(Z)-O-Methylsuberenol

Details

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Internal ID 5d63b276-8225-4968-91a2-06f427ba5c1e
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-methoxy-6-[(Z)-3-methoxy-3-methylbut-1-enyl]chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H18O4/c1-16(2,19-4)8-7-12-9-11-5-6-15(17)20-14(11)10-13(12)18-3/h5-10H,1-4H3/b8-7-
InChI Key IMRSLPQVHDFZJC-FPLPWBNLSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H18O4
Molecular Weight 274.31 g/mol
Exact Mass 274.12050905 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.24
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-O-Methylsuberenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.9280 92.80%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6503 65.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8768 87.68%
OATP1B3 inhibitior + 0.9883 98.83%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8268 82.68%
P-glycoprotein inhibitior - 0.5544 55.44%
P-glycoprotein substrate - 0.8028 80.28%
CYP3A4 substrate - 0.5277 52.77%
CYP2C9 substrate - 0.6661 66.61%
CYP2D6 substrate - 0.8370 83.70%
CYP3A4 inhibition + 0.6149 61.49%
CYP2C9 inhibition - 0.7675 76.75%
CYP2C19 inhibition + 0.6955 69.55%
CYP2D6 inhibition - 0.8717 87.17%
CYP1A2 inhibition + 0.8528 85.28%
CYP2C8 inhibition - 0.7733 77.33%
CYP inhibitory promiscuity + 0.6814 68.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Danger 0.4240 42.40%
Eye corrosion - 0.9750 97.50%
Eye irritation + 0.7063 70.63%
Skin irritation - 0.8027 80.27%
Skin corrosion - 0.9798 97.98%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7916 79.16%
Micronuclear + 0.5700 57.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.8703 87.03%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5645 56.45%
Acute Oral Toxicity (c) II 0.5019 50.19%
Estrogen receptor binding + 0.9763 97.63%
Androgen receptor binding + 0.6989 69.89%
Thyroid receptor binding + 0.5927 59.27%
Glucocorticoid receptor binding + 0.7065 70.65%
Aromatase binding + 0.9234 92.34%
PPAR gamma + 0.8336 83.36%
Honey bee toxicity - 0.7921 79.21%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9887 98.87%

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 93.67% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.23% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.16% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.74% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.95% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.37% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.44% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 84.60% 94.73%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.82% 85.30%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.23% 99.17%

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 14212557
LOTUS LTS0090006
wikiData Q105115905