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N-(2,2-di(1H-indol-3-yl)ethyl)benzamide is a complex organic compound with the molecular formula C24H20N2O. It is characterized by a benzamide group attached to a central ethyl chain, which is further connected to two indole rings. This structure endows the compound with unique chemical and physical properties. Indole rings are known for their presence in various natural products and pharmaceuticals, contributing to a range of biological activities. The specific arrangement of atoms in N-(2,2-di(1H-indol-3-yl)ethyl)benzamide may influence its potential applications in fields such as medicinal chemistry, where it could be explored for its interactions with biological targets. The compound's synthesis and study can provide insights into the development of new drugs or materials with specific therapeutic or functional properties.

3770-68-1

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3770-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3770-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3770-68:
(6*3)+(5*7)+(4*7)+(3*0)+(2*6)+(1*8)=101
101 % 10 = 1
So 3770-68-1 is a valid CAS Registry Number.

3770-68-1Downstream Products

3770-68-1Relevant academic research and scientific papers

Streptindole and Its Derivatives as Novel Antiviral and Anti-Phytopathogenic Fungus Agents

Ding, Xin,Gao, Yongyue,Kang, Jin,Ma, Dejun,Wang, Qingmin,Wang, Ziwen,Zhang, Mingjun

, p. 7839 - 7849 (2020)

Plant diseases caused by plant viruses and pathogens seriously affect the production and storage of food crops. With the emergence of drug resistance, it is very difficult to control. Natural products are the source of new drug discovery. Here, the natural product streptindole was found to have good antiviral activity against tobacco mosaic virus (TMV) and fungicidal activities against 14 kinds of phytopathogenic fungi. A series of derivatives of streptindole were designed, synthesized, and evaluated for their antiviral and fungicidal activities. Compounds 4, 5, 11, 12c, 12d, 13d, and 13i-13l showed higher anti-TMV activities than ribavirin (inhibitory rate: 38, 37, and 40% at 500 μg/mL for inactivation, curative, and protection activity in vivo, respectively), among which compound 12d (inhibitory rate: 57, 55, and 53% at 500 μg/mL for inactivation, curative, and protection activity in vivo, respectively) with excellent antiviral activity was further evaluated for the mode of action. The mechanism research revealed that 12d can break the three-dimensional structure of TMV coat protein (CP) through hydrogen bonds, thus inhibiting the assembly of virus particles. The molecular docking result showed that compound 12d did exhibit strong interaction with TMV CP. The derivatives of streptindole also displayed broad-spectrum fungicidal activities. The current study provided valuable insights into the antiviral and fungicidal activities of streptindole derivatives.

Application of alkaloid streptindole and derivatives thereof in prevention and control of plant viruses and pathogenic bacteria

-

, (2021/07/01)

The invention relates to an application of alkaloid streptindole and derivatives thereof in control of plant virus pathogens. It is found that streptindole and derivatives I-1 to I-14 thereof show good anti-plant virus pathogen activity for the first time

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