8-(3,4-Dihydroxy-3-methylbut-1-enyl)-7-methoxychromen-2-one

Details

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Internal ID 9a50ff9f-fa98-4eaf-af27-2db442ce3031
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 8-(3,4-dihydroxy-3-methylbut-1-enyl)-7-methoxychromen-2-one
SMILES (Canonical) CC(CO)(C=CC1=C(C=CC2=C1OC(=O)C=C2)OC)O
SMILES (Isomeric) CC(CO)(C=CC1=C(C=CC2=C1OC(=O)C=C2)OC)O
InChI InChI=1S/C15H16O5/c1-15(18,9-16)8-7-11-12(19-2)5-3-10-4-6-13(17)20-14(10)11/h3-8,16,18H,9H2,1-2H3
InChI Key XVVRFNCLKCYMPH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O5
Molecular Weight 276.28 g/mol
Exact Mass 276.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.56
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 8-(3,4-Dihydroxy-3-methylbut-1-enyl)-7-methoxychromen-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 + 0.9252 92.52%
Caco-2 + 0.5387 53.87%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6304 63.04%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.9213 92.13%
OATP1B3 inhibitior + 0.9354 93.54%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5628 56.28%
P-glycoprotein inhibitior - 0.8865 88.65%
P-glycoprotein substrate - 0.8359 83.59%
CYP3A4 substrate - 0.5399 53.99%
CYP2C9 substrate - 0.6485 64.85%
CYP2D6 substrate - 0.8442 84.42%
CYP3A4 inhibition - 0.6591 65.91%
CYP2C9 inhibition - 0.9203 92.03%
CYP2C19 inhibition - 0.7559 75.59%
CYP2D6 inhibition - 0.8302 83.02%
CYP1A2 inhibition - 0.5899 58.99%
CYP2C8 inhibition - 0.6001 60.01%
CYP inhibitory promiscuity - 0.8366 83.66%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6392 63.92%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.6342 63.42%
Skin irritation - 0.8027 80.27%
Skin corrosion - 0.9497 94.97%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4054 40.54%
Micronuclear + 0.5674 56.74%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8027 80.27%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.6007 60.07%
Acute Oral Toxicity (c) III 0.5832 58.32%
Estrogen receptor binding + 0.9129 91.29%
Androgen receptor binding + 0.7405 74.05%
Thyroid receptor binding - 0.5587 55.87%
Glucocorticoid receptor binding + 0.8437 84.37%
Aromatase binding + 0.7804 78.04%
PPAR gamma + 0.7810 78.10%
Honey bee toxicity - 0.9308 93.08%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9102 91.02%

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 95.49% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.72% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 91.39% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.76% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.58% 94.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.45% 86.92%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.65% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.55% 99.23%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 80.85% 98.00%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.26% 96.90%

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.
Boenninghausenia albiflora
Citrus × aurantium
Murraya paniculata

Cross-Links

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PubChem 156495
LOTUS LTS0131251
wikiData Q105343210