CNS 5161 | 160754-76-7

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: CNS 5161
• 英文别名: N-(2-chloro-5-methylthiophenyl)-N'-(3-methylthiophenyl)-N'-methylguanidine；N'-[2-chloro-5-(methylthio)phenyl]-N-methyl-N-[3-(methylthio)phenyl]-guanidine；N-(2-chloro-5-methylthiophenyl)-N'-(3-methylthiophenyl)-N'-methyl-guanidine；3-(2-Chloro-5-(methylthio)phenyl)-1-methyl-1-(3-(methylthio)phenyl)guanidine；2-(2-chloro-5-methylsulfanylphenyl)-1-methyl-1-(3-methylsulfanylphenyl)guanidine
• CAS: 160754-76-7
• 化学式: C₁₆H₁₈ClN₃S₂
• 分子量: 351.924
• InChiKey: JHVHEDNLONERHY-UHFFFAOYSA-N

物化性质

• 沸点：
  465.4±55.0 °C(Predicted)
• 密度：
  1.25±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  22
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  92.2
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  2-氯-5-(甲硫基)苯甲酸 在 aluminum (III) chloride 、 potassium tert-butylate 、 三乙胺 作用下， 以 乙醇 、 氯苯 、 甲苯 、 叔丁醇 为溶剂， 反应 9.08h， 生成 CNS 5161
  参考文献：
  名称：

  WO2006/136846

  摘要：

  公开号：

文献信息

• [EN] (R)-4-((4-((4-(TETRAHYDROFURAN-3-YLOXY)BENZO[D]ISOXAZOL-3-YLOXY)METHYL)PIPERIDIN-1-YL)METHYL)TETRAHYDRO-2H-PYRAN-4-OL, A PARTIAL AGONIST OF 5-HT4 RECEPTORS<br/>[FR] (R)-4-((4-((4-(TÉTRAHYDROFURAN-3-YLOXY)BENZO[D]ISOXAZOL-3-YLOXY)MÉTHYL) PIPÉRIDIN-1-YL)MÉTHYL)TÉTRAHYDRO-2H-PYRAN-4-OLE, AGONISTE PARTIEL DES RÉCEPTEURS 5-HT4
  申请人：PFIZER

  公开号：WO2011101774A1

  公开（公告）日：2011-08-25

  (R)-4-((4-((4-(tetrahydrofuran-3-yloxy)benzo[d]isoxazol-3- yloxy)methyl)piperidin-1-yl)methyl)tetrahydro-2H-pyran-4-ol and its use in treating neurodegenerative disorders, is described herein.

  (R)-4-((4-((4-(四氢呋喃-3-氧基)苯并[d]异噁唑-3-氧基)甲基)哌啶-1-基)甲基)四氢-2H-吡喃-4-醇及其在治疗神经退行性疾病中的用途在此描述。
• [EN] INDOLE COMPOUNDS AND METHODS FOR TREATING VISCERAL PAIN<br/>[FR] COMPOSÉS D'INDOLE ET PROCÉDÉS DE TRAITEMENT DE LA DOULEUR VISCÉRALE
  申请人：NEURAXON INC

  公开号：WO2009062319A1

  公开（公告）日：2009-05-22

  The invention features methods of treating visceral pain or a condition in a mammal caused by the action of nitric oxide synthase (NOS) or by the action of serotonin 5HT1D/1B receptors, by administering to a patient in need thereof a therapeutically effective amount of an indole compound of Formula (I), or a pharmaceutically acceptable salt or prodrug thereof. The methods of the invention may further comprise the administration of additional therapeutic agent. The invention also features new compounds of Formula (I), pharmaceutical compositions thereof, and methods of resolving enantiomeric mixtures.

  该发明涉及治疗哺乳动物体内因一氧化氮合酶（NOS）或5-羟色胺受体5HT1D/1B的作用引起的内脏疼痛或疾病的方法，通过向需要治疗的患者施用式(I)的吲哚化合物的治疗有效量，或其药学上可接受的盐或前药。该发明的方法还可以包括额外治疗剂的施用。该发明还涉及式(I)的新化合物、其药物组合物以及解决对映体混合物的方法。
• 3,5 - SUBSTITUTED INDOLE COMPOUNDS HAVING NOS AND NOREPINEPHRINE REUPTAKE INHIBITORY ACTIVITY
  申请人：Annedi Subhash C.

  公开号：US20090131503A1

  公开（公告）日：2009-05-21

  The present invention relates to novel 3,5-substituted indole compounds of Formula (I) having nitric oxide synthase (NOS) inhibitory activity together with inhibitory activity at the norepinephrine transporter (NET), to pharmaceutical and diagnostic compositions containing them, and to their medical use.

  本发明涉及具有一氧化氮合酶（NOS）抑制活性以及对去甲肾上腺素转运蛋白（NET）具有抑制活性的新型3,5-取代吲哚化合物（I）的公式，以及含有它们的药用和诊断组合物，以及它们的医疗用途。
• Substituted benzimidazole compounds with dual NOS inhibitory activity and mu opioid agonist activity
  申请人：Renton Paul

  公开号：US20080214613A1

  公开（公告）日：2008-09-04

  The present invention relates to benzimidazole compounds having dual nitric oxide synthase (NOS) inhibitory activity and agonist activity at the mu-opioid receptor, to pharmaceutical and diagnostic compositions containing them, and to their medical use, particularly as compounds for the treatment or prevention of chronic pain, acute pain, migraine, and neuropathic pain.

  本发明涉及具有双重一氧化氮合酶（NOS）抑制活性和μ-阿片受体激动活性的苯并咪唑化合物，以及包含它们的药物和诊断组合物，以及它们的医学用途，特别是作为治疗或预防慢性疼痛、急性疼痛、偏头痛和神经病性疼痛的化合物。
• AMINOCYCLOBUTANE DERIVATIVES, METHOD FOR PREPARING SAME AND THE USE THEREOF AS DRUGS
  申请人：PIERRE FABRE MEDICAMENT

  公开号：US20150315132A1

  公开（公告）日：2015-11-05

  The present inventions concerns derivatives of aminocyclobutane, particularly as NMDA receptor antagonists, their application in human therapy and their method of preparation. These compounds correspond to the general formula (1): wherein: X 1 represents a hydrogen atom or fluorine atom; X 2 is a hydrogen atom or fluorine atom or chlorine atom; R1 represents a hydrogen atom or fluorine atom or chlorine atom or methyl group or methoxy group or cyano group; R2 represents independently or together a methyl group or ethyl group.

  目前的发明涉及氨基环丁烷的衍生物，特别是作为NMDA受体拮抗剂，在人类治疗中的应用以及它们的制备方法。这些化合物对应于一般式（1）：其中：X1代表氢原子或氟原子；X2是氢原子或氟原子或氯原子；R1代表氢原子或氟原子或氯原子或甲基基团或甲氧基团或氰基；R2独立或一起代表甲基基团或乙基基团。