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Journal articles on the topic '2-amino-propanamide'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Macháček, Vladimír, Makky M. M. Hassanien, Vojeslav Štěrba, and Antonín Lyčka. "Formation of the Meisenheimer spiro adduct of N-(2,4,6-trinitrophenyl)alanine methylamide and its rearrangement to 2-amino-N-methyl-N-(2,4,6-trinitrophenyl)propanamide." Collection of Czechoslovak Chemical Communications 51, no. 9 (1986): 1972–85. http://dx.doi.org/10.1135/cccc19861972.

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N-(2,4,6-trinitrophenyl)alanine methylamide (I) undergoes base-catalyzed cyclization in methanol to give the spiro adduct II. In aniline-anilinium chloride buffers, the spiro adduct is protonated at the oxygen atom of 2-nitro group to give the neutral compound III. In 4-bromoaniline buffers or by action of methanolic hydrogen chloride, the compound III is opened to E and Z isomers of 2-amino-N-methyl-N-(2,4,6-trinitrophenyl)propanamide hydrochloride (IV). The rate-limiting step of cyclization of compound Z-IV to compound III consists in the isomerization Z-IV → E-IV. At higher pH values (aceta

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2

Manolov, Stanimir, Iliyan Ivanov, Dimitar Bojilov, and Paraskev Nedialkov. "2-(2-Fluoro-[1,1′-biphenyl]-4-yl)-N-(4-methyl-2-oxo-2H-chromen-7-yl)propanamide." Molbank 2023, no. 3 (2023): M1682. http://dx.doi.org/10.3390/m1682.

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Herein, we report the synthesis of 2-(2-fluoro-[1,1′-biphenyl]-4-yl)-N-(4-methyl-2-oxo-2H-chromen-7-yl)propanamide in the reaction between 7-amino-4-methyl-2H-chromen-2-one and (±)-flurbiprofen. The newly-obtained bio-functional hybrid compound was fully characterized via 1H, 13C NMR, UV, and mass spectral data.

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3

Sravya, Gundala, Ummadi Nagarjuna, Venkatapuram Padmavathi, Galla Rajitha, Sakuri Chandi priya, and Adivireddy Padmaja. "Synthesis, Antioxidant and Anti-inflammatory Activities of 5-((styrylsulfonyl) methyl)-1,3,4-Oxadiazol / Thiadiazol-2-amine Derivatives." Letters in Drug Design & Discovery 16, no. 11 (2019): 1233–47. http://dx.doi.org/10.2174/1570180816666181102114529.

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Background: A new class of 5-(styrylsulfonylmethyl)-1,3,4-oxadiazol-2-amine and 5- (styrylsulfonylmethyl)-1,3,4-thiadiazol-2-amine derivatives were prepared by derivatization of amino function. Methods: All the synthesized compounds were tested for antioxidant and anti-inflammatory activities. Results: The 2-amino-3-chloro-N-(5-(4-methylstyrylsulfonylmethyl)-1,3,4-oxadiazol-2-yl)-propanamide (12b) and 3-chloro-N-(5-(4-methylstyrylsulfonylmethyl)-1,3,4-oxadiazol-2-yl)-butanamide (14b) displayed significant antioxidant activity, greater than the standard Ascorbic acid. Conclusion: Moreover, 12b

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4

Zareva, Sonya. "Solid-state linear-dichroic infrared (IR-LD) spectroscopic and theoretical characterization of 2-[(2-ethoxy-3,4-dioxocyclobut-1-en-yl)amino]propanamide." Open Chemistry 4, no. 4 (2006): 695–707. http://dx.doi.org/10.2478/s11532-006-0034-0.

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Abstract2-[(2-Ethoxy-3,4-dioxocyclobut-1-en-yl)amino]propanamide (N-alaninamidoamide of squaric acid ethyl ester) has been characterized structurally and spectroscopically by ab initio calculations and IR-LD spectroscopy of oriented crystals suspended in a nematic liquid crystal. The results are compared with single crystal X-ray structures illustrating the possibilities of this experimental approach to obtaining structural information as well as assigning IR bands.

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5

Yu-hua, Zhang, Duan Chun-sheng, Fu Hui, et al. "Theoretical study on the influence of formamide on the optical rotation of 2-amino-propanamide." Journal of Indian Chemical Society Vol. 88, Apr 2011 (2011): 525–30. https://doi.org/10.5281/zenodo.5766678.

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College of Chemistry & Chemical Engineering, China University of Petroleum, Shangdong, Qingdao 266555, People's Republic of China <em>E-mail</em> : zhengyu@mail.qfnu.edu.cn, niceuu@163.com Department of Chemistry, Qufu Normal University, Shandong, Qufu 273165, People's Republic of China lnstitute of Vocational and Adult Edttcation of Qufu Normal University, Shandong 273165, People's Republic of China <em>Manuscript received 28 May 2010, accepted 16 August 2010</em> Five stationary points of formamlde-2-amino propionamide complexes have been optimized at the B3LYP/6- 311++G (2d,

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6

Rima, Ghassoub, Jacques Satgé, Rodolphe Dagiral, et al. "Synthesis and Radioprotective Activity of New Organosilicon and Germanium Compounds." Metal-Based Drugs 5, no. 3 (1998): 139–46. http://dx.doi.org/10.1155/mbd.1998.139.

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Silathiazolidine and metalladithioacetals (M = Si, Ge) have been prepared by the interaction of dialkyldichloro- or bis(diethylamino)dialkylsilanes and -germanes with 3-[N-(2- thioethyl)]amino-propanamide (WR-2529) and [1-thioethyl-2-(1-naphtylmethyl)]-2- imidazoline. The study of these compounds in the field of chemical radioprotection has shown a notable decrease in the toxicity and a rather large increase in the radioprotective activity of these new derivatives in comparison with the starting organic compounds.

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7

Tüzün, Işıl, Ayten Y. Karataş, Özge Şeşenoğlu, Ayhan S. Demir, and Gülay Özcengiz. "2-Amino-N-(2-furylmethyl)propanamide as a novel alanylglycine equivalent synthesized by bacilysin synthetase." Enzyme and Microbial Technology 33, no. 5 (2003): 725–28. http://dx.doi.org/10.1016/s0141-0229(03)00209-6.

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8

Sedlák, Miloš, Jiří Hanusek, Radim Bína, Jaromír Kaválek, and Vladimír Macháček. "Kinetics and Mechanism of the Formation and Decomposition of Imidazolin-4-ones from 2-(N-Benzoylamino)alkanamides in Aqueous Medium." Collection of Czechoslovak Chemical Communications 64, no. 10 (1999): 1629–40. http://dx.doi.org/10.1135/cccc19991629.

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The cyclization reactions of substituted 2-(N-benzoyl-N-methyl)aminoalkanamides 1a-1g have been studied in aqueous medium. The Hammett reaction constant is ρ = 1.4 for the cyclization reactions of compounds 1a-1e in sodium hydroxide solutions. 2-[N-Methyl- N-(4-nitrobenzoyl)amino]-2-(4-nitrophenyl)propanamide (1g) is cyclized to imidazolinone 2g in aqueous amine buffers of pH 9-11.5; the reaction is subject to specific base catalysis in these media, and the rate-limiting step is the formation of a tetrahedral intermediate. In sodium hydroxide solution, the primary cyclization product is hydrol

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9

Jonuškienė, Ilona, Rima Stankevičienė, Kristina Kantminienė, and Ingrida Tumosienė. "The Influence of Phytohormones on Antioxidative and Antibacterial Activities in Callus Cultures of Hypericum perforatum L." Agriculture 13, no. 8 (2023): 1543. http://dx.doi.org/10.3390/agriculture13081543.

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Natural extracts of Hypericum perforatum L. are widely used in the pharmaceutical industry due to their antiviral, antioxidant, antibacterial, antidiabetic, and antidepressant activities. Plant biotechnological methods are gaining more attention as efficient and biosustainable approaches for the production of high value compounds by using plant callus cultures in vitro. The aim of this research was to evaluate the influence of phytohormones on the formation of Hypericum perforatum L. callus culture, to explore antioxidant and antibacterial activities, and to determine the amounts of phytochemi

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10

Tumosienė, Ingrida, Kristina Kantminienė, Arnas Klevinskas, Vilma Petrikaitė, Ilona Jonuškienė, and Vytautas Mickevičius. "Antioxidant and Anticancer Activity of Novel Derivatives of 3-[(4-Methoxyphenyl)amino]propanehydrazide." Molecules 25, no. 13 (2020): 2980. http://dx.doi.org/10.3390/molecules25132980.

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Series of novel 3-[(4-methoxyphenyl)amino]propanehydrazide derivatives bearing semicarbazide, thiosemicarbazide, thiadiazole, triazolone, triazolethione, thiophenyltriazole, furan, thiophene, naphthalene, pyrrole, isoindoline-1,3-dione, oxindole, etc. moieties were synthesized and their molecular structures were confirmed by IR, 1H-, 13C-NMR spectroscopy and mass spectrometry data. The antioxidant activity of the synthesized compounds was screened by DPPH radical scavenging method. The antioxidant activity of N-(1,3-dioxoisoindolin-2-yl)-3-((4-methoxyphenyl)amino)propanamide and 3-((4-methoxyp

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11

Bhowmik, Prasanta C. "Smooth Crabgrass (Digitaria ischaemum) Control in Kentucky Bluegrass (Poa pratensis) Turf with Herbicides Applied Preemergence." Weed Technology 1, no. 2 (1987): 145–48. http://dx.doi.org/10.1017/s0890037x00029341.

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In field experiments, preemergence applications of bensulide {O,O-bis(1-methylethyl)S-[2-[(phenylsulfonyl)amino] ethyl] phosphorodithioate} or DCPA (dimethyl-2,3,5,6-tetrachloro-1,4-benzenedicarboxylate) at 11.2 kg ai/ha controlled smooth crabgrass [Digitaria ischaemum(Schreb. ex Schweig.)Schreb. ex Muhl. #3DIGIS] selectively in turf. Granular and liquid formulations of bensulide performed similarly. Napropamide [N,N-diethyl-2-(1-naphthalenyloxy)propanamide] granules when applied alone at 1.1 to 3.4 kg ai/ha were partially effective, but when combined with 5.6 kg ai/ha bensulide, controlled sm

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12

Patten, Timothy E., Christina Troeltzsch, and Marilyn M. Olmstead. "Copper(I) and -(II) Complexes of Neutral and DeprotonatedN-(2,6-Diisopropylphenyl)-3-[bis(2-pyridylmethyl)amino]propanamide." Inorganic Chemistry 44, no. 25 (2005): 9197–206. http://dx.doi.org/10.1021/ic0505697.

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13

Berchielli-Robertson, D. L., C. H. Gilliam, and D. C. Fare. "Preemergence Herbicide Control of Eclipta alba in Container-grown Plants." HortScience 24, no. 5 (1989): 779–81. http://dx.doi.org/10.21273/hortsci.24.5.779.

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Abstract Preemergence herbicides were evaluated for control of yerba-de-tago [Eclipta alba (L.) Hasskarl] and for phytotoxicity to four container-grown landscape species. Herbicides providing excellent control (less than one weed/pot) were chlorimuron at 0.035 and 0.07 kg·ha-1, chlorimuron + metribuzin at 0.075 + 0.485 kg·ha-1, and oryzalin at 4.5 and 9.0 kg·ha-1. Injury within 30 days after treatment occurred with applications of oxyfluorfen, lactofen, and fomesafen at the × 1 and × 2 rates on Ilex vomitoria Ait. ‘Nana’ (dwarf yaupon), Rhododendron satsuki ‘Pink Gumpo’ (‘Pink Gumpo’ azalea),

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14

Turner, D. L., S. S. Sharpe, and Ray Dickens. "Herbicide Effects on Tensile Strength and Rooting of Centipedegrass Sod." HortScience 25, no. 5 (1990): 541–44. http://dx.doi.org/10.21273/hortsci.25.5.541.

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“Effects of selected herbicides on sod tensile strength and rooting of mature and immature turf of common centipedegrass [Eremochloa ophiuroides (Munro.) Hack] were studied in field experiments. Herbicides evaluated were atrazine, atrazine + tridiphane, bensulide, DCPA, DPX-6316, imazapyr, imazaquin, napropamide, oxadiazon, pendimethalin, sethoxydim, simazine, and sulfometuron. At 2, 4, and 8 weeks after treatment (WAT), sod tensile strength was determined, and root length and number were measured 7 to 10 days later. In 1986 sod tensile strength was not affected, but in 1987 the tensile streng

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15

Dotsenko, Victor V., Nawras T. Jassim, Azamat Z. Temerdashev, Zainab R. Abdul-Hussein, Nicolai A. Aksenov, and Inna V. Aksenova. "New 6′-Amino-5′-cyano-2-oxo-1,2-dihydro-1′H-spiro[indole-3,4′-pyridine]-3′-carboxamides: Synthesis, Reactions, Molecular Docking Studies and Biological Activity." Molecules 28, no. 7 (2023): 3161. http://dx.doi.org/10.3390/molecules28073161.

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The purpose of this work was to prepare new isatin- and monothiomalondiamide-based indole derivatives, as well as to study the properties of the new compounds. The four-component reaction of 5-R-isatins (R = H, CH3), malononitrile, monothiomalonamide (3-amino-3-thioxo- propanamide) and triethylamine in hot EtOH yields a mixture of isomeric triethylammonium 6′-amino-3′-(aminocarbonyl)-5′-cyano-2-oxo-1,2-dihydro-1′H- and 6′-amino-3′-(aminocarbonyl)- 5′-cyano-2-oxo-1,2-dihydro-3′H-spiro[indole-3,4′-pyridine]-2′-thiolates. The reactivity and structure of the products was studied. We found that oxi

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16

Kornylov, A. Yu, A. A. Krysko, O. L. Krysko, and S. E. Sambursky. "SYNTHESIS METHOD OF OPTICALLY PURE ENANTIOMERS OF 5-ARYL SUBSTITUTED3-METHYL‑7- NITRO‑1,2-DIHYDRO‑3H‑1,4-BENZODIAZEPIN‑2-ONES." Odesa National University Herald. Chemistry 27, no. 2(82) (2022): 76–82. http://dx.doi.org/10.18524/2304-0947.2022.2(82).264890.

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The aim of this work is to develop a simple, fast and efficient method for the synthesis of optically pure enantiomers of some 5-aryl-substituted 3-methyl‑7-nitro‑1,2-dihydro‑3H‑1,4-benzodiazepin‑2-ones using simple reagents. In the course of the study, we found that the interaction of 2-amino‑5-nitrobenzophenone or 2-amino‑2’-chloro‑5-nitrobenzophenone with optically active L- or D‑α-alanine N‑carboxyanhydrides in the presence of two equivalents of trifluoroacetic acid does not leads to the formation of the corresponding reaction intermediates (2-amino-N-(2-benzoylphenyl)propanamide), even wh

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17

Gilbertz, D. A., and B. J. Johnson. "Response of Bedding Plants and Weeds to Herbicides." Journal of Environmental Horticulture 5, no. 4 (1987): 158–62. http://dx.doi.org/10.24266/0738-2898-5.4.158.

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Preemergence and postemergence herbicides were evaluated for summer weed control and for phytotoxicity of 6 commonly used annual bedding plant species. Dacthal (dimethyl 2,3,5,6-tetrachloro-1,4-benzenedicarboxylate), Enide (N,N-dimethyl-a-phenyl benzene acetamide), Devrinol (N,N-diethyl-2-(1-naphthalenyloxy) propanamide), Surflan (4-(dipropylamino)-3,5-dinitro-benzenesulfonamide), Ronstar (3-[2,4-dichloro-5-(1-methylethoxy)phenyl]-5-1(1,1-dimethylethy1)-1,3,4-oxadiazol-2-(3H)-one), Kerb (3,5-dichloro(N-l, 1-dimethyl-2-propynyl)benzamide), and Treflan (2,6-dinitro-N,N-dipropyl-4-(trifluoromethy

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18

Buvailo, Andrii I., Anna V. Pavlishchuk, Larysa V. Penkova, Natalia V. Kotova та Matti Haukka. "Bis{(E)-3-[2-(hydroxyimino)propanamido]-2,2-dimethylpropan-1-aminium} bis[μ-(E)-N-(3-amino-2,2-dimethylpropyl)-2-(hydroxyimino)propanamido(2−)]bis{[(E)-N-(3-amino-2,2-dimethylpropyl)-2-(hydroxyimino)propanamide]copper(II)} bis((E)-{3-[2-(hydroxyimino)propanamido]-2,2-dimethylpropyl}carbamate) acetonitrile disolvate". Acta Crystallographica Section E Structure Reports Online 68, № 12 (2012): m1480—m1481. http://dx.doi.org/10.1107/s160053681204620x.

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19

Wilcox-Lee, Darlene, and Daniel T. Drost. "Tillage Reduces Yield and Crown, Fern, and Bud Growth in a Mature Asparagus Planting." Journal of the American Society for Horticultural Science 116, no. 6 (1991): 937–41. http://dx.doi.org/10.21273/jashs.116.6.937.

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Asparagus officinalis L. cv. Centennial established with transplants in 1983 was maintained with tillage or a no-till (NT) system to evaluate effects of tillage on yield and plant growth in a mature asparagus planting. Metribuzin or metribuzin + napropamide at 1.12 and 1.68 kg a.i./ha, respectively, were used for weed control in both tillage regimes. Marketable yields were assessed for 5 years. In 1989, in addition to yield data, destructive harvests of entire plants were made every 3 weeks from March to November to evaluate the effect of tillage on fern, crown, and bud growth, and carbohydrat

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20

Jackson, Graham E., Fatin M. Elmagbari, Ahmed N. Hammouda, and Raffaele P. Bonomo. "Solution equilibria and the X-ray structure of Cu(ii) complexation with 3-amino-N-(pyridin-2-ylmethyl)propanamide, a pseudo-mimic of human serum albumin." Dalton Transactions 45, no. 42 (2016): 17010–19. http://dx.doi.org/10.1039/c6dt02974d.

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21

Holt, Neal W., and Jim H. Hunter. "Annual Canarygrass (Phalaris canariensis) Tolerance and Weed Control Following Herbicide Application." Weed Science 35, no. 5 (1987): 673–77. http://dx.doi.org/10.1017/s004317450006077x.

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Field studies were conducted in Saskatchewan to evaluate the effect of herbicides on annual canarygrass (Phalaris canariensisL.) and associated weeds. Bromoxynil (3,5-dibromo-4-hydroxybenzonitrile) at 0.35 kg ai/ha, tank mixes of bromoxynil at 0.28 kg/ha plus the ester of MCPA [(4-chloro-2-methylphenoxy)acetic acid] at 0.28 kg ae/ha, linuron [N′-(3,4-dichlorophenyl)-N-methoxy-N-methylurea] at 0.28 kg ai/ha plus MCPA amine at 0.56 kg/ha, or propanil [N-(3,4-dichlorophenyI)propanamide] at 1.0 kg ai/ha plus MCPA ester at 0.28 kg/ha resulted in annual canarygrass seed and dry matter yields equal t

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22

Umesh, Kumar. "CNS Disorders: Treatment Approach with Novel Derivatives of Coumarins in Experimental Albino Mice." Research and Review Drugs and Drugs Development 1, no. 2 (2019): 1–20. https://doi.org/10.5281/zenodo.3066784.

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<strong><em>Aim</em></strong><strong><em>:</em></strong><em> The present study was aimed to assess the treatment of CNS disorders of the novel coumarin (Benzopyran-2-one) derivatives i.e., 2- (4-isobutylphenyl) -N- (4-methyl-2-oxo-2H-chromen-7-yl) propanamide (comp-I), 2-(2-(2,6- dichlorophenylamino) phenyl) –N- (4- methyl-2-oxo-2H-chromen-7-yl) acetamide (comp-II) and 2-(1-(4-chlorobenzoyl)-6-methoxy-2-methyl-1H-indol-3-yl)-N-(4-methyl-2-oxo-2H-chromen-7-yl) acetamide (comp-III) by using the various pharmacological activities i.e., anti-convulsant, anxiolytic, spontaneous motor activity

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23

Leporati, Enrico. "Design of transition metal chelates with biological activity. Potentiometric study of complex formation equilibria between 2-amino-N-hydroxy-3-(p-hydroxyphenyl) propanamide and nickel(II), copper(II), and hydrogen ions in aqueous solution." Journal of the Chemical Society, Dalton Transactions, no. 6 (1987): 1409. http://dx.doi.org/10.1039/dt9870001409.

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NYAITONDI, OMBUNA DINAH, RUTH NDUTA WANJAU, HUDSON NYAMBAKA, and AHMED HASSANALI. "Anti-bacterial properties and GC-MS analysis of extracts and essential oils of selected plant product." Biofarmasi Journal of Natural Product Biochemistry 16, no. 1 (2018): 44–58. http://dx.doi.org/10.13057/biofar/f160105.

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Nyaitondi OD, Wanjau R, Nyambaka H, Hassanali A. 2018. Anti-bacterial properties and GC-MS analysis of extracts and essential oils of selected plant product. Biofarmasi J Nat Prod Biochem 16: 44-58. Plants are traditionally used for the treatment of bacterial infections though they are not clinically regulated due to lack of awareness and sufficient data to support the reported therapeutic claims. Some plants used as food and vegetables are hardly considered in such studies. This study aimed to investigate the antibacterial properties associated with garlic, ginger, turmeric, lemon, and onion

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Lacivita, Enza, Madia Letizia Stama, Jun Maeda, et al. "Radiosynthesis and in vivo Evaluation of Carbon-11 (2S)-3-(1H-Indol-3-yl)-2-{[(4-methoxyphenyl)carbamoyl]amino}-N-{[1-(5-methoxypyridin-2-yl)cyclohexyl]methyl}propanamide: An Attempt to Visualize Brain Formyl Peptide Receptors in Mouse Models of Neuroinfl." Chemistry & Biodiversity 13, no. 7 (2016): 875–83. http://dx.doi.org/10.1002/cbdv.201500281.

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Thomas, David R., Ellen M. Soffin, Claire Roberts, et al. "SB-699551-A (3-cyclopentyl-N-[2-(dimethylamino)ethyl]-N-[(4′-{[(2-phenylethyl)amino]methyl}-4-biphenylyl)methyl]propanamide dihydrochloride), a novel 5-ht5A receptor-selective antagonist, enhances 5-HT neuronal function: Evidence for an autoreceptor role for the 5-ht5A receptor in guinea pig brain." Neuropharmacology 51, no. 3 (2006): 566–77. http://dx.doi.org/10.1016/j.neuropharm.2006.04.019.

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Manjunatha, K. S., N. D. Satyanarayan, and S. Harishkumar. "ANTIMICROBIAL AND IN SILICO ADMET SCREENING OF NOVEL (E)-N-(2-(1H-INDOL-3-YL-AMINO) VINYL)-3-(1-METHYL-1H-INDOL-3-YL)-3-PHENYLPROPANAMIDE DERIVATIVES." International Journal of Pharmacy and Pharmaceutical Sciences 8, no. 10 (2016): 251. http://dx.doi.org/10.22159/ijpps.2016v8i10.13957.

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<p><strong>Objective: </strong>Synthesis, <em>in silico</em> absorption, distribution, metabolism, excretion, toxicity (ADMET) and <em>in vitro</em> antimicrobial screening of (<em>E</em>)-<em>N</em>-(2-(1<em>H</em>-indol-3-ylamino) vinyl)-3-(1-methyl-1<em>H</em>-indol-3-yl)-3-phenylpropanamide derivatives.<strong></strong></p><p><strong>Methods: </strong>(<em>E</em>)-<em>N</em>-(2-(1<em>H</em>-indol-3-ylamino) vinyl)-3-(1-methyl-1&lt

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Ying, Junwu, Junwu Ying, Shuang Liang, et al. "Route design and development for an anthranilic diamide compound containing 2-methyl-2-amino-propanamide group as a potential insecticide." Arkivoc 2024, no. 8 (2024). http://dx.doi.org/10.24820/ark.5550190.p012.185.

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Liu, Ying, Xiang-Guang Meng, Jian-Mei Li, Xiao-Hong Li, and Wei-Feng Yu. "Efficient hydrolysis of glucose-1-phosphate catalyzed by metallomicelles with histidine residue." Chemical Papers 68, no. 5 (2014). http://dx.doi.org/10.2478/s11696-013-0492-8.

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AbstractPhosphate esters play an important role in genetic information transfer, cell signal transduction, energy transmission and metabolic processes of living beings. Efficient catalytic hydrolysis of phosphate esters is still an attractive and challenging problem. Here, a new 2-amino-N-dodecyl-3-(1H-imidazol-5-yl)propanamide (L2) surfactant was synthesized and its metallomicelles of La3+, Cu2+, Co2+, and Zn2+ complexes were used as mimic metalloenzymes to catalyze the hydrolysis of glucose-1-phosphate (G1P) in a buffer solution at 35°C. The metallomicelle systems can efficiently catalyze th

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"Docking Studies of Lipase (Mflip1) from Malassezia furfur (Robin) with Propanamide, N-methyl-2-amino and 1-Propanol, 3-(dimethylamino) Predicting Inhibitory Activity." International Journal of Pharmaceutical Research 12, no. 1 (2020). http://dx.doi.org/10.31838/ijpr/2020.12.01.011.

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Kailas Patil, Harshada, Hetakshi Vilas Patil, Mohit Sunil Pawar, et al. "Safinamide Mesylate: Analytical and Chromatographic Methodologies." Asian Journal of Pharmaceutical Analysis, May 10, 2025, 153–59. https://doi.org/10.52711/2231-5675.2025.00024.

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Safinamide Mesylate (SAF) (S1), also known as (S)-2-(4-((3-Fluorobenzyl) oxy) benzyl) amino) propanamide methane sulfonate, is a recently developed medicine to treat Parkinson's disease (PD). Safinamide is a third-generation reversible MAO-B inhibitor, which also blocks sodium voltage-sensitive channels and modulates stimulated release of glutamate. Safinamide used to supplement levodopa/carbidopa for Parkinson's disease therapy during "off" episodes. According to the literature, there are many methods for the analysis of Safinamide Mesylate, so we gather all methods in one review. Safinamide

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LEPORATI, E. "ChemInform Abstract: Design of Transition Metal Chelates with Biological Activity. Potentiometric Study of Complex Formation Equilibria Between 2-Amino-N-hydroxy-3-(p-hydroxyphenyl)propanamide and Nickel(II), Copper(II), and Hydrogen Ions in Aqueous Solut." ChemInform 18, no. 39 (1987). http://dx.doi.org/10.1002/chin.198739066.

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