1197-55-3
1197-55-3
Chemical Structure
4-Aminophenylacetic acid
- CAS No.: 1197-55-3
- Formula:C8H9NO2
- Molecular Weight:151.16
IUPAC Name: 2-(4-aminophenyl)acetic acid
InChIKey: CSEWAUGPAQPMDC-UHFFFAOYSA-N
SMILES: O=C(CC1=CC=C(C=C1)N)O
Biological Activity: 4-Aminophenylacetic acid is a kind of biological materials or organic compounds that are widely used in life science research[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-Aminophenylacetic acid | 99.26% | 4-Aminophenylacetic acid is a kind of biological materials or organic compounds that are widely used in life science research. | ||||||||||||||||||||
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4-Aminobenzoic acid (Standard) | 99.96% | 4-Aminobenzoic acid (Standard) is the analytical standard of 4-Aminobenzoic acid. This product is intended for research and analytical applications. 4-Aminobenzoic acid is an intermediate in the synthesis of folic acid by bacteria, plants and fungi. | ||||||||||||||||||||
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4-Hydroxyphenylacetic acid | 99.96% | 4-hydroxyphenylacetic acid, a major microbiota-derived metabolite of polyphenols, is involved in the antioxidative action. 4-hydroxyphenylacetic acid induces expression of Nrf2. | ||||||||||||||||||||
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4-(Hydroxymethyl)phenylacetic acid | 97.0% | 4-(Hydroxymethyl)phenylacetic acid can serve as the main body of insoluble polypeptide. 4-(Hydroxymethyl)phenylacetic acid can react with DEPBT and 4-acetylaniline to form amide intermediates. 4-(Hydroxymethyl)phenylacetic acid is a metabolite produced by the metabolism of flavonoids such as quercetin by colonic microbiota. 4-(Hydroxymethyl)phenylacetic acid significantly inhibits 6-MP oxidation and has no significant inhibition on xanthine oxidation. | ||||||||||||||||||||
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2-(4-Cyanophenyl)acetic acid | 98.0% | 2-(4-Cyanophenyl)acetic acid is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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3-Aminophenylacetic acid | 98.03% | 3-Aminophenylacetic acid is an organic compound. | ||||||||||||||||||||
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4-Chlorophenylacetic acid | 99.94% | 4-Chlorophenylacetic acid is an aromatase antagonist. 4-Chlorophenylacetic acid inhibits estrogen-induced breast tumorigenesis by blocking estrogen conversion. 4-Chlorophenylacetic acid also serves as the sole carbon and energy source for Pseudomonas sp. CBS3; it is degraded via dechlorination and aromatic ring cleavage pathways, and induces the synthesis of protocatechuate 2,3-dioxygenase. 4-Chlorophenylacetic acid can be applied to studies related to estrogen-induced breast tumors and bacterial degradation pathways. | ||||||||||||||||||||
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4-(4-Aminophenyl)butanoic acid | 98.64% | 4-(4-Aminophenyl)butanoic acid is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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3-(4-Aminophenyl)propionic acid | 3-(4-Aminophenyl)propionic acid is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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p-(Methoxycarbonylmethyl)aniline | p-(Methoxycarbonylmethyl)aniline is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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4-(Chloromethyl)phenylacetic Acid | 4-(Chloromethyl)phenylacetic Acid is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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