3-(2-Hydroperoxypropan-2-yl)-4a,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-one

Details

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Internal ID e80d4938-dadd-4e48-a0e9-aeb245e13401
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name 3-(2-hydroperoxypropan-2-yl)-4a,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O3/c1-10-6-5-7-11-8-13(16)12(9-15(10,11)4)14(2,3)18-17/h8-10,17H,5-7H2,1-4H3
InChI Key ZNFUKMGHJDXGCN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O3
Molecular Weight 250.33 g/mol
Exact Mass 250.15689456 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.52
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 3-(2-Hydroperoxypropan-2-yl)-4a,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.8613 86.13%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6611 66.11%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9181 91.81%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8247 82.47%
P-glycoprotein inhibitior - 0.9224 92.24%
P-glycoprotein substrate - 0.8570 85.70%
CYP3A4 substrate + 0.6021 60.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8736 87.36%
CYP3A4 inhibition - 0.8631 86.31%
CYP2C9 inhibition - 0.6365 63.65%
CYP2C19 inhibition - 0.6486 64.86%
CYP2D6 inhibition - 0.9148 91.48%
CYP1A2 inhibition - 0.6451 64.51%
CYP2C8 inhibition - 0.7757 77.57%
CYP inhibitory promiscuity - 0.7353 73.53%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8143 81.43%
Carcinogenicity (trinary) Non-required 0.4824 48.24%
Eye corrosion - 0.9805 98.05%
Eye irritation - 0.7448 74.48%
Skin irritation - 0.5346 53.46%
Skin corrosion - 0.9312 93.12%
Ames mutagenesis + 0.6029 60.29%
Human Ether-a-go-go-Related Gene inhibition - 0.6423 64.23%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.6448 64.48%
skin sensitisation - 0.5396 53.96%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.4691 46.91%
Acute Oral Toxicity (c) III 0.6456 64.56%
Estrogen receptor binding + 0.5662 56.62%
Androgen receptor binding + 0.5953 59.53%
Thyroid receptor binding + 0.7396 73.96%
Glucocorticoid receptor binding - 0.5218 52.18%
Aromatase binding - 0.5740 57.40%
PPAR gamma - 0.7098 70.98%
Honey bee toxicity - 0.9288 92.88%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9929 99.29%

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 99.03% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.95% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.42% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.14% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.05% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.42% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.59% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.35% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.46% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.79% 93.04%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.58% 92.94%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.54% 93.03%
CHEMBL1902 P62942 FK506-binding protein 1A 83.63% 97.05%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.60% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.29% 91.07%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.22% 82.69%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.99% 96.77%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.50% 97.14%

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.
Senecio reicheanus

Cross-Links

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PubChem 14830798
LOTUS LTS0036876
wikiData Q105380040