Chinensin

Details

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Internal ID e2add80d-2254-48bb-9a4a-6de436f2f673
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 5-(3,4-dimethoxyphenyl)-8H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one
SMILES (Canonical) COC1=C(C=C(C=C1)C2=C3C=C4C(=CC3=CC5=C2C(=O)OC5)OCO4)OC
SMILES (Isomeric) COC1=C(C=C(C=C1)C2=C3C=C4C(=CC3=CC5=C2C(=O)OC5)OCO4)OC
InChI InChI=1S/C21H16O6/c1-23-15-4-3-11(6-16(15)24-2)19-14-8-18-17(26-10-27-18)7-12(14)5-13-9-25-21(22)20(13)19/h3-8H,9-10H2,1-2H3
InChI Key PJLRAQVYTOCNHT-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C21H16O6
Molecular Weight 364.30 g/mol
Exact Mass 364.09468823 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.92
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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31888-76-3

2D Structure

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2D Structure of Chinensin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 + 0.8831 88.31%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7625 76.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9547 95.47%
OATP1B3 inhibitior + 0.9649 96.49%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8634 86.34%
P-glycoprotein inhibitior + 0.7548 75.48%
P-glycoprotein substrate - 0.8145 81.45%
CYP3A4 substrate + 0.5346 53.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8360 83.60%
CYP3A4 inhibition + 0.9348 93.48%
CYP2C9 inhibition + 0.9716 97.16%
CYP2C19 inhibition + 0.9766 97.66%
CYP2D6 inhibition + 0.6561 65.61%
CYP1A2 inhibition + 0.5380 53.80%
CYP2C8 inhibition + 0.4932 49.32%
CYP inhibitory promiscuity + 0.9546 95.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Warning 0.4177 41.77%
Eye corrosion - 0.9817 98.17%
Eye irritation - 0.5730 57.30%
Skin irritation - 0.7884 78.84%
Skin corrosion - 0.9637 96.37%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3840 38.40%
Micronuclear + 0.7674 76.74%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.6507 65.07%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.7066 70.66%
Acute Oral Toxicity (c) III 0.7135 71.35%
Estrogen receptor binding + 0.8685 86.85%
Androgen receptor binding + 0.7890 78.90%
Thyroid receptor binding + 0.7227 72.27%
Glucocorticoid receptor binding + 0.9298 92.98%
Aromatase binding - 0.5191 51.91%
PPAR gamma + 0.6456 64.56%
Honey bee toxicity - 0.8020 80.20%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9709 97.09%

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
CHEMBL230 P35354 Cyclooxygenase-2 96.75% 89.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.29% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.79% 85.14%
CHEMBL240 Q12809 HERG 93.65% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.49% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.35% 98.95%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 92.54% 96.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.04% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.80% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.58% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.10% 92.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.08% 96.77%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 91.04% 92.38%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 88.79% 98.21%
CHEMBL2535 P11166 Glucose transporter 85.64% 98.75%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 85.49% 85.00%
CHEMBL1951 P21397 Monoamine oxidase A 85.40% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.12% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.77% 96.09%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 84.51% 96.00%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 82.72% 82.67%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.04% 94.80%
CHEMBL1907 P15144 Aminopeptidase N 82.03% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 81.44% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.13% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.93% 92.94%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.64% 97.36%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.63% 94.03%
CHEMBL4302 P08183 P-glycoprotein 1 80.51% 92.98%

Cross-Links

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PubChem 5315827
NPASS NPC231323
LOTUS LTS0215418
wikiData Q104396776