(3b,5a,25R)-3-Hydroxyspirostan-6-one 3-[2-acetylarabinosyl-(1->6)-glucoside]

Details

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Internal ID 34a0f3b5-12f1-4e2d-b943-b6d96f3f04fd
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
IUPAC Name [4,5-dihydroxy-2-[[3,4,5-trihydroxy-6-(5',7,9,13-tetramethyl-19-oxospiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-2-yl]methoxy]oxan-3-yl] acetate
SMILES (Canonical) CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)OC(=O)C)O)O)O)C)C)C)OC1
SMILES (Isomeric) CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)OC(=O)C)O)O)O)C)C)C)OC1
InChI InChI=1S/C40H62O14/c1-18-6-11-40(50-15-18)19(2)30-28(54-40)14-24-22-13-26(42)25-12-21(7-9-38(25,4)23(22)8-10-39(24,30)5)52-36-34(47)33(46)32(45)29(53-36)17-49-37-35(51-20(3)41)31(44)27(43)16-48-37/h18-19,21-25,27-37,43-47H,6-17H2,1-5H3
InChI Key LYOWCAVVHJOCKI-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C40H62O14
Molecular Weight 766.90 g/mol
Exact Mass 766.41395665 g/mol
Topological Polar Surface Area (TPSA) 200.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.83
H-Bond Acceptor 14
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3b,5a,25R)-3-Hydroxyspirostan-6-one 3-[2-acetylarabinosyl-(1->6)-glucoside]

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5742 57.42%
Caco-2 - 0.8855 88.55%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7904 79.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8575 85.75%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.7868 78.68%
P-glycoprotein inhibitior + 0.7309 73.09%
P-glycoprotein substrate + 0.5430 54.30%
CYP3A4 substrate + 0.7517 75.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8751 87.51%
CYP3A4 inhibition - 0.9098 90.98%
CYP2C9 inhibition - 0.9285 92.85%
CYP2C19 inhibition - 0.9100 91.00%
CYP2D6 inhibition - 0.9643 96.43%
CYP1A2 inhibition - 0.9395 93.95%
CYP2C8 inhibition + 0.6702 67.02%
CYP inhibitory promiscuity - 0.9766 97.66%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6192 61.92%
Eye corrosion - 0.9914 99.14%
Eye irritation - 0.9186 91.86%
Skin irritation - 0.6063 60.63%
Skin corrosion - 0.9394 93.94%
Ames mutagenesis - 0.7270 72.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7013 70.13%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.9441 94.41%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8771 87.71%
Acute Oral Toxicity (c) I 0.7619 76.19%
Estrogen receptor binding + 0.8475 84.75%
Androgen receptor binding + 0.6858 68.58%
Thyroid receptor binding - 0.6360 63.60%
Glucocorticoid receptor binding + 0.6121 61.21%
Aromatase binding + 0.6491 64.91%
PPAR gamma + 0.7086 70.86%
Honey bee toxicity - 0.6273 62.73%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9228 92.28%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.90% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.38% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.52% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.24% 97.25%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.21% 96.77%
CHEMBL5255 O00206 Toll-like receptor 4 93.44% 92.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.90% 94.45%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 92.41% 93.04%
CHEMBL1914 P06276 Butyrylcholinesterase 91.02% 95.00%
CHEMBL5957 P21589 5'-nucleotidase 90.47% 97.78%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.27% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.09% 96.95%
CHEMBL325 Q13547 Histone deacetylase 1 89.63% 95.92%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.89% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.74% 86.33%
CHEMBL226 P30542 Adenosine A1 receptor 87.65% 95.93%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.34% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.34% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.05% 95.89%
CHEMBL2581 P07339 Cathepsin D 85.66% 98.95%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.80% 95.50%
CHEMBL5028 O14672 ADAM10 83.06% 97.50%
CHEMBL340 P08684 Cytochrome P450 3A4 82.54% 91.19%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.12% 95.89%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.72% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.56% 95.71%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.16% 96.90%

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.
Allium chinense

Cross-Links

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PubChem 74029744
LOTUS LTS0079699
wikiData Q105159464