Company Name: |
Shanghai YuanYe Biotechnology Co., Ltd.
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Tel: |
021-61312847; 18021002903 |
Email: |
3008007409@qq.com |
Products Intro: |
Product Name:SEC inhibitor KL-2 CAS:900308-51-2 Purity:98% Package:5mg Remarks:S89687
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SEC inhibitor KL-2 manufacturers
- SEC inhibitor KL-2
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- $32.00 / 1mg
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2025-06-12
- CAS:900308-51-2
- Min. Order:
- Purity: 98.03%
- Supply Ability: 10g
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| SEC inhibitor KL-2 Basic information |
Product Name: | SEC inhibitor KL-2 | Synonyms: | KL2;KL-2;KL 2;2-Butenamide, N-(5-chloro-2-methylphenyl)-4-(4-fluorophenyl)-2-hydroxy-4-oxo-;N-(5-Chloro-2-methylphenyl)-4-(4-fluorophenyl)-2-hydroxy-4-oxobut-2-enamide;SEC inhibitor KL-2, 10 mM in DMSO | CAS: | 900308-51-2 | MF: | C17H13ClFNO3 | MW: | 333.74 | EINECS: | | Product Categories: | | Mol File: | 900308-51-2.mol |  |
| SEC inhibitor KL-2 Chemical Properties |
Boiling point | 521.1±50.0 °C(Predicted) | density | 1.400±0.06 g/cm3(Predicted) | storage temp. | Store at -20°C | solubility | Soluble in DMSO | pka | 8.09±0.50(Predicted) | form | Solid | color | Light yellow to yellow |
| SEC inhibitor KL-2 Usage And Synthesis |
Uses | SEC inhibitor KL-2 (KL-2), a peptidomimetic lead compound, is a potent, selective super elongation complex (SEC) inhibitor and disrupts the interaction between the SEC scaffolding protein AFF4 and P-TEFb, resulting in impaired release of Pol II from promoter-proximal pause sites and a reduced average rate of processive transcription elongation. SEC inhibitor KL-2 exhibits an dose-dependent inhibitory effect on AFF4-CCNT1 interaction with a Ki of 1.50 μM[1]. | Biochem/physiol Actions | Disruptor of SEC (super elongation complex) | in vivo | SEC inhibitor KL-2 (10 mg/kg, i.p., once daily for 15 days) delays tumor growth and prolonged survival in the MDA231-LM2 xenograft tumor model in nude mice[1]. Animal Model: | MDA231-LM2 xenograft tumor model in nude mice[1] | Dosage: | 10 mg/kg | Administration: | Intraperitoneal injection (i.p.), once daily for 15 days | Result: | Significantly delayed tumor growth and increased survival of mice. |
| References | [1] Liang K, et al. Targeting Processive Transcription Elongation via SEC Disruption for MYC-Induced CancerTherapy. Cell. 2018 Oct 18;175(3):766-779. DOI:10.1016/j.cell.2018.09.027 |
| SEC inhibitor KL-2 Preparation Products And Raw materials |
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