A1506
Anthranilic acid
Synonym(s):
2-AA, 2-Aminobenzoic acid
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About This Item
Linear Formula:
2-(H2N)C6H4CO2H
CAS Number:
Molecular Weight:
137.14
Beilstein/REAXYS Number:
471803
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
Recommended Products
vapor density
4.7 (vs air)
form
solid
mp
144-148 °C (lit.)
solubility
ethanol: soluble, clear to slightly hazy
SMILES string
Nc1ccccc1C(O)=O
InChI
1S/C7H7NO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,8H2,(H,9,10)
InChI key
RWZYAGGXGHYGMB-UHFFFAOYSA-N
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Application
Used for non-selective, efficient fluorescent labeling of glycans.
replaced by
Product No.
Description
Pricing
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk_germany
WGK 1
flash_point_f
302.0 °F - closed cup
flash_point_c
150 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Jun Soma et al.
Nephron, 92(3), 693-698 (2002-10-10)
Tranilast, N-(3,4-dimethoxycinnamoyl) anthranilic acid, suppresses collagen synthesis by various cells, including macrophages and fibroblasts, by interfering with the actions of transforming growth factor-beta 1. We investigated the effect of tranilast on progression of diabetic nephropathy (DN), since this process is
Sangram S Kale et al.
Organic & biomolecular chemistry, 10(42), 8426-8433 (2012-09-25)
Structural modulation of Ant-Pro (anthranilic acid-proline) oligomers has been carried out by chirality alteration of the proline residues. The results suggest that the chirality altered oligomers show well-defined helical conformation featuring nine-membered hydrogen bonding interactions - without compromising conformational rigidity.
Li Gu et al.
The Analyst, 138(18), 5461-5469 (2013-07-26)
In this work, we report a competitive sensor performing "double recognition" for the specific capture of dopamine (DA) with the combination of boronic acid functional groups and molecularly imprinted cavities based on poly(aniline-co-anthranilic acid) (PANANA) as the support material. This
Stuart W Haynes et al.
Journal of the American Chemical Society, 134(42), 17444-17447 (2012-10-04)
Members of the asperlicin family of fungal metabolites produced by Aspergillus alliaceus are known potent CCK(A) antagonists. Herein, we report the identification of the gene cluster responsible for directing their biosynthesis. We validate and probe the pathway by genetic manipulation
S Ahmad
Drug metabolism reviews, 10(1), 1-14 (1979-01-01)
Research in recent years has considerably enhanced our understanding of the membrane-bound cytochrome P-450-catalyzed biotransformations in organisms. A remarkable similarity has become apparent between diversified animal groups with respect to the components and functional roles of the cytochrome P-450 systems.
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