跳转至内容
Merck
CN

SBR00013

Sigma-Aldrich

放线菌素D,现配溶液

from Streptomyces sp., 2 mg/mL in DMSO

别名:

放线菌素 D 溶液 来源于链霉菌 属, 放线菌素 IV, 更生霉素

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C62H86N12O16
CAS号:
分子量:
1255.42
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.76

生物来源

Streptomyces sp.

质量水平

描述

Ready Made Solution

表单

liquid

储存条件

protect from light

浓度

2 mg/mL in DMSO

颜色

dark orange

抗生素抗菌谱

neoplastics

作用机制

DNA synthesis | interferes

储存温度

−20°C

SMILES字符串

N21C(CCC2)C(=O)N(CC(=O)N(C(C(=O)OC(C(C(=O)NC(C1=O)C(C)C)NC(=O)c3c4nc5c(c([c](c(c5[o]c4c(cc3)C)C)=O)N)C(=O)NC6C(OC(=O)C(N(C(=O)CN(C(=O)C7N(CCC7)C(=O)C(NC6=O)C(C)C)C)C)C(C)C)C)C)C(C)C)C)C

InChI

1S/C62H86N12O16/c1-27(2)42-59(84)73-23-17-19-36(73)57(82)69(13)25-38(75)71(15)48(29(5)6)61(86)88-33(11)44(55(80)65-42)67-53(78)35-22-21-31(9)51-46(35)64-47-40(41(63)50(77)32(10)52(47)90-51)54(79)68-45-34(12)89-62(87)49(30(7)8)72(16)39(76)26-70(14)58(83)37-20-18-24-74(37)60(85)43(28(3)4)66-56(45)81/h21-22,27-30,33-34,36-37,42-45,48-49H,17-20,23-26,63H2,1-16H3,(H,65,80)(H,66,81)(H,67,78)(H,68,79)

InChI key

RJURFGZVJUQBHK-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

应用

<ul>
<li><strong>Regulation of Immune Checkpoints in Cancer:</strong> Actinomycin D is pivotal in studying the ADAR-mediated RNA editing processes that regulate PVR immune checkpoints in colorectal cancer, thus demonstrating its crucial role in cancer immunotherapy research and providing insights into novel therapeutic targets (Qian et al., 2024).</li>
<li><strong>Chemotherapy and Immunotherapy Combination:</strong> The use of Actinomycin D in combined chemotherapy highlights its effectiveness in salvaging multi-chemotherapy agent and avelumab resistant choriocarcinoma, showcasing its potential in overcoming resistance to treatment in gynecological cancers (Lehmann et al., 2023).</li>
<li><strong>Advancements in Dental Medicine:</strong> Actinomycin D is used in regulating gene expression crucial for tissue regeneration and repair in dental health and it is also used to determine RNA stability assay (Pan et al., 2023).</li>
<li><strong>Cancer Progression Research:</strong> The study on hypoxia-induced lncRNA in hepatocellular carcinoma progression, where RNA-binding proteins play a critical role, aligns with Actinomycin D′s application in transcriptional inhibition and its influence on mRNA stability, essential for understanding cancer biology and developing targeted therapies (Tuo et al., 2023).</li>
</ul>

生化/生理作用

放线菌素D是一种抑制细胞增殖的抗肿瘤抗生素。它是抗肿瘤细胞凋亡的细胞毒性诱导剂。该化合物通过与双链DNA形成稳定的复合物(通过脱氧鸟苷残基)以非特异性方式抑制细胞增殖,从而抑制DNA引发的RNA合成。它还会导致DNA的单链断裂。

放线菌素D已被证明是逆转录中负链转移步骤的抑制剂,因此可用于研究和抑制HIV复制。还显示它可以抑制依托泊苷(拓扑异构酶II的抑制剂)诱导的PC12细胞程序性细胞死亡。

在细胞培养中,放线菌素D用作选择剂。已经研究了放线菌素D与核糖体RNA中酵母的结合。研究了各种大肠埃希菌菌株对放线菌素D的敏感性和结合机理。放线菌素D在分子生物学中也用作阻断RNA聚合酶进展的DNA嵌入剂。

包装

1ML

注意

放线菌素D溶液对光非常敏感。

制备说明

使用前,可将2 mg/mL溶液在适当的缓冲液中进一步稀释。

象形图

Health hazard

警示用语:

Danger

危险声明

危险分类

Carc. 1B

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

188.6 °F - closed cup

闪点(°C)

87 °C - closed cup


从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Dawson, R.M.C., et al., Eds.
Data for Biochemical Research, 256-257 (1986)
J Guo et al.
Journal of virology, 72(8), 6716-6724 (1998-07-11)
In this report we demonstrate that human immunodeficiency virus type 1 (HIV-1) minus-strand transfer, assayed in vitro and in endogenous reactions, is greatly inhibited by actinomycin D. Previously we showed that HIV-1 nucleocapsid (NC) protein (a nucleic acid chaperone catalyzing
W R Davis et al.
Biochemistry, 37(40), 14213-14221 (1998-10-07)
Actinomycin D was found to be a potent inhibitor of HIV-1 reverse transcriptase catalyzed DNA strand transfer reactions. Using an oligonucleotide model system, actinomycin D inhibition of DNA strand transfer was examined to elucidate the mechanism of inhibition and further
The binding of actinomycin D and F to bacterial DNA.
L F Cavalieri et al.
Biochimica et biophysica acta, 166(3), 722-725 (1968-10-29)
M Nakajima et al.
Neuroscience letters, 176(2), 161-164 (1994-08-01)
A rat pheochromocytoma cell line (PC12 cells) died within 24 h in the presence of etoposide (1-40 micrograms/ml), an inhibitor of topoisomerase II. This cytotoxic effect was prevented by either nerve growth (NGF) or epidermal growth factor (EGF). Cycloheximide and

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门