AR-C 118925XX structure
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Common Name | AR-C 118925XX | ||
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CAS Number | 216657-60-2 | Molecular Weight | 537.592 | |
Density | 1.5±0.1 g/cm3 | Boiling Point | N/A | |
Molecular Formula | C28H23N7O3S | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of AR-C 118925XXAR-C118925XX is a selective P2Y2 receptor antagonist. AR-C118925XX inhibits ATP-induced IL-6 production and phosphorylation of p38. AR-C118925XX also inhibits Bleomycin (HY-108345)-induced dermal fibrosis in mice. AR-C118925XX also inhibits ATP-induced tumor growth[1][2]. |
Name | AR-C118925XX |
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Synonym | More Synonyms |
Description | AR-C118925XX is a selective P2Y2 receptor antagonist. AR-C118925XX inhibits ATP-induced IL-6 production and phosphorylation of p38. AR-C118925XX also inhibits Bleomycin (HY-108345)-induced dermal fibrosis in mice. AR-C118925XX also inhibits ATP-induced tumor growth[1][2]. |
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Related Catalog | |
Target |
P2Y2 Receptor |
In Vivo | AR-C118925XX (i.p.) 抑制 Bleomycin 对小鼠真皮厚度的增加[1]。 |
References |
Density | 1.5±0.1 g/cm3 |
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Molecular Formula | C28H23N7O3S |
Molecular Weight | 537.592 |
Exact Mass | 537.158325 |
LogP | 4.78 |
Index of Refraction | 1.756 |
AR-C118925XX |
2-Furancarboxamide, 5-[[5-(2,8-dimethyl-5H-dibenzo[a,d]cyclohepten-5-yl)-3,4-dihydro-2-oxo-4-thioxo-1(2H)-pyrimidinyl]methyl]-N-1H-tetrazol-5-yl- |
5-{[5-(2,8-Dimethyl-5H-dibenzo[a,d][7]annulen-5-yl)-2-oxo-4-thioxo-3,4-dihydro-1(2H)-pyrimidinyl]methyl}-N-(1H-tetrazol-5-yl)-2-furamide |