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METHYL INDOLE-3-CARBOXYLATE, 99%
Кат. №: 395307-25G
Производитель: Sigma-Aldrich
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METHYL INDOLE-3-CARBOXYLATE, 99%
Main image
Кат. №: 395307-25G
Производитель: Sigma-Aldrich
Кол-во:
Фасовка:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
METHYL INDOLE-3-CARBOXYLATE, 99%
Кат. №: 395307-25G
Производитель: Sigma-Aldrich
Кол-во:
Фасовка:
Цена по запросу
Товар оформляется под заказ
Description General description Methyl indole-3-carboxylate (3-Methoxycarbonylindole, 3-Carbomethoxyindole, Methyl indolyl-3-carboxylate) has been extracted from the marine Streptomyces sp. 060524. Its crystal structure indicates the presence of inter­molecular N-H…O hydrogen bond. It is also obtained during the isolation of sorazinones A and B from Sorangium cellulosum strain Soce895. It undergoes regioselective dibromination with bromine in acetic acid to afford methyl 5,6-dibromoindole-3-carboxylate. Application Reactant for preparation of: • Nitric oxide synthase (nNOS) inhibitorS • Protein kinase c alpha (PKCα) inhibitors • Inhibitors of the C-terminal domain of RNA polymerase II as antitumor agents • Kinase insert domain receptor (KDR) inhibitors • Organocatalysts for the anti-Mannich reaction • Very late antigen-4 (VLA-4) antagonists • Inhibitors of Human 5-Lipoxygenase • Serotonin 5-HT4 receptor antagonists • Hyaluronidase inhibitors Reactant for: • Enantioselective Meerwein-Eschenmoser Claisen rearrangement reactions† Packaging 25 g in glass bottle
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Building Blocks, C10, Chemical Synthesis, Heterocyclic Building Blocks, Indoles More... Quality Level
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Description General description Methyl indole-3-carboxylate (3-Methoxycarbonylindole, 3-Carbomethoxyindole, Methyl indolyl-3-carboxylate) has been extracted from the marine Streptomyces sp. 060524. Its crystal structure indicates the presence of inter­molecular N-H…O hydrogen bond. It is also obtained during the isolation of sorazinones A and B from Sorangium cellulosum strain Soce895. It undergoes regioselective dibromination with bromine in acetic acid to afford methyl 5,6-dibromoindole-3-carboxylate. Application Reactant for preparation of: • Nitric oxide synthase (nNOS) inhibitorS • Protein kinase c alpha (PKCα) inhibitors • Inhibitors of the C-terminal domain of RNA polymerase II as antitumor agents • Kinase insert domain receptor (KDR) inhibitors • Organocatalysts for the anti-Mannich reaction • Very late antigen-4 (VLA-4) antagonists • Inhibitors of Human 5-Lipoxygenase • Serotonin 5-HT4 receptor antagonists • Hyaluronidase inhibitors Reactant for: • Enantioselective Meerwein-Eschenmoser Claisen rearrangement reactions† Packaging 25 g in glass bottle
Related Categories
Building Blocks, C10, Chemical Synthesis, Heterocyclic Building Blocks, Indoles More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.