Dec-2-en-4,6-diynal

Details

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Internal ID 27801c11-940b-4f55-97ff-d4bf557c9eb5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name dec-2-en-4,6-diynal
SMILES (Canonical) CCCC#CC#CC=CC=O
SMILES (Isomeric) CCCC#CC#CC=CC=O
InChI InChI=1S/C10H10O/c1-2-3-4-5-6-7-8-9-10-11/h8-10H,2-3H2,1H3
InChI Key BYWJFYMWAKEDNZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O
Molecular Weight 146.19 g/mol
Exact Mass 146.073164938 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.55
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Dec-2-en-4,6-diynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.7973 79.73%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Plasma membrane 0.5127 51.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8982 89.82%
OATP1B3 inhibitior + 0.9369 93.69%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9128 91.28%
P-glycoprotein inhibitior - 0.9814 98.14%
P-glycoprotein substrate - 0.8715 87.15%
CYP3A4 substrate - 0.5889 58.89%
CYP2C9 substrate - 0.7984 79.84%
CYP2D6 substrate - 0.8408 84.08%
CYP3A4 inhibition - 0.9757 97.57%
CYP2C9 inhibition - 0.8871 88.71%
CYP2C19 inhibition - 0.9061 90.61%
CYP2D6 inhibition - 0.9652 96.52%
CYP1A2 inhibition + 0.5789 57.89%
CYP2C8 inhibition - 0.9447 94.47%
CYP inhibitory promiscuity - 0.6879 68.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.4992 49.92%
Eye corrosion + 0.9842 98.42%
Eye irritation + 0.9495 94.95%
Skin irritation + 0.8421 84.21%
Skin corrosion - 0.7594 75.94%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6469 64.69%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.5766 57.66%
skin sensitisation + 0.9356 93.56%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.7283 72.83%
Acute Oral Toxicity (c) III 0.7636 76.36%
Estrogen receptor binding - 0.7616 76.16%
Androgen receptor binding - 0.7310 73.10%
Thyroid receptor binding - 0.5236 52.36%
Glucocorticoid receptor binding - 0.7616 76.16%
Aromatase binding - 0.7164 71.64%
PPAR gamma - 0.5627 56.27%
Honey bee toxicity - 0.8596 85.96%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.7750 77.50%

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 90.40% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 89.99% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.11% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.71% 92.86%
CHEMBL221 P23219 Cyclooxygenase-1 83.53% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.03% 96.00%
CHEMBL255 P29275 Adenosine A2b receptor 81.55% 98.59%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.82% 89.34%

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.
Grindelia hirsutula

Cross-Links

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PubChem 163050570
LOTUS LTS0184044
wikiData Q104949982