9-(2-Hydroxy-3-methoxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

Details

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Internal ID 5b7b1fed-e6cd-4280-8441-b0b283a73d51
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Furanocoumarins > Psoralens
IUPAC Name 9-(2-hydroxy-3-methoxy-3-methylbutoxy)furo[3,2-g]chromen-7-one
SMILES (Canonical) CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)OC
SMILES (Isomeric) CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)OC
InChI InChI=1S/C17H18O6/c1-17(2,20-3)12(18)9-22-16-14-11(6-7-21-14)8-10-4-5-13(19)23-15(10)16/h4-8,12,18H,9H2,1-3H3
InChI Key ICVVBGAHOQMQEJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O6
Molecular Weight 318.32 g/mol
Exact Mass 318.11033829 g/mol
Topological Polar Surface Area (TPSA) 78.10 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.70
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-(2-Hydroxy-3-methoxy-3-methylbutoxy)furo[3,2-g]chromen-7-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9787 97.87%
Caco-2 + 0.5119 51.19%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7012 70.12%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9346 93.46%
OATP1B3 inhibitior + 0.8027 80.27%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6672 66.72%
P-glycoprotein inhibitior - 0.5812 58.12%
P-glycoprotein substrate - 0.8256 82.56%
CYP3A4 substrate - 0.5429 54.29%
CYP2C9 substrate - 0.6755 67.55%
CYP2D6 substrate - 0.8103 81.03%
CYP3A4 inhibition - 0.7614 76.14%
CYP2C9 inhibition - 0.8086 80.86%
CYP2C19 inhibition - 0.7335 73.35%
CYP2D6 inhibition - 0.8080 80.80%
CYP1A2 inhibition - 0.7056 70.56%
CYP2C8 inhibition - 0.6987 69.87%
CYP inhibitory promiscuity - 0.8485 84.85%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4927 49.27%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.8776 87.76%
Skin irritation - 0.8010 80.10%
Skin corrosion - 0.9590 95.90%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5054 50.54%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.6651 66.51%
skin sensitisation - 0.7670 76.70%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.8435 84.35%
Acute Oral Toxicity (c) III 0.5220 52.20%
Estrogen receptor binding + 0.7746 77.46%
Androgen receptor binding + 0.7927 79.27%
Thyroid receptor binding + 0.6806 68.06%
Glucocorticoid receptor binding + 0.6074 60.74%
Aromatase binding + 0.6479 64.79%
PPAR gamma + 0.7579 75.79%
Honey bee toxicity - 0.8723 87.23%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.8206 82.06%

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
CHEMBL2581 P07339 Cathepsin D 97.46% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.78% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.39% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.81% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.53% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 89.82% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.53% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.35% 95.56%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.36% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.37% 96.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.75% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.52% 93.65%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.79% 95.71%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.61% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.49% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.20% 96.09%
CHEMBL4208 P20618 Proteasome component C5 80.16% 90.00%

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.
Prangos pabularia

Cross-Links

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PubChem 483515
LOTUS LTS0062876
wikiData Q105111189