Weight | 137.138 g/mol |
---|---|
Formula | C7H7NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
anthranilic acid
anthranilate · sodium anthranilate · anthranilic acid, calcium (2:1) salt
14342-65-5, 15442-49-6, 118-92-3, 97675-38-2, 1321-11-5, 98072-80-1
Score:
#458 in Biochemistry
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#1479 in Biology
,
#1736 in Chemistry
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- Nonselective and Efficient Fluorescent Labeling of Glycans Using 2-Amino Benzamide and Anthranilic Acid (Analytical Biochemistry, 1995)
- Identification and characterization of genes for a second anthranilate synthase in Pseudomonas aeruginosa: interchangeability of the two anthranilate synthases and evolutionary implications. (Journal of Bacteriology, 1990)
- High resolution and high sensitivity methods for oligosaccharide mapping and characterization by normal phase high performance liquid chromatography following derivatization with highly fluorescent anthranilic acid (Glycobiology, 1998)
- Pharmacological properties of N-(3',4'-dimethoxycinnamoyl) anthranilic acid (N-5'), a new anti-atopic agent. (British Journal of Pharmacology, 1976)
- Two anthranilate synthase genes in Arabidopsis: defense-related regulation of the tryptophan pathway. (The Plant Cell, 1992)
- Synthesis of anthranilic acid derivatives through iron-catalyzed ortho amination of aromatic carboxamides with N-chloroamines. (Journal of the American Chemical Society, 2014)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - anthranilate
- sodium anthranilate
- anthranilic acid, calcium (2:1) salt
- anthranilic acid, monosodium salt
- anthranilic acid, dihydrochloride
- anthranilic acid, hydrochloride
- 2-aminobenzoic acid
- anthranilic acid, cadmium salt
- anthranilic acid, monolithium salt
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SMILESC1=CC=C(C(=C1)C(=O)O)N
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InChIKeyRWZYAGGXGHYGMB-UHFFFAOYSA-N
- Pubchem - anthranilic acid
- Wikipedia - anthranilic acid
Anthranilic acid (o-amino-benzoic acid, 2-aminobenzoic acid, 2-AA, 2AA, AA) is an aromatic acid with the formula C6H4(NH2)(CO2H). The molecule consists of a substituted benzene ring, hence is classed as aromatic, with two adjacent, or "ortho-" functional groups, a carboxylic acid and an amine. The compound is consequently amphoteric.
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