beta-Chenopodiol-6-acetate

Details

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Internal ID 52fb08cf-89dc-4049-8829-85b241764998
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name [(1R,2R,4aR,8aS)-2-(2-hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H28O3/c1-11-7-6-9-17(5)10-8-13(16(3,4)19)15(14(11)17)20-12(2)18/h13-15,19H,1,6-10H2,2-5H3/t13-,14-,15+,17-/m1/s1
InChI Key QIVOSAOEZNYGQW-PNBKFKSVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H28O3
Molecular Weight 280.40 g/mol
Exact Mass 280.20384475 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.46
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of beta-Chenopodiol-6-acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.6805 68.05%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8061 80.61%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.8833 88.33%
OATP1B3 inhibitior - 0.2566 25.66%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9483 94.83%
P-glycoprotein inhibitior - 0.8341 83.41%
P-glycoprotein substrate - 0.9150 91.50%
CYP3A4 substrate + 0.6142 61.42%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate - 0.8744 87.44%
CYP3A4 inhibition - 0.7570 75.70%
CYP2C9 inhibition + 0.5432 54.32%
CYP2C19 inhibition + 0.5487 54.87%
CYP2D6 inhibition - 0.9470 94.70%
CYP1A2 inhibition - 0.6278 62.78%
CYP2C8 inhibition - 0.7032 70.32%
CYP inhibitory promiscuity - 0.8499 84.99%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Non-required 0.5329 53.29%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.6532 65.32%
Skin irritation + 0.5407 54.07%
Skin corrosion - 0.9668 96.68%
Ames mutagenesis - 0.7723 77.23%
Human Ether-a-go-go-Related Gene inhibition - 0.7232 72.32%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.5464 54.64%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7186 71.86%
Acute Oral Toxicity (c) III 0.5888 58.88%
Estrogen receptor binding + 0.6624 66.24%
Androgen receptor binding - 0.5411 54.11%
Thyroid receptor binding + 0.5193 51.93%
Glucocorticoid receptor binding + 0.6713 67.13%
Aromatase binding - 0.7090 70.90%
PPAR gamma - 0.6625 66.25%
Honey bee toxicity - 0.8286 82.86%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 1.0000 100.00%

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 96.75% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.86% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.01% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.73% 94.45%
CHEMBL2581 P07339 Cathepsin D 88.00% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.99% 93.04%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.87% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.84% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.73% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 83.11% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.96% 97.09%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.21% 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.
Dysphania botrys

Cross-Links

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PubChem 162931109
LOTUS LTS0242163
wikiData Q105222424