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Merck

I4883

Sigma-Aldrich

布洛芬

≥98% (GC), powder, COX inhibitor

别名:

2-(4-异丁苯)丙酸, Motrin, Rebugen, 布洛芬, α-甲基-4-(异丁基)苯乙酸, (±)-2-(4-异丁基苯基)丙酸

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About This Item

经验公式(希尔记法):
C13H18O2
CAS号:
分子量:
206.28
EC號碼:
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

产品名称

布洛芬, ≥98% (GC)

生物源

synthetic (organic)

化驗

≥98% (GC)

形狀

powder

mp

77-78  °C

溶解度

ethanol: 50 mg/mL, clear, colorless to faintly yellow

SMILES 字串

CC(C)Cc1ccc(cc1)C(C)C(O)=O

InChI

1S/C13H18O2/c1-9(2)8-11-4-6-12(7-5-11)10(3)13(14)15/h4-7,9-10H,8H2,1-3H3,(H,14,15)

InChI 密鑰

HEFNNWSXXWATRW-UHFFFAOYSA-N

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一般說明

布洛芬是一种非类固醇抗炎药(NSAID),常用来止痛、消炎、退烧。它会抑制多种抗高血压药物作用,包括β肾上腺素能阻滞剂、血管紧张素转换酶抑制剂、血管紧张素受体阻滞剂和利尿剂。布洛芬在脑脊液中以未结合状态存在,在关节炎患者中会积聚在炎症关节的滑膜液中。

應用

布洛芬用于:
  • 研究其对新生儿肺发育的血管和肺影响
  • 研究其对人胆管癌细胞株凋亡、增殖和组织学变化的影响
  • 在萜类治疗性低共溶体系(therapeutic deep eutectic system)制备中,研究其物化、抗菌和抗癌特性。

生化/生理作用

环加氧酶 (COX) 抑制剂,对 COX-1 的抑制活性大于对 COX-2 的抑制活性。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Jennifer S Chen et al.
bioRxiv : the preprint server for biology (2020-10-01)
Identifying drugs that regulate severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and its symptoms has been a pressing area of investigation during the coronavirus disease 2019 (COVID-19) pandemic. Nonsteroidal anti-inflammatory drugs (NSAIDs), which are frequently used for the relief
Mateusz P Czub et al.
Journal of medicinal chemistry, 63(13), 6847-6862 (2020-05-30)
Every day, hundreds of millions of people worldwide take nonsteroidal anti-inflammatory drugs (NSAIDs), often in conjunction with multiple other medications. In the bloodstream, NSAIDs are mostly bound to serum albumin (SA). We report the crystal structures of equine serum albumin
Tzu-Feng Wang et al.
Cells, 11(3) (2022-02-16)
Parkinson's disease (PD) is an age-related neurodegenerative disease caused by a selective loss of dopaminergic (DA) neurons in the substantia nigra (SN). Microglial activation is implicated in the pathogenesis of PD. This study aimed to characterize the role of microglial
Morshed A Chowdhury et al.
Journal of medicinal chemistry, 52(6), 1525-1529 (2009-03-20)
A novel class of 1-(4-methanesulfonylphenyl and 4-aminosulfonylphenyl)-5-[4-(1-difluoromethyl-1,2-dihydropyrid-2-one)]-3-trifluoromethyl-1H-pyrazole hybrid cyclooxygenase-2 (COX-2)/5-lipoxygenase (5-LOX) inhibitory anti-inflammatory agents was designed. Replacement of the tolyl ring present in celecoxib by the N-difluoromethyl-1,2-dihydropyrid-2-one moiety provided compounds showing dual selective COX-2/5-LOX inhibitory activities. 1-(4-Aminosulfonylphenyl)-5-[4-(1-difluoromethyl-1,2-dihydropyrid-2-one)]-3-trifluoromethyl-1H-pyrazole exhibited good anti-inflammatory
Bart Van Overmeire et al.
Lancet (London, England), 364(9449), 1945-1949 (2004-11-30)
Ibuprofen is used for treatment and prevention of patent ductus arteriosus in low-birthweight infants. Its effects on regional circulations differ from those of indometacin. Because prophylactic indometacin reduces the frequency of severe intraventricular haemorrhage and patent ductus arteriosus, we aimed

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