000 01550 a2200433 4500
005 20250515091634.0
264 0 _c20080303
008 200803s 0 0 eng d
022 _a1464-3405
024 7 _a10.1016/j.bmcl.2007.09.063
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTao, Zhi-Fu
245 0 0 _aMacrocyclic ureas as potent and selective Chk1 inhibitors: an improved synthesis, kinome profiling, structure-activity relationships, and preliminary pharmacokinetics.
_h[electronic resource]
260 _bBioorganic & medicinal chemistry letters
_cDec 2007
300 _a6593-601 p.
_bdigital
500 _aPublication Type: Comparative Study; Journal Article
650 0 4 _aAnimals
650 0 4 _aCatalysis
650 0 4 _aCheckpoint Kinase 1
650 0 4 _aHeLa Cells
650 0 4 _aHumans
650 0 4 _aMacrocyclic Compounds
_xchemical synthesis
650 0 4 _aMice
650 0 4 _aProtein Kinase Inhibitors
_xchemical synthesis
650 0 4 _aProtein Kinases
_xpharmacokinetics
650 0 4 _aStructure-Activity Relationship
650 0 4 _aUrea
_xchemical synthesis
700 1 _aChen, Zehan
700 1 _aBui, Mai-Ha
700 1 _aKovar, Peter
700 1 _aJohnson, Eric
700 1 _aBouska, Jennifer
700 1 _aZhang, Haiying
700 1 _aRosenberg, Saul
700 1 _aSowin, Thomas
700 1 _aLin, Nan-Horng
773 0 _tBioorganic & medicinal chemistry letters
_gvol. 17
_gno. 23
_gp. 6593-601
856 4 0 _uhttps://doi.org/10.1016/j.bmcl.2007.09.063
_zAvailable from publisher's website
999 _c17456531
_d17456531