cis-4-Heptenal

Details

Top
Internal ID 8218d454-37a3-47b1-8f56-8d638d7d2dca
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (Z)-hept-4-enal
SMILES (Canonical) CCC=CCCC=O
SMILES (Isomeric) CC/C=C\CCC=O
InChI InChI=1S/C7H12O/c1-2-3-4-5-6-7-8/h3-4,7H,2,5-6H2,1H3/b4-3-
InChI Key VVGOCOMZRGWHPI-ARJAWSKDSA-N
Popularity 101 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H12O
Molecular Weight 112.17 g/mol
Exact Mass 112.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.93
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
6728-31-0
cis-4-Hepten-1-al
(Z)-Hept-4-enal
(Z)-4-heptenal
4-Heptenal, (Z)-
(Z)-4-Hepten-1-al
(4Z)-4-Heptenal
4-Heptenal, (4Z)-
Hept-cis-4-enal
4-Heptenal, cis-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of cis-4-Heptenal

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.8626 86.26%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Plasma membrane 0.5982 59.82%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.8588 85.88%
OATP1B3 inhibitior + 0.9203 92.03%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9225 92.25%
P-glycoprotein inhibitior - 0.9872 98.72%
P-glycoprotein substrate - 0.9639 96.39%
CYP3A4 substrate - 0.7160 71.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7983 79.83%
CYP3A4 inhibition - 0.9802 98.02%
CYP2C9 inhibition - 0.9199 91.99%
CYP2C19 inhibition - 0.9561 95.61%
CYP2D6 inhibition - 0.9697 96.97%
CYP1A2 inhibition + 0.6011 60.11%
CYP2C8 inhibition - 0.9867 98.67%
CYP inhibitory promiscuity - 0.7659 76.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.6407 64.07%
Eye corrosion + 0.9914 99.14%
Eye irritation + 0.9866 98.66%
Skin irritation + 0.7884 78.84%
Skin corrosion - 0.9675 96.75%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7806 78.06%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation + 0.9334 93.34%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.9288 92.88%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5433 54.33%
Acute Oral Toxicity (c) III 0.8647 86.47%
Estrogen receptor binding - 0.9724 97.24%
Androgen receptor binding - 0.9389 93.89%
Thyroid receptor binding - 0.8664 86.64%
Glucocorticoid receptor binding - 0.8434 84.34%
Aromatase binding - 0.8774 87.74%
PPAR gamma - 0.7984 79.84%
Honey bee toxicity - 0.9395 93.95%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.7821 78.21%

Targets

Top

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.13% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.39% 89.34%
CHEMBL2581 P07339 Cathepsin D 81.36% 98.95%

Plants that contains it

Top
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.
Capsella bursa-pastoris
Senna alexandrina

Cross-Links

Top
PubChem 5362814
NPASS NPC145022