9,12,15-Octadecatrienal

Details

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Internal ID 2cef1a93-4f07-442b-b5cd-a3a7b5dddeef
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (9E,12E,15E)-octadeca-9,12,15-trienal
SMILES (Canonical) CCC=CCC=CCC=CCCCCCCCC=O
SMILES (Isomeric) CC/C=C/C/C=C/C/C=C/CCCCCCCC=O
InChI InChI=1S/C18H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h3-4,6-7,9-10,18H,2,5,8,11-17H2,1H3/b4-3+,7-6+,10-9+
InChI Key TUCMDDWTBVMRTP-IUQGRGSQSA-N
Popularity 5 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) 5.77
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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(9E,12E,15E)-octadeca-9,12,15-trienal
26537-71-3
TEAL
LMFA06000102
SCHEMBL910331
DTXSID00880768
CHEBI:183591
TUCMDDWTBVMRTP-IUQGRGSQSA-N
(9E,12E,15E)-9,12,15-Octadecatrienal #

2D Structure

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2D Structure of 9,12,15-Octadecatrienal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.8320 83.20%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Plasma membrane 0.5982 59.82%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.7350 73.50%
OATP1B3 inhibitior + 0.9203 92.03%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.5645 56.45%
P-glycoprotein inhibitior - 0.7734 77.34%
P-glycoprotein substrate - 0.9044 90.44%
CYP3A4 substrate - 0.6248 62.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7983 79.83%
CYP3A4 inhibition - 0.9802 98.02%
CYP2C9 inhibition - 0.9199 91.99%
CYP2C19 inhibition - 0.9561 95.61%
CYP2D6 inhibition - 0.9697 96.97%
CYP1A2 inhibition + 0.6011 60.11%
CYP2C8 inhibition - 0.9517 95.17%
CYP inhibitory promiscuity - 0.7659 76.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.6407 64.07%
Eye corrosion + 0.9914 99.14%
Eye irritation + 0.9267 92.67%
Skin irritation + 0.7884 78.84%
Skin corrosion - 0.9675 96.75%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7545 75.45%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6967 69.67%
skin sensitisation + 0.9334 93.34%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.9288 92.88%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.6396 63.96%
Acute Oral Toxicity (c) III 0.8647 86.47%
Estrogen receptor binding + 0.5946 59.46%
Androgen receptor binding - 0.8108 81.08%
Thyroid receptor binding + 0.7199 71.99%
Glucocorticoid receptor binding - 0.6433 64.33%
Aromatase binding - 0.5643 56.43%
PPAR gamma + 0.7552 75.52%
Honey bee toxicity - 0.9700 97.00%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.7821 78.21%

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
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 94.35% 90.75%
CHEMBL2581 P07339 Cathepsin D 91.26% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.87% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.72% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.22% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 81.86% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.85% 96.00%
CHEMBL1781 P11387 DNA topoisomerase I 81.25% 97.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.11% 89.34%
CHEMBL2664 P23526 Adenosylhomocysteinase 80.48% 86.67%

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.
Artemisia capillaris
Mentha arvensis
Mentha canadensis
Zingiber officinale

Cross-Links

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PubChem 5283384
NPASS NPC189331