2,6,7-Trimethoxyphenanthren-4-ol

Details

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Internal ID 14f4f356-e835-4f2a-a7fd-ebc3a87964d9
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 2,6,7-trimethoxyphenanthren-4-ol
SMILES (Canonical) COC1=CC(=C2C(=C1)C=CC3=CC(=C(C=C32)OC)OC)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)C=CC3=CC(=C(C=C32)OC)OC)O
InChI InChI=1S/C17H16O4/c1-19-12-6-11-5-4-10-7-15(20-2)16(21-3)9-13(10)17(11)14(18)8-12/h4-9,18H,1-3H3
InChI Key OJXFCMHKFIMBEM-UHFFFAOYSA-N
Popularity 0 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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There are no found synonyms.

2D Structure

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2D Structure of 2,6,7-Trimethoxyphenanthren-4-ol

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 + 0.9399 93.99%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7055 70.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9139 91.39%
OATP1B3 inhibitior + 0.9640 96.40%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6471 64.71%
P-glycoprotein inhibitior - 0.7113 71.13%
P-glycoprotein substrate - 0.8288 82.88%
CYP3A4 substrate - 0.6002 60.02%
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 + 0.7273 72.73%
CYP inhibitory promiscuity - 0.5444 54.44%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8428 84.28%
Carcinogenicity (trinary) Non-required 0.4995 49.95%
Eye corrosion - 0.9802 98.02%
Eye irritation + 0.8732 87.32%
Skin irritation - 0.6611 66.11%
Skin corrosion - 0.9777 97.77%
Ames mutagenesis + 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3605 36.05%
Micronuclear + 0.5918 59.18%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.8628 86.28%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7357 73.57%
Acute Oral Toxicity (c) III 0.4423 44.23%
Estrogen receptor binding + 0.9341 93.41%
Androgen receptor binding + 0.6093 60.93%
Thyroid receptor binding + 0.8390 83.90%
Glucocorticoid receptor binding + 0.8097 80.97%
Aromatase binding + 0.8416 84.16%
PPAR gamma + 0.6479 64.79%
Honey bee toxicity - 0.9455 94.55%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.7451 74.51%
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 96.31% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.92% 92.94%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.24% 99.15%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 91.01% 91.79%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.98% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.33% 95.56%
CHEMBL2535 P11166 Glucose transporter 89.13% 98.75%
CHEMBL4208 P20618 Proteasome component C5 88.76% 90.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.03% 89.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.10% 93.99%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.03% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.86% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.19% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.05% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.88% 96.00%
CHEMBL1951 P21397 Monoamine oxidase A 82.56% 91.49%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.08% 92.68%

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 22753768
LOTUS LTS0092739
wikiData Q105193339