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Merck
CN

SML3299

Sigma-Aldrich

S-Ketorolac

≥98% (HPLC)

别名:

(-)-Ketorolac, (1S)-5-Benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid, (S)-Ketorolac

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关于此项目

经验公式(希尔记法):
C15H13NO3
化学文摘社编号:
分子量:
255.27
MDL编号:
UNSPSC代码:
51111800
NACRES:
NA.77
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质量水平

方案

≥98% (HPLC)

表单

powder

旋光性

[α]/D -165 to -185°, c = 0.5 in methanol

颜色

white to beige

溶解性

DMSO: 2 mg/mL, clear

储存温度

2-8°C

SMILES字符串

[n]21c(ccc2C(=O)c3ccccc3)[C@H](CC1)C(=O)O

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-/m0/s1

InChI key

OZWKMVRBQXNZKK-NSHDSACASA-N

生化/生理作用

S-Ketorolac is an active enantiomer of nonsteroidal anti-inflammatory drug Ketorolac. S-Ketorolac is a selective and potent cyclooxygenase 1/2 (COX-1/2) inhibitor which exhibits anti-inflammatory activities. It is significantly more potent than non-selective COX inhibitors indomethacin or diclofenac.
selective and potent COX-1/2 inhibitor

象形图

Skull and crossbones

警示用语:

Danger

危险声明

危险分类

Acute Tox. 3 Oral

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Pyry A Välitalo et al.
British journal of clinical pharmacology, 83(9), 1966-1975 (2017-04-22)
Although ketorolac analgesia is linked only to the S-enantiomer, there is limited information on the stereo-selective pharmacokinetics of this agent. We studied the stereo-selective pharmacokinetics of ketorolac in a pooled dataset of two studies, with women at delivery and 4-5 months
M F Jett et al.
The Journal of pharmacology and experimental therapeutics, 288(3), 1288-1297 (1999-02-23)
The marked analgesic efficacy of ketorolac in humans, relative to other nonsteroidal anti-inflammatory drugs (NSAIDs), has lead to speculation as to whether additional non-NSAID mechanism(s) contribute to its analgesic actions. To evaluate this possibility, we characterized (R,S)-ketorolac's pharmacological properties in
Laurie G Hudson et al.
Cancers, 11(8) (2019-07-28)
Cytoreductive surgery and chemotherapy are cornerstones of ovarian cancer treatment, yet disease recurrence remains a significant clinical issue. Surgery can release cancer cells into the circulation, suppress anti-tumor immunity, and induce inflammatory responses that support the growth of residual disease.

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