[(8R,9R,10R)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] (Z)-but-2-enoate

Details

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Internal ID 470992f5-1353-4d3e-8bfb-01df17b95229
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name [(8R,9R,10R)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] (Z)-but-2-enoate
SMILES (Canonical) CC=CC(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC
SMILES (Isomeric) C/C=C\C(=O)O[C@@H]1C2=CC(=C(C(=C2C3=C(C4=C(C=C3C[C@H]([C@@]1(C)O)C)OCO4)OC)OC)OC)OC
InChI InChI=1S/C27H32O9/c1-8-9-19(28)36-26-16-12-17(30-4)22(31-5)25(33-7)21(16)20-15(10-14(2)27(26,3)29)11-18-23(24(20)32-6)35-13-34-18/h8-9,11-12,14,26,29H,10,13H2,1-7H3/b9-8-/t14-,26-,27-/m1/s1
InChI Key IYXMASSPEGXSSL-PQKSVOEBSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C27H32O9
Molecular Weight 500.50 g/mol
Exact Mass 500.20463259 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.22
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(8R,9R,10R)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] (Z)-but-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 + 0.9939 99.39%
Caco-2 + 0.7289 72.89%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.6510 65.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8728 87.28%
OATP1B3 inhibitior + 0.9245 92.45%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9599 95.99%
P-glycoprotein inhibitior + 0.8744 87.44%
P-glycoprotein substrate - 0.6407 64.07%
CYP3A4 substrate + 0.6772 67.72%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8866 88.66%
CYP3A4 inhibition + 0.8589 85.89%
CYP2C9 inhibition + 0.5797 57.97%
CYP2C19 inhibition + 0.5379 53.79%
CYP2D6 inhibition - 0.7148 71.48%
CYP1A2 inhibition - 0.7954 79.54%
CYP2C8 inhibition + 0.6642 66.42%
CYP inhibitory promiscuity + 0.5219 52.19%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4143 41.43%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9094 90.94%
Skin irritation - 0.7533 75.33%
Skin corrosion - 0.9502 95.02%
Ames mutagenesis - 0.5108 51.08%
Human Ether-a-go-go-Related Gene inhibition - 0.3623 36.23%
Micronuclear + 0.5774 57.74%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.7239 72.39%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.8640 86.40%
Acute Oral Toxicity (c) III 0.4686 46.86%
Estrogen receptor binding + 0.8867 88.67%
Androgen receptor binding - 0.5106 51.06%
Thyroid receptor binding + 0.6652 66.52%
Glucocorticoid receptor binding + 0.8292 82.92%
Aromatase binding + 0.5293 52.93%
PPAR gamma + 0.8024 80.24%
Honey bee toxicity - 0.6587 65.87%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5545 55.45%
Fish aquatic toxicity + 0.9947 99.47%

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 99.01% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.97% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.85% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.63% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.09% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.58% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.73% 92.62%
CHEMBL2413 P32246 C-C chemokine receptor type 1 89.58% 89.50%
CHEMBL261 P00915 Carbonic anhydrase I 88.06% 96.76%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.95% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.90% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.23% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 85.60% 91.19%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.11% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.67% 100.00%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 83.91% 82.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.05% 95.89%
CHEMBL4208 P20618 Proteasome component C5 81.95% 90.00%
CHEMBL2535 P11166 Glucose transporter 80.96% 98.75%

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.
Schisandra rubriflora

Cross-Links

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PubChem 163195115
LOTUS LTS0246477
wikiData Q105123041