08% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.37% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.01% 94.00%
CHEMBL2581 P07339 Cathepsin D 82.43% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.22% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.20% 99.17%

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 101289916
NPASS NPC170656