G-1
G-1 is a selective agonist for GPER. It acts by blocking tubulin polymerization.
仅供研究使用。 我们不向患者出售。
化学信息
| 名称 | G-1 |
|---|---|
| Iupac 化学名称 | Syn-1-[4-(6-bromobenzo[1,3] dioxol-5yl)-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinolin-8-yl]-ethanone |
| 同义词 | G-1; G 1; G1; |
| 英文同义词 | G-1; G 1; G1; |
| 分子式 | C21H18BrNO3 |
| 分子量 | 412.28 |
| Smile | CC(C1=CC2=C(NC(C3=C(Br)C=C(OCO4)C4=C3)C5C2C=CC5)C=C1)=O |
| InChiKey | VHSVKVWHYFBIFJ-UHFFFAOYSA-N |
| InChi | InChI=1S/C21H18BrNO3/c1-11(24)12-5-6-18-15(7-12)13-3-2-4-14(13)21(23-18)16-8-19-20(9-17(16)22)26-10-25-19/h2-3,5-9,13-14,21,23H,4,10H2,1H3 |
| Cas号 | 881639-98-1 |
| 相关CAS号 |
订购信息
| 包装 | 价格 | 库存 | 纯度 | 备货期 |
|---|---|---|---|---|
| 大货 | 询价 | 询价 | 询价 |
| 外观性状 | 固体粉末 |
|---|---|
| 纯度 | 98% Min. |
| 存储 | 干燥、黑暗，短期（日至周）0-4摄氏度，长期（月至年）0-20摄氏度。 |
| 可溶性 | 可溶于DMSO |
| 处理方式 | |
| 运输条件 | 作为非危险化学品在环境温度下装运。这种产品在正常运输和海关工作期间可以稳定几周 |
| 海关编码 |
| Targets | |
|---|---|
| Mechanism | |
| Cell study | |
| Animal study | |
| Clinical study |
1: Thomas P. Rapid steroid hormone actions initiated at the cell surface and the receptors that mediate them with an emphasis on recent progress in fish models. Gen Comp Endocrinol. 2012 Feb 1;175(3):367-83. doi: 10.1016/j.ygcen.2011.11.032. Epub 2011 Nov 29. Review. PubMed PMID: 22154643; PubMed Central PMCID: PMC3264783.
2: Revankar CM, Mitchell HD, Field AS, Burai R, Corona C, Ramesh C, Sklar LA, Arterburn JB, Prossnitz ER. Synthetic estrogen derivatives demonstrate the functionality of intracellular GPR30. ACS Chem Biol. 2007 Aug 17;2(8):536-44. Epub 2007 Jul 27. PubMed PMID: 17655271.
3: Song RX, Fan P, Yue W, Chen Y, Santen RJ. Role of receptor complexes in the extranuclear actions of estrogen receptor alpha in breast cancer. Endocr Relat Cancer. 2006 Dec;13 Suppl 1:S3-13. Review. PubMed PMID: 17259556.
4: Revankar CM, Cimino DF, Sklar LA, Arterburn JB, Prossnitz ER. A transmembrane intracellular estrogen receptor mediates rapid cell signaling. Science. 2005 Mar 11;307(5715):1625-30. Epub 2005 Feb 10. PubMed PMID: 15705806.
