Versicoumarin A

Details

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Internal ID cc1fa2ea-48c9-455d-bf00-b4cb3c3068ee
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name (2R)-6-methoxy-2,8,8-trimethyl-2,9-dihydro-1H-pyrano[4,3-f]chromene-4,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H18O5/c1-8-5-9-10(15(18)20-8)6-12(19-4)14-13(9)11(17)7-16(2,3)21-14/h6,8H,5,7H2,1-4H3/t8-/m1/s1
InChI Key KWFWITMTZVXDQD-MRVPVSSYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H18O5
Molecular Weight 290.31 g/mol
Exact Mass 290.11542367 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.54
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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CHEMBL3800350

2D Structure

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2D Structure of Versicoumarin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9765 97.65%
Caco-2 + 0.7555 75.55%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7148 71.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9082 90.82%
OATP1B3 inhibitior + 0.9692 96.92%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7267 72.67%
P-glycoprotein inhibitior - 0.8847 88.47%
P-glycoprotein substrate - 0.7562 75.62%
CYP3A4 substrate + 0.6283 62.83%
CYP2C9 substrate - 0.5853 58.53%
CYP2D6 substrate - 0.8323 83.23%
CYP3A4 inhibition - 0.7651 76.51%
CYP2C9 inhibition - 0.9086 90.86%
CYP2C19 inhibition - 0.7500 75.00%
CYP2D6 inhibition - 0.8467 84.67%
CYP1A2 inhibition - 0.5974 59.74%
CYP2C8 inhibition - 0.7337 73.37%
CYP inhibitory promiscuity - 0.8889 88.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5529 55.29%
Eye corrosion - 0.9751 97.51%
Eye irritation + 0.6992 69.92%
Skin irritation - 0.8423 84.23%
Skin corrosion - 0.9536 95.36%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6023 60.23%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.6532 65.32%
skin sensitisation - 0.8106 81.06%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.6338 63.38%
Acute Oral Toxicity (c) III 0.7108 71.08%
Estrogen receptor binding - 0.5193 51.93%
Androgen receptor binding - 0.6092 60.92%
Thyroid receptor binding + 0.5169 51.69%
Glucocorticoid receptor binding - 0.4854 48.54%
Aromatase binding - 0.7304 73.04%
PPAR gamma + 0.5683 56.83%
Honey bee toxicity - 0.5845 58.45%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9281 92.81%

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 97.76% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.27% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.18% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.77% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.47% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.70% 85.14%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 90.41% 97.14%
CHEMBL2535 P11166 Glucose transporter 89.63% 98.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.55% 96.77%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.02% 96.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.26% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.97% 94.00%
CHEMBL1902 P62942 FK506-binding protein 1A 85.84% 97.05%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.50% 92.94%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 83.74% 96.00%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 83.55% 95.53%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.48% 99.23%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 82.32% 82.38%
CHEMBL1907 P15144 Aminopeptidase N 82.28% 93.31%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 82.17% 82.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.24% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.69% 91.07%
CHEMBL1937 Q92769 Histone deacetylase 2 80.57% 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.
There are no matching plants.

Cross-Links

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PubChem 101890346
LOTUS LTS0200564
wikiData Q77310199