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Merck
CN

104051

吡啶酰胺

98%

别名:

2-吡啶甲酰胺

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关于此项目

经验公式(希尔记法):
C6H6N2O
化学文摘社编号:
分子量:
122.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
215-921-5
MDL number:
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产品名称

吡啶酰胺, 98%

InChI key

IBBMAWULFFBRKK-UHFFFAOYSA-N

InChI

1S/C6H6N2O/c7-6(9)5-3-1-2-4-8-5/h1-4H,(H2,7,9)

SMILES string

NC(=O)c1ccccn1

assay

98%

mp

110 °C (dec.) (lit.)

functional group

amide

Quality Level

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Application

以吡啶酰胺为模板制备分子印迹聚合物 。在一项研究中,吡啶酰胺被用于评估吡啶酰胺从HClO 4 中的铬(III) - 吡啶酰胺络合物中释放的动力学和机理。

Biochem/physiol Actions

吡啶酰胺是大鼠胰岛细胞核多聚(ADP-核糖)合成酶的潜在抑制剂 。吡啶酰胺充当二齿配体并与镧系元素硝酸盐,硫氰酸盐和高氯酸盐形成配合物

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Manuela Jörg et al.
ChemMedChem, 16(1), 216-233 (2020-08-28)
This study investigated the structure-activity relationships of 4-phenylpyridin-2-one and 6-phenylpyrimidin-4-one M1 muscarinic acetylcholine receptor (M1 mAChRs) positive allosteric modulators (PAMs). The presented series focuses on modifications to the core and top motif of the reported leads, MIPS1650 (1) and MIPS1780
Protection by picolinamide, a novel inhibitor of poly (ADP-ribose) synthetase, against both streptozotocin-induced depression of proinsulin synthesis and reduction of NAD content in pancreatic islets.
H Yamamoto et al.
Biochemical and biophysical research communications, 95(1), 474-481 (1980-07-16)
Lanthanide complexes with picolinamide.
Condorelli G, et al.
J. Inorg. Nucl. Chem., 36(12), 3763-3766 (1974)
Mark Turlington et al.
Journal of medicinal chemistry, 56(20), 7976-7996 (2013-09-21)
Positive allosteric modulators (PAMs) of metabotropic glutamate receptor 5 (mGlu5) represent a promising therapeutic strategy for the treatment of schizophrenia. Both allosteric agonism and high glutamate fold-shift have been implicated in the neurotoxic profile of some mGlu5 PAMs; however, these
Hemant Bhutani et al.
Journal of pharmaceutical and biomedical analysis, 39(5), 892-899 (2005-06-28)
Rifampicin and isoniazid are known to interact with each other in solid formulation environment to yield isonicotinyl hydrazone (HYD). In earlier studies, this reaction was indicated to be catalyzed by pyrazinamide and ethambutol hydrochloride, the two other co-drugs present in

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