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Merck
CN

D6135

Sigma-Aldrich

Distamycin A hydrochloride from Streptomyces distallicus

≥90% (TLC)

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About This Item

经验公式(希尔记法):
C22H27N9O4 · HCl
CAS号:
分子量:
517.97
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:

方案

≥90% (TLC)

作用机制

DNA synthesis | interferes

储存温度

−20°C

SMILES字符串

Cl.Cn1cc(NC=O)cc1C(=O)Nc2cc(C(=O)Nc3cc(C(=O)NCCC(N)=N)n(C)c3)n(C)c2

生化/生理作用

Reported to specifically inhibit the initiation of RNA synthesis.

象形图

Exclamation mark

警示用语:

Warning

危险声明

预防措施声明

危险分类

Skin Sens. 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Terri G Edwards et al.
Antiviral research, 91(2), 177-186 (2011-06-15)
Human papillomavirus (HPV) causes cervical cancer and other hyperproliferative diseases. There currently are no approved antiviral drugs for HPV that directly decrease viral DNA load and that have low toxicity. We report the potent anti-HPV activity of two N-methylpyrrole-imidazole polyamides
Gaetano Marverti et al.
Amino acids, 42(2-3), 641-653 (2011-08-05)
Acquired resistance to cisplatin (cDDP) is a multifactorial process that represents one of the main problems in ovarian cancer therapy. Distamycin A is a minor groove DNA binder whose toxicity has limited its use and prompted the synthesis of derivatives
Vivian Chagas da Silveira et al.
Journal of inorganic biochemistry, 105(12), 1692-1703 (2011-11-22)
Previous studies on copper(II) complexes with oxindole-Schiff base ligands have shown their potential antitumor activity towards different cells, inducing apoptosis through a preferential attack to DNA and/or mitochondria. Herein, we better characterize the interactions between some of these copper(II) complexes
Mariko Asagi et al.
Biophysical chemistry, 149(1-2), 34-39 (2010-04-17)
Distamycin A (Dst) is an antibiotic which binds to the minor groove of double-stranded DNA at A/T-rich regions. We have examined the affinity and mode of Dst binding to DNA duplexes containing a conserved A/T core and variable terminal A/T
Austin E Smith et al.
Biochemistry, 50(38), 8107-8116 (2011-08-23)
The molecular mechanism for the displacement of HMGA1 proteins from DNA is integral to disrupting their cellular function, which is linked to many metastatic cancers. Chemical shift and NOESY NMR experiments provide structural evidence for the displacement of an AT

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