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Journal articles on the topic 'Benzoyl glycine'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Mistry, Rakesh N., and K. R. Desai. "Studies on Synthesis of Some Novel Heterocyclic Azlactone Derivatives and Imidazolinone Derivatives and their Antimicrobial Activity." E-Journal of Chemistry 2, no. 1 (2005): 42–51. http://dx.doi.org/10.1155/2005/542938.

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p- Methyl benzoic acid on reaction with phosphorus pentachloride gives p - methyl benzoyl chloride derivative which on condensation with glycine gives p - methyl benzoyl glycine derivative. Now, this p - methyl benzoyl glycine derivative on condensation with various substituted aldehydes gives corresponding substituted 4 - [aryl methylidine] - 2 - [p - methyl phenyl] - oxazole - 5 - one derivatives [1(a-j)]. Further, these derivatives [1(a-j)] on condensation with 4 , 4’ - diamino diphenyl sulphone gives corresponding substituted imidazolinone - dibenzsulphone derivatives [2(a-j)], on condensa

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2

Abdulsattar, Raghad, and Basima M. Sarhan. "Synthesis and Characterization of Some New Metals Complexes of ((4 Methoxy Benzoyl) Carbamothioyl) Glycine." Pakistan Journal of Medical and Health Sciences 16, no. 4 (2022): 930–34. http://dx.doi.org/10.53350/pjmhs22164930.

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A new ligand ( 4- methoxy benzoyl ) carbamothioyl ) Glycine (MCG) is synthesized by reaction of (4- methoxy benzoyl isothiocyanate) with Glycine(1:1). It is characterized by micro elemental analysis (C.H.N.S.), FT-IR, (UV-Vis) and 1H and 13CNMR spectra. Some metals ions complexes of this ligand were prepared and characterized byFT-IR,UV-Visible spectra, conductivity measurements, magnetic susceptibility and atomic absorption. From results obtained, the following formula [M(MCG)2] where M2+ = Mn, Co, Ni, Cu, Zn, , Cd and Hg, the proposed molecular structure for these complexes as tetrahedral ge

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3

Awaluddin, Almah Bt, and Stuart McLean. "Conjugation of benzoic acid in marsupials." Australian Journal of Zoology 33, no. 5 (1985): 693. http://dx.doi.org/10.1071/zo9850693.

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The urinary metabolites of benzoic acid have been studied in seven marsupial species and the rat. Benzoic acid was excreted mainly as the glycine conjugate, hippuric acid, with smaller, though variable, amounts as benzoyl glucuronide. Thus the overall pattern of metabolism was similar to that found in most other mammals. All species formed significant amounts of a recently discovered metabolite of benzoic acid, 0-hydroxyphenylpropionic acid, suggesting that the metabolic pathway for its formation, involving the addition of a two-carbon fragment, may occur generally in other species.

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4

Nagaraja, H. S., V. Upadhyaya, P. Mohan Rao, P. Sreeramana Aithal, and A. P. Bhat. "Organic nonlinear optical crystals of benzoyl glycine." Journal of Crystal Growth 193, no. 4 (1998): 674–78. http://dx.doi.org/10.1016/s0022-0248(98)00483-7.

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5

Dutta, Arpita, Suven Das, Purak Das, Suvendu Maity, and Prasanta Ghosh. "Fibril formation through self-assembly of a simple glycine derivative and X-ray diffraction study." Zeitschrift für Kristallographie - Crystalline Materials 235, no. 1-2 (2020): 47–51. http://dx.doi.org/10.1515/zkri-2019-0062.

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AbstractN-(N-benzoyl glycinyl)-N,N′-dicyclohexylurea was synthesised by conjugating N-benzoyl glycine and dicyclohexylcarbodiimide (DCC) using triethylamine as base catalyst. A single crystal X-ray diffraction study reveals that the compound self-assembles into a supramolecular sheet structure by intermolecular N–H · · · O, C–H · · · O hydrogen bonding and non-bonding van der Waals interactions. A high resolution transmission electronic microscopic (HR-TEM) image of the compound exhibits formation of fibrils in the solid state.

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6

Rádl, Stanislav, Petr Hezký, Petr Konvička, and Ivan Krejčí. "Synthesis and Analgesic Activity of Some Substituted 1-Benzofurans and 1-Benzothiophenes." Collection of Czechoslovak Chemical Communications 65, no. 7 (2000): 1093–108. http://dx.doi.org/10.1135/cccc20001093.

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2-Benzoyl- and 2-(pyridylcarbonyl)-1-benzofuran-3-amines were prepared from 2-hydroxybenzonitrile and corresponding bromoethanone derivatives. 2-Benzoyl- and 2-(pyridylcarbonyl)-1-benzothiophene-3-amines were prepared analogously from 2-sulfanylbenzonitrile. 2-Benzoyl-1-benzofuran-3-amine treated with acetic anhydride or ethyl chloroformate provided the corresponding N-acetyl or N-ethoxycarbonyl derivatives. These N-activated compounds were alkylated with ethyl bromoacetate to provide ethyl N-acetyl-N-(2-benzoyl-1-benzofuran-3-yl)glycinate and ethyl N-(2-benzoyl-1-benzofuran-3-yl)-N-ethoxycarb

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7

Leßmann, Frank, Lothar Beyer, Rainer Richter, and Reinhard Meusinger. "N-Benzoylthiocarbamoyl Amino Acid Ethyl Esters as Chelate Ligands for Transition Metal Ions." Zeitschrift für Naturforschung B 53, no. 9 (1998): 981–90. http://dx.doi.org/10.1515/znb-1998-0909.

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Abstract The reactions of benzoyl isothiocyanate with amino acid ethyl esters (N-butyl glycine ethyl ester, (S)-(-)-proline ethyl ester) give N-benzoylthiocarbamoyl amino acid ethyl esters. Apart from the expected N-benzoylthiocarbamoyl (S)-(-)-proline ethyl ester the racemic N-benzoyl thiocarbamoyl (R)/(S)-proline ethyl ester is formed because of base catalyzed racemization of the educt (S)-(-)-proline ethyl ester during the reaction of (S)-(-)-proline ethyl ester hydrochloride with triethylamine. The structures of both compounds were established by X-ray crystal structure analysis and speci

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8

Alex, A. V., and J. Philip. "Ultrasonic measurement of the elastic properties of benzoyl glycine single crystals." Pramana 62, no. 1 (2004): 87–94. http://dx.doi.org/10.1007/bf02704428.

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9

Rohwer, Johann M., Chantelle Schutte, and Rencia van der Sluis. "Functional Characterisation of Three Glycine N-Acyltransferase Variants and the Effect on Glycine Conjugation to Benzoyl–CoA." International Journal of Molecular Sciences 22, no. 6 (2021): 3129. http://dx.doi.org/10.3390/ijms22063129.

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The glycine conjugation pathway in humans is involved in the metabolism of natural substrates and the detoxification of xenobiotics. The interactions between the various substrates in this pathway and their competition for the pathway enzymes are currently unknown. The pathway consists of a mitochondrial xenobiotic/medium-chain fatty acid: coenzyme A (CoA) ligase (ACSM2B) and glycine N-acyltransferase (GLYAT). The catalytic mechanism and substrate specificity of both of these enzymes have not been thoroughly characterised. In this study, the level of evolutionary conservation of GLYAT missense

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10

Thondorf, Iris, Wolfgang Brandt, Angela Stockel, and Hans-Ulrich Demuth. "Modeling of the Reaction Mechanism of the Decomposition of a New Class of Mechanism-Based Protease Inhibitors." Protein & Peptide Letters 3, no. 2 (1996): 113–18. http://dx.doi.org/10.2174/092986650302220614120916.

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Abstract: Investigating the hydrolytic stability of mechanism-based inhibitors such as peptidyl 0-acyl hydroxamates we found that peptidyl hydroxamates with proline in P1-position are up to 3 orders of magnitude more stable than those with other residues in this position. Semiempirical AMI calculations have been carried out for the comparison of proline and glycine containing hydroxamates and on their corresponding anions. The theoretical calculations indicate an interaction between the N-terminal amide hydrogen with the negatively charged carboxamide function of the glycine anions. Such an ar

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11

Corry, Alan J., Alok Goel, Steven R. Alley, et al. "N-ortho-Ferrocenyl benzoyl dipeptide esters: Synthesis, structural characterization and in vitro anti-cancer activity of N-{ortho-(ferrocenyl)benzoyl}-glycine-l-alanine ethyl ester and N-{ortho-(ferrocenyl)benzoyl}-l-alanine-glycine ethyl ester." Journal of Organometallic Chemistry 692, no. 6 (2007): 1405–10. http://dx.doi.org/10.1016/j.jorganchem.2006.10.018.

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12

Nagaraja, H. S., F. Ohnesorge, D. K. Avasthi, R. Neumann, and P. Mohan Rao. "Scanning force microscopy of ion-irradiated organic single crystals of benzoyl glycine." Applied Physics A Materials Science & Processing 71, no. 3 (2000): 337–41. http://dx.doi.org/10.1007/s003390000592.

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13

Patel, Vaishali, Mansi Patel, Niralee Velhal, Kinjal Parmar, and Janki Patel. "Analytical Method Development and Validation for the Spectrophotometric Estimation of Hipuuric Acid Prodrug (Methenamine Hippurate)." INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE 14, no. 01 (2023): 76–80. http://dx.doi.org/10.25258/ijpqa.14.1.13.

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Hippuric acid, pronounced as n-benzoyl glycine, is utilized in the study of nutrition, small bioactive molecules, amino acid derivatives, peptide synthesis, chemical synthesis, cell biology, and chemical biology. It can be found in urine and is produced when glycine and benzoic acid combine. Treatment of urinary tract infections (UTIs) is challenging due to the development of resistant bacterial strains brought on by repeated use of antibiotics and chemotherapy. Methenamine hippurate as a pharmaceutical dosage form hasn’t been the subject of any published research, hence a UV-visible spectroph

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14

Schuhmann, Elfriede, Christian Robl, and Wolfgang Beck. "Metallkomplexe mit biologisch wichtigen Liganden, LXXIV [1]. Metallorganische Verbindungen von 2-(3-Thienyl)glycin und dessen Derivaten / Metal Complexes with Biologically Important Ligands, LXXIV [1]. Organometallic Compounds of 2-(3-Thienyl)glycine and Derivatives thereof." Zeitschrift für Naturforschung B 49, no. 11 (1994): 1569–79. http://dx.doi.org/10.1515/znb-1994-1120.

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N.O-Chelate complexes of R,S-2-(3-thienyl)glycinate (L) have been obtained: ML2 (M = Ni, Cu), (n-Bu3P)(Cl)M(L) (M = Pd. Pt), (η3-C3H5)Pd(L), C6H4CH,CHNMe2Pd(L), (η6-p-cymene)(Cl)Ru(L), (η5-C5Me5)(Cl)M(L) (M = Rh, Ir) and (η5-C5H5)(OC)2Mo(L). The methyl ester of R,S-2-(3-thienvl)glycine (L') forms the complexes trans-CT2PdL′2, cis- Cl2Pt(L')2, (η-Bu3P)(Cl2)M(L') (M = Pd, Pt) and (η5-C5Me5)(Cl)2M(L') (M = Rh, Ir) in which the ligand L' is coordinated through the amino group. The structures of (η3-C3H5)Pd(L) and of (η5-C5Me5)(Cl2)Ir(L') have been determined by X-ray diffraction. N- Benzoyl-2-(3-t

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15

Prem Anand, D., M. Gulam Mohamed, S. A. Rajasekar, S. Selvakumar, A. Joseph Arul Pragasam, and P. Sagayaraj. "Growth and characterization of pure, benzophenone and iodine doped benzoyl glycine single crystals." Materials Chemistry and Physics 97, no. 2-3 (2006): 501–5. http://dx.doi.org/10.1016/j.matchemphys.2005.08.055.

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16

Chattopadhyay, Tapan K., Rex A. Palmer, Peter A. Timmins, and Mogens F. Lehmann. "Crystal and molecular structure of benzoyl-l-leucyl-glycine ethyl ester (l-LEUGLY)." Journal of Crystallographic and Spectroscopic Research 17, no. 6 (1987): 783–97. http://dx.doi.org/10.1007/bf01160742.

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17

Dmitrieva, Alena V., Oleg A. Levitskiy, Yuri K. Grishin, and Tatiana V. Magdesieva. "A new oxidatively stable ligand for the chiral functionalization of amino acids in Ni(II)–Schiff base complexes." Beilstein Journal of Organic Chemistry 19 (April 27, 2023): 566–74. http://dx.doi.org/10.3762/bjoc.19.41.

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A new oxidatively stable (S)-N-benzylproline-derived ligand ((S)-N-(2-benzoyl-5-tert-butylphenyl)-1-benzylpyrrolidine-2-carboxamide) and its Ni(II)–Schiff base complexes formed of glycine, serine, and dehydroalanine are reported. A bulky tert-butyl substituent in the phenylene fragment precludes unwanted oxidative dimerization of the Schiff base complex, making it suitable for targeted electrochemically induced oxidative modification of the amino acid side chain. Experimental and DFT studies showed that the additional tert-butyl group increases the dispersion interactions in the Ni coordinatio

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18

R., M. Kedar S. A. Deshmukh. "SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF 1-(4-CHLOROPHENYL)-2-(3-SULPHOXYPHENYL-4-(4-SUBSTITUTED BENZYLIDENE)-5-IMIDAZOLONES." INDO AMERICAN JOURNAL OF PHARMACEUTICAL RESEARCH 07, no. 01 (2017): 7526–31. https://doi.org/10.5281/zenodo.1007273.

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Imidazolones are believed to be associated with several pharmacological activities. Their significance lies in the fact that they show diverse biological activities. Which include anticancer, anticonvulsant, antiparkinsonian, CNS depressant, antimicrobial, antihelmintic, anti HIV, anti-inflammatory etc.However no work is reported on imidazolone from substituted benzoyl glycine.Therefore it was thought interesting to attempt synthesis of imidazolones containing new substituent and study there antimicrobial activity In the proposed work, we have reported eight newly synthesized sulphoxy substitu

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19

Angus, R. H., P. R. Carey, H. Lee, A. C. Storer, and K. I. Varughese. "The structure and resonance Raman spectra – structure correlations for N-benzoyl-DL-alanine ethyl dithioester." Canadian Journal of Chemistry 63, no. 8 (1985): 2169–75. http://dx.doi.org/10.1139/v85-356.

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An X-ray crystallographic analysis of N-benzoyl-DL-alanine ethyl dithioester demonstrates that it takes up a B-type conformation comparable to that found for N-acylglycine dithioesters in the crystalline state. B-conformations are characterized by small N—C—C—S(thiol) torsional angles resulting from an [Formula: see text](thiol) interaction. In the present case the N—C—C—S torsional angle is −23° and the [Formula: see text] distance 2.830 Å. A Raman spectroscopic study of a single crystal and a resonance Raman (RR) spectroscopic study of powdered N-benzoyl-DL-alanine ethyl dithioester establis

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20

WANG, MAW-LING, CHIN-CHOU OU, and JING-JER JWO. "STUDY OF THE REACTION OF GLYCINE AND BENZOYL CHLORIDE UNDER INVERSE PHASE TRANSFER CATALYSIS." Chemical Engineering Communications 179, no. 1 (2000): 233–52. http://dx.doi.org/10.1080/00986440008912198.

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21

Jayarama, A., H. J. Ravindra, and S. M. Dharmaprakash. "Crystal growth, characterization, structural characteristics and second harmonic generation in N-benzoyl glycine crystals." Materials Chemistry and Physics 113, no. 1 (2009): 91–95. http://dx.doi.org/10.1016/j.matchemphys.2008.06.063.

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22

Deepa, C., and M. Anbuchezhiyan. "Evolving NLO effect, mechanical, thermal, and dielectric study of N-Benzoyl glycine doped L-Threonine." Materials Today: Proceedings 46 (2021): 3409–12. http://dx.doi.org/10.1016/j.matpr.2020.11.590.

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23

Bayya, Chandraprakash, and Sarangapani Manda. "Synthesis, Characterization and Anticancer Activity of (5,1-Substituted)-3-(indoline-4-(thiophene-2-yl-methylene)-2-(p-tolyl)-2-methylene)-4,3-dihydro-1H-imidazole-5-one Derivatives." Asian Journal of Chemistry 33, no. 9 (2021): 2027–32. http://dx.doi.org/10.14233/ajchem.2021.23271.

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The synthesis of novel imidazole-5-one derivatives (5a-j) was allowed in a conventional method by way of Erlenmeyer and Schiff base mechanism. Compound 2a was synthesized by Erlenmeyer reaction of N-(4-methoxy benzoyl)glycine with 2-thiophene-carboxaldehyde in the presence of acetic anhydride and anhydrous sodium acetate. Finally, it undergoes dehydration reaction with Schiff bases of isatin derivatives (4a-j) to yield final compounds 5a-j. The organic potentials of the newly synthesized imidazole-5-one derivatives have been evaluated for their in vitro anticancer activity by MTT assay method.

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24

Zabadal, Miroslav, Dominik Heger, Petr Klán, and Zdeněk Kříž. "Intramolecular Triplet-Triplet Energy Transfer in Short Flexible Bichromophoric Amino Acids, Dipeptides and Carboxylic Acid Diester." Collection of Czechoslovak Chemical Communications 69, no. 4 (2004): 776–96. http://dx.doi.org/10.1135/cccc20040776.

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Efficiencies of the intramolecular triplet-triplet energy transfer (ITET) in various bichromophoric amino acids (glycine, valine, phenylalanine, and sarcosine), dipeptides (glycylglycine, phenylalanylphenylalanine), and a simple diester, with the benzoyl and naphthyl terminal groups serving as donor and acceptor, respectively, have been determined by the steady-state photokinetic measurements. The magnitude of the transfer rate constants (>108 s-1) and the number of bonds separating the chromophores (8 or 11 atoms) suggest a through-space exothermic exchange mechanism in all cases. The infl

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25

Kishore kumar, T., S. Janarthanan, M. Victor Antony Raj, S. Pandi, P. Sagayaraj, and D. Prem Anand. "Photoconductivity, dielectric and thermal investigations of pure, benzophenone- and iodine-doped benzoyl glycine NLO single crystals." Journal of Physics and Chemistry of Solids 69, no. 11 (2008): 2634–38. http://dx.doi.org/10.1016/j.jpcs.2008.06.002.

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26

Nagaraja, H. S., R. Neumann, and P. Mohan Rao. "Ion-induced craters on the surface of benzoyl glycine single-crystals studied by scanning force microscopy." Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 185, no. 1-4 (2001): 66–70. http://dx.doi.org/10.1016/s0168-583x(01)00756-x.

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27

Sajan, D., H. J. Ravindra, Neeraj Misra, and I. Hubert Joe. "Intramolecular charge transfer and hydrogen bonding interactions of nonlinear optical material N-benzoyl glycine: Vibrational spectral study." Vibrational Spectroscopy 54, no. 1 (2010): 72–80. http://dx.doi.org/10.1016/j.vibspec.2010.06.007.

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28

Singh, Man, and Sushila Chauhan. "Preparation, molecular weight determination and structural studies of (polyvinylpyrrolidone)-oximate silico-benzoyl glycine copolymer with IR spectroscopy." Natural Product Research 21, no. 5 (2007): 426–35. http://dx.doi.org/10.1080/14786410600600474.

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29

Goel, Alok, David Savage, Steven R. Alley, et al. "The synthesis and structural characterization of N-para-ferrocenyl benzoyl dipeptide esters: The X-ray crystal structure of N-{para-(ferrocenyl)benzoyl}-l-alanine-glycine ethyl ester." Journal of Organometallic Chemistry 691, no. 22 (2006): 4686–93. http://dx.doi.org/10.1016/j.jorganchem.2006.08.002.

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30

Varughese, K. A., R. H. Angus, P. R. Carey, H. Lee, and A. C. Storer. "The structure and resonance Raman spectra – structure correlations for methyloxycarbonyl-L-phenylalanyl-L-alanine ethyl dithioester." Canadian Journal of Chemistry 64, no. 8 (1986): 1668–73. http://dx.doi.org/10.1139/v86-274.

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The structure of methyloxycarbonyl-L-phenylalanyl-L-alanine ethyl dithioester has been determined by X-ray crystallographic analysis. The N—C—C—S(thiol) and C—N—C—C(S) torsional angles are 141(1)° and −69(2)°, respectively. Consequently, the N and thiono (C=S) sulfur atoms are in close contact and the [Formula: see text](thiono) distance is 3.078(5) Å. The structure is a perturbed A conformer, which we designate A′, by analogy to a previously characterised A conformer (Huber etal., Biochemistry, 21 3109 (1982)). The [Formula: see text] angles for the Phe residue are −87(2) and 151(2)°, respect

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31

Singh, Man, and Sushila Chauhan. "Synthesis and molecular weight and structural determinations of (polyvinylpyrrolidone)- oximate-silico-benzoyl glycine copolymer with IR and NMR spectroscopy." Journal of Applied Polymer Science 104, no. 5 (2007): 3261–68. http://dx.doi.org/10.1002/app.25681.

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32

Fareed, Ghulam, Nighat Afza, Ali Versiani, et al. "Synthesis, spectroscopic characterization and pharmacological evaluation of oxazolone derivatives." Journal of the Serbian Chemical Society 78, no. 8 (2013): 1127–34. http://dx.doi.org/10.2298/jsc120917126f.

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A series of 4-aryl methylidene-2-phenyl/methyl-5-(4H)-oxazolone derivatives (2-7) have been synthesized using the reported method by condensation of aldehydes with N-benzoyl / N-acetyl glycine in the presence of zinc oxide as a catalyst and acetic anhydride at room temperature in ethanol. The compounds (2-6) are new derivatives. The structures of compounds were evaluated on the basis of 1H-NMR, 13C-NMR, EIMS, FT-IR and elemental analysis. All the compounds were screened for their antibacterial and urease inhibition activity. Antibacterial activity was tested by agar well diffusion method using

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33

Saadi, Lina, and Shaimaa Adnan. "Synthesis, Antibacterial and Antioxidant Evaluation of 2-Substituted-4-arylidene-5(4<i>H</i>)-oxazolone Derivatives." Indonesian Journal of Chemistry 23, no. 5 (2023): 1463. http://dx.doi.org/10.22146/ijc.83052.

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In this research, the synthesis of new substituted oxazolone derivatives is described via Erlenmeyer synthesis of N-acyl amino acid. Firstly, the azo derivative 1 was prepared by coupling the diazonium salt of 3-amino-4-methoxybenzoic acid with 4,5-dichloroimidazole in sodium hydroxide solution. Benzoyl chloride derivative 2, the key intermediate of the synthesis, was synthesized by the acylation of azo-carboxylic acid derivative 1 with thionyl chloride. The resulting acyl chloride derivative reacted with glycine in a basic catalyst to form a hippuric acid derivative 3. After that, oxazolone d

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34

Singh, Man, and Sushila Chauhan. "Preparation, molecular weight determination and structural studies of (polyvinylpyrrolidone)-oximate silico-benzoyl glycine copolymer with IR spectroscopy at pH 7." Physics and Chemistry of Liquids 45, no. 4 (2007): 443–52. http://dx.doi.org/10.1080/00319100601152683.

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35

Raad, Marwa, Khalaf Farris Alsamarrai, and Yehya Kamal Al-Bayati. "Synthesis, Characterization of Chlropheniramine maleate– Molecularly Imprinted Polymers and Their Application as Sensors for the Determination of the Drug in Some Pharmaceutical Preparations." Ibn AL- Haitham Journal For Pure and Applied Science 30, no. 3 (2017): 44. http://dx.doi.org/10.30526/30.3.1601.

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New chlropheniramine maleate (CPM) selective electrochemical membranes were prepared by using chlropheniramine maleate -molecularly imprinted polymers. MIP was prepared by bulk polymerization using 2-hydroxyethyl methacrylate (2-HEMA) as monomer, ethylene glycol dimethacrylate (EGDMA) as a cross-linker and a benzoyl peroxide (BPO) as an initiator at 600C. Three CPM-MIP electrodes were constructed by using tri-tolyl Phosphate (ToCP), tris (2- ethyl hexyl) Phosphate (TEHP) and tributyl Phosphate (TBP) as plasticizers in PVC matrix.Electrode parameters including slopes, working concentrations ph.

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36

Sherry, Ratna. "Polarographic Studies of Mixed Complexes of Pb(II) with m -Nitro Benzoyl Glycine and Succinate Ions using NaNO3 as Supporting Electrolyte." RESEARCH REVIEW International Journal of Multidisciplinary 6, no. 1 (2021): 296–302. https://doi.org/10.31305/rrijm.2021.v06.i01.056.

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37

Goel, Alok, David Savage, Steven R. Alley, et al. "The synthesis and structural characterization of novel N-meta-ferrocenyl benzoyl dipeptide esters: The X-ray crystal structure and in vitro anti-cancer activity of N-{meta-ferrocenyl)benzoyl}-l-alanine-glycine ethyl ester." Journal of Organometallic Chemistry 692, no. 6 (2007): 1292–99. http://dx.doi.org/10.1016/j.jorganchem.2006.09.057.

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38

Xavier, T. S., Peter T. M. Kenny, D. Manimaran, and I. Hubert Joe. "FT-IR and Raman spectroscopic and DFT studies of anti-cancer active molecule N-{(meta-ferrocenyl) Benzoyl} – l -Alanine – Glycine ethyl ester." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 145 (June 2015): 523–30. http://dx.doi.org/10.1016/j.saa.2015.02.087.

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39

Khambhati, Vivek H., Hamed K. Abbas, Michael Sulyok, Maria Tomaso-Peterson, and W. Thomas Shier. "First Report of the Production of Mycotoxins and Other Secondary Metabolites by Macrophomina phaseolina (Tassi) Goid. Isolates from Soybeans (Glycine max L.) Symptomatic with Charcoal Rot Disease." Journal of Fungi 6, no. 4 (2020): 332. http://dx.doi.org/10.3390/jof6040332.

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Macrophomina phaseolina (Tassi) Goid., the causal agent of charcoal rot disease of soybean, is capable of causing disease in more than 500 other commercially important plants. This fungus produces several secondary metabolites in culture, including (-)-botryodiplodin, phaseolinone and mellein. Given that independent fungal isolates may differ in mycotoxin and secondary metabolite production, we examined a collection of 89 independent M. phaseolina isolates from soybean plants with charcoal rot disease using LC-MS/MS analysis of culture filtrates. In addition to (-)-botryodiplodin and mellein,

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Lee, H., R. H. Angus, A. C. Storer, and P. R. Carey. "Structure of enzyme-bound substrates: resonance Raman and kinetic evidence for differential enzyme-substrate contacts in N-(Pentafluoro-benzoyl)glycine dithioacyl and thioacyl papain." Journal of Molecular Structure 214 (December 1989): 1–13. http://dx.doi.org/10.1016/0022-2860(89)80002-x.

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Titov, Oleksii, and Viktor Brygadyrenko. "Influence of Synthetic Flavorings on the Migration Activity of Tribolium confusum and Sitophilus granarius." Ekológia (Bratislava) 40, no. 2 (2021): 163–77. http://dx.doi.org/10.2478/eko-2021-0019.

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Abstract Flavorings and volatile biologically active substances, used by humans for various purposes, may potentially have fumigating, repellent, or attractive effects on various species of anthropod storage pests. Tribolium confusum Jacquelin du Val, 1863 (Tenebrionidae) and Sitophilus granarius (Linnaeus, 1758) (Curculionidae) are the two most abundant pests of grain and grain products; the damage they cause to stored products of horticulture is 5–20% of the total yield of grain crops. In the experiment, we video-recorded migratory activity of beetles and evaluated it according to standard t

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Romoff, Todd T., Bernardo G. Ignacio, Noel Mansour, et al. "Large-Scale Synthesis of the Glycine Schiff Base Ni(II) Complex Derived from (S)- and (R)-N-(2-Benzoyl-4-chlorophenyl)-1-[(3,4-dichlorophenyl)methyl]-2-pyrrolidinecarboxamide." Organic Process Research & Development 24, no. 2 (2020): 294–300. http://dx.doi.org/10.1021/acs.oprd.9b00399.

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Seebach, Dieter, David D. Miller, Stefan Müller, and Theodor Weber. "The Chiral Glycine Enolate Derivative from 1-Benzoyl-2-(tert-butyl)-3-methyl-1,3-imidazolidin-4-one is Alkylated in the 5-Position with Relative Topicitylk. Preliminary Communication." Helvetica Chimica Acta 68, no. 4 (1985): 949–52. http://dx.doi.org/10.1002/hlca.19850680418.

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Miguez, João Pedro, Roberto Fernandez-Lafuente, Olga Luisa Tavano, and Adriano Aguiar Mendes. "The Immobilization and Stabilization of Trypsin from the Porcine Pancreas on Chitosan and Its Catalytic Performance in Protein Hydrolysis." Catalysts 13, no. 10 (2023): 1344. http://dx.doi.org/10.3390/catal13101344.

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In this study, trypsin from the porcine pancreas was immobilized on a heterofunctional support prepared by activating chitosan (Chit) hydrogel with glutaraldehyde (GA), then functionalizing it with glycine (Chit–GA–Gly). The catalytic performance of the immobilized trypsin in the hydrolysis reactions was compared with the catalytic performance of the immobilized enzyme on glutaraldehyde-activated chitosan (Chit–GA) and chitosan hydrogel (Chit). The maximum concentration of immobilized protein on Chit–GA–Gly was approximately 16 mg·g−1 at pH 9.0 (5 mmol·L−1 buffer sodium carbonate) at 25 °C fro

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Odhiambo, Ogweno Paulicarp, Celestine Makobe, Viviene Matiru, and Wycliffe Masanta. "Antimicrobial Action of Sambacus nigra, Symphytum officinale, Urtica dioica, and Mentha pulegium Plant Compounds against Antibiotic Resistant Streptococcus pneumoniae." East African Journal of Health and Science 7, no. 1 (2024): 95–111. http://dx.doi.org/10.37284/eajhs.7.1.1743.

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Infections by Streptococcus pneumoniae are among the leading causes of illness and death in children below 5 years, people with underlying debilitating medical conditions, and the elderly worldwide. Over the past three decades, antimicrobial resistance in S. pneumoniae has drastically increased, with resistance reported in Penicillin, erythromycin, trimethoprim/sulfamethoxazole, vancomycin, tetracycline, chloramphenicol and ofloxacin. This phenomenon has necessitated a continuous search for alternative compounds against S. pneumoniae, such as Plants. The objective was to investigate antimicrob

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Wei, Yuyang, and Wenbin Zhang. "Potential Cycling Effects on Activities of Nickel-Mediated Benzyl Alcohol and Glycine Electrooxidation in Alkaline Solutions." Catalysts 10, no. 1 (2020): 119. http://dx.doi.org/10.3390/catal10010119.

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Nickel electrodes under continuous potential cycling were applied for the electrooxidation of benzyl alcohol and glycine in KOH solutions, and their activities were measured and compared by cyclic voltammetry. It is shown that intrinsic activities of both reactions decrease with the increasing catalyst loadings, and a more significant decreasing trend was observed in glycine electrooxidation when compared to benzyl alcohol electrooxidation. These phenomena may be explained by an increasing of mass loading induced a decrease of the catalyst surface conductivity, structure changes of Ni(OH)2 fro

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Nicholas, Sumesh. "The tripeptideN-Cbz-βGly-Gly-Gly-Obz". Acta Crystallographica Section E Crystallographic Communications 71, № 4 (2015): o240—o241. http://dx.doi.org/10.1107/s2056989015004272.

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The title peptide,N-benzyloxycarbonyl-β-glycylglycylglycine benzyl ester, C22H25N3O6, contains a non-proteinogenic amino acid residue, β-glycine, which is a homologated analogue of glycine. In the molecular structure, β-glycine adopts an extended conformation with atransconformation about its Cβ—Cαbond. The second glycine residue adopts an extended conformation while the third glycine residue adopts a helical conformation. In the crystal, three N—H...O hydrogen bonds, two involving the same carbonyl O atom as acceptor, results in an infinite two-dimensional network parallel to thebcplane.

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Wu, HaiYan, Edward P. Masler, Steven T. Rogers, Ching Chen, and David J. Chitwood. "Benzyl isothiocyanate affects development, hatching and reproduction of the soybean cyst nematode Heterodera glycines." Nematology 16, no. 4 (2014): 495–504. http://dx.doi.org/10.1163/15685411-00002781.

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Benzyl isothiocyanate (BITC), prepared in 1% methanol and applied at micro-molar doses, decreased Heterodera glycines infective second-stage juvenile (J2) movement, hatching and reproduction on soybean, Glycine max. Direct exposure of J2 to 30 μM BITC caused an immediate decrease (17%) in J2 movement relative to 1% methanol controls, and within 3 h exposure eliminated >99% of movement. Continuous exposure of H. glycines eggs to 30 μM or 60 μM BITC significantly decreased percentage hatch of J2 measured at 7 days (30 μM, 15.8 ± 2.4%; 60 μM, 7.9 ± 2.2%) relative to controls (44.9 ± 4.1%). Con

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Doi, M., K. Kinoshita, A. Asano, R. Yoneda, T. Kurihara, and T. Ishida. "N-Benzyl-N-(tert-butyloxycarbonyl)glycine, anN-Substituted Glycine (Peptoid) Monomer." Acta Crystallographica Section C Crystal Structure Communications 54, no. 8 (1998): 1164–65. http://dx.doi.org/10.1107/s0108270198002741.

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Martin, Tellis A., and William T. Comer. "N-[[(Mercaptoacetyl)amino]benzoyl]glycines mucolytic agents." Journal of Medicinal Chemistry 28, no. 7 (1985): 910–14. http://dx.doi.org/10.1021/jm00145a011.

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