(3R)-3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-5,7-dimethoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

Details

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Internal ID 8ecacacb-69c8-4f53-bc94-2623f62040ca
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavans > Isoflavanones > 3-prenylated isoflavanones
IUPAC Name (3R)-3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-5,7-dimethoxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H32O6/c1-15(2)7-9-18-21(28)12-11-17(25(18)29)20-14-33-23-13-22(31-5)19(10-8-16(3)4)27(32-6)24(23)26(20)30/h7-8,11-13,20,28-29H,9-10,14H2,1-6H3/t20-/m0/s1
InChI Key AXLJPECJCPNXRX-FQEVSTJZSA-N
Popularity 4 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 6.20
Atomic LogP (AlogP) 5.49
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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SCHEMBL29907989

2D Structure

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2D Structure of (3R)-3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-5,7-dimethoxy-6-(3-methylbut-2-enyl)-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 + 0.9739 97.39%
Caco-2 + 0.5426 54.26%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7651 76.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9288 92.88%
OATP1B3 inhibitior + 0.8986 89.86%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9681 96.81%
P-glycoprotein inhibitior + 0.8410 84.10%
P-glycoprotein substrate - 0.6991 69.91%
CYP3A4 substrate + 0.5987 59.87%
CYP2C9 substrate - 0.7880 78.80%
CYP2D6 substrate - 0.7350 73.50%
CYP3A4 inhibition - 0.6805 68.05%
CYP2C9 inhibition + 0.8632 86.32%
CYP2C19 inhibition + 0.8982 89.82%
CYP2D6 inhibition + 0.5249 52.49%
CYP1A2 inhibition + 0.9338 93.38%
CYP2C8 inhibition + 0.5854 58.54%
CYP inhibitory promiscuity + 0.9300 93.00%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7589 75.89%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.8006 80.06%
Skin irritation - 0.8018 80.18%
Skin corrosion - 0.9513 95.13%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6957 69.57%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8424 84.24%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.8372 83.72%
Acute Oral Toxicity (c) III 0.6060 60.60%
Estrogen receptor binding + 0.9033 90.33%
Androgen receptor binding + 0.8166 81.66%
Thyroid receptor binding + 0.6411 64.11%
Glucocorticoid receptor binding + 0.7848 78.48%
Aromatase binding - 0.5698 56.98%
PPAR gamma + 0.8117 81.17%
Honey bee toxicity - 0.7649 76.49%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9899 98.99%

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 99.74% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.31% 94.45%
CHEMBL2581 P07339 Cathepsin D 94.33% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.31% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.86% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.64% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.51% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.57% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.84% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.05% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.40% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.92% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 84.77% 91.19%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.90% 95.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.78% 97.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.15% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 82.77% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.76% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.13% 94.00%
CHEMBL4208 P20618 Proteasome component C5 81.67% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.53% 99.23%
CHEMBL1929 P47989 Xanthine dehydrogenase 81.08% 96.12%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.76% 96.00%

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.
Glycyrrhiza aspera
Glycyrrhiza uralensis
Glycyrrhiza uralensis

Cross-Links

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PubChem 46232311
NPASS NPC145467
LOTUS LTS0259427
wikiData Q104920630