Didymocalyxin B

Details

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Internal ID 1e4b72ae-3346-49d2-8177-925698d46116
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > 2-Hydroxychalcones
IUPAC Name (E)-1-[2,6-dihydroxy-4,5-dimethoxy-7-[(E)-3-phenylprop-2-enoyl]-1-benzofuran-3-yl]-3-phenylprop-2-en-1-one
SMILES (Canonical) COC1=C(C(=C(C2=C1C(=C(O2)O)C(=O)C=CC3=CC=CC=C3)C(=O)C=CC4=CC=CC=C4)O)OC
SMILES (Isomeric) COC1=C(C(=C(C2=C1C(=C(O2)O)C(=O)/C=C/C3=CC=CC=C3)C(=O)/C=C/C4=CC=CC=C4)O)OC
InChI InChI=1S/C28H22O7/c1-33-26-23-21(19(29)15-13-17-9-5-3-6-10-17)28(32)35-25(23)22(24(31)27(26)34-2)20(30)16-14-18-11-7-4-8-12-18/h3-16,31-32H,1-2H3/b15-13+,16-14+
InChI Key QNVPSFXWYIBJBF-WXUKJITCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H22O7
Molecular Weight 470.50 g/mol
Exact Mass 470.13655304 g/mol
Topological Polar Surface Area (TPSA) 106.00 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.65
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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CHEBI:185695
LMPK12120331
(E)-1-[2,6-dihydroxy-4,5-dimethoxy-7-[(E)-3-phenylprop-2-enoyl]-1-benzouran-3-yl]-3-phenylprop-2-en-1-one

2D Structure

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2D Structure of Didymocalyxin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9830 98.30%
Caco-2 - 0.5856 58.56%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7131 71.31%
OATP2B1 inhibitior - 0.5691 56.91%
OATP1B1 inhibitior + 0.8614 86.14%
OATP1B3 inhibitior + 0.8606 86.06%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8572 85.72%
P-glycoprotein inhibitior + 0.9000 90.00%
P-glycoprotein substrate - 0.8663 86.63%
CYP3A4 substrate - 0.5122 51.22%
CYP2C9 substrate - 0.8044 80.44%
CYP2D6 substrate - 0.8462 84.62%
CYP3A4 inhibition - 0.6613 66.13%
CYP2C9 inhibition + 0.7275 72.75%
CYP2C19 inhibition + 0.5843 58.43%
CYP2D6 inhibition - 0.7948 79.48%
CYP1A2 inhibition + 0.5985 59.85%
CYP2C8 inhibition + 0.8331 83.31%
CYP inhibitory promiscuity + 0.6942 69.42%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Danger 0.5244 52.44%
Eye corrosion - 0.9846 98.46%
Eye irritation - 0.6824 68.24%
Skin irritation - 0.7221 72.21%
Skin corrosion - 0.9575 95.75%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6972 69.72%
Micronuclear + 0.9000 90.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7867 78.67%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7741 77.41%
Acute Oral Toxicity (c) II 0.5084 50.84%
Estrogen receptor binding + 0.8226 82.26%
Androgen receptor binding + 0.8039 80.39%
Thyroid receptor binding + 0.6012 60.12%
Glucocorticoid receptor binding + 0.7572 75.72%
Aromatase binding - 0.4906 49.06%
PPAR gamma + 0.8010 80.10%
Honey bee toxicity - 0.8861 88.61%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5755 57.55%
Fish aquatic toxicity + 0.9915 99.15%

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 98.25% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.62% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.48% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.20% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.49% 93.99%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.81% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 86.47% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.20% 89.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 85.76% 94.08%
CHEMBL3194 P02766 Transthyretin 85.17% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.61% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.03% 99.17%
CHEMBL2581 P07339 Cathepsin D 82.13% 98.95%

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.
Didymocarpus albicalyx

Cross-Links

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PubChem 6313586
LOTUS LTS0034720
wikiData Q76324150