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

Details

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Internal ID a8b7475e-3837-4fca-a96a-b7937ff972ca
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)ethyl]-6,15-dihydroxy-5-methoxy-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(CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OC)C)O5)C)O)C
SMILES (Isomeric) CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(CCC4C3CC5C6(C4(C(=O)CC(C6O)OC)C)O5)C)O)C
InChI InChI=1S/C29H42O7/c1-14-11-20(35-25(32)15(14)2)16(3)28(33)10-8-18-17-12-23-29(36-23)24(31)21(34-6)13-22(30)27(29,5)19(17)7-9-26(18,28)4/h16-21,23-24,31,33H,7-13H2,1-6H3
InChI Key JIOWYOZENBWYAC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H42O7
Molecular Weight 502.60 g/mol
Exact Mass 502.29305367 g/mol
Topological Polar Surface Area (TPSA) 106.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.34
H-Bond Acceptor 7
H-Bond Donor 2
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)ethyl]-6,15-dihydroxy-5-methoxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-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 + 0.9558 95.58%
Caco-2 - 0.7129 71.29%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6587 65.87%
OATP2B1 inhibitior - 0.7138 71.38%
OATP1B1 inhibitior + 0.8647 86.47%
OATP1B3 inhibitior + 0.9230 92.30%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6874 68.74%
BSEP inhibitior + 0.7560 75.60%
P-glycoprotein inhibitior + 0.6124 61.24%
P-glycoprotein substrate + 0.5283 52.83%
CYP3A4 substrate + 0.7309 73.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8953 89.53%
CYP3A4 inhibition - 0.7693 76.93%
CYP2C9 inhibition - 0.7968 79.68%
CYP2C19 inhibition - 0.8517 85.17%
CYP2D6 inhibition - 0.9450 94.50%
CYP1A2 inhibition - 0.7257 72.57%
CYP2C8 inhibition + 0.5795 57.95%
CYP inhibitory promiscuity - 0.9622 96.22%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5786 57.86%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9388 93.88%
Skin irritation - 0.5278 52.78%
Skin corrosion - 0.9198 91.98%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4743 47.43%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.6086 60.86%
skin sensitisation - 0.8455 84.55%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.8097 80.97%
Acute Oral Toxicity (c) I 0.4113 41.13%
Estrogen receptor binding + 0.7115 71.15%
Androgen receptor binding + 0.7881 78.81%
Thyroid receptor binding - 0.5109 51.09%
Glucocorticoid receptor binding + 0.7166 71.66%
Aromatase binding + 0.7296 72.96%
PPAR gamma + 0.6682 66.82%
Honey bee toxicity - 0.6808 68.08%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9633 96.33%

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
CHEMBL1914 P06276 Butyrylcholinesterase 94.53% 95.00%
CHEMBL1937 Q92769 Histone deacetylase 2 93.11% 94.75%
CHEMBL4302 P08183 P-glycoprotein 1 93.10% 92.98%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.55% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.43% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.73% 95.56%
CHEMBL204 P00734 Thrombin 90.88% 96.01%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.29% 96.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.99% 97.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.22% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.59% 91.11%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.07% 91.07%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.33% 94.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.09% 82.69%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.29% 97.25%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.08% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.94% 86.33%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 83.71% 97.33%
CHEMBL5103 Q969S8 Histone deacetylase 10 83.45% 90.08%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.83% 96.38%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.14% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.06% 93.56%
CHEMBL1902 P62942 FK506-binding protein 1A 80.77% 97.05%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.74% 100.00%

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.
Tubocapsicum anomalum

Cross-Links

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PubChem 73306782
LOTUS LTS0228458
wikiData Q105129242