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CAS | 172889-26-8 |
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Couple Type | Inhibitor |
Purity | ≥98% (TLC) |

Alternative Name | AG1879, 4-Amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine |
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CAS | 172889-27-9 |
Couple Type | Inhibitor |
Purity | ≥98% (TLC) |
pp242 . hydrate
ENZ-CHM132
Inhibitor of both mTORC1 and mTORC2. Induces cell death in human and murine leukemia cells.

Alternative Name | PP-242, 2-[4-Amino-1-(1-methylethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-1H-indol-5-ol, 2-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)-1H-indol-5-ol |
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CAS | 1092351-67-1 |
Couple Type | Inhibitor |
Purity | ≥99% (HPLC) |

Purity | ≥98% |
---|

Alternative Name | Peroxisome proliferator activated receptor α |
---|---|
Application | Gel Shift, IP, WB |
Host | Mouse |
Isotype | IgG2b |
Species Reactivity | Human, Mouse, Rat |

Alternative Name | Peroxisome proliferator activated receptor γ2 |
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Application | FUNC, Gel Supershift, ICC, IHC, WB |
Host | Rabbit |
Species Reactivity | Mouse |

Alternative Name | 1-Hydroxy-4-phosphono-oxy-2,2,6,6-tetramethylpiperidine . HCl |
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Purity | ≥99% (EPR) |

Alternative Name | IGF-IR Inhibitor, N-(5-Chloro-2-methoxyphenyl)-N’-(2-methyl-4-quinolinyl)urea |
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CAS | 196868-63-0 |
Couple Type | Inhibitor |
Purity | ≥98% (HPLC (UV)) |

CAS | 92623-83-1 |
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Couple Type | Inhibitor |
Purity | ≥98% (TLC) |

Alternative Name | 2-(Cyclohexylcarbonyl)-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isoquinolin-4-one |
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CAS | 55268-74-1 |
Couple Type | Activator |
Purity | ≥98% (HPLC) |

Alternative Name | U-14975 |
---|---|
CAS | 1434-54-4 |
Couple Type | Activator, Ligand |
Purity | ≥99% (HPLC) |

Application | ELISA, ICC, IHC (PS), WB |
---|---|
Host | Mouse |
Isotype | IgG1 |
Species Reactivity | Human, Mouse, Primate, Rat |

Application | ELISA, ICC, WB |
---|---|
Host | Mouse |
Isotype | IgG1 |
Species Reactivity | Human, Monkey, Mouse, Rat |

Alternative Name | Celastrol methyl ester |
---|---|
CAS | 1258-84-0 |
Couple Type | Inhibitor |
Purity | ≥97% (HPLC) |
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