cis-6-Nonenal

Details

Top
Internal ID 037b62f6-62a0-497a-9942-c482923b4d72
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (Z)-non-6-enal
SMILES (Canonical) CCC=CCCCCC=O
SMILES (Isomeric) CC/C=C\CCCCC=O
InChI InChI=1S/C9H16O/c1-2-3-4-5-6-7-8-9-10/h3-4,9H,2,5-8H2,1H3/b4-3-
InChI Key RTNPCOBSXBGDMO-ARJAWSKDSA-N
Popularity 46 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H16O
Molecular Weight 140.22 g/mol
Exact Mass 140.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.71
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

Top
2277-19-2
(Z)-Non-6-enal
(Z)-6-Nonenal
cis-6-Nonen-1-al
6-Nonenal, (6Z)-
(6Z)-non-6-enal
6-Nonenal, cis-
(6Z)-6-Nonenal
6-NONENAL, (Z)-
FEMA No. 3580
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of cis-6-Nonenal

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.9193 91.93%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Plasma membrane 0.5982 59.82%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.8338 83.38%
OATP1B3 inhibitior + 0.9203 92.03%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8752 87.52%
P-glycoprotein inhibitior - 0.9848 98.48%
P-glycoprotein substrate - 0.9311 93.11%
CYP3A4 substrate - 0.6634 66.34%
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 - 0.9785 97.85%
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 + 0.9899 98.99%
Skin irritation + 0.7884 78.84%
Skin corrosion - 0.9675 96.75%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6292 62.92%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation + 0.9334 93.34%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9288 92.88%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.5704 57.04%
Acute Oral Toxicity (c) III 0.8647 86.47%
Estrogen receptor binding - 0.9405 94.05%
Androgen receptor binding - 0.9005 90.05%
Thyroid receptor binding - 0.7473 74.73%
Glucocorticoid receptor binding - 0.8088 80.88%
Aromatase binding - 0.8870 88.70%
PPAR gamma - 0.5771 57.71%
Honey bee toxicity - 0.9582 95.82%
Biodegradation - 0.6000 60.00%
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
CHEMBL2581 P07339 Cathepsin D 88.09% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.72% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.63% 96.09%
CHEMBL2664 P23526 Adenosylhomocysteinase 82.42% 86.67%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 82.31% 90.75%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.61% 89.34%
CHEMBL1781 P11387 DNA topoisomerase I 80.83% 97.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.28% 95.56%

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.
Artemisia capillaris

Cross-Links

Top
PubChem 5362720
NPASS NPC104688