(2R)-5,7-dihydroxy-2-[(2R)-5-hydroxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-2,3-dihydrochromen-4-one

Details

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Internal ID 65e490c8-bb7b-4e3b-9bbb-2b307a40d495
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Flavanones
IUPAC Name (2R)-5,7-dihydroxy-2-[(2R)-5-hydroxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H26O6/c1-14(2)5-4-9-25(3)10-8-16-18(27)7-6-17(24(16)31-25)21-13-20(29)23-19(28)11-15(26)12-22(23)30-21/h5-8,10-12,21,26-28H,4,9,13H2,1-3H3/t21-,25-/m1/s1
InChI Key BVVVHQJFODXUQX-PXDATVDWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H26O6
Molecular Weight 422.50 g/mol
Exact Mass 422.17293854 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 5.30
Atomic LogP (AlogP) 5.42
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-5,7-dihydroxy-2-[(2R)-5-hydroxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-2,3-dihydrochromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9724 97.24%
Caco-2 - 0.6512 65.12%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7364 73.64%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.8400 84.00%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9571 95.71%
P-glycoprotein inhibitior + 0.7300 73.00%
P-glycoprotein substrate - 0.5071 50.71%
CYP3A4 substrate + 0.6712 67.12%
CYP2C9 substrate - 0.7981 79.81%
CYP2D6 substrate - 0.8063 80.63%
CYP3A4 inhibition - 0.5340 53.40%
CYP2C9 inhibition + 0.5524 55.24%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.8045 80.45%
CYP1A2 inhibition + 0.5313 53.13%
CYP2C8 inhibition + 0.5890 58.90%
CYP inhibitory promiscuity + 0.7633 76.33%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6480 64.80%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.6584 65.84%
Skin irritation - 0.7209 72.09%
Skin corrosion - 0.9274 92.74%
Ames mutagenesis - 0.5837 58.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6456 64.56%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.7684 76.84%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.5535 55.35%
Acute Oral Toxicity (c) III 0.5525 55.25%
Estrogen receptor binding + 0.8822 88.22%
Androgen receptor binding + 0.7117 71.17%
Thyroid receptor binding + 0.6197 61.97%
Glucocorticoid receptor binding + 0.8318 83.18%
Aromatase binding + 0.7030 70.30%
PPAR gamma + 0.7515 75.15%
Honey bee toxicity - 0.7592 75.92%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9794 97.94%

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 99.64% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.00% 94.45%
CHEMBL1929 P47989 Xanthine dehydrogenase 97.67% 96.12%
CHEMBL2581 P07339 Cathepsin D 96.37% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.50% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.74% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 93.25% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.09% 95.56%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 90.90% 83.10%
CHEMBL226 P30542 Adenosine A1 receptor 90.72% 95.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.38% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.77% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.06% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.90% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.79% 97.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 87.32% 96.38%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.99% 99.15%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.88% 90.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.81% 100.00%
CHEMBL4208 P20618 Proteasome component C5 86.08% 90.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.14% 95.71%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.16% 94.80%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.78% 93.40%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.19% 92.62%
CHEMBL236 P41143 Delta opioid receptor 80.03% 99.35%

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.
Morus alba

Cross-Links

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PubChem 163081794
LOTUS LTS0152870
wikiData Q104946941