7-Hydroxy-6-methyl-4-propan-2-ylchromen-2-one

Details

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Internal ID 8ac4e1a9-9fa3-4026-917f-5ba0f5251fc5
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 7-hydroxy-6-methyl-4-propan-2-ylchromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14O3/c1-7(2)9-5-13(15)16-12-6-11(14)8(3)4-10(9)12/h4-7,14H,1-3H3
InChI Key UFVKXIXGJJWITR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O3
Molecular Weight 218.25 g/mol
Exact Mass 218.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.93
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxy-6-methyl-4-propan-2-ylchromen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.8955 89.55%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7706 77.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9496 94.96%
OATP1B3 inhibitior + 0.9777 97.77%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8703 87.03%
P-glycoprotein inhibitior - 0.9284 92.84%
P-glycoprotein substrate - 0.9154 91.54%
CYP3A4 substrate - 0.5701 57.01%
CYP2C9 substrate + 0.6157 61.57%
CYP2D6 substrate - 0.8705 87.05%
CYP3A4 inhibition - 0.9670 96.70%
CYP2C9 inhibition - 0.7447 74.47%
CYP2C19 inhibition - 0.8809 88.09%
CYP2D6 inhibition - 0.9573 95.73%
CYP1A2 inhibition + 0.8300 83.00%
CYP2C8 inhibition - 0.9262 92.62%
CYP inhibitory promiscuity - 0.8389 83.89%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9713 97.13%
Carcinogenicity (trinary) Non-required 0.6348 63.48%
Eye corrosion - 0.9835 98.35%
Eye irritation + 0.8881 88.81%
Skin irritation - 0.5686 56.86%
Skin corrosion - 0.9831 98.31%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7575 75.75%
Micronuclear + 0.7359 73.59%
Hepatotoxicity - 0.5573 55.73%
skin sensitisation - 0.8663 86.63%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.5719 57.19%
Acute Oral Toxicity (c) III 0.6091 60.91%
Estrogen receptor binding - 0.5098 50.98%
Androgen receptor binding + 0.6082 60.82%
Thyroid receptor binding - 0.5218 52.18%
Glucocorticoid receptor binding + 0.7031 70.31%
Aromatase binding + 0.6217 62.17%
PPAR gamma + 0.6494 64.94%
Honey bee toxicity - 0.8621 86.21%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9700 97.00%

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 98.17% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.83% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.75% 99.15%
CHEMBL2581 P07339 Cathepsin D 93.03% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.89% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 92.17% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 92.11% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 89.15% 93.65%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.39% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.46% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.26% 94.45%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 82.55% 83.57%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.46% 93.56%

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.
Macrothelypteris torresiana

Cross-Links

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PubChem 13831855
LOTUS LTS0228564
wikiData Q104945503