1219802-18-2
1219802-18-2
Chemical Structure
Quinoline-2-carboxylic acid-d6
- CAS No.: 1219802-18-2
- Formula:C10HD6NO2
- Molecular Weight:179.21
IUPAC Name: quinoline-2-carboxylic-d6 acid
InChIKey: LOAUVZALPPNFOQ-MZWXYZOWSA-N
SMILES: OC(C1=NC2=C(C([2H])=C([2H])C([2H])=C2[2H])C([2H])=C1[2H])=O
Biological Activity: Quinoline-2-carboxylic acid-d6 is the deuterium labeled Quinoline-2-carboxylic acid (HY-W002011). Quinoline-2-carboxylic acid exhibits antidiabetic activity. Quinoline-2-carboxylic acid can be used as drug intermediate for synthesis of various active compounds[1][2].
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Quinoline-2-carboxylic acid-d6 | Quinoline-2-carboxylic acid-d6 is the deuterium labeled Quinoline-2-carboxylic acid (HY-W002011). Quinoline-2-carboxylic acid exhibits antidiabetic activity. Quinoline-2-carboxylic acid can be used as drug intermediate for synthesis of various active compounds. | |||||||||||||||||||||
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Quinoline-2-carboxylic acid (Standard) | 99.96% | Quinoline-2-carboxylic acid exhibits antidiabetic activity. Quinoline-2-carboxylic acid can be used as drug intermediate for synthesis of various active compounds. | ||||||||||||||||||||
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Quinoline-2-carboxylic acid | 99.99% | Quinoline-2-carboxylic acid exhibits antidiabetic activity. Quinoline-2-carboxylic acid can be used as drug intermediate for synthesis of various active compounds. | ||||||||||||||||||||
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References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief]
- [2]. Lee H W, et al., Quinoline-2-carboxylic acid isolated from Ephedra pachyclada and its structural derivatives show inhibitory effects against α-glucosidase and α-amylase[J]. Journal of the Korean Society for Applied Biological Chemistry, 2014, 57: 441-444.
