4,6,9-Trimethoxyphenanthropolone

Details

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Internal ID 94033031-4f39-4322-8bf7-dd629cd40fac
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 2,5,11-trimethoxy-3,8-dimethylcyclohepta[a]naphthalen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20O4/c1-11-6-13-8-18(23-4)14-7-12(2)17(22-3)9-15(14)20(13)19(24-5)10-16(11)21/h6-10H,1-5H3
InChI Key DRHLTPUTOAKXAP-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 4.10
Atomic LogP (AlogP) 4.00
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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4,6,9-trimethoxyphenanthropolone

2D Structure

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2D Structure of 4,6,9-Trimethoxyphenanthropolone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9214 92.14%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7161 71.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9508 95.08%
OATP1B3 inhibitior + 0.9848 98.48%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8703 87.03%
P-glycoprotein inhibitior - 0.4780 47.80%
P-glycoprotein substrate - 0.8730 87.30%
CYP3A4 substrate - 0.5217 52.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7332 73.32%
CYP3A4 inhibition + 0.6034 60.34%
CYP2C9 inhibition - 0.8902 89.02%
CYP2C19 inhibition - 0.5334 53.34%
CYP2D6 inhibition - 0.9484 94.84%
CYP1A2 inhibition + 0.9612 96.12%
CYP2C8 inhibition - 0.8458 84.58%
CYP inhibitory promiscuity + 0.6479 64.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8155 81.55%
Carcinogenicity (trinary) Non-required 0.5503 55.03%
Eye corrosion - 0.9691 96.91%
Eye irritation + 0.8269 82.69%
Skin irritation - 0.7499 74.99%
Skin corrosion - 0.9868 98.68%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7220 72.20%
Micronuclear + 0.6618 66.18%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.9384 93.84%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.4915 49.15%
Acute Oral Toxicity (c) II 0.5452 54.52%
Estrogen receptor binding + 0.9125 91.25%
Androgen receptor binding + 0.5997 59.97%
Thyroid receptor binding + 0.7488 74.88%
Glucocorticoid receptor binding + 0.7641 76.41%
Aromatase binding + 0.7443 74.43%
PPAR gamma + 0.7842 78.42%
Honey bee toxicity - 0.8129 81.29%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9849 98.49%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.78% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.67% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.47% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 88.73% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.02% 91.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.99% 97.36%
CHEMBL2535 P11166 Glucose transporter 83.83% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.42% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.28% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.15% 93.99%
CHEMBL230 P35354 Cyclooxygenase-2 82.18% 89.63%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.07% 89.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.38% 86.33%

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 44557155
LOTUS LTS0158523
wikiData Q104987417