beta-D-Glucopyranoside, (1beta,3beta,22alpha,25S)-1,3,22-trihydroxyfurost-5-en-26-yl

Details

Top
Internal ID e7c1fca7-21aa-44fc-9910-107eb032bdb1
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins
IUPAC Name (1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,14,16-triol
SMILES (Canonical) CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)C)C)OC1(CCC(C)COC6C(C(C(C(O6)CO)O)O)O)O
SMILES (Isomeric) C[C@H]1[C@H]2[C@H](C[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC=C5[C@@]4([C@@H](C[C@@H](C5)O)O)C)C)O[C@@]1(CC[C@H](C)CO[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)O
InChI InChI=1S/C33H54O10/c1-16(15-41-30-29(39)28(38)27(37)24(14-34)42-30)7-10-33(40)17(2)26-23(43-33)13-22-20-6-5-18-11-19(35)12-25(36)32(18,4)21(20)8-9-31(22,26)3/h5,16-17,19-30,34-40H,6-15H2,1-4H3/t16-,17-,19+,20+,21-,22-,23-,24+,25+,26-,27+,28-,29+,30+,31-,32-,33+/m0/s1
InChI Key XVRUZUGQEQHLOB-QQMVAJSHSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C33H54O10
Molecular Weight 610.80 g/mol
Exact Mass 610.37169792 g/mol
Topological Polar Surface Area (TPSA) 169.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.46
H-Bond Acceptor 10
H-Bond Donor 7
Rotatable Bonds 7

Synonyms

Top
beta-D-Glucopyranoside, (1beta,3beta,22alpha,25S)-1,3,22-trihydroxyfurost-5-en-26-yl
145645-63-2

2D Structure

Top
2D Structure of beta-D-Glucopyranoside, (1beta,3beta,22alpha,25S)-1,3,22-trihydroxyfurost-5-en-26-yl

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7571 75.71%
Caco-2 - 0.8669 86.69%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7376 73.76%
OATP2B1 inhibitior - 0.5812 58.12%
OATP1B1 inhibitior + 0.8765 87.65%
OATP1B3 inhibitior + 0.8994 89.94%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.6638 66.38%
P-glycoprotein inhibitior + 0.6592 65.92%
P-glycoprotein substrate + 0.6085 60.85%
CYP3A4 substrate + 0.7431 74.31%
CYP2C9 substrate - 0.8020 80.20%
CYP2D6 substrate - 0.8336 83.36%
CYP3A4 inhibition - 0.9268 92.68%
CYP2C9 inhibition - 0.9182 91.82%
CYP2C19 inhibition - 0.9234 92.34%
CYP2D6 inhibition - 0.9343 93.43%
CYP1A2 inhibition - 0.9102 91.02%
CYP2C8 inhibition + 0.6445 64.45%
CYP inhibitory promiscuity - 0.9302 93.02%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5116 51.16%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9354 93.54%
Skin irritation + 0.4929 49.29%
Skin corrosion - 0.9426 94.26%
Ames mutagenesis - 0.8337 83.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6796 67.96%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.7050 70.50%
skin sensitisation - 0.9214 92.14%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.8079 80.79%
Acute Oral Toxicity (c) I 0.5904 59.04%
Estrogen receptor binding + 0.6636 66.36%
Androgen receptor binding + 0.7019 70.19%
Thyroid receptor binding - 0.5813 58.13%
Glucocorticoid receptor binding - 0.4806 48.06%
Aromatase binding + 0.6724 67.24%
PPAR gamma + 0.5723 57.23%
Honey bee toxicity - 0.6419 64.19%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9176 91.76%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.84% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.24% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 96.75% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.31% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 93.41% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 91.25% 95.89%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.82% 92.86%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.18% 93.56%
CHEMBL221 P23219 Cyclooxygenase-1 89.01% 90.17%
CHEMBL2996 Q05655 Protein kinase C delta 88.50% 97.79%
CHEMBL2581 P07339 Cathepsin D 88.38% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.28% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.91% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.43% 94.45%
CHEMBL242 Q92731 Estrogen receptor beta 86.17% 98.35%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 85.74% 89.05%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.82% 96.61%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.19% 95.89%
CHEMBL4581 P52732 Kinesin-like protein 1 83.87% 93.18%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 83.71% 98.46%
CHEMBL1871 P10275 Androgen Receptor 83.44% 96.43%
CHEMBL3401 O75469 Pregnane X receptor 83.35% 94.73%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.75% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 81.93% 92.50%
CHEMBL2360 P00492 Hypoxanthine-guanine phosphoribosyltransferase 80.72% 87.38%
CHEMBL2094135 Q96BI3 Gamma-secretase 80.12% 98.05%

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.
Nolina microcarpa
Rhodiola rosea

Cross-Links

Top
PubChem 15719188
NPASS NPC40974
LOTUS LTS0267690
wikiData Q105343105