2-Cyclohexen-1-one, 4-hydroxy-3-methyl-6-(1-methylethyl)-

Details

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Internal ID ee6e55c0-65e9-4f98-818b-d21640ac6f8d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name 4-hydroxy-3-methyl-6-propan-2-ylcyclohex-2-en-1-one
SMILES (Canonical) CC1=CC(=O)C(CC1O)C(C)C
SMILES (Isomeric) CC1=CC(=O)C(CC1O)C(C)C
InChI InChI=1S/C10H16O2/c1-6(2)8-5-9(11)7(3)4-10(8)12/h4,6,8-9,11H,5H2,1-3H3
InChI Key HEJGMQATUPGCRD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H16O2
Molecular Weight 168.23 g/mol
Exact Mass 168.115029749 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.54
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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141978-04-3
4-Hydroxy-6-isopropyl-3-methyl-2-cyclohexen-1-one
DTXSID30340744

2D Structure

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2D Structure of 2-Cyclohexen-1-one, 4-hydroxy-3-methyl-6-(1-methylethyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7248 72.48%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.7883 78.83%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9655 96.55%
OATP1B3 inhibitior + 0.9697 96.97%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9692 96.92%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.8400 84.00%
CYP3A4 substrate - 0.6229 62.29%
CYP2C9 substrate - 0.7735 77.35%
CYP2D6 substrate - 0.8566 85.66%
CYP3A4 inhibition - 0.8888 88.88%
CYP2C9 inhibition - 0.9560 95.60%
CYP2C19 inhibition - 0.8405 84.05%
CYP2D6 inhibition - 0.8993 89.93%
CYP1A2 inhibition - 0.8683 86.83%
CYP2C8 inhibition - 0.9967 99.67%
CYP inhibitory promiscuity - 0.8713 87.13%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.6768 67.68%
Carcinogenicity (trinary) Non-required 0.7171 71.71%
Eye corrosion - 0.8344 83.44%
Eye irritation + 0.7601 76.01%
Skin irritation + 0.7674 76.74%
Skin corrosion - 0.8763 87.63%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7045 70.45%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6533 65.33%
skin sensitisation + 0.8759 87.59%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.7819 78.19%
Acute Oral Toxicity (c) III 0.7637 76.37%
Estrogen receptor binding - 0.9293 92.93%
Androgen receptor binding - 0.8085 80.85%
Thyroid receptor binding - 0.8171 81.71%
Glucocorticoid receptor binding - 0.7710 77.10%
Aromatase binding - 0.9492 94.92%
PPAR gamma - 0.8845 88.45%
Honey bee toxicity - 0.9292 92.92%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.7898 78.98%

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 93.08% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.79% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.42% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.46% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.23% 97.25%
CHEMBL4208 P20618 Proteasome component C5 80.96% 90.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.25% 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.
Chrysactinia mexicana
Foeniculum vulgare

Cross-Links

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PubChem 566981
LOTUS LTS0163918
wikiData Q82110543