7-(Hydroxymethyl)-9-methoxy-1-methylphenanthrene-3,6-diol

Details

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Internal ID cfa2f6ea-d7ad-4936-9710-04c4c59dd959
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 7-(hydroxymethyl)-9-methoxy-1-methylphenanthrene-3,6-diol
SMILES (Canonical) CC1=CC(=CC2=C3C=C(C(=CC3=C(C=C12)OC)CO)O)O
SMILES (Isomeric) CC1=CC(=CC2=C3C=C(C(=CC3=C(C=C12)OC)CO)O)O
InChI InChI=1S/C17H16O4/c1-9-3-11(19)5-13-12(9)7-17(21-2)15-4-10(8-18)16(20)6-14(13)15/h3-7,18-20H,8H2,1-2H3
InChI Key CZTMVNXXZPVJSQ-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) 69.90 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(Hydroxymethyl)-9-methoxy-1-methylphenanthrene-3,6-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9801 98.01%
Caco-2 + 0.6700 67.00%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7159 71.59%
OATP2B1 inhibitior - 0.5632 56.32%
OATP1B1 inhibitior + 0.9193 91.93%
OATP1B3 inhibitior + 0.9364 93.64%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6859 68.59%
P-glycoprotein inhibitior - 0.9147 91.47%
P-glycoprotein substrate - 0.7792 77.92%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate + 0.3970 39.70%
CYP3A4 inhibition - 0.6967 69.67%
CYP2C9 inhibition - 0.6841 68.41%
CYP2C19 inhibition + 0.6440 64.40%
CYP2D6 inhibition - 0.8628 86.28%
CYP1A2 inhibition + 0.9208 92.08%
CYP2C8 inhibition + 0.4923 49.23%
CYP inhibitory promiscuity + 0.6989 69.89%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8610 86.10%
Carcinogenicity (trinary) Non-required 0.7187 71.87%
Eye corrosion - 0.9836 98.36%
Eye irritation + 0.7616 76.16%
Skin irritation - 0.7810 78.10%
Skin corrosion - 0.9361 93.61%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4193 41.93%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.7824 78.24%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6531 65.31%
Acute Oral Toxicity (c) III 0.6723 67.23%
Estrogen receptor binding + 0.8501 85.01%
Androgen receptor binding + 0.5751 57.51%
Thyroid receptor binding + 0.6475 64.75%
Glucocorticoid receptor binding + 0.8183 81.83%
Aromatase binding + 0.8202 82.02%
PPAR gamma + 0.7853 78.53%
Honey bee toxicity - 0.8665 86.65%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9138 91.38%

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 97.91% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.68% 95.56%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 93.22% 89.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.44% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.26% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.04% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.78% 92.62%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 88.65% 91.79%
CHEMBL1255126 O15151 Protein Mdm4 87.47% 90.20%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.53% 99.15%
CHEMBL2535 P11166 Glucose transporter 85.49% 98.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.37% 91.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.61% 86.33%
CHEMBL4581 P52732 Kinesin-like protein 1 81.52% 93.18%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.28% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 80.00% 94.73%

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.
Tannodia perrieri

Cross-Links

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PubChem 10826894
LOTUS LTS0162688
wikiData Q104973144