alpha-Alasken-8-one

Details

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Internal ID 98934adf-9b5b-4fd0-a6f7-b7a15ddde921
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones
IUPAC Name (1R,5S)-1,8-dimethyl-4-propan-2-ylidenespiro[4.5]dec-8-en-3-one
SMILES (Canonical) CC1CC(=O)C(=C(C)C)C12CCC(=CC2)C
SMILES (Isomeric) C[C@@H]1CC(=O)C(=C(C)C)[C@]12CCC(=CC2)C
InChI InChI=1S/C15H22O/c1-10(2)14-13(16)9-12(4)15(14)7-5-11(3)6-8-15/h5,12H,6-9H2,1-4H3/t12-,15-/m1/s1
InChI Key ZZDZYXINURVBJN-IUODEOHRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.05
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of alpha-Alasken-8-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.9481 94.81%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.4975 49.75%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.9290 92.90%
OATP1B3 inhibitior + 0.9090 90.90%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7036 70.36%
P-glycoprotein inhibitior - 0.9511 95.11%
P-glycoprotein substrate - 0.8518 85.18%
CYP3A4 substrate + 0.5091 50.91%
CYP2C9 substrate - 0.8116 81.16%
CYP2D6 substrate - 0.8716 87.16%
CYP3A4 inhibition - 0.9265 92.65%
CYP2C9 inhibition - 0.9270 92.70%
CYP2C19 inhibition - 0.8389 83.89%
CYP2D6 inhibition - 0.9632 96.32%
CYP1A2 inhibition - 0.8567 85.67%
CYP2C8 inhibition - 0.9554 95.54%
CYP inhibitory promiscuity - 0.8929 89.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.4869 48.69%
Eye corrosion - 0.9561 95.61%
Eye irritation + 0.7552 75.52%
Skin irritation + 0.8425 84.25%
Skin corrosion - 0.9835 98.35%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7090 70.90%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6391 63.91%
skin sensitisation + 0.9105 91.05%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.5806 58.06%
Acute Oral Toxicity (c) III 0.5180 51.80%
Estrogen receptor binding - 0.9815 98.15%
Androgen receptor binding - 0.7584 75.84%
Thyroid receptor binding - 0.6129 61.29%
Glucocorticoid receptor binding - 0.8336 83.36%
Aromatase binding - 0.8173 81.73%
PPAR gamma - 0.6327 63.27%
Honey bee toxicity - 0.8462 84.62%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9810 98.10%

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 94.15% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.67% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.47% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.25% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.64% 97.25%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.32% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.32% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.77% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.09% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.55% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.31% 90.71%

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.
Calypogeia fissa
Nekemias grossedentata

Cross-Links

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PubChem 15894374
NPASS NPC11148
LOTUS LTS0171591
wikiData Q105386716