Octadeca-2,9,16-trien-12,14-diynal

Details

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Internal ID 4a8c9ae2-d987-4ca0-9910-24e0c3c6b9d9
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name octadeca-2,9,16-trien-12,14-diynal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h2-3,9-10,16-18H,8,11-15H2,1H3
InChI Key NOWARHAZBDFDNT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H22O
Molecular Weight 254.40 g/mol
Exact Mass 254.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.22
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Octadeca-2,9,16-trien-12,14-diynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.5976 59.76%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Plasma membrane 0.4527 45.27%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.8011 80.11%
OATP1B3 inhibitior + 0.9444 94.44%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7034 70.34%
P-glycoprotein inhibitior - 0.8159 81.59%
P-glycoprotein substrate - 0.8062 80.62%
CYP3A4 substrate + 0.5163 51.63%
CYP2C9 substrate - 0.8021 80.21%
CYP2D6 substrate - 0.8588 85.88%
CYP3A4 inhibition - 0.9688 96.88%
CYP2C9 inhibition - 0.8451 84.51%
CYP2C19 inhibition - 0.9201 92.01%
CYP2D6 inhibition - 0.9743 97.43%
CYP1A2 inhibition + 0.5072 50.72%
CYP2C8 inhibition - 0.7803 78.03%
CYP inhibitory promiscuity - 0.6795 67.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.5036 50.36%
Eye corrosion + 0.9925 99.25%
Eye irritation - 0.5563 55.63%
Skin irritation + 0.7646 76.46%
Skin corrosion - 0.7589 75.89%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3763 37.63%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5967 59.67%
skin sensitisation + 0.9132 91.32%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.9065 90.65%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.6707 67.07%
Acute Oral Toxicity (c) III 0.8681 86.81%
Estrogen receptor binding + 0.6342 63.42%
Androgen receptor binding - 0.6015 60.15%
Thyroid receptor binding + 0.5831 58.31%
Glucocorticoid receptor binding - 0.6351 63.51%
Aromatase binding + 0.5896 58.96%
PPAR gamma + 0.7302 73.02%
Honey bee toxicity - 0.8862 88.62%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.7400 74.00%
Fish aquatic toxicity + 0.8543 85.43%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 89.28% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.12% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.89% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.81% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.01% 95.56%

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.
Senecio brevilorus

Cross-Links

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PubChem 163008195
LOTUS LTS0226574
wikiData Q105182842