Virescenoside V

Details

Top
Internal ID 81fce6b2-a2fd-49d4-af66-d61e2d86201e
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides
IUPAC Name (1S,2R,3R,4aS,4bR,7R,10aR)-7-ethenyl-2,3-dihydroxy-1,4a,7-trimethyl-1-[[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H40O9/c1-5-24(2)7-6-14-13(9-24)15(28)8-18-25(14,3)10-16(29)22(33)26(18,4)12-34-23-21(32)20(31)19(30)17(11-27)35-23/h5,9,14,16-23,27,29-33H,1,6-8,10-12H2,2-4H3/t14-,16+,17+,18+,19+,20+,21-,22-,23+,24-,25+,26+/m0/s1
InChI Key QPUZIMJVFNBYQT-JHSKIDNSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C26H40O9
Molecular Weight 496.60 g/mol
Exact Mass 496.26723285 g/mol
Topological Polar Surface Area (TPSA) 157.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.06
H-Bond Acceptor 9
H-Bond Donor 6
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Virescenoside V

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7632 76.32%
Caco-2 - 0.8024 80.24%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7868 78.68%
OATP2B1 inhibitior - 0.7218 72.18%
OATP1B1 inhibitior + 0.8621 86.21%
OATP1B3 inhibitior - 0.3249 32.49%
MATE1 inhibitior - 0.9812 98.12%
OCT2 inhibitior - 0.7026 70.26%
BSEP inhibitior + 0.7641 76.41%
P-glycoprotein inhibitior - 0.5832 58.32%
P-glycoprotein substrate - 0.7772 77.72%
CYP3A4 substrate + 0.6815 68.15%
CYP2C9 substrate - 0.7975 79.75%
CYP2D6 substrate - 0.8765 87.65%
CYP3A4 inhibition - 0.8267 82.67%
CYP2C9 inhibition - 0.8882 88.82%
CYP2C19 inhibition - 0.8542 85.42%
CYP2D6 inhibition - 0.9420 94.20%
CYP1A2 inhibition - 0.8238 82.38%
CYP2C8 inhibition - 0.5609 56.09%
CYP inhibitory promiscuity - 0.9605 96.05%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7097 70.97%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9594 95.94%
Skin irritation - 0.5506 55.06%
Skin corrosion - 0.9451 94.51%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6506 65.06%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.8088 80.88%
skin sensitisation - 0.8998 89.98%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6146 61.46%
Acute Oral Toxicity (c) III 0.7177 71.77%
Estrogen receptor binding + 0.6463 64.63%
Androgen receptor binding + 0.6613 66.13%
Thyroid receptor binding + 0.5337 53.37%
Glucocorticoid receptor binding + 0.6790 67.90%
Aromatase binding + 0.7465 74.65%
PPAR gamma + 0.6000 60.00%
Honey bee toxicity - 0.7190 71.90%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9653 96.53%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.40% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.50% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.77% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.79% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.73% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.12% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.90% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.97% 100.00%
CHEMBL1977 P11473 Vitamin D receptor 88.55% 99.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.15% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 86.92% 94.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.50% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.51% 89.00%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 82.88% 95.83%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.37% 91.24%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.00% 89.34%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.23% 96.61%
CHEMBL5028 O14672 ADAM10 80.17% 97.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.07% 86.33%

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.
There are no matching plants.

Cross-Links

Top
PubChem 139583852
LOTUS LTS0259502
wikiData Q75068284