16-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-7,15-dihydroxy-10,14,16-trimethyl-17-oxapentacyclo[13.2.2.01,14.02,11.05,10]nonadec-4-en-9-one

Details

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Internal ID f087bef5-8aee-45ba-9542-5c36bc71f8d1
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name 16-(4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl)-7,15-dihydroxy-10,14,16-trimethyl-17-oxapentacyclo[13.2.2.01,14.02,11.05,10]nonadec-4-en-9-one
SMILES (Canonical) CC1=C(C(=O)OC(C1)C2(C3(CCC4(C3(CCC5C4CC=C6C5(C(=O)CC(C6)O)C)C)O2)O)C)C
SMILES (Isomeric) CC1=C(C(=O)OC(C1)C2(C3(CCC4(C3(CCC5C4CC=C6C5(C(=O)CC(C6)O)C)C)O2)O)C)C
InChI InChI=1S/C28H38O6/c1-15-12-22(33-23(31)16(15)2)26(5)28(32)11-10-27(34-26)20-7-6-17-13-18(29)14-21(30)25(17,4)19(20)8-9-24(27,28)3/h6,18-20,22,29,32H,7-14H2,1-5H3
InChI Key HWAGUKMIVWYXPY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H38O6
Molecular Weight 470.60 g/mol
Exact Mass 470.26683893 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 16-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)-7,15-dihydroxy-10,14,16-trimethyl-17-oxapentacyclo[13.2.2.01,14.02,11.05,10]nonadec-4-en-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9842 98.42%
Caco-2 - 0.6016 60.16%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8428 84.28%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.8930 89.30%
OATP1B3 inhibitior + 0.9146 91.46%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7321 73.21%
BSEP inhibitior + 0.8445 84.45%
P-glycoprotein inhibitior - 0.4790 47.90%
P-glycoprotein substrate + 0.5218 52.18%
CYP3A4 substrate + 0.7083 70.83%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8975 89.75%
CYP3A4 inhibition - 0.7364 73.64%
CYP2C9 inhibition - 0.9232 92.32%
CYP2C19 inhibition - 0.9396 93.96%
CYP2D6 inhibition - 0.9613 96.13%
CYP1A2 inhibition - 0.8810 88.10%
CYP2C8 inhibition + 0.4749 47.49%
CYP inhibitory promiscuity - 0.9596 95.96%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.4791 47.91%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9384 93.84%
Skin irritation + 0.6504 65.04%
Skin corrosion - 0.8962 89.62%
Ames mutagenesis - 0.5637 56.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5394 53.94%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.7283 72.83%
skin sensitisation - 0.8709 87.09%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.6891 68.91%
Acute Oral Toxicity (c) I 0.8110 81.10%
Estrogen receptor binding + 0.8217 82.17%
Androgen receptor binding + 0.7724 77.24%
Thyroid receptor binding + 0.5367 53.67%
Glucocorticoid receptor binding + 0.7945 79.45%
Aromatase binding + 0.7635 76.35%
PPAR gamma + 0.5806 58.06%
Honey bee toxicity - 0.8235 82.35%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9855 98.55%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.54% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.31% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.40% 97.25%
CHEMBL204 P00734 Thrombin 88.23% 96.01%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.20% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.50% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.38% 93.04%
CHEMBL1937 Q92769 Histone deacetylase 2 87.37% 94.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.31% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.81% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.16% 94.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.15% 93.40%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.18% 82.69%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.01% 93.03%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.31% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.94% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.91% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.29% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.73% 93.99%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.29% 93.56%

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.
Ajuga parviflora
Withania coagulans

Cross-Links

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PubChem 73106250
LOTUS LTS0054040
wikiData Q104888907