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2-氯-6-环丙基氨基吡嗪 | 941294-47-9

中文名称
2-氯-6-环丙基氨基吡嗪
中文别名
(6-氯吡嗪-2)-环丙胺;2-氯-6-环丙胺基吡嗪
英文名称
6-chloro-N-cyclopropylpyrazin-2-amine
英文别名
——
2-氯-6-环丙基氨基吡嗪化学式
CAS
941294-47-9
化学式
C7H8ClN3
mdl
——
分子量
169.614
InChiKey
TYAIEHCRGITGEM-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):
    1.6
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    37.8
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2933990090

SDS

SDS:9ed91f35e2ed3e809f6da3dc6ef092d1
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 2-Chloro-6-cyclopropylaminopyrazine
Synonyms: 6-Chloro-N-cyclopropylpyrazin-2-amine; (6-chloropyrazin-2-yl)cyclopropylamine

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

Section 3. Composition/information on ingredients.
Ingredient name: 2-Chloro-6-cyclopropylaminopyrazine
CAS number: 941294-47-9

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, refrigerated.
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: C7H8ClN3
Molecular weight: 169.6

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 chloride.

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

反应信息

  • 作为反应物:
    描述:
    2-氯-6-环丙基氨基吡嗪六甲基二锡四(三苯基膦)钯 作用下, 以 1,4-二氧六环 为溶剂, 反应 2.0h, 生成 N-cyclopropyl-6-(trimethylstannyl)pyrazin-2-amine
    参考文献:
    名称:
    [EN] AZOLE COMPOUNDS AS PIM INHIBITORS
    [FR] COMPOSÉS D'AZOLE UTILISÉS EN TANT QU'INHIBITEURS DES PIM
    摘要:
    该发明涉及公式I和Ia的双环化合物及其盐。在某些实施例中,该发明涉及Pim-1和/或Pim-2和/或Pim-3蛋白激酶活性或酶功能的抑制剂或调节剂。在更进一步的实施例中,该发明涉及包含本文所披露的化合物的药物组合物,以及它们在预防和治疗Pim激酶相关疾病和病症,尤其是癌症中的用途。
    公开号:
    WO2012129338A1
  • 作为产物:
    描述:
    2,6-二氯吡嗪环丙胺potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 0.5h, 以36%的产率得到2-氯-6-环丙基氨基吡嗪
    参考文献:
    名称:
    KMU-1170, a Novel Multi-Protein Kinase Inhibitor, Suppresses Inflammatory Signal Transduction in THP-1 Cells and Human Osteoarthritic Fibroblast-Like Synoviocytes by Suppressing Activation of NF-κB and NLRP3 Inflammasome Signaling Pathway
    摘要:
    蛋白激酶调节蛋白磷酸化,参与基本的细胞过程,如炎症反应。在这项研究中,我们发现了一种新型的多蛋白激酶抑制剂,KMU-1170,它是吲哚啉-2-酮的衍生物,并研究了其在THP-1细胞和人类骨关节炎纤维样滑膜细胞(FLS)中抑制炎症信号传导的机制。我们证明,在THP-1细胞中,KMU-1170抑制了脂多糖(LPS)诱导的诱导型一氧化氮合酶(iNOS)和环氧合酶-2(COX-2)的上调,并且进一步抑制了LPS诱导的转化生长因子-β激活激酶1、JNK、ERK、NF-κB抑制因子α/β(IKKα/β)和NF-κB p65的磷酸化,以及NF-κB p65的核转位。此外,KMU-1170抑制了LPS诱导的IL-1β、TNF-α和IL-6等促炎细胞因子的上调,显著地抑制了在THP-1细胞中LPS诱导的NLRP3炎症小体的上调。重要的是,KMU-1170减轻了人类骨关节炎FLS中LPS介导的炎症反应,如IL-1β、TNF-α、IL-6、iNOS和COX-2的上调以及IKKα/β和NF-κB p65的磷酸化。总的来说,这些结果表明KMU-1170抑制了炎症信号传导,可能成为潜在的抗炎药物。
    DOI:
    10.3390/ijms22031194
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文献信息

  • Azole Compounds as PIM Inhibitors
    申请人:Wang Hui-Ling
    公开号:US20140187553A1
    公开(公告)日:2014-07-03
    The invention relates to bicyclic compounds of formulas I and Ia, and salts thereof. In some embodiments, the invention relates to inhibitors or modulators of Pim-1 and/or Pim-2, and/or Pim-3 protein kinase activity or enzyme function. In still further embodiments, the invention relates to pharmaceutical compositions comprising compounds disclosed herein, and their use in the prevention and treatment of Pim kinase related conditions and diseases, preferably cancer.
    本发明涉及式I和Ia及其盐的双环化合物。在某些实施例中,本发明涉及Pim-1和/或Pim-2以及/或Pim-3蛋白激酶活性或酶功能的抑制剂或调节剂。在更进一步的实施例中,本发明涉及包含本文所披露的化合物的制药组合物及其在预防和治疗Pim激酶相关疾病和条件,优选为癌症中的应用。
  • Azole compounds as PIM inhibitors
    申请人:Wang Hui-Ling
    公开号:US09321756B2
    公开(公告)日:2016-04-26
    The invention relates to bicyclic compounds of formulas I and Ia, and salts thereof. In some embodiments, the invention relates to inhibitors or modulators of Pim-1 and/or Pim-2, and/or Pim-3 protein kinase activity or enzyme function. In still further embodiments, the invention relates to pharmaceutical compositions comprising compounds disclosed herein, and their use in the prevention and treatment of Pim kinase related conditions and diseases, preferably cancer.
    本发明涉及公式I和Ia的双环化合物及其盐。在某些实施例中,本发明涉及Pim-1和/或Pim-2和/或Pim-3蛋白激酶活性或酶功能的抑制剂或调节剂。在更进一步的实施例中,本发明涉及包含所述化合物的药物组合物,以及它们在预防和治疗Pim激酶相关疾病和疾病,尤其是癌症方面的应用。
  • AZOLE COMPOUNDS AS PIM INHIBITORS
    申请人:Amgen Inc.
    公开号:EP2688886A1
    公开(公告)日:2014-01-29
  • US9321756B2
    申请人:——
    公开号:US9321756B2
    公开(公告)日:2016-04-26
  • [EN] AZOLE COMPOUNDS AS PIM INHIBITORS<br/>[FR] COMPOSÉS D'AZOLE UTILISÉS EN TANT QU'INHIBITEURS DES PIM
    申请人:AMGEN INC
    公开号:WO2012129338A1
    公开(公告)日:2012-09-27
    The invention relates to bicyclic compounds of formulas I and Ia, and salts thereof. In some embodiments, the invention relates to inhibitors or modulators of Pim-1 and/or Pim-2, and/or Pim-3 protein kinase activity or enzyme function. In still further embodiments, the invention relates to pharmaceutical compositions comprising compounds disclosed herein, and their use in the prevention and treatment of Pim kinase related conditions and diseases, preferably cancer.
    该发明涉及公式I和Ia的双环化合物及其盐。在某些实施例中,该发明涉及Pim-1和/或Pim-2和/或Pim-3蛋白激酶活性或酶功能的抑制剂或调节剂。在更进一步的实施例中,该发明涉及包含本文所披露的化合物的药物组合物,以及它们在预防和治疗Pim激酶相关疾病和病症,尤其是癌症中的用途。
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