beta-D-Galactopyranoside, (1beta,3beta,25S)-3-hydroxyspirost-5-en-1-yl 6-deoxy-2-O-(6-deoxy-alpha-D-mannopyranosyl)-

Details

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Internal ID e9ea31ff-65cc-4753-adc3-b717342587fe
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
IUPAC Name (2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-2-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-6-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol
SMILES (Canonical) CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)C)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1
SMILES (Isomeric) C[C@H]1CC[C@@]2([C@H]([C@H]3[C@@H](O2)C[C@@H]4[C@@]3(CC[C@H]5[C@H]4CC=C6[C@@]5([C@@H](C[C@@H](C6)O)O[C@H]7[C@@H]([C@H]([C@H]([C@H](O7)C)O)O)O[C@H]8[C@@H]([C@@H]([C@H]([C@@H](O8)C)O)O)O)C)C)C)OC1
InChI InChI=1S/C39H62O12/c1-17-9-12-39(46-16-17)18(2)28-26(51-39)15-25-23-8-7-21-13-22(40)14-27(38(21,6)24(23)10-11-37(25,28)5)49-36-34(32(44)30(42)20(4)48-36)50-35-33(45)31(43)29(41)19(3)47-35/h7,17-20,22-36,40-45H,8-16H2,1-6H3/t17-,18-,19-,20+,22+,23+,24-,25-,26-,27+,28-,29-,30-,31+,32-,33+,34+,35-,36-,37-,38-,39+/m0/s1
InChI Key OWGURJWJHWYCIQ-KJXSMTROSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C39H62O12
Molecular Weight 722.90 g/mol
Exact Mass 722.42412741 g/mol
Topological Polar Surface Area (TPSA) 177.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.39
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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beta-D-Galactopyranoside, (1beta,3beta,25S)-3-hydroxyspirost-5-en-1-yl 6-deoxy-2-O-(6-deoxy-alpha-D-mannopyranosyl)-
CHEMBL291743
DTXSID701113219
(1beta,3beta,25S)-3-Hydroxyspirost-5-en-1-yl 6-deoxy-2-O-(6-deoxy-alpha-D-mannopyranosyl)-beta-D-galactopyranoside

2D Structure

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2D Structure of beta-D-Galactopyranoside, (1beta,3beta,25S)-3-hydroxyspirost-5-en-1-yl 6-deoxy-2-O-(6-deoxy-alpha-D-mannopyranosyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9110 91.10%
Caco-2 - 0.8721 87.21%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7118 71.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8906 89.06%
OATP1B3 inhibitior + 0.9561 95.61%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.5740 57.40%
P-glycoprotein inhibitior + 0.7026 70.26%
P-glycoprotein substrate + 0.5252 52.52%
CYP3A4 substrate + 0.7490 74.90%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8129 81.29%
CYP3A4 inhibition - 0.9134 91.34%
CYP2C9 inhibition - 0.9241 92.41%
CYP2C19 inhibition - 0.9494 94.94%
CYP2D6 inhibition - 0.9206 92.06%
CYP1A2 inhibition - 0.8639 86.39%
CYP2C8 inhibition + 0.7485 74.85%
CYP inhibitory promiscuity - 0.9315 93.15%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4723 47.23%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9257 92.57%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9358 93.58%
Ames mutagenesis - 0.8454 84.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7797 77.97%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.8000 80.00%
skin sensitisation - 0.8809 88.09%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7165 71.65%
Acute Oral Toxicity (c) I 0.4129 41.29%
Estrogen receptor binding + 0.7095 70.95%
Androgen receptor binding + 0.7182 71.82%
Thyroid receptor binding - 0.6039 60.39%
Glucocorticoid receptor binding + 0.5562 55.62%
Aromatase binding + 0.7054 70.54%
PPAR gamma + 0.6635 66.35%
Honey bee toxicity - 0.5455 54.55%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9484 94.84%

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 98.11% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.28% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 95.00% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.66% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.83% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.36% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.18% 86.33%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 90.34% 95.89%
CHEMBL1914 P06276 Butyrylcholinesterase 87.17% 95.00%
CHEMBL332 P03956 Matrix metalloproteinase-1 86.81% 94.50%
CHEMBL221 P23219 Cyclooxygenase-1 86.64% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.25% 95.89%
CHEMBL5255 O00206 Toll-like receptor 4 84.06% 92.50%
CHEMBL2243 O00519 Anandamide amidohydrolase 83.78% 97.53%
CHEMBL3401 O75469 Pregnane X receptor 83.76% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.37% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.49% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.38% 92.62%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.11% 86.00%

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.
Beaucarnea recurvata
Dracaena surculosa

Cross-Links

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PubChem 21630158
LOTUS LTS0181241
wikiData Q105202004