(Z)-7-Dodecenal

Details

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Internal ID 01749e78-cc8d-45f7-bc6b-fda8c07a3979
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (Z)-dodec-7-enal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h5-6,12H,2-4,7-11H2,1H3/b6-5-
InChI Key HTUHYXDEKCWDCI-WAYWQWQTSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C12H22O
Molecular Weight 182.30 g/mol
Exact Mass 182.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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(Z)-dodec-7-enal
7Z-Dodecenal
63851-40-1
7-dodecenal, Z
7-Dodecenal, (Z)-
SCHEMBL27893229
HTUHYXDEKCWDCI-WAYWQWQTSA-N
LMFA06000162
A901993

2D Structure

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2D Structure of (Z)-7-Dodecenal

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 + 0.8870 88.70%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Plasma membrane 0.6886 68.86%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.8393 83.93%
OATP1B3 inhibitior + 0.9089 90.89%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6817 68.17%
P-glycoprotein inhibitior - 0.9691 96.91%
P-glycoprotein substrate - 0.9159 91.59%
CYP3A4 substrate - 0.6549 65.49%
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 - 0.9652 96.52%
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 + 0.9911 99.11%
Skin irritation + 0.8698 86.98%
Skin corrosion - 0.9034 90.34%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5660 56.60%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6191 61.91%
skin sensitisation + 0.9027 90.27%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9177 91.77%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6653 66.53%
Acute Oral Toxicity (c) III 0.8534 85.34%
Estrogen receptor binding - 0.8861 88.61%
Androgen receptor binding - 0.8005 80.05%
Thyroid receptor binding - 0.5754 57.54%
Glucocorticoid receptor binding - 0.6901 69.01%
Aromatase binding - 0.7613 76.13%
PPAR gamma - 0.5967 59.67%
Honey bee toxicity - 0.9832 98.32%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.7300 73.00%
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 93.40% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.71% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.70% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 91.56% 89.63%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.87% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.06% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.81% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 85.05% 97.00%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.24% 92.86%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.56% 89.34%
CHEMBL2664 P23526 Adenosylhomocysteinase 82.42% 86.67%
CHEMBL221 P23219 Cyclooxygenase-1 81.04% 90.17%

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.
Valeriana jatamansi

Cross-Links

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PubChem 6430185
NPASS NPC157250