2,3-Dihydrowithanolide E

Details

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Internal ID 8fd79c7e-a175-48c1-b16b-c6b917e4fdc4
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name 15-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-12,15-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one
SMILES (Canonical) CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC5C6(C4(C(=O)CCC6)C)O5)C)O)O)O)C
SMILES (Isomeric) CC1=C(C(=O)OC(C1)C(C)(C2(CCC3(C2(CCC4C3CC5C6(C4(C(=O)CCC6)C)O5)C)O)O)O)C
InChI InChI=1S/C28H40O7/c1-15-13-20(34-22(30)16(15)2)25(5,31)28(33)12-11-26(32)18-14-21-27(35-21)9-6-7-19(29)24(27,4)17(18)8-10-23(26,28)3/h17-18,20-21,31-33H,6-14H2,1-5H3
InChI Key OILCCDVXJXTPHF-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C28H40O7
Molecular Weight 488.60 g/mol
Exact Mass 488.27740361 g/mol
Topological Polar Surface Area (TPSA) 117.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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CHEBI:175793
5b,6b-Epoxy-14a,17b,20S-trihydroxy-1-oxo-22R-with-24-enolide
15-[1-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-12,15-dihydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one

2D Structure

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2D Structure of 2,3-Dihydrowithanolide E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8604 86.04%
Caco-2 - 0.6410 64.10%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6273 62.73%
OATP2B1 inhibitior - 0.7149 71.49%
OATP1B1 inhibitior + 0.8765 87.65%
OATP1B3 inhibitior + 0.9400 94.00%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6374 63.74%
BSEP inhibitior + 0.8060 80.60%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate + 0.5659 56.59%
CYP3A4 substrate + 0.7066 70.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8970 89.70%
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 + 0.5680 56.80%
CYP inhibitory promiscuity - 0.9803 98.03%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5958 59.58%
Eye corrosion - 0.9902 99.02%
Eye irritation - 0.9260 92.60%
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 + 0.6563 65.63%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.6160 61.60%
skin sensitisation - 0.8271 82.71%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.6829 68.29%
Acute Oral Toxicity (c) I 0.3666 36.66%
Estrogen receptor binding + 0.7406 74.06%
Androgen receptor binding + 0.7609 76.09%
Thyroid receptor binding + 0.5291 52.91%
Glucocorticoid receptor binding + 0.7315 73.15%
Aromatase binding + 0.7949 79.49%
PPAR gamma + 0.6038 60.38%
Honey bee toxicity - 0.8432 84.32%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9759 97.59%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.71% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.59% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.48% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.65% 95.56%
CHEMBL1914 P06276 Butyrylcholinesterase 91.72% 95.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 91.00% 93.04%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.14% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.20% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.71% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.61% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.99% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.64% 92.94%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 87.33% 91.79%
CHEMBL2039 P27338 Monoamine oxidase B 86.14% 92.51%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.13% 97.14%
CHEMBL1902 P62942 FK506-binding protein 1A 84.25% 97.05%
CHEMBL259 P32245 Melanocortin receptor 4 84.13% 95.38%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.00% 82.69%
CHEMBL230 P35354 Cyclooxygenase-2 83.70% 89.63%
CHEMBL3401 O75469 Pregnane X receptor 82.37% 94.73%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.82% 93.03%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.62% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.73% 94.00%
CHEMBL1871 P10275 Androgen Receptor 80.64% 96.43%
CHEMBL5028 O14672 ADAM10 80.04% 97.50%

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.
Physalis angulata

Cross-Links

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PubChem 131751517
LOTUS LTS0178410
wikiData Q104399690