2'-Methoxykurarinone

Details

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Internal ID 90d7bd3c-b3c8-47e8-a4fd-ecb68fdcea6f
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name 7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H32O6/c1-15(2)7-8-17(16(3)4)11-20-21(29)13-25(32-6)26-22(30)14-24(33-27(20)26)19-10-9-18(28)12-23(19)31-5/h7,9-10,12-13,17,24,28-29H,3,8,11,14H2,1-2,4-6H3
InChI Key KTAQQSUPNZAWEY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H32O6
Molecular Weight 452.50 g/mol
Exact Mass 452.21988874 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.91
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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SCHEMBL15386077
FT-0775578

2D Structure

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2D Structure of 2'-Methoxykurarinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.5375 53.75%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8008 80.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8466 84.66%
OATP1B3 inhibitior + 0.8539 85.39%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9476 94.76%
P-glycoprotein inhibitior + 0.8228 82.28%
P-glycoprotein substrate + 0.5112 51.12%
CYP3A4 substrate + 0.6536 65.36%
CYP2C9 substrate - 0.7880 78.80%
CYP2D6 substrate - 0.7350 73.50%
CYP3A4 inhibition - 0.7153 71.53%
CYP2C9 inhibition + 0.7785 77.85%
CYP2C19 inhibition + 0.9169 91.69%
CYP2D6 inhibition - 0.7029 70.29%
CYP1A2 inhibition + 0.7535 75.35%
CYP2C8 inhibition + 0.6522 65.22%
CYP inhibitory promiscuity + 0.8659 86.59%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.7241 72.41%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.8255 82.55%
Skin irritation - 0.7957 79.57%
Skin corrosion - 0.9500 95.00%
Ames mutagenesis - 0.5537 55.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7078 70.78%
Micronuclear - 0.5041 50.41%
Hepatotoxicity + 0.7302 73.02%
skin sensitisation - 0.8007 80.07%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5113 51.13%
Acute Oral Toxicity (c) III 0.6421 64.21%
Estrogen receptor binding + 0.8620 86.20%
Androgen receptor binding + 0.6477 64.77%
Thyroid receptor binding + 0.6769 67.69%
Glucocorticoid receptor binding + 0.8694 86.94%
Aromatase binding + 0.6236 62.36%
PPAR gamma + 0.6986 69.86%
Honey bee toxicity - 0.6898 68.98%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9925 99.25%

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 98.55% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.91% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.21% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.47% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.94% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.76% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.59% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.55% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.41% 85.14%
CHEMBL2535 P11166 Glucose transporter 88.39% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 87.97% 94.73%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.57% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.23% 89.00%
CHEMBL340 P08684 Cytochrome P450 3A4 85.16% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.74% 97.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.07% 99.15%
CHEMBL1902 P62942 FK506-binding protein 1A 82.26% 97.05%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.12% 94.00%
CHEMBL4040 P28482 MAP kinase ERK2 81.27% 83.82%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.86% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.70% 90.71%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.38% 89.62%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.36% 92.62%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.19% 97.14%

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.
Sophora flavescens

Cross-Links

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PubChem 25252741
LOTUS LTS0141983
wikiData Q105145683