ChemicalBook--->CAS DataBase List--->41438-38-4

41438-38-4

41438-38-4 Structure

41438-38-4 Structure
IdentificationBack Directory
[Name]

2,4-DIETHYLPYRIDINE DICARBOXYLATE
[CAS]

41438-38-4
[Synonyms]

2,4-DPD
Ai3-17897
Diethyl-2,4-pdc
2,4-Pdc diethyl ester
2,4-Pyridinedicarboxylic
DIETHYL 2,4-PYRIDINECARBOXYLATE
Diethyl 2,4-pyridinedicarboxylate
2,4-DIETHYLPYRIDINE DICARBOXYLATE
diethyl pyridine-2,4-dicarboxylate
diethyl 2,4-pyridinedicarboxylic acid
2,4-DIETHYL PYRIDINE-2,4-DICARBOXYLATE
2,4-pyridinedicarboxylicacid,ethylester
2,4-PYRIDINEDICARBOXYLIC ACID DIETHYL ESTER
pyridine-2,4-dicarboxylic acid diethyl ester
2,4-pyridine dicarboxylic acid 2,4-diethyl ester
2,4-Pyridinedicarboxylic acid, diethyl ester Pyridine-2,4-Dicarboxylic Acid Diethyl Ester
[EINECS(EC#)]

680-341-5
[Molecular Formula]

C11H13NO4
[MDL Number]

MFCD00152168
[MOL File]

41438-38-4.mol
[Molecular Weight]

223.23
Chemical PropertiesBack Directory
[Melting point ]

31 °C
[Boiling point ]

330.9±22.0 °C(Predicted)
[density ]

1.165±0.06 g/cm3(Predicted)
[vapor pressure ]

0.022Pa at 25℃
[storage temp. ]

2-8°C
[solubility ]

≤50mg/ml in ethanol;20mg/ml in DMSO;30mg/ml in dimethyl formamide
[form ]

Crystalline
[pka]

-0.69±0.10(Predicted)
[color ]

White to Almost white
[LogP]

1.92 at 20℃ and pH7.82
[Surface tension]

56.3mN/m at 1g/L and 19.7℃
[CAS DataBase Reference]

41438-38-4
Safety DataBack Directory
[HS Code ]

2933.39.9200
Hazard InformationBack Directory
[Uses]

Diethyl pyridine-2,4-dicarb is a potent prolyl 4-hydroxylase-directed proinhibitor. Diethyl pyridine-2,4-dicarb inhibits prolyl hydroxylation and procollagen processing in chick-embryo calvaria[1].
[Biological Activity]

2,4-dpd is a cell permeable, competitive inhibitor of the oxygen-sensing enzyme hif-α prolyl hydroxylase (hif-ph) [1].hypoxia-inducible factor (hif) is a transcription factor with a key role in cellular responses to hypoxia in a variety of organisms. the hif system plays an important role in angiogenesis, erythropoiesis, energy utilization, glucose/energy metabolism, tumour development, and ischaemic/hypoxic disease. genetic or pharmacological inactivation of the hif hydroxylases results in a constitutive activation of the hif pathway with little or even absent regulation by oxygen remaining. the oxygen-sensing enzyme hif-α prolyl hydroxylase catalyzes hydroxylation of specific prolyl and asparaginyl residues in the regulatory hif-α subunits [2].exposure to 2,4-dpd limited prolyl 4-hydroxylase activity in c. elegans., where their esters are hydrolyzed to form competitors of a -ketoglutarate. 2,4-dpd showed dramatic effects among the progeny. when exposed to a high level of 2,4-dpd (2.7 mm), all progeny died regardless of genotype of c. elegans. the dead embryos arrested at the twofold stage [1].
[storage]

Store at -20°C
[References]

[1] friedman l, higgin j j, moulder g, et al. prolyl 4-hydroxylase is required for viability and morphogenesis in caenorhabditis elegans[j]. proceedings of the national academy of sciences, 2000, 97(9): 4736-4741.
[2] schofield c j, ratcliffe p j. signalling hypoxia by hif hydroxylases[j]. biochemical and biophysical research communications, 2005, 338(1): 617-626.
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