cis,cis-7,10,-Hexadecadienal

Details

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Internal ID 8a66dcb4-a4b9-493f-9eaa-bda7851a6ff6
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (7Z,10Z)-hexadeca-7,10-dienal
SMILES (Canonical) CCCCCC=CCC=CCCCCCC=O
SMILES (Isomeric) CCCCC/C=C\C/C=C\CCCCCC=O
InChI InChI=1S/C16H28O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h6-7,9-10,16H,2-5,8,11-15H2,1H3/b7-6-,10-9-
InChI Key WIWVOAOSGQCJSL-HZJYTTRNSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C16H28O
Molecular Weight 236.39 g/mol
Exact Mass 236.214015512 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.22
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 12

Synonyms

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(7Z,10Z)-7,10-Hexadecadienal
SCHEMBL10613675
DTXSID60880840
WIWVOAOSGQCJSL-HZJYTTRNSA-N
(7Z,10Z)-7,10-Hexadecadienal #
56829-23-3

2D Structure

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2D Structure of cis,cis-7,10,-Hexadecadienal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9060 90.60%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Plasma membrane 0.6168 61.68%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior - 0.3466 34.66%
OATP1B3 inhibitior + 0.8896 88.96%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6773 67.73%
P-glycoprotein inhibitior - 0.8754 87.54%
P-glycoprotein substrate - 0.8968 89.68%
CYP3A4 substrate - 0.6291 62.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7983 79.83%
CYP3A4 inhibition - 0.9832 98.32%
CYP2C9 inhibition - 0.9391 93.91%
CYP2C19 inhibition - 0.9524 95.24%
CYP2D6 inhibition - 0.9654 96.54%
CYP1A2 inhibition + 0.8016 80.16%
CYP2C8 inhibition - 0.9312 93.12%
CYP inhibitory promiscuity - 0.8166 81.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.7077 70.77%
Eye corrosion + 0.9897 98.97%
Eye irritation + 0.9077 90.77%
Skin irritation + 0.9083 90.83%
Skin corrosion - 0.8898 88.98%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5216 52.16%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6066 60.66%
skin sensitisation + 0.9219 92.19%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.9954 99.54%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5410 54.10%
Acute Oral Toxicity (c) III 0.6225 62.25%
Estrogen receptor binding - 0.5942 59.42%
Androgen receptor binding - 0.8115 81.15%
Thyroid receptor binding + 0.7055 70.55%
Glucocorticoid receptor binding - 0.6577 65.77%
Aromatase binding - 0.7207 72.07%
PPAR gamma + 0.8418 84.18%
Honey bee toxicity - 0.9874 98.74%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.8753 87.53%
Fish aquatic toxicity + 0.9569 95.69%

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
CHEMBL230 P35354 Cyclooxygenase-2 97.15% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.06% 92.08%
CHEMBL2581 P07339 Cathepsin D 94.80% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.45% 85.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.10% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.53% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.40% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.29% 97.29%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 86.81% 90.75%
CHEMBL1781 P11387 DNA topoisomerase I 85.39% 97.00%
CHEMBL221 P23219 Cyclooxygenase-1 83.97% 90.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.00% 89.34%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.70% 91.81%
CHEMBL3401 O75469 Pregnane X receptor 82.46% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.89% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.85% 96.00%
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.
Uncaria macrophylla

Cross-Links

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PubChem 5365665
NPASS NPC287128