2349356-09-6
中文名稱(chēng)
化合物 T30600
英文名稱(chēng)
BSJ-03-204
CAS
2349356-09-6
分子式
C43H48N10O8
分子量
832.9
MOL 文件
2349356-09-6.mol
更新日期
2026/06/12 17:40:22
2349356-09-6 結(jié)構(gòu)式
基本信息
中文別名
化合物 T30600 英文別名
BSJ-03-204Acetamide, N-[4-[4-[6-[(6-acetyl-8-cyclopentyl-7,8-dihydro-5-methyl-7-oxopyrido[2,3-d]pyrimidin-2-yl)amino]-3-pyridinyl]-1-piperazinyl]butyl]-2-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1,3-dioxo-1H-isoindol-4-yl]oxy]-
物理化學(xué)性質(zhì)
密度1.397±0.06 g/cm3(Predicted)
儲(chǔ)存條件-20°C, protect from light
溶解度溶于二甲基亞砜
酸度系數(shù)(pKa)10.68±0.40(Predicted)
形態(tài)Solid
顏色Light yellow to green yellow
化合物 T30600價(jià)格(試劑級(jí))
| 報(bào)價(jià)日期 | 產(chǎn)品編號(hào) | 產(chǎn)品名稱(chēng) | CAS號(hào) | 包裝 | 價(jià)格 |
| 2026/06/05 | HY-136250 | 化合物 T30600 BSJ-03-204 | 2349356-09-6 | 1 mg | 1591元 |
| 2026/06/05 | HY-136250 | 化合物 T30600 BSJ-03-204 | 2349356-09-6 | 5mg | 3500元 |
| 2026/06/05 | HY-136250 | 化合物 T30600 BSJ-03-204 | 2349356-09-6 | 10mg | 5800元 |
常見(jiàn)問(wèn)題列表
生物活性
BSJ-03-204 是一種有效的，選擇性的基于 Palbociclib (HY-50767) 的 CDK4/6 雙重降解劑 (PROTAC)，對(duì) CDK4/D1 和 CDK6/D1 的 IC50 分別為 26.9 nM 和 10.4 nM。BSJ-03-204 不誘導(dǎo) IKZF1/3 降解，具有抗癌活性。靶點(diǎn)
|
CDK4/D1 26.9 nM (IC 50 ) |
CDK6/D1 10.4 nM (IC 50 ) |
體外研究
BSJ-03-204 (0.0001-100 μM; for 3 or 4 days) has potent anti-proliferative effects on MCL cell lines.
BSJ-03-204 (1 μM; for 1 day) potently induces a G1 arrest.
BSJ-03-204 (0.1-5 μM; for 4 hours) only resultes in degradation of CDK4/6 in WT cells, not IKZF1/3.
Cell Proliferation Assay
| Cell Line: | MCL cell lines (Jeko-1, Mino, Granta-519, Rec-1, and Maver-1 cells) |
| Concentration: | 0.0001-100 μM |
| Incubation Time: | For 3 or 4 days |
| Result: | Had potent anti-proliferative effects on mantle cell lymphoma (MCL) cell lines. |
Cell Cycle Analysis
| Cell Line: | Granta-519 cells |
| Concentration: | 1 μM |
| Incubation Time: | For 1 day |
| Result: | Potently induced a G1 arrest. |
Western Blot Analysis
| Cell Line: | Wildtype (WT) or Crbn -/- Jurkat cells |
| Concentration: | 0.1, 0.5, 1, 5 μM |
| Incubation Time: | For 4 hours |
| Result: | Only resulted in degradation of CDK4/6 in WT cells, not IKZF1/3. |