5,10-Pentadecadienal

Details

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Internal ID e7a5a6a0-f0bd-416d-993f-137867877a19
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (5E,10E)-pentadeca-5,10-dienal
SMILES (Canonical) CCCCC=CCCCC=CCCCC=O
SMILES (Isomeric) CCCC/C=C/CCC/C=C/CCCC=O
InChI InChI=1S/C15H26O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h5-6,10-11,15H,2-4,7-9,12-14H2,1H3/b6-5+,11-10+
InChI Key QVECBYWMAHQYNQ-RINXSNKBSA-N
Popularity 1 reference 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 4.60
Atomic LogP (AlogP) 4.83
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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5,10-Pentadecadienal, (Z,Z)-
(5Z,10Z)-5,10-Pentadecadienal
LMFA06000086
QVECBYWMAHQYNQ-RINXSNKBSA-N

2D Structure

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2D Structure of 5,10-Pentadecadienal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.8995 89.95%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Plasma membrane 0.6886 68.86%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.7729 77.29%
OATP1B3 inhibitior + 0.9089 90.89%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6128 61.28%
P-glycoprotein inhibitior - 0.9306 93.06%
P-glycoprotein substrate - 0.9037 90.37%
CYP3A4 substrate - 0.6553 65.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7983 79.83%
CYP3A4 inhibition - 0.9791 97.91%
CYP2C9 inhibition - 0.9259 92.59%
CYP2C19 inhibition - 0.9387 93.87%
CYP2D6 inhibition - 0.9662 96.62%
CYP1A2 inhibition + 0.7881 78.81%
CYP2C8 inhibition - 0.9664 96.64%
CYP inhibitory promiscuity - 0.8093 80.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.7102 71.02%
Eye corrosion + 0.9924 99.24%
Eye irritation + 0.9604 96.04%
Skin irritation + 0.8698 86.98%
Skin corrosion - 0.9034 90.34%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4460 44.60%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6676 66.76%
skin sensitisation + 0.9027 90.27%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.9177 91.77%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.7220 72.20%
Acute Oral Toxicity (c) III 0.8534 85.34%
Estrogen receptor binding - 0.6925 69.25%
Androgen receptor binding - 0.7948 79.48%
Thyroid receptor binding + 0.7288 72.88%
Glucocorticoid receptor binding - 0.6611 66.11%
Aromatase binding - 0.8071 80.71%
PPAR gamma + 0.7049 70.49%
Honey bee toxicity - 0.9829 98.29%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9470 94.70%

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 92.06% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.30% 99.17%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.17% 98.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.04% 92.08%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.93% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.25% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.53% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 80.36% 94.73%
CHEMBL1781 P11387 DNA topoisomerase I 80.27% 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.
Abies nebrodensis

Cross-Links

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PubChem 5283372
LOTUS LTS0226026
wikiData Q76294037