2-[6-[14-[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraenoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol

Details

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Internal ID 737d1034-5d1b-41cb-b38a-9164ec9c67c7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Diterpene glycosides
IUPAC Name 2-[6-[14-[3,4-dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraenoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol
SMILES (Canonical) CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC(=CCCC(=CCCC(=CCCC(C)(C=C)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)C)O)O)O)O)O)C)C)C)CO)O)O)O
SMILES (Isomeric) CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC(=CCCC(=CCCC(=CCCC(C)(C=C)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)C)O)O)O)O)O)C)C)C)CO)O)O)O
InChI InChI=1S/C44H74O20/c1-8-44(7,64-43-37(56)33(52)39(27(19-46)61-43)63-42-35(54)31(50)29(48)25(6)59-42)17-11-16-22(3)13-9-12-21(2)14-10-15-23(4)20-57-40-36(55)32(51)38(26(18-45)60-40)62-41-34(53)30(49)28(47)24(5)58-41/h8,12,15-16,24-43,45-56H,1,9-11,13-14,17-20H2,2-7H3
InChI Key KSLNLJXEBIKDEN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C44H74O20
Molecular Weight 923.00 g/mol
Exact Mass 922.47734475 g/mol
Topological Polar Surface Area (TPSA) 317.00 Ų
XlogP -1.30
Atomic LogP (AlogP) -1.55
H-Bond Acceptor 20
H-Bond Donor 12
Rotatable Bonds 21

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-[6-[14-[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraenoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7609 76.09%
Caco-2 - 0.8712 87.12%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.7499 74.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8867 88.67%
OATP1B3 inhibitior + 0.8497 84.97%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9349 93.49%
P-glycoprotein inhibitior + 0.7362 73.62%
P-glycoprotein substrate - 0.6567 65.67%
CYP3A4 substrate + 0.6559 65.59%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8353 83.53%
CYP3A4 inhibition - 0.9053 90.53%
CYP2C9 inhibition - 0.8932 89.32%
CYP2C19 inhibition - 0.8577 85.77%
CYP2D6 inhibition - 0.9408 94.08%
CYP1A2 inhibition - 0.8637 86.37%
CYP2C8 inhibition + 0.5450 54.50%
CYP inhibitory promiscuity - 0.9168 91.68%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6738 67.38%
Eye corrosion - 0.9872 98.72%
Eye irritation - 0.9056 90.56%
Skin irritation - 0.6626 66.26%
Skin corrosion - 0.9555 95.55%
Ames mutagenesis - 0.5854 58.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7837 78.37%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.6799 67.99%
skin sensitisation - 0.8651 86.51%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.6612 66.12%
Acute Oral Toxicity (c) III 0.6586 65.86%
Estrogen receptor binding + 0.8057 80.57%
Androgen receptor binding + 0.6503 65.03%
Thyroid receptor binding + 0.5460 54.60%
Glucocorticoid receptor binding + 0.7267 72.67%
Aromatase binding + 0.6878 68.78%
PPAR gamma + 0.7612 76.12%
Honey bee toxicity - 0.5077 50.77%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9398 93.98%

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 96.94% 91.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 93.22% 97.36%
CHEMBL3401 O75469 Pregnane X receptor 92.21% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.57% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.57% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.54% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.91% 99.17%
CHEMBL2581 P07339 Cathepsin D 86.56% 98.95%
CHEMBL3589 P55263 Adenosine kinase 86.27% 98.05%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.05% 97.29%
CHEMBL1951 P21397 Monoamine oxidase A 82.69% 91.49%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.34% 92.08%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.71% 96.61%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.65% 89.00%

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.
Nicotiana obtusifolia

Cross-Links

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PubChem 162865965
LOTUS LTS0060513
wikiData Q105145483