| 货号 | 包装规格 | 操作 |
|---|---|---|
| SML3025-5MG | 5 mg | |
| SML3025-25MG | 25 mg |
≥98%（HPLC）
BAY-784 is an orally available, non-toxic, potent, and selective antagonist of human Gonadotropin-Releasing Hormone Receptor [hGnRH-R], which is potently active in other species including rate, dogs and cynomolgus monkey. It partially lowered plasma luteinizing hormone levels in humans. BAY-784 exhibits favorable drug metabolism and pharmacokinetic (DMPK) profile thus is suitable for in vivo studies.
orally available, non-toxic, potent, and selective antagonist of human Gonadotropin-Releasing Hormone Receptor [hGnRH-R]
| 英文名称 | BAY-784 |
| CAS 号 | 1631164-24-3 |
| 经验分子式 | C29H26ClF4N3O5S2 |
| 分子量 | 672.11 |
| UNSPSC | 12352200 |
| NACRES | NA.77 |
| InChI | 1 S/C29 H26 ClF 4 N3 O 5S 2/C30-23-14-19（含硫化合物）（29（32，33）34）15-35-24（23）16-36-27（38）18-3-8-25-22（13-18）（9-11-43（39，40）12-10-28）26（17-1-2-17）37（25）44（41，42）21-6-4-20（31）5-7-21/h3- 8，13 -15，17，26H，1- 2，9 -12，16H2，（H，36，38）/t 26-/m0/s1 |
| InChI key | PZGSYNNVPNLHQG-SANMLTNESA-N |
| SMILES字符串 | O=S(CCC1(C2=C(N3S(C4=CC=C(F)C=C4)(=O)=O)C=CC(C(NCC5=C(Cl)C=C(C(F)(F)F)C=N5)=O)=C2)[C@@H]3C6CC6)(CC1)=O |
| 含量测定 | ≥98%（HPLC） |
| 形态 | 粉末 |
| 光学活性 | [α]/D -120 to -100°, c = 0.5 in chloroform-d |
| 颜色 | 白色至米色 |
| 溶解性 | DMSO: 2 mg/mL，清澈 |
| 储存温度 | 2-8°C |
| 质量等级 | 100 |
| 包装规格（货号 SML3025-5MG） | 5 mg |
| 包装规格（货号 SML3025-25MG） | 25 mg |
