Tag: 209.629

Synthesis, characterization and antimicrobial evaluation of N-(4-oxo-2phenyl/ thiophenylquinazolin-3(4H)-yl)-1H-indole-2 or 3-carboxamide derivatives was written by Chaudhary, Aniruddh Prasad;Shukla, Akhilesh Kumar;Kant, Padam. And the article was included in Chemistry & Biology Interface in 2018.Recommanded Product: 87802-11-7 This article mentions the following:

A series of novel N-(4-oxo-2phenyl/thiophenylquinazolin-3(4H)-yl)-1H-indole-2 or 3-carboxamide derivatives were prepared and screened for their antimicrobial activities against different strains of bacteria and fungi. The most potent antibacterial and antifungal activity was exhibited by compound with halogen substituted ring in the resp. series compared to the compounds bearing other electron donating or withdrawing groups. The synthesized compounds were characterized with the help of spectroscopic techniques including IR, ₁H-NMR, ₁₃C-NMR and Mass spectra. In the experiment, the researchers used many compounds, for example, Methyl 5-chloro-1H-indole-2-carboxylate (cas: 87802-11-7Recommanded Product: 87802-11-7).

Methyl 5-chloro-1H-indole-2-carboxylate (cas: 87802-11-7) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. Moreover, it is known that it controls biofilm formation. However, the role of indole in the cell has not been fully elucidated.Recommanded Product: 87802-11-7

Referemce:
Indole alkaloid derivatives as building blocks of natural products from聽Bacillus thuringiensis聽and聽Bacillus velezensis聽and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Synthesis, characterization and antimicrobial evaluation of N-(4-oxo-2phenyl/ thiophenylquinazolin-3(4H)-yl)-1H-indole-2 or 3-carboxamide derivatives was written by Chaudhary, Aniruddh Prasad;Shukla, Akhilesh Kumar;Kant, Padam. And the article was included in Chemistry & Biology Interface in 2018.Recommanded Product: 87802-11-7 This article mentions the following:

A series of novel N-(4-oxo-2phenyl/thiophenylquinazolin-3(4H)-yl)-1H-indole-2 or 3-carboxamide derivatives were prepared and screened for their antimicrobial activities against different strains of bacteria and fungi. The most potent antibacterial and antifungal activity was exhibited by compound with halogen substituted ring in the resp. series compared to the compounds bearing other electron donating or withdrawing groups. The synthesized compounds were characterized with the help of spectroscopic techniques including IR, ₁H-NMR, ₁₃C-NMR and Mass spectra. In the experiment, the researchers used many compounds, for example, Methyl 5-chloro-1H-indole-2-carboxylate (cas: 87802-11-7Recommanded Product: 87802-11-7).

Methyl 5-chloro-1H-indole-2-carboxylate (cas: 87802-11-7) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. Moreover, it is known that it controls biofilm formation. However, the role of indole in the cell has not been fully elucidated.Recommanded Product: 87802-11-7

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Synthesis, characterization and antimicrobial evaluation of N-(4-oxo-2phenyl/ thiophenylquinazolin-3(4H)-yl)-1H-indole-2 or 3-carboxamide derivatives was written by Chaudhary, Aniruddh Prasad;Shukla, Akhilesh Kumar;Kant, Padam. And the article was included in Chemistry & Biology Interface in 2018.Recommanded Product: 87802-11-7 This article mentions the following:

A series of novel N-(4-oxo-2phenyl/thiophenylquinazolin-3(4H)-yl)-1H-indole-2 or 3-carboxamide derivatives were prepared and screened for their antimicrobial activities against different strains of bacteria and fungi. The most potent antibacterial and antifungal activity was exhibited by compound with halogen substituted ring in the resp. series compared to the compounds bearing other electron donating or withdrawing groups. The synthesized compounds were characterized with the help of spectroscopic techniques including IR, ₁H-NMR, ₁₃C-NMR and Mass spectra. In the experiment, the researchers used many compounds, for example, Methyl 5-chloro-1H-indole-2-carboxylate (cas: 87802-11-7Recommanded Product: 87802-11-7).

Methyl 5-chloro-1H-indole-2-carboxylate (cas: 87802-11-7) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. Moreover, it is known that it controls biofilm formation. However, the role of indole in the cell has not been fully elucidated.Recommanded Product: 87802-11-7

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Synthesis, characterization and antimicrobial evaluation of N-(4-oxo-2phenyl/ thiophenylquinazolin-3(4H)-yl)-1H-indole-2 or 3-carboxamide derivatives was written by Chaudhary, Aniruddh Prasad;Shukla, Akhilesh Kumar;Kant, Padam. And the article was included in Chemistry & Biology Interface in 2018.Recommanded Product: 87802-11-7 This article mentions the following:

A series of novel N-(4-oxo-2phenyl/thiophenylquinazolin-3(4H)-yl)-1H-indole-2 or 3-carboxamide derivatives were prepared and screened for their antimicrobial activities against different strains of bacteria and fungi. The most potent antibacterial and antifungal activity was exhibited by compound with halogen substituted ring in the resp. series compared to the compounds bearing other electron donating or withdrawing groups. The synthesized compounds were characterized with the help of spectroscopic techniques including IR, ₁H-NMR, ₁₃C-NMR and Mass spectra. In the experiment, the researchers used many compounds, for example, Methyl 5-chloro-1H-indole-2-carboxylate (cas: 87802-11-7Recommanded Product: 87802-11-7).

Methyl 5-chloro-1H-indole-2-carboxylate (cas: 87802-11-7) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. Moreover, it is known that it controls biofilm formation. However, the role of indole in the cell has not been fully elucidated.Recommanded Product: 87802-11-7

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles