3-amino-4-nitro-[2]naphthoic acid | 498546-32-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 3-amino-4-nitro-[2]naphthoic acid
• 英文别名: 3-Amino-4-nitro-[2]naphthoesaeure；3-Amino-4-nitro-2-naphthalenecarboxylic Acid；3-Amino-4-nitronaphthalene-2-carboxylic acid
• CAS: 498546-32-0
• 化学式: C₁₁H₈N₂O₄
• 分子量: 232.196
• InChiKey: VWOXDFIGNUTZAK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  17
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  109
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  3-amino-4-nitro-[2]naphthoic acid 在 硫酸 、 水 、 溶剂黄146 、 sodium nitrite 作用下， 生成 3-carboxy-1-hydroxy-naphthalene-2-diazonium-betaine
  参考文献：
  名称：

  Egg Production, Fertility, and Hatchability of Breeder Hens Receiving Dietary Phytase

  摘要：

  An experiment was conducted to determine whether supplemental dietary phytase could support egg production, egg shell quality, fertility, and hatchability in broiler breeder hens on a diet with marginal available phosphorus. During the production period, 27 to 60 wk of age, individually caged broiler breeder hens; were fed four diets with two available phosphorus (AP) concentrations (0.1 and 0.3%) and two phytase levels [0 and 300 phytase units (FTU)/kg]. Phytase increased overall hen-day egg production by 9.8%, as compared with hens consuming a low phosphorus diet without added phytase. Addition of phytase significantly reduced hen mortality regardless of AP levels. Phytase improved bone mineral content and bone density of hens at both AP levels. Supplemental phytase had no significant effect on egg weight or egg specific gravity. The results suggest the possibility of a detrimental interaction of phytase with the 0.1 AP level on hatchability.

  DOI：

  10.1093/japr/12.3.264
• 作为产物：
  描述：

  3-(乙酰氨基)-2-萘甲酸 在 盐酸 、 溴 、 硝酸 、 溶剂黄146 、 sodium nitrite 作用下， 生成 3-amino-4-nitro-[2]naphthoic acid
  参考文献：
  名称：

  198.氨基羟基萘甲酸。第二部分 尝试从3-氨基-2-萘甲酸合成7-氨基-4-羟基-2-萘甲酸（“羧基j-酸”）

  摘要：

  DOI：

  10.1039/jr9500000961

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。
• Adcock,W.; Wells,P.R., Australian Journal of Chemistry, 1965, vol. 18, p. 1351 - 1364
  作者：Adcock,W.、Wells,P.R.

  DOI：——

  日期：——
• 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：——