间氨基苯甲酸结构式
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常用名 | 间氨基苯甲酸 | 英文名 | 3-Aminobenzoic acid |
|---|---|---|---|---|
| CAS号 | 99-05-8 | 分子量 | 137.136 | |
| 密度 | 1.3±0.1 g/cm3 | 沸点 | 352.5±25.0 °C at 760 mmHg | |
| 分子式 | C7H7NO2 | 熔点 | 178-180 °C(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 167.0±23.2 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
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One-pot enzymatic conversion of carbon dioxide and utilization for improved microbial growth.
Environ. Sci. Technol. 49(7) , 4466-72, (2015) We developed a process for one-pot CO2 conversion and utilization based on simple conversion of CO2 to bicarbonate at ambient temperature with no energy input, by using the cross-linking-based composites of carboxylated polyaniline nanofibers (cPANFs) and car... |
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Synthesis and evaluation of novel aromatic substrates and competitive inhibitors of GABA aminotransferase.
Bioorg. Med. Chem. Lett. 18 , 3122-5, (2008) The design, synthesis, and evaluation of novel gamma-aminobutyric acid aminotransferase (GABA-AT) inhibitors and inactivators can lead to the discovery of new GABA-related therapeutics. To this end, a series of aromatic amino acid compounds was synthesized to... |
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Selective Gating of Neuronal Activity by Intrinsic Properties in Distinct Motor Rhythms.
J. Neurosci. 35 , 9799-810, (2015) Many neural circuits show fast reconfiguration following altered sensory or modulatory inputs to generate stereotyped outputs. In the motor circuit of Xenopus tadpoles, I study how certain voltage-dependent ionic currents affect firing thresholds and contribu... |
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Differential 12C-/13C-isotope dansylation labeling and fast liquid chromatography/mass spectrometry for absolute and relative quantification of the metabolome.
Anal. Chem. 81(10) , 3919-32, (2009) We report a new quantitative metabolome profiling technique based on differential (12)C-/(13)C-isotope dansylation labeling of metabolites, fast liquid chromatography (LC) separation and electrospray ionization Fourier-transform ion cyclotron resonance mass s... |
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Three-dimensional quantitative structure-activity relationship analyses of substrates of the human proton-coupled amino acid transporter 1 (hPAT1).
Bioorg. Med. Chem. 19 , 6409-18, (2011) The proton-coupled amino acid transporter hPAT1 has recently gained much interest due to its ability to transport small drugs thereby allowing their oral administration. A three-dimensional quantitative structure-activity relationship (3D QSAR) study has been... |
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Aerobic biodegradation of 3-aminobenzoate by gram-negative bacteria involves intermediate formation of 5-aminosalicylate as ring-cleavage substrate.
FEMS Microbiol. Lett. 122(1-2) , 137-43, (1994) The aerobic metabolism of 3-aminobenzoate by bacteria was studied. Bacterial strains degrading 3-aminobenzoate were obtained by enrichment with 3-aminobenzoate (strain Ia3) or 5-aminosalicylate (strains BN9 and 5AS1). During growth with 3-aminobenzoate, strai... |
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Involvement of poly(ADP-ribose) synthetase in acoustic trauma of the cochlea.
Tohoku J. Exp. Med. 200(4) , 195-202, (2003) We investigated effects of poly(ADP-ribose) synthetase (PARS) inhibitors on acoustic trauma. Albino guinea pigs were intravenously given 3-aminobenzamide, nicotinamide or 3-aminobenzoic acid (an inactive analog of 3-aminobenzamide) just prior to exposure to a... |
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N-acetylation and N-formylation of m-aminobenzoic acid by cell suspension cultures of Solanum laciniatum.
J. Asian Nat. Prod. Res. 2(4) , 305-9, (2000) Two new biotransformation products, N-acetyl-m-aminobenzoic acid and N-formyl-m-aminobenzoic acid were isolated from cell suspension cultures of Solanum laciniatum following administration of m-aminobenzoic acid, and their structures were elucidated using one... |
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Characterization of the superinduction of the c-myc proto-oncogene in fibroblasts by benzamide derivatives.
Mol. Cell Biochem. 124(2) , 175-81, (1993) In mouse fibroblasts stimulated from quiescence into proliferation by serum the induction of expression of the c-myc proto-oncogene is strongly stimulated by 3-methoxybenzamide. Similar superinduction effects are seen with related compounds such as 3-aminoben... |
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4-aminometyl-3-nitrobenzoic acid--a photocleavable linker for oligonucleotides containing combinatorial libraries.
Nucleosides Nucleotides Nucleic Acids 24(9) , 1333-43, (2005) We detail the design, synthesis, and characterization of an o-nitrobenzyl-based photolabile linker containing amine and carboxyl anchor groups. A model nucleoside monomer modified with an imidazole residue and a precursor unit linked to a heterocyclic base th... |