说明: UPGL00004是一种有效的谷氨酰胺酶C(GAC)抑制剂(IC50=29nM;Kd=27nM)。UPGL00004强烈抑制高度侵袭性三阴性乳腺癌细胞系的增殖。 Information UPGL00004 UPGL00004 is a potent glutaminase C (GAC) inhibitor with an IC50 of 29 nM, showing high selectivity for GAC over GLS2. Targets glutaminase C (Cell-free assay) 29 nM In vitro UPGL00004 potently inhibits the growth of triple negative breast cancer cells, as well as tumor growth when combined with the anti-VEGF antibody bevacizumab. In vivo UPGL00004 potently suppresses tumor growth in a patient-derived xenograft model for breast cancer, when combined with the anti-angiogenesis, anti-VEGF monoclonal antibody bevacizumab. Cell Research(from reference) Cell lines:Breast cancer cells Concentrations:0-10 μM Incubation Time:6 days
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UPGL00004
CAS number:1890169-95-5 molecular formula:C25H26N8O2S2
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| Chinese alias | - | ||
| English alias | 2-Phenyl-N-(5-(4-((5-(2-phenylacetamido)-1,3,4-thiadiazol-2-yl)amino)piperidin-1-yl)-1,3,4-thiadiazol-2-yl)acetamide | N-[5-[4-[[5-[(2-Phenylacetyl)amino]-1,3,4-thiadiazol-2-yl]amino]-1-piperidinyl]-1,3,4-thiadiazol-2-yl]benzeneacetamide | ||
| CAS number | 1890169-95-5 | molecular formula | C25H26N8O2S2 |
| molecular weight | 534.66 g/mol | Exact mass | ≥98% |
| PSA | 182.000 Ų | logp | 3.091 |
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