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AP-22161 selectively binds the Src SH2 domain by targeting highly conserved phosphotyrosine binding to cysteine residues in the pocket. AP-22161 selectively inhibits Src SH2 binding and can be used to inhibit osteoclast absorption.
AP-22161 selectively binds the Src SH2 domain by targeting highly conserved phosphotyrosine binding to cysteine residues in the pocket. AP-22161 selectively inhibits Src SH2 binding and can be used to inhibit osteoclast absorption.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
25 mg | ¥ 21,600 | 10-14周 | |
50 mg | ¥ 28,800 | 10-14周 | |
100 mg | ¥ 37,500 | 10-14周 |
产品描述 | AP-22161 selectively binds the Src SH2 domain by targeting highly conserved phosphotyrosine binding to cysteine residues in the pocket. AP-22161 selectively inhibits Src SH2 binding and can be used to inhibit osteoclast absorption. |
别名 | UNII-G7VE62573J, SCHEMBL7243003, G7VE62573J, AP22161, AP 22161 |
分子量 | 577.67 |
分子式 | C32H39N3O7 |
CAS No. | 268741-42-0 |
密度 | no data available |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
版权所有©2015-2024 TargetMol Chemicals Inc.保留所有权利.
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