2-Nonene-4,6,8-triynal

Details

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Internal ID 3884903f-decb-42f6-9d28-38b63b1d9c25
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (E)-non-2-en-4,6,8-triynal
SMILES (Canonical) C#CC#CC#CC=CC=O
SMILES (Isomeric) C#CC#CC#C/C=C/C=O
InChI InChI=1S/C9H4O/c1-2-3-4-5-6-7-8-9-10/h1,7-9H/b8-7+
InChI Key YZDIZAOHDWYDBH-BQYQJAHWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H4O
Molecular Weight 128.13 g/mol
Exact Mass 128.026214747 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.38
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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(E)-non-2-en-4,6,8-triynal
LMFA06000050
non-2-ene-4,6,8-triynal
CHEBI:73737
Q27144077

2D Structure

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2D Structure of 2-Nonene-4,6,8-triynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 + 0.5769 57.69%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.3599 35.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9054 90.54%
OATP1B3 inhibitior + 0.9580 95.80%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9341 93.41%
P-glycoprotein inhibitior - 0.9764 97.64%
P-glycoprotein substrate - 0.9707 97.07%
CYP3A4 substrate - 0.6219 62.19%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate - 0.8385 83.85%
CYP3A4 inhibition - 0.9784 97.84%
CYP2C9 inhibition - 0.8993 89.93%
CYP2C19 inhibition - 0.9212 92.12%
CYP2D6 inhibition - 0.9719 97.19%
CYP1A2 inhibition - 0.6947 69.47%
CYP2C8 inhibition - 0.9568 95.68%
CYP inhibitory promiscuity - 0.8075 80.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7383 73.83%
Carcinogenicity (trinary) Non-required 0.5056 50.56%
Eye corrosion + 0.9964 99.64%
Eye irritation + 0.9700 97.00%
Skin irritation + 0.9250 92.50%
Skin corrosion + 0.9901 99.01%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7904 79.04%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.6303 63.03%
skin sensitisation + 0.9286 92.86%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.7319 73.19%
Acute Oral Toxicity (c) II 0.8445 84.45%
Estrogen receptor binding - 0.8268 82.68%
Androgen receptor binding - 0.8157 81.57%
Thyroid receptor binding - 0.7898 78.98%
Glucocorticoid receptor binding - 0.7810 78.10%
Aromatase binding - 0.7517 75.17%
PPAR gamma - 0.7509 75.09%
Honey bee toxicity - 0.6109 61.09%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.3934 39.34%

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 80.98% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.68% 95.56%

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.
Asparagus falcatus

Cross-Links

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PubChem 5283343
LOTUS LTS0195973
wikiData Q104959290