7,4'-DI-O-Methylisoxanthohumol

Details

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Internal ID 7e2cecfd-08dc-414e-a9c4-4beb0944e27b
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name (2S)-5,7-dimethoxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical) CC(=CCC1=C2C(=C(C=C1OC)OC)C(=O)CC(O2)C3=CC=C(C=C3)OC)C
SMILES (Isomeric) CC(=CCC1=C2C(=C(C=C1OC)OC)C(=O)C[C@H](O2)C3=CC=C(C=C3)OC)C
InChI InChI=1S/C23H26O5/c1-14(2)6-11-17-20(26-4)13-21(27-5)22-18(24)12-19(28-23(17)22)15-7-9-16(25-3)10-8-15/h6-10,13,19H,11-12H2,1-5H3/t19-/m0/s1
InChI Key MRUCPTGFOUAUDY-IBGZPJMESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H26O5
Molecular Weight 382.40 g/mol
Exact Mass 382.17802393 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.93
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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7,4'-DI-O-METHYLISOXANTHOHUMOL

2D Structure

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2D Structure of 7,4'-DI-O-Methylisoxanthohumol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.9413 94.13%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7626 76.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8902 89.02%
OATP1B3 inhibitior + 0.9465 94.65%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9426 94.26%
P-glycoprotein inhibitior + 0.9446 94.46%
P-glycoprotein substrate - 0.8464 84.64%
CYP3A4 substrate + 0.5913 59.13%
CYP2C9 substrate - 0.8008 80.08%
CYP2D6 substrate - 0.7156 71.56%
CYP3A4 inhibition - 0.5329 53.29%
CYP2C9 inhibition + 0.7247 72.47%
CYP2C19 inhibition + 0.9268 92.68%
CYP2D6 inhibition - 0.8409 84.09%
CYP1A2 inhibition + 0.7939 79.39%
CYP2C8 inhibition - 0.6415 64.15%
CYP inhibitory promiscuity + 0.9410 94.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9713 97.13%
Carcinogenicity (trinary) Non-required 0.6845 68.45%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.8791 87.91%
Skin irritation - 0.8090 80.90%
Skin corrosion - 0.9739 97.39%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7961 79.61%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.8016 80.16%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6148 61.48%
Acute Oral Toxicity (c) III 0.7206 72.06%
Estrogen receptor binding + 0.8853 88.53%
Androgen receptor binding + 0.6988 69.88%
Thyroid receptor binding + 0.6441 64.41%
Glucocorticoid receptor binding + 0.8131 81.31%
Aromatase binding - 0.6057 60.57%
PPAR gamma + 0.7470 74.70%
Honey bee toxicity - 0.7943 79.43%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9876 98.76%

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 98.41% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.87% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.40% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.04% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.75% 97.09%
CHEMBL4208 P20618 Proteasome component C5 92.62% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.48% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.16% 86.33%
CHEMBL2581 P07339 Cathepsin D 90.14% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.99% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.46% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 86.39% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.06% 94.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.21% 96.12%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.15% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.96% 96.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.38% 86.92%
CHEMBL2535 P11166 Glucose transporter 83.03% 98.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 76311725
LOTUS LTS0230642
wikiData Q105170933