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Tubercidin/杀结核菌素 {[allProObj[0].p_purity_real_show]}

货号:A118999 同义名: 结核菌素 / 7-Deazaadenosine; 7-DZA

Tubercidin是一种腺苷类似物,抑制DNA复制及RNA和蛋白质合成,具有抗真菌和抗病毒活性。

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+
Tubercidin/杀结核菌素 化学结构 CAS号:69-33-0
Tubercidin/杀结核菌素 化学结构
CAS号:69-33-0
Tubercidin/杀结核菌素 3D分子结构
CAS号:69-33-0
Tubercidin/杀结核菌素 化学结构 CAS号:69-33-0
Tubercidin/杀结核菌素 3D分子结构 CAS号:69-33-0
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Tubercidin/杀结核菌素 纯度/质量文件 产品仅供科研

货号:A118999 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, Kd: 42.1 nM

Leucyl-tRNA synthetase, IC50: 46.11 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。

Tubercidin/杀结核菌素 生物活性

描述 Tubercidin, also known as 7-Deazaadenosine, is an antibiotic derived from Streptomyces tubercidicus. It demonstrates inhibitory action against Streptococcus faecalis, with an IC50 of 0.02 μM[1]. This compound acts by integrating into DNA or RNA, which results in the inhibition of DNA replication, as well as RNA and protein synthesis[2]. Tubercidin is also identified as a mild inhibitor of adenosine phosphorylase, affecting the phosphorylation processes of adenosine and AMP[1]. In a concentration range of 0-10 nM over 14 days, Tubercidin exerts a dose-dependent suppressive effect on both myeloid and erythroid progenitor cells in human bone marrow, with IC50 values of 3.4 nM for CFU-GM and 3.7 nM for BFU-E[3].

Tubercidin/杀结核菌素 细胞实验

Cell Line
Concentration Treated Time Description References
Marc-145 cells 500 nM 24 hours Evaluate the inhibitory effect of Tubercidin on PRRSV replication Microbiol Spectr. 2024 Mar 5;12(3):e0347923
Marc-145 cells 150-500 nM 48 hours Evaluate the cytotoxicity of Tubercidin on Marc-145 cells Microbiol Spectr. 2024 Mar 5;12(3):e0347923
Leishmania major Friedlin (LmjF) parasites 0.9 and 1.8 µM 72 hours To evaluate the antiparasitic activity of Tubercidin against LmjF parasites. Results showed that Tubercidin has significant antiparasitic activity against LmjF parasites. PLoS Negl Trop Dis. 2016 Sep 8;10(9):e0004972

Tubercidin/杀结核菌素 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Nude mice SCLC xenograft model Subcutaneous injection 5 mg/kg 3 times per week for 3 weeks To evaluate the anti-tumor effect of Tubercidin in the SCLC xenograft model. The results showed that Tubercidin treatment significantly inhibited the growth of DMS 114 tumors in nude mice, with the tumor volume and weight in the treatment group being significantly smaller than those in the control group. J Cell Mol Med. 2022 May;26(9):2557-2565

Tubercidin/杀结核菌素 动物研究

Animal study When administered via intraperitoneal injection at a dosage of 5 mg/kg for 10 days, particularly in conjunction with NBMPR-P, Tubercidin shields mice from its own lethal effects, enabling the treatment to be repeated with a 100% survival rate[3].

Tubercidin/杀结核菌素 参考文献

[1]Bloch A, et al. On the mode of action of 7-deaza-adenosine (Tubercidin). Biochim Biophys Acta. 1967 Mar 29;138(1):10-25.

[2]Bergstrom DE, et al. Antiviral activity of C-5 substituted tubercidin analogues. J Med Chem. 1984 Mar;27(3):285-92.

[3]Kouni MH, et al. Prevention of tubercidin host toxicity by nitrobenzylthioinosine 5'-monophosphate for the treatment of schistosomiasis. Antimicrob Agents Chemother. 1989 Jun;33(6):824-7.

Tubercidin/杀结核菌素 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.76mL

0.75mL

0.38mL

18.78mL

3.76mL

1.88mL

37.56mL

7.51mL

3.76mL

Tubercidin/杀结核菌素 技术信息

CAS号69-33-0
分子式C11H14N4O4
分子量 266.25
SMILES Code NC1=C2C(N([C@H]3[C@@H]([C@@H]([C@@H](CO)O3)O)O)C=C2)=NC=N1
MDL No. MFCD00056012
别名 结核菌素 ;7-Deazaadenosine; 7-DZA; U 10071; Tubercidine; TBC; Sparsomycin A; SKI 26996; B 120121; Antibiotic XK 101-1; NSC 56408
运输蓝冰
InChI Key HDZZVAMISRMYHH-KCGFPETGSA-N
Pubchem ID 6245
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry,2-8°C

溶解方案

DMSO: 30 mg/mL(112.67 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 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
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