IMT1B

(Synonyms: LDC203974)
目录号: PL03656 纯度: ≥98%
IMT1B (LDC203974) 是一种具有口服活性的,非竞争性的,特异性的线粒体 RNA 聚合酶 (POLRMT) 别构抑制剂,可抑制线粒体 DNA (mtDNA) 的表达。IMT1B 具有抗肿瘤作用。
CAS No. :2304621-06-3
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PL03656-5mg 5mg ¥2145.00 请登录
PL03656-10mg 10mg ¥3475.00 请登录
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PL03656-50mg 50mg ¥7555.00 请登录
PL03656-100mg 100mg ¥9865.00 请登录
PL03656-1 mL x 10 mM (in DMSO) 1 mL x 10 mM (in DMSO) ¥2225.00 请登录
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中文名称
IMT1B
英文名称
IMT1B
英文别名
LDC203974(IMT1B);(S)-1-((R)-2-((4-(2-Chloro-4-fluorophenyl)-2-oxo-2H-chromen-7-yl)oxy)propanoyl)piperidine-3-carboxylic acid;IMT1B
Cas No.
2304621-06-3
分子式
C24H21ClFNO6
分子量
473.88
包装储存
Powder -20°C 3 years;4°C 2 years
详情描述

IMT1B (LDC203974) 是一种具有口服活性的,非竞争性的,特异性的线粒体 RNA 聚合酶 (POLRMT) 别构抑制剂,可抑制线粒体 DNA (mtDNA) 的表达。IMT1B 具有抗肿瘤作用。

产品详情
IMT1B (LDC203974) 是一种具有口服活性的,非竞争性的,特异性的线粒体 RNA 聚合酶 (POLRMT) 别构抑制剂,可抑制线粒体 DNA (mtDNA) 的表达。IMT1B 具有抗肿瘤作用。
生物活性
IMT1B (LDC203974) is an orally active, noncompetitive and specific allosteric inhibitor of mitochondrial RNA polymerase (POLRMT) and inhibits mitochondrial DNA (mtDNA) expression. IMT1B has anti-tumour effects.
性状
Solid
IC50 & Target[1][2]
POLRMT
体外研究(In Vitro)
IMT1B is a noncompetitive inhibitor that causes a conformational change of POLRMT, which blocks substrate binding and transcription in a dose-dependent way in vitro.
IMT1B (0.01 nM-10 μM; 72-168 hours) dose-dependently decreases in cell viability in A2780, A549 and HeLa cells.
IMT1B depletes cellular metabolites.
IMT1B increases the levels of mono- and diphosphate nucleotides that results in a considerable increase in the AMP/ATP ratio and levels of phosphorylated AMPK.
has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
IMT1B (100 mg/kg; p.o.; daily; for four weeks) significantly reduces tumour size in mice containing xenografts.
IMT1B reduces mtDNA transcript levels and respiratory-chain subunit levels in tumours.
IMT1B exhibits good oral bioavailability (mice 101 %) and C max (mice 5149 ng/mL) following oral administration (mice 10 mg/kg).
IMT1B exhibits elimination half-life (mice 1.88 h) due to plasma clearance (mice 0.44 L/h/kg) following intravenous administration (mice 1 mg/kg).
has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Nina A Bonekamp, et al. Small-molecule inhibitors of human mitochondrial DNA transcription. Nature. 2020 Dec;588(7839):712-716.
溶解度数据
In Vitro: DMSO : 250 mg/mL (527.56 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)
[1]. Nina A Bonekamp, et al. Small-molecule inhibitors of human mitochondrial DNA transcription. Nature. 2020 Dec;588(7839):712-716.

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2