beta-Triticene

Details

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Internal ID 191f3ec5-d991-4bad-939b-9922a947358c
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (2Z,4E)-pentadeca-2,4-dienal
SMILES (Canonical) CCCCCCCCCCC=CC=CC=O
SMILES (Isomeric) CCCCCCCCCC/C=C/C=C\C=O
InChI InChI=1S/C15H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h11-15H,2-10H2,1H3/b12-11+,14-13-
InChI Key WJGSBYJVUWVJLB-WCYNZMGESA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 6.00
Atomic LogP (AlogP) 4.83
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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(2E,4Z)-2,4-Pentadecadienal
b-Triticene
CHEBI:172313
(2Z,4E)-pentadeca-2,4-dienal

2D Structure

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2D Structure of beta-Triticene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.9295 92.95%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Plasma membrane 0.5260 52.60%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.8399 83.99%
OATP1B3 inhibitior + 0.9016 90.16%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6892 68.92%
P-glycoprotein inhibitior - 0.9001 90.01%
P-glycoprotein substrate - 0.9338 93.38%
CYP3A4 substrate - 0.6245 62.45%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8597 85.97%
CYP3A4 inhibition - 0.9911 99.11%
CYP2C9 inhibition - 0.9285 92.85%
CYP2C19 inhibition - 0.9519 95.19%
CYP2D6 inhibition - 0.9653 96.53%
CYP1A2 inhibition + 0.7244 72.44%
CYP2C8 inhibition - 0.9204 92.04%
CYP inhibitory promiscuity - 0.7617 76.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6467 64.67%
Eye corrosion + 0.9927 99.27%
Eye irritation + 0.9830 98.30%
Skin irritation + 0.9187 91.87%
Skin corrosion - 0.8516 85.16%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3798 37.98%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5701 57.01%
skin sensitisation + 0.9648 96.48%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.9954 99.54%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.6381 63.81%
Acute Oral Toxicity (c) III 0.8135 81.35%
Estrogen receptor binding - 0.7082 70.82%
Androgen receptor binding + 0.5681 56.81%
Thyroid receptor binding + 0.7864 78.64%
Glucocorticoid receptor binding - 0.6804 68.04%
Aromatase binding - 0.6319 63.19%
PPAR gamma + 0.6790 67.90%
Honey bee toxicity - 0.9804 98.04%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.9053 90.53%
Fish aquatic toxicity + 0.9804 98.04%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.99% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 94.12% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.50% 92.86%
CHEMBL2581 P07339 Cathepsin D 92.26% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.38% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.80% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.41% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.53% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.79% 91.81%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.38% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 81.81% 94.73%
CHEMBL1781 P11387 DNA topoisomerase I 81.71% 97.00%

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.
Triticum aestivum

Cross-Links

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PubChem 131751101
LOTUS LTS0045766
wikiData Q105306770