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3-羟基-N-2-吡啶-2-萘胺 | 24445-26-9

中文名称
3-羟基-N-2-吡啶-2-萘胺
中文别名
——
英文名称
3-hydroxy-naphthalene-2-carboxylic acid pyridin-2-ylamide
英文别名
3-Hydroxy-n-pyridin-2-yl-2-naphthamide;3-hydroxy-N-pyridin-2-ylnaphthalene-2-carboxamide
3-羟基-N-2-吡啶-2-萘胺化学式
CAS
24445-26-9
化学式
C16H12N2O2
mdl
MFCD06335042
分子量
264.283
InChiKey
PHRLXUJXDQNSFA-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:
    412.5±25.0 °C(Predicted)
  • 密度:
    1.361±0.06 g/cm3(Predicted)
  • 溶解度:
    0.5 [ug/mL]

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    62.2
  • 氢给体数:
    2
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2933399090

SDS

SDS:f05918c50f2b561521f44eb8b94b23b4
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反应信息

  • 作为产物:
    描述:
    2-羟基-3-萘甲酸正丁基锂硫酸 作用下, 以 四氢呋喃正己烷丙酮 为溶剂, 反应 13.5h, 生成 3-羟基-N-2-吡啶-2-萘胺
    参考文献:
    名称:
    Structure–activity relationship studies of naphthol AS-E and its derivatives as anticancer agents by inhibiting CREB-mediated gene transcription
    摘要:
    CREB (cyclic AMP-response element binding protein) is a downstream transcription factor of a multitude of signaling pathways emanating from receptor tyrosine kinases or G-protein coupled receptors. CREB is not activated until it is phosphorylated at Ser133 and its subsequent binding to CREB-binding protein (CBP) through kinase-inducible domain (KID) in CREB and KID-interacting (KIX) domain in CBP. Tumor tissues from various organs present higher level of expression and activation of CREB. Thus CREB has been proposed as a promising cancer drug target. We previously described naphthol AS-E (1a) as a small molecule inhibitor of CREB-mediated gene transcription in living cells. Here we report the structure-activity relationship (SAR) studies of la by modifying the appendant phenyl ring. All the compounds were evaluated for in vitro inhibition of KIX-KID interaction, cellular inhibition of CREB-mediated gene transcription and inhibition of proliferation of four cancer cell lines (A549, MCF-7, MDA-MB-231 and MDA-MB-468). SAR indicated that a small and electron-withdrawing group was preferred at the para-position for KIX-KID interaction inhibition. Compound la was selected for further biological characterization and it was found that la down-regulated the expression of endogenous CREB target genes. Expression of a constitutively active CREB mutant, VP16-CREB in MCF-7 cells rendered the cells resistant to la, suggesting that CREB was critical in mediating its anticancer activity. Furthermore, la was not toxic to normal human cells. Collectively, these data support that la represents a structural template for further development into potential cancer therapeutics with a novel mechanism of action. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2012.09.056
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文献信息

  • [EN] NAPHTHAMIDES AS ANTICANCER AGENTS<br/>[FR] NAPHTHAMIDES EN TANT QU'AGENTS ANTI-CANCÉREUX
    申请人:UNIV OREGON HEALTH & SCIENCE
    公开号:WO2010048302A1
    公开(公告)日:2010-04-29
    A compound (particularly useful for inhibiting cancer) according to formula (I): or a pharmaceutically acceptable salt thereof, wherein: x is 0 or 1; R1-R6 are each independently H, -CN, -NO2, -NO, -OH, halogen, hydroxyalkyl, carboxyl, substituted carboxyl, aminocarbonyl, alkoxy, carbonyl or substituted carbonyl; R7 is H, alkyl, alkyl amino, aminoacyl, hydroxyacyl, heteroaryl, heterocycloalkyi, alkyl heteroaryl or alkyl heterocycloalkyl; R8 is H or alkyl; A is O or N; and Ar is an aryl, substituted aryl, heteroaryl, or substituted heleroaryl, provided that if R7 is H then Ar is aryl substituted with alkyl amino.
    一种化合物(特别适用于抑制癌症),其化学式为(I)或其药学上可接受的盐,其中:x为0或1;R1-R6各自独立地为H,-CN,-NO2,-NO,-OH,卤素,羟基烷基,羧基,取代羧基,氨基甲酰基,烷氧基,羰基或取代羰基;R7为H,烷基,烷基氨基,氨基酰基,羟基酰基,杂环芳基,杂环环烷基,烷基杂环芳基或烷基杂环环烷基;R8为H或烷基;A为O或N;Ar为芳基,取代芳基,杂环芳基或取代杂环芳基,但如果R7为H,则Ar为取代烷基氨基的芳基。
  • PIGMENT COMPOSITION, INKJET RECORDING INK, COLORING COMPOSITION FOR COLOR FILTER, AND COLOR FILTER
    申请人:HIGASHI Masahiro
    公开号:US20120001133A1
    公开(公告)日:2012-01-05
    A pigment composition including (A) an azo pigment represented by formula (1), and at least one selected from the group consisting of (B) a coloring agent represented by formula (2), and (C) at least one selected from the group consisting of an additive represented by formula (3) and an additive represented by formula (4).
    一种颜料组合物,包括(A)由式(1)表示的偶氮颜料,以及至少从由式(2)表示的着色剂组成的群体中选择的一种,和/或至少从由式(3)表示的添加剂和由式(4)表示的添加剂组成的群体中选择的一种。
  • Naphthalene carboxamides as inhibitors of human cytomegalovirus DNA polymerase
    作者:Valerie A Vaillancourt、Michele M Cudahy、Sandra A Staley、Roger J Brideau、Steven J Conrad、Mary L Knechtel、Nancee L Oien、Janet L Wieber、Yoshihiko Yagi、Michael W Wathen
    DOI:10.1016/s0960-894x(00)00402-9
    日期:2000.9
    ortho-Hydroxynaphthalene carboxamides have been identified as inhibitors of HCMV DNA polymerase. SAR investigations have demonstrated that both the amide and hydroxy functionalities are required for activity. Substitution on the naphthalene ring has led to inhibitors with submicromolar IC(50)s against HCMV polymerase. These compounds have been found to be >100-fold selective for inhibition of HCMV polymerase versus human alpha polymerase and display antiviral activity in a cell-based plaque reduction assay. (C) 2000 Elsevier Science Ltd. All rights reserved.
  • JPS6321645A
    申请人:——
    公开号:JPS6321645A
    公开(公告)日:1988-01-29
  • US8202327B2
    申请人:——
    公开号:US8202327B2
    公开(公告)日:2012-06-19
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