Withaperuvin G

Details

Top
Internal ID ac2c69bd-a20f-4275-8bfd-c6a75da49c89
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name 16-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-13,16-dihydroxy-2,17-dimethyl-5,9-dioxahexacyclo[10.7.0.02,8.04,6.08,10.013,17]nonadecan-3-one
SMILES (Canonical) CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC5C6(C4(C(=O)C7C(C6)O7)C)O5)C)O)O)O)C
SMILES (Isomeric) CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC5C6(C4(C(=O)C7C(C6)O7)C)O5)C)O)O)O)C
InChI InChI=1S/C28H38O8/c1-13-10-18(35-22(30)14(13)2)25(5,31)28(33)9-8-26(32)16-11-19-27(36-19)12-17-20(34-17)21(29)24(27,4)15(16)6-7-23(26,28)3/h15-20,31-33H,6-12H2,1-5H3
InChI Key FHBPSLRPQVOBMG-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C28H38O8
Molecular Weight 502.60 g/mol
Exact Mass 502.25666817 g/mol
Topological Polar Surface Area (TPSA) 129.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.97
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
2b,3b
5,6b-Diepoxy-14,17b,20R-trihydroxy-1-oxo-5b,22R-with-24-enolide

2D Structure

Top
2D Structure of Withaperuvin G

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8604 86.04%
Caco-2 - 0.6944 69.44%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6273 62.73%
OATP2B1 inhibitior - 0.7156 71.56%
OATP1B1 inhibitior + 0.8845 88.45%
OATP1B3 inhibitior + 0.9400 94.00%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6374 63.74%
BSEP inhibitior + 0.6635 66.35%
P-glycoprotein inhibitior - 0.4542 45.42%
P-glycoprotein substrate + 0.6681 66.81%
CYP3A4 substrate + 0.7121 71.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8964 89.64%
CYP3A4 inhibition - 0.7750 77.50%
CYP2C9 inhibition - 0.8408 84.08%
CYP2C19 inhibition - 0.8738 87.38%
CYP2D6 inhibition - 0.9484 94.84%
CYP1A2 inhibition - 0.8267 82.67%
CYP2C8 inhibition + 0.5297 52.97%
CYP inhibitory promiscuity - 0.9803 98.03%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5958 59.58%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9265 92.65%
Skin irritation + 0.5274 52.74%
Skin corrosion - 0.9055 90.55%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4402 44.02%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.6482 64.82%
skin sensitisation - 0.8271 82.71%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.7596 75.96%
Acute Oral Toxicity (c) I 0.3666 36.66%
Estrogen receptor binding + 0.7411 74.11%
Androgen receptor binding + 0.7687 76.87%
Thyroid receptor binding + 0.5581 55.81%
Glucocorticoid receptor binding + 0.7120 71.20%
Aromatase binding + 0.7583 75.83%
PPAR gamma + 0.6467 64.67%
Honey bee toxicity - 0.7951 79.51%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9759 97.59%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.09% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.32% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.20% 91.11%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 92.76% 97.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.62% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.30% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.07% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.44% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.93% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.25% 89.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.87% 93.04%
CHEMBL3401 O75469 Pregnane X receptor 85.85% 94.73%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.22% 93.56%
CHEMBL1871 P10275 Androgen Receptor 84.97% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.93% 96.09%
CHEMBL259 P32245 Melanocortin receptor 4 84.72% 95.38%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.27% 96.61%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.43% 95.89%
CHEMBL2996 Q05655 Protein kinase C delta 81.79% 97.79%
CHEMBL299 P17252 Protein kinase C alpha 81.72% 98.03%
CHEMBL1914 P06276 Butyrylcholinesterase 81.42% 95.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.08% 91.03%
CHEMBL2094135 Q96BI3 Gamma-secretase 80.71% 98.05%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.11% 100.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.10% 93.03%

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.
Physalis peruviana

Cross-Links

Top
PubChem 131751505
LOTUS LTS0032276
wikiData Q104995163