14 articles for Y Demizu
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
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
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
Design and synthesis of estrogen receptor ligands with a 4-heterocycle-4-phenylheptane skeleton.

Nagasaki University
Efficient synthesis of a multi-substituted diphenylmethane skeleton as a steroid mimetic.

National Institute of Health Sciences