7beta-Acetoxywithanolide D

Details

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Internal ID fbbcc1bc-cc54-4b1e-99ba-21183791f4e0
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name [(1S,2R,6S,7R,9R,10R,11S,12S,15S,16S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-1-hydroxyethyl]-6-hydroxy-2,16-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-10-yl] acetate
SMILES (Canonical) CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3C(C5C6(C4(C(=O)C=CC6O)C)O5)OC(=O)C)C)O)C
SMILES (Isomeric) CC1=C(C(=O)O[C@H](C1)[C@@](C)([C@H]2CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3[C@H]([C@@H]5[C@]6([C@@]4(C(=O)C=C[C@@H]6O)C)O5)OC(=O)C)C)O)C
InChI InChI=1S/C30H40O8/c1-14-13-22(37-26(34)15(14)2)29(6,35)19-8-7-17-23-18(11-12-27(17,19)4)28(5)20(32)9-10-21(33)30(28)25(38-30)24(23)36-16(3)31/h9-10,17-19,21-25,33,35H,7-8,11-13H2,1-6H3/t17-,18-,19-,21-,22+,23-,24+,25+,27-,28-,29+,30+/m0/s1
InChI Key SHUUIGOWNXWQBK-RYJNYAFDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H40O8
Molecular Weight 528.60 g/mol
Exact Mass 528.27231823 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.04
H-Bond Acceptor 8
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 7beta-Acetoxywithanolide D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9472 94.72%
Caco-2 - 0.7426 74.26%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7545 75.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8566 85.66%
OATP1B3 inhibitior + 0.8329 83.29%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6624 66.24%
BSEP inhibitior + 0.6010 60.10%
P-glycoprotein inhibitior + 0.7277 72.77%
P-glycoprotein substrate - 0.5084 50.84%
CYP3A4 substrate + 0.7539 75.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9020 90.20%
CYP3A4 inhibition - 0.8569 85.69%
CYP2C9 inhibition - 0.8226 82.26%
CYP2C19 inhibition - 0.8734 87.34%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.6090 60.90%
CYP2C8 inhibition + 0.5273 52.73%
CYP inhibitory promiscuity - 0.9368 93.68%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6038 60.38%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9390 93.90%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9144 91.44%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7262 72.62%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.5783 57.83%
skin sensitisation - 0.8326 83.26%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity + 0.6119 61.19%
Acute Oral Toxicity (c) IV 0.3696 36.96%
Estrogen receptor binding + 0.8264 82.64%
Androgen receptor binding + 0.7509 75.09%
Thyroid receptor binding + 0.5458 54.58%
Glucocorticoid receptor binding + 0.7479 74.79%
Aromatase binding + 0.7609 76.09%
PPAR gamma + 0.6598 65.98%
Honey bee toxicity - 0.7610 76.10%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9871 98.71%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.97% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.30% 95.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 91.97% 97.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.47% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.18% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.05% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.21% 99.23%
CHEMBL2581 P07339 Cathepsin D 87.60% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.34% 93.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.04% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.60% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.48% 89.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.90% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 84.54% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.84% 94.00%
CHEMBL5028 O14672 ADAM10 83.35% 97.50%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.29% 90.93%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.07% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.55% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.75% 100.00%
CHEMBL1902 P62942 FK506-binding protein 1A 80.75% 97.05%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.67% 94.45%
CHEMBL1871 P10275 Androgen Receptor 80.55% 96.43%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 80.51% 97.33%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.48% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.07% 95.71%

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.
Eriolarynx australis
Iochroma arborescens

Cross-Links

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PubChem 5315458
NPASS NPC226419
LOTUS LTS0194994
wikiData Q105253213