NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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pyridine-2,4-dicarboxylic acid
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IUPAC Traditional name
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pyridine-2,4-dicarboxylic acid
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2,4-pyridinedicarboxylic acid
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Synonyms
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2,4-Pyridinedicarboxylic acid
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Lutidinic acid
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Lutidinic acid
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2,4-Pyridinedicarboxylic acid
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pyridine-2,4-dicarboxylic acid
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Pyridine-2,4-dicarboxylic acid
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2,4-吡啶二羧酸
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吡啶-2,4-二羧酸水合物
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CAS Number
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EC Number
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MDL Number
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MFCD00006296
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MFCD00149413
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Beilstein Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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3.180665
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H Acceptors
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5
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H Donor
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2
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LogD (pH = 5.5)
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-3.3716452
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LogD (pH = 7.4)
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-6.2329383
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Log P
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0.45658952
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Molar Refractivity
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38.0415 cm3
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Polarizability
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14.275565 Å3
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Polar Surface Area
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87.49 Å2
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Rotatable Bonds
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2
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Lipinski's Rule of Five
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true
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DETAILS
DETAILS
Sigma Aldrich
Sigma Aldrich -
04473
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Application 2,4-Pyridinedicarboxylic acid is an in vitro and in cell inhibitor, as well as a known inhibitor of the histone lysine demethylases. 2,4-Pyridinedicarboxylic acid has been used in a study to determine that ruthenium(II) complexes exert antimetastatic effects on several tumor cell lines in vitro, achieved mostly by the effect on cell adhesion, migration and angiogenesis. . 2,4-Pyridinedicarboxylic acid has been used in a study to develop an assay that represents the first report of a RapidFire mass spectrometery assay for an epigenetics target. |
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Aldrich Library of FT-IR Spectra, 1st edn., 1985, 2, 790D, (ir)
- • Aldrich Library of NMR Spectra, 9, 45A, (pmr)
- • Jerchel, D. et al., Annalen, 1958, 613, 153, (synth)
- • Lukes, R. et al., Coll. Czech. Chem. Comm., 1961, 26, 2727, (synth)
- • Oliveto, E.P., Chem. Heterocycl. Compd., (Part 3), 1962, 14, 179, (bibl)
- • Pollak, P.I. et al., Chem. Heterocycl. Compd., Suppl. 3, 1974, 14, (bibl)
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PATENTS
PATENTS
PubChem Patent
Google Patent