喷昔洛韦|T1643|TargetMol

Penciclovir
39809-25-1

￥786 500mg 起订

￥328 100mg 起订

￥476 200mg 起订

上海更新日期：2025-03-12

TargetMol中国（陶术生物）

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产品详情:

中文名称：: 喷昔洛韦

英文名称：: Penciclovir

CAS号：: 39809-25-1

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：: 99.1%

产品类别：: 抑制剂

货号：: T1643

Product Introduction

Bioactivity

名称	Penciclovir
描述	Penciclovir (BRL 39123) is a Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor. In HSV infected cells, penciclovir is phosphorylated by viral thymidine kinase and subsequently converted by cellular kinases into the active metabolite, penciclovir triphosphate, which competitively inhibits viral HSV polymerase by blocking deoxyguanosine triphosphate substrate binding. As a result, herpes viral DNA synthesis and replication are selectively inhibited.
细胞实验	Penciclovir is dissolved with DMSO and diluted with appropriate media[2]. Human breast cancer cell lines MCF-7 and MDA-MB-435, glioblastoma U87 mg, and embryonic kidney cells 293T are cultured at 37°C in a humidified atmosphere containing 5% CO2 in Iscove's modified Dulbecco medium or Leibovitz's L-medium and 5% fetal bovine serum (FBS). The assays are performed with slight modifications. In brief, cells are seeded into 24-well plates (5×104 cells/well) and infected 48 h later with 103 particles per cell of unmodified virus (Adtk), PEGylated virus (PEG-Adtk), or RGD-PEG-modified virus (RGD-PEG-Adtk) in triplicates in culture medium with 2% FBS and incubated for 4 h at 37°C. The incubation medium is then replaced by normal medium and cells are further incubated for 48 h. Cells are harvested and lysed with 500 μL of TK lysis buffer that contained 0.5% Nonidet P-40 (NP-40), 20 mM N-(2-hydroxyethyl) piperazine-N′-(2-ethanesulfonic acid) (HEPES) (pH 7.6), 2 mM Mg(OAc)2, 1 mM dithiothreitol, and 50 μM thymidine. The supernatant is collected after centrifugation. The samples are kept at -80°C until use. The modified and unmodified adenovirus protein concentrations are determined by the Micro BCA assay. One microgram of cell extract is incubated with HSV1-tk substrate 8-3H-Penciclovir (8-3 H-PCV). The phosphorylated tracer is separated from unphosphorylated 8-3 H-PCV with DE-81 filters. TK activity is expressed as the percentage of conversion of substrate per minute per microgram protein[2].
体内活性	Penciclovir具有抗多种病毒疱疹的活性,如抗HHV-6A（IC50：37.9 μM）和HHV-6B（IC50：77.8 μM）。Penciclovir具有抗Ⅰ型和Ⅱ型单纯疱疹病毒的体外活性,且对水痘带状疱疹病毒也有较好作用,却不影响未感染细胞中DNA的合成。作为鸟嘌呤类似物,Penciclovir毒性低、选择性高。Penciclovir由细胞激酶转化成三磷酸盐的活性形式,与脱氧鸟苷三磷酸竞争性抑制病毒DNA聚合酶,进而抑制病毒感染细胞的DNA合成。单纯疱疹病毒Ⅰ型的相关研究显示,Penciclovir使细胞凋亡,但造成的基因毒性较小。
存储条件	Powder: -20°C for 3 years \| In solvent: -80°C for 1 year \| Shipping with blue ice.
溶解度	H2O : 1 mg/mL (3.94 mM) DMSO : 50 mg/mL (197.43 mM), Sonication is recommended. Ethanol : < 1 mg/mL (insoluble or slightly soluble)
关键字	VSA671 \| BRL-39123 \| mortality \| inhibit \| HSV \| no-toxic \| Inhibitor \| anti-herpesvirus \| VSA-671 \| BRL39123 \| Penciclovir \| Herpes simplex virus
相关产品	Oxyresveratrol \| Acyclovir \| Adenosine 5'-monophosphate monohydrate \| Levamisole hydrochloride \| Chlorhexidine diacetate \| Metronidazole \| Artemisinin \| EIDD-1931 \| Methyl 2-amino-5-bromobenzoate \| Idoxuridine \| L-Lysine \| Ribavirin
相关库	抑制剂库 \| 经典已知活性库 \| 已知活性化合物库 \| FDA 上市药物库 \| 抗病毒库 \| 药物功能重定位化合物库

喷昔洛韦|||VSA 671|||BRL 39123|TargetMol

上海陶术生物科技有限公司为美国Target Molecule Corp. ( Target Mol ) 在上海建立的全资子公司。我们与美国波士顿、德国慕尼黑的同事一起，为北美、欧洲和亚洲从事药物研发和生物学研究的科学家提供优质的产品和专业的服务。公司下设筛选事业部，化学事业部，生物事业部和新材料部。从虚拟筛选到实体化合物分子供应；从商业化产品销售到个性化定制合成；从对明确靶点的分子筛选到对明确分子的多靶点筛选，从高通量筛选到化学结构优化，我们都可以满足您的科研用品及技术服务的需求。经过在中国市场五年的精心耕耘，我们已成为筛选化合物领域优秀的供应商，为超过五百家学校和各类企业提供了品质卓越的小分子化合物和药物筛

成立日期	(12年)
注册资本	566.2651万人民币
员工人数	100-500人
年营业额	￥ 1亿以上
经营模式	贸易,试剂,定制,服务
主营行业	化学试剂,生物活性小分子