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1,3,6,7-tetramethyl-(1H,3H)-pteridine-2,4-dione | 2625-25-4

中文名称
——
中文别名
——
英文名称
1,3,6,7-tetramethyl-(1H,3H)-pteridine-2,4-dione
英文别名
1,3,6,7-tetramethyllumazine;1,3,6,7-tetramethyl-1H-pteridine-2,4-dione;1,3,6,7-Tetramethyl-1H-pteridin-2,4-dion;1,3,6,7-Tetramethyl-2,4(1H,3H)-pteridindion;1,3,6,7-Tetramethylpteri-2,4-dion;1,3,6,7-Tetramethyl-lumazin;1,3,6,7-Tetramethylpteridine-2,4(1h,3h)-dione;1,3,6,7-tetramethylpteridine-2,4-dione
1,3,6,7-tetramethyl-(1H,3H)-pteridine-2,4-dione化学式
CAS
2625-25-4
化学式
C10H12N4O2
mdl
MFCD02167492
分子量
220.231
InChiKey
RIUBVVOTTNDDIR-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

  • 熔点:
    164-166.5 °C
  • 沸点:
    400.9±55.0 °C(Predicted)
  • 密度:
    1.292±0.06 g/cm3(Predicted)
  • 溶解度:
    0.05 M

计算性质

  • 辛醇/水分配系数(LogP):
    0.1
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    66.4
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:76751a872f1beaddaef3a609ec38d3b4
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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

点击查看最新优质反应信息

文献信息

  • Immunosuppressive effects of pteridine derivatives
    申请人:——
    公开号:US20030236255A1
    公开(公告)日:2003-12-25
    Novel poly-substituted pteridinediones (lumazines), and mono- or polysubstituted 2-thiolumazines, 4-thiolumazines or 2,4-dithiolumazines, having disclosed substituents in positions 1, 3, 6 and 7 of the pteridine ring, and pharmaceutically acceptable salts thereof, are useful as biologically active ingredients in preparing pharmaceutical compositions especially for the treatment or prevention of a CNS disorder, a cell proliferative disorder, a viral infection, an immune or auto-immune disorder or a transplant rejection. Combinations of the pteridine derivatives of the invention with an immunosuppressant or immunomodulator drug, an antineoplastic drug or an antiviral agent, providing potential synergistic effects, are also disclosed.
    新型多取代的喹啉二酮(卢马嗪),以及单取代或多取代的2-硫代卢马嗪,4-硫代卢马嗪或2,4-二硫代卢马嗪,在喹啉环的1、3、6和7位上具有已披露的取代基,并且其药学上可接受的盐,在制备药物组合物中作为生物活性成分特别用于治疗或预防中枢神经系统疾病、细胞增殖障碍、病毒感染、免疫或自身免疫障碍或移植排斥。本发明的喹啉衍生物与免疫抑制剂或免疫调节剂药物、抗肿瘤药物或抗病毒药物的组合,提供潜在的协同效应。
  • Synthesis and structural studies on three-dimensionally hydrogen-bonded metal perchlorate complexes with 1,3-dimethyllumazine and 1,3,6,7-tetramethyllumazine. Crystal structure of diaqua-bis(1,3,6,7-tetramethyl-pteridine2,4(1H,3H)-dione-O4,N5) copper(II) perchlorate dihydrate
    作者:Francisco Hueso-Ureña、Sonia B. Jiménez-Pulido、Miguel N. Moreno-Carretero、Miguel Quirós-Olozábal、Juan M. Salas-Peregrín
    DOI:10.1016/s0020-1693(97)05722-8
    日期:1998.2
    the equatorial plane consisting of two N(5) and two O(4) atoms of pteridine ligands: the two axial sites are occupied by two oxygen atoms from the coordinated water molecules. The monomeric units together with non-coordinated water molecules and perchlorate anions are involved in a complex three-dimensional H-bonds network, the pteridine moieties being packed following planes roughly parallel to b axis
    在水溶液中,M II(ClO 4)2(MnMn,Co,Ni,Cu,Zn,Cd和Hg)与1.3-二甲基lum嗪9DLM反应)和1,3,6,7-四甲基(嗪(DLMD)(lumazine =(1 H,3 H)-pteridin-2,4-dione)生成通式为Mp II(ClO 4)2(LM)2 · n H 2 O的配合物。技术(元素分析和热重分析),光谱方法(IR,13 C和11 H NMR,UV-VIS-NIR,电子顺磁共振)和磁测量(77–290 K)。对复合物[Cu(DLMD)2(H 2 O)2 ](ClO 4)2 ·2H 2 O进行了单晶X射线衍射研究。该化合物在单斜晶系中结晶。P 2 1 / c空间组,Z = 2,带有和R对于4648个独立反射和224个参数,= 0.0728。金属离子占据中心并表现出扭曲的八面体配位。配位八面体被展平,赤道面由蝶啶配体的两个N(5)和两个O(4)原子
  • Synthesis and structural studies on 1:1 metal complexes with 1,3–dimethyllumazine and 1,3,6,7–tetramethyllumazine. Crystal structure of two dichloro copper (II) and mercury (II) compounds and a polymeric chloro–nitrato bridged–mercury (II) complex
    作者:Francisco Hueso-Ureña、Sonia B. Jiménez-Pulido、Miguel N. Moreno-Carretero、Españapós-Olozá、Miguel Quirós-Olozábal、Juan M. Salas-Peregrín
    DOI:10.1016/s0277-5387(98)00122-3
    日期:1998.9
    These units are weakly paired through long interactions of each metal centre with chloride ions of a neighbour molecule (Hg···Cl 3.664 A) . The mixed complex 3 displays a polymeric structure in which the nitrate groups act as bridging bifurcate ligands between two Hg (II) ions through only one of their three oxygen atoms. The coordination polyhedron around the Hg (II) ion must be described as a trigonal
    摘要在绝对甲醇介质中,已分离出八种新的通式为M II X 2 L·nH 2 O的1:1金属络合物(L = 1,3-二甲基鲁嗪(DLM)或1,3,6,7-四甲基鲁嗪(L = 1,3-6,7-四甲基鲁嗪( DLMD); M = Cu,Cd,Hg,Pd和Pt; X = Cl-或NO-3)。用于结构表征的实验技术为热法(TG和DSC)和光谱法(IR,13 C和1 H–NMR和EPR)和磁法(77–290 K)。对[CuCl 2(DLMD)(H 2 O)]·H 2 O(1),[HgCl 2(DLMD)](2)和[HgCl(NO 3) )(DLMD)](3)。在所有络合物中,源自戊嗪的配体似乎都通过N5和O4原子以双齿形式配位。配合物1显示单体五配位结构,其中配位多面体可以最好地描述为三角双锥体。赤道平面被两个氯原子(Cu–Cl 2.268和2.261 A)和有机配体(Cu–O(4)2.294 A)中
  • Immunosuppresive effects of pteridine derivatives
    申请人:Waer Jozef Albert Mark
    公开号:US20070043000A1
    公开(公告)日:2007-02-22
    Novel poly-substituted pteridinediones (lumazines), and mono- or polysubstituted 2-thiolumazines, 4-thiolumazines or 2,4-dithiolumazines, having disclosed substituents in positions 1, 3, 6 and 7 of the pteridine ring, and pharmaceutically acceptable salts thereof, are useful as biologically active ingredients in preparing pharmaceutical compositions especially for the treatment or prevention of a CNS disorder, a cell proliferative disorder, a viral infection, an immune or auto-immune disorder or a transplant rejection. Combinations of the pteridine derivatives of the invention with an immunosuppressant or immunomodulator drug, an antineoplastic drug or an antiviral agent, providing potential synergistic effects, are also disclosed.
    新型多取代噻唑并二酮(吕马嗪),以及单取代或多取代的2-硫吕马嗪、4-硫吕马嗪或2,4-二硫吕马嗪,在噻嗪环的1、3、6和7位上具有已披露的取代基,以及其药学上可接受的盐,可用作制备药物组合物的活性成分,尤其适用于治疗或预防中枢神经系统疾病、细胞增殖紊乱、病毒感染、免疫或自身免疫性疾病或移植排斥。本发明的噻唑衍生物与免疫抑制剂或免疫调节剂、抗肿瘤药物或抗病毒药物的组合,提供潜在的协同作用。
  • Tada, Masaru; Totoki, Shintaro, Journal of Heterocyclic Chemistry, 1988, vol. 25, p. 1295 - 1299
    作者:Tada, Masaru、Totoki, Shintaro
    DOI:——
    日期:——
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