160660
喹哪啶酸
98%
别名:
2-喹啉羧酸
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关于此项目
经验公式（希尔记法）:
C10H7NO2
化学文摘社编号:
分子量:
173.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-218-3
Beilstein/REAXYS Number:
126322
MDL number:
产品名称
喹哪啶酸, 98%
InChI key
LOAUVZALPPNFOQ-UHFFFAOYSA-N
InChI
1S/C10H7NO2/c12-10(13)9-6-5-7-3-1-2-4-8(7)11-9/h1-6H,(H,12,13)
SMILES string
OC(=O)c1ccc2ccccc2n1
assay
98%
form
solid
mp
156-158 °C (lit.)
functional group
carboxylic acid
Quality Level
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General description
喹啉酸也称为喹啉-2-羧酸。已报告微波辅助合成喹啉酸取代苯胺的方法。抑制丙酮酸盐的氧化，α-大鼠肝线粒体中的酮戊二酸、谷氨酸和柠檬酸。喹啉酸是色氨酸降解的代谢产物，抑制灌注肝脏中的糖异生。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Total synthesis of thiostrepton, part 2: construction of the quinaldic acid macrocycle and final stages of the synthesis.
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Ergothioneine is believed not to be synthesized by man but it accumulates to high concentrations in some mammalian cells as a result of dietary intake. Ergothioneine is known to chelate divalent metal ions with high affinity. Other substances which are
Mode of action of hypoglycemic agents. 3. Studies on 5-methoxy indole-2-carboxylic acid and quinaldic acid.
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The Journal of biological chemistry, 245(20), 5297-5303 (1970-10-25)
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Biological chemistry Hoppe-Seyler, 374(6), 363-376 (1993-06-01)
Serratia marcecens 2CC-1 utilizes quinaldic acid (quinoline 2-carboxylic acid) as sole source of carbon, nitrogen and energy. Growth of strain 2CC-1 on quinaldic acid as well as on nicotinic acid and hypoxanthine was inhibited completely by the molybdate antagonist tungstate
Zhao-Qing Du et al.
Journal of Cancer, 11(15), 4614-4624 (2020-06-04)
Platelet-derived growth receptor α (PDGFRα) is a key factor in many pathophysiological processes. The expression level of PDGFRα is significantly elevated in the early stage of liver development and maintained at a lower level in adult normal livers. In this
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