(1S,2S,3'S,4S,4'R,6S,7S,8S,9R,10S,13S,14R)-7-hydroxy-3',4',8,10,14-pentamethylspiro[5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicosa-15,18-diene-6,5'-oxolane]-2',17-dione

Details

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Internal ID 8e69a017-601a-44be-ba7e-4ad3fa0cd77a
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroid lactones > Withanolides and derivatives
IUPAC Name (1S,2S,3'S,4S,4'R,6S,7S,8S,9R,10S,13S,14R)-7-hydroxy-3',4',8,10,14-pentamethylspiro[5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicosa-15,18-diene-6,5'-oxolane]-2',17-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H38O5/c1-14-16(3)28(33-25(14)31)24(30)15(2)23-22(32-28)13-21-19-7-6-17-12-18(29)8-10-26(17,4)20(19)9-11-27(21,23)5/h8,10,12,14-16,19-24,30H,6-7,9,11,13H2,1-5H3/t14-,15-,16+,19+,20-,21-,22-,23-,24-,26-,27-,28-/m0/s1
InChI Key JJXDFSOHRJHKGE-SEXHSVSSSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C28H38O5
Molecular Weight 454.60 g/mol
Exact Mass 454.27192431 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.44
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,2S,3'S,4S,4'R,6S,7S,8S,9R,10S,13S,14R)-7-hydroxy-3',4',8,10,14-pentamethylspiro[5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicosa-15,18-diene-6,5'-oxolane]-2',17-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9837 98.37%
Caco-2 - 0.6459 64.59%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7971 79.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8463 84.63%
OATP1B3 inhibitior + 0.9284 92.84%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5271 52.71%
BSEP inhibitior + 0.9078 90.78%
P-glycoprotein inhibitior - 0.4384 43.84%
P-glycoprotein substrate - 0.5858 58.58%
CYP3A4 substrate + 0.7671 76.71%
CYP2C9 substrate - 0.8178 81.78%
CYP2D6 substrate - 0.8875 88.75%
CYP3A4 inhibition - 0.7742 77.42%
CYP2C9 inhibition - 0.9556 95.56%
CYP2C19 inhibition - 0.9725 97.25%
CYP2D6 inhibition - 0.9603 96.03%
CYP1A2 inhibition - 0.6527 65.27%
CYP2C8 inhibition + 0.6117 61.17%
CYP inhibitory promiscuity - 0.9708 97.08%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.4139 41.39%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9693 96.93%
Skin irritation + 0.6485 64.85%
Skin corrosion - 0.8415 84.15%
Ames mutagenesis - 0.8470 84.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6500 65.00%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8395 83.95%
Respiratory toxicity + 0.9444 94.44%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.8089 80.89%
Acute Oral Toxicity (c) III 0.4064 40.64%
Estrogen receptor binding + 0.8064 80.64%
Androgen receptor binding + 0.8285 82.85%
Thyroid receptor binding + 0.6515 65.15%
Glucocorticoid receptor binding + 0.7643 76.43%
Aromatase binding + 0.7225 72.25%
PPAR gamma + 0.5378 53.78%
Honey bee toxicity - 0.6391 63.91%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9835 98.35%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.61% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 96.51% 100.00%
CHEMBL1871 P10275 Androgen Receptor 96.12% 96.43%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.46% 91.11%
CHEMBL218 P21554 Cannabinoid CB1 receptor 93.48% 96.61%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.09% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 90.68% 95.93%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.51% 89.00%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 88.84% 89.05%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.81% 97.09%
CHEMBL332 P03956 Matrix metalloproteinase-1 85.77% 94.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.69% 92.94%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.90% 97.25%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 84.89% 97.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.70% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.99% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.16% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.73% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.59% 95.89%
CHEMBL2581 P07339 Cathepsin D 80.37% 98.95%

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.
There are no matching plants.

Cross-Links

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PubChem 73356967
LOTUS LTS0179225
wikiData Q105130029