Bisabol-1-one

Details

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Internal ID b4506610-6615-4da5-bd98-ba861dc58109
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 5-methyl-2-(6-methylheptan-2-yl)cyclohexan-1-one
SMILES (Canonical) CC1CCC(C(=O)C1)C(C)CCCC(C)C
SMILES (Isomeric) CC1CCC(C(=O)C1)C(C)CCCC(C)C
InChI InChI=1S/C15H28O/c1-11(2)6-5-7-13(4)14-9-8-12(3)10-15(14)16/h11-14H,5-10H2,1-4H3
InChI Key KCRFTEABMBVXDT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28O
Molecular Weight 224.38 g/mol
Exact Mass 224.214015512 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.45
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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KCRFTEABMBVXDT-UHFFFAOYSA-N

2D Structure

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2D Structure of Bisabol-1-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 + 0.5695 56.95%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.7462 74.62%
OATP2B1 inhibitior - 0.8471 84.71%
OATP1B1 inhibitior + 0.9647 96.47%
OATP1B3 inhibitior + 0.9468 94.68%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7472 74.72%
P-glycoprotein inhibitior - 0.9254 92.54%
P-glycoprotein substrate - 0.5220 52.20%
CYP3A4 substrate - 0.5350 53.50%
CYP2C9 substrate - 0.6168 61.68%
CYP2D6 substrate - 0.7682 76.82%
CYP3A4 inhibition - 0.9626 96.26%
CYP2C9 inhibition - 0.8942 89.42%
CYP2C19 inhibition - 0.9385 93.85%
CYP2D6 inhibition - 0.9390 93.90%
CYP1A2 inhibition - 0.7078 70.78%
CYP2C8 inhibition - 0.9847 98.47%
CYP inhibitory promiscuity - 0.9374 93.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.7299 72.99%
Eye corrosion + 0.6681 66.81%
Eye irritation + 0.7800 78.00%
Skin irritation + 0.7436 74.36%
Skin corrosion - 0.8298 82.98%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7218 72.18%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation + 0.9505 95.05%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6084 60.84%
Acute Oral Toxicity (c) III 0.8966 89.66%
Estrogen receptor binding - 0.7792 77.92%
Androgen receptor binding - 0.5806 58.06%
Thyroid receptor binding - 0.7776 77.76%
Glucocorticoid receptor binding - 0.7142 71.42%
Aromatase binding - 0.6231 62.31%
PPAR gamma - 0.9063 90.63%
Honey bee toxicity - 0.9399 93.99%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9351 93.51%

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
CHEMBL2581 P07339 Cathepsin D 97.56% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.10% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.07% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.52% 90.71%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.28% 94.80%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.92% 93.56%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 86.67% 96.47%
CHEMBL1907 P15144 Aminopeptidase N 86.01% 93.31%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.70% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.29% 86.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.95% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.58% 91.11%
CHEMBL4588 P22894 Matrix metalloproteinase 8 81.83% 94.66%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 80.54% 98.33%

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.
Ozothamnus ledifolius

Cross-Links

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PubChem 91750162
LOTUS LTS0213584
wikiData Q105138902