Licodione base + 2Prenyl

Details

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Internal ID 88505f69-c270-4b33-80e7-ba7b96d7c9fd
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > 3-prenylated chalcones
IUPAC Name (Z)-1-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-3-hydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H28O5/c1-15(2)5-7-17-11-18(9-10-21(17)26)22(27)13-24(29)20-12-19(8-6-16(3)4)23(28)14-25(20)30/h5-6,9-14,26-28,30H,7-8H2,1-4H3/b22-13-
InChI Key FFPFIAFZJXSGDK-XKZIYDEJSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C25H28O5
Molecular Weight 408.50 g/mol
Exact Mass 408.19367399 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.60
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

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SCHEMBL30266564
LMPK12120378

2D Structure

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2D Structure of Licodione base + 2Prenyl

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 - 0.6012 60.12%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7934 79.34%
OATP2B1 inhibitior + 0.5747 57.47%
OATP1B1 inhibitior + 0.9445 94.45%
OATP1B3 inhibitior + 0.9138 91.38%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8990 89.90%
P-glycoprotein inhibitior + 0.6376 63.76%
P-glycoprotein substrate - 0.8510 85.10%
CYP3A4 substrate - 0.6469 64.69%
CYP2C9 substrate - 0.7867 78.67%
CYP2D6 substrate - 0.8526 85.26%
CYP3A4 inhibition + 0.5746 57.46%
CYP2C9 inhibition + 0.9246 92.46%
CYP2C19 inhibition + 0.9412 94.12%
CYP2D6 inhibition - 0.7114 71.14%
CYP1A2 inhibition + 0.9313 93.13%
CYP2C8 inhibition - 0.6849 68.49%
CYP inhibitory promiscuity + 0.9233 92.33%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7872 78.72%
Carcinogenicity (trinary) Non-required 0.7577 75.77%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.5200 52.00%
Skin irritation - 0.7601 76.01%
Skin corrosion - 0.9035 90.35%
Ames mutagenesis - 0.6354 63.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7944 79.44%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.6235 62.35%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6434 64.34%
Acute Oral Toxicity (c) III 0.7107 71.07%
Estrogen receptor binding + 0.9347 93.47%
Androgen receptor binding + 0.7486 74.86%
Thyroid receptor binding + 0.6788 67.88%
Glucocorticoid receptor binding + 0.8890 88.90%
Aromatase binding + 0.7836 78.36%
PPAR gamma + 0.8856 88.56%
Honey bee toxicity - 0.9505 95.05%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 1.0000 100.00%

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 97.56% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.17% 86.33%
CHEMBL2581 P07339 Cathepsin D 90.46% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 87.89% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.75% 99.17%
CHEMBL4208 P20618 Proteasome component C5 84.38% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.14% 95.56%
CHEMBL3194 P02766 Transthyretin 84.02% 90.71%
CHEMBL221 P23219 Cyclooxygenase-1 83.53% 90.17%
CHEMBL2535 P11166 Glucose transporter 82.23% 98.75%

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
Glycyrrhiza glabra
Glycyrrhiza inflata
Glycyrrhiza uralensis

Cross-Links

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PubChem 42607642
NPASS NPC179222
LOTUS LTS0090907
wikiData Q104994608