Electrooxidation is an efficient method for treating effluents with high concentrations of ammoniacal nitrogen and organic matter (R), in the presence of chloride ions (Cl-). The present study aimed at degrading ammoniacal nitrogen and organic matter from an effluent generated at a fertilizer storage port terminal. For this purpose, a batch electrochemical reactor with mechanical agitation was used, with a Ti/RuO2 anode. The parameters studied were the current density that varied in 20, 40 and 60 mA cm-2, the concentration of chloride ions that was 0.04, 0.74, 0.90 to 0.81 mol L-1 and the electrolysis time that varied from 4.0, 5.0, 7.0 and 8.0 h. A 22 experimental design was conducted to determine the significance level of the parameters studied. The results obtained indicated the removal of 99.99% of N-NH3 and 75.60% of total organic carbon (TOC) when a current density of 60 mA cm-2 and a Cl- concentration of 35.5 g L-1 were applied, after 4.0 h of electrolysis. R, R , (R) Cl. Cl . (Cl-) terminal purpose used TiRuO2 TiRuO Ti RuO2 RuO Ti/RuO anode 20 4 6 cm2, cm2 cm 2, 2 004 0 04 0.04 074 74 0.74 090 90 0.9 081 81 0.8 L1 L 1 L- 50 5 5.0 70 7 7. 80 8 8. 9999 99 99.99 NNH3 NNH N NH3 NH N-NH 7560 75 75.60 TOC (TOC cm- 355 35 35. applied 4. (R (Cl- 00 0.0 07 0.7 09 9 0. 08 5. 999 99.9 756 75.6 3 (Cl 99. 75.

Hair can provide chemical information about drug use. This study employed matrix-assisted laser desorption ionization mass spectrometry (MALDI-MS) to detect drugs in hair samples. The technique was used to detect cocaine (COC, molecular weight (Mw) = 303.14 Da) and its main metabolites, benzoylecgonine (BZE, Mw = 289.13 Da), cocaethylene (COCE, Mw = 317.16 Da) and ecgonine methyl ester (EME, Mw = 199.12 Da) in hair strands using 2,5-dihydroxybenzoic acid (DHB, 7.0 mg mL-1) and α-cyano-4-hydroxycinnamic acid (CHCA, at concentrations of 1.5, 3.0, 7.0, and 10 mg mL-1) as the evaluated matrices. Among these, CHCA was selected. Subsequently, the qualitative results obtained by MALDI(+) MS were correlated with the quantitative analyses of gas chromatography-mass spectrometry (GC-MS), demonstrating a significant correlation in responses (70%), with the detection of analytes by MALDI(+) MS even at low concentrations, determined by GC-MS. The concentration ranges obtained by GC MS analysis were from 0.6 to 4.1 ng mg-1 of COC, and from 0.05 to 0.4 ng mg-1 of COCE. The effect of pre-washing on the detection of COC and its metabolites was also evaluated, and the results indicated less influence from the pre-washing stage and confirmed the reduction in COC detection in hair exposed to bleaching. use matrixassisted matrix assisted MALDIMS MALDI (MALDI-MS samples (COC (Mw 30314 303 14 303.1 Da BZE, BZE (BZE 28913 289 13 289.1 Da, , COCE, COCE (COCE 31716 317 16 317.1 EME, EME (EME 19912 199 12 199.1 2,5dihydroxybenzoic 25dihydroxybenzoic dihydroxybenzoic 2,5 2 5 DHB, DHB (DHB 70 7 0 7. mL1 mL 1 mL-1 αcyano4hydroxycinnamic αcyanohydroxycinnamic α cyano 4 hydroxycinnamic CHCA, (CHCA 15 1.5 30 3 3.0 matrices these selected Subsequently MALDI+ + MALDI(+ chromatographymass chromatography GCMS, GCMS (GC-MS) 70%, 70% (70%) GCMS. MS. GC-MS 06 6 0. 41 4. mg1 mg- 005 05 0.0 04 prewashing pre washing bleaching 3031 303. 2891 28 289. 3171 31 317. 1991 19 199. 5dihydroxybenzoic 25 2, mL- αcyano 1. 3. MALDI( (GC-MS (70% 00 (70 (7 (

A series of novel thieno[2,3-d]pyrimidine derivatives were designed, synthesized and evaluated for their biological ability. 2-Amino-4,7-dihydro-5H-thieno[2,3-d]pyrano-3-cyanonitrile was synthesized by Gewald reaction using pyranone as substrate, malonitrile and sulfur powder as raw materials and triethylamine as base at room temperature. Subsequent amination with N,N-dimethylformamide dimethyl acetal (DMF-DMA) gave N'-(3-cyano-4,7-dihydro-5H-thieno[2,3-c]pyran-2-yl)-N,N-dimethylmethanimidamide. In this article, the 23 thieno[2,3-d] pyrimidines were obtained by Dimroth rearrangement condensation with different anilines, 16 of them being new compounds. Meanwhile, all compounds were assessed for breast cancer MDA-MB-231 cell line bioactivity with paclitaxel (PTX) as the positive control, and all compounds in the series showed inhibitory effects on breast cancer cell MDA-MB-231. The IC50 of compound l against MDA-MB-231 is 27.6 μM, which is similar to that of PTX with an IC50 of 29.3 μM. This means that compound l exhibits comparable inhibitory activity to PTX in MDA-MB-231 cells and may be considered as a potential anti-MDA-MB-231 inhibitor. thieno2,3dpyrimidine thieno23dpyrimidine thienodpyrimidine thieno 2,3 d pyrimidine 2 3 designed ability 2Amino4,7dihydro5Hthieno2,3dpyrano3cyanonitrile 2Amino47dihydro5Hthieno23dpyrano3cyanonitrile AminodihydroHthienodpyranocyanonitrile Amino 4,7 dihydro 5H pyrano cyanonitrile 4 7 H substrate temperature N,Ndimethylformamide NNdimethylformamide N,N dimethylformamide N DMFDMA DMF DMA (DMF-DMA N3cyano4,7dihydro5Hthieno2,3cpyran2ylN,Ndimethylmethanimidamide. N3cyano47dihydro5Hthieno23cpyran2ylNNdimethylmethanimidamide NcyanodihydroHthienocpyranylNNdimethylmethanimidamide cyano c pyran yl dimethylmethanimidamide. dimethylmethanimidamide N'-(3-cyano-4,7-dihydro-5H-thieno[2,3-c]pyran-2-yl)-N,N-dimethylmethanimidamide article thieno2,3d thieno23d thienod thieno[2,3-d anilines 1 Meanwhile MDAMB231 MDAMB MDA MB 231 MDA-MB-23 (PTX control MDAMB231. 231. IC IC5 276 27 6 27. μM 293 29 29. antiMDAMB231 antiMDAMB anti anti-MDA-MB-23 inhibitor thieno2 3dpyrimidine dpyrimidine 2, 2Amino4 7dihydro5Hthieno2 3dpyrano3cyanonitrile Hthieno dpyrano 47 4, Ndimethylformamide NN N3cyano4 3cpyran2ylN Ndimethylmethanimidamide cpyran ylN N3cyano4,7dihydro5Hthieno2,3cpyran2ylN,Ndimethylmethanimidamide ylNNdimethylmethanimidamide 3d MDAMB23 MDA-MB-2 antiMDAMB23 anti-MDA-MB-2 2Amino dihydroHthieno 7dihydro5Hthieno dpyranocyanonitrile Ncyano N3cyano cpyranylN MDAMB2 MDA-MB- antiMDAMB2 anti-MDA-MB- MDA-MB anti-MDA-MB

Citronellyl esters present broad applications in the cosmetic, pharmaceutical, and food industries due to their organoleptic and biological properties. Lipase-catalyzed acylation of citronellol has been a suitable way to obtain these natural esters on a high scale. This work describes the lipase-catalyzed acylation of citronellol through esterification and transesterification with linear acylating agents (C3-C18) using Novozym®435 as a biocatalyst. The results show that all esters achieved not less than 91% conversion from an esterification model, showing a good reaction profile. Citronellyl propionate and laurate were selected for study in a transesterification reaction model, and it resulted in a lower reaction time for ester conversions. As an example, we highlight citronellyl propionate production, which approximately 10 g L-1 of the product was obtained after 1.5 h of esterification compared to 2 min by transesterification. The final esters were purified with high purity (≥ 90%) and identified by gas chromatography-mass spectrometry (GC-MS), and their structures were elucidated by 1H and 13C nuclear magnetic resonance (NMR). Enzyme recycling was evaluated and Novozym®435 was able to be applied for at least 20 cycles. Results demonstrated the efficiency of acylation reactions catalyzed by this enzyme and showed the potential of the methodology for the production and purification of flavor esters. cosmetic pharmaceutical properties Lipasecatalyzed Lipase scale lipasecatalyzed lipase C3C18 CC C3 C18 C (C3-C18 Novozym435 Novozym 435 Novozym®43 biocatalyst 91 model profile conversions example 1 L1 L L- 15 5 1. ≥ ( 90% 90 chromatographymass chromatography mass GCMS, GCMS GC MS , (GC-MS) H NMR. NMR . (NMR) cycles C3C1 C1 (C3-C1 Novozym43 43 Novozym®4 9 (GC-MS (NMR C3C (C3-C Novozym4 4 Novozym®

This study investigated the removal of contaminants in water by adsorption on thermoplastic starch (TPS) and kraft lignin (KL) composites. A study on the desorption of methylene blue (MB) and methyl orange (MO) dyes in water was also carried out, followed by the photodegradation of solutions containing dissolved dyes. Initially, the surface morphology of the TPS and TPS-KL films was analyzed by scanning electron microscopy, revealing advantageous characteristics for efficient adsorption of contaminants. Fourier transform infrared spectroscopy (FTIR) analysis made it possible to characterize the TPS and TPS-KL composites. The results demonstrate the reversibility of the process and confirm the lack of permanent chemical modification in the polymer matrix, indicating that the adsorption/desorption process is physical rather than chemical. This suggests that the adsorbent material can be reused without losing its fundamental structural properties. Furthermore, the study allows for verification of the chemical changes on the surfaces of the materials involved. Ultraviolet-visible spectroscopy (UV-Vis) results show that for MO, both substrates exhibited low adsorption capacity, with efficiency values close to 20%. In contrast, for MB, both composite materials displayed excellent dye adsorption rates, achieving efficiencies of 78% or higher. The photodegradation of adsorbed dyes revealed promising results. (TPS KL (KL composites MB (MB MO (MO out Initially TPSKL microscopy FTIR (FTIR matrix adsorptiondesorption properties Furthermore involved Ultravioletvisible Ultraviolet visible UVVis UV Vis (UV-Vis capacity 20 20% contrast rates 78 higher 2 7

Asphaltene aggregation mechanism is still a nebulous and controversial issue. Many authors argue that the aggregation of its components is due to π-stacking interactions, nonetheless, alkyl chains, heteroatoms, and even acidic groups are also constituents of asphaltenes and can play an important role in the chemistry of asphaltene. Excimers from pyrene are easily detected by fluorescence and were used in the current study to probe the effect of the side chain on the π-stacking capacity of pyrene. Pyrene was acylated with acyl chains varying from two to twelve carbon atoms, and the effect of the variation of the acyl chain length on excimer formation was followed by fluorescence emission spectroscopy. The results revealed that as the side chain grows from two to twelve carbon atoms the excimer/monomer ratio decreases and the excimer heat of formation drops from ΔH = -6.00 to -1.29 kcal mol-1. Further, the crystal structure of octanoyl pyrene (PC8) indicates that in the crystal structure, the aromatic moiety faces the acyl chain. This result was corroborated by density functional theory (DFT) calculations. Finally, the results were compared with two different asphaltenes and indicate that π-stacking cannot be assumed as the main driving force for asphaltene aggregation. issue πstacking π stacking interactions nonetheless heteroatoms spectroscopy excimermonomer monomer 6.00 600 6 00 -6.0 1.29 129 1 29 -1.2 mol1. mol1 mol 1. mol-1 Further PC8 PC (PC8 DFT (DFT calculations Finally 6.0 60 0 -6. 1.2 12 2 -1. mol- (PC 6. -6 -1 -

Brazil is home to a rich biodiversity of native edible fruits renowned for their health-promoting compounds and flavors. Among these, Eugenia uniflora L. (Brazilian pitanga) is particularly notable. The fruit varies in color from yellow to purple and is prized for its intense aroma and versatile taste profile. However, information about the compounds responsible for their nutritional and sensory potential is still limited. This study analyzed volatile compounds and metabolites in yellow, red and purple pitanga fruits (Eugenia uniflora) at various ripening stages, exploiting a metabolomics approach. Yellow pitanga had 30 volatile compounds, with esters (40%), terpenes (26.67%) and aldehydes (16.67%) constituting 83.34% of identified volatile compounds. Red pitanga featured 26 volatile compounds, primarily terpenes and esters (each 30.77%) and aldehydes (15.38%), making up 76.92%. Purple pitanga contained 39 volatile compounds, with terpenes and esters (each 35.90%) and aldehydes (17.95%), totaling 89.75% of identified volatile compounds. Across all pitanga types, 124 metabolites were identified, including saturated fatty acids (17.74%), terpenes (17.74%) and sugars (16.93%), constituting 52.41% of identified metabolites. Future studies should provide nutritional information, consumption methods and industrial applications for pitanga fruits, focusing on sensory analysis, health benefits, preservation and breeding to enhance bioactive compounds and flavor. healthpromoting promoting flavors these L Brazilian notable profile However limited stages approach 3 40%, 40 40% , (40%) 26.67% 2667 67 (26.67% 16.67% 1667 16 (16.67% 8334 83 34 83.34 2 each 30.77% 3077 77 15.38%, 1538 15.38% 15 38 (15.38%) 7692 76 92 76.92% 35.90% 3590 35 90 17.95%, 1795 17.95% 17 95 (17.95%) 8975 89 75 89.75 types 12 17.74%, 1774 17.74% 74 (17.74% 16.93%, 1693 16.93% 93 (16.93%) 5241 52 41 52.41 analysis benefits flavor 4 (40% 26.67 266 6 (26.67 16.67 166 1 (16.67 833 8 83.3 30.77 307 7 153 15.38 (15.38% 769 9 76.92 35.90 359 179 17.95 (17.95% 897 89.7 177 17.74 (17.74 169 16.93 (16.93% 524 5 52.4 (40 26.6 (26.6 16.6 (16.6 83. 30.7 15.3 (15.38 76.9 35.9 17.9 (17.95 89. 17.7 (17.7 16.9 (16.93 52. (4 26. (26. 16. (16. 30. 15. (15.3 76. 35. 17. (17.9 (17. (16.9 ( (26 (16 (15. (17 (2 (1 (15

This study details the preparation, antileishmanial assay, and in silico analysis of twenty 2-hydroxy-3-(1,2,3-triazolyl)propyl vanillin derivatives. These compounds were synthesized in three steps and evaluated against Leishmania infantum, Leishmania amazonensis, and Leishmania braziliensis promastigotes. Compounds 3s and 3t were the most effective, showing good activity against all Leishmania species tested. Molecular docking indicated that all compounds bind favorably to the sterol 14α-demethylase (CYP51) enzyme from L. infantum. ADMET (absorption, distribution, metabolism, excretion and toxicity) analysis indicated good oral bioavailability, non blood-brain barrier penetration, and high gastrointestinal absorption. Posaconazole and compounds 3e, 3s, and 3t remained stable in the CYP51 binding region during 100 ns molecular dynamics (MD) simulations. Root mean square deviation (RMSD) and root mean square fluctuations (RMSF) analyses from the MD trajectory revealed significant conformational fluctuations of the CYP51 N-terminal, suggesting occasional expulsion of 3e, potentially explaining its higher IC50 (half-maximal inhibitory concentration) values. Pairwise decomposition analyses from molecular mechanics Poisson-Boltzmann surface area (MM/PBSA) calculations highlighted the importance of hydrophobic residues in interacting with the synthesized derivatives. preparation assay 2hydroxy31,2,3triazolylpropyl 2hydroxy3123triazolylpropyl hydroxytriazolylpropyl 2 hydroxy 3 1,2,3 triazolyl propyl 1 derivatives infantum amazonensis promastigotes s t effective tested 14αdemethylase αdemethylase 14α demethylase α CYP (CYP51 L absorption, absorption (absorption distribution metabolism toxicity bioavailability bloodbrain blood brain penetration 3e e CYP5 10 (MD simulations RMSD (RMSD RMSF (RMSF Nterminal, Nterminal N terminal, terminal N-terminal IC IC5 halfmaximal half maximal concentration values PoissonBoltzmann Poisson Boltzmann MM/PBSA MMPBSA MM PBSA (MM/PBSA 2hydroxy31 3triazolylpropyl triazolylpropyl 123 1,2, (CYP5 2hydroxy3 12 1,2 (CYP 2hydroxy 1,

Since Locher proposed the concept of boron neutron capture therapy (BNCT) in 1936, it has become a great challenge in the field of medicinal chemistry. The great dare has been to obtain boron-containing compounds that selectively accumulate in the organ to be irradiated. Polyhedral boron clusters (PBC) have been considered attractive moieties for the development of BNCT-agents due to their large contribution of boron per molecule. Various issues arose in the first efforts to develop PBC during the 1940-1950s that prevented their application in BNCT clinical trials, such as a lack of selectivity and low boron tumor-accumulation. Currently, the most studied PBC in BNCT are the icosahedral dicarba-closo-dodecaboranes (C2B10H12) commonly referred to carboranes and, to a lesser extent, their mono-anionic derivatives resulting from the loss of a B-vertex, commonly known as nido-carborane, and their metal complexes, known as metallacarboranes. This review will cover the medicinal chemistry of PBC for BNCT. (BNCT 1936 boroncontaining containing irradiated (PBC BNCTagents agents molecule 19401950s s 1940 1950s trials tumoraccumulation. tumoraccumulation tumor accumulation. accumulation tumor-accumulation Currently dicarbaclosododecaboranes dicarba closo dodecaboranes C2B10H12 CBH C B H (C2B10H12 extent monoanionic mono anionic Bvertex, Bvertex vertex, vertex B-vertex nidocarborane, nidocarborane nido carborane, carborane nido-carborane complexes metallacarboranes 193 194 C2B10H1 (C2B10H1 19 C2B10H (C2B10H 1

The past 30 years have been transformative in the landscape of drug discovery, and certainly one of the most ground-breaking areas was kinase research. Since its start in the mid-1990s, kinase studies have reached notable hallmarks, ranging from the development of the first inhibitor, to innovative treatment options for a range of diseases. Today, kinases remain a pivotal protein class in drug discovery. Contemporarily, the Brazilian medicinal chemistry scene has also evolved, and followed up to such trends in the global landscape of research. Notably, the creation of the Summer School of Pharmaceutical and Medicinal Chemistry (EVQFM, in portuguese) in 1995, and its subsequent 30 consecutive editions, has raised the interest and knowledge of multiple generations in Brazil. This review aims to briefly outline the history of kinase inhibitor research, some of its landmarks, and highlight some of the contributions of Brazilian researchers to this important field of medicinal chemistry. 3 discovery groundbreaking ground breaking research mid1990s, mid1990s mids mid 1990s, 1990s s mid-1990s hallmarks diseases Today Contemporarily evolved Notably EVQFM, EVQFM (EVQFM portuguese 1995 editions Brazil landmarks 199 19 1

The microwave-assisted interesterification of babassu oil with methyl, ethyl and butyl acetates was carried out via acid catalysis, using sulfuric, phosphoric, methanesulfonic and acetic acids for the production of biodiesel with triacetin as an additive. Dielectric measurements in the range of 0.3 to 13 GHz of pure reactants and reactions media lead to a clear understanding of the interaction between the medium and microwave irradiation, allowing achieving optimal conditions in terms of microwave power, kind and catalyst concentration, reactant molar ratios, and temperatures. Using ethyl acetate, reactions were carried out at various oil to acetate molar ratio (1:12 to 1:72) using sulfuric acid (0.5% m/mT) as a catalyst. For 1:60 molar ratio, the experiments were carried out with 0.5 to 2% m/mT sulfuric acid. The kind of catalyst and the applied microwave power to mass ratio were investigated using H3PO4, CH3COOH and CH3SO3H. The best catalytic activities were achieved with H2SO4 and CH3SO3H. It was found that under microwave or conventional heating the reactivity follows the ethyl→methyl→butyl trend. The best results were achieved using ethyl acetate with H2SO4 which yields 91.1% biodiesel and 18.3% triacetin in 120 min under microwave heating while using CH3SO3H yields 80.1% biodiesel and 11.2% triacetin. microwaveassisted assisted methyl catalysis phosphoric additive 03 0 3 0. 1 irradiation concentration ratios temperatures 112 12 (1:1 172 72 1:72 0.5% 05 5 (0.5 mmT m mT 160 60 1:6 2 H3PO4 HPO H PO CHCOOH CH COOH CHSOH SO HSO H2SO ethylmethylbutyl trend 911 91 91.1 183 18 18.3 801 80 80.1 11 11.2 (1: 17 7 1:7 (0. 16 6 1: H3PO 9 91. 18. 8 80. 11. (1 (0 (

This research explores the concentration of black carbon (BC) in particulate matter (PM10 and PM2.5) from ten monitoring stations in the Metropolitan Region of Rio de Janeiro (MRRJ), Bonsucesso (BS), Botafogo (BOT), Copacabana (COP), Gavea (GAV), Gericino (GER), Lagoa (LAG), Recreio dos Bandeirantes (REC), Santa Cruz (SC), Castelo (CAS) and Urca (URC), covering a range of pollution sources (vehicular, industrial, and residential). PM samples were collected using filter units every week from January 2018 to December 2019. Results revealed high concentrations of PM10 in BS (86 ± 22 µg m3) and PM2.5 in REC (30 ± 11 µg m3). Likewise, both monitoring stations exceeded the international limits. In 2019, BC in PM10 decreased in the following order: BS > CAS > GER > BOT > SC > GAV. For 2018, BC in PM2.5 decreased as follows REC > LAG > SC, while 2019 REC > GAV > LAG > COP > URC. REC and BS have industrial and commercial activities and intense vehicular traffic. During the period of study, average BC concentrations in PM10 and PM2.5 were 3.3 ± 1.5 and 1.9 ± 0.70 µg m3, respectively. These findings indicate that BC concentrations should be monitored and regulated in locations with high levels of traffic-related air pollution for offering new insights and guiding efforts to minimize emissions and enhance public health. (BC (PM1 PM25 PM2 5 MRRJ, MRRJ , (MRRJ) BS, (BS) BOT, (BOT) COP, (COP) GAV, (GAV) GER, (GER) LAG, (LAG) REC, (REC) (SC) (CAS URC, URC (URC) vehicular, (vehicular residential. residential . residential) 201 PM1 86 (8 2 m3 m PM2. 30 (3 1 m3. Likewise limits order traffic study 33 3 3. 15 1. 19 9 070 0 70 0.7 respectively trafficrelated related health (PM (MRRJ (BS (BOT (COP (GAV (GER (LAG (REC (SC (URC 20 8 ( 07 7 0.

This study investigates the potential of Morita-Baylis-Hillman adducts derived from carvacrol as anticancer agents. The synthesis process, involving the reaction of aromatic aldehydes with carvacrol acrylate as a Michael acceptor, resulted in stable adducts with impressive yields ranging from 60 to 92%, achieved within a maximum reaction time of 24 h. Through a screening process utilizing 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) test, compound 6, identified as the acrylate/2-naphthyl adduct, emerged as the most active within the series among twelve compounds tested. Specifically, compound 6 exhibited a remarkably potent impact on neuroblastoma cell lines, particularly SH-SY5Y cells, with half-maximal inhibitory concentration (IC50) of 8.7 µM after 72 h (42 times more potent than carvacrol, IC50 = 374.1 μM). The exploration of the selectivity index (SI) against normal cell lines demonstrated an outstanding SI of 4.28 compared to other compounds. Mechanistic studies on SH-SY5Y cells revealed a concentration-dependent apoptotic effect attributed to caspase 3/7 activation. In silico modeling showcased favorable pharmacokinetic properties for compound 6, including effective absorption after oral administration. Assessment of toxicity of compound 6 profile using brine shrimp and the Irwin test indicated low toxicity, highlighting its potential for future anticancer agent development. MoritaBaylisHillman Morita Baylis Hillman agents acceptor 92 92% 2 34,5dimethylthiazol2yl2,5diphenyltetrazolium 345dimethylthiazol2yl25diphenyltetrazolium dimethylthiazolyldiphenyltetrazolium 3 4,5 dimethylthiazol yl 2,5 diphenyltetrazolium 4 5 MTT (MTT acrylate/2naphthyl acrylate2naphthyl acrylatenaphthyl acrylate/2 naphthyl adduct tested Specifically SHSY5Y SHSYY SH SY5Y SY Y halfmaximal half maximal IC (IC50 87 8 7 8. 42 (4 IC5 3741 374 1 374. μM. μM . μM) (SI 428 28 4.2 concentrationdependent dependent 37 3/ activation administration development 9 34 5dimethylthiazol2yl2 5diphenyltetrazolium 45 4, 25 2, 2naphthyl acrylate2 acrylate/ SHSY SYY (IC5 ( 4. dimethylthiazolyl 5dimethylthiazol2yl (IC