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3-(3-(4-phenoxymethyl-benzyl)-isoxazol-5-yl)-pyridin-2-ylamine | 936340-59-9

中文名称
——
中文别名
——
英文名称
3-(3-(4-phenoxymethyl-benzyl)-isoxazol-5-yl)-pyridin-2-ylamine
英文别名
3-[3-[[4-(phenoxymethyl)phenyl]methyl]-1,2-oxazol-5-yl]pyridin-2-amine
3-(3-(4-phenoxymethyl-benzyl)-isoxazol-5-yl)-pyridin-2-ylamine化学式
CAS
936340-59-9
化学式
C22H19N3O2
mdl
——
分子量
357.412
InChiKey
AJADWUCBVIBVNM-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

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    74.2
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    manogepixN-甲基吗啉盐酸 、 sodium hydride 作用下, 以 1,4-二氧六环 、 mineral oil 为溶剂, 反应 2.4h, 生成 3-(3-(4-phenoxymethyl-benzyl)-isoxazol-5-yl)-pyridin-2-ylamine
    参考文献:
    名称:
    Gwt1 抑制剂 manogepix (APX001A) 类似物的合成和对隐球菌属的体外评估。
    摘要:
    Fosmanogepix (APX001) 是一流的前药分子,目前正处于侵袭性真菌感染的 2 期临床试验阶段。活性部分 manogepix (APX001A) 抑制新型真菌蛋白 Gwt1。Gwt1 催化 GPI 锚生物合成途径的早期步骤。在这里,我们描述了 292 种新的和 24 种先前描述的类似物的合成和评估,这些类似物是使用一系列高级中间体合成的,以允许快速模拟。与 manogepix 相比,几种化合物对新生隐球菌和格特隐球菌的抗真菌活性显着提高(8 到 32 倍)。进一步的体外表征确定了三种类似物,这些类似物具有与 manogepix 相似的初步安全性和体外特征,并且对隐球菌属具有优异的活性。
    DOI:
    10.1016/j.bmcl.2019.126713
点击查看最新优质反应信息

文献信息

  • PYRIDINE DERIVATIVES SUBSTITUTED BY HETEROCYCLIC RING AND PHOSPHONOAMINO GROUP, AND ANTI-FUNGAL AGENT CONTAINING SAME
    申请人:Tanaka Keigo
    公开号:US20090082403A1
    公开(公告)日:2009-03-26
    Anti-fungal agent having excellent anti-fungal action physicochemical properties including safety and water solubility. Compound represented by formula (I), or salt thereof: wherein R 1 represents hydrogen, halogen, amino, R 11 —NH— wherein R 11 represents C 1-6 alkyl, hydroxy C 1-6 alkyl, C 1-6 alkoxy C 1-6 alkyl, or C 1-6 alkoxycarbonyl C 1-6 alkyl, R 12 —(CO)—NH— wherein R 12 represents C 1-6 alkyl group or C 1-6 alkoxy C 1-6 alkyl, C 1-6 alkyl, hydroxy C 1-6 alkyl, cyano C 1-6 alkyl, C 1-6 alkoxy, or C 1-6 alkoxy C 1-6 alkyl or a phosphonoamino group; R 2 represents hydrogen, C 1-6 alkyl, amino, or a di C 1-6 alkylamino group or a phosphonoamino group; one of X and Y is nitrogen while the other is nitrogen or oxygen; ring A represents a 5- or 6-member heteroaryl ring or a benzene ring which may have a halogen atom or 1 or 2 C 1-6 alkyl groups; Z represents a single bond, a methylene group, an ethylene group, oxygen, sulfur, —CH 2 O—, —OCH 2 —, —NH—, —CH 2 NH—, —NHCH 2 —, —CH 2 S—, or —SCH 2 —; R 3 represents hydrogen or halogen or C 1-6 alkyl, C 3-8 cycloalkyl, C 6-10 aryl, a 5- or 6-member heteroaryl group or a 5- or 6-member nonaromatic heterocyclic group which may have 1 or 2 substituents; and R 4 represents hydrogen or halogen; provided that either R 1 or R 2 represents a phosphonoamino group.
    抗真菌剂具有优异的抗真菌作用物理化学性质,包括安全性和水溶性。化合物由式(I)表示,或其盐: 其中R1代表氢,卤素,氨基,R11—NH—其中R11代表C1-6烷基,羟基C1-6烷基,C1-6烷氧基C1-6烷基,或C1-6烷氧羰基C1-6烷基,R12—(CO)—NH—其中R12代表C1-6烷基或C1-6烷氧基C1-6烷基,C1-6烷基,羟基C1-6烷基,氰基C1-6烷基,C1-6烷氧基,或C1-6烷氧基C1-6烷基或磷酰氨基团;R2代表氢,C1-6烷基,氨基,或二C1-6烷基氨基团或磷酰氨基团;X和Y中的一个是氮,另一个是氮或氧;环A代表5-或6-成员杂芳基环或可能具有卤素原子或1或2个C1-6烷基基团的苯环;Z代表单键,亚甲基基团,乙烯基团,氧,硫,—CH2O—,—OCH2—,—NH—,—CH2NH—,—NHCH2—,—CH2S—,或—SCH2—;R3代表氢或卤素或C1-6烷基,C3-8环烷基,C6-10芳基,5-或6-成员杂芳基团或可能具有1或2个取代基的5-或6-成员非芳香杂环基;和R4代表氢或卤素;前提是R1或R2中的一个代表磷酰氨基团。
  • Heterocycles substituted pyridine derivatives and antifungal agent containing thereof
    申请人:Tanaka Keigo
    公开号:US20070105904A1
    公开(公告)日:2007-05-10
    An object of the present invention is to provide an antifungal agent which has excellent antifungal effects and is superior in terms of its physical properties, safety and metabolic stability. According to the present invention, there is disclosed a compound represented by the following formula (I), or a salt thereof: wherein R 1 represents a hydrogen atom, a halogen atom, an amino group, a C 1-6 alkyl group, a C 1-6 alkoxy group or a C 1-6 alkoxy C 1-6 alkyl group; R 2 represents a hydrogen atom, a C 1-6 alkyl group, an amino group or a di C 1-6 alkylamino group; one of X and Y is a nitrogen atom while the other is a nitrogen atom or an oxygen atom; ring A represents a 5- or 6-member heteroaryl ring or a benzene ring which may have a halogen atom, or 1 or 2 C 1-6 alkyl groups; Z represents a single bond, a methylene group, an ethylene group, an oxygen atom, a sulfur atom, —CH 2 O—, —OCH 2 —, —NH—, —CH 2 NH—, —NHCH 2 —, —CH 2 S—, or —SCH 2 —; R 3 represents a hydrogen atom, a halogen atom, a C 1-6 alkyl group, a C 3-8 cycloalkyl group, a C 6-10 aryl group, a 5- or 6-member heteroaryl group, or 5- or 6-member non-aromatic heterocyclic group which may have 1 or 2 substituents; and R 4 represents a hydrogen atom or a halogen atom.
    本发明的一个目的是提供一种具有优异的抗真菌效果并在其物理性质、安全性和代谢稳定性方面优越的抗真菌剂。根据本发明,公开了以下式(I)所代表的化合物或其盐: 其中R1代表氢原子、卤素原子、氨基、C1-6烷基、C1-6烷氧基或C1-6烷氧基C1-6烷基;R2代表氢原子、C1-6烷基、氨基或二C1-6烷基氨基中的一个;X和Y中的一个是氮原子,另一个是氮原子或氧原子;环A代表一个5-或6-成员杂芳基环或可能具有卤素原子、1个或2个C1-6烷基的苯环;Z代表一个单键、一个亚甲基基、一个乙烯基、一个氧原子、一个硫原子、-CH2O-、-OCH2-、-NH-、-CH2NH-、-NHCH2-、-CH2S-或-SCH2-;R3代表氢原子、卤素原子、C1-6烷基、C3-8环烷基、C6-10芳基、一个5-或6-成员杂芳基、或可能具有1个或2个取代基的5-或6-成员非芳香杂环基;R4代表氢原子或卤素原子。
  • HETEROCYCLES SUBSTITUTED PYRIDINE DERIVATIVES AND ANTIFUNGAL AGENT CONTAINING THEREOF
    申请人:TANAKA Keigo
    公开号:US20120029023A1
    公开(公告)日:2012-02-02
    An object of the present invention is to provide an antifungal agent which has excellent antifungal effects and is superior in terms of its physical properties, safety and metabolic stability. According to the present invention, there is disclosed a compound represented by the following formula (I), or a salt thereof: wherein R 1 , R 2 , X, Y, ring A, Z, R 3 and R 4 are as defined in the specification.
    本发明的目的是提供一种具有优异的抗真菌效果且在物理性质、安全性和代谢稳定性方面优越的抗真菌剂。根据本发明,公开了下式(I)所表示的化合物或其盐:其中R1、R2、X、Y、环A、Z、R3和R4如规范中所定义。
  • AGRICULTURAL COMPOSITION
    申请人:Matsuzaki Yuichi
    公开号:US20110201649A1
    公开(公告)日:2011-08-18
    Provided is an agricultural composition comprising a compound represented by the formula (I) or a salt thereof or a hydrate thereof, for controlling a plant disease due to a plant pathogen: [wherein, G represents a di-valent aromatic hetero 5-membered ring optionally having a halogen atom or C1 to 3 alkyl group (with the proviso that a hetero atom of the aromatic hetero 5-membered ring is a nitrogen atom, oxygen atom or sulfur atom), R 1 represents a hydrogen atom or amino group, R 2 , R 3 and R 4 represent each independently a hydrogen atom or the like, and E represents an optionally substituted 5 to 10-membered heterocyclic group or C6-10 aryl group.].
    提供的是一种农业组合物,包括由式(I)或其盐或水合物表示的化合物,用于控制由植物病原体引起的植物病害:[其中,G代表一个二价芳香杂环五元环,可选地具有卤原子或C1至3烷基(前提是芳香杂环五元环的杂原子是氮原子、氧原子或硫原子),R1代表氢原子或氨基,R2、R3和R4分别独立地代表氢原子或类似物,E代表可选地取代的5到10元杂环基或C6-10芳基。]。
  • Pyridine derivatives substituted by heterocyclic ring and phosphonoamino group, and anti-fungal agent containing same
    申请人:Tanaka Keigo
    公开号:US08507530B2
    公开(公告)日:2013-08-13
    Anti-fungal agent having excellent anti-fungal action physicochemical properties including safety and water solubility. Compound represented by formula (I), or salt thereof: wherein R1 represents hydrogen, halogen, amino, R11—NH— wherein R11 represents C1-6 alkyl, hydroxy C1-6 alkyl, C1-6 alkoxy C1-6 alkyl, or C1-6alkoxycarbonyl C1-6 alkyl, R12—(CO)—NH— wherein R12 represents C1-6 alkyl group or C1-6 alkoxy C1-6 alkyl, C1-6 alkyl, hydroxy C1-6 alkyl, cyano C1-6 alkyl, C1-6 alkoxy, or C1-6 alkoxy C1-6 alkyl or a phosphonoamino group; R2 represents hydrogen, C1-6 alkyl, amino, or a di C1-6 alkylamino group or a phosphonoamino group; one of X and Y is nitrogen while the other is nitrogen or oxygen; ring A represents a 5- or 6-member heteroaryl ring or a benzene ring which may have a halogen atom or 1 or 2 C1-6 alkyl groups; Z represents a single bond, a methylene group, an ethylene group, oxygen, sulfur, —CH2O—, —OCH2—, —NH—, —CH2NH—, —NHCH2—, —CH2S—, or —SCH2—; R3 represents hydrogen or halogen or C1-6 alkyl, C3-8 cycloalkyl, C6-10 aryl, a 5- or 6-member heteroaryl group or a 5- or 6-member nonaromatic heterocyclic group which may have 1 or 2 substituents; and R4 represents hydrogen or halogen; provided that either R1 or R2 represents a phosphonoamino group.
    具有优异的抗真菌作用、安全性和水溶性的抗真菌剂。化合物的化学式(I)或其盐:其中,R1代表氢、卤素、氨基、R11—NH—,其中R11代表C1-6烷基、羟基C1-6烷基、C1-6烷氧基C1-6烷基或C1-6烷氧羰基C1-6烷基,R12—(CO)—NH—,其中R12代表C1-6烷基或C1-6烷氧基C1-6烷基、C1-6烷基、羟基C1-6烷基、氰基C1-6烷基、C1-6烷氧基或C1-6烷氧羰基C1-6烷基或磷酸氨基基;R2代表氢、C1-6烷基、氨基或二C1-6烷基氨基基或磷酸氨基基;X和Y中的一个是氮,另一个是氮或氧;环A代表一个5-或6-成员的杂环芳基环或苯环,其中可能有一个卤素原子或1或2个C1-6烷基基团;Z代表单键、亚甲基基团、乙烯基团、氧原子、硫原子、—CH2O—、—OCH2—、—NH—、—CH2NH—、—NHCH2—、—CH2S—或—SCH2—;R3代表氢、卤素或C1-6烷基、C3-8环烷基、C6-10芳基、一个5-或6-成员的杂环芳基或一个5-或6-成员的非芳杂环基团,其中可能有1或2个取代基;R4代表氢或卤素;但R1或R2之一代表磷酸氨基基团。
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