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Etodolac(AY-24236)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Etodolac(AY-24236)图片
CAS NO:41340-25-4
规格:≥98%
包装与价格:
包装价格(元)
500mg电议
1g电议
2g电议
5g电议
10g电议
25g电议

产品介绍
理化性质和储存条件
Molecular Weight (MW)287.35
FormulaC17H21NO3
CAS No.41340-25-4
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 58 mg/mL (201.8 mM)
Water: <1 mg/mL
Ethanol: 58 mg/mL (201.8 mM)
Other info

Chemical Name: (RS)-2-(1,8-Diethyl-4,9-dihydro-3H-pyrano[3,4-b]indol-1-yl)acetic acid

InChi Key: NNYBQONXHNTVIJ-UHFFFAOYSA-N

InChi Code: InChI=1S/C17H21NO3/c1-3-11-6-5-7-12-13-8-9-21-17(4-2,10-14(19)20)16(13)18-15(11)12/h5-7,18H,3-4,8-10H2,1-2H3,(H,19,20)

SMILES Code: O=C(O)CC1(CC)OCCC2=C1NC3=C2C=CC=C3CC

SynonymsAY 24,236, Lodine, AY24,236, AY24236, Etodolic Acid, AY 24236, AY-24,236, AY-24236, Ramodar, Ultradol
实验参考方法
In Vitro

In vitro activity: Etodolac markedly inhibits ICl, vol activation by TNFα as well as subsequent apoptotic events such as apoptotic cell volume decrease (AVD) and elevation of caspase-3/7 activity in isolated rabbit articular chondrocytes.


In Vivo
Etodolac attenuates paclitaxel-induced peripheral neuropathy by a COX-independent pathway in a mouse model of mechanical allodynia. Etodolac and other NSAIDs inhibits paw swelling and causes gastric mucosal lesions in adjuvant arthritic rats in a dose-dependent manner. Etodolac shows the highest UD(50) value and safety index among these NSAIDs in arthritic rats. Etodolac also shows the highest UD(50) value and safety index, except when its effects are assessed by acetic acid-induced writhing in normal rats. Etodolac dose-dependently inhibits the development of gastric cancer, and no cancer is detected at a dose of 30 mg/kg/day. Etodolac does not affect the extent of inflammatory cell infiltration or oxidative DNA damage, but it significantly inhibits mucosal cell proliferation and dose-dependently represses the development of intestinal metaplasia in the stomachs of Helicobacter pylori (Hp)-infected Mongolian gerbils (MGs). Etodolac alleviates heat-evoked hyperalgesia in the CCI rats and the increase in number of TRAP-positive multinucleated osteoclasts on the CCI-side is abrogated, however, it does not inhibit the decrease of bone mineral content (BMC) and bone mineral density (BMD) on the CCI-side.
Animal modelMice
Formulation & Dosage30 mg/kg
References

Int J Mol Sci. 2013 Sep 30;14(10):19705-15; J Pharmacol Exp Ther. 2012 Jul;342(1):53-60.