2',4',6'-Trihydroxy-3',5'-diprenyldihydrochalcone

Details

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Internal ID 18c65d9e-f525-46cc-8439-b5581b8c2e5e
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > 2-Hydroxy-dihydrochalcones
IUPAC Name 3-phenyl-1-[2,4,6-trihydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]propan-1-one
SMILES (Canonical) CC(=CCC1=C(C(=C(C(=C1O)C(=O)CCC2=CC=CC=C2)O)CC=C(C)C)O)C
SMILES (Isomeric) CC(=CCC1=C(C(=C(C(=C1O)C(=O)CCC2=CC=CC=C2)O)CC=C(C)C)O)C
InChI InChI=1S/C25H30O4/c1-16(2)10-13-19-23(27)20(14-11-17(3)4)25(29)22(24(19)28)21(26)15-12-18-8-6-5-7-9-18/h5-11,27-29H,12-15H2,1-4H3
InChI Key LHAWAPWIXXDHPB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H30O4
Molecular Weight 394.50 g/mol
Exact Mass 394.21440943 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 6.80
Atomic LogP (AlogP) 5.64
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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LMPK12120486

2D Structure

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2D Structure of 2',4',6'-Trihydroxy-3',5'-diprenyldihydrochalcone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 - 0.6408 64.08%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8753 87.53%
OATP2B1 inhibitior - 0.5683 56.83%
OATP1B1 inhibitior + 0.7900 79.00%
OATP1B3 inhibitior + 0.9223 92.23%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9504 95.04%
P-glycoprotein inhibitior + 0.6395 63.95%
P-glycoprotein substrate - 0.8166 81.66%
CYP3A4 substrate - 0.5610 56.10%
CYP2C9 substrate - 0.7958 79.58%
CYP2D6 substrate - 0.8207 82.07%
CYP3A4 inhibition + 0.6225 62.25%
CYP2C9 inhibition + 0.7639 76.39%
CYP2C19 inhibition + 0.8603 86.03%
CYP2D6 inhibition - 0.6837 68.37%
CYP1A2 inhibition + 0.8576 85.76%
CYP2C8 inhibition - 0.6052 60.52%
CYP inhibitory promiscuity + 0.8110 81.10%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8462 84.62%
Carcinogenicity (trinary) Non-required 0.7671 76.71%
Eye corrosion - 0.9908 99.08%
Eye irritation + 0.6301 63.01%
Skin irritation - 0.7600 76.00%
Skin corrosion - 0.9106 91.06%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7475 74.75%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.5848 58.48%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.8310 83.10%
Acute Oral Toxicity (c) III 0.6171 61.71%
Estrogen receptor binding + 0.9209 92.09%
Androgen receptor binding + 0.5362 53.62%
Thyroid receptor binding + 0.6017 60.17%
Glucocorticoid receptor binding + 0.8637 86.37%
Aromatase binding + 0.6198 61.98%
PPAR gamma + 0.9566 95.66%
Honey bee toxicity - 0.9325 93.25%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9969 99.69%

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
CHEMBL2581 P07339 Cathepsin D 97.23% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.02% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 94.15% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 92.68% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.88% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.45% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.17% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.10% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.82% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.32% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.20% 99.17%

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.
Helichrysum polycladum
Metalasia cymbifolia

Cross-Links

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PubChem 42607680
LOTUS LTS0150191
wikiData Q105151668