(15-Hydroxy-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.01,16.04,21.05,9]henicosa-4(21),5(9),10,16,18-pentaen-12-yl) 2-methylbut-2-enoate

Details

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Internal ID 22abcd55-48b6-401f-a34e-b79d37be9dd5
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name (15-hydroxy-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.01,16.04,21.05,9]henicosa-4(21),5(9),10,16,18-pentaen-12-yl) 2-methylbut-2-enoate
SMILES (Canonical) CC=C(C)C(=O)OC1C(C(C(C2=CC(=C(C(=O)C23COC4=C3C1=CC5=C4OCO5)OC)OC)O)C)C
SMILES (Isomeric) CC=C(C)C(=O)OC1C(C(C(C2=CC(=C(C(=O)C23COC4=C3C1=CC5=C4OCO5)OC)OC)O)C)C
InChI InChI=1S/C27H30O9/c1-7-12(2)26(30)36-21-14(4)13(3)20(28)16-9-17(31-5)23(32-6)25(29)27(16)10-33-24-19(27)15(21)8-18-22(24)35-11-34-18/h7-9,13-14,20-21,28H,10-11H2,1-6H3
InChI Key XUIUDMCZUMRZDC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H30O9
Molecular Weight 498.50 g/mol
Exact Mass 498.18898253 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.26
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (15-Hydroxy-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.01,16.04,21.05,9]henicosa-4(21),5(9),10,16,18-pentaen-12-yl) 2-methylbut-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9811 98.11%
Caco-2 + 0.5821 58.21%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7801 78.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8809 88.09%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9658 96.58%
P-glycoprotein inhibitior + 0.8611 86.11%
P-glycoprotein substrate + 0.5334 53.34%
CYP3A4 substrate + 0.6650 66.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8669 86.69%
CYP3A4 inhibition + 0.7447 74.47%
CYP2C9 inhibition + 0.7537 75.37%
CYP2C19 inhibition + 0.6722 67.22%
CYP2D6 inhibition - 0.7577 75.77%
CYP1A2 inhibition - 0.6959 69.59%
CYP2C8 inhibition + 0.4842 48.42%
CYP inhibitory promiscuity + 0.7556 75.56%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Danger 0.5127 51.27%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.9287 92.87%
Skin irritation - 0.7283 72.83%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5523 55.23%
Micronuclear + 0.7174 71.74%
Hepatotoxicity - 0.5091 50.91%
skin sensitisation - 0.6673 66.73%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5822 58.22%
Acute Oral Toxicity (c) III 0.3598 35.98%
Estrogen receptor binding + 0.8361 83.61%
Androgen receptor binding + 0.6796 67.96%
Thyroid receptor binding + 0.6056 60.56%
Glucocorticoid receptor binding + 0.9036 90.36%
Aromatase binding + 0.5399 53.99%
PPAR gamma + 0.7521 75.21%
Honey bee toxicity - 0.6595 65.95%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9802 98.02%

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 98.64% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.14% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.99% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.47% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.29% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.96% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.52% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 91.26% 94.80%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.71% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.20% 89.00%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 89.41% 98.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 89.38% 91.07%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.87% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.20% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.78% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 85.06% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.29% 100.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.88% 95.50%
CHEMBL2535 P11166 Glucose transporter 82.61% 98.75%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.70% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.46% 97.14%
CHEMBL3401 O75469 Pregnane X receptor 80.41% 94.73%

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.
Kadsura heteroclita

Cross-Links

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PubChem 162926705
LOTUS LTS0266206
wikiData Q105342336