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Cidofovir/西多福韦 {[allProObj[0].p_purity_real_show]}

货号:A370831 同义名: GS 0504; HPMPC

Cidofovir 是一种抗 CMV 化合物,通过选择性抑制病毒 DNA 聚合酶,抑制 CMV 复制,从而防止病毒复制和转录。

HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Cidofovir/西多福韦 化学结构 CAS号:113852-37-2
Cidofovir/西多福韦 化学结构
CAS号:113852-37-2
Cidofovir/西多福韦 3D分子结构
CAS号:113852-37-2
Cidofovir/西多福韦 化学结构 CAS号:113852-37-2
Cidofovir/西多福韦 3D分子结构 CAS号:113852-37-2
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Cidofovir/西多福韦 纯度/质量文件 产品仅供科研

货号:A370831 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 DNA synthesis helicase RdRp ribonucleotide reductase tRNA synthetase YB-1 其他靶点 纯度
Fexinidazole 98%
Daptomycin 98%
Blasticidin S·HCl 98%
Metronidazole 98%
Daunorubicin HCl +++

DNA synthesis, Ki: 20 nM

98%
Triglycidyl isocyanurate p53 98+%
Nedaplatin 99%+
Oxolinic acid 98+%
Bendamustine 98+%
Trifluridine 98%
Robinetin 99%+
Carboplatin 99%
Cidofovir 99%
Cisplatin 99%
Cytarabine ++++

DNA synthesis, IC50: 16 nM

98%
Acelarin ++++

DNA synthesis, EC50: 0.2 nM

99%+
Oxaliplatin 98%
YK-4-279 99%+
ML216 +

BLMfull-length, IC50: 2.98 μM

BLM636-1298, IC50: 0.97 μM

99%+
RK-33 98%
Brr2-IN-3 99%+
Phen-DC3 Trifluoromethanesulfonate 95%
Favipiravir 99%
Suramin sodium salt ++

RdRp, IC50: 0.26 μM

99%+
Clofarabine ++

Ribonucleotide reductase, IC50: 65 nM

97%
Didox 98%
(E)-3-AP 99%
Halofuginone +++

prolyl-tRNA synthetase, Ki: 18.3nM

99%+
BC-LI-0186 +++

Leucyl-tRNA synthetase, IC50: 46.11 nM

Leucyl-tRNA synthetase, Kd: 42.1 nM

98%
SU056 +

YB-1, IC50: 1.73 μM

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Cidofovir/西多福韦 生物活性

靶点
  • DNA synthesis

描述 Cidofovir is a synthetic nucleotide analog with potent antiviral activity against a wide range of herpes viruses. In A549 cells, the analysis of 50% inhibitory dose (ID50) of cidofovir dihydrate in different strains and serotypes of adenovirus showed that the mean ID50 values for Ad5 wide-type, Ad5 McEwen, Ad14 and Ad8 are 9.5, 7.3, 5.4, and 4.7 μg/mL, respectively[2]. In MRC-5 cells, the ED50 values of cidofovir dihydrate against Hmc wild type, SC16, BW-S, BW-R, MS wild type are 6.5 ± 2.5, 9.3 ± 1.8, 8.5 ± 1.0, 1.1 ± 0.9, and 9.1 ± 1.8 μM, respectively[3].. A graded decrease in the severity of acute conjunctivitis was observed in rabbits received the treatment of 0.1% cidofovir dihydrate, whereas the concentrations at 0.5% and 1% caused a moderate grade of acute conjunctivitis. A significantly reduction in Ad5 ocular titers was shown in 0.5% and 1% cidofovir dihydrate-treated groups compared to the placebo group. The duration of viral ocular shedding in 0.1%, 0.5%, and 1% cidofovir dihydrate-treated groups were 6, 4, and 4 days, compared to 7-day duration in placebo group. The mean ELISA antibody titer was decreased by 0.5% and 1% cidofovir dihydrate 21 days post the inoculation[3].

Cidofovir/西多福韦 细胞实验

Cell Line
Concentration Treated Time Description References
293T cells 0, 50, 100, 200, 500 and 1000 μg/mL 24 h Evaluate the cytocompatibility of blank HPMPC and RPMPC nanogels, results showed negligible toxicity to 293T cells at the high concentration of 1000 μg/mL Acta Pharm Sin B. 2021 Feb;11(2):560-571.
HepG2 cells 0, 50, 100, 200, 500 and 1000 μg/mL 24 h Evaluate the cytocompatibility of blank HPMPC and RPMPC nanogels, results showed negligible toxicity to HepG2 cells and 293T cells at the high concentration of 1000 μg/mL Acta Pharm Sin B. 2021 Feb;11(2):560-571.
MA104 cells 50-400 µM 12 h To evaluate the inhibitory effect of cidofovir on HBoV1 replication, results showed that 400 µM cidofovir inhibited approximately 50% of viral replication. J Virol. 2025 Feb 25;99(2):e0153924.
3T12 fibroblast cells 42 µg/ml 18 h To assess the inhibitory effect of cidofovir on γHV68 viral DNA synthesis, results showed that cidofovir significantly inhibited viral DNA synthesis. Cell Host Microbe. 2010 Jun 25;7(6):516-26.
CRFK cells 1.9 to 976 μM 72 or 96 h Evaluate the antiviral effect of cidofovir on FHV-1 infection, calculated EC50 as 26.5±9.9 μM mSphere. 2017 Apr 5;2(2):e00039-17.

Cidofovir/西多福韦 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
BALB/c nude mice Humanized subcutaneous liver cancer model Intravenous injection 2 mg/kg Injected on Days 0 and 6, lasting for 14 days Evaluate the anti-tumor effect of DOX-loaded HPMPC nanogels, results showed the HPMPC@DOX group exhibited the strongest tumor growth inhibition effect, with significantly lower tumor weight compared to other groups Acta Pharm Sin B. 2021 Feb;11(2):560-571.
Mice B6 mice Intraperitoneal injection 600 µg Single dose, 2 days post infection Inhibits Orthopoxvirus replication and prevents mousepox in aged mice J Exp Med. 2010 Oct 25;207(11):2369-81

Cidofovir/西多福韦 临床研究

NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT02227641 Patients Undergoing Allogeneic... 展开 >> Stem Cell Transplantation 收起 << Phase 1 Phase 2 Unknown March 2017 Germany ... 展开 >> Medical Center Augsburg Recruiting Augsburg, Germany, 86156 Contact: Christoph Schmid, MD, PhD    0049 821 4002736       Principal Investigator: Christoph Schmid, MD, PhD          Charité University Hospital Berlin Recruiting Berlin, Germany, 13353 Contact: Armin H Gerbitz, MD, PhD    ++49 30 450565256    armin.gerbitz@charite.de    Contact: Lutz Uharek, MD, PhD       lutz.uharek@charite.de    Sub-Investigator: Lutz Uharek, MD, PhD          Principal Investigator: Armin Gerbitz, MD, PhD          Universitiy Hospital Erlangen Recruiting Erlangen, Germany, 91054 Contact: Anita Kremer, MD, PhD    ++49 9131 8543183    anita.kremer@uk-erlangen.de    Contact: Bernd Spriewald, MD, PhD    ++49 9131 8543116    bernd.spriewald@uk-erlangen.de    Sub-Investigator: Katja San Niccolo, MD          University of Mainz Recruiting Mainz, Germany, 55131 Contact: Eva Wagner, MD          Principal Investigator: Eva Wagner, MD          University of Munich LMU Recruiting Munich, Germany, 81377 Contact: Johanna Tischer, MD    0049 89 70954240       Principal Investigator: Johanna Tischer, MD          University of Regensburg Not yet recruiting Regensburg, Germany, 93053 Contact: Ernst Holler, MD, PhD    0049 941 9445570       Principal Investigator: Ernst Holler, MD, PhD 收起 <<
NCT03532035 Adenovirus Phase 2 Not yet recruiting December 20, 2019 -
NCT00078533 Cytomegalovirus Infections Phase 1 Completed - United States, Texas ... 展开 >> Houston Methodist Hospital Houston, Texas, United States, 77030 Texas Children's Hospital Houston, Texas, United States, 77030 收起 <<

Cidofovir/西多福韦 参考文献

[1]Li SB, Yang ZH, et al. Activity of(S)-1-(3-hydroxy-2-phosphonylmethoxypropyl)cytosine (HPMPC) against guinea pig cytomegalovirus infection in cultured cells and in guinea pigs. Antiviral Res. 1990 May;13(5):237-52.

[2]Snoeck R, Sakuma T, et al.(S)-1-(3-hydroxy-2-phosphonylmethoxypropyl)cytosine, a potent and selective inhibitor of human cytomegalovirus replication. Antimicrob Agents Chemother. 1988 Dec;32(12):1839-44.

[3]de Oliveira CB, Stevenson D, LaBree L, McDonnell PJ, Trousdale MD. Evaluation of Cidofovir (HPMPC, GS-504) against adenovirus type 5 infection in vitro and in a New Zealand rabbit ocular model. Antiviral Res. 1996 Jul;31(3):165-72. doi: 10.1016/0166-3542(95)00962-0. PMID: 8811201.

Cidofovir/西多福韦 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.58mL

0.72mL

0.36mL

17.91mL

3.58mL

1.79mL

35.82mL

7.16mL

3.58mL

Cidofovir/西多福韦 技术信息

CAS号113852-37-2
分子式C8H14N3O6P
分子量 279.19
SMILES Code OC[C@@H](OCP(O)(O)=O)CN1C=CC(N)=NC1=O
MDL No. MFCD00866936
别名 GS 0504; HPMPC; (S)-1-(3-hydroxy-2-phosphonylmethoxypropyl)cytosine; (S)-HPMPC
运输蓝冰
InChI Key VWFCHDSQECPREK-LURJTMIESA-N
Pubchem ID 60613
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Keep in dark place, sealed in dry, store in freezer, under -20°C

溶解方案

H2O: 3 mg/mL(10.75 mM),配合低频超声助溶

配制的工作液建议现用现配,短期内尽快用完。 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案 一
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