(6S)-2,6-dimethylocta-1,7-dien-3-one

Details

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Internal ID 3855d3c7-a290-4c40-8c3d-6f796d066940
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Alpha-branched alpha,beta-unsaturated ketones
IUPAC Name (6S)-2,6-dimethylocta-1,7-dien-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O/c1-5-9(4)6-7-10(11)8(2)3/h5,9H,1-2,6-7H2,3-4H3/t9-/m1/s1
InChI Key VVGFGPNQFFVNKV-SECBINFHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6S)-2,6-dimethylocta-1,7-dien-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.7236 72.36%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Nucleus 0.3810 38.10%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9438 94.38%
OATP1B3 inhibitior + 0.9241 92.41%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8224 82.24%
P-glycoprotein inhibitior - 0.9776 97.76%
P-glycoprotein substrate - 0.9524 95.24%
CYP3A4 substrate - 0.6647 66.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8251 82.51%
CYP3A4 inhibition - 0.9433 94.33%
CYP2C9 inhibition - 0.9476 94.76%
CYP2C19 inhibition - 0.8846 88.46%
CYP2D6 inhibition - 0.9464 94.64%
CYP1A2 inhibition - 0.5174 51.74%
CYP2C8 inhibition - 0.9909 99.09%
CYP inhibitory promiscuity - 0.7724 77.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.6176 61.76%
Eye corrosion + 0.8108 81.08%
Eye irritation + 0.9629 96.29%
Skin irritation + 0.8427 84.27%
Skin corrosion - 0.8631 86.31%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7319 73.19%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.9269 92.69%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5617 56.17%
Acute Oral Toxicity (c) III 0.7464 74.64%
Estrogen receptor binding - 0.9689 96.89%
Androgen receptor binding - 0.8916 89.16%
Thyroid receptor binding - 0.8900 89.00%
Glucocorticoid receptor binding - 0.8087 80.87%
Aromatase binding - 0.8967 89.67%
PPAR gamma - 0.7201 72.01%
Honey bee toxicity - 0.8967 89.67%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.7660 76.60%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.61% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.79% 99.17%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 84.64% 98.75%
CHEMBL2581 P07339 Cathepsin D 84.34% 98.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.90% 94.33%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.55% 91.24%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.06% 89.34%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.65% 96.47%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.12% 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.
Tagetes minuta

Cross-Links

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PubChem 101678764
LOTUS LTS0270331
wikiData Q105297651