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质量水平
方案
≥95% (HPLC)
表单
powder
旋光性
[α]/D +162 to +178°, c = 1 in methanol
颜色
white to beige
溶解性
DMSO: 25 mg/mL, clear
储存温度
−20°C
SMILES字符串
O=C(O)[C@H]1C2=CC=C(C(C3=CC=CC=C3)=O)N2CC1
InChI
1S/C15H13NO3/c17-14(10-4-2-1-3-5-10)13-7-6-12-11(15(18)19)8-9-16(12)13/h1-7,11H,8-9H2,(H,18,19)/t11-/m1/s1
InChI key
OZWKMVRBQXNZKK-LLVKDONJSA-N
生化/生理作用
R-酮咯酸是Rho家族GTPases Cdc42（细胞分裂控制蛋白42）和Rac1（与Ras相关的C3肉毒杆菌毒素底物1）的一种有效选择性的变构抑制剂，可调节对肿瘤转移至关重要的下游GTPase依赖性生理反应。 R-酮咯酸可显著抑制卵巢癌细胞的粘附、迁移和侵袭。
酮咯酸（（rac）-5-苯甲酰基-1,2-3H-吡咯并[1,2a]吡咯1-羧酸）是一种非甾体类抗炎药（NSAID）。它被用作外消旋混合物，其包含1:1的R（+）和S（−）立体异构体。它被广泛用于儿童的肠外镇痛药。酮咯酸可用作非麻醉性镇痛药。它可阻止中枢神经系统外围的前列腺素的合成。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
Enantiomer?selective pharmacokinetics and metabolism of ketorolac in children.
Kauffman RE, et al.
Clinical Pharmacology and Therapeutics, 65(4), 382-388 (1999)
Tudor I Oprea et al.
Drug discovery today. Therapeutic strategies, 8(3-4), 61-69 (2012-03-01)
Academia and small business research units are poised to play an increasing role in drug discovery, with drug repurposing as one of the major areas of activity. Here we summarize project status for a number of drugs or classes of
The pharmacokinetics of ketorolac enantiomers following intramuscular administration of the racemate.
Hayball PJ, et al.
British Journal of Clinical Pharmacology, 37(1), 75-78 (1994)
Yuna Guo et al.
Molecular cancer therapeutics, 14(10), 2215-2227 (2015-07-25)
Cdc42 (cell division control protein 42) and Rac1 (Ras-related C3 botulinum toxin substrate 1) are attractive therapeutic targets in ovarian cancer based on established importance in tumor cell migration, adhesion, and invasion. Despite a predicted benefit, targeting GTPases has not
Tudor I Oprea et al.
PloS one, 10(11), e0142182-e0142182 (2015-11-13)
Rho family GTPases (including Rac, Rho and Cdc42) collectively control cell proliferation, adhesion and migration and are of interest as functional therapeutic targets in numerous epithelial cancers. Based on high throughput screening of the Prestwick Chemical Library® and cheminformatics we
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