2,6-Dimethyloct-7-en-4-one

Details

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Internal ID 1a6ce1c2-407d-41c1-a4d4-60aadd7bf878
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name 2,6-dimethyloct-7-en-4-one
SMILES (Canonical) CC(C)CC(=O)CC(C)C=C
SMILES (Isomeric) CC(C)CC(=O)CC(C)C=C
InChI InChI=1S/C10H18O/c1-5-9(4)7-10(11)6-8(2)3/h5,8-9H,1,6-7H2,2-4H3
InChI Key VUSBHGLIAQXBSW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O
Molecular Weight 154.25 g/mol
Exact Mass 154.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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2,6-Dimethyloct-7-en-4-one
Dihydrotagetone
1879-00-1
7-Octen-4-one, 2,6-dimethyl-
EINECS 217-532-6
2,6-Dimethyl-7-octen-4-one
SCHEMBL6903513
DTXSID70883766
(+)-2,6-Dimethyl-7-octen-4-one
AKOS017341560
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,6-Dimethyloct-7-en-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.7268 72.68%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4179 41.79%
OATP2B1 inhibitior - 0.8605 86.05%
OATP1B1 inhibitior + 0.9354 93.54%
OATP1B3 inhibitior + 0.9401 94.01%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8371 83.71%
P-glycoprotein inhibitior - 0.9766 97.66%
P-glycoprotein substrate - 0.9741 97.41%
CYP3A4 substrate - 0.6795 67.95%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.7855 78.55%
CYP3A4 inhibition - 0.9011 90.11%
CYP2C9 inhibition - 0.9182 91.82%
CYP2C19 inhibition - 0.8681 86.81%
CYP2D6 inhibition - 0.9493 94.93%
CYP1A2 inhibition - 0.7043 70.43%
CYP2C8 inhibition - 0.9913 99.13%
CYP inhibitory promiscuity - 0.8342 83.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6483 64.83%
Carcinogenicity (trinary) Non-required 0.5793 57.93%
Eye corrosion + 0.9673 96.73%
Eye irritation + 0.9871 98.71%
Skin irritation + 0.7376 73.76%
Skin corrosion - 0.9337 93.37%
Ames mutagenesis - 0.8637 86.37%
Human Ether-a-go-go-Related Gene inhibition - 0.7625 76.25%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.9514 95.14%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5991 59.91%
Acute Oral Toxicity (c) III 0.5677 56.77%
Estrogen receptor binding - 0.9846 98.46%
Androgen receptor binding - 0.8875 88.75%
Thyroid receptor binding - 0.8776 87.76%
Glucocorticoid receptor binding - 0.8101 81.01%
Aromatase binding - 0.8526 85.26%
PPAR gamma - 0.9289 92.89%
Honey bee toxicity - 0.9067 90.67%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity + 0.6999 69.99%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.16% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.92% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.93% 98.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.63% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.46% 94.45%

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.
Elsholtzia ciliata
Mosla chinensis
Tagetes minuta

Cross-Links

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PubChem 102706
NPASS NPC139178
LOTUS LTS0191959
wikiData Q67879926