7-(3-Methylbut-1-enoxy)-8-(3-methylbut-1-enyl)chromen-2-one

Details

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Internal ID 40ef3f18-e5cc-4f39-9aa8-418697bf9b40
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-(3-methylbut-1-enoxy)-8-(3-methylbut-1-enyl)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H22O3/c1-13(2)5-8-16-17(21-12-11-14(3)4)9-6-15-7-10-18(20)22-19(15)16/h5-14H,1-4H3
InChI Key DXPRZCMFCUTDCS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H22O3
Molecular Weight 298.40 g/mol
Exact Mass 298.15689456 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 5.10
Atomic LogP (AlogP) 5.01
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(3-Methylbut-1-enoxy)-8-(3-methylbut-1-enyl)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 + 0.9964 99.64%
Caco-2 + 0.8567 85.67%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7283 72.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9246 92.46%
OATP1B3 inhibitior + 0.9872 98.72%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8381 83.81%
P-glycoprotein inhibitior + 0.6848 68.48%
P-glycoprotein substrate - 0.8875 88.75%
CYP3A4 substrate - 0.5915 59.15%
CYP2C9 substrate - 0.6318 63.18%
CYP2D6 substrate - 0.8560 85.60%
CYP3A4 inhibition - 0.8783 87.83%
CYP2C9 inhibition - 0.5394 53.94%
CYP2C19 inhibition + 0.6909 69.09%
CYP2D6 inhibition - 0.9352 93.52%
CYP1A2 inhibition + 0.9437 94.37%
CYP2C8 inhibition - 0.8282 82.82%
CYP inhibitory promiscuity + 0.7557 75.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9813 98.13%
Carcinogenicity (trinary) Non-required 0.4784 47.84%
Eye corrosion - 0.9658 96.58%
Eye irritation - 0.6915 69.15%
Skin irritation - 0.7294 72.94%
Skin corrosion - 0.9858 98.58%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7179 71.79%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.7949 79.49%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.4918 49.18%
Acute Oral Toxicity (c) III 0.5712 57.12%
Estrogen receptor binding + 0.8843 88.43%
Androgen receptor binding + 0.7496 74.96%
Thyroid receptor binding + 0.5173 51.73%
Glucocorticoid receptor binding + 0.5939 59.39%
Aromatase binding + 0.9500 95.00%
PPAR gamma + 0.5326 53.26%
Honey bee toxicity - 0.8018 80.18%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9930 99.30%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.03% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.46% 96.00%
CHEMBL2581 P07339 Cathepsin D 92.07% 98.95%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 87.89% 85.30%
CHEMBL3401 O75469 Pregnane X receptor 87.28% 94.73%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 83.86% 83.57%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.29% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.67% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.62% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 80.80% 94.75%

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.
Skimmia reevesiana

Cross-Links

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PubChem 163192777
LOTUS LTS0173263
wikiData Q104991136