Yinyanghuo E

Details

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Internal ID 2fcba5d3-c924-4711-a4ab-f1f70717423d
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Pyranoflavonoids
IUPAC Name 5,7-dihydroxy-2-(8-hydroxy-2,2-dimethylchromen-6-yl)chromen-4-one
SMILES (Canonical) CC1(C=CC2=C(O1)C(=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C(=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)C
InChI InChI=1S/C20H16O6/c1-20(2)4-3-10-5-11(6-15(24)19(10)26-20)16-9-14(23)18-13(22)7-12(21)8-17(18)25-16/h3-9,21-22,24H,1-2H3
InChI Key FIKLOAGOJKGOFT-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H16O6
Molecular Weight 352.30 g/mol
Exact Mass 352.09468823 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.76
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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5,7-dihydroxy-2-(8-hydroxy-2,2-dimethylchromen-6-yl)chromen-4-one
RefChem:195648
174286-26-1
SCHEMBL4224539
LMPK12110731

2D Structure

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2D Structure of Yinyanghuo E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9756 97.56%
Caco-2 + 0.6167 61.67%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7479 74.79%
OATP2B1 inhibitior - 0.5608 56.08%
OATP1B1 inhibitior + 0.9215 92.15%
OATP1B3 inhibitior + 0.9545 95.45%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5743 57.43%
P-glycoprotein inhibitior - 0.4895 48.95%
P-glycoprotein substrate - 0.6428 64.28%
CYP3A4 substrate + 0.6194 61.94%
CYP2C9 substrate - 0.6192 61.92%
CYP2D6 substrate - 0.8382 83.82%
CYP3A4 inhibition + 0.7907 79.07%
CYP2C9 inhibition + 0.8016 80.16%
CYP2C19 inhibition + 0.6139 61.39%
CYP2D6 inhibition - 0.8096 80.96%
CYP1A2 inhibition - 0.5177 51.77%
CYP2C8 inhibition + 0.7118 71.18%
CYP inhibitory promiscuity + 0.7465 74.65%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5709 57.09%
Eye corrosion - 0.9888 98.88%
Eye irritation + 0.5790 57.90%
Skin irritation - 0.7085 70.85%
Skin corrosion - 0.9262 92.62%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5130 51.30%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.7621 76.21%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5106 51.06%
Acute Oral Toxicity (c) III 0.7187 71.87%
Estrogen receptor binding + 0.8999 89.99%
Androgen receptor binding + 0.7225 72.25%
Thyroid receptor binding + 0.6931 69.31%
Glucocorticoid receptor binding + 0.8099 80.99%
Aromatase binding + 0.7735 77.35%
PPAR gamma + 0.8737 87.37%
Honey bee toxicity - 0.8066 80.66%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9503 95.03%

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 98.91% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.84% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.84% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.70% 85.14%
CHEMBL2581 P07339 Cathepsin D 92.96% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.94% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.59% 95.56%
CHEMBL3194 P02766 Transthyretin 87.53% 90.71%
CHEMBL2039 P27338 Monoamine oxidase B 85.93% 92.51%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.63% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 85.00% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.29% 99.23%
CHEMBL4208 P20618 Proteasome component C5 84.17% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.73% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.59% 86.33%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.13% 94.42%

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.
Epimedium brevicornu
Epimedium sagittatum

Cross-Links

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PubChem 5315397
NPASS NPC258994
LOTUS LTS0086325
wikiData Q104995748