17422-33-2
17422-33-2
Chemical Structure
6-Chloroindole
- CAS No.: 17422-33-2
- Formula:C8H6ClN
- Molecular Weight:151.59
IUPAC Name: 6-chloro-1H-indole
InChIKey: YTYIMDRWPTUAHP-UHFFFAOYSA-N
SMILES: ClC1=CC2=C(C=C1)C=CN2
Biological Activity: 6-Chloroindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
| Cat. No. | Nom du produit | Pureté | Description | Pricing | |||||||||||||||||||
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6-Chloroindole | 6-Chloroindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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5-Bromoindole | 99.97% | 5-Bromoindole is an antibacterial agent with a MIC of 200 μg/mL. 5-Bromoindole inhibits biofilm and curli formation, reduces swarming motility and swimming motility. 5-Bromoindole can be used for the research of enterohemorrhagic escherichia coli o157:h7 infection. | ||||||||||||||||||||
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5-Fluoroindole | 99.88% | 5-Fluoroindole is an orally active fluorinated indole derivative and antibacterial agent. 5-Fluoroindole induces ROS accumulation and triggers Apoptosis. 5-Fluoroindole inhibits the growth of pan-susceptible Mycobacterium tuberculosis (Mtb) H37Rv strains. 5-Fluoroindole has significant bactericidal activity against Pseudomonas syringae pv. actinidiae (Psa) with an EC50 of 15.34 μg/mL. 5-Fluoroindole introduces fluorine labeling for protein research. 5-Fluoroindole can be used in the study of tuberculosis and kiwifruit bacterial canker. | ||||||||||||||||||||
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6-Bromoindole | 99.91% | 6-Bromoindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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5-Hydroxyindole | 99.94% | 5-Hydroxyindole is an orally active hydroxylated indole and tryptophan metabolite. 5-Hydroxyindole activates α7 nicotinic acetylcholine receptors and acts on intestinal L-type calcium channels. 5-Hydroxyindole slows down the desensitization of 5-HT3 receptor-mediated ion currents in cells. 5-Hydroxyindole causes convulsions and loss of consciousness. 5-Hydroxyindole is used in the study of neuroblastoma, schizophrenia, and diseases related to intestinal motility disorders. | ||||||||||||||||||||
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6-Aminoindole | 6-Aminoindole is an electron donor. A novel proton transfer hydrogen-bonded complex is formed between 6-aminoindole and Picric acid. | |||||||||||||||||||||
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5-Methylindole | 99.90% | 5-Methylindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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6-Fluoroindole | 99.74% | 6-Fluoroindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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6-Hydroxyindole (Standard) | ≥98% | 6-Hydroxyindole (Standard) is the analytical standard of 6-Hydroxyindole (HY-W002438). This product is intended for research and analytical applications. 6-Hydroxyindole is an orally active, endogenous long-acting OATP1B1 inhibitor. 6-Hydroxyindole does not alter the cell surface expression or subcellular localization of OATP1B1. 6-Hydroxyindole protects cells against Ferroptosis. 6-Hydroxyindole possesses intrinsic radical-trapping antioxidant activity. 6-Hydroxyindole serves as a component of oxidative hair dyes. 6-Hydroxyindole can be used in research related to renal failure and neurodegenerative diseases. | ||||||||||||||||||||
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5-Chloroindole | 99.79% | 5-Chloroindole is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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1H-Indol-5-amine | 98.0% | 1H-Indol-5-amine (5-Aminoindole) is an organic compound containing an indole ring structure and belongs to the class of indole derivatives. 1H-Indol-5-amine can serve as a key intermediate for the synthesis of other active compounds. | ||||||||||||||||||||
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