(17S,23S)-17,23-epoxy-3beta,7beta-dihydroxy-11,15-dioxo-5alpha-lanosta-8-en-26,23-olide

Details

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Internal ID ba5c9390-fc6a-4f9b-825c-50ddde5f29d8
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H42O7/c1-15-11-29(36-24(15)35)12-16(2)30(37-29)14-21(34)28(7)23-17(31)10-19-25(3,4)20(33)8-9-26(19,5)22(23)18(32)13-27(28,30)6/h15-17,19-20,31,33H,8-14H2,1-7H3/t15-,16+,17-,19-,20-,26-,27-,28-,29-,30-/m0/s1
InChI Key KGDKFJWOCHUNLY-ZVEHTUBCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H42O7
Molecular Weight 514.60 g/mol
Exact Mass 514.29305367 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (17S,23S)-17,23-epoxy-3beta,7beta-dihydroxy-11,15-dioxo-5alpha-lanosta-8-en-26,23-olide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 - 0.6318 63.18%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8400 84.00%
OATP2B1 inhibitior - 0.7159 71.59%
OATP1B1 inhibitior + 0.8692 86.92%
OATP1B3 inhibitior + 0.8486 84.86%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.5647 56.47%
BSEP inhibitior + 0.8380 83.80%
P-glycoprotein inhibitior + 0.6481 64.81%
P-glycoprotein substrate - 0.5553 55.53%
CYP3A4 substrate + 0.6763 67.63%
CYP2C9 substrate - 0.8007 80.07%
CYP2D6 substrate - 0.8822 88.22%
CYP3A4 inhibition - 0.6666 66.66%
CYP2C9 inhibition - 0.8745 87.45%
CYP2C19 inhibition - 0.9481 94.81%
CYP2D6 inhibition - 0.9645 96.45%
CYP1A2 inhibition - 0.8432 84.32%
CYP2C8 inhibition + 0.5087 50.87%
CYP inhibitory promiscuity - 0.9339 93.39%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Danger 0.4352 43.52%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9214 92.14%
Skin irritation + 0.6433 64.33%
Skin corrosion - 0.8962 89.62%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4855 48.55%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.6404 64.04%
skin sensitisation - 0.7626 76.26%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity + 0.6929 69.29%
Acute Oral Toxicity (c) I 0.6968 69.68%
Estrogen receptor binding + 0.7052 70.52%
Androgen receptor binding + 0.7377 73.77%
Thyroid receptor binding + 0.5985 59.85%
Glucocorticoid receptor binding + 0.8082 80.82%
Aromatase binding + 0.7696 76.96%
PPAR gamma + 0.6461 64.61%
Honey bee toxicity - 0.6956 69.56%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9944 99.44%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.09% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.79% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.62% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.53% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.40% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.58% 99.23%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 87.41% 88.84%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.48% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.00% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.98% 82.69%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.85% 86.00%
CHEMBL1937 Q92769 Histone deacetylase 2 84.96% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.50% 89.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 83.91% 85.30%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 83.59% 96.38%
CHEMBL259 P32245 Melanocortin receptor 4 82.96% 95.38%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.47% 93.04%
CHEMBL2996 Q05655 Protein kinase C delta 80.26% 97.79%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 146684144
LOTUS LTS0164319
wikiData Q105140700