7-(2-Hydroxy-3-methylbut-3-enoxy)chromen-2-one

Details

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Internal ID ea1c5af8-4f03-4315-9413-dc0aa72a27e2
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-(2-hydroxy-3-methylbut-3-enoxy)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H14O4/c1-9(2)12(15)8-17-11-5-3-10-4-6-14(16)18-13(10)7-11/h3-7,12,15H,1,8H2,2H3
InChI Key XCYOSEWDYYJJIX-UHFFFAOYSA-N
Popularity 0 references 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) 55.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.11
H-Bond Acceptor 4
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 7-(2-Hydroxy-3-methylbut-3-enoxy)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 + 0.9899 98.99%
Caco-2 + 0.8270 82.70%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6275 62.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8522 85.22%
OATP1B3 inhibitior + 0.9249 92.49%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7061 70.61%
P-glycoprotein inhibitior - 0.8959 89.59%
P-glycoprotein substrate - 0.8923 89.23%
CYP3A4 substrate - 0.5371 53.71%
CYP2C9 substrate - 0.8377 83.77%
CYP2D6 substrate - 0.8156 81.56%
CYP3A4 inhibition - 0.6240 62.40%
CYP2C9 inhibition - 0.8037 80.37%
CYP2C19 inhibition + 0.5219 52.19%
CYP2D6 inhibition - 0.8343 83.43%
CYP1A2 inhibition + 0.6618 66.18%
CYP2C8 inhibition - 0.8899 88.99%
CYP inhibitory promiscuity - 0.5243 52.43%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6636 66.36%
Eye corrosion - 0.9766 97.66%
Eye irritation - 0.5818 58.18%
Skin irritation - 0.7203 72.03%
Skin corrosion - 0.9559 95.59%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4740 47.40%
Micronuclear + 0.5392 53.92%
Hepatotoxicity - 0.5050 50.50%
skin sensitisation - 0.6484 64.84%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6309 63.09%
Acute Oral Toxicity (c) III 0.6106 61.06%
Estrogen receptor binding + 0.6467 64.67%
Androgen receptor binding + 0.6605 66.05%
Thyroid receptor binding - 0.6548 65.48%
Glucocorticoid receptor binding + 0.6774 67.74%
Aromatase binding + 0.7760 77.60%
PPAR gamma + 0.7833 78.33%
Honey bee toxicity - 0.8697 86.97%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7550 75.50%
Fish aquatic toxicity + 0.9725 97.25%

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 96.90% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.81% 98.95%
CHEMBL2039 P27338 Monoamine oxidase B 94.78% 92.51%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.68% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.90% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 92.68% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 92.18% 94.73%
CHEMBL4208 P20618 Proteasome component C5 89.01% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.38% 96.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.75% 86.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.28% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.68% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.16% 85.14%

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 calycinum

Cross-Links

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PubChem 163040345
LOTUS LTS0223397
wikiData Q105325552