5,6-Dideuteriohexanal

Details

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Internal ID d3774b4c-40a5-4b9a-b757-ebf92533aece
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name 5,6-dideuteriohexanal
SMILES (Canonical) CCCCCC=O
SMILES (Isomeric) [2H]CC([2H])CCCC=O
InChI InChI=1S/C6H12O/c1-2-3-4-5-6-7/h6H,2-5H2,1H3/i1D,2D
InChI Key JARKCYVAAOWBJS-QDNHWIQGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12O
Molecular Weight 102.17 g/mol
Exact Mass 102.101368494 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.77
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,6-Dideuteriohexanal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.6910 69.10%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.3488 34.88%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.9327 93.27%
OATP1B3 inhibitior + 0.9272 92.72%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9361 93.61%
P-glycoprotein inhibitior - 0.9874 98.74%
P-glycoprotein substrate - 0.9254 92.54%
CYP3A4 substrate - 0.6107 61.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7756 77.56%
CYP3A4 inhibition - 0.9882 98.82%
CYP2C9 inhibition - 0.9407 94.07%
CYP2C19 inhibition - 0.9544 95.44%
CYP2D6 inhibition - 0.9600 96.00%
CYP1A2 inhibition + 0.7073 70.73%
CYP2C8 inhibition - 0.9872 98.72%
CYP inhibitory promiscuity - 0.8874 88.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.7099 70.99%
Eye corrosion + 0.9962 99.62%
Eye irritation + 0.9503 95.03%
Skin irritation + 0.9203 92.03%
Skin corrosion - 0.8580 85.80%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6021 60.21%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation + 0.7360 73.60%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.8913 89.13%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6222 62.22%
Acute Oral Toxicity (c) III 0.8676 86.76%
Estrogen receptor binding - 0.8898 88.98%
Androgen receptor binding - 0.9478 94.78%
Thyroid receptor binding - 0.8092 80.92%
Glucocorticoid receptor binding - 0.5631 56.31%
Aromatase binding - 0.7789 77.89%
PPAR gamma - 0.6720 67.20%
Honey bee toxicity - 0.8255 82.55%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.7793 77.93%

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 95.40% 89.63%
CHEMBL2581 P07339 Cathepsin D 93.37% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.71% 92.08%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 88.07% 85.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.48% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.45% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.61% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.81% 92.86%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.62% 89.34%
CHEMBL2664 P23526 Adenosylhomocysteinase 82.42% 86.67%
CHEMBL3401 O75469 Pregnane X receptor 81.76% 94.73%

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.
Conioselinum anthriscoides

Cross-Links

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PubChem 11115998
NPASS NPC274787