



| 货号 | 包装规格 | 操作 |
|---|---|---|
| A1221-5MG | 5 mg |
≥ 98%,结晶固体或过冷液体
AH6809 has been used:
as a prostaglandin E2 receptor 1 & 2 (EP1/2) antagonist to analyze its effects on cyclooxygenase-2 /prostaglandin E2 (COX-2/PGE2) signaling in the angiogenic feedback of endothelial cells to hypoxiaPMID 22050691as an EP2 antagonist to study its effects on tumor angiogenesis in human prostate cancer cell linesPMID 18829529as an EP2 antagonist to analyze its effects on overexpression of amyloid precursor protein (APP)PMID 15193769
AH 6809在拮抗非小细胞肺癌细胞系的增殖中起作用。PMID 11891031
DP/EP前列腺素类受体拮抗剂;对DP受体具有最高亲和力,但也可作为鼠EP 1和EP 2前列腺素类受体的弱拮抗剂。
该化合物在《受体分类和信号转导手册》的前列腺素受体页面上有介绍。要浏览其他手册页面,请点击这里。
| 英文名称 | AH6809 |
| CAS 号 | 33458-93-4 |
| 经验分子式 | C17H14O5 |
| 分子量 | 298.29 |
| NACRES | NA.77 |
| UNSPSC | 12352200 |
| MDL 号 | MFCD08056083 |
| InChI key | AQFFXPQJLZFABJ-UHFFFAOYSA-N |
| SMILES字符串 | CC(C)Oc1ccc2c(Oc3ccc(cc3C2 = O)C(O)= O)c1 |
| InChI | 1S/C17H14O5/c1-9(2)21-11-4-5-12-15(8-11)22-14-6-3-10(17(19)20)7-13(14)16(12)18/h3-9H,1-2H3,(H,19,20) |
| 含量测定 | ≥98% |
| 形态 | 结晶固体或过冷液体 |
| 溶解性 | 乙醇:可溶性2.5 mg/mL; DMSO或DMF:可溶性8 mg/mL |
| 质量等级 | 100 |
| 包装规格(货号 A1221-5MG) | 5 mg |