| 货号:AG-CR1-3673-M001 | 规格:1 mg | 目录价:¥360 |
| 货号:AG-CR1-3673-M005 | 规格:5 mg | 目录价:¥1320 |
| 货号:AG-CR1-3673-M025 | 规格:25 mg | 目录价:¥4560 |
产品详情
* 以下信息仅供参考,详情请以原厂网站为准
产品名称:
Delanzomib [CEP-18770]
别名:
NPH 007098; CT 47098; CIP 18770; [(1R)-1-[[(2S,3R)-3-Hydroxy-2-[(6-phenylpyridine-2-carbonyl)amino]butanoyl]amino]-3-methylbutyl]boronic acid
产品描述:
Potent, selective, reversible orally bioavailable proteasome inhibitor. Synthetic P2 threonine boronic acid. Targets the chymotrypsin-like beta5 subunit of the constitutive 20S proteasome (IC50=3.8nM). Cross-reacts and inhibits the caspase-like/peptidyl-glutamyl peptide-hydrolyzing (PGPH) beta1 subunit (IC50=~70nM). Displays similar potency for the chymotrypsin-like activity of the proteasome compared to bortezomib. Exhibits a favorable cytotoxicity profile toward normal human epithelial cells, bone marrow progenitors and bone marrow-derived stromal cells relative to bortezomib (Prod. No. AG-CR1-3602). Anticancer compound effective against multiple myeloma in vivo. In vitro, blocks the growth of representative human solid and hematological tumor cell lines (IC50s=5.6-34nM). Shown to down-modulate NF-kappaB, induce apoptosis, inhibit angiogenesis and M-CSF-RANKL-induced osteoclastogenesis.
保存温度:
+4°C
运输温度:
Ambient
预期分子量:
413.3
产品形式:
solid
产地:
瑞士
纯度:
>95% (1H-NMR)
CAS号:
847499-27-8
分子式:
C21H28BN3O5
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