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Merck

P2116

Sigma-Aldrich

吡非尼酮

≥97% (HPLC), powder, antifibrotic agent

别名:

5-甲基-1-苯基-2-(1H)-吡啶酮

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About This Item

经验公式(希尔记法):
C12H11NO
CAS号:
分子量:
185.22
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

product name

吡非尼酮, ≥97% (HPLC)

化驗

≥97% (HPLC)

形狀

powder

溶解度

H2O: >10 mg/mL at 60 °C (warming for 30 minutes)
DMSO: >20 mg/mL

起源

Shionogi

SMILES 字串

O=C(C=CC(C)=C1)N1C2=CC=CC=C2

InChI

1S/C12H11NO/c1-10-7-8-12(14)13(9-10)11-5-3-2-4-6-11/h2-9H,1H3

InChI 密鑰

ISWRGOKTTBVCFA-UHFFFAOYSA-N

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一般說明

吡非尼酮(5-甲基-1-苯基-2-[1H]-吡啶酮)是合成的吡啶 衍生物。

應用

吡非尼酮用于:
  • 作为兔的术后滴眼剂,分析其抗纤维化作用,改进青光眼滤过手术
  • 作为抗瘢痕形成剂,检查其是否影响兔植入青光眼引流装置(GDD)后的异物反应
  • 在人眼眶成纤维细胞(hOF)原代培养物中测试其抗纤维化潜力
  • 作为肿瘤坏死因子(TNFα)抑制剂,研究其在缺氧中的作用

生化/生理作用

吡非尼酮可抑制胶原生成和成纤维细胞增殖。在多种肺纤维化动物模型和临床试验中显示出抗纤维化和抗炎属性。
吡非尼酮用于治疗特发性肺纤维化(IPF)。有助于减少肺功能下降引起的衰弱,延长无进展生存期。吡非尼酮可抑制人Tenon′s 囊成纤维细胞胶原蛋白的增殖和收缩。

特點和優勢

该化合物由 Shionogi 开发。如需浏览其他制药公司开发的化合物和批准的药物/候选药物列表,请点击此处

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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CX3CL1 (fractalkine) and TNF alpha production by perfused human placental lobules under normoxic and hypoxic conditions in vitro: the importance of CX3CR1 signaling
Szukiewicz D, et al.
Inflammation Research, 63(3), 179-189 (2014)
Huzaifa I Adamali et al.
Drug design, development and therapy, 6, 261-272 (2012-10-12)
Over the past decade, there has been a cohesive effort from patients, physicians, clinical and basic scientists, and the pharmaceutical industry to find definitive treatments for idiopathic pulmonary fibrosis (IPF). As understanding of disease behavior and pathogenesis has improved, the
Pirfenidone safety and adverse event management in idiopathic pulmonary fibrosis
Lancaster L H, et al.
European Respiratory Review, 26(146), 170057-170057 (2017)
Arata Azuma
Therapeutic advances in respiratory disease, 6(2), 107-114 (2012-02-16)
Pirfenidone is the first antifibrotic agent to be approved for the treatment of pulmonary fibrosis. Idiopathic pulmonary fibrosis (IPF) is one of the idiopathic interstitial pneumonias with the worst prognoses; approximately half of patients die within 3-5 years, and the
K Huber et al.
Histochemistry and cell biology, 142(4), 361-371 (2014-05-16)
The aim of this study was to establish an ex vivo model for a faster optimisation of sample preparation procedures, for example matrix choice, in matrix-assisted laser desorption/ionisation (MALDI) drug imaging studies. The ionisation properties of four drugs, afatinib, erlotinib

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