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    • 10. 发明授权
    • Process for identifying RXR-receptor-agonist compounds
    • 识别RXR-受体 - 激动剂化合物的方法
    • US5696104A
    • 1997-12-09
    • US665866
    • 1996-06-19
    • Michel DemarchezAndre Jomard
    • Michel DemarchezAndre Jomard
    • A61K49/00A61K31/59A61K31/19A61K31/20
    • A61K49/0006
    • The present invention relates to a process for identifying RXR-agonist molecules, characterized in that it comprises the following steps: (i) a sufficient amount of a compound which is an active ligand for at least one receptor of the super-family of steroidal/thyroidal receptors, other than an RXR-receptor-specific ligand, and which can heterodimerize with the RXRs, is applied topically to a part of the skin of a mammal, (ii) a molecule capable of having an RXR-agonist activity is administered systemically or topically to this same mammal, or to this same part of the skin of the mammal, before, during or after step (i), and (iii) the response on that part of the skin of the mammal thus treated is evaluated.
    • 本发明涉及一种鉴定RXR激动剂分子的方法,其特征在于其包括以下步骤:(i)足量的化合物,其为甾体/超氧化物歧化酶超家族的至少一种受体的活性配体, 不同于RXR受体特异性配体的甲状腺受体,可与RXR异源二聚化,局部应用于哺乳动物皮肤的一部分,(ii)能够具有RXR-激动剂活性的分子被全身施用 或局部给予该相同的哺乳动物,或在步骤(i)之前,期间或之后的哺乳动物皮肤的相同部分,和(iii)评估对该治疗的哺乳动物的该部分皮肤的反应。