7-Hydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)-5-methoxychromen-4-one

Details

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Internal ID 79fe1dd2-f632-4e12-83fd-f007e1beb105
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 8-prenylated flavones
IUPAC Name 7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)-5-methoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H32O7/c1-15(2)16(9-10-27(3,4)31)11-19-20(29)13-24(33-6)25-21(30)14-23(34-26(19)25)18-8-7-17(28)12-22(18)32-5/h7-8,12-14,16,28-29,31H,1,9-11H2,2-6H3
InChI Key ZAIBANKMNGFRNX-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C27H32O7
Molecular Weight 468.50 g/mol
Exact Mass 468.21480336 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 5.17
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxy-2-(4-hydroxy-2-methoxyphenyl)-8-(5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl)-5-methoxychromen-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 + 0.9936 99.36%
Caco-2 - 0.5639 56.39%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7838 78.38%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.8165 81.65%
OATP1B3 inhibitior + 0.8692 86.92%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9544 95.44%
P-glycoprotein inhibitior + 0.7821 78.21%
P-glycoprotein substrate + 0.7012 70.12%
CYP3A4 substrate + 0.6469 64.69%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.7784 77.84%
CYP3A4 inhibition + 0.5659 56.59%
CYP2C9 inhibition - 0.5358 53.58%
CYP2C19 inhibition + 0.5120 51.20%
CYP2D6 inhibition - 0.8861 88.61%
CYP1A2 inhibition + 0.5761 57.61%
CYP2C8 inhibition + 0.6388 63.88%
CYP inhibitory promiscuity - 0.5677 56.77%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7062 70.62%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.8203 82.03%
Skin irritation - 0.7593 75.93%
Skin corrosion - 0.9398 93.98%
Ames mutagenesis + 0.5563 55.63%
Human Ether-a-go-go-Related Gene inhibition + 0.8497 84.97%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.7925 79.25%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5273 52.73%
Acute Oral Toxicity (c) III 0.3543 35.43%
Estrogen receptor binding + 0.8646 86.46%
Androgen receptor binding + 0.7664 76.64%
Thyroid receptor binding + 0.6616 66.16%
Glucocorticoid receptor binding + 0.8616 86.16%
Aromatase binding + 0.8046 80.46%
PPAR gamma + 0.7788 77.88%
Honey bee toxicity - 0.6816 68.16%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9960 99.60%

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 98.67% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.94% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 96.98% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.22% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.78% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.87% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.74% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.99% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.38% 85.14%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 88.12% 90.93%
CHEMBL3401 O75469 Pregnane X receptor 87.85% 94.73%
CHEMBL2413 P32246 C-C chemokine receptor type 1 85.78% 89.50%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.62% 99.15%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.02% 96.95%
CHEMBL3194 P02766 Transthyretin 83.13% 90.71%
CHEMBL1907 P15144 Aminopeptidase N 83.06% 93.31%
CHEMBL1811 P34995 Prostanoid EP1 receptor 82.93% 95.71%
CHEMBL2535 P11166 Glucose transporter 82.69% 98.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.37% 97.14%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.09% 89.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.94% 95.89%

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.
Allium victorialis
Sophora flavescens

Cross-Links

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PubChem 5320098
NPASS NPC229191
LOTUS LTS0197979
wikiData Q105369882