[16-[3-[5-[4-[3,5-Dihydroxy-4-methoxy-6-(sulfooxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-6-(sulfooxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4-hydroxy-5-sulfooxyoxan-2-yl]oxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-en-4-yl] acetate

Details

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Internal ID bfb0d813-a541-447d-9800-dfc006605143
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Oligosaccharides > Oligosaccharide sulfates
IUPAC Name [16-[3-[5-[4-[3,5-dihydroxy-4-methoxy-6-(sulfooxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-6-(sulfooxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4-hydroxy-5-sulfooxyoxan-2-yl]oxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-en-4-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C56H90O32S3/c1-24(2)12-11-17-55(9)46-29(80-26(4)57)20-54(8)28-13-14-33-52(5,6)34(16-18-53(33,7)27(28)15-19-56(46,54)51(65)87-55)83-50-45(37(60)32(21-76-50)88-91(72,73)74)86-47-39(62)38(61)42(25(3)79-47)84-49-41(64)44(36(59)31(82-49)23-78-90(69,70)71)85-48-40(63)43(75-10)35(58)30(81-48)22-77-89(66,67)68/h13,24-25,27,29-50,58-64H,11-12,14-23H2,1-10H3,(H,66,67,68)(H,69,70,71)(H,72,73,74)
InChI Key GHVTXBCGOPYFKA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C56H90O32S3
Molecular Weight 1371.50 g/mol
Exact Mass 1370.4577342 g/mol
Topological Polar Surface Area (TPSA) 493.00 Ų
XlogP -0.90
Atomic LogP (AlogP) -0.29
H-Bond Acceptor 29
H-Bond Donor 10
Rotatable Bonds 22

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [16-[3-[5-[4-[3,5-Dihydroxy-4-methoxy-6-(sulfooxymethyl)oxan-2-yl]oxy-3,5-dihydroxy-6-(sulfooxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4-hydroxy-5-sulfooxyoxan-2-yl]oxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icos-1(20)-en-4-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8724 87.24%
Caco-2 - 0.8592 85.92%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.5854 58.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8106 81.06%
OATP1B3 inhibitior + 0.9220 92.20%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9373 93.73%
P-glycoprotein inhibitior + 0.7437 74.37%
P-glycoprotein substrate + 0.7850 78.50%
CYP3A4 substrate + 0.7533 75.33%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8815 88.15%
CYP3A4 inhibition - 0.8688 86.88%
CYP2C9 inhibition - 0.7471 74.71%
CYP2C19 inhibition - 0.7166 71.66%
CYP2D6 inhibition - 0.8706 87.06%
CYP1A2 inhibition - 0.7451 74.51%
CYP2C8 inhibition + 0.7767 77.67%
CYP inhibitory promiscuity - 0.8530 85.30%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.5332 53.32%
Eye corrosion - 0.9799 97.99%
Eye irritation - 0.8965 89.65%
Skin irritation - 0.7603 76.03%
Skin corrosion - 0.9152 91.52%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7049 70.49%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8504 85.04%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.8817 88.17%
Acute Oral Toxicity (c) III 0.5780 57.80%
Estrogen receptor binding + 0.6535 65.35%
Androgen receptor binding + 0.7575 75.75%
Thyroid receptor binding + 0.7125 71.25%
Glucocorticoid receptor binding + 0.8162 81.62%
Aromatase binding + 0.7073 70.73%
PPAR gamma + 0.8195 81.95%
Honey bee toxicity - 0.6331 63.31%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9930 99.30%

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 98.74% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.69% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.55% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.42% 94.45%
CHEMBL2179 P04062 Beta-glucocerebrosidase 95.17% 85.31%
CHEMBL1937 Q92769 Histone deacetylase 2 93.57% 94.75%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 92.01% 95.89%
CHEMBL226 P30542 Adenosine A1 receptor 91.97% 95.93%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.84% 96.77%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 91.68% 96.38%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.93% 95.56%
CHEMBL3714130 P46095 G-protein coupled receptor 6 90.76% 97.36%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.62% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.57% 89.00%
CHEMBL5255 O00206 Toll-like receptor 4 88.99% 92.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 88.94% 94.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.27% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 88.12% 91.19%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 88.08% 89.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.07% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.70% 97.14%
CHEMBL4581 P52732 Kinesin-like protein 1 87.67% 93.18%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.47% 96.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.99% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.61% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.47% 97.09%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.29% 100.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.07% 90.08%
CHEMBL1871 P10275 Androgen Receptor 85.02% 96.43%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.92% 99.23%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 84.51% 98.75%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 84.21% 91.03%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.04% 93.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.60% 82.69%
CHEMBL332 P03956 Matrix metalloproteinase-1 82.41% 94.50%
CHEMBL5028 O14672 ADAM10 81.99% 97.50%
CHEMBL3401 O75469 Pregnane X receptor 80.32% 94.73%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.23% 95.71%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 73657258
LOTUS LTS0178977
wikiData Q105008766