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3-Acetylamino-4-nitro-[2]naphthoesaeure | 498546-30-8

中文名称
——
中文别名
——
英文名称
3-Acetylamino-4-nitro-[2]naphthoesaeure
英文别名
3-acetylamino-4-nitro-[2]naphthoic acid;4-Nitro-3-acetamino-naphthoesaeure-(2);3-Acetamido-4-nitro-2-naphthalenecarboxylic Acid;3-acetamido-4-nitronaphthalene-2-carboxylic acid
3-Acetylamino-4-nitro-[2]naphthoesaeure化学式
CAS
498546-30-8
化学式
C13H10N2O5
mdl
——
分子量
274.233
InChiKey
YOQXFEZGJHTIMT-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):
    2.3
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    112
  • 氢给体数:
    2
  • 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
  • 下游产品
    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

  • Benzo[b]pyrano[3,2-h]acridin-7-one compounds
    申请人:LES LABORATOIRES SERVIER
    公开号:US20040063702A1
    公开(公告)日:2004-04-01
    A method for treating a living body afflicted with a cancer selected from lung and ovarian carcinoma, comprising the step of administering to the living animal body an amount of a compound selected from those of formula (I): 1 wherein: X and Y represent group selected from hydrogen, halogen, mercapto, cyano, nitro, alkyl, trihaloalkyl, trihaloalkylcarbonylamino, —ORa, —NRaRb, —NRa—C(O)-T 1 , —O—C(O)-T 1 , —O-T 2 -NRaRb, —O-T 2 -ORa, —NRa-T 2 -NRaRb, —NRa-T 2 -ORa and —NRa-T 2 -CO 2 Ra wherein Ra, Rb, T 1 , T 2 are as defined in the description, or X and Y together form a methylenedioxy or ethylenedioxy, R 1 represents hydrogen or alkyl, R 2 represents a group selected from hydrogen, —ORa, —NRaRb, —NRa—C(O)-T 1 , —O—C(O)-T 1 , —O-T 2 -NRaRb, —O-T 2 -ORa, —NRa-T 2 -NRaRb, —NRa-T 2 -ORa and —NRa-T 2 -CO 2 Ra wherein Ra, Rb, T 1 and T 2 are as defined hereinbefore, R 3 and R 4 represent hydrogen or alkyl, W represents a group of formula —CH(R 5 )—CH(R 6 )—, —CH═C(R 7 )—, —C(R 7 )═CH— or —C(O)—CH(R 8 )— wherein R 5 , R 6 , R 7 and R 8 are as defined in the description, their isomers and N-oxides, and addition salts thereof with a pharmaceutically acceptable acid or base, and medicinal products containing the same are useful in the treatment of cancer.
    一种治疗患有肺癌和卵巢癌的生物体的方法,包括向生物体内注射一定量的化合物,所述化合物的选择公式为(I)中的一种:其中,X和Y代表从氢、卤素、巯基、氰基、硝基、烷基、三卤代烷基、三卤代烷基羰基氨基、-ORa、-NRaRb、-NRa-C(O)-T1、-O-C(O)-T1、-O-T2-NRaRb、-O-T2-ORa、-NRa-T2-NRaRb、-NRa-T2-ORa和-NRa-T2-CO2Ra中选择的基团,其中Ra、Rb、T1和T2如上所述,或X和Y共同形成亚甲二氧基或乙二氧基,R1代表氢或烷基,R2代表从氢、-ORa、-NRaRb、-NRa-C(O)-T1、-O-C(O)-T1、-O-T2-NRaRb、-O-T2-ORa、-NRa-T2-NRaRb、-NRa-T2-ORa和-NRa-T2-CO2Ra中选择的基团,其中Ra、Rb、T1和T2如上所述,R3和R4代表氢或烷基,W代表公式-CH(R5)-CH(R6)-、-CH═C(R7)-、-C(R7)═CH-或-C(O)-CH(R8)-中的一种基团,其中R5、R6、R7和R8如上所述,它们的异构体和N-氧化物,以及与药学上可接受的酸或碱形成的加合物盐,和含有它们的药物制剂在癌症治疗中有用。
  • New benzo [b] pyrano [3,2-h] acridin-7-one compounds
    申请人:——
    公开号:US20030073841A1
    公开(公告)日:2003-04-17
    A compound selected from those of formula (I): 1 wherein: X and Y represent group selected from hydrogen, halogen, mercapto, cyano, nitro, alkyl, trihaloalkyl, trihaloalkylcarbonylamino, —ORa, —NRaRb, —NRa—C(O)-T 1 , —O—C(O)-T 1 , —O-T 2 -NRaRb, —O-T 2 ORa, —NRa-T 2 NRaRb, —NRa-T 2 -ORa and —NRa-T 2 -CO 2 Ra wherein Ra, Rb, T 1 , T 2 are as defined in the description, or X and Y together form a methylenedioxy or ethylenedioxy, R 1 represents hydrogen or alkyl, R 2 represents a group selected from hydrogen, —ORa, —NRaRb, —NRa—C(O)-T 1 , —O—C(O)-T 1 , —O-T 2 -NRaRb, —O-T 2 -ORa, —NRa-T 2 -NRaRb, —NRa-T 2 -ORa and —NRa-T 2 -CO 2 Ra wherein Ra, Rb, T 1 and T 2 are as defined hereinbefore, R 3 and R 4 represent hydrogen or alkyl, W represents a group of formula —CH(R 5 )—CH(R 6 )—, —CH═C(R 7 )—, —C(R 7 )═CH— or —C(O)—CH(R 8 )— wherein R 5 , R 6 , R 7 and R 8 are as defined in the description, their isomers and N-oxides, and addition salts thereof with a pharmaceutically acceptable acid or base, and medicinal products containing the same which are useful in the treatment of cancer.
    从式(I)中选择的化合物:其中,X和Y代表氢,卤素,巯基,氰基,硝基,烷基,三卤代烷基,三卤代烷基羰基氨基,-ORa,-NRaRb,-NRa-C(O)-T1,-O-C(O)-T1,-O-T2-NRaRb,-O-T2ORa,-NRa-T2NRaRb,-NRa-T2-ORa和-NRa-T2-CO2Ra,其中Ra,Rb,T1,T2如描述中所定义,或X和Y共同形成甲基二氧或乙基二氧基,R1代表氢或烷基,R2代表从氢,-ORa,-NRaRb,-NRa-C(O)-T1,-O-C(O)-T1,-O-T2-NRaRb,-O-T2-ORa,-NRa-T2-NRaRb,-NRa-T2-ORa和-NRa-T2-CO2Ra中选择的基团,其中Ra,Rb,T1和T2如前所述定义,R3和R4代表氢或烷基,W代表式为-CH(R5)-CH(R6)-,-CH═C(R7)-,-C(R7)═CH-或-C(O)-CH(R8)的基团,其中R5,R6,R7和R8如描述中所定义,它们的异构体和N-氧化物,以及与药学上可接受的酸或碱形成的加合物盐,以及含有它们的医药产品,可用于癌症的治疗。
  • Benzo[b]pyrano[3,2-h]acridin-7-one compounds
    申请人:Les Laboratories Servier
    公开号:US06642248B2
    公开(公告)日:2003-11-04
    A compound selected from those of formula (I): wherein: X and Y represent group selected from hydrogen, halogen, mercapto, cyano, nitro, alkyl, trihaloalkyl, trihaloalkylcarbonylamino, —ORa, —NRaRb, —NRa—C(O)—T1, —O—C(O)—T1, —O—T2-NRaRb, —O—T2-ORa, —NRa—T2-NRaRb, —NRa—T2-ORa and —NRa—T2-CO2Ra wherein Ra, Rb, T1, T2 are as defined in the description, R1 represents hydrogen or alkyl, R2 represents a group selected from hydrogen, —ORa, —NRaRb, —NRa—C(O)—T1, —O—C(O)—T1, —O—T2-NRaRb, —O—T2-ORa, —NRa—T2-NRaRb, —NRa—T2-ORa and —NRa—T2-CO2Ra wherein Ra, Rb, T1 and T2 are as defined hereinbefore, R3 and R4 represent hydrogen or alkyl, W represents a group of formula —CH(R5)—CH(R6)—, —CH═C(R7)—, —C(R7)═CH— or —C(O)—CH(R8)— wherein R5, R6, R7 and R8 are as defined in the description, their isomers and N-oxides, and addition salts thereof with a pharmaceutically acceptable acid or base, and medicinal products containing the same which are useful in the treatment of cancer.
    从式(I)所选的化合物:其中:X和Y代表从氢,卤素,巯基,氰基,硝基,烷基,三卤代烷基,三卤代烷基羰基氨基,—ORa,—NRaRb,—NRa—C(O)—T1,—O—C(O)—T1,—O—T2-NRaRb,—O—T2-ORa,—NRa—T2-NRaRb,—NRa—T2-ORa和—NRa—T2-CO2Ra中选择的基团,其中Ra,Rb,T1,T2如描述中所定义,R1代表氢或烷基,R2代表从氢,—ORa,—NRaRb,—NRa—C(O)—T1,—O—C(O)—T1,—O—T2-NRaRb,—O—T2-ORa,—NRa—T2-NRaRb,—NRa—T2-ORa和—NRa—T2-CO2Ra中选择的基团,其中Ra,Rb,T1和T2如前述所定义,R3和R4代表氢或烷基,W代表式—CH(R5)—CH(R6)—,—CH═C(R7)—,—C(R7)═CH—或—C(O)—CH(R8)—中的基团,其中R5,R6,R7和R8如描述中所定义,其异构体和N-氧化物,以及与药学上可接受的酸或碱形成的加成盐,以及含有它们的药物制剂,用于治疗癌症。
  • Nikuni et al., Memoirs of the Institute of Scientific and Industrial Research, Osaka University, 1948, vol. 6, p. 84
    作者:Nikuni et al.
    DOI:——
    日期:——
  • US6642248B2
    申请人:——
    公开号:US6642248B2
    公开(公告)日:2003-11-04
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