6-(4-Hydroxy-3-methyl-2-butenyl)-7-hydroxy coumarin

Details

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Internal ID 43116f0d-0156-451d-91a4-0716c3edf6d5
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 7-hydroxy-6-(4-hydroxy-3-methylbut-2-enyl)chromen-2-one
SMILES (Canonical) CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)CO
SMILES (Isomeric) CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)CO
InChI InChI=1S/C14H14O4/c1-9(8-15)2-3-10-6-11-4-5-14(17)18-13(11)7-12(10)16/h2,4-7,15-16H,3,8H2,1H3
InChI Key JUOLTTLEQHQQED-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H14O4
Molecular Weight 246.26 g/mol
Exact Mass 246.08920892 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.98
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(4-Hydroxy-3-methyl-2-butenyl)-7-hydroxy coumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9797 97.97%
Caco-2 + 0.6244 62.44%
Blood Brain Barrier - 0.7072 70.72%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7456 74.56%
OATP2B1 inhibitior - 0.5806 58.06%
OATP1B1 inhibitior + 0.9106 91.06%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6312 63.12%
P-glycoprotein inhibitior - 0.9396 93.96%
P-glycoprotein substrate - 0.8016 80.16%
CYP3A4 substrate - 0.6020 60.20%
CYP2C9 substrate - 0.5903 59.03%
CYP2D6 substrate - 0.8263 82.63%
CYP3A4 inhibition - 0.6981 69.81%
CYP2C9 inhibition + 0.5111 51.11%
CYP2C19 inhibition + 0.6690 66.90%
CYP2D6 inhibition - 0.7527 75.27%
CYP1A2 inhibition + 0.7886 78.86%
CYP2C8 inhibition - 0.8471 84.71%
CYP inhibitory promiscuity + 0.6976 69.76%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.6936 69.36%
Eye corrosion - 0.9903 99.03%
Eye irritation + 0.6445 64.45%
Skin irritation - 0.7278 72.78%
Skin corrosion - 0.9522 95.22%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5571 55.71%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8136 81.36%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6161 61.61%
Acute Oral Toxicity (c) III 0.3759 37.59%
Estrogen receptor binding + 0.8369 83.69%
Androgen receptor binding + 0.5722 57.22%
Thyroid receptor binding - 0.5719 57.19%
Glucocorticoid receptor binding + 0.8980 89.80%
Aromatase binding + 0.7282 72.82%
PPAR gamma + 0.8227 82.27%
Honey bee toxicity - 0.9536 95.36%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 1.0000 100.00%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3242 O43570 Carbonic anhydrase XII 770 nM
Ki
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.77% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.83% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 92.03% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.90% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 85.20% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.03% 94.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.51% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.12% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.04% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.38% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.23% 89.00%

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.
Aegle marmelos
Phellodendron chinense var. glabriusculum

Cross-Links

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PubChem 78157935
LOTUS LTS0201060
wikiData Q105135342