2,4-Dimethylpentanal

Details

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Internal ID d6457025-49ab-4071-95e4-bc22ff16d262
Taxonomy Organic oxygen compounds > Organic oxides
IUPAC Name 2,4-dimethylpentanal
SMILES (Canonical) CC(C)CC(C)C=O
SMILES (Isomeric) CC(C)CC(C)C=O
InChI InChI=1S/C7H14O/c1-6(2)4-7(3)5-8/h5-7H,4H2,1-3H3
InChI Key GPTMCJMLSOIYGU-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C7H14O
Molecular Weight 114.19 g/mol
Exact Mass 114.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.87
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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27944-79-2
Pentanal, 2,4-dimethyl-
Valeraldehyde, 2,4-dimethyl-
5DE7YF56LC
NSC-523741
NSC523741
Pentanal,4-dimethyl-
Valeraldehyde,4-dimethyl-
UNII-5DE7YF56LC
SCHEMBL195346
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4-Dimethylpentanal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.6328 63.28%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.4754 47.54%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.9286 92.86%
OATP1B3 inhibitior + 0.9550 95.50%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9313 93.13%
P-glycoprotein inhibitior - 0.9823 98.23%
P-glycoprotein substrate - 0.9404 94.04%
CYP3A4 substrate - 0.7383 73.83%
CYP2C9 substrate - 0.5862 58.62%
CYP2D6 substrate - 0.7805 78.05%
CYP3A4 inhibition - 0.9822 98.22%
CYP2C9 inhibition - 0.9621 96.21%
CYP2C19 inhibition - 0.9692 96.92%
CYP2D6 inhibition - 0.9513 95.13%
CYP1A2 inhibition - 0.8607 86.07%
CYP2C8 inhibition - 0.9936 99.36%
CYP inhibitory promiscuity - 0.9233 92.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6283 62.83%
Carcinogenicity (trinary) Non-required 0.6062 60.62%
Eye corrosion + 1.0000 100.00%
Eye irritation + 0.9864 98.64%
Skin irritation + 0.8124 81.24%
Skin corrosion - 0.8786 87.86%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7874 78.74%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.7802 78.02%
skin sensitisation + 0.8587 85.87%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.5858 58.58%
Acute Oral Toxicity (c) III 0.6642 66.42%
Estrogen receptor binding - 0.9399 93.99%
Androgen receptor binding - 0.8253 82.53%
Thyroid receptor binding - 0.9001 90.01%
Glucocorticoid receptor binding - 0.9177 91.77%
Aromatase binding - 0.8637 86.37%
PPAR gamma - 0.9031 90.31%
Honey bee toxicity - 0.8883 88.83%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.3945 39.45%

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 92.60% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 87.82% 89.63%
CHEMBL3837 P07711 Cathepsin L 87.50% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.15% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 85.00% 93.31%
CHEMBL268 P43235 Cathepsin K 84.10% 96.85%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.80% 89.34%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.38% 90.24%
CHEMBL221 P23219 Cyclooxygenase-1 82.35% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.69% 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.
Foeniculum vulgare

Cross-Links

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PubChem 34072
NPASS NPC238004