PYRIDINE-2,4-DICARBOXYLIC ACID MONOHYDRATE

PYRIDINE-2,4-DICARBOXYLIC ACID MONOHYDRATE Property

Melting point:

246-248 °C (dec.)(lit.)

storage temp. 

Store at -20°C

solubility 

DMSO: 1.4 mg/ml; PBS (pH 7.2): 0.2 mg/ml

form 

A crystalline solid

BRN 

131631

Safety

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

26

WGK Germany 

3

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

PYRIDINE-2,4-DICARBOXYLIC ACID MONOHYDRATE Chemical Properties,Usage,Production

Description

2,4-Pyridinedicarboxylic Acid (2,4-PDCA) is a compound that structurally mimics 2-oxoglutarate (2-OG, also known as α-ketoglutarate) and chelates zinc, thus affecting a range of enzymes. As a 2-OG mimic, it blocks the activity of 2-OG oxygenases, which include certain lysine demethylases and a variety of hydroxylases (e.g., prolyl, collagen, lysyl). 2,4-PDCA inhibits several Jumonji domain-containing lysine demethylases when used at low micromolar concentrations. Through its effects on hydroxylases, including prolyl hydroxlase 1 (IC₅₀ = 1.5 μM), 2,4-PDCA modulates hypoxia-inducible factor turnover, collagen synthesis, and plant cell wall formation. It can inhibit zinc-dependent enzymes, like metallo-β-lactamase. 2,4-PDCA also affects and is translocated by organic anion transporters.

References

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[2] M KRISTIAN KOSKI. The active site of an algal prolyl 4-hydroxylase has a large structural plasticity.[J]. The Journal of Biological Chemistry, 2007: 37112-37123. DOI: 10.1074/jbc.m706554200
[3] MUKRAM M. MACKEEN. Small-Molecule-Based Inhibition of Histone Demethylation in Cells Assessed by Quantitative Mass Spectrometry[J]. Journal of Proteome Research, 2010, 9 8: 4082-4092. DOI: 10.1021/pr100269b
[4] ULRIKE LEURS. Inhibitor scaffold for the histone lysine demethylase KDM4C (JMJD2C)[J]. Bioorganic & Medicinal Chemistry Letters, 2012, 22 18: Pages 5811-5813. DOI: 10.1016/j.bmcl.2012.07.091
[5] OLIVER N F KING. Quantitative high-throughput screening identifies 8-hydroxyquinolines as cell-active histone demethylase inhibitors.[J]. PLoS ONE, 2010: e15535. DOI: 10.1371/journal.pone.0015535
[6] LINE H. KRISTENSEN. Studies of H3K4me3 demethylation by KDM5B/Jarid1B/PLU1 reveals strong substrate recognition in vitro and identifies 2,4-pyridine-dicarboxylic acid as an in vitro and in cell inhibitor[J]. The FEBS journal, 2012, 279 11: 1905-1914. DOI: 10.1111/j.1742-4658.2012.08567.x
[7] SHOHEI HAMADA. Design, Synthesis, Enzyme-Inhibitory Activity, and Effect on Human Cancer Cells of a Novel Series of Jumonji Domain-Containing Protein 2 Histone Demethylase Inhibitors[J]. Journal of Medicinal Chemistry, 2010, 53 15: 5629-5638. DOI: 10.1021/jm1003655
[8] L E HORSFALL. Competitive inhibitors of the CphA metallo-beta-lactamase from Aeromonas hydrophila.[J]. Antimicrobial Agents and Chemotherapy, 2007: 2136-2142. DOI: 10.1128/aac.00866-06
[9] YOHANNES HAGOS. α-Ketoglutarate-related inhibitors of HIF prolyl hydroxylases are substrates of renal organic anion transporters 1 (OAT1) and 4 (OAT4).[J]. Pflugers Archiv?: European journal of physiology, 2012, 464 4: 367-374. DOI: 10.1007/s00424-012-1140-9