[6-[[6,16-Dihydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-4-hydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] hydrogen sulfate

Details

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Internal ID 3e01f08f-27b8-4143-a6cb-c93de2a92d5c
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
IUPAC Name [6-[[6,16-dihydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-4-hydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] hydrogen sulfate
SMILES (Canonical) CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)OS(=O)(=O)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O
SMILES (Isomeric) CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)OS(=O)(=O)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O
InChI InChI=1S/C44H72O21S/c1-18(16-58-39-36(52)35(51)32(48)27(15-45)61-39)8-11-44(54)19(2)30-26(64-44)14-25-23-7-6-21-12-22(46)13-29(43(21,5)24(23)9-10-42(25,30)4)62-41-38(33(49)28(17-59-41)65-66(55,56)57)63-40-37(53)34(50)31(47)20(3)60-40/h6,18-20,22-41,45-54H,7-17H2,1-5H3,(H,55,56,57)
InChI Key LNSGTQVVVSIYJG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C44H72O21S
Molecular Weight 969.10 g/mol
Exact Mass 968.42868047 g/mol
Topological Polar Surface Area (TPSA) 339.00 Ų
XlogP -0.90
Atomic LogP (AlogP) -1.39
H-Bond Acceptor 20
H-Bond Donor 11
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [6-[[6,16-Dihydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-4-hydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] hydrogen sulfate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8092 80.92%
Caco-2 - 0.8826 88.26%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.4852 48.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8420 84.20%
OATP1B3 inhibitior + 0.9326 93.26%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.6771 67.71%
BSEP inhibitior + 0.8947 89.47%
P-glycoprotein inhibitior + 0.7439 74.39%
P-glycoprotein substrate + 0.7431 74.31%
CYP3A4 substrate + 0.7610 76.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8516 85.16%
CYP3A4 inhibition - 0.8294 82.94%
CYP2C9 inhibition - 0.7656 76.56%
CYP2C19 inhibition - 0.7252 72.52%
CYP2D6 inhibition - 0.8709 87.09%
CYP1A2 inhibition - 0.7468 74.68%
CYP2C8 inhibition + 0.7601 76.01%
CYP inhibitory promiscuity - 0.8878 88.78%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.5258 52.58%
Eye corrosion - 0.9793 97.93%
Eye irritation - 0.9070 90.70%
Skin irritation - 0.7370 73.70%
Skin corrosion - 0.9080 90.80%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7622 76.22%
Micronuclear + 0.5800 58.00%
Hepatotoxicity - 0.6820 68.20%
skin sensitisation - 0.8439 84.39%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.9051 90.51%
Acute Oral Toxicity (c) III 0.5719 57.19%
Estrogen receptor binding + 0.8357 83.57%
Androgen receptor binding + 0.7227 72.27%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7229 72.29%
Aromatase binding + 0.6472 64.72%
PPAR gamma + 0.7977 79.77%
Honey bee toxicity - 0.5714 57.14%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5255 52.55%
Fish aquatic toxicity + 0.9828 98.28%

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
CHEMBL226 P30542 Adenosine A1 receptor 98.69% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.69% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.94% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 94.73% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.65% 97.09%
CHEMBL2581 P07339 Cathepsin D 93.60% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.57% 89.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 92.83% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 91.80% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.36% 93.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.18% 96.00%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 90.22% 98.46%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.04% 95.56%
CHEMBL333 P08253 Matrix metalloproteinase-2 89.23% 96.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.07% 86.33%
CHEMBL5255 O00206 Toll-like receptor 4 87.94% 92.50%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 87.49% 92.86%
CHEMBL4581 P52732 Kinesin-like protein 1 86.91% 93.18%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.55% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.55% 97.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.73% 94.45%
CHEMBL2842 P42345 Serine/threonine-protein kinase mTOR 85.43% 92.78%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 85.20% 89.67%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.17% 96.61%
CHEMBL2179 P04062 Beta-glucocerebrosidase 84.76% 85.31%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.72% 92.88%
CHEMBL1871 P10275 Androgen Receptor 83.17% 96.43%
CHEMBL3401 O75469 Pregnane X receptor 83.04% 94.73%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.85% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.44% 100.00%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 82.21% 96.90%
CHEMBL5028 O14672 ADAM10 81.64% 97.50%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 81.47% 95.00%
CHEMBL4588 P22894 Matrix metalloproteinase 8 81.34% 94.66%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.30% 97.29%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 81.17% 95.83%
CHEMBL1937 Q92769 Histone deacetylase 2 81.08% 94.75%
CHEMBL332 P03956 Matrix metalloproteinase-1 80.43% 94.50%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.03% 97.25%

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.
Ruscus colchicus

Cross-Links

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PubChem 162908322
LOTUS LTS0011538
wikiData Q105154467