N-(1H-benzimidazol-2-yl)-3-pyrrol-1-ylbenzamide manufacturers
- MKI-1
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- $61.00
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2026-07-14
- CAS:1190277-80-5
- Purity: 99.81%
- Supply Ability: 10g
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| | N-(1H-benzimidazol-2-yl)-3-pyrrol-1-ylbenzamide Basic information |
| Product Name: | N-(1H-benzimidazol-2-yl)-3-pyrrol-1-ylbenzamide | | Synonyms: | N-(1H-benzimidazol-2-yl)-3-pyrrol-1-ylbenzamide;MKI-1;Benzamide, N-1H-benzimidazol-2-yl-3-(1H-pyrrol-1-yl)-;MKI-1/MASTL Kinase Inhibitor-1;N-(1H-Benzo[d]imidazol-2-yl)-3-(1H-pyrrol-1-yl)benzamide;MKI-1, 10 mM in DMSO;N-1H-Benzimidazol-2-yl-3-(1H-pyrrol-1-yl)benzamide | | CAS: | 1190277-80-5 | | MF: | C18H14N4O | | MW: | 302.33 | | EINECS: | | | Product Categories: | | | Mol File: | 1190277-80-5.mol |  |
| | N-(1H-benzimidazol-2-yl)-3-pyrrol-1-ylbenzamide Chemical Properties |
| density | 1.31±0.1 g/cm3(Predicted) | | pka | 10.56±0.10(Predicted) | | form | Solid | | color | Off-white to light yellow |
| | N-(1H-benzimidazol-2-yl)-3-pyrrol-1-ylbenzamide Usage And Synthesis |
| Uses | MKI-1, an inhibitor of MASTL (microtubule-associated serine/threonine kinase-like) with an IC50 of 9.9 μM, exerts antitumor and radiosensitizer activities through PP2A activation in breast cancer[1]. | | in vivo | MKI-1 (50 mg/kg, ip, twice a week) reduces tumor growth and enhances the radiosensitivity of BT549 xenograft model in response to 6 Gy irradiation compared with the control group, with no notable changes in body weight, suggesting the absence of gross toxicity in the treated mice[1].
| Animal Model: | Five-week-old female BALB/c nude mice (BT549 cells)[1]. | | Dosage: | 50 mg/kg. | | Administration: | Twice per week by intraperitoneal (i.p.) injection. | | Result: | Reduced tumor growth. |
| | References | [1] Ah-Young Kim, et al. MKI-1, a Novel Small-Molecule Inhibitor of MASTL, Exerts Antitumor and Radiosensitizer Activities Through PP2A Activation in Breast cancer. Front Oncol. 2020 Sep 29;10:571601. DOI:10.3389/fonc.2020.571601 |
| | N-(1H-benzimidazol-2-yl)-3-pyrrol-1-ylbenzamide Preparation Products And Raw materials |
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