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thioflavin T | 20096-11-1

中文名称
——
中文别名
——
英文名称
thioflavin T
英文别名
2-[4-(Dimethylamino)phenyl]-3,6-dimethyl-1,3-benzothiazol-3-ium;4-(3,6-dimethyl-1,3-benzothiazol-3-ium-2-yl)-N,N-dimethylaniline
thioflavin T化学式
CAS
20096-11-1
化学式
C17H19N2S
mdl
——
分子量
283.417
InChiKey
FXEKRIDRIFBJOR-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):
    4.7
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    35.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    cucurbit[14]uril 、 thioflavin T 为溶剂, 生成
    参考文献:
    名称:
    碱性土阳离子介导的硫代黄素T与葫芦丝的光致发光配合物[14]尿
    摘要:
    我们第一次报道了碱土金属离子介导的硫代黄素T(ThT)与扭曲葫芦[14] uril(tQ [14])的固体光致发光配合物。与tQ [14]的相互作用增强了水溶液中ThT的荧光。实际上,随着tQ [14]的增加,ThT的荧光强度迅速增加,直到tQ [14]:ThT的比率为15。有趣的是,在更低的tQ [14]:ThT的比率(1:1)下,引入了碱土金属阳离子(AE 2+)进入tQ [14] -ThT相互作用系统导致ThT的荧光猝灭,Mg 2+除外阳离子,导致最初的荧光增强,然后ThT逐渐荧光猝灭。在较高的tQ [14]:ThT比(1:15)下,将碱土金属阳离子引入tQ [14] -ThT相互作用系统导致固体tQ [14] / ThT / AE 2+相互作用产物沉淀,它发出强烈的蓝色荧光,但Sr 2+阳离子除外,它显示ThT的荧光猝灭而没有任何固体沉淀。因此,TQ [14] -ThT交互系统显示
    DOI:
    10.1039/c7nj04115b
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文献信息

  • 2-ARYLBENZOTHIOPHENE DERIVATIVES OR PHARCEUTICALLY ACCEPTABLE SALTS THEREOF, PREPARATION METHOD THEREOF, AND PHARCEUTICAL COMPOSITION FOR THE DIAGNOSIS OR TREATMENT OF DEGENERATIVE BRAIN DISEASE CONTAINING THE SAME AS ACTIVE INGREDIENT
    申请人:Chi Dae Yoon
    公开号:US20100261727A1
    公开(公告)日:2010-10-14
    2-arylbenzothiophene derivatives or pharmaceutically acceptable salts thereof, a preparation method thereof, and a pharmaceutical composition for the diagnosis or treatment of degenerative brain disease containing the same as an active ingredient. Since the 2-arylbenzothiophene derivatives of Formula 1 have a relatively high binding affinity for β-amyloid, they can be used as diagnostic reagents for diagnosing Alzheimer's disease at an early stage by non-invasive techniques when they are labeled with radioisotopes: wherein R 1 -R 4 , V, W, X, Y and Z are as defined in the Detailed Descript of the specification. Further, when the pharmaceutical composition containing the 2-arylbenzothiophene derivative binds with a low-molecular weight β-amyloid peptide binding compound, generation of malignant high-molecular weight β-amyloid deposits is minimized. Accordingly, the pharmaceutical composition can be used as a therapeutic agent of degenerative brain disease such as Alzheimer's disease.
    2-芳基苯并噻吩生物或其药用可接受盐,其制备方法,以及包含其作为活性成分的用于诊断或治疗退行性脑疾病的药物组合物。由于式1中的2-芳基苯并噻吩生物具有相对较高的β-淀粉样蛋白结合亲和力,因此当它们与放射性同位素标记时,它们可以作为诊断试剂用于通过非侵入性技术早期诊断阿尔茨海默病: 其中R1-R4,V,W,X,Y和Z如规范的详细描述中所定义。此外,当含有2-芳基苯并噻吩生物的药物组合物与低分子量β-淀粉样蛋白结合化合物结合时,最小化了恶性高分子量β-淀粉样蛋白沉积物的生成。因此,该药物组合物可用作治疗阿尔茨海默病等退行性脑疾病的治疗剂。
  • Benzylideneaniline derivatives and their radioisotope labeled compounds for binding and imaging of beta-amyloid plaques
    申请人:Jeong Jae Min
    公开号:US20070122341A1
    公开(公告)日:2007-05-31
    Benzylideneaniline derivatives of formula 1 wherein R1-R5 are independently selected from hydrogen, C 1 -C 4 alkyl and F (at least one of them is F) and each R 6 -R 10 are independently selected from hydrogen, C 1 -C 4 alkyl, OH, OCH 3 , NH 2 , NHCH 3 and N(CH 3 ) 2 (at least one of them is OH, OCH 3 , NH 2 , NHCH 3 or N(CH 3 ) 2 ) are disclosed. Benzylideneaniline derivatives according to the present invention have high affinity to β-amyloid plaques. Thus, they can cross the blood-brain-barrier (BBB) and bind to β-amyloid plaques after administration into the body, making them useful for treatment, prevention, or imaging of Alzheimer's disease.
    公开了公式1的苯甲醛苯胺生物,其中R1-R5分别选自、C1-C4烷基和F(它们中至少有一个是F),每个R6-R10分别选自、C1-C4烷基、OH、O 、NH2、NH 和N(CH3)2(它们中至少有一个是OH、O 、NH2、NH 或N( )2)。根据本发明的苯甲醛苯胺生物具有高亲和力β-淀粉样斑块。因此,它们可以穿过血脑屏障(BBB),在体内给药后结合β-淀粉样斑块,使其用于治疗、预防或成像阿尔茨海默病。
  • Basic Yellow Dyes as Dye Component for Optical Data Recording Media
    申请人:Steffanut Pascal
    公开号:US20090018318A1
    公开(公告)日:2009-01-15
    The present invention relates to the use of Basic Yellow dyes as dye component for optical data recording media. In a preferred aspect the present invention relates to Basic Yellow dyes together with a metalazo complex dye as dye components for optical data recording media. In a more preferred aspect, the invention relates to a write once read many (WORM) type optical data recording medium capable of recording and reproducing information with radiation of blue laser of preferably 405 nm, which employs a Basic Yellow dye together with a metalazo complex dye and a further recording dye in the optical layer.
    本发明涉及将基本黄染料用作光学数据记录介质的染料组分。在一个首选方面,本发明涉及基本黄染料属偶络合染料作为光学数据记录介质的染料组分。在更首选的方面,该发明涉及一种一次性写入多次读取(WORM)类型的光学数据记录介质,能够使用蓝光激光(最好为405纳米)记录和再现信息,该介质在光学层中使用基本黄染料属偶络合染料以及另一种记录染料
  • 3-hydroxy-cyclohex-2-enone based azo dyes, and their use with anionic azo metal complex dyes
    申请人:Clariant International Ltd.
    公开号:EP1925642A1
    公开(公告)日:2008-05-28
    The present invention relates to the use of 3-hydroxy-cyclohex-2-enone azo based dyes and/or of azo metal complex dyes made thereof, and to compositions comprising 3-hydroxy-cyclohex-2-enone azo based dyes and anionic azo metal complex dyes with cationic basic yellow dyes in optical layers for optical data recording, preferably for optical data recording using a laser with a wavelength up to 450 nm. The invention further relates to a write once read many (WORM) type optical data recording medium capable of recording and reproducing information with radiation of blue laser, which employs a 3-hydroxy-cyclohex-2-enone azo based dye and/or an azo metal complex dye made thereof, or a composition comprising a 3-hydroxy-cyclohex-2-enone azo based dye and a anionic azo metal complex dye with a cationic basic yellow dye in the optical layer.
    本发明涉及使用3-羟基环己-2-染料和/或由此制成的偶属络合物染料,以及包含3-羟基环己-2-染料和带有阳离子基本黄染料的阴离子偶属络合物染料的组合物,在光学层中用于光学数据记录,最好用于使用波长高达450纳米的激光进行光学数据记录。该发明还涉及一种一次写多次读(WORM)型光学数据记录介质,能够使用蓝激光记录和复制信息,该介质采用3-羟基环己-2-染料和/或由此制成的偶属络合物染料,或者包含3-羟基环己-2-染料和光学层中的带有阳离子基本黄染料的阴离子偶属络合物染料的组合物。
  • (3-FLUORO-2-HYDROXY)PROPYL-FUNCTIONALIZED ARYL DERIVATIVES OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME AS ACTIVE INGREDIENT FOR THE DIAGNOSIS OR TREATMENT OF NEURODEGENERATIVE BRAIN DISEASES
    申请人:Chi Dae-Yoon
    公开号:US20120214994A1
    公开(公告)日:2012-08-23
    The present invention relates to (3-fluoro-2-hydroxy)propyl-functionalized aryl derivatives or to the pharmaceutically acceptable salt thereof, to a method for preparing same, and to a pharmaceutical composition containing same as active ingredients for the diagnosis or treatment of neurodegenerative brain diseases. The aryl derivatives of the present invention are (3-fluoro-2-hydroxy)propyl-functionalized to increase the polarity thereof, and therefore the drugs containing the aryl derivatives can easily permeate into the cerebrovascular membrane, thus increasing the effectiveness of the drugs. As the aryl derivatives of the present invention strongly bind to β-amyloid, the aryl derivatives, when labeled with radioisotope, can be used as a diagnostic agent for non-invasively diagnosing early Alzheimer's disease. Further, the aryl derivatives of the present invention bind to low molecular β-amyloid peptide conjugates to inhibit the generation of malignant high molecular β-amyloid plaque, and thus can be effectively used as a therapeutic agent for neurodegenerative brain diseases such as Alzheimer's disease.
    本发明涉及(3--2-羟基)丙基官能化芳基衍生物或其药用可接受的盐,以及制备该衍生物的方法,以及含有该衍生物作为活性成分的药物组合物,用于诊断或治疗神经退行性脑疾病。本发明的芳基衍生物经(3--2-羟基)丙基官能化以增加其极性,因此含有该芳基衍生物的药物可以轻松渗透到脑血管膜中,从而增加药物的有效性。由于本发明的芳基衍生物与β-淀粉样蛋白结合强,因此当该芳基衍生物标记放射性同位素时,可用作无创诊断早期阿尔茨海默病的诊断剂。此外,本发明的芳基衍生物与低分子量β-淀粉样肽结合以抑制恶性高分子量β-淀粉样斑块的生成,因此可以有效用作治疗阿尔茨海默病等神经退行性脑疾病的治疗剂。
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同类化合物

(1Z)-1-(3-乙基-5-羟基-2(3H)-苯并噻唑基)-2-丙酮 齐拉西酮砜 齐帕西酮-d8 阳离子蓝NBLH 阳离子荧光黄4GL 锂2-(4-氨基苯基)-5-甲基-1,3-苯并噻唑-7-磺酸酯 铜酸盐(4-),[2-[2-[[2-[3-[[4-氯-6-[乙基[4-[[2-(硫代氧代)乙基]磺酰]苯基]氨基]-1,3,5-三嗪-2-基]氨基]-2-(羟基-kO)-5-硫代苯基]二氮烯基-kN2]苯基甲基]二氮烯基-kN1]-4-硫代苯酸根(6-)-kO]-,(1:4)氢,(SP-4-3)- 铜羟基氟化物 钾2-(4-氨基苯基)-5-甲基-1,3-苯并噻唑-7-磺酸酯 钠3-(2-{(Z)-[3-(3-磺酸丙基)-1,3-苯并噻唑-2(3H)-亚基]甲基}[1]苯并噻吩并[2,3-d][1,3]噻唑-3-鎓-3-基)-1-丙烷磺酸酯 邻氯苯骈噻唑酮 西贝奈迪 螺[3H-1,3-苯并噻唑-2,1'-环戊烷] 螺[3H-1,3-苯并噻唑-2,1'-环己烷] 葡萄属英A 草酸;N-[1-[4-(2-苯基乙基)哌嗪-1-基]丙-2-基]-2-丙-2-基氧基-1,3-苯并噻唑-6-胺 苯酰胺,N-2-苯并噻唑基-4-(苯基甲氧基)- 苯酚,3-[[2-(三苯代甲基)-2H-四唑-5-基]甲基]- 苯胺,N-(3-苯基-2(3H)-苯并噻唑亚基)- 苯碳杂氧杂脒,N-1,2-苯并异噻唑-3-基- 苯甲酸,4-(6-辛基-2-苯并噻唑基)- 苯甲基2-甲基哌啶-1,2-二羧酸酯 苯并噻唑正离子,2-[3-(1,3-二氢-1,3,3-三甲基-2H-吲哚-2-亚基)-1-丙烯-1-基]-3-乙基-,碘化(1:1) 苯并噻唑正离子,2-[2-[4-(二甲氨基)苯基]乙烯基]-3-乙基-6-甲基-,碘化 苯并噻唑正离子,2-[(2-乙氧基-2-羰基乙基)硫代]-3-甲基-,溴化 苯并噻唑啉 苯并噻唑三氯金(III) 苯并噻唑-d4 苯并噻唑-7-乙酸 苯并噻唑-6-腈 苯并噻唑-5-羧酸 苯并噻唑-5-硼酸频哪醇酯 苯并噻唑-4-醛 苯并噻唑-4-乙酸 苯并噻唑-2-磺酸钠 苯并噻唑-2-磺酸 苯并噻唑-2-磺酰氟 苯并噻唑-2-甲醛 苯并噻唑-2-甲酸 苯并噻唑-2-甲基甲胺 苯并噻唑-2-基磺酰氯 苯并噻唑-2-基甲基-乙基-胺 苯并噻唑-2-基叠氮化物 苯并噻唑-2-基-邻甲苯-胺 苯并噻唑-2-基-己基-胺 苯并噻唑-2-基-(4-氯-苯基)-胺 苯并噻唑-2-基-(4-氟-苯基)-胺 苯并噻唑-2-基-(4-乙氧基-苯基)-胺 苯并噻唑-2-基-(2-甲氧基-苯基)-胺 苯并噻唑-2-基-(2,6-二甲基-苯基)-胺