4-Hydroxy-2-methyl-5-(6-methylhepta-1,5-dien-2-yl)cyclohex-2-en-1-one

Details

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Internal ID a55ddf45-eaa2-4357-86ad-6ef5c100d5bd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4-hydroxy-2-methyl-5-(6-methylhepta-1,5-dien-2-yl)cyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O2/c1-10(2)6-5-7-11(3)13-9-14(16)12(4)8-15(13)17/h6,8,13,15,17H,3,5,7,9H2,1-2,4H3
InChI Key OCULPYOOSGFLRB-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 3.20
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-2-methyl-5-(6-methylhepta-1,5-dien-2-yl)cyclohex-2-en-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 + 0.9955 99.55%
Caco-2 + 0.6486 64.86%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8571 85.71%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9159 91.59%
OATP1B3 inhibitior + 0.9138 91.38%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.8504 85.04%
P-glycoprotein inhibitior - 0.9179 91.79%
P-glycoprotein substrate - 0.8675 86.75%
CYP3A4 substrate - 0.5377 53.77%
CYP2C9 substrate - 0.7735 77.35%
CYP2D6 substrate - 0.8566 85.66%
CYP3A4 inhibition - 0.7103 71.03%
CYP2C9 inhibition - 0.8328 83.28%
CYP2C19 inhibition - 0.7743 77.43%
CYP2D6 inhibition - 0.8770 87.70%
CYP1A2 inhibition - 0.7883 78.83%
CYP2C8 inhibition - 0.9424 94.24%
CYP inhibitory promiscuity - 0.7723 77.23%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8628 86.28%
Carcinogenicity (trinary) Non-required 0.7056 70.56%
Eye corrosion - 0.9155 91.55%
Eye irritation - 0.5819 58.19%
Skin irritation + 0.5289 52.89%
Skin corrosion - 0.9664 96.64%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4648 46.48%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.7582 75.82%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5797 57.97%
Acute Oral Toxicity (c) III 0.7747 77.47%
Estrogen receptor binding - 0.8024 80.24%
Androgen receptor binding - 0.7778 77.78%
Thyroid receptor binding - 0.6709 67.09%
Glucocorticoid receptor binding - 0.6038 60.38%
Aromatase binding - 0.8580 85.80%
PPAR gamma - 0.6532 65.32%
Honey bee toxicity - 0.7787 77.87%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9821 98.21%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.30% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.08% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.80% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.13% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 83.15% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.90% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.05% 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.
Cryptomeria japonica

Cross-Links

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PubChem 75953544
LOTUS LTS0178633
wikiData Q105189587