Scaffold hopping of fused piperidine-type NK3 receptor antagonists to reduce environmental impact

被引:1
|
作者
Yamamoto, Koki [1 ]
Inuki, Shinsuke [1 ]
Ohno, Hiroaki [1 ]
Oishi, Shinya [1 ]
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan
关键词
Environmental impact; Fezolinetant; GnRH; NK3; receptor; Scaffold hopping; WATER TREATMENT-PLANT; HUMAN NEUROKININ-3 RECEPTOR; PHARMACEUTICALS; KISSPEPTIN; SECRETION; HORMONES; FATE; GNRH; PHOTODEGRADATION; IDENTIFICATION;
D O I
10.1016/j.bmc.2019.03.059
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neurokinin-3 receptor (NK3R) plays a pivotal role in the release of gonadotropin-releasing hormone in the hypothalamus-pituitary-gonadal (HPG) axis. To develop novel NK3R antagonists with less environmental toxicity, a series of heterocyclic scaffolds for the triazolopiperazine substructure in an NK3R antagonist fezoli-netant were designed and synthesized. An isoxazolo[3,4-c]piperidine derivative exhibited moderate NK3R antagonistic activity and favorable properties that were decomposable under environmental conditions.
引用
收藏
页码:2019 / 2026
页数:8
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    Rosenblum, Stuart B.
    Kozlowski, Joseph A.
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    Panocka, I
    Massi, M
    Lapo, I
    Swiderski, T
    Kowalczyk, M
    Sadowski, B
    PEPTIDES, 2001, 22 (07) : 1037 - 1042
  • [38] Novel histamine H3 receptor antagonists based on the 4-[(1H-imidazol-4-yl)methyl]piperidine scaffold
    Vaccaro, WD
    Sher, R
    Berlin, M
    Shih, NY
    Aslanian, R
    Schwerdt, JH
    McCormick, KD
    Piwinski, JJ
    West, RE
    Anthes, JC
    Williams, SM
    Wu, RL
    She, HS
    Rivelli, MA
    Mutter, JC
    Corboz, MR
    Hey, JA
    Favreau, L
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (02) : 395 - 399
  • [39] In vitro and in vivo comparison of two non-peptide tachykinin NK3 receptor antagonists: Improvements in efficacy achieved through enhanced brain penetration or altered pharmacological characteristics
    Dawson, Lee A.
    Langmead, Christopher J.
    Dada, Adeshola
    Watson, Jeannette M.
    Wu, Zining
    de la Flor, Raul
    Jones, Gareth A.
    Cluderay, Jane E.
    Southam, Eric
    Murkitt, Graham S.
    Hill, Mark D.
    Jones, Declan N. C.
    Davies, Ceri H.
    Hagan, Jim J.
    Smith, Paul W.
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2010, 627 (1-3) : 106 - 114
  • [40] Hyperresponsiveness to the tachykinin NK1 receptor agonist [SAR9, Met(O2)11]SP after IL-1β pretreatment and passive sensitization of human isolated bronchi:: Effects of tachykinin NK2 and NK3 receptor antagonists.
    Vincent, F
    Naline, E
    Molimard, M
    Daoui, S
    Vilain, P
    Emonds-Alt, X
    Advenier, C
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 159 (03) : A281 - A281