[(8S,9S,10S,11R)-8-benzoyl-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-11-yl] benzoate

Details

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Internal ID 0dc8105c-7e27-4291-ae57-e4950b5bef08
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name [(8S,9S,10S,11R)-8-benzoyl-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-11-yl] benzoate
SMILES (Canonical) CC1C(C2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)C(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3)OC(=O)C6=CC=CC=C6
SMILES (Isomeric) C[C@H]1[C@H](C2=CC3=C(C(=C2C4=C(C(=C(C=C4[C@@H]([C@@]1(C)O)C(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3)OC(=O)C6=CC=CC=C6
InChI InChI=1S/C37H36O10/c1-20-31(47-36(39)22-15-11-8-12-16-22)24-18-26-33(46-19-45-26)35(44-6)28(24)27-23(17-25(41-3)32(42-4)34(27)43-5)29(37(20,2)40)30(38)21-13-9-7-10-14-21/h7-18,20,29,31,40H,19H2,1-6H3/t20-,29+,31+,37-/m0/s1
InChI Key OCDIGISLRCLKAH-JPVSHXBVSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C37H36O10
Molecular Weight 640.70 g/mol
Exact Mass 640.23084734 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP 6.60
Atomic LogP (AlogP) 6.38
H-Bond Acceptor 10
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(8S,9S,10S,11R)-8-benzoyl-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-11-yl] benzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9776 97.76%
Caco-2 - 0.6486 64.86%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7489 74.89%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8827 88.27%
OATP1B3 inhibitior + 0.9193 91.93%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9931 99.31%
P-glycoprotein inhibitior + 0.9331 93.31%
P-glycoprotein substrate - 0.6012 60.12%
CYP3A4 substrate + 0.6723 67.23%
CYP2C9 substrate - 0.7962 79.62%
CYP2D6 substrate - 0.8610 86.10%
CYP3A4 inhibition + 0.7544 75.44%
CYP2C9 inhibition + 0.7083 70.83%
CYP2C19 inhibition - 0.6021 60.21%
CYP2D6 inhibition - 0.7853 78.53%
CYP1A2 inhibition - 0.8281 82.81%
CYP2C8 inhibition + 0.8146 81.46%
CYP inhibitory promiscuity - 0.5349 53.49%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9343 93.43%
Carcinogenicity (trinary) Non-required 0.3943 39.43%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.8878 88.78%
Skin irritation - 0.7986 79.86%
Skin corrosion - 0.9581 95.81%
Ames mutagenesis - 0.5354 53.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7602 76.02%
Micronuclear + 0.7674 76.74%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.7502 75.02%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7657 76.57%
Acute Oral Toxicity (c) III 0.4753 47.53%
Estrogen receptor binding + 0.8418 84.18%
Androgen receptor binding + 0.7479 74.79%
Thyroid receptor binding + 0.6652 66.52%
Glucocorticoid receptor binding + 0.8147 81.47%
Aromatase binding + 0.5367 53.67%
PPAR gamma + 0.7701 77.01%
Honey bee toxicity - 0.7889 78.89%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5649 56.49%
Fish aquatic toxicity + 0.9662 96.62%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.64% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.22% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.76% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.41% 96.77%
CHEMBL2535 P11166 Glucose transporter 92.55% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.20% 95.56%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 90.11% 89.44%
CHEMBL2581 P07339 Cathepsin D 88.72% 98.95%
CHEMBL4208 P20618 Proteasome component C5 87.10% 90.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.92% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.89% 89.00%
CHEMBL5028 O14672 ADAM10 85.78% 97.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.60% 97.14%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 84.33% 83.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.10% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.87% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.86% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 83.68% 91.19%

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 propinqua

Cross-Links

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PubChem 45270920
LOTUS LTS0248712
wikiData Q105189318