9-Methoxy-5-(3-methylbut-2-enoxy)furo[3,2-g]chromen-7-one

Details

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Internal ID 079de0a6-0356-4193-95ba-3e7e5f5afdfc
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Furanocoumarins > Psoralens > 8-methoxypsoralens
IUPAC Name 9-methoxy-5-(3-methylbut-2-enoxy)furo[3,2-g]chromen-7-one
SMILES (Canonical) CC(=CCOC1=CC(=O)OC2=C1C=C3C=COC3=C2OC)C
SMILES (Isomeric) CC(=CCOC1=CC(=O)OC2=C1C=C3C=COC3=C2OC)C
InChI InChI=1S/C17H16O5/c1-10(2)4-6-20-13-9-14(18)22-16-12(13)8-11-5-7-21-15(11)17(16)19-3/h4-5,7-9H,6H2,1-3H3
InChI Key TYIHPYDDANTUSP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O5
Molecular Weight 300.30 g/mol
Exact Mass 300.09977361 g/mol
Topological Polar Surface Area (TPSA) 57.90 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.89
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-Methoxy-5-(3-methylbut-2-enoxy)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 + 0.9927 99.27%
Caco-2 + 0.8325 83.25%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7539 75.39%
OATP2B1 inhibitior - 0.8650 86.50%
OATP1B1 inhibitior + 0.9512 95.12%
OATP1B3 inhibitior + 0.8002 80.02%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7286 72.86%
P-glycoprotein inhibitior + 0.5909 59.09%
P-glycoprotein substrate - 0.7893 78.93%
CYP3A4 substrate - 0.5343 53.43%
CYP2C9 substrate - 0.6794 67.94%
CYP2D6 substrate - 0.8509 85.09%
CYP3A4 inhibition + 0.6951 69.51%
CYP2C9 inhibition + 0.5477 54.77%
CYP2C19 inhibition + 0.8984 89.84%
CYP2D6 inhibition + 0.6410 64.10%
CYP1A2 inhibition + 0.8169 81.69%
CYP2C8 inhibition - 0.5833 58.33%
CYP inhibitory promiscuity + 0.8888 88.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5570 55.70%
Eye corrosion - 0.9740 97.40%
Eye irritation - 0.7713 77.13%
Skin irritation - 0.7660 76.60%
Skin corrosion - 0.9703 97.03%
Ames mutagenesis - 0.6054 60.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6830 68.30%
Micronuclear - 0.5226 52.26%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.6640 66.40%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.7094 70.94%
Acute Oral Toxicity (c) III 0.5497 54.97%
Estrogen receptor binding + 0.8635 86.35%
Androgen receptor binding + 0.7936 79.36%
Thyroid receptor binding + 0.5439 54.39%
Glucocorticoid receptor binding + 0.7388 73.88%
Aromatase binding + 0.7143 71.43%
PPAR gamma + 0.8178 81.78%
Honey bee toxicity - 0.8627 86.27%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9855 98.55%

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 98.30% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.13% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.44% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 94.47% 94.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.03% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.02% 86.33%
CHEMBL2581 P07339 Cathepsin D 90.44% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.39% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.12% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 87.50% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.47% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.92% 96.00%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 82.18% 95.83%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.70% 92.62%

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.
Angelica dahurica
Angelica sinensis
Angelica taiwaniana
Apium graveolens
Conioselinum anthriscoides
Hansenia weberbaueriana
Niphogeton ternata
Thamnosma rhodesica

Cross-Links

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PubChem 53398727
NPASS NPC89591