Schottenol glucoside

Details

Top
Internal ID 9eefcae4-d4b5-41d2-bbd3-5b3eef87247e
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Stigmastanes and derivatives
IUPAC Name (2R,3R,4S,5S,6R)-2-[[(3S,5S,9R,10S,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C
SMILES (Isomeric) CC[C@H](CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)C)C)C(C)C
InChI InChI=1S/C35H60O6/c1-7-22(20(2)3)9-8-21(4)26-12-13-27-25-11-10-23-18-24(14-16-34(23,5)28(25)15-17-35(26,27)6)40-33-32(39)31(38)30(37)29(19-36)41-33/h11,20-24,26-33,36-39H,7-10,12-19H2,1-6H3/t21-,22-,23+,24+,26-,27+,28+,29-,30-,31+,32-,33-,34+,35-/m1/s1
InChI Key XWPUVGRUJWXYTP-PYUVDJBBSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C35H60O6
Molecular Weight 576.80 g/mol
Exact Mass 576.43898963 g/mol
Topological Polar Surface Area (TPSA) 99.40 Ų
XlogP 7.50
Atomic LogP (AlogP) 5.85
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 9

Synonyms

Top
61376-86-1
(2R,3R,4S,5S,6R)-2-[[(3S,5S,9R,10S,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
Schottenol beta-D-glucoside
beta-D-Glucopyranoside, (3beta,5alpha)-stigmast-7-en-3-yl
DTXSID701249602
(3beta,5alpha)-Stigmast-7-en-3-yl beta-D-glucopyranoside

2D Structure

Top
2D Structure of Schottenol glucoside

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8941 89.41%
Caco-2 - 0.8039 80.39%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7468 74.68%
OATP2B1 inhibitior - 0.5779 57.79%
OATP1B1 inhibitior + 0.8629 86.29%
OATP1B3 inhibitior + 0.8152 81.52%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.5930 59.30%
P-glycoprotein inhibitior + 0.6309 63.09%
P-glycoprotein substrate - 0.5618 56.18%
CYP3A4 substrate + 0.6897 68.97%
CYP2C9 substrate - 0.8025 80.25%
CYP2D6 substrate - 0.8264 82.64%
CYP3A4 inhibition - 0.7938 79.38%
CYP2C9 inhibition - 0.7682 76.82%
CYP2C19 inhibition - 0.8388 83.88%
CYP2D6 inhibition - 0.9187 91.87%
CYP1A2 inhibition - 0.8052 80.52%
CYP2C8 inhibition - 0.6373 63.73%
CYP inhibitory promiscuity - 0.7103 71.03%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6820 68.20%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9340 93.40%
Skin irritation - 0.5678 56.78%
Skin corrosion - 0.9452 94.52%
Ames mutagenesis - 0.8070 80.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7075 70.75%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.6307 63.07%
skin sensitisation - 0.8978 89.78%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7657 76.57%
Acute Oral Toxicity (c) III 0.6774 67.74%
Estrogen receptor binding + 0.6906 69.06%
Androgen receptor binding + 0.5761 57.61%
Thyroid receptor binding - 0.5497 54.97%
Glucocorticoid receptor binding + 0.5756 57.56%
Aromatase binding + 0.5459 54.59%
PPAR gamma + 0.5596 55.96%
Honey bee toxicity - 0.7514 75.14%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9772 97.72%

Targets

Top

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.21% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.48% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.15% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.31% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.65% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.47% 95.89%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 89.78% 94.23%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.62% 93.56%
CHEMBL1977 P11473 Vitamin D receptor 88.55% 99.43%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.97% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.37% 92.62%
CHEMBL2581 P07339 Cathepsin D 85.36% 98.95%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.89% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.36% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.70% 86.33%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.99% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 82.71% 95.93%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.35% 96.21%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.34% 96.00%

Plants that contains it

Top
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.
Camellia sinensis
Ipomopsis aggregata
Prunella vulgaris

Cross-Links

Top
PubChem 124879
LOTUS LTS0147059
wikiData Q105343704