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1-(4-溴苯基磺酰)哌啶-4-酮 | 929000-54-4

中文名称
1-(4-溴苯基磺酰)哌啶-4-酮
中文别名
1-((4-溴苯基)磺酰)哌啶-4-酮;1-(4-溴苯基磺酰基)哌啶-4-酮
英文名称
1-(4-bromophenylsulfonyl)piperidin-4-one
英文别名
1-(4-bromobenzenesulfonyl)piperidin-4-one;1-((4-Bromophenyl)sulfonyl)piperidin-4-one;1-(4-bromophenyl)sulfonylpiperidin-4-one
1-(4-溴苯基磺酰)哌啶-4-酮化学式
CAS
929000-54-4
化学式
C11H12BrNO3S
mdl
MFCD09258649
分子量
318.191
InChiKey
CVRKCAXMZOAGQZ-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):
    1.2
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.363
  • 拓扑面积:
    62.8
  • 氢给体数:
    0
  • 氢受体数:
    4

安全信息

  • 储存条件:
    | 室温 |

SDS

SDS:a2df6c30362f58487995782b2d79c230
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 1-(4-Bromophenylsulfonyl)piperidin-4-one
Synonyms:

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

Section 3. Composition/information on ingredients.
Ingredient name: 1-(4-Bromophenylsulfonyl)piperidin-4-one
CAS number: 929000-54-4

Section 4. First aid measures
Skin contact: Immediately wash skin with copious amounts of water for at least 15 minutes while removing
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact: Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation: Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Ingestion: Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

Section 5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

Section 6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution: Wear approved mask/respirator
Hand precaution: Wear suitable gloves/gauntlets
Skin protection: Wear suitable protective clothing
Eye protection: Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

Section 7. Handling and storage
Handling: This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Store in closed vessels.
Storage:

Section 8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

Section 9. Physical and chemical properties
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C11H12BrNO3S
Molecular weight: 318.2

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, nitrogen oxides, hydrogen bromide, sulfur oxides.

Section 11. Toxicological information
No data.

Section 12. Ecological information
No data.

Section 13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

Section 14. Transportation information
Non-harzardous for air and ground transportation.

Section 15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

  • 下游产品
    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:
    描述:
    1-(4-溴苯基磺酰)哌啶-4-酮草酰氯溶剂黄146二甲基亚砜 作用下, 以 二氯甲烷 为溶剂, 反应 4.25h, 生成 C18H25BrN2O3S
    参考文献:
    名称:
    TASIN类似物的设计和合成,它们专门针对具有突变性腺瘤性息肉病大肠菌(APC)的结直肠癌细胞系。
    摘要:
    尽管靶向抗癌疗法取得了进展,但仍没有针对小分子结肠直肠癌(CRC)发育和进程的小分子疗法,这是导致癌症死亡的第二大原因。我们先前披露了截短性腺瘤性结肠炎(APC)选择性抑制剂1(TASIN-1)的发现,这是一种小分子,可通过抑制腺瘤性息肉病(APC)肿瘤抑制基因中的截短突变而特异性靶向结直肠癌细胞系胆固醇的生物合成。在这里,我们报告了TASIN类似物的集合及其对结肠癌细胞系和等基因细胞系对活性的报告,报告了APC依赖选择性的状态。鉴定出许多有效的和选择性的类似物,包括具有良好代谢稳定性和药代动力学特性的化合物。本文报道的化合物代表了首个基因型选择性系列,该系列特异性靶向大多数CRC患者中存在的apc突变,并充当结肠癌靶向治疗的翻译平台。
    DOI:
    10.1021/acs.jmedchem.9b00532
  • 作为产物:
    描述:
    4-氧代哌啶酮盐酸盐4-溴苯磺酰氯potassium carbonate 作用下, 以 氯仿 为溶剂, 反应 20.0h, 以82%的产率得到1-(4-溴苯基磺酰)哌啶-4-酮
    参考文献:
    名称:
    TASIN类似物的设计和合成,它们专门针对具有突变性腺瘤性息肉病大肠菌(APC)的结直肠癌细胞系。
    摘要:
    尽管靶向抗癌疗法取得了进展,但仍没有针对小分子结肠直肠癌(CRC)发育和进程的小分子疗法,这是导致癌症死亡的第二大原因。我们先前披露了截短性腺瘤性结肠炎(APC)选择性抑制剂1(TASIN-1)的发现,这是一种小分子,可通过抑制腺瘤性息肉病(APC)肿瘤抑制基因中的截短突变而特异性靶向结直肠癌细胞系胆固醇的生物合成。在这里,我们报告了TASIN类似物的集合及其对结肠癌细胞系和等基因细胞系对活性的报告,报告了APC依赖选择性的状态。鉴定出许多有效的和选择性的类似物,包括具有良好代谢稳定性和药代动力学特性的化合物。本文报道的化合物代表了首个基因型选择性系列,该系列特异性靶向大多数CRC患者中存在的apc突变,并充当结肠癌靶向治疗的翻译平台。
    DOI:
    10.1021/acs.jmedchem.9b00532
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文献信息

  • NOVEL ANALGESIC THAT BINDS FILAMIN A
    申请人:Burns Barbier Lindsay
    公开号:US20100280057A1
    公开(公告)日:2010-11-04
    A compound, composition and method are disclosed that can provide analgesia. A contemplated compound has a structure that corresponds to Formula I, wherein R 1 and R 2 are substituents, and n, W, X and Y are defined within.
    揭示了一种可以提供镇痛作用的化合物、组合物和方法。一个考虑中的化合物具有与式I对应的结构,其中R1和R2是取代基,n、W、X和Y在其中被定义。
  • [EN] THERAPEUTICS TARGETING MUTANT ADENOMATOUS POLYPOSIS COLI (APC) FOR THE TREATMENT OF CANCER<br/>[FR] AGENTS THÉRAPEUTIQUES CIBLANT LA POLYPOSE ADÉNOMATEUSE COLIQUE (APC) MUTANTE POUR LE TRAITEMENT DU CANCER
    申请人:UNIV TEXAS
    公开号:WO2020117972A1
    公开(公告)日:2020-06-11
    The present disclosure reports an extensive medicinal chemistry evaluation of a large collection of Truncating APC-Selective Inhibitor (TASIN) compounds. The compounds were evaluated for activity against a series of colon cancer cell lines with and without truncating APC-mutations, as well as in an isogenic cell line pair reporting on the status of APC- dependent selectivity. A number of very potent and selective compounds were identified, including compounds with good metabolic stability and PK properties. The small molecules reported herein thus represent a first-in-class genotype-selective series that specifically target ape mutations present in the vast majority of CRC patients, and therefore serves as a translational platform towards a potential targeted therapy for colon cancer.
    本披露报告了对大量截断APC-选择性抑制剂(TASIN)化合物的广泛药物化学评估。这些化合物针对一系列结肠癌细胞系进行了活性评估,包括具有截断APC突变和不具有截断APC突变的细胞系,以及在报告APC依赖性选择性状况的同源细胞系对。鉴定了一些非常有效和选择性的化合物,包括具有良好代谢稳定性和药代动力学性质的化合物。因此,本文报道的小分子代表了一种首创的基因型选择性系列,专门针对存在于绝大多数结直肠癌患者中的猿类突变,因此可作为一个转化平台,朝着结肠癌的潜在靶向治疗迈进。
  • FATTY ACID SYNTHASE INHIBITORS
    申请人:Adams Nicholas D.
    公开号:US20130237535A1
    公开(公告)日:2013-09-12
    This invention relates to the use of spirocyclic piperidine derivatives for the modulation, notably the inhibition of the activity or function of fatty acid synthase (FAS). Suitably, the present invention relates to the use of spirocyclic piperidines in the treatment of cancer.
    本发明涉及使用螺环状哌啶生物来调节脂肪酸合成酶(FAS)的活性或功能,尤其是抑制其活性或功能。适当地,本发明涉及使用螺环状哌啶生物治疗癌症。
  • Filamin a binding anti-inflammatory and analgesic
    申请人:Pain Therapeutics, Inc.
    公开号:EP2918587A2
    公开(公告)日:2015-09-16
    A compound or its pharmaceutically acceptable salt, composition and method are disclosed that can provide analgesia and reduce inflammation. A contemplated compound has a structure that corresponds to Formula II, wherein the R group substituents, D, F, X, W and A are defined within.
    本发明公开了一种化合物或其药学上可接受的盐、组合物和方法,可提供镇痛和减轻炎症。一种考虑使用的化合物具有与式 II 相对应的结构,其中 R 基取代基、D、F、X、W 和 A 在式 II 中定义。
  • FILAMIN A-BINDING ANTI-INFLAMMATORY ANALGESIC
    申请人:Pain Therapeutics, Inc.
    公开号:EP2498600B1
    公开(公告)日:2016-03-02
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