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[3,3']bi[1,2,4]triazinyl | 855244-43-8

中文名称
——
中文别名
——
英文名称
[3,3']bi[1,2,4]triazinyl
英文别名
3,3'-BI-1,2,4-Triazine;3-(1,2,4-triazin-3-yl)-1,2,4-triazine
[3,3']bi[1,2,4]triazinyl化学式
CAS
855244-43-8
化学式
C6H4N6
mdl
MFCD09702453
分子量
160.138
InChiKey
KRWGPAQDPHZSRD-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    452.3±28.0 °C(Predicted)
  • 密度:
    1.403±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.8
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    77.3
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 草酸醛 作用下, 生成 [3,3']bi[1,2,4]triazinyl
    参考文献:
    名称:
    Dedichen, 1936, # 5, p. 26
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • COMPLEXES FOR USE IN METATHESIS REACTIONS
    申请人:Hoveyda Amir H.
    公开号:US20120302710A1
    公开(公告)日:2012-11-29
    The present invention relates generally to metal complexes, methods for preparation and uses of the same.
    本发明涉及属配合物的一般性质,其制备方法以及其用途。
  • 1,2,4-TRIAZINE-4-AMINE DERIVATIVES
    申请人:Congreve Miles Stuart
    公开号:US20130029963A1
    公开(公告)日:2013-01-31
    According to the invention there is provided a compound of formula A1 which may be useful in the treatment of a condition or disorder ameliorated by the inhibition of the A 1 -A 2b or, particularly, the A 2a receptor wherein the compound of formula A1 has the structure, wherein, A represents Cy 1 or Het A ; Cy 1 represents a 5- to 14-membered aromatic, fully saturated or partially unsaturated carbocyclic ring system comprising one, two or three rings, which Cy 1 group is optionally substituted by one or more R 4a substituents; Het A represents a 5- to 14-membered heterocyclic group that may be aromatic, fully saturated or partially unsaturated, and which contains one or more heteroatoms selected from O, S and N, which heterocyclic group may comprise one, two or three rings and which HetA group is optionally substituted by one or more R4b substituents; B represents a Cy 2 or Het B ; Cy 2 represents a 3- to 10-membered aromatic, fully saturated or partially unsaturated carbocyclic ring system comprising one or two rings, which Cy 2 group is optionally substituted by one or more R 4c substituents; Het B represents a 3- to 10-membered heterocyclic group that may be aromatic, fully saturated or partially unsaturated, and which contains one or more heteroatoms selected from O, S and N, which heterocyclic group may comprise one or two rings and which Het B group is optionally substituted by one or more R 4d substituents.
    根据本发明提供了一种A1式化合物,该化合物可能有用于治疗通过抑制A1-A2bor,特别是A2a受体而改善的疾病或疾病状态,其中A1式化合物具有以下结构,其中A代表Cy1或HetA;Cy1代表一个5到14个成员的芳香族、完全饱和或部分不饱和的碳环状环系,包括一个、两个或三个环,该Cy1基团可以被一个或多个R4a取代;HetA代表一个5到14个成员的杂环基团,可能是芳香族、完全饱和或部分不饱和的,并且其中包含一个或多个从O、S和N中选择的杂原子,该杂环基团可以包括一个、两个或三个环,该HetA基团可以被一个或多个R4b取代;B代表Cy2或HetB;Cy2代表一个3到10个成员的芳香族、完全饱和或部分不饱和的碳环状环系,包括一个或两个环,该Cy2基团可以被一个或多个R4c取代;HetB代表一个3到10个成员的杂环基团,可能是芳香族、完全饱和或部分不饱和的,并且其中包含一个或多个从O、S和N中选择的杂原子,该杂环基团可以包括一个或两个环,该HetB基团可以被一个或多个R4d取代。
  • Vanilloid receptor ligands and their use in treatments
    申请人:Amgen Inc.
    公开号:EP1775295A1
    公开(公告)日:2007-04-18
    Compounds having the general structure formula (I) and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, bums, allergic skin reactions, pruritus, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders.
    具有通式(I)结构的化合物 以及含有它们的组合物,用于治疗急性、炎症性和神经性疼痛、牙痛、一般头痛、偏头痛、丛集性头痛、混合血管性和非血管性综合征、紧张性头痛、一般炎症、关节炎、风湿性疾病、骨关节炎、炎症性肠道疾病、炎症性眼部疾病、炎症性或不稳定型膀胱疾病、牛皮癣、伴有炎症成分的皮肤不适、慢性炎症、炎症性疼痛及相关的痛觉减退和痛觉过敏、神经性疼痛及相关的痛觉减退和痛觉过敏、糖尿病神经病变性疼痛、因痛症、交感神经维持性疼痛、失代偿综合征、哮喘、上皮组织损伤或功能障碍、单纯疱疹、呼吸道、泌尿生殖道、胃肠道或血管部位的内脏运动障碍、伤口、溃疡、十二指肠溃疡、腹泻、坏死剂引起的胃病变、毛发生长、血管运动性或过敏性鼻炎、支气管病变或膀胱病变。
  • 1,2,4-triazine-4-amine derivatives
    申请人:Heptares Therapeutics Limited
    公开号:US10988455B2
    公开(公告)日:2021-04-27
    According to the invention there is provided a compound of formula A1 which may be useful in the treatment of a condition or disorder ameliorated by the inhibition of the A1-A2b or, particularly, the A2a receptor wherein the compound of formula A1 has the structure, wherein, A represents Cy1 or HetA; Cy1 represents a 5- to 14-membered aromatic, fully saturated or partially unsaturated carbocyclic ring system comprising one, two or three rings, which Cy1 group is optionally substituted by one or more R4a substituents; HetA represents a 5- to 14-membered heterocyclic group that may be aromatic, fully saturated or partially unsaturated, and which contains one or more heteroatoms selected from O, S and N, which heterocyclic group may comprise one, two or three rings and which HetA group is optionally substituted by one or more R4b substituents; B represents a Cy2 or HetB; Cy2 represents a 3- to 10-membered aromatic, fully saturated or partially unsaturated carbocyclic ring system comprising one or two rings, which Cy2 group is optionally substituted by one or more R4c substituents; HetB represents a 3- to 10-membered heterocyclic group that may be aromatic, fully saturated or partially unsaturated, and which contains one or more heteroatoms selected from O, S and N, which heterocyclic group may comprise one or two rings and which HetB group is optionally substituted by one or more R4d substituents.
    根据本发明,提供了一种式 A1 的化合物,该化合物可用于治疗通过抑制 A1-A2b 或特别是 A2a 受体而改善的病症或紊乱,其中式 A1 的化合物具有如下结构,其中,A 代表 Cy1 或 HetA;Cy1 代表 5 至 14 元芳香族、完全饱和或部分不饱和的碳环系统,该碳环系统由一个、两个或三个环组成,该 Cy1 基团任选被一个或多个 R4a 取代基取代;HetA 代表 5 至 14 元杂环基团,可以是芳香族、完全饱和或部分不饱和的杂环基团,含有一个或多个选自 O、S 和 N 的杂原子,该杂环基团可以包括一个、两个或三个环,该 HetA 基团任选被一个或多个 R4b 取代基取代;B 代表 Cy2 或 HetB;Cy2 代表由一个或两个环组成的 3 至 10 元芳香族、完全饱和或 部分不饱和碳环系统,其 Cy2 基团可任选被一个或多个 R4c 取代基取代;HetB 代表 3 至 10 元杂环基团,可以是芳香族、完全饱和或部分不饱和的杂环基团,其中含有一个或多个选自 O、S 和 N 的杂原子,该杂环基团可包括一个或两个环,该 HetB 基团可任选被一个或多个 R4d 取代基取代。
  • US8546500B2
    申请人:——
    公开号:US8546500B2
    公开(公告)日:2013-10-01
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