000 01425 a2200397 4500
005 20250514184313.0
264 0 _c20041222
008 200412s 0 0 eng d
022 _a0960-894X
024 7 _a10.1016/j.bmcl.2004.02.053
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHuang, Charles Q
245 0 0 _aDesign, synthesis, and SAR of 2-dialkylamino-4-arylpyrimidines as potent and selective corticotropin-releasing factor(1) (CRF(1)) receptor antagonists.
_h[electronic resource]
260 _bBioorganic & medicinal chemistry letters
_cMay 2004
300 _a2083-6 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAnimals
650 0 4 _aCHO Cells
650 0 4 _aCricetinae
650 0 4 _aDrug Design
650 0 4 _aPyrimidines
_xchemical synthesis
650 0 4 _aRats
650 0 4 _aReceptors, Corticotropin-Releasing Hormone
_xantagonists & inhibitors
650 0 4 _aStructure-Activity Relationship
650 0 4 _aCRF Receptor, Type 1
700 1 _aGrigoriadis, Dimitri E
700 1 _aLiu, Zhengyu
700 1 _aMcCarthy, James R
700 1 _aRamphal, John
700 1 _aWebb, Thomas
700 1 _aWhitten, Jeffrey P
700 1 _aXie, Michael Y
700 1 _aChen, Chen
773 0 _tBioorganic & medicinal chemistry letters
_gvol. 14
_gno. 9
_gp. 2083-6
856 4 0 _uhttps://doi.org/10.1016/j.bmcl.2004.02.053
_zAvailable from publisher's website
999 _c14794589
_d14794589