4-oxo-27-TBDMS Withaferin A

Details

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Internal ID 8845047c-ba54-47e1-a69f-ff4e7898c788
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name (1S,2R,7S,9R,11S,12S,15R,16S)-15-[(1S)-1-[(2R)-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-ene-3,6-dione
SMILES (Canonical) CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6=O)C)O5)C)CO[Si](C)(C)C(C)(C)C
SMILES (Isomeric) CC1=C(C(=O)O[C@H](C1)[C@@H](C)[C@H]2CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3C[C@@H]5[C@]6([C@@]4(C(=O)C=CC6=O)C)O5)C)CO[Si](C)(C)C(C)(C)C
InChI InChI=1S/C34H50O6Si/c1-19-16-26(39-30(37)22(19)18-38-41(8,9)31(3,4)5)20(2)23-10-11-24-21-17-29-34(40-29)28(36)13-12-27(35)33(34,7)25(21)14-15-32(23,24)6/h12-13,20-21,23-26,29H,10-11,14-18H2,1-9H3/t20-,21-,23+,24-,25-,26+,29+,32+,33-,34+/m0/s1
InChI Key RZWFBNOFUAHADD-VTYRCZOESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C34H50O6Si
Molecular Weight 582.80 g/mol
Exact Mass 582.33766584 g/mol
Topological Polar Surface Area (TPSA) 82.20 Ų
XlogP 0.00
Atomic LogP (AlogP) 6.59
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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1214886-31-3
(1S,2R,7S,9R,11S,12S,15R,16S)-15-[(1S)-1-[(2R)-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-4-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-ene-3,6-dione
27-TBDMS-4-Dehydrowithaferin A
(5beta,6beta,22R)-27-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-5,6-epoxy-22-hydroxy-1,4-dioxo-ergosta-2,24-dien-26-oic acid, delta-lactone
C34H50O6Si
orb1694436
CHEMBL2047419
HY-N10355
AKOS040754751
PD069707
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-oxo-27-TBDMS Withaferin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8762 87.62%
Caco-2 - 0.7389 73.89%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6504 65.04%
OATP2B1 inhibitior - 0.8620 86.20%
OATP1B1 inhibitior + 0.8709 87.09%
OATP1B3 inhibitior + 0.9561 95.61%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9788 97.88%
P-glycoprotein inhibitior + 0.8480 84.80%
P-glycoprotein substrate + 0.6594 65.94%
CYP3A4 substrate + 0.7420 74.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8907 89.07%
CYP3A4 inhibition - 0.8325 83.25%
CYP2C9 inhibition - 0.7895 78.95%
CYP2C19 inhibition - 0.8169 81.69%
CYP2D6 inhibition - 0.9079 90.79%
CYP1A2 inhibition - 0.7470 74.70%
CYP2C8 inhibition + 0.6711 67.11%
CYP inhibitory promiscuity - 0.9072 90.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6000 60.00%
Eye corrosion - 0.9802 98.02%
Eye irritation - 0.9158 91.58%
Skin irritation - 0.7367 73.67%
Skin corrosion - 0.9303 93.03%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7470 74.70%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.5717 57.17%
skin sensitisation - 0.7942 79.42%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6749 67.49%
Acute Oral Toxicity (c) III 0.3619 36.19%
Estrogen receptor binding + 0.7850 78.50%
Androgen receptor binding + 0.7731 77.31%
Thyroid receptor binding + 0.6068 60.68%
Glucocorticoid receptor binding + 0.8268 82.68%
Aromatase binding + 0.7762 77.62%
PPAR gamma + 0.6620 66.20%
Honey bee toxicity - 0.6988 69.88%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.9819 98.19%

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 96.54% 97.25%
CHEMBL2581 P07339 Cathepsin D 93.81% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.33% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.45% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.38% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.01% 94.00%
CHEMBL230 P35354 Cyclooxygenase-2 90.97% 89.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.78% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.10% 97.14%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.93% 85.14%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.73% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.88% 99.23%
CHEMBL5103 Q969S8 Histone deacetylase 10 85.52% 90.08%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.54% 100.00%
CHEMBL2179 P04062 Beta-glucocerebrosidase 83.91% 85.31%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.66% 90.93%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.21% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 82.89% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.65% 91.11%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.38% 96.38%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 81.73% 97.33%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.46% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.10% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.75% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 80.22% 94.75%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.18% 82.69%

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.
Withania aristata

Cross-Links

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PubChem 66572431
LOTUS LTS0125963
wikiData Q105248646