3,6,9-Trimethoxyphenanthropolone

Details

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Internal ID 7f84adce-6858-419e-93e6-281cf1e0c117
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Tanshinones, isotanshinones, and derivatives
IUPAC Name 2,5,10-trimethoxy-3,8-dimethylcyclohepta[a]naphthalen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20O4/c1-11-7-16-15(10-17(11)22-3)14-9-19(24-5)20(21)12(2)6-13(14)8-18(16)23-4/h6-10H,1-5H3
InChI Key GBUYBLVESLNEQP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O4
Molecular Weight 324.40 g/mol
Exact Mass 324.13615911 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.00
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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3,6,9-trimethoxyphenanthropolone

2D Structure

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2D Structure of 3,6,9-Trimethoxyphenanthropolone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.9349 93.49%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.7274 72.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9628 96.28%
OATP1B3 inhibitior + 0.9720 97.20%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8543 85.43%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.8751 87.51%
CYP3A4 substrate - 0.5491 54.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7000 70.00%
CYP3A4 inhibition + 0.7768 77.68%
CYP2C9 inhibition - 0.8259 82.59%
CYP2C19 inhibition + 0.6553 65.53%
CYP2D6 inhibition - 0.9272 92.72%
CYP1A2 inhibition + 0.9422 94.22%
CYP2C8 inhibition - 0.8748 87.48%
CYP inhibitory promiscuity + 0.5956 59.56%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8930 89.30%
Carcinogenicity (trinary) Non-required 0.4916 49.16%
Eye corrosion - 0.9612 96.12%
Eye irritation + 0.8056 80.56%
Skin irritation - 0.7263 72.63%
Skin corrosion - 0.9860 98.60%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6944 69.44%
Micronuclear + 0.6318 63.18%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.9185 91.85%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.4882 48.82%
Acute Oral Toxicity (c) III 0.4795 47.95%
Estrogen receptor binding + 0.8810 88.10%
Androgen receptor binding + 0.5562 55.62%
Thyroid receptor binding + 0.6785 67.85%
Glucocorticoid receptor binding + 0.5991 59.91%
Aromatase binding + 0.7396 73.96%
PPAR gamma + 0.5422 54.22%
Honey bee toxicity - 0.8292 82.92%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9813 98.13%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.37% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 90.87% 94.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.45% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.91% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.87% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.50% 91.11%
CHEMBL2535 P11166 Glucose transporter 85.01% 98.75%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.20% 89.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.89% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.74% 96.00%

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.
Strophioblachia fimbricalyx

Cross-Links

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PubChem 44557154
LOTUS LTS0054315
wikiData Q105006097