16 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Synthesis and evaluation of raloxifene derivatives as a selective estrogen receptor down-regulator.
National Institute of Health Sciences
Effects of alkyl side chains and terminal hydrophilicity on vitamin D receptor (VDR) agonistic activity based on the diphenylpentane skeleton.
National Institute of Health Sciences
Structural development of stabilized helical peptides as inhibitors of estrogen receptor (ER)-mediated transcription.
National Institute of Health Sciences
Synthesis and evaluation of tamoxifen derivatives with a long alkyl side chain as selective estrogen receptor down-regulators.
National Institute of Health Sciences
Structural development of stapled short helical peptides as vitamin D receptor (VDR)-coactivator interaction inhibitors.
National Institute of Health Sciences
Development of stapled short helical peptides capable of inhibiting vitamin D receptor (VDR)-coactivator interactions.
National Institute of Health Sciences
(2S,2'R)-analogue of LG190178 is a major active isomer.
National Institute of Health Sciences
Design, synthesis and X-ray crystallographic study of new nonsecosteroidal vitamin D receptor ligands.
National Institute of Health Sciences
Structure-activity relationship study of PROTACs against hematopoietic prostaglandin D
National Institute of Health Sciences
Synthesis of digalactosyl diacylglycerols and their structure-inhibitory activity on human lanosterol synthase.
National Institute of Health Sciences
Discovery of a Highly Potent and Selective Degrader Targeting Hematopoietic Prostaglandin D Synthase via In Silico Design.
National Institute of Health Sciences
Synthesis of Norgestomet and its 17β-isomer and evaluation of their agonistic activities against progesterone receptor.
National Institute of Health Sciences
Development of a Hematopoietic Prostaglandin D Synthase-Degradation Inducer.
National Institute of Health Sciences
Structural development of non-secosteroidal vitamin D receptor (VDR) ligands without any asymmetric carbon.
National Institute of Health Sciences
Development of Protein Degradation Inducers of Androgen Receptor by Conjugation of Androgen Receptor Ligands and Inhibitor of Apoptosis Protein Ligands.
National Institute of Health Sciences