5,8-Dihydroxy-3-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-(3-hydroxy-3-methylbutyl)chromen-4-one

Details

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Internal ID 51d7c36b-7209-4a44-b676-e03bd59d85c3
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavans > Isoflavanones > 6-prenylated isoflavanones
IUPAC Name 5,8-dihydroxy-3-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-(3-hydroxy-3-methylbutyl)chromen-4-one
SMILES (Canonical) CC1(C=CC2=CC(=C(C=C2O1)O)C3=COC4=C(C=C(C(=C4C3=O)O)CCC(C)(C)O)O)C
SMILES (Isomeric) CC1(C=CC2=CC(=C(C=C2O1)O)C3=COC4=C(C=C(C(=C4C3=O)O)CCC(C)(C)O)O)C
InChI InChI=1S/C25H26O7/c1-24(2,30)7-5-14-10-18(27)23-20(21(14)28)22(29)16(12-31-23)15-9-13-6-8-25(3,4)32-19(13)11-17(15)26/h6,8-12,26-28,30H,5,7H2,1-4H3
InChI Key KQZGQDSCCWMZCT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H26O7
Molecular Weight 438.50 g/mol
Exact Mass 438.16785316 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.46
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,8-Dihydroxy-3-(7-hydroxy-2,2-dimethylchromen-6-yl)-6-(3-hydroxy-3-methylbutyl)chromen-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 + 0.9840 98.40%
Caco-2 - 0.7222 72.22%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7524 75.24%
OATP2B1 inhibitior + 0.5759 57.59%
OATP1B1 inhibitior + 0.8524 85.24%
OATP1B3 inhibitior + 0.9139 91.39%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9287 92.87%
BSEP inhibitior + 0.8984 89.84%
P-glycoprotein inhibitior + 0.6458 64.58%
P-glycoprotein substrate - 0.5734 57.34%
CYP3A4 substrate + 0.6524 65.24%
CYP2C9 substrate - 0.5959 59.59%
CYP2D6 substrate - 0.8238 82.38%
CYP3A4 inhibition - 0.7447 74.47%
CYP2C9 inhibition - 0.7602 76.02%
CYP2C19 inhibition - 0.7797 77.97%
CYP2D6 inhibition - 0.8898 88.98%
CYP1A2 inhibition - 0.6940 69.40%
CYP2C8 inhibition + 0.6749 67.49%
CYP inhibitory promiscuity - 0.7294 72.94%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5866 58.66%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.7120 71.20%
Skin irritation - 0.7215 72.15%
Skin corrosion - 0.9136 91.36%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6973 69.73%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.8130 81.30%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.5902 59.02%
Acute Oral Toxicity (c) III 0.4986 49.86%
Estrogen receptor binding + 0.9395 93.95%
Androgen receptor binding + 0.7443 74.43%
Thyroid receptor binding + 0.7190 71.90%
Glucocorticoid receptor binding + 0.8842 88.42%
Aromatase binding + 0.7871 78.71%
PPAR gamma + 0.9024 90.24%
Honey bee toxicity - 0.8624 86.24%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9760 97.60%

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 99.73% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.38% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.66% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.54% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 90.91% 94.73%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.76% 96.77%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.88% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.50% 93.99%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.60% 97.25%
CHEMBL4208 P20618 Proteasome component C5 85.58% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.39% 95.56%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.88% 80.78%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.83% 95.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.83% 99.23%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.48% 89.34%

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.
Eriosema kraussianum

Cross-Links

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PubChem 102510321
LOTUS LTS0077504
wikiData Q105144892