9,10-Dihydro-2,7-dihydroxy-1,3,5-trimethoxyphenanthrene

Details

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Internal ID ee4c9f6e-a944-42c2-bf72-ff5b0385daba
Taxonomy Benzenoids > Phenanthrenes and derivatives > Hydrophenanthrenes
IUPAC Name 1,3,5-trimethoxy-9,10-dihydrophenanthrene-2,7-diol
SMILES (Canonical) COC1=CC(=CC2=C1C3=CC(=C(C(=C3CC2)OC)O)OC)O
SMILES (Isomeric) COC1=CC(=CC2=C1C3=CC(=C(C(=C3CC2)OC)O)OC)O
InChI InChI=1S/C17H18O5/c1-20-13-7-10(18)6-9-4-5-11-12(15(9)13)8-14(21-2)16(19)17(11)22-3/h6-8,18-19H,4-5H2,1-3H3
InChI Key OPQXRVWHTHJRDR-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H18O5
Molecular Weight 302.32 g/mol
Exact Mass 302.11542367 g/mol
Topological Polar Surface Area (TPSA) 68.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9,10-Dihydro-2,7-dihydroxy-1,3,5-trimethoxyphenanthrene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9595 95.95%
Caco-2 + 0.8783 87.83%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7689 76.89%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9030 90.30%
OATP1B3 inhibitior + 0.9375 93.75%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6057 60.57%
P-glycoprotein inhibitior - 0.8877 88.77%
P-glycoprotein substrate - 0.8291 82.91%
CYP3A4 substrate + 0.5734 57.34%
CYP2C9 substrate - 0.6180 61.80%
CYP2D6 substrate + 0.5879 58.79%
CYP3A4 inhibition - 0.8776 87.76%
CYP2C9 inhibition - 0.7003 70.03%
CYP2C19 inhibition + 0.5468 54.68%
CYP2D6 inhibition - 0.8701 87.01%
CYP1A2 inhibition + 0.9059 90.59%
CYP2C8 inhibition + 0.7086 70.86%
CYP inhibitory promiscuity + 0.5722 57.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7720 77.20%
Carcinogenicity (trinary) Non-required 0.5340 53.40%
Eye corrosion - 0.9845 98.45%
Eye irritation + 0.6850 68.50%
Skin irritation - 0.6675 66.75%
Skin corrosion - 0.9229 92.29%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6451 64.51%
Micronuclear - 0.6200 62.00%
Hepatotoxicity - 0.5039 50.39%
skin sensitisation - 0.8589 85.89%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.6601 66.01%
Acute Oral Toxicity (c) III 0.5920 59.20%
Estrogen receptor binding + 0.7648 76.48%
Androgen receptor binding - 0.5448 54.48%
Thyroid receptor binding + 0.6936 69.36%
Glucocorticoid receptor binding + 0.7058 70.58%
Aromatase binding + 0.5548 55.48%
PPAR gamma + 0.6326 63.26%
Honey bee toxicity - 0.9312 93.12%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6151 61.51%
Fish aquatic toxicity + 0.9314 93.14%

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 98.91% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.39% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.87% 86.33%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 90.61% 92.68%
CHEMBL1951 P21397 Monoamine oxidase A 90.35% 91.49%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 89.82% 98.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.07% 99.17%
CHEMBL2535 P11166 Glucose transporter 88.76% 98.75%
CHEMBL2056 P21728 Dopamine D1 receptor 88.34% 91.00%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 88.29% 91.79%
CHEMBL4208 P20618 Proteasome component C5 87.76% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.02% 95.56%
CHEMBL242 Q92731 Estrogen receptor beta 85.46% 98.35%
CHEMBL2581 P07339 Cathepsin D 83.25% 98.95%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.70% 96.21%
CHEMBL5747 Q92793 CREB-binding protein 81.68% 95.12%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.42% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.89% 95.89%
CHEMBL217 P14416 Dopamine D2 receptor 80.80% 95.62%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.75% 94.03%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.10% 94.00%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 80.01% 95.78%

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 decipiens

Cross-Links

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PubChem 129856049
LOTUS LTS0207978
wikiData Q105196522