Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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.
パッケージサイズ | 在庫状況 | 単価(税別) |
---|---|---|
25 mg | 約10-14 週間 | ¥ 693,000 |
50 mg | 約10-14 週間 | ¥ 913,500 |
100 mg | 約10-14 週間 | ¥ 1,262,500 |
説明 | 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. |
別名 | AP22161, G7VE62573J, UNII-G7VE62573J, SCHEMBL7243003, AP 22161 |
分子量 | 577.67 |
分子式 | C32H39N3O7 |
CAS No. | 268741-42-0 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
You can also refer to dose conversion for different animals. 詳細
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AP-22161 268741-42-0 AP22161 G7VE62573J UNII-G7VE62573J SCHEMBL 7243003 SCHEMBL7243003 AP 22161 SCHEMBL-7243003 Inhibitor inhibitor inhibit