(Z)-Tagetenone

Details

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Internal ID 4139c076-dafa-4fd0-9694-d56da93044c3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (5Z)-2,6-dimethylocta-2,5,7-trien-4-one
SMILES (Canonical) CC(=CC(=O)C=C(C)C=C)C
SMILES (Isomeric) CC(=CC(=O)/C=C(/C)\C=C)C
InChI InChI=1S/C10H14O/c1-5-9(4)7-10(11)6-8(2)3/h5-7H,1H2,2-4H3/b9-7-
InChI Key XUINKEIPBTYUJP-CLFYSBASSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.65
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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cis-Ocimenone
(Z)-Ocimenone
cis-Tagetenone
SCHEMBL2133992
XUINKEIPBTYUJP-CLFYSBASSA-N
DTXSID001317682
33746-71-3
(z)-2,6-dimethylocta-2,5,7-trien-4-one
Q67880201

2D Structure

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2D Structure of (Z)-Tagetenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.8813 88.13%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4677 46.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9521 95.21%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8511 85.11%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.9711 97.11%
CYP3A4 substrate - 0.6350 63.50%
CYP2C9 substrate - 0.7786 77.86%
CYP2D6 substrate - 0.8821 88.21%
CYP3A4 inhibition - 0.9163 91.63%
CYP2C9 inhibition - 0.8968 89.68%
CYP2C19 inhibition - 0.7842 78.42%
CYP2D6 inhibition - 0.9402 94.02%
CYP1A2 inhibition - 0.8133 81.33%
CYP2C8 inhibition - 0.9869 98.69%
CYP inhibitory promiscuity - 0.6830 68.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6083 60.83%
Carcinogenicity (trinary) Non-required 0.5743 57.43%
Eye corrosion + 0.9633 96.33%
Eye irritation + 0.9915 99.15%
Skin irritation + 0.8343 83.43%
Skin corrosion - 0.6298 62.98%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7499 74.99%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.9372 93.72%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.6658 66.58%
Acute Oral Toxicity (c) II 0.4730 47.30%
Estrogen receptor binding - 0.9535 95.35%
Androgen receptor binding - 0.8111 81.11%
Thyroid receptor binding - 0.8201 82.01%
Glucocorticoid receptor binding - 0.7091 70.91%
Aromatase binding - 0.8116 81.16%
PPAR gamma - 0.8640 86.40%
Honey bee toxicity - 0.8235 82.35%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity + 0.7818 78.18%

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 87.00% 96.09%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 84.00% 82.05%
CHEMBL4040 P28482 MAP kinase ERK2 82.82% 83.82%
CHEMBL340 P08684 Cytochrome P450 3A4 81.96% 91.19%
CHEMBL2581 P07339 Cathepsin D 80.50% 98.95%

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.
Cantinoa mutabilis
Daucus carota
Lippia javanica
Seriphidium herba-alba
Tagetes minuta

Cross-Links

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PubChem 6428432
LOTUS LTS0060931
wikiData Q67880201