[(2S,3S,4S,5R,6S)-5-hydroxy-2-methyl-6-[[(1R,3S,5S,6S,7R,19S,21R,23R,24R,25S,26R,28S,30S,31S,32R,33R)-24,25,31,32-tetrahydroxy-5,23,30-trimethyl-33-[(2S)-2-methylbutanoyl]oxy-9-oxo-19-pentyl-2,4,8,20,22,27,29-heptaoxatetracyclo[26.2.2.13,7.021,26]tritriacontan-6-yl]oxy]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (2S)-2-methylbutanoate

Details

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Internal ID f06c5e6b-4cce-4f7b-89c8-688b990c9c2f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides
IUPAC Name [(2S,3S,4S,5R,6S)-5-hydroxy-2-methyl-6-[[(1R,3S,5S,6S,7R,19S,21R,23R,24R,25S,26R,28S,30S,31S,32R,33R)-24,25,31,32-tetrahydroxy-5,23,30-trimethyl-33-[(2S)-2-methylbutanoyl]oxy-9-oxo-19-pentyl-2,4,8,20,22,27,29-heptaoxatetracyclo[26.2.2.13,7.021,26]tritriacontan-6-yl]oxy]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (2S)-2-methylbutanoate
SMILES (Canonical) CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC(=O)C(C)CC)OC3C(OC(C(C3O)O)OC4C(C(C(OC4O1)C)O)O)C)C)OC5C(C(C(C(O5)C)OC(=O)C(C)CC)OC6C(C(C(C(O6)C)O)O)O)O
SMILES (Isomeric) CCCCC[C@H]1CCCCCCCCCC(=O)O[C@@H]2[C@H]([C@@H](O[C@H]([C@@H]2OC(=O)[C@@H](C)CC)O[C@H]3[C@@H](O[C@H]([C@@H]([C@@H]3O)O)O[C@@H]4[C@H]([C@H]([C@H](O[C@H]4O1)C)O)O)C)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC(=O)[C@@H](C)CC)O[C@H]6[C@@H]([C@@H]([C@H]([C@@H](O6)C)O)O)O)O
InChI InChI=1S/C56H96O24/c1-11-14-20-23-33-24-21-18-16-15-17-19-22-25-34(57)74-48-45(78-54-42(65)46(44(31(9)71-54)75-50(66)26(4)12-2)79-52-40(63)37(60)35(58)28(6)68-52)32(10)72-56(49(48)76-51(67)27(5)13-3)77-43-30(8)70-53(41(64)39(43)62)80-47-38(61)36(59)29(7)69-55(47)73-33/h26-33,35-49,52-56,58-65H,11-25H2,1-10H3/t26-,27-,28-,29+,30-,31-,32-,33-,35-,36-,37+,38-,39-,40+,41+,42+,43-,44-,45-,46-,47+,48+,49+,52-,53-,54-,55-,56-/m0/s1
InChI Key XYFRDSCAGIKHED-QLFFLOGESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C56H96O24
Molecular Weight 1153.30 g/mol
Exact Mass 1152.62915392 g/mol
Topological Polar Surface Area (TPSA) 333.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 2.46
H-Bond Acceptor 24
H-Bond Donor 8
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2S,3S,4S,5R,6S)-5-hydroxy-2-methyl-6-[[(1R,3S,5S,6S,7R,19S,21R,23R,24R,25S,26R,28S,30S,31S,32R,33R)-24,25,31,32-tetrahydroxy-5,23,30-trimethyl-33-[(2S)-2-methylbutanoyl]oxy-9-oxo-19-pentyl-2,4,8,20,22,27,29-heptaoxatetracyclo[26.2.2.13,7.021,26]tritriacontan-6-yl]oxy]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (2S)-2-methylbutanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5000 50.00%
Caco-2 - 0.8668 86.68%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6926 69.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8363 83.63%
OATP1B3 inhibitior + 0.8309 83.09%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9772 97.72%
P-glycoprotein inhibitior + 0.7399 73.99%
P-glycoprotein substrate + 0.6761 67.61%
CYP3A4 substrate + 0.6970 69.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8899 88.99%
CYP3A4 inhibition - 0.7800 78.00%
CYP2C9 inhibition - 0.9333 93.33%
CYP2C19 inhibition - 0.8567 85.67%
CYP2D6 inhibition - 0.9416 94.16%
CYP1A2 inhibition - 0.9042 90.42%
CYP2C8 inhibition + 0.6263 62.63%
CYP inhibitory promiscuity - 0.9756 97.56%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7479 74.79%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.9012 90.12%
Skin irritation - 0.7208 72.08%
Skin corrosion - 0.9249 92.49%
Ames mutagenesis - 0.6578 65.78%
Human Ether-a-go-go-Related Gene inhibition + 0.7967 79.67%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5665 56.65%
skin sensitisation - 0.8982 89.82%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.9215 92.15%
Acute Oral Toxicity (c) III 0.6582 65.82%
Estrogen receptor binding + 0.8235 82.35%
Androgen receptor binding + 0.6220 62.20%
Thyroid receptor binding + 0.5391 53.91%
Glucocorticoid receptor binding + 0.7284 72.84%
Aromatase binding + 0.5922 59.22%
PPAR gamma + 0.7576 75.76%
Honey bee toxicity - 0.7840 78.40%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6228 62.28%
Fish aquatic toxicity + 0.9527 95.27%

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
CHEMBL2581 P07339 Cathepsin D 99.05% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.40% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.53% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.85% 97.25%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 93.72% 96.38%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 92.62% 90.24%
CHEMBL3359 P21462 Formyl peptide receptor 1 92.41% 93.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.90% 92.62%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 91.82% 96.47%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 91.68% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.21% 90.71%
CHEMBL5255 O00206 Toll-like receptor 4 89.46% 92.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.29% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 88.24% 94.33%
CHEMBL4072 P07858 Cathepsin B 87.76% 93.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.07% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.86% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 86.13% 91.19%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 84.43% 98.75%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 84.02% 83.00%
CHEMBL1968 P07099 Epoxide hydrolase 1 83.31% 98.57%
CHEMBL3401 O75469 Pregnane X receptor 83.28% 94.73%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.89% 96.77%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 82.27% 95.64%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.54% 97.09%
CHEMBL2514 O95665 Neurotensin receptor 2 80.60% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.48% 95.56%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.17% 96.90%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 80.01% 82.50%

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.
Ipomoea murucoides

Cross-Links

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PubChem 162962058
LOTUS LTS0113169
wikiData Q105344463