7-(2,3-Dihydroxy-3-methylbutoxy)chromen-2-one

Details

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Internal ID 60f332e2-4c14-4c30-921b-82a6ec446f41
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-(2,3-dihydroxy-3-methylbutoxy)chromen-2-one
SMILES (Canonical) CC(C)(C(COC1=CC2=C(C=C1)C=CC(=O)O2)O)O
SMILES (Isomeric) CC(C)(C(COC1=CC2=C(C=C1)C=CC(=O)O2)O)O
InChI InChI=1S/C14H16O5/c1-14(2,17)12(15)8-18-10-5-3-9-4-6-13(16)19-11(9)7-10/h3-7,12,15,17H,8H2,1-2H3
InChI Key GHSFVCDUBWHKCG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O5
Molecular Weight 264.27 g/mol
Exact Mass 264.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.30
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(2,3-Dihydroxy-3-methylbutoxy)chromen-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 + 0.9645 96.45%
Caco-2 + 0.6814 68.14%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7604 76.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8708 87.08%
OATP1B3 inhibitior + 0.8851 88.51%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5665 56.65%
P-glycoprotein inhibitior - 0.9288 92.88%
P-glycoprotein substrate - 0.8881 88.81%
CYP3A4 substrate - 0.5386 53.86%
CYP2C9 substrate - 0.6661 66.61%
CYP2D6 substrate - 0.8264 82.64%
CYP3A4 inhibition - 0.9550 95.50%
CYP2C9 inhibition - 0.9233 92.33%
CYP2C19 inhibition - 0.8786 87.86%
CYP2D6 inhibition - 0.9060 90.60%
CYP1A2 inhibition + 0.5440 54.40%
CYP2C8 inhibition - 0.8740 87.40%
CYP inhibitory promiscuity - 0.9348 93.48%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6263 62.63%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.8509 85.09%
Skin irritation - 0.8117 81.17%
Skin corrosion - 0.9557 95.57%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6854 68.54%
Micronuclear - 0.5167 51.67%
Hepatotoxicity - 0.5425 54.25%
skin sensitisation - 0.8242 82.42%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7453 74.53%
Acute Oral Toxicity (c) III 0.7186 71.86%
Estrogen receptor binding + 0.7368 73.68%
Androgen receptor binding + 0.7160 71.60%
Thyroid receptor binding + 0.5727 57.27%
Glucocorticoid receptor binding + 0.6707 67.07%
Aromatase binding + 0.7180 71.80%
PPAR gamma + 0.7642 76.42%
Honey bee toxicity - 0.9200 92.00%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9148 91.48%

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
CHEMBL2039 P27338 Monoamine oxidase B 97.89% 92.51%
CHEMBL2581 P07339 Cathepsin D 96.66% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.81% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.54% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 93.74% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.13% 99.17%
CHEMBL4208 P20618 Proteasome component C5 86.65% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.63% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.20% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.36% 86.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.40% 86.92%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.21% 95.71%
CHEMBL1951 P21397 Monoamine oxidase A 81.49% 91.49%
CHEMBL1907 P15144 Aminopeptidase N 81.46% 93.31%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.17% 100.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.48% 93.65%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.01% 99.15%

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.
Coleonema album

Cross-Links

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PubChem 101779265
LOTUS LTS0098555
wikiData Q105008703