Withanosideiv

Details

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Internal ID 575b7b92-47af-4de6-979c-2c75e9b555f8
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives > Withanolide glycosides and derivatives
IUPAC Name 2-[1-[1-hydroxy-10,13-dimethyl-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethyl]-5-(hydroxymethyl)-4-methyl-2,3-dihydropyran-6-one
SMILES (Canonical) CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC=C5C4(C(CC(C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)C)C)CO
SMILES (Isomeric) CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC=C5C4(C(CC(C5)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)C)C)CO
InChI InChI=1S/C40H62O15/c1-17-11-26(53-36(50)22(17)14-41)18(2)23-7-8-24-21-6-5-19-12-20(13-29(43)40(19,4)25(21)9-10-39(23,24)3)52-38-35(49)33(47)31(45)28(55-38)16-51-37-34(48)32(46)30(44)27(15-42)54-37/h5,18,20-21,23-35,37-38,41-49H,6-16H2,1-4H3
InChI Key VUQQGHSDHGOYRH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C40H62O15
Molecular Weight 782.90 g/mol
Exact Mass 782.40887127 g/mol
Topological Polar Surface Area (TPSA) 245.00 Ų
XlogP 1.00
Atomic LogP (AlogP) -0.19
H-Bond Acceptor 15
H-Bond Donor 9
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Withanosideiv

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7838 78.38%
Caco-2 - 0.8855 88.55%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8076 80.76%
OATP2B1 inhibitior - 0.8696 86.96%
OATP1B1 inhibitior + 0.8441 84.41%
OATP1B3 inhibitior - 0.2313 23.13%
MATE1 inhibitior - 0.9412 94.12%
OCT2 inhibitior - 0.6776 67.76%
BSEP inhibitior + 0.8113 81.13%
P-glycoprotein inhibitior + 0.7200 72.00%
P-glycoprotein substrate + 0.6087 60.87%
CYP3A4 substrate + 0.7563 75.63%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8853 88.53%
CYP3A4 inhibition - 0.9495 94.95%
CYP2C9 inhibition - 0.9335 93.35%
CYP2C19 inhibition - 0.9392 93.92%
CYP2D6 inhibition - 0.9467 94.67%
CYP1A2 inhibition - 0.9243 92.43%
CYP2C8 inhibition + 0.6747 67.47%
CYP inhibitory promiscuity - 0.9590 95.90%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6109 61.09%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9191 91.91%
Skin irritation + 0.5259 52.59%
Skin corrosion - 0.9457 94.57%
Ames mutagenesis - 0.7044 70.44%
Human Ether-a-go-go-Related Gene inhibition + 0.8060 80.60%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.7158 71.58%
skin sensitisation - 0.9254 92.54%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.4565 45.65%
Estrogen receptor binding + 0.8330 83.30%
Androgen receptor binding + 0.7511 75.11%
Thyroid receptor binding - 0.6192 61.92%
Glucocorticoid receptor binding + 0.6324 63.24%
Aromatase binding + 0.6776 67.76%
PPAR gamma + 0.7166 71.66%
Honey bee toxicity - 0.6844 68.44%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9296 92.96%

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 95.28% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.99% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.74% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 94.35% 94.75%
CHEMBL5103 Q969S8 Histone deacetylase 10 93.70% 90.08%
CHEMBL226 P30542 Adenosine A1 receptor 93.26% 95.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.39% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.29% 97.25%
CHEMBL1871 P10275 Androgen Receptor 91.88% 96.43%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 91.18% 95.89%
CHEMBL2581 P07339 Cathepsin D 91.15% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.48% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 89.74% 93.04%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.59% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.01% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.48% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.66% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.94% 94.45%
CHEMBL5028 O14672 ADAM10 85.32% 97.50%
CHEMBL3401 O75469 Pregnane X receptor 84.42% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.46% 96.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.68% 95.89%
CHEMBL5255 O00206 Toll-like receptor 4 81.00% 92.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.89% 93.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.23% 97.14%

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.
Withania somnifera

Cross-Links

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PubChem 72982317
LOTUS LTS0055230
wikiData Q105297375