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Journal articles on the topic '3-Aminobutanoic acid'

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Published: 5 June 2025

Last updated: 2 August 2025

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1

M., Sivasankaran Nair, Kalalakshmi G., and Sankaranarayana Pillai M. "Mixed ligand complex formation of copper(II) with 2,5-diaminovaleric acid and some amino acids." Journal of Indian Chemical Society Vol. 76, Jun 1999 (1999): 310–11. https://doi.org/10.5281/zenodo.5852299.

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Department of Chemistry, Manonmaniam Sundaranar University, Abishekapatti, Tirunelveli-627 012, India Department of Chemistry, S. T. Hindu College, Nagercoil-629 002, India <em>Manuscript received 18 August 1998, revised 20 January 1999, accepted 16 February 1999</em> The stability and structure of the mixed ligand complexes formed by <strong>Cu<sup>ll</sup> </strong>with DL-2,5-diaminovaleric acid (dava) as ligand (<strong>A</strong>) and DL-2-aminobutanoic acid (2aba), DL-3-aminobutanoic acid (3aba), DL-4-aminobutanoic acid (4aba) and DL-4-amino-3- hydroxybutanoic acid (abba) as ligands (<st

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2

Ramírez G., Joaquín Guillermo, Melissa Muñoz A., Luis Fernando Patiño H., and Juan Gonzalo Morales O. "Banana Moko disease management with resistance inducers and chlorine dioxide." Agronomía Colombiana 33, no. 2 (2015): 194–202. http://dx.doi.org/10.15446/agron.colomb.v33n2.48663.

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The plant disease Moko, caused by Ralstonia solanacearum, is the most important bacterial disease in banana and plantain crops worldwide. In the present study, chlorine dioxide and seven resistance inducers in banana plants (Musa sp.) infected with this bacterium were evaluated under greenhouse conditions. For the evaluation of chlorine dioxide, three doses were used (10, 30 and 50 mg L-1). The evaluation of the resistance inducers included the following: sodium salicylate 0.4 g L-1; hydrogen peroxide 1 mM; potassium phosphite 1.5 mL L-1; 3-aminobutanoic acid 1.0 g L-1; methyl jasmonate 0.2 g

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3

Monka, N. Y., L. R. Zhurakhivska, M. S. Kurka, G. B. Shiуan, Yu М. Semenchuk, and V. I. Lubenets. "Synthesis of thiosulphonate and amino acid derivatives of benzochinone and predicted screening of their biological activity." Chemistry, Technology and Application of Substances 4, no. 2 (2021): 40–46. http://dx.doi.org/10.23939/ctas2021.02.040.

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Quinoid derivatives are attractive not only as interesting synthons for synthesis, but also as potential biologically active substances, so it is important to modify the compounds of the quinone series with different pharmacoform fragments. In this work, the structural design of chlorine and bromanyl disulfur-containing fragments, namely thiosulfonate, and chloranyl – a fragment of 4- aminobutanoic acid. Methods of synthesis were developed and physicochemical characteristics of thiosulfonate and amino acid derivatives were studied: 2,5-bis (thiosulfonate) -3,6-halogen -1,4- benzoquinones and 2

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4

Parthasarathy, R., T. Xie, M. G. Wolfersberger, and W. R. Harvey. "Substrate structure and amino acid/K+ symport in brush-border membrane vesicles from larval Manduca sexta midgut." Journal of Experimental Biology 197, no. 1 (1994): 237–50. http://dx.doi.org/10.1242/jeb.197.1.237.

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The effects of amino acid sidechain length, substituent position and c chirality on amino acid/K+ symport have been examined in rapid filtration experiments on brush-border membrane vesicles prepared from larval Manduca sexta midgut. Cis-inhibition and trans-stimulation protocols were used to examine the effects of amino acid analogs on the uptake of alanine, phenylalanine, leucine and lysine, which are cotransported with K+ by a zwitterionic symporter at the high pH characteristic of the midgut in vivo. The symporter was found to translocate both L- and D-stereoisomers of alanine, leucine and

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5

Emeka, Ugoala, Ndukwe George, and Ayo Rachael. "Isolation and Characterisation of Some Microalgae Bioactive Molecules." ALGERIAN JOURNAL OF NATURAL PRODUCTS 4, no. 3 (2016): 323–47. https://doi.org/10.5281/zenodo.200210.

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This study involved the isolation, structure elucidation, and biological screening of secondary metabolites in freshwater microalgae for bioactive and chemically novel compounds. Isolates were fractionated and purified from the methanol, ethyl acetate, dichloromethane, petroleum ether and aqueous extracts of microalgae via column chromatography technique over silica gel using a gradient mixture of solvents. The chemical structures of isolated compounds have been elucidated using Solid-state cross polarization (CP) and magic angle spinning (MAS) <sup>13</sup>C-NMR spectroscopic technique at spe

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6

Shashikala, Yalagi. "Study of vibrational spectra of zwitterionic 3-Aminobutanoic acid, as supported by DFT calculations." World Journal of Advanced Research and Reviews 16, no. 3 (2022): 1122–31. https://doi.org/10.5281/zenodo.7904051.

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3-Aminobutanoic acid is an unnatural amino acid and by analogy with other amino acids, is represented in its zwitterionic form by R-CH(COO¯)NH<sub>3</sub><sup>+</sup> (where side group R<strong> = </strong>aryl, alkyl or any other group) in solid phase. Experimental IR and Raman modes near 3029, 2871, 1577, 1288 cm<sup>-1</sup> measured for 3ABA are strongly in favor of the zwitterionic dimer structure formed of –N-H∙∙∙O–C bonding between –NH<sub>3</sub><sup>+ </sup>and anion – CO<sub>2</sub>¯ groups. Zwitterionic monomer and

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7

Weiß, Markus, Tobias Brinkmann, and Harald Gröger. "Towards a greener synthesis of (S)-3-aminobutanoic acid: process development and environmental assessment." Green Chemistry 12, no. 9 (2010): 1580. http://dx.doi.org/10.1039/c002721a.

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8

Shashikala Yalagi. "Study of vibrational spectra of zwitterionic 3-Aminobutanoic acid, as supported by DFT calculations." World Journal of Advanced Research and Reviews 16, no. 3 (2022): 1122–31. http://dx.doi.org/10.30574/wjarr.2022.16.3.1487.

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3-Aminobutanoic acid is an unnatural amino acid and by analogy with other amino acids, is represented in its zwitterionic form by R-CH(COO¯)NH3+ (where side group R = aryl, alkyl or any other group) in solid phase. Experimental IR and Raman modes near 3029, 2871, 1577, 1288 cm-1 measured for 3ABA are strongly in favor of the zwitterionic dimer structure formed of –N-H∙∙∙O–C bonding between –NH3+ and anion – CO2¯ groups. Zwitterionic monomer and dimer structures at B3LYP/6-311++G(d,p) level are computed. It has been found that the stable zwitterionic monomer and dimer structures are possible

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9

Bismondo, Arturo, Luigi Rizzo, Plinio Di Bernardo, and Pier Luigi Zanonato. "Uranyl(VI) complexes of 3-aminopropanoic acid and 4-aminobutanoic acid in aqueous solution: a potentiometric and calorimetric study." Journal of the Chemical Society, Dalton Transactions, no. 4 (1987): 695. http://dx.doi.org/10.1039/dt9870000695.

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10

Bismondo, A., U. Casellato, S. Sitran та R. Graziani. "Preparation and characterization of some uranyl complexes of amino acids. The crystal structure of [UO2(γ-aminobutanoic acid)3] (NO3)2". Inorganica Chimica Acta 110, № 3 (1985): 205–10. http://dx.doi.org/10.1016/s0020-1693(00)82308-7.

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11

Juaristi, Eusebio, Jaime Escalante, Bernd Lamatsch, and Dieter Seebach. "Enantioselective synthesis of .beta.-amino acids. 2. Preparation of the like stereoisomers of 2-methyl- and 2-benzyl-3-aminobutanoic acid." Journal of Organic Chemistry 57, no. 8 (1992): 2396–98. http://dx.doi.org/10.1021/jo00034a037.

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12

Seebach, Dieter, Jennifer L. Matthews, Anton Meden, Thomas Wessels, Christian Baerlocher, and Lynne B. McCusker. "Cyclo-?-peptides: Structure and tubular stacking of cyclic tetramers of 3-aminobutanoic acid as determined from powder diffraction data." Helvetica Chimica Acta 80, no. 1 (1997): 173–82. http://dx.doi.org/10.1002/hlca.19970800116.

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13

Zha, Xiaoyu, Gaowen Li, Ling Zhang, Qun Chen, and Qing Xia. "Identification of active compounds in Ophiopogonis Radix from different geographical origins by UPLC-Q/TOF-MS combined with GC-MS approaches." Open Life Sciences 17, no. 1 (2022): 865–80. http://dx.doi.org/10.1515/biol-2022-0096.

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Abstract Ophiopogonis Radix, also known as Maidong in Chinese, is largely produced in the Sichuan and Zhejiang provinces: “Chuan-maidong (CMD)” and “Zhe-maidong (ZMD),” respectively. This study aimed to distinguish and evaluate the quality of CMD and ZMD. In this study, the tubers of CMD and ZMD were investigated using UPLC-Q/TOF-MS, GC-MS, and LC-MS methods, respectively. Overall, steroidal saponins, homoisoflavonoids, amino acids, and nucleosides were quickly identified. Furthermore, multivariate statistical analysis revealed that CMD and ZMD could be separated. Moreover, CMD showed higher l

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14

JUARISTI, E., J. ESCALANTE, B. LAMATSCH та D. SEEBACH. "ChemInform Abstract: Enantioselective Synthesis of β-Amino Acids. Part 2. Preparation of the Like Stereoisomers of 2-Methyl- and 2-Benzyl-3-aminobutanoic Acid." ChemInform 23, № 34 (2010): no. http://dx.doi.org/10.1002/chin.199234279.

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15

SCALONI, Andrea, Mauro DALLA SERRA, Pietro AMODEO, et al. "Structure, conformation and biological activity of a novel lipodepsipeptide from Pseudomonas corrugata: cormycin A1." Biochemical Journal 384, no. 1 (2004): 25–36. http://dx.doi.org/10.1042/bj20040422.

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Cationic lipodepsipeptides from Pseudomonas spp. have been characterized for their structural and antimicrobial properties. In the present study, the structure of a novel lipodepsipeptide, cormycin A, produced in culture by the tomato pathogen Pseudomonas corrugata was elucidated by combined protein chemistry, mass spectrometry and two-dimensional NMR procedures. Its peptide moiety corresponds to L-Ser-D-Orn-L-Asn-D-Hse-L-His-L-aThr-Z-Dhb-L-Asp(3-OH)-L-Thr(4-Cl) [where Orn represents ornithine, Hse is homoserine, aThr is allo-threonine, Z-Dhb is 2,3-dehydro-2-aminobutanoic acid, Asp(3-OH) is 3

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16

Kuriyama, Shigeaki, Yoshie Inomata, Yumiko Arai, and Frank Scott Howell. "Characterization and crystal structure of cadmium(II) halide complexes with amino acids and their derivatives: VII. Crystal structures of aquadibromo(3-aminopropanoic acid)cadmium(II), dichloro(4-aminobutanoic acid)cadmium(II), diaquabis(aminohexanoic acid)cadmium(II) tetrachlorocadmium(II), and dibromo(azetidine-3-carboxylic acid)cadmium(II)." Journal of Inorganic Biochemistry 100, no. 8 (2006): 1299–307. http://dx.doi.org/10.1016/j.jinorgbio.2006.03.003.

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17

Cox, Geoffrey G., та Laurence M. Harwood. "Synthesis of homochiral α-amino acids by reductive amination of α-ketoacids via 3-substituted- 5-phenyl-3,4-dehydromorpholin-2-ones: Synthesis of (S)- and (R)-2-aminobutanoic acid". Tetrahedron: Asymmetry 5, № 9 (1994): 1669–72. http://dx.doi.org/10.1016/0957-4166(94)80077-4.

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18

SEEBACH, D., J. L. MATTHEWS, A. MEDEN, T. WESSELS, C. BAERLOCHER та L. B. MCCUSKER. "ChemInform Abstract: Cyclo-β-peptides: Structure and Tubular Stacking of Cyclic Tetramers (I), (II), and (III) of 3-Aminobutanoic Acid as Determined from Powder Diffraction Data." ChemInform 28, № 18 (2010): no. http://dx.doi.org/10.1002/chin.199718235.

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19

COX, G. G., та L. M. HARWOOD. "ChemInform Abstract: Synthesis of Homochiral α-Amino Acids by Reductive Amination of . alpha.-Ketoacids via 3-Substituted-5-phenyl-3,4-dehydromorpholin-2- ones: Synthesis of (S)- and (R)-2-Aminobutanoic Acid." ChemInform 26, № 7 (2010): no. http://dx.doi.org/10.1002/chin.199507225.

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20

Oksana, Mishchenko, Palagina Natalia, Larianovskaya Yuliia, Gorbach Tatyana, Khomenko Viktor, and Yasna Nataliia. "Influence of a new derivative of 4-aminobutanoic acid on the level of neuromediatory aminoacids, neuromediators and the state of the rats' hypocamp in conditions of brain ischemia." ScienceRise: Pharmaceutical Science, no. 2(30) (April 30, 2021): 64–71. https://doi.org/10.15587/2519-4852.2021.230305.

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<strong>The aim:</strong> to investigate the effect of a new derivative of 4-aminobutanoic acid (compounds KGM-5) on the level of neurotransmitters and neurotransmitter amino acids and the structural-functional state of the hippocampus of rats with acute cerebrovascular accident (ACVA). <strong>Materials and methods.</strong> ACVA was reproduced in rats by occlusion of the left carotid artery under anesthesia (sodium thiopental (35 mg/kg) intraperitoneally (i/p). 5 groups of animals were used: intact control (IC, n=6), untreated animals with ACVA (CP, n=13); animals with ACVA (n=14),

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21

Juaristi, Eusebio, and Jaime Escalante. "Enantioselective synthesis of .beta.-amino acids. 4. 1,2 Asymmetric induction in the alkylation of 1-benzoyl-3,6(S)-dimethylperhydropyrimidin-4-one. Preparation of the like and unlike stereoisomers of 2-methyl- and 2-benzyl-3(S)-aminobutanoic acid." Journal of Organic Chemistry 58, no. 8 (1993): 2282–85. http://dx.doi.org/10.1021/jo00060a051.

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22

Andruszkiewicz, Ryszard, and Richard B. Silverman. "A Convenient Synthesis of 3-Alkyl-4-aminobutanoic Acids." Synthesis 1989, no. 12 (1989): 953–55. http://dx.doi.org/10.1055/s-1989-27443.

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23

"A novel process for producing optically active 3-aminobutanoic acid and the ester intermediates." Process Biochemistry 32, no. 1 (1997): 72–73. http://dx.doi.org/10.1016/s0032-9592(97)87454-7.

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24

Mohanlal, Smitha, Diprupa Saha, Shubhant Pandey, Rudresh Acharya, and Nagendra K. Sharma. "Synthesis of R‐GABA Derivatives via Pd(II) Catalyzed Enantioselective C(sp3)‐H Arylation and Virtual Validation with GABAB1 Receptor for Potential leads." Chemistry – An Asian Journal, March 18, 2024. http://dx.doi.org/10.1002/asia.202400064.

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GABA (γ‐amino butyric acid) analogues like baclofen, tolibut, phenibut, etc., are well‐known GABAB1 inhibitors and pharmaceutically important drugs. However, there is a huge demand for more chiral GABA aryl analogues with promising pharmacological actions. Here, we demonstrate the chiral ligand acetyl‐protected amino quinoline (APAQ) mediated enantioselective synthesis of GABAB1 inhibitor drug scaffolds from easily accessible GABA via Pd‐catalyzed C(sp3)‐H activation. The synthetic methodology shows moderate to good yields, up to 74% of ee. We have successfully demonstrated the deprotection an

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25

BISMONDO, A., L. RIZZO, P. DI BERNARDO, and P. L. ZANONATO. "ChemInform Abstract: Uranyl(VI) Complexes of 3-Aminopropanoic Acid and 4-Aminobutanoic Acid in Aqueous Solution: a Potentiometric and Calorimetric Study." ChemInform 18, no. 31 (1987). http://dx.doi.org/10.1002/chin.198731265.

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26

"Biological and Pharmacokinetic Studies with β-Peptides". CHIMIA 52, № 12 (1998): 734. http://dx.doi.org/10.2533/chimia.1998.734.

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Interactions and cleavage reactions of β-amino acids and β-oligopeptides (up to nine residues, carrying the side chains of Ala, Val, Leu, Ile, Phe, Ser, Lys, and Hop) with biological systems, such as the most potent peptidases (pronase, proteinase K, 20S proteasome), microorganisms (Pseudomonas aeruginosa and Pseudomonas putida), and mammalian blood (intravenous application to rats) have been investigated and compared with ?-peptides. The results are: i) the three peptidases do not cleave β-peptides at all (within 24 h), and they are not inhibited by a β-peptide; ii) except for certain 3-amino

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27

Boča, Roman, Richard Imrich, Juraj Štofko, Beáta Vranovičová, and Cyril Rajnák. "Molecular properties of linear amino acids in water." Amino Acids 56, no. 1 (2024). http://dx.doi.org/10.1007/s00726-023-03365-3.

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AbstractFour linear amino acids of increased separation of the carboxyl and amino groups, namely glycine (aminoacetic acid), β-alanine (3-aminopropanoic acid), GABA (4-aminobutanoic acid) and DAVA (5-aminopentanoic acid), have been studied by quantum chemical ab initio and DFT methods including the solvent effect in order to get electronic structure and molecular descriptors, such as ionisation energy, electron affinity, molecular electronegativity, chemical hardness, electrophilicity index, dipole moment, quadrupole moment and dipole polarizability. Thermodynamic functions (zero-point energy,

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28

ANDRUSZKIEWICZ, R., and R. B. SILVERMAN. "ChemInform Abstract: A Convenient Synthesis of 3-Alkyl-4-aminobutanoic Acids." ChemInform 21, no. 19 (1990). http://dx.doi.org/10.1002/chin.199019126.

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29

Jeong, Mi-Jeong, Byoung Joon Ko, and Joo Yeol Kim. "Mass spectrometry-based metabolomics study for delay tomato fruit ripening by sound waves." Journal of Analytical Science and Technology 14, no. 1 (2023). http://dx.doi.org/10.1186/s40543-023-00384-3.

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AbstractTomato (Solanum lycopersicum L.) is one of the most consumed vegetables worldwide. The ripening of tomato is performed for its freshness and represented by color and gene expression. In our previous study, we performed molecular analyses on tomato ripening with and without sound-wave treatment. In the present study, we performed metabolomics analysis of ripening tomatoes with and without sound-wave treatment to expand our knowledge of tomato ripening. To achieve this goal, tomatoes at 7, 10, and 14 d of ripening were selected and analyzed via liquid chromatography–mass spectrometry (LC

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30

Moreira, Ryan, Michael Noden, and Scott D. Taylor. "Synthesis of Azido Acids and Their Application in the Preparation of Complex Peptides." Synthesis, November 9, 2020. http://dx.doi.org/10.1055/s-0040-1707314.

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AbstractAzido acids are important synthons for the synthesis of complex peptides. As a protecting group, the azide moiety is atom-efficient, easy to install and can be reduced in the presence of many other protecting groups, making it ideal for the synthesis of branched and/or cyclic peptides. α-Azido acids are less bulky than urethane-protected counterparts and react more effectively in coupling reactions of difficult-to-form peptide and ester bonds. Azido acids can also be used to form azoles on complex intermediates. This review covers the synthesis of azido acids and their application to t

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