(5E,9R,10E)-6,12-dimethyl-9-propan-2-yltrideca-5,10,12-trien-2-one

Details

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Internal ID f4dbf64e-f3bd-4314-95f1-748ddca14bdc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (5E,9R,10E)-6,12-dimethyl-9-propan-2-yltrideca-5,10,12-trien-2-one
SMILES (Canonical) CC(C)C(CCC(=CCCC(=O)C)C)C=CC(=C)C
SMILES (Isomeric) CC(C)[C@@H](CC/C(=C/CCC(=O)C)/C)/C=C/C(=C)C
InChI InChI=1S/C18H30O/c1-14(2)10-12-18(15(3)4)13-11-16(5)8-7-9-17(6)19/h8,10,12,15,18H,1,7,9,11,13H2,2-6H3/b12-10+,16-8+/t18-/m1/s1
InChI Key HXPJEKSKJRYDGV-VZEKCIGISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H30O
Molecular Weight 262.40 g/mol
Exact Mass 262.229665576 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.49
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5E,9R,10E)-6,12-dimethyl-9-propan-2-yltrideca-5,10,12-trien-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 + 0.8898 88.98%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Nucleus 0.4086 40.86%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9344 93.44%
OATP1B3 inhibitior + 0.9096 90.96%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5148 51.48%
P-glycoprotein inhibitior - 0.8698 86.98%
P-glycoprotein substrate - 0.8172 81.72%
CYP3A4 substrate - 0.5160 51.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8213 82.13%
CYP3A4 inhibition - 0.9440 94.40%
CYP2C9 inhibition - 0.8869 88.69%
CYP2C19 inhibition - 0.8717 87.17%
CYP2D6 inhibition - 0.9589 95.89%
CYP1A2 inhibition - 0.5211 52.11%
CYP2C8 inhibition - 0.9400 94.00%
CYP inhibitory promiscuity - 0.7799 77.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.6013 60.13%
Eye corrosion + 0.6452 64.52%
Eye irritation - 0.7069 70.69%
Skin irritation + 0.7843 78.43%
Skin corrosion - 0.9688 96.88%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7427 74.27%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.9188 91.88%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6277 62.77%
Acute Oral Toxicity (c) III 0.8434 84.34%
Estrogen receptor binding - 0.8880 88.80%
Androgen receptor binding - 0.8901 89.01%
Thyroid receptor binding + 0.5444 54.44%
Glucocorticoid receptor binding - 0.6625 66.25%
Aromatase binding - 0.8593 85.93%
PPAR gamma - 0.4877 48.77%
Honey bee toxicity - 0.8171 81.71%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9654 96.54%

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 91.65% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.65% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.54% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.24% 89.34%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.90% 96.47%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.14% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 82.89% 94.73%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.88% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.12% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.89% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.84% 91.11%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.22% 82.05%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.13% 94.33%

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.
Nicotiana tabacum

Cross-Links

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PubChem 122361523
LOTUS LTS0024771
wikiData Q105035096