2-Tetradeca-5,12-dien-8,10-diynyloctadeca-2,9,16-trien-12,14-diynal

Details

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Internal ID 6a99c075-69e0-4bef-8c20-a11ffaaf7187
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name 2-tetradeca-5,12-dien-8,10-diynyloctadeca-2,9,16-trien-12,14-diynal
SMILES (Canonical) CC=CC#CC#CCC=CCCCCCC=C(CCCCC=CCC#CC#CC=CC)C=O
SMILES (Isomeric) CC=CC#CC#CCC=CCCCCCC=C(CCCCC=CCC#CC#CC=CC)C=O
InChI InChI=1S/C32H38O/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32(31-33)29-27-25-23-21-19-16-14-12-10-8-6-4-2/h3-6,17-19,21,30-31H,15-16,20,22-29H2,1-2H3
InChI Key IYHLMHGYSZIORH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H38O
Molecular Weight 438.60 g/mol
Exact Mass 438.292265831 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 9.60
Atomic LogP (AlogP) 7.68
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Tetradeca-5,12-dien-8,10-diynyloctadeca-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 + 0.9899 98.99%
Caco-2 - 0.7664 76.64%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.4199 41.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7746 77.46%
OATP1B3 inhibitior + 0.9462 94.62%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8203 82.03%
P-glycoprotein inhibitior + 0.7116 71.16%
P-glycoprotein substrate - 0.7665 76.65%
CYP3A4 substrate + 0.5352 53.52%
CYP2C9 substrate - 0.7984 79.84%
CYP2D6 substrate - 0.8360 83.60%
CYP3A4 inhibition - 0.9317 93.17%
CYP2C9 inhibition - 0.8753 87.53%
CYP2C19 inhibition - 0.8988 89.88%
CYP2D6 inhibition - 0.9525 95.25%
CYP1A2 inhibition - 0.6361 63.61%
CYP2C8 inhibition - 0.6571 65.71%
CYP inhibitory promiscuity - 0.5471 54.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.5329 53.29%
Eye corrosion + 0.9229 92.29%
Eye irritation - 0.8514 85.14%
Skin irritation + 0.6853 68.53%
Skin corrosion - 0.8114 81.14%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8259 82.59%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.6039 60.39%
skin sensitisation + 0.9407 94.07%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.5365 53.65%
Acute Oral Toxicity (c) III 0.8931 89.31%
Estrogen receptor binding + 0.7026 70.26%
Androgen receptor binding - 0.6271 62.71%
Thyroid receptor binding + 0.6198 61.98%
Glucocorticoid receptor binding - 0.5875 58.75%
Aromatase binding - 0.4897 48.97%
PPAR gamma + 0.6464 64.64%
Honey bee toxicity - 0.9133 91.33%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6124 61.24%
Fish aquatic toxicity + 0.9133 91.33%

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 94.98% 99.17%
CHEMBL1829 O15379 Histone deacetylase 3 85.39% 95.00%
CHEMBL1951 P21397 Monoamine oxidase A 83.91% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 83.82% 94.73%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.55% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.06% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.57% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.31% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.68% 94.45%

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.
Centaurea macrocephala

Cross-Links

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PubChem 163005831
LOTUS LTS0140389
wikiData Q105122755