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L-798106
产品别名
244101-02-8
L-798106
(2E)-N-[(5-bromo-2-methoxyphenyl)sulfonyl]-3-[2-(2-naphthalenylmethyl)phenyl]-2-propenamide
结构式
基本信息
Empirical Formula【经验(实验)分子式】 | C27H22BrNO4S |
Molecular weight | 536.44 |
MDL number | MFCD08272644 |
PubChem Substance ID【PubChem化学物质编号】 | 329817411 |
Application【应用】 | L-798106, a selective prostanoid receptor EP3 antagonist, is used in prostanoid receptor signaling studies that regulate COX-2 levels and the central excitatory effects of PGE(2) on PVN neurons. |
Biochem/physiol Actions【生化/生理作用】 | L-798106 was among the first prostanoid receptor EP3-selective antagonists. It has been used in multiple studies to tease out EP3 agonist activity, both in vitro and in vivo. It successfully blocks the actions of sulprostone, an EP3-selective agonist, and it helped show that the vascular contraction effect of PGE2 is due to its prostanoid EP3 agonist activity. |
Features and Benefits【特点和优势】 | This compound was developed by Merck & Co., Inc., Kenilworth, NJ, U.S.. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here. |
产品性质
Quality Level【质量水平】 | 100 |
Assay【测定】 | ≥98% (HPLC) |
form【形式】 | powder |
solubility【溶解性】 | DMSO: >20 mg/mL |
originator【创始人】 | Merck & Co., Inc., Kenilworth, NJ, U.S. |
storage temp.【储存温度】 | 2-8℃ |
SMILES string | COc1ccc(Br)cc1S(=O)(=O)NC(=O)\C=C\c2ccccc2Cc3ccc4ccccc4c3 |
InChI | 1S/C27H22BrNO4S/c1-33-25-14-13-24(28)18-26(25)34(31,32)29-27(30)15-12-21-7-3-5-9-23(21)17-19-10-11-20-6-2-4-8-22(20)16-19/h2-16,18H,17H2,1H3,(H,29,30)/b15-12+ |
InChI key | ODTKFNUPVBULRJ-NTCAYCPXSA-N |
packaging【包装】 | 5, 25 mg in glass bottle |
安全信息
Hazard Statements | H413 |
Precautionary Statements | P273 - P501 |
Hazard Classifications【危险分类】 | Aquatic Chronic 4 |
Storage Class Code【储存分类代码】 | 13 - Non Combustible Solids |
WGK | WGK 3 |