7-Hydroxy-2,3,4-trimethoxyphenanthrene

Details

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Internal ID bc5899f9-b05a-4cdb-b0c3-64a866712107
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 5,6,7-trimethoxyphenanthren-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H16O4/c1-19-14-9-11-5-4-10-8-12(18)6-7-13(10)15(11)17(21-3)16(14)20-2/h4-9,18H,1-3H3
InChI Key XOYDRISJWPIZCQ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O4
Molecular Weight 284.31 g/mol
Exact Mass 284.10485899 g/mol
Topological Polar Surface Area (TPSA) 47.90 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.72
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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7-hydroxy-2,3,4-trimethoxyphenanthrene

2D Structure

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2D Structure of 7-Hydroxy-2,3,4-trimethoxyphenanthrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9328 93.28%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7055 70.55%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.8807 88.07%
OATP1B3 inhibitior + 0.9640 96.40%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6395 63.95%
P-glycoprotein inhibitior - 0.8033 80.33%
P-glycoprotein substrate - 0.6810 68.10%
CYP3A4 substrate - 0.5714 57.14%
CYP2C9 substrate - 0.7933 79.33%
CYP2D6 substrate + 0.4916 49.16%
CYP3A4 inhibition - 0.6931 69.31%
CYP2C9 inhibition - 0.9575 95.75%
CYP2C19 inhibition - 0.6790 67.90%
CYP2D6 inhibition - 0.8844 88.44%
CYP1A2 inhibition + 0.9154 91.54%
CYP2C8 inhibition + 0.8487 84.87%
CYP inhibitory promiscuity - 0.5444 54.44%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8428 84.28%
Carcinogenicity (trinary) Non-required 0.4995 49.95%
Eye corrosion - 0.9802 98.02%
Eye irritation + 0.8929 89.29%
Skin irritation - 0.6611 66.11%
Skin corrosion - 0.9777 97.77%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3868 38.68%
Micronuclear + 0.5918 59.18%
Hepatotoxicity + 0.5697 56.97%
skin sensitisation - 0.8628 86.28%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7772 77.72%
Acute Oral Toxicity (c) III 0.4423 44.23%
Estrogen receptor binding + 0.8816 88.16%
Androgen receptor binding + 0.7887 78.87%
Thyroid receptor binding + 0.8083 80.83%
Glucocorticoid receptor binding + 0.6864 68.64%
Aromatase binding + 0.7679 76.79%
PPAR gamma + 0.5387 53.87%
Honey bee toxicity - 0.9271 92.71%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7151 71.51%
Fish aquatic toxicity + 0.9529 95.29%

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 95.42% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 92.19% 98.35%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.81% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.79% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.51% 89.62%
CHEMBL2535 P11166 Glucose transporter 88.93% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.08% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.24% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.30% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.21% 95.56%
CHEMBL1255126 O15151 Protein Mdm4 83.55% 90.20%
CHEMBL213 P08588 Beta-1 adrenergic receptor 83.40% 95.56%
CHEMBL4208 P20618 Proteasome component C5 80.73% 90.00%

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.
Dioscorea communis

Cross-Links

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PubChem 11997529
LOTUS LTS0250528
wikiData Q105338022