[2-[5-Acetyloxy-2-[3,7-dimethyl-8-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyocta-2,6-dienoxy]-3-hydroxy-6-methyloxan-4-yl]oxy-5-hydroxy-6-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 8-hydroxy-2,6-dimethylocta-2,6-dienoate

Details

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Internal ID 7e088ffe-1b03-44e7-bf51-5dbcd8848b80
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name [2-[5-acetyloxy-2-[3,7-dimethyl-8-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyocta-2,6-dienoxy]-3-hydroxy-6-methyloxan-4-yl]oxy-5-hydroxy-6-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 8-hydroxy-2,6-dimethylocta-2,6-dienoate
SMILES (Canonical) CC1C(C(C(C(O1)OCC(=CCCC(=CCOC2C(C(C(C(O2)C)OC(=O)C)OC3C(C(C(C(O3)C)O)OC4C(C(C(C(O4)C)O)O)O)OC(=O)C(=CCCC(=CCO)C)C)O)C)C)O)O)O
SMILES (Isomeric) CC1C(C(C(C(O1)OCC(=CCCC(=CCOC2C(C(C(C(O2)C)OC(=O)C)OC3C(C(C(C(O3)C)O)OC4C(C(C(C(O4)C)O)O)O)OC(=O)C(=CCCC(=CCO)C)C)O)C)C)O)O)O
InChI InChI=1S/C46H74O21/c1-21(16-18-47)13-11-15-24(4)42(57)65-41-39(66-45-36(55)34(53)31(50)26(6)61-45)32(51)27(7)62-46(41)67-40-37(56)44(63-28(8)38(40)64-29(9)48)58-19-17-22(2)12-10-14-23(3)20-59-43-35(54)33(52)30(49)25(5)60-43/h14-17,25-28,30-41,43-47,49-56H,10-13,18-20H2,1-9H3
InChI Key JBRRGJXTNQIPEO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C46H74O21
Molecular Weight 963.10 g/mol
Exact Mass 962.47225936 g/mol
Topological Polar Surface Area (TPSA) 309.00 Ų
XlogP 0.20
Atomic LogP (AlogP) -0.16
H-Bond Acceptor 21
H-Bond Donor 9
Rotatable Bonds 20

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [2-[5-Acetyloxy-2-[3,7-dimethyl-8-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyocta-2,6-dienoxy]-3-hydroxy-6-methyloxan-4-yl]oxy-5-hydroxy-6-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 8-hydroxy-2,6-dimethylocta-2,6-dienoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7338 73.38%
Caco-2 - 0.8697 86.97%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8541 85.41%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8629 86.29%
OATP1B3 inhibitior + 0.8778 87.78%
MATE1 inhibitior - 0.9012 90.12%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9461 94.61%
P-glycoprotein inhibitior + 0.7382 73.82%
P-glycoprotein substrate - 0.5903 59.03%
CYP3A4 substrate + 0.6769 67.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8946 89.46%
CYP3A4 inhibition - 0.7923 79.23%
CYP2C9 inhibition - 0.8340 83.40%
CYP2C19 inhibition - 0.8045 80.45%
CYP2D6 inhibition - 0.8852 88.52%
CYP1A2 inhibition - 0.7633 76.33%
CYP2C8 inhibition + 0.5085 50.85%
CYP inhibitory promiscuity - 0.9119 91.19%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6980 69.80%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9025 90.25%
Skin irritation - 0.6933 69.33%
Skin corrosion - 0.9595 95.95%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6980 69.80%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.6463 64.63%
skin sensitisation - 0.8913 89.13%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5137 51.37%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6384 63.84%
Acute Oral Toxicity (c) III 0.6931 69.31%
Estrogen receptor binding + 0.7964 79.64%
Androgen receptor binding + 0.5703 57.03%
Thyroid receptor binding + 0.5815 58.15%
Glucocorticoid receptor binding + 0.7814 78.14%
Aromatase binding + 0.5454 54.54%
PPAR gamma + 0.8134 81.34%
Honey bee toxicity - 0.7028 70.28%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5145 51.45%
Fish aquatic toxicity + 0.9722 97.22%

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 95.70% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.98% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.22% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 89.56% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.51% 89.00%
CHEMBL2581 P07339 Cathepsin D 87.76% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.89% 86.33%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.24% 94.33%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 82.92% 97.47%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.91% 96.00%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.46% 97.36%
CHEMBL5255 O00206 Toll-like receptor 4 81.79% 92.50%
CHEMBL340 P08684 Cytochrome P450 3A4 81.17% 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.
Vangueria agrestis

Cross-Links

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PubChem 162914465
LOTUS LTS0053216
wikiData Q105124540