UAMC-NH2isaderivativeofUAMCwithaaminobutoxygroup,whichisusefultosynthesieUAMCconjugate.UAMC-,alsoknownasSP-,isanovelpotentandselectiveinhibitoroffibroblastactivationprotein(fap),displayinglownanomolarinhibitorypotencyandhighselectivityagainsttherelateddipeptidylpeptidases(dpps)dppiv,dpp9,dppii,andprolyloligopeptidase(prep).
UAMC-NH2是UAMC的衍生物，具有氨基丁氧基，可用于合成UAMC1缀合物。UAMC-，也称为SP-，是一种新型的成纤维细胞激活蛋白（fap）的强效选择性抑制剂，对相关的二肽基肽酶（dpps）dppiv、dpp9、dppii和脯氨酰寡肽酶（prep）显示出低纳摩尔抑制力和高选择性。
Name:UAMC-NH2CAS#:UnknownChemicalFormula:C21H23F2N5O3ExactMass:.MolecularWeight:.ElementalAnalysis:C,58.46;H,5.37;F,8.81;N,16.23;O,11.12
Thisproductisnotinstock,whichmaybeavailablebycustomsynthesis
陕西新研博美UAMC-NH2