2007
DOI: 10.1016/j.bmcl.2006.10.071
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Synthesis and SAR of potent and selective androgen receptor antagonists: 5,6-Dichloro-benzimidazole derivatives

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Cited by 35 publications
(14 citation statements)
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“…JNJ-37654032 was identified as part of an extended program to discover nonsteroidal, orally bioavailable small molecules with anabolic effects on muscle and minimal androgenic effects on prostate [17][18][19]. It is one of the enantiomers of a benzimidazole analog reported previously ( Fig.…”
Section: In Vitro Propertiesmentioning
confidence: 97%
See 1 more Smart Citation
“…JNJ-37654032 was identified as part of an extended program to discover nonsteroidal, orally bioavailable small molecules with anabolic effects on muscle and minimal androgenic effects on prostate [17][18][19]. It is one of the enantiomers of a benzimidazole analog reported previously ( Fig.…”
Section: In Vitro Propertiesmentioning
confidence: 97%
“…Our laboratory has identified several distinct chemical classes of nonsteroidal SARM [13][14][15][16][17][18][19][20][21][22][23]. These compounds were identified by screening in orchidectomized immature male rats.…”
Section: Introductionmentioning
confidence: 99%
“…Our laboratory has identified several distinct chemical classes of nonsteroidal SARM [15][16][17][18][19][20][21][22][23][24][25]. These compounds were identified by screening in orchidectomized immature male rats.…”
Section: Introductionmentioning
confidence: 99%
“…Although all the positions of the benzimidazole ring can be substituted with a variety of chemical entities, most of the biologically active benzimidazole derivatives, obtained up to now, have functional groups at 1‐, 2‐, and/or 5‐ (or 6‐) positions . Literature survey reveals that 5,6‐dichlorobenzimidazole derivatives are very important for their pharmacological activities like antitumor, antioxidant, antiurease, antiparasitic, and antilipase (Scheme ) .…”
Section: Introductionmentioning
confidence: 99%