(3S,4S,5S,6S)-2-[(2S,3R,4R,5S,6R)-6-(3,33-dimethylpentatriacontan-18-yloxy)-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID 8f0b3d19-b89a-4b28-a64d-8aaadae8d0d4
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl glycosides > Alkyl glycosides > Simplexides
IUPAC Name (3S,4S,5S,6S)-2-[(2S,3R,4R,5S,6R)-6-(3,33-dimethylpentatriacontan-18-yloxy)-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C49H96O11/c1-5-37(3)31-27-23-19-15-11-7-9-13-17-21-25-29-33-39(34-30-26-22-18-14-10-8-12-16-20-24-28-32-38(4)6-2)57-48-46(56)44(54)47(41(36-51)59-48)60-49-45(55)43(53)42(52)40(35-50)58-49/h37-56H,5-36H2,1-4H3/t37?,38?,39?,40-,41-,42+,43-,44+,45-,46-,47-,48+,49?/m0/s1
InChI Key OZRMWRKSVGENOC-ZOMXCWEZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C49H96O11
Molecular Weight 861.30 g/mol
Exact Mass 860.69526387 g/mol
Topological Polar Surface Area (TPSA) 179.00 Ų
XlogP 14.00
Atomic LogP (AlogP) 9.01
H-Bond Acceptor 11
H-Bond Donor 7
Rotatable Bonds 38

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,4S,5S,6S)-2-[(2S,3R,4R,5S,6R)-6-(3,33-dimethylpentatriacontan-18-yloxy)-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-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 - 0.8062 80.62%
Caco-2 - 0.8579 85.79%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.9000 90.00%
Subcellular localzation Mitochondria 0.7561 75.61%
OATP2B1 inhibitior - 0.5737 57.37%
OATP1B1 inhibitior + 0.8993 89.93%
OATP1B3 inhibitior + 0.8813 88.13%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.6434 64.34%
P-glycoprotein inhibitior + 0.6595 65.95%
P-glycoprotein substrate - 0.8054 80.54%
CYP3A4 substrate + 0.5813 58.13%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8361 83.61%
CYP3A4 inhibition - 0.8147 81.47%
CYP2C9 inhibition - 0.8809 88.09%
CYP2C19 inhibition - 0.8219 82.19%
CYP2D6 inhibition - 0.9326 93.26%
CYP1A2 inhibition - 0.8965 89.65%
CYP2C8 inhibition - 0.8465 84.65%
CYP inhibitory promiscuity - 0.9195 91.95%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7120 71.20%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.8862 88.62%
Skin irritation - 0.8260 82.60%
Skin corrosion - 0.9687 96.87%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6486 64.86%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.8500 85.00%
skin sensitisation - 0.9305 93.05%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.7507 75.07%
Acute Oral Toxicity (c) III 0.5933 59.33%
Estrogen receptor binding + 0.7371 73.71%
Androgen receptor binding + 0.6091 60.91%
Thyroid receptor binding - 0.5471 54.71%
Glucocorticoid receptor binding - 0.5979 59.79%
Aromatase binding + 0.6494 64.94%
PPAR gamma + 0.6547 65.47%
Honey bee toxicity - 0.7783 77.83%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7735 77.35%
Fish aquatic toxicity + 0.8187 81.87%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 94.84% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.86% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 92.66% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.78% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.40% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.89% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.31% 99.17%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.83% 96.47%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.24% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 86.96% 94.73%
CHEMBL2996 Q05655 Protein kinase C delta 84.16% 97.79%
CHEMBL5255 O00206 Toll-like receptor 4 83.96% 92.50%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.96% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.47% 97.25%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 81.23% 97.47%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 80.89% 95.58%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.74% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.60% 96.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.17% 96.61%
CHEMBL2885 P07451 Carbonic anhydrase III 80.01% 87.45%

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.
There are no matching plants.

Cross-Links

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PubChem 71719044
LOTUS LTS0185330
wikiData Q105204058