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  • 麦冬皂苷D|T6S1255|TargetMol

麦冬皂苷D|T6S1255|TargetMol

Ophiopogonin-D
41753-55-3
578 1mg 起订
853 2mg 起订
1450 5mg 起订
上海 更新日期:2024-09-29

TargetMol中国(陶术生物)

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联系人:邵小姐
手机:4008200310 拨打
邮箱:marketing@tsbiochem.com

产品详情:

中文名称:
麦冬皂苷D
英文名称:
Ophiopogonin-D
CAS号:
41753-55-3
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.
纯度规格:
≥98%
产品类别:
抑制剂
货号:
T6S1255

Product Introduction

Bioactivity

名称Ophiopogonin-D
描述Ophiopogonin-D significantly inhibited the in vitro and in vivo growth of prostate cells via RIPK1. Ophiopogonin-D may be developed as a potential anti-prostate cancer agent.
细胞实验The CCK-8 assay was used to assess the viability of prostate cancer cells.?The cell morphology was examined by an ultrastructural analysis via transmission electron microscopy.?Cells in apoptosis (early and late stages) were detected using an Annexin V-FITC/propidium iodide kit with a FACSCaliber flow cytometer.?JC-1, a cationic lipophilic probe, was employed to measure the mitochondrial membrane potential (MMP) of PC3 cells.?Changes in the protein expression of RIPK1, C-RIPK1, caspase 8, cleaved-caspase 8, Bim, Bid, caspase 10, and cleaved-caspase 10 were evaluated by Western blotting.?The mRNA expression of Bim was examined by quantitative real-time reverse transcription polymerase chain reaction.?Z-VAD-FMK (a caspase inhibitor) and necrostatin-1 (a specific inhibitor of RIPK1) were utilized to determine whether the cell death was mediated by RIPK1 or caspases[1].
动物实验One week after tumor cell inoculation, mice bearing palpable tumors were randomly divided into control and treatment groups (8 mice/group).?OPD′ was dissolved in the vehicle, PEG400:Saline:Ethanol (400:300:200, v/v/v), and administered (via i.p. injection) at doses of 2.5 or 5.0 mg/kg bodyweight 5 days a week for 24 days.?The control group received vehicle only.?The mice were sacrificed by cervical dislocation on Day 24, and the tumor tissues were removed and weighed[1].
体外活性Ophiopogonin D(OPD) 对PC3细胞展现了强大的抗肿瘤活性。通过RIPK1相关途径诱导细胞凋亡,提高了RIPK1和Bim的蛋白表达水平,降低了cleaved-RIPK1、caspase 8、cleaved-caspase 8、Bid、caspase 10、及cleaved-caspase 10的水平。OPD还增加了Bim的mRNA表达。当细胞预先用necrostatin-1[1]处理时,Bim的蛋白表达水平降低。
体内活性Ophiopogonin D(OPD)′ 以5mg/kg剂量治疗,自治疗第6天起显著抑制肿瘤生长(p = 0.034)。研究结束时(第24天),切除、拍照并称重肿瘤组织。以5mg/kg OPD′治疗结果在第24天与对照治疗相比,肿瘤生长抑制显著(p = 0.000),约79.8%。5.0 mg/kg剂量的肿瘤生长抑制作用明显强于2.5 mg/kg剂量(p = 0.000)。所有组别均未发现显著的体重减轻[1]。
存储条件Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度DMSO : 30 mg/mL (35.09 mM)
关键字Ophiopogonin D | Ophiopogonin-D | OphiopogoninD
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麦冬皂苷D|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 (12年)
注册资本 566.265100万人民币
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 天然产物,生化试剂,分子生物学,分子砌块,生物技术服务

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