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  • 化合物 PTG-0861|T61337|TargetMol

化合物 PTG-0861|T61337|TargetMol

PTG-0861
13800 50mg 起订
17500 100mg 起订
10600 25mg 起订
上海 更新日期:2025-11-17

TargetMol中国(陶术生物)

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联系人:邵小姐
手机:15002134094 拨打
邮箱:marketing@targetmol.cn

产品详情:

中文名称:
化合物 PTG-0861
英文名称:
PTG-0861
CAS号:
2494082-34-5
品牌:
TargetMol
产地:
美国
保存条件:
Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
产品类别:
抑制剂
货号:
T61337

Product Introduction

Bioactivity

名称PTG-0861
描述PTG-0861 is a highly specific inhibitor of histone deacetylase 6 (HDAC6), demonstrating an impressive IC50 value of 5.92 nm. This compound effectively triggers apoptosis and holds potential for research pertaining to acute myeloid leukemia, multiple myeloma, and other hematological cancers [1].
体外活性PTG-0861 (compound 54) (0.1-5 μM, 6 hours) stimulates the expression of acetylated a-tubulin and has inhibitory activity against HDAC6 with the IC 50 value of 0.59 μM [1]. PTG-0861 (compound 54) (0-4 μM, 18 hours) can induce apoptosis in a dose-dependent manner and has some cytotoxic effect [1]. Western Blot Analysis [1] Cell Line: MV4-11 cells Concentration: 0.1-5 μM Incubation Time: 6 hours Result: Induced the accumulation of acetylated a-tubulin expression at 500 nM. Immunofluorescence [1] Cell Line: HeLa cells Concentration: 0-2 μM Incubation Time: 6 hours Result: Increased levels of acetylated a-tubulin at 0.1 μM. Apoptosis Analysis [1] Cell Line: MV4-11 cells Concentration: 0-4 μM Incubation Time: 18 hours Result: Induced about 18% cells late apoptosis at 4 μM while at low dose 0.25 μM only about 5%. Cell Cytotoxicity Assay [1] Cell Line: Hematological cancer cell lines MV4-11, MM.1S, and RPMI 8226 Concentration: 1.24-4.94 μM Incubation Time: 72 hours Result: Showed cytotoxic effects on MV4-11, MM.1S, and RPMI 8226 with the IC 50 value of 1.85 μM,1.9 μM,4.94 μM, respectively. Cell Line: Concentration: Incubation Time: Result: Result: The pharmacokinetic parameters of PTG-0861 in vitro Parameter PTG-0861 Percent Remaining (%) 0 min 100.00 Percent Remaining (%) 30 min 96.41 Percent Remaining (%) 60 min 97.98 Percent Remaining (%) 120 min 97.08 T1/2 (min) ∞ T1/2 (min) 50.85 ± 3.37 CLint (mL/min/106 cells) 27.32 ± 1.81 -Log Pe 5.66 ± 0.02 Papp (A-B) (10 6, cm/s) 1.33 ± 0.03 Papp (B-A) (10 6, cm/s) 0.94 ± 0.13 Efflux Ratio 0.71 ± 0.08
体内活性PTG-0861 (compound 54) (oral administration, 20 mg/kg, everyday, 5 days) has no effect on weight and no obvious toxicity in CD1 mice [1]. Animal Model: CD1 mice [1] Dosage: 20 mg/kg Administration: Oral administration; everyday; 5 days Result: No weight loss in mice and no obvious toxicity. Animal Model: Male CD1 mice [1] Dosage: 20 mg/kg Administration: Intraperitoneal injection; once Result: The pharmacokinetic parameters of PTG-0861 in vivo Parameter PTG-0861 half-life 0.25 h C max 526 ng/mL AUC last 190 h ng/mL AUC inf 219 h ng/mL AUC Extr(%) 0.324 MRT(h) 0.350 AUC/D(h mg/mL) 9.5
存储条件Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
相关产品Sodium citrate | L-Methionine | Gefitinib | Cysteamine hydrochloride | Alginic acid | Metronidazole | Dextran sulfate sodium salt (MW 5000) | Citric Acid Triammonium | Stavudine | Cystamine dihydrochloride | L-Ascorbic acid sodium salt | Sodium 4-phenylbutyrate
PTG-0861|TargetMol

公司简介

TargetMol Chemicals Inc. 总部位于马萨诸塞州波士顿,致力于为全球生化领域科学家的研究提供专业的产品和服务。TargetMol?品牌的客户群分布于40多个国家和地区,已发展成为全球知名的化合物库和小分子化合物研究供应商。 TargetMol?可提供160多种满足不同需求的化合物库,以及多种类型的生化试剂产品,包括12000多种抑制剂、16000多种天然产物和各类多肽、抗体、生命科学试剂盒等,此外,我们还建设有CADD(计算机辅助药物设计)研究中心、药理实验室、药化合成平台三大技术中心,全方位满足客户的定制需求。 凭借我们优质的产品和服务、快速高效的全球供应链和专业的技术支持,我们将有效帮助您缩短研发周期,取得更成功的结果。

成立日期 (13年)
注册资本 589.8595万人民币
员工人数 100-500人
年营业额 ¥ 1亿以上
经营模式 贸易,工厂,试剂,定制,服务
主营行业 中间体,天然产物,生物化工,化学试剂,生物技术服务

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