2,6,10-Trimethyldodeca-2,6,9,11-tetraenal

Details

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Internal ID 996b3015-94a5-46e4-abe5-048dba380a1b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2,6,10-trimethyldodeca-2,6,9,11-tetraenal
SMILES (Canonical) CC(=CCC=C(C)C=C)CCC=C(C)C=O
SMILES (Isomeric) CC(=CCC=C(C)C=C)CCC=C(C)C=O
InChI InChI=1S/C15H22O/c1-5-13(2)8-6-9-14(3)10-7-11-15(4)12-16/h5,8-9,11-12H,1,6-7,10H2,2-4H3
InChI Key PFSTYGCNVAVZBK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.38
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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PFSTYGCNVAVZBK-UHFFFAOYSA-N
FT-0622201

2D Structure

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2D Structure of 2,6,10-Trimethyldodeca-2,6,9,11-tetraenal

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 + 0.8419 84.19%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Nucleus 0.3952 39.52%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.9051 90.51%
OATP1B3 inhibitior + 0.9117 91.17%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.7155 71.55%
P-glycoprotein inhibitior - 0.9396 93.96%
P-glycoprotein substrate - 0.9321 93.21%
CYP3A4 substrate - 0.5899 58.99%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8311 83.11%
CYP3A4 inhibition - 0.9621 96.21%
CYP2C9 inhibition - 0.9069 90.69%
CYP2C19 inhibition - 0.9090 90.90%
CYP2D6 inhibition - 0.9580 95.80%
CYP1A2 inhibition - 0.6252 62.52%
CYP2C8 inhibition - 0.9567 95.67%
CYP inhibitory promiscuity - 0.7753 77.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.5737 57.37%
Eye corrosion + 0.8158 81.58%
Eye irritation + 0.9151 91.51%
Skin irritation + 0.8359 83.59%
Skin corrosion - 0.9345 93.45%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5284 52.84%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5177 51.77%
skin sensitisation + 0.9156 91.56%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.5790 57.90%
Acute Oral Toxicity (c) III 0.8525 85.25%
Estrogen receptor binding - 0.8401 84.01%
Androgen receptor binding - 0.8780 87.80%
Thyroid receptor binding - 0.7348 73.48%
Glucocorticoid receptor binding + 0.6154 61.54%
Aromatase binding - 0.5830 58.30%
PPAR gamma + 0.6928 69.28%
Honey bee toxicity - 0.8626 86.26%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9902 99.02%

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
CHEMBL2581 P07339 Cathepsin D 91.03% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.65% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.18% 96.09%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.13% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.98% 95.56%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.49% 93.10%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.37% 91.11%

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.
Citrus × aurantium
Citrus maxima
Citrus trifoliata
Elsholtzia ciliata
Mosla chinensis

Cross-Links

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PubChem 21064
NPASS NPC53809