CAS: 681136-29-8; Jnj-1661010

该化合物是一种化学化合物,其结构复杂,包括一个管状环和硫氨酸酯混合物;该化合物通常具有与管状子衍生物和硫氨酸化合物有关的特性,例如潜在的生物活动和与各种生物目标互动的能力;它可能具有有机溶剂中中溶性以及水溶解性有限等特征,许多有机化合物都常见. 苯基化合物的存在表明有芳香相互作用的潜力,可能影响其再活性和结合性.此外,这种性质的化合物往往因其药用特性而受到调查,包括抗微生物,抗炎炎炎,或抗癌活动. 熔点,沸点和光谱数据等具体特征需要经验性测量或文献参考,以精确值.

结构式图片

上下游产品

1-(3-phenyl-[1,2,4]thiadiazol-5-yl)piperazine phenyl is°Cyanate 4-(3-Chloro-[1,2,4]thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide phenylboronic acid

合成工艺路线路线简述

  • 合成目标产物 Jnj 1661010 主要起始原料 3-Phenyl-5-Piperazino-1,2,4-Thiadiazole And Phenyl Isocyanate
  • (文献来源)合成步骤主要原料 3-Phenyl-5-Piperazino-1,2,4-Thiadiazole 和 Phenyl Isocyanate
📜4-(3-Chloro-[1,2,4]Thiadiazol-5-yl)-Piperazine-1-Carboxylic Acid Phenylamide,苯硼酸 反应生成 N-苯基-4-(3-苯基-1,2,4-噻二唑-5-基)-1-哌嗪甲酰胺
参考文献:N-Heteroarylpiperazinyl Ureas As Modulators Of Fatty Acid Amide Hydrolase
标题:N-Heteroarylpiperazinyl Ureas As Modulators Of Fatty Acid Amide Hydrolase
摘要:描述了某些n-杂环芳基哌嗪基脲化合物,这些化合物可用作faah抑制剂.这些化合物可以用于制备药物组合物,并用于治疗由脂肪酰胺水解酶(Faah)活性介导的疾病状态,紊乱和情况的方法.因此,这些化合物可以用于治疗焦虑,疼痛,炎症,睡眠障碍,进食障碍或运动障碍(如多发性硬化症).

海关参考信息

专利信息


专利号:US-12194020-B2
优先权日:2017-12-22
标 题:Reversing baldness through cannabinoid receptor activation
发明人:POSTREL RICHARD
权利人:POSTREL RICHARD
摘要:This invention reverses male pattern baldness by shocking dormant hair follicles out of their androgen induced hibernation phase back to the active hair-growing anagenic phase. The invention integrates two functions: 1) It blocks synthesis of compounds holding the follicles in the telogenic/hibernating phase and 2) It stimulates synthesis of compounds animating the hair-growing/anagenic phase in the follicular activity cycle. One preferred embodiment comprises an enzyme inhibitor blocking the conversion of testosterone to dihydrotestosterone (DHT), a flavonoid simultaneously increasing synthesis of prostaglandins alternative to prostaglandin D2, and a selected cannabinoid compound stimulating restore the hair follicle to its normal growth cycle. This novel trimodal therapy restores the hair follicles to their normal cycling processes and maintains these restorative properties so long as this rebalance in maintained.

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献


1: Karbarz MJ, Luo L, Chang L, Tham CS, Palmer JA, Wilson SJ, Wennerholm ML, Brown SM, Scott BP, Apodaca RL, Keith JM, Wu J, Breitenbucher JG, Chaplan SR, Webb M. Biochemical and biological properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a mechanism-based inhibitor of fatty acid amide hydrolase. Anesth Analg. 2009 Jan;108(1):316-29. doi: 10.1213/ane.0b013e31818c7cbd.

合成参考文献


参考文献:10.1016/j.bmcl.2011.06.096
摘要:Otrubova K, Ezzili C, Boger DL. The discovery and development of inhibitors of fatty acid amide hydrolase (FAAH). Bioorganic & Medicinal Chemistry Letters. 2011 Aug;21(16):4674–85. doi: 10.1016/j.bmcl.2011.06.096.
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