1-Nonenal

Details

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Internal ID ecbca7c8-9b7c-42c4-8909-be70256b516a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ketenes
IUPAC Name non-1-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H16O/c1-2-3-4-5-6-7-8-9-10/h8H,2-7H2,1H3
InChI Key MMQWFMBMXXWRKD-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16O
Molecular Weight 140.22 g/mol
Exact Mass 140.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.80
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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SCHEMBL2038808

2D Structure

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2D Structure of 1-Nonenal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.9501 95.01%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Plasma membrane 0.5260 52.60%
OATP2B1 inhibitior - 0.8526 85.26%
OATP1B1 inhibitior + 0.9177 91.77%
OATP1B3 inhibitior + 0.9016 90.16%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9242 92.42%
P-glycoprotein inhibitior - 0.9870 98.70%
P-glycoprotein substrate - 0.9195 91.95%
CYP3A4 substrate - 0.6813 68.13%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7128 71.28%
CYP3A4 inhibition - 0.9911 99.11%
CYP2C9 inhibition - 0.9285 92.85%
CYP2C19 inhibition - 0.9519 95.19%
CYP2D6 inhibition - 0.9653 96.53%
CYP1A2 inhibition + 0.7244 72.44%
CYP2C8 inhibition - 0.9386 93.86%
CYP inhibitory promiscuity - 0.7617 76.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6467 64.67%
Eye corrosion + 0.9927 99.27%
Eye irritation + 0.9756 97.56%
Skin irritation + 0.9187 91.87%
Skin corrosion - 0.8516 85.16%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5138 51.38%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6107 61.07%
skin sensitisation + 0.9648 96.48%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9954 99.54%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.6554 65.54%
Acute Oral Toxicity (c) III 0.8135 81.35%
Estrogen receptor binding - 0.9350 93.50%
Androgen receptor binding - 0.8246 82.46%
Thyroid receptor binding - 0.7106 71.06%
Glucocorticoid receptor binding - 0.8464 84.64%
Aromatase binding - 0.7832 78.32%
PPAR gamma - 0.7831 78.31%
Honey bee toxicity - 0.9720 97.20%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.9018 90.18%
Fish aquatic toxicity + 0.9804 98.04%

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 95.99% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.93% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.07% 92.86%
CHEMBL2581 P07339 Cathepsin D 92.61% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.25% 85.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.08% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.50% 97.29%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.02% 91.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.88% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.02% 89.34%
CHEMBL221 P23219 Cyclooxygenase-1 83.49% 90.17%
CHEMBL1907 P15144 Aminopeptidase N 81.12% 93.31%

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.
Gossypium hirsutum

Cross-Links

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PubChem 3015503
LOTUS LTS0133574
wikiData Q105167996