2,3,7-Trimethoxyphenazine

Details

Top
Internal ID c4c082a6-da65-4c85-b311-91f5b3af63c6
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name 2,3,7-trimethoxyphenazine
SMILES (Canonical) COC1=CC2=NC3=CC(=C(C=C3N=C2C=C1)OC)OC
SMILES (Isomeric) COC1=CC2=NC3=CC(=C(C=C3N=C2C=C1)OC)OC
InChI InChI=1S/C15H14N2O3/c1-18-9-4-5-10-11(6-9)17-13-8-15(20-3)14(19-2)7-12(13)16-10/h4-8H,1-3H3
InChI Key JLAONHHPFOHTJH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H14N2O3
Molecular Weight 270.28 g/mol
Exact Mass 270.10044231 g/mol
Topological Polar Surface Area (TPSA) 53.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2,3,7-Trimethoxyphenazine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.8999 89.99%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.7845 78.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9463 94.63%
OATP1B3 inhibitior + 0.9700 97.00%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.4930 49.30%
P-glycoprotein inhibitior - 0.8153 81.53%
P-glycoprotein substrate - 0.8462 84.62%
CYP3A4 substrate - 0.6343 63.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3777 37.77%
CYP3A4 inhibition - 0.5910 59.10%
CYP2C9 inhibition - 0.9529 95.29%
CYP2C19 inhibition + 0.5525 55.25%
CYP2D6 inhibition - 0.8048 80.48%
CYP1A2 inhibition + 0.8722 87.22%
CYP2C8 inhibition + 0.4574 45.74%
CYP inhibitory promiscuity + 0.6546 65.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5027 50.27%
Eye corrosion - 0.9907 99.07%
Eye irritation + 0.9486 94.86%
Skin irritation - 0.8141 81.41%
Skin corrosion - 0.9723 97.23%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4079 40.79%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.9259 92.59%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.6548 65.48%
Acute Oral Toxicity (c) III 0.5698 56.98%
Estrogen receptor binding + 0.8657 86.57%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.8880 88.80%
Glucocorticoid receptor binding + 0.8705 87.05%
Aromatase binding + 0.9251 92.51%
PPAR gamma - 0.6162 61.62%
Honey bee toxicity - 0.9622 96.22%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.7900 79.00%
Fish aquatic toxicity - 0.6285 62.85%

Targets

Top

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
CHEMBL3714130 P46095 G-protein coupled receptor 6 92.63% 97.36%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.52% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.14% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.86% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.78% 96.00%
CHEMBL4208 P20618 Proteasome component C5 88.44% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.75% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 87.41% 93.31%
CHEMBL5747 Q92793 CREB-binding protein 85.09% 95.12%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.37% 91.11%
CHEMBL2535 P11166 Glucose transporter 83.28% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.10% 99.17%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 80.41% 92.38%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.16% 92.94%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.02% 99.15%

Plants that contains it

Top
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

Top
PubChem 21856873
NPASS NPC209217