추천 제품
Quality Level
분석
≥98% (HPLC)
양식
powder
색상
white to tan
solubility
DMSO: ≥20 mg/mL
저장 온도
2-8°C
SMILES string
CON(C)C(=O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)c2cc3cc(Cl)ccc3[nH]2
InChI
1S/C21H22ClN3O4/c1-25(29-2)21(28)19(26)17(10-13-6-4-3-5-7-13)24-20(27)18-12-14-11-15(22)8-9-16(14)23-18/h3-9,11-12,17,19,23,26H,10H2,1-2H3,(H,24,27)/t17-,19+/m0/s1
InChI key
WEQLRDLTRCEUHG-PKOBYXMFSA-N
관련 카테고리
애플리케이션
CP-316819 has been used as a positive control to study the inhibitory activity against glycogen phosphorylase in vitro.
생화학적/생리학적 작용
CP-316819 belongs to the family of indole-2-carboxamide series of phosphorylase inhibitors. It has an ability to regulate interaction of glycogen targeting subunit (GL) 16mer peptide with phosphorylase a.
CP-316819 is a glycogen phosphorylase inhibitor
CP-316819 is a potent glycogen phosphorylase inhibitor. (IC50 = 40 nM against human liver GPα.) Under low glucose conditions, CP-316819 facilitates glycogen utilization in the brain, prevents neuronal cell death and maintains brain electrical currents.
법적 정보
Sold for research purposes under agreement from Pfizer Inc.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Oral
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
The hepatic PP1 glycogen-targeting subunit interaction with phosphorylase a can be blocked by C-terminal tyrosine deletion or an indole drug
Kelsall LR, et al.
Febs Letters, 581(24), 4749-4753 (2007)
Synthesis and Antidiabetic Activity of Thiazolo [2, 3-f] Purine Derivatives and Their Analogs
Spasov AA, et al.
Pharmaceutical Chemistry Journal, 51(7), 533-539 (2017)
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