摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-amino-5-phenylselenophene-2-carboxamide | 1252925-91-9

中文名称
——
中文别名
——
英文名称
3-amino-5-phenylselenophene-2-carboxamide
英文别名
3-Amino-5-phenylselenophene-2-carboxamide
3-amino-5-phenylselenophene-2-carboxamide化学式
CAS
1252925-91-9
化学式
C11H10N2OSe
mdl
——
分子量
265.173
InChiKey
QQXGSAZRJNQJLN-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:
    423.9±45.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.09
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    69.1
  • 氢给体数:
    2
  • 氢受体数:
    2

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

  • 作为反应物:
    参考文献:
    名称:
    [EN] SUBSTITUTED 4-(ARYLAMINO) SELENOPHENOPYRIMIDINE COMPOUNDS AND METHODS OF USE THEREOF
    [FR] COMPOSÉS 4-(ARYLAMINO) SÉLÉNOPHÉNOPYRIMIDINE SUBSTITUÉS ET LEURS PROCÉDÉS D'UTILISATION
    摘要:
    公开号:
    WO2012077135A3
  • 作为产物:
    描述:
    3-amino-5-phenyl-2-selenophenecarbonitrile 、 sodium hydroxide 作用下, 以 乙醇 为溶剂, 反应 0.75h, 以67%的产率得到3-amino-5-phenylselenophene-2-carboxamide
    参考文献:
    名称:
    [EN] ANTI-CANCER DRUGS, AND USES RELATING FOR MALIGNANT MELANOMA AND OTHER CANCERS
    [FR] MÉDICAMENTS ANTICANCÉREUX ET UTILISATIONS LIÉES À DES MÉLANOMES MALINS ET À D'AUTRES CANCERS
    摘要:
    硒吡喃三氮烯类似物,它们的组成物,互变异构体,立体异构体,多晶形态,水合物,溶剂合物,以及药学上可接受的盐和它们的混合物可用于治疗转移性恶性黑色素瘤和其他癌症。硒吡喃三氮烯类似物具有一般式(I)或(II):其中取代基R1、R2、R3、R6和R7如规范中所述。其他可用这些化合物治疗的癌症包括但不限于恶性黑色素瘤、白血病、淋巴瘤(霍奇金病和非霍奇金病)、肉瘤(尤因肉瘤)、脑肿瘤、中枢神经系统(CNS)转移瘤、胶质瘤、癌症如乳腺癌、前列腺癌、肺癌(小细胞和非小细胞)、结肠癌、胰腺癌、头颈癌和口咽鳞状细胞癌。
    公开号:
    WO2010125575A1
点击查看最新优质反应信息

文献信息

  • ANTI-CANCER DRUGS, AND USES RELATING FOR MALIGNANT MELANOMA AND OTHER CANCERS
    申请人:GOKARAJU Ganga Raju
    公开号:US20100272678A1
    公开(公告)日:2010-10-28
    Selenopheno triazene analogs, their compositions, tautomeric forms, stereoisomers, polymorphs, hydrates, solvates, and pharmaceutically acceptable salts and mixtures thereof are useful for the treatment of metastatic malignant melanoma and other cancers. The selenopheno triazene analogs have the general formulae (I) or (II): wherein the substituents R 1 , R 2 , R 3 , R 6 , and R 7 are as described in the specification. Other cancers include which may be treated with these compounds include, but are not limited to, malignant melanoma, leukemia, lymphomas (Hodgkins and non-Hodgkins), sarcomas (Ewing's sarcoma), brain tumors, central nervous system (CNS) metastases, gliomas, carcinomas such as breast cancer, prostate cancer, lung cancer (small cell and non-small cell), colon cancer, pancreatic cancer, Head and Neck cancers and oropharyngeal squamous cell carcinoma.
    硒吡嗪三唑类似物,它们的组成物,互变异构体,立体异构体,多晶形态,水合物,溶剂合物,以及其药用可接受的盐和混合物对于治疗转移性恶性黑色素瘤和其他癌症是有用的。硒吡嗪三唑类似物具有一般式(I)或(II):其中取代基R1、R2、R3、R6和R7如规范中所述。这些化合物可用于治疗的其他癌症包括但不限于恶性黑色素瘤、白血病、淋巴瘤(霍奇金病和非霍奇金病)、肉瘤(尤因肉瘤)、脑肿瘤、中枢神经系统(CNS)转移、胶质瘤、癌症如乳腺癌、前列腺癌、肺癌(小细胞和非小细胞)、结肠癌、胰腺癌、头颈癌和口咽鳞状细胞癌。
  • Anti-cancer drugs, and uses relating for malignant melanoma and other cancers
    申请人:Kasina Laila Innova Pharmaceuticals Private Limited
    公开号:US08143237B2
    公开(公告)日:2012-03-27
    Selenopheno triazene analogs, their compositions, tautomeric forms, stereoisomers, polymorphs, hydrates, solvates, and pharmaceutically acceptable salts and mixtures thereof are useful for the treatment of metastatic malignant melanoma and other cancers. The selenopheno triazene analogs have the general formulae (I) or (II): wherein the substituents R1, R2, R3, R6, and R7 are as described in the specification. Other cancers include which may be treated with these compounds include, but are not limited to, malignant melanoma, leukemia, lymphomas (Hodgkins and non-Hodgkins), sarcomas (Ewing's sarcoma), brain tumors, central nervous system (CNS) metastases, gliomas, carcinomas such as breast cancer, prostate cancer, lung cancer (small cell and non-small cell), colon cancer, pancreatic cancer, Head and Neck cancers and oropharyngeal squamous cell carcinoma.
    Selenopheno triazene类似物,它们的组成,互变异构体,立体异构体,多晶体,水合物,溶剂物和药学上可接受的盐以及它们的混合物,可用于治疗转移性恶性黑色素瘤和其他癌症。 Selenopheno triazene类似物具有一般式(I)或(II):其中取代基R1,R2,R3,R6和R7如规范中所述。其他可能使用这些化合物治疗的癌症包括但不限于恶性黑色素瘤,白血病,淋巴瘤(霍奇金氏和非霍奇金氏),肉瘤(尤因肉瘤),脑肿瘤,中枢神经系统(CNS)转移,胶质瘤,如乳腺癌,前列腺癌,肺癌(小细胞和非小细胞),结肠癌,胰腺癌,头颈癌和咽喉鳞状细胞癌。
  • SUBSTITUTED 4-(SELENOPHEN-2(OR-3)-YLAMINO)PYRIMIDINE COMPOUNDS AND METHODS OF USE THEREOF
    申请人:KASINA LAILA INNOVA PHARMACEUTICALS PRIVATE LIMITED
    公开号:US20130266563A1
    公开(公告)日:2013-10-10
    Selenophene compounds of formula (I) are described herein. In the compounds of Formula (I), ring A is a 6-membered aromatic fused ring, optionally containing one, two or three nitrogen atoms; a 5-membered heteroaromatic fused ring; or a mono- or bicyclic saturated heterocyclic fused ring having at least one ring member selected from the group consisting of N, O, S, SO and SO 2 ; Y in ring B is nitrogen or substituted carbon; X is NR 6 , O, S, S(O), or S(O) 2 . R 1 , R 2 , R 3 , R 4 , and R 6 are defined in the specification. Selenophene compounds of formula (I) may be used in methods of treating cell proliferative disorders, particularly cancer. Pharmaceutical compositions containing selenophene compounds of formula (I) may be used for treatment, inhibition, or control of cancer.
    本文描述了化学式(I)的硒杂苯化合物。在化合物的式(I)中,环A是一个6元芳香融合环,可选地包含一个、两个或三个氮原子;一个5元杂芳融合环;或者一个含有至少一个环成员选自N、O、S、SO和SO2的单环或双环饱和杂环融合环;环B中的Y为氮或取代的碳;X为NR6、O、S、S(O)或S(O)2。R1、R2、R3、R4和R6在说明书中有定义。化学式(I)的硒杂苯化合物可用于治疗细胞增殖性疾病,特别是癌症。含有化学式(I)的硒杂苯化合物的制药组合物可用于治疗、抑制或控制癌症。
  • Substituted 4-(selenophen-2(or-3)-ylamino)pyrimidine compounds and methods of use thereof
    申请人:Kasina Laila Innova Pharmaceuticals Private Limited
    公开号:US08815879B2
    公开(公告)日:2014-08-26
    Selenophene compounds of formula (I) are described herein. In the compounds of Formula (I), ring A is a 6-membered aromatic fused ring, optionally containing one, two or three nitrogen atoms; a 5-membered heteroaromatic fused ring; or a mono- or bicyclic saturated heterocyclic fused ring having at least one ring member selected from the group consisting of N, O, S, SO and SO2; Y in ring B is nitrogen or substituted carbon; X is NR6, O, S, S(O), or S(O)2. R1, R2, R3, R4, and R6 are defined in the specification. Selenophene compounds of formula (I) may be used in methods of treating cell proliferative disorders, particularly cancer. Pharmaceutical compositions containing selenophene compounds of formula (I) may be used for treatment, inhibition, or control of cancer.
    本文描述了公式(I)的硒杂苯化合物。在公式(I)的化合物中,环A是一个6元芳香融合环,可选地含有一个、两个或三个氮原子;一个5元杂芳融合环;或者是至少有一个环成员选自N、O、S、SO和SO2的单环或双环饱和杂环融合环;环B中的Y是氮或取代的碳;X是NR6、O、S、S(O)或S(O)2。R1、R2、R3、R4和R6在规范中有定义。公式(I)的硒杂苯化合物可用于治疗细胞增殖性疾病,特别是癌症。含有公式(I)的硒杂苯化合物的制药组合物可用于治疗、抑制或控制癌症。
  • [EN] ANTI-CANCER DRUGS, AND USES RELATING FOR MALIGNANT MELANOMA AND OTHER CANCERS<br/>[FR] MÉDICAMENTS ANTICANCÉREUX ET UTILISATIONS LIÉES À DES MÉLANOMES MALINS ET À D'AUTRES CANCERS
    申请人:KASINA LAILA INNOVA PHARMACEUT
    公开号:WO2010125575A1
    公开(公告)日:2010-11-04
    Selenopheno triazene analogs, their compositions, tautomeric forms, stereoisomers, polymorphs, hydrates, solvates, and pharmaceutically acceptable salts and mixtures thereof are useful for the treatment of metastatic malignant melanoma and other cancers. The selenopheno triazene analogs have the general formulae (I) or (II): wherein the substituents R1, R2, R3, R6, and R7 are as described in the specification. Other cancers include which may be treated with these compounds include, but are not limited to, malignant melanoma, leukemia, lymphomas (Hodgkins and non-Hodgkins), sarcomas (Ewing's sarcoma), brain tumors, central nervous system (CNS) metastases, gliomas, carcinomas such as breast cancer, prostate cancer, lung cancer (small cell and non-small cell), colon cancer, pancreatic cancer, Head and Neck cancers and oropharyngeal squamous cell carcinoma.
    硒吡喃三氮烯类似物,它们的组成物,互变异构体,立体异构体,多晶形态,水合物,溶剂合物,以及药学上可接受的盐和它们的混合物可用于治疗转移性恶性黑色素瘤和其他癌症。硒吡喃三氮烯类似物具有一般式(I)或(II):其中取代基R1、R2、R3、R6和R7如规范中所述。其他可用这些化合物治疗的癌症包括但不限于恶性黑色素瘤、白血病、淋巴瘤(霍奇金病和非霍奇金病)、肉瘤(尤因肉瘤)、脑肿瘤、中枢神经系统(CNS)转移瘤、胶质瘤、癌症如乳腺癌、前列腺癌、肺癌(小细胞和非小细胞)、结肠癌、胰腺癌、头颈癌和口咽鳞状细胞癌。
查看更多

同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸 麦撒奎 鹅膏氨酸 鹅膏氨酸 鸦胆子酸A甲酯 鸦胆子酸A 鸟氨酸缩合物