8-Hydroxy-2,6,9,9-tetramethylcycloundeca-2,6,10-trien-1-one

Details

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Internal ID e9f1c436-60e7-4ecd-a9f5-30053a67af72
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 8-hydroxy-2,6,9,9-tetramethylcycloundeca-2,6,10-trien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-11-6-5-7-12(2)13(16)8-9-15(3,4)14(17)10-11/h7-10,14,17H,5-6H2,1-4H3
InChI Key PXEHDVGCVODKBI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O2
Molecular Weight 234.33 g/mol
Exact Mass 234.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 2
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 8-Hydroxy-2,6,9,9-tetramethylcycloundeca-2,6,10-trien-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 + 0.9953 99.53%
Caco-2 + 0.9358 93.58%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5811 58.11%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.9575 95.75%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.7112 71.12%
P-glycoprotein inhibitior - 0.9436 94.36%
P-glycoprotein substrate - 0.9173 91.73%
CYP3A4 substrate + 0.5485 54.85%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.8720 87.20%
CYP3A4 inhibition - 0.8198 81.98%
CYP2C9 inhibition - 0.8085 80.85%
CYP2C19 inhibition - 0.7497 74.97%
CYP2D6 inhibition - 0.8657 86.57%
CYP1A2 inhibition - 0.5851 58.51%
CYP2C8 inhibition - 0.9270 92.70%
CYP inhibitory promiscuity - 0.7638 76.38%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8428 84.28%
Carcinogenicity (trinary) Non-required 0.5771 57.71%
Eye corrosion - 0.9383 93.83%
Eye irritation + 0.5581 55.81%
Skin irritation + 0.7890 78.90%
Skin corrosion - 0.8716 87.16%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5308 53.08%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.8072 80.72%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.6547 65.47%
Acute Oral Toxicity (c) III 0.8319 83.19%
Estrogen receptor binding - 0.8038 80.38%
Androgen receptor binding - 0.7758 77.58%
Thyroid receptor binding - 0.6930 69.30%
Glucocorticoid receptor binding - 0.6471 64.71%
Aromatase binding - 0.5597 55.97%
PPAR gamma - 0.6043 60.43%
Honey bee toxicity - 0.9213 92.13%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9125 91.25%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.07% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.35% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.48% 91.11%
CHEMBL4208 P20618 Proteasome component C5 87.04% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.77% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.54% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.70% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.31% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.81% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 73238363
LOTUS LTS0046736
wikiData Q104195506