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关于此项目
经验公式(希尔记法):
C13H18O2
化学文摘社编号:
分子量:
206.28
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
239-784-6
MDL number:
Quality Level
agency
USP/NF, meets USP testing specifications
form
solid
application(s)
pharmaceutical (small molecule)
SMILES string
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 key
HEFNNWSXXWATRW-UHFFFAOYSA-N
Gene Information
human ... ALB(213), ALOX5(240), CYP1A2(1544), CYP2C9(1559), IL8RA(3577), PTGS1(5742), PTGS2(5743)
mouse ... Alox5(11689)
rat ... Alox5(25290), Ptgs1(24693)
Application
- A Case of Erythema Nodosum in a 20-Year-Old Female During the Postpartum Period.:详细报道1例布洛芬参与治疗结节性红斑的临床病例。说明本品的治疗应用及相关风险(Nguyen M et al., 2024)。
- Coracoclavicular Joint Arthrosis - An Uncommon Cause of Shoulder Pain.:研究用布洛芬治疗罕见关节病相关的疼痛。加深了解骨科疾病中的疼痛管理(Graça NNJ et al., 2024)。
Biochem/physiol Actions
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。
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
R O Day et al.
Clinical pharmacology and therapeutics, 43(5), 480-487 (1988-05-01)
The simultaneous disposition of the enantiomers of ibuprofen in synovial fluid and plasma was studied in eight patients with arthritis. Concentrations of the active S-enantiomer in synovial fluid exceeded those of the R-enantiomer at all times in all patients with
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
Zhangjian Huang et al.
Journal of medicinal chemistry, 54(5), 1356-1364 (2011-02-02)
The carboxylic acid group of the anti-inflammatory (AI) drugs indo-methacin, (S)-naproxen and ibuprofen was covalently linked via a two-carbon ethyl spacer to a sulfohydroxamic acid moiety (CH(2)CH(2)SO(2)NHOH) to furnish a group of hybrid ester prodrugs that release nitric oxide (NO)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| I7905-10G | 04061833858400 |
| I7905-1G | 04061833858417 |
| I7905-5G | 04061833858424 |
