8-methoxy-9-phenyl-2,3-dihydro-1H-phenalene-1,4-diol

Details

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Internal ID 60ec75fb-ac55-400c-a059-49561b301e86
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 8-methoxy-9-phenyl-2,3-dihydro-1H-phenalene-1,4-diol
SMILES (Canonical) COC1=C(C2=C3C(=C(C=CC3=C1)O)CCC2O)C4=CC=CC=C4
SMILES (Isomeric) COC1=C(C2=C3C(=C(C=CC3=C1)O)CCC2O)C4=CC=CC=C4
InChI InChI=1S/C20H18O3/c1-23-17-11-13-7-9-15(21)14-8-10-16(22)20(18(13)14)19(17)12-5-3-2-4-6-12/h2-7,9,11,16,21-22H,8,10H2,1H3
InChI Key SACCSROMZNBAMO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O3
Molecular Weight 306.40 g/mol
Exact Mass 306.125594432 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.20
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-methoxy-9-phenyl-2,3-dihydro-1H-phenalene-1,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 - 0.5339 53.39%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.9161 91.61%
OATP2B1 inhibitior - 0.8493 84.93%
OATP1B1 inhibitior + 0.9435 94.35%
OATP1B3 inhibitior + 0.9518 95.18%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7539 75.39%
P-glycoprotein inhibitior - 0.6533 65.33%
P-glycoprotein substrate - 0.7997 79.97%
CYP3A4 substrate + 0.5518 55.18%
CYP2C9 substrate - 0.7818 78.18%
CYP2D6 substrate + 0.5806 58.06%
CYP3A4 inhibition - 0.8484 84.84%
CYP2C9 inhibition + 0.5486 54.86%
CYP2C19 inhibition + 0.7210 72.10%
CYP2D6 inhibition - 0.8894 88.94%
CYP1A2 inhibition + 0.8894 88.94%
CYP2C8 inhibition + 0.7695 76.95%
CYP inhibitory promiscuity - 0.5835 58.35%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7511 75.11%
Carcinogenicity (trinary) Non-required 0.4206 42.06%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.7623 76.23%
Skin irritation - 0.6102 61.02%
Skin corrosion - 0.9162 91.62%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3721 37.21%
Micronuclear - 0.6241 62.41%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8522 85.22%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7165 71.65%
Acute Oral Toxicity (c) III 0.6102 61.02%
Estrogen receptor binding + 0.9010 90.10%
Androgen receptor binding + 0.8115 81.15%
Thyroid receptor binding + 0.6818 68.18%
Glucocorticoid receptor binding + 0.8435 84.35%
Aromatase binding + 0.5950 59.50%
PPAR gamma + 0.8218 82.18%
Honey bee toxicity - 0.8861 88.61%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.8472 84.72%

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 98.62% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.98% 86.33%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 92.85% 91.79%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.55% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.33% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.18% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.74% 99.15%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.45% 93.99%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.75% 99.17%
CHEMBL4208 P20618 Proteasome component C5 84.53% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.87% 94.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.59% 94.03%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 102484716
LOTUS LTS0062599
wikiData Q105248761