3,5,6,7-Tetramethoxyphenanthrene-2-ol

Details

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Internal ID 442f3c7d-e163-4eb6-b0da-46fe33d82e45
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 3,5,6,7-tetramethoxyphenanthren-2-ol
SMILES (Canonical) COC1=C(C(=C2C(=C1)C=CC3=CC(=C(C=C32)OC)O)OC)OC
SMILES (Isomeric) COC1=C(C(=C2C(=C1)C=CC3=CC(=C(C=C32)OC)O)OC)OC
InChI InChI=1S/C18H18O5/c1-20-14-9-12-10(7-13(14)19)5-6-11-8-15(21-2)17(22-3)18(23-4)16(11)12/h5-9,19H,1-4H3
InChI Key LPCCNSGUTPIMPZ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C18H18O5
Molecular Weight 314.30 g/mol
Exact Mass 314.11542367 g/mol
Topological Polar Surface Area (TPSA) 57.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.73
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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SCHEMBL14439528
BDBM50469835

2D Structure

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2D Structure of 3,5,6,7-Tetramethoxyphenanthrene-2-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 + 0.9360 93.60%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7055 70.55%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.9028 90.28%
OATP1B3 inhibitior + 0.9640 96.40%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7963 79.63%
P-glycoprotein inhibitior - 0.6993 69.93%
P-glycoprotein substrate - 0.8665 86.65%
CYP3A4 substrate - 0.5876 58.76%
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 + 0.7223 72.23%
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 + 0.8626 86.26%
Skin irritation - 0.6611 66.11%
Skin corrosion - 0.9777 97.77%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4324 43.24%
Micronuclear + 0.5918 59.18%
Hepatotoxicity - 0.5803 58.03%
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 - 0.8359 83.59%
Acute Oral Toxicity (c) III 0.4423 44.23%
Estrogen receptor binding + 0.9177 91.77%
Androgen receptor binding + 0.6164 61.64%
Thyroid receptor binding + 0.7990 79.90%
Glucocorticoid receptor binding + 0.7535 75.35%
Aromatase binding + 0.7842 78.42%
PPAR gamma + 0.6505 65.05%
Honey bee toxicity - 0.9397 93.97%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.7051 70.51%
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 96.74% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.31% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.79% 89.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.12% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.80% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.74% 95.56%
CHEMBL2535 P11166 Glucose transporter 86.58% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.61% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.20% 99.17%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.90% 92.94%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.84% 99.15%
CHEMBL4208 P20618 Proteasome component C5 81.04% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.93% 96.00%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 80.12% 91.79%

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.
Combretum caffrum
Combretum psidioides

Cross-Links

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PubChem 11141545
LOTUS LTS0249404
wikiData Q105155029