2-[6-[16-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol

Details

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Internal ID 93e269b4-4f17-4f64-bfe9-bff9b6f70e31
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Diterpene glycosides
IUPAC Name 2-[6-[16-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-yl]oxy-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)OC(C)(CCC=C(C)CCC=C(C)CCC=C(C)COC3C(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)CO)O)O)O)C=C)CO)O)O)O
SMILES (Isomeric) CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC(C)(CCC=C(C)CCC=C(C)CCC=C(C)COC3C(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)CO)O)O)O)C=C)CO)O)O)O
InChI InChI=1S/C44H74O21/c1-7-44(6,65-42-37(57)34(54)38(27(19-47)62-42)63-40-35(55)31(51)28(48)24(5)59-40)16-10-15-22(3)12-8-11-21(2)13-9-14-23(4)20-58-43-39(33(53)30(50)26(18-46)61-43)64-41-36(56)32(52)29(49)25(17-45)60-41/h7,11,14-15,24-43,45-57H,1,8-10,12-13,16-20H2,2-6H3
InChI Key CWAXZXSFUDEMIX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C44H74O21
Molecular Weight 939.00 g/mol
Exact Mass 938.47225936 g/mol
Topological Polar Surface Area (TPSA) 337.00 Ų
XlogP -1.20
Atomic LogP (AlogP) -2.58
H-Bond Acceptor 21
H-Bond Donor 13
Rotatable Bonds 22

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-[6-[16-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraen-3-yl]oxy-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 - 0.7291 72.91%
Caco-2 - 0.8696 86.96%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.9143 91.43%
Subcellular localzation Mitochondria 0.7906 79.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8738 87.38%
OATP1B3 inhibitior + 0.8227 82.27%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.9134 91.34%
P-glycoprotein inhibitior + 0.7345 73.45%
P-glycoprotein substrate - 0.6385 63.85%
CYP3A4 substrate + 0.6646 66.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8353 83.53%
CYP3A4 inhibition - 0.9241 92.41%
CYP2C9 inhibition - 0.8670 86.70%
CYP2C19 inhibition - 0.8488 84.88%
CYP2D6 inhibition - 0.9426 94.26%
CYP1A2 inhibition - 0.8844 88.44%
CYP2C8 inhibition + 0.5837 58.37%
CYP inhibitory promiscuity - 0.9295 92.95%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6905 69.05%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9053 90.53%
Skin irritation - 0.6920 69.20%
Skin corrosion - 0.9559 95.59%
Ames mutagenesis - 0.5854 58.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8448 84.48%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.7299 72.99%
skin sensitisation - 0.8837 88.37%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.7620 76.20%
Acute Oral Toxicity (c) III 0.6191 61.91%
Estrogen receptor binding + 0.7990 79.90%
Androgen receptor binding + 0.6179 61.79%
Thyroid receptor binding + 0.5485 54.85%
Glucocorticoid receptor binding + 0.7043 70.43%
Aromatase binding + 0.6676 66.76%
PPAR gamma + 0.7470 74.70%
Honey bee toxicity - 0.5417 54.17%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9493 94.93%

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 97.06% 91.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 94.64% 97.36%
CHEMBL3401 O75469 Pregnane X receptor 92.86% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.88% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.09% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.60% 86.33%
CHEMBL3589 P55263 Adenosine kinase 88.56% 98.05%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.32% 99.17%
CHEMBL2581 P07339 Cathepsin D 87.36% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.61% 97.29%
CHEMBL1951 P21397 Monoamine oxidase A 81.61% 91.49%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.54% 92.08%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 80.07% 97.47%

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 attenuata

Cross-Links

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PubChem 73240539
LOTUS LTS0112078
wikiData Q104971132