Methyl 4-(8-hydroxy-7-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate

Details

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Internal ID a13a04ce-7e94-46c4-a0ce-c3ecde1f53c0
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins
IUPAC Name methyl 4-(8-hydroxy-7-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate
SMILES (Canonical) CC(=CCC1=CC2=C(C(=C(C=C2)OC)O)OC1=O)C(=O)OC
SMILES (Isomeric) CC(=CCC1=CC2=C(C(=C(C=C2)OC)O)OC1=O)C(=O)OC
InChI InChI=1S/C16H16O6/c1-9(15(18)21-3)4-5-11-8-10-6-7-12(20-2)13(17)14(10)22-16(11)19/h4,6-8,17H,5H2,1-3H3
InChI Key KXEJCMRLSGMAAK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O6
Molecular Weight 304.29 g/mol
Exact Mass 304.09468823 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.17
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 4-(8-hydroxy-7-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9793 97.93%
Caco-2 + 0.8004 80.04%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5989 59.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9144 91.44%
OATP1B3 inhibitior + 0.8936 89.36%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5069 50.69%
P-glycoprotein inhibitior - 0.6682 66.82%
P-glycoprotein substrate - 0.7513 75.13%
CYP3A4 substrate + 0.5083 50.83%
CYP2C9 substrate - 0.5802 58.02%
CYP2D6 substrate - 0.8534 85.34%
CYP3A4 inhibition - 0.8934 89.34%
CYP2C9 inhibition - 0.8564 85.64%
CYP2C19 inhibition - 0.5139 51.39%
CYP2D6 inhibition - 0.8458 84.58%
CYP1A2 inhibition + 0.5648 56.48%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.5498 54.98%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5901 59.01%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.8035 80.35%
Skin irritation - 0.7236 72.36%
Skin corrosion - 0.9726 97.26%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5943 59.43%
Micronuclear + 0.5818 58.18%
Hepatotoxicity + 0.6855 68.55%
skin sensitisation - 0.8535 85.35%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6316 63.16%
Acute Oral Toxicity (c) III 0.4522 45.22%
Estrogen receptor binding + 0.8318 83.18%
Androgen receptor binding + 0.5846 58.46%
Thyroid receptor binding - 0.5408 54.08%
Glucocorticoid receptor binding + 0.7613 76.13%
Aromatase binding + 0.8230 82.30%
PPAR gamma + 0.6406 64.06%
Honey bee toxicity - 0.9168 91.68%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9911 99.11%

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 98.81% 91.11%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 93.00% 98.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.90% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.76% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 91.78% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.30% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 90.91% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.71% 94.45%
CHEMBL2581 P07339 Cathepsin D 88.15% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.97% 95.56%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.78% 85.30%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.76% 92.62%
CHEMBL4208 P20618 Proteasome component C5 83.09% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.99% 96.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.24% 96.95%
CHEMBL2535 P11166 Glucose transporter 82.10% 98.75%
CHEMBL4040 P28482 MAP kinase ERK2 81.91% 83.82%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.28% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.14% 99.23%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.72% 89.34%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.30% 91.07%

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.
Phebalium clavatum

Cross-Links

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PubChem 85402031
LOTUS LTS0249092
wikiData Q105147301