Oprozomib (ONX-0912)

产品编号: DC2010 Featured
Oprozomib (ONX-0912)
结构式
935888-69-0
此产品仅供科研所需,我们不出售给病人
​我们将匹配市场上最好的价格给您
Email:order@dcbio.cn
免费咨询电话:4008862077
我们的合作伙伴:
  • 20
  • 19
  • 18
  • 17
  • 16
  • 15
  • 14
  • 12
  • 11
  • 10
  • 9
  • 8
  • 13
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
中国地区超过5000个高品质化合物库存
应用领域
Oprozomib (ONX 0912; PR047)是口服生物相容性的抑制剂,能抑制20S proteasome(20S蛋白酶体)β5/LMP7的CT-L活性,IC50为36 nM/82 nM。
Cas No.: 935888-69-0
名称: L-Serinamide, O-methyl-N-[(2-methyl-5-thiazolyl)carbonyl]-L-seryl-O-methyl-N-[(1S)-2-[(2R)-2-methyl-2-oxiranyl]-2-oxo-1-(phenylmethyl)ethyl]-
别名: Oprozomib, ONX0912
SMILES: CC1=NC=C(S1)C(=O)N[C@@H](COC)C(=O)N[C@@H](COC)C(=O)N[C@@H](CC2=CC=CC=C2)C(=O)[C@]3(CO3)C
分子式: C25H32N4O7S
分子量: 532.61
纯度:
保存条件: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description:
In Vivo:
In Vitro:
References: Description of Oprozomib (ONX 0912): ONX 0912 is an orally bioavailable proteasome inhibitor with potential antineoplastic activity. ONX 0912 inhibits the activity of the proteasome, thereby blocking the targeted proteolysis normally per Formed by the proteasome; this may result in an accumulation of unwanted or misfolded proteins. Disruption of various cell signaling pathways may follow, eventually leading to the induction of apoptosis and inhibition of tumor growth. Proteasomes are large protease complexes that degrade unneeded or damaged proteins that have been ubiquitinated. Check For active clinical trials or closed clinical trials using this agent. (NCI Thesaurus). For the detailed information about the solubility of Oprozomib (ONX-0912) in water, the solubility of Oprozomib (ONX-0912) in DMSO, the solubility of Oprozomib (ONX-0912) in PBS buffer, the animal experiment(test) of Oprozomib (ONX-0912),the in vivo,in vitro and clinical trial test of Oprozomib (ONX-0912),the cell experiment(test) of Oprozomib (ONX-0912),the IC50, EC50 and Affinity of Oprozomib (ONX-0912), please contact DC Chemicals.
Kinase Assay:
Cell Assay:
Animal Administration:
References:
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
产品编号 产品名称 应用领域
DC8481 Delanzomib(CEP-18770) Delanzomib(CEP-18770)是口服活性的蛋白酶体糜蛋白酶样活性抑制剂,能下调核内NF-kappaB活性。
DC5089 Ixazomib Citrate (MLN-9708) Ixazomib citrate (MLN9708) 是 20S蛋白酶体胰凝乳蛋白酶样蛋白水解β5位点的可逆抑制剂,IC50 为3.4 nM和Ki为0.93 nM。
DC2010 Oprozomib (ONX-0912) Oprozomib (ONX 0912; PR047)是口服生物相容性的抑制剂,能抑制20S proteasome(20S蛋白酶体)β5/LMP7的CT-L活性,IC50为36 nM/82 nM。
DC1027 Bortezomib (Velcade,MG-341,PS-341) Bortezomib (PS-341) 是一种可逆性和选择性的蛋白酶体抑制剂,通过靶向苏氨酸残基有效抑制 20S 蛋白酶体 (Ki=0.6 nM)。Bortezomib 破坏细胞周期、诱导细胞凋亡以及抑制核因子 NF-κB。Bortezomib 具有抗肿瘤活性。
DC1002 Carfilzomib (PR-171) Carfilzomib是不可逆的蛋白酶体 (proteasome) 抑制剂,其在ANBL-6和RPMI 8226细胞中的 IC50 为5 nM。