15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-6,15-dihydroxy-5-methoxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-11-en-3-one

Details

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Internal ID e1f860eb-bc80-463b-bb2d-a5a20ed87eb2
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]-6,15-dihydroxy-5-methoxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-11-en-3-one
SMILES (Canonical) CC1=C(C(=O)OC(C1)C(C)(C2(CCC3=C4CC5C6(O5)C(C(CC(=O)C6(C4CCC32C)C)OC)O)O)O)C
SMILES (Isomeric) CC1=C(C(=O)OC(C1)C(C)(C2(CCC3=C4CC5C6(O5)C(C(CC(=O)C6(C4CCC32C)C)OC)O)O)O)C
InChI InChI=1S/C29H40O8/c1-14-11-21(36-24(32)15(14)2)27(5,33)28(34)10-8-17-16-12-22-29(37-22)23(31)19(35-6)13-20(30)26(29,4)18(16)7-9-25(17,28)3/h18-19,21-23,31,33-34H,7-13H2,1-6H3
InChI Key MMLYMHIYQXEBTR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H40O8
Molecular Weight 516.60 g/mol
Exact Mass 516.27231823 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP 0.20
Atomic LogP (AlogP) 2.52
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-1-hydroxyethyl]-6,15-dihydroxy-5-methoxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-11-en-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9397 93.97%
Caco-2 - 0.6771 67.71%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7212 72.12%
OATP2B1 inhibitior - 0.7141 71.41%
OATP1B1 inhibitior + 0.8720 87.20%
OATP1B3 inhibitior + 0.9292 92.92%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6874 68.74%
BSEP inhibitior + 0.6407 64.07%
P-glycoprotein inhibitior + 0.6242 62.42%
P-glycoprotein substrate - 0.5135 51.35%
CYP3A4 substrate + 0.7202 72.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8927 89.27%
CYP3A4 inhibition - 0.7771 77.71%
CYP2C9 inhibition - 0.7796 77.96%
CYP2C19 inhibition - 0.8345 83.45%
CYP2D6 inhibition - 0.9415 94.15%
CYP1A2 inhibition - 0.7307 73.07%
CYP2C8 inhibition + 0.5364 53.64%
CYP inhibitory promiscuity - 0.9748 97.48%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5546 55.46%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9286 92.86%
Skin irritation - 0.5280 52.80%
Skin corrosion - 0.9171 91.71%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4829 48.29%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.6367 63.67%
skin sensitisation - 0.8498 84.98%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.9015 90.15%
Acute Oral Toxicity (c) I 0.2948 29.48%
Estrogen receptor binding + 0.6836 68.36%
Androgen receptor binding + 0.7682 76.82%
Thyroid receptor binding + 0.5143 51.43%
Glucocorticoid receptor binding + 0.7344 73.44%
Aromatase binding + 0.7832 78.32%
PPAR gamma + 0.6621 66.21%
Honey bee toxicity - 0.7789 77.89%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9708 97.08%

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
CHEMBL204 P00734 Thrombin 99.39% 96.01%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.27% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.80% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.93% 99.23%
CHEMBL1902 P62942 FK506-binding protein 1A 92.93% 97.05%
CHEMBL230 P35354 Cyclooxygenase-2 92.19% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.05% 95.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 90.54% 97.14%
CHEMBL1871 P10275 Androgen Receptor 89.19% 96.43%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.93% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.83% 94.00%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 87.84% 97.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.52% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.29% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.80% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.04% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.66% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 85.25% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 85.23% 94.75%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.21% 92.68%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.90% 92.62%
CHEMBL2581 P07339 Cathepsin D 83.26% 98.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.71% 91.07%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.25% 100.00%
CHEMBL1907 P15144 Aminopeptidase N 81.40% 93.31%
CHEMBL259 P32245 Melanocortin receptor 4 81.29% 95.38%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.46% 93.04%

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 cinerascens
Physalis lagascae

Cross-Links

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PubChem 74039195
LOTUS LTS0017601
wikiData Q105167877