Tag: M.W=100-150

Authors Devi, P; Bishnoi, A; Singh, V in MAIK NAUKA/INTERPERIODICA/SPRINGER published article about in [Devi, P.; Bishnoi, A.] Univ Lucknow, Dept Chem, Lucknow 226007, Uttar Pradesh, India; [Singh, V.] Inst Engn & Technol, Dept Biotechnol, Lucknow 226021, Uttar Pradesh, India in 2021, Cited 37. Name: 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

A highly efficient method for the multicomponent synthesis of substituted 4H-pyrido[1,2-a]pyrimidine-2-hydroxy-4-one derivatives, starting from 4H-pyrido[1,2-a]primidine-2-hydroxy-4-one, beta-naphthol, and substituted aromatic aldehydes, in moderate to good yields has been developed. The structure of the pyridopyrimidine derivatives was established by spectral methods. In vitro antibacterial activity of the newly synthesized compounds was evaluated against highly pathogenic Gram-positive [Staphylococcus aureus (MTCC 96)] and Gram-negative [Pseudomonas aeruginosa (MTCC 424), Salmonella typhi (MTCC 537), Klebsiella pneumoniae (MTCC 424), Escherichia coli (MTCC 64) and Chromobacterium violaceum] bacteria.

Name: 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Devi, P; Bishnoi, A; Singh, V or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Product Details of 100-51-6. Recently I am researching about PHENOLIC-COMPOUNDS; PHASE ADVANCES; ANTAGONISTS; DERIVATIVES; ACTIVATION; MT1, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81773612]; Program of Yunling Scholar; Youth Innovation Promotion Association, CAS [2013252]; Applied Basic Research Programs of Yunnan Province [2017FB137]. Published in PERGAMON-ELSEVIER SCIENCE LTD in OXFORD ,Authors: Chen, SY; Geng, CA; Ma, YB; Huang, XY; Yang, XT; Su, LH; He, XF; Li, TZ; Deng, ZT; Gao, Z; Zhang, XM; Chen, JJ. The CAS is 100-51-6. Through research, I have a further understanding and discovery of Benzyl Alcohol

Gastrodia elata is a famous traditional Chinese herb with medicinal and edible application. In this study, nine polybenzyls (1-9), including six new ones (2-5, 7 and 9), were isolated from the EtOAc extract of G. elata. Five compounds 1, 3, 4, 6 and 8 were found to activate melatonin receptors. Especially, compound 1 showed agonistic effects on MT1 and MT2 receptors with EC50 values of 237 and 244 mu M. For better understanding their structure-activity relationships (SARs), ten polybenzyl analogs were further synthesized and assayed for their activities on melatonin receptors. Preliminary SARs study suggested that two para-hydroxy groups were the key pharmacophore for maintaining activity. Molecular docking simulations verified that compound 1 could strongly interact with MT2 receptor by bonding to Phe 118, Gly 121, His 208, Try 294 and Ala 297 residues.

About Benzyl Alcohol, If you have any questions, you can contact Chen, SY; Geng, CA; Ma, YB; Huang, XY; Yang, XT; Su, LH; He, XF; Li, TZ; Deng, ZT; Gao, Z; Zhang, XM; Chen, JJ or concate me.. Product Details of 100-51-6

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Recently I am researching about CARBON NITRIDE SEMICONDUCTORS; ADSORPTION PROPERTIES; ORGANIC FRAMEWORKS; AROMATIC ALCOHOLS; BUILDING-BLOCKS; STORAGE; CAPTURE; WATER, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [51703031]. Published in ELSEVIER SCIENCE BV in AMSTERDAM ,Authors: Xu, CY; Qian, L; Lin, JY; Guo, ZY; Yan, D; Zhan, HB. The CAS is 100-51-6. Through research, I have a further understanding and discovery of Benzyl Alcohol. Product Details of 100-51-6

Heptazine units with highly rich nitrogen sites were employed to fabricate a new porous organic polymer (POP-HE) via direct coupling of 2,5,8-trichloro-s-heptazine and 4,4′,4 ”,4”’-(ethene-1,1,2,2-tetrayl)tetraaniline with the mild base N, N’-diisopropylethylamine (DIPEA) in tetrahydrofuran (THF) solution. POP-HE displays good CO2 uptake capacity (50.6 cm(3) g(-1), 10 wt%, 1 bar/273 K) and highly selectively adsorptive separation of CO2 over CH4 under ambient conditions. Impressively, at 273 K, the predicted IAST selectivity of POP-HE is 47.0-13.4 for the natural gas mixture (CO2/CH4 = 5:95) at pressures varying from 0 to 1 atm. Meanwhile, the result of calculated band gap value based on Tauc plot motivated us to investigate its photocatalytic activity. POP-HE was applied as heterogeneous photocatalyst for visible light-induced selective oxidation of benzyl alcohol to benzaldehyde, and exhibited great conversion of 33.6% under irradiation of white LED light, which is much higher than that of g-C3N4. Moreover, POP-HE can be recycled up to three times without significant decrease in catalytic activity.

Product Details of 100-51-6. About Benzyl Alcohol, If you have any questions, you can contact Xu, CY; Qian, L; Lin, JY; Guo, ZY; Yan, D; Zhan, HB or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Recently I am researching about COVALENT POLYMER NETWORKS; SILICA, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [51673016]; Molecular Foundry – Office of Science, Office of Basic Energy Sciences, of the U.S. Department of EnergyUnited States Department of Energy (DOE) [DE-AC02-05 CH11231]; Beijing Natural Science FoundationBeijing Natural Science Foundation [2194083]. Computed Properties of C8H8O2. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: He, CF; Shi, SW; Wang, D; Helms, BA; Russell, TP. The CAS is 99-93-4. Through research, I have a further understanding and discovery of 4′-Hydroxyacetophenone

Vitrimers are network polymers that undergo associative bond exchange reactions in the condensed phase above a threshold temperature, dictated by the exchangeable bonds comprising the vitrimer. For vitrimers, chemistries reliant on poorly nudeophilic bond exchange partners (e.g., hydroxy-functionalized alkanes) or poorly electrophilic exchangeable bonds, catalysts are required to lower the threshold temperature, which is undesirable in that catalyst leaching or deactivation diminishes its influence over time and may compromise reuse. Here we show how to access catalyst-free bond exchange reactions in catalyst-dependent polyester vitrimers by obviating conventional ester bonds in favor of oxime-esters. Poly(oxime-ester) (POE) vitrimers are synthesized using thiol-ene click chemistry, affording high stretchability and malleability. POE vitrimers are readily recycled with little degradation of their initial mechanical properties, suggesting exciting opportunities for sustainable plastics.

Computed Properties of C8H8O2. About 4′-Hydroxyacetophenone, If you have any questions, you can contact He, CF; Shi, SW; Wang, D; Helms, BA; Russell, TP or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Authors Srividya, N; Lange, I; Hartmann, M; Li, QR; Mirzaei, M; Lange, BM in AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC published article about COENZYME-A-SYNTHETASE; COA SYNTHETASE; ESCHERICHIA-COLI; ARABIDOPSIS-THALIANA; ANALYSIS REVEALS; BIOSYNTHESIS; ACID; IDENTIFICATION; LIGASES; GROWTH in [Lange, Bernd Markus] Washington State Univ, Inst Biol Chem, Pullman, WA 99164 USA; Washington State Univ, MJ Murdock Metabol Lab, Pullman, WA 99164 USA; [Hartmann, Michael] Univ Dusseldorf, Dept Mol Ecophysiol Plants, Univ Str 1, D-40225 Dusseldorf, Germany; [Li Qunrui] CP Pharmaceut Grp, Jia 3 Yongandongli, Beijing 100022, Peoples R China; [Mirzaei, Maryam] Tarbiat Modares Univ, Tehran 14115111, Iran in 2020, Cited 41. HPLC of Formula: C5H8O2. The Name is (E)-2-Methylbut-2-enoic acid. Through research, I have a further understanding and discovery of 80-59-1

Taxol (paclitaxel) is a very widely used anticancer drug, but its commercial sources mainly consist of stripped bark or suspension cultures of members of the plant genus Taxus. Taxol accumulates as part of a complex mixture of chemical analogs, termed taxoids, which complicates its production in pure form, highlighting the need for metabolic engineering approaches for high-level Taxol production in cell cultures or microbial hosts. Here, we report on the characterization of acyl-activating enzymes (AAEs) that catalyze the formation of CoA esters of different organic acids relevant for the N-substitution of the 3-phenylisoserine side chain of taxoids. On the basis of similarities to AAE genes of known function from other organisms, we identified candidate genes in publicly available transcriptome data sets obtained with Taxus ? media. We cloned 17 AAE genes, expressed them heterologously in Escherichia coli, purified the corresponding recombinant enzymes, and performed in vitro assays with 27 organic acids as potential substrates. We identified TmAAE1 and TmAAE5 as the most efficient enzymes for the activation of butyric acid (Taxol D side chain), TmAAE13 as the best candidate for generating a CoA ester of tiglic acid (Taxol B side chain), TmAAE3 and TmAAE13 as suitable for the activation of 4-methylbutyric acid (N-debenzoyl-N-(2-methylbutyryl)taxol side chain), TmAAE15 as a highly efficient candidate for hexanoic acid activation (Taxol C side chain), and TmAAE4 as suitable candidate for esterification of benzoic acid with CoA (Taxol side chain). This study lays important groundwork for metabolic engineering efforts aimed at improving Taxol production in cell cultures.

HPLC of Formula: C5H8O2. About (E)-2-Methylbut-2-enoic acid, If you have any questions, you can contact Srividya, N; Lange, I; Hartmann, M; Li, QR; Mirzaei, M; Lange, BM or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Authors Kamei, Y; Seino, Y; Yamaguchi, Y; Yoshino, T; Maeda, S; Kojima, M; Matsunaga, S in NATURE RESEARCH published article about in [Kamei, Yuji; Seino, Yusuke; Yamaguchi, Yuto; Yoshino, Tatsuhiko; Kojima, Masahiro; Matsunaga, Shigeki] Hokkaido Univ, Fac Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan; [Maeda, Satoshi] Hokkaido Univ, Inst Chem React Design & Discovery WPI ICReDD, Sapporo, Hokkaido 0010021, Japan; [Maeda, Satoshi] Hokkaido Univ, Fac Sci, Sapporo, Hokkaido 0600810, Japan; [Maeda, Satoshi] JST, ERATO Maeda Artificial Intelligence Chem React De, Sapporo, Hokkaido 0600810, Japan; [Matsunaga, Shigeki] Hokkaido Univ, Global Stn Biosurfaces & Drug Discovery, Sapporo, Hokkaido 0600812, Japan in 2021, Cited 70. Name: (E)-2-Methylbut-2-enoic acid. The Name is (E)-2-Methylbut-2-enoic acid. Through research, I have a further understanding and discovery of 80-59-1

Hydrogen atom transfer (HAT) hydrogenation has recently emerged as an indispensable method for the chemoselective reduction of unactivated alkenes. However, the hitherto reported systems basically require stoichiometric amounts of silanes and peroxides, which prevents wider applications, especially with respect to sustainability and safety concerns. Herein, we report a silane- and peroxide-free HAT hydrogenation using a combined cobalt/photoredox catalysis and ascorbic acid (vitamin C) as a sole stoichiometric reactant. A cobalt salophen complex is identified as the optimal cocatalyst for this environmentally benign HAT hydrogenation in aqueous media, which exhibits high functional-group tolerance. In addition to its applicability in the late-stage hydrogenation of amino-acid derivatives and drug molecules, this method offers unique advantage in direct transformation of unprotected sugar derivatives and allows the HAT hydrogenation of unprotected C-glycoside in higher yield compared to previously reported HAT hydrogenation protocols. The proposed mechanism is supported by experimental and theoretical studies. Hydrogen atom transfer (HAT) hydrogenation of alkenes usually requires stoichiometric silanes and peroxides. Here, the authors report a silane- and peroxide-free HAT hydrogenation method using a combined cobalt/photoredox catalysis and vitamin C as a sole stoichiometric reactant.

About (E)-2-Methylbut-2-enoic acid, If you have any questions, you can contact Kamei, Y; Seino, Y; Yamaguchi, Y; Yoshino, T; Maeda, S; Kojima, M; Matsunaga, S or concate me.. Name: (E)-2-Methylbut-2-enoic acid

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Computed Properties of C8H8O2. In 2021 J IRAN CHEM SOC published article about ANTIMICROBIAL ACTIVITY; ANALGESIC ACTIVITY; HETEROCYCLES in [Elkanzi, Nadia A. A.; Alruwaili, May M.; Alruwaili, Enas D.; Almamtrfi, Rahaf W.; Alsharary, Hadeel Kh.] Jouf Univ, Coll Sci, Chem Dept, POB 2014, Sakaka, Saudi Arabia; [Elkanzi, Nadia A. A.] Aswan Univ, Fac Sci, Chem Dept, POB 81528, Aswan, Egypt; [Hrichi, Hajer] Carthage Univ, Ctr Urbain Nord, Natl Inst Appl Sci & Technol, BPN 676, Tunis 1080, Tunisia; [Bakr, Rania B.; Hendawy, O.] Jouf Univ, Coll Pharm, Dept Pharmacol, Sakaka 2014, Aljouf, Saudi Arabia; [Bakr, Rania B.] Beni Suef Univ, Fac Pharm, Dept Pharmaceut Organ Chem, Bani Suwayf 62514, Egypt; [Hendawy, O.] Beni Suef Univ, Fac Med, Dept Clin Pharmacol, Bani Suwayf, Egypt in 2021, Cited 34. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.

In the current study, a new series of pyrazole derivatives4a-d,5a-dand6a-dpossessing 1,5,10,10a-tetrahydrobenzo[g]quinoline-3-carbonitrile moiety were synthesized by treating chalcones (3a-d) with hydrazine monohydrate/acetic anhydride, hydrazine monohydrate/formic acid and 4-chlorophenylhydrazine in ethanol, respectively. These reactions proceeded smoothly with satisfactory yields, and the obtained compounds were characterized using FTIR,H-1-NMR,C-13-NMR and elemental analyses. All the synthesized compounds were subjected to antibacterial activity againstBacillus subtilis,Staphylococcus aureus,Escherichia coli, andPseudomonas aeruginosabacteria and molecular docking studies. The antibacterial studies showed that all compounds exhibited good to excellent antibacterial activity against the tested bacterial strains. The structure-activity relationship studies revealed that the compounds3b,4b,5band6bbearing a chlorine atom at the para position of the phenyl group attached to pyrazole moiety in displayed the highest antibacterial activity against all the tested bacteria exceeding the standard drug ampicillin. Moreover, the molecular docking results showed that the highest scores docking have been obtained from the most active antibacterial compounds3b,3d,4b,4d,4c,5band6bwith good energy binding score within the active site of topoisomerase II DNA gyrase enzymes (PDB ID: 2XCS), suggesting that they can act by the inhibition of DNA replication. These compounds are auspicious candidates as antibacterial agents that would deserve further investigations.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Elkanzi, NAA; Hrichi, H; Bakr, RB; Hendawy, O; Alruwaili, MM; Alruwaili, ED; Almamtrfi, RW; Alsharary, HK or concate me.. Computed Properties of C8H8O2

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

In 2021 EUR J MED CHEM published article about PHASE-II TRIAL; CARBOXYLESTERASE ISOZYMES; DERIVATIVES; PROBE; IRINOTECAN; LOPERAMIDE; DISCOVERY; SUBSTRATE; PROGRESS in [Huo, Peng-Chao; Guan, Xiao-Qing; Song, Yun-Qing; Sun, Meng-Ru; He, Rong-Jing; Zou, Li-Wei; Xue, Li-Juan; Shi, Jin-Hui; Ge, Guang-Bo] Shanghai Univ Tradit Chinese Med, Inst Interdisciplinary Integrat Med Res, Shanghai, Peoples R China; [Huo, Peng-Chao; Zhang, Nan] Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Peoples R China; [Liu, Peng; Liu, Zhi-Guo] Wenzhou Med Univ, Chem Biol Res Ctr, Sch Pharmaceut Sci, Wenzhou, Zhejiang, Peoples R China in 2021, Cited 36. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5. Recommanded Product: 123-11-5

Human carboxylesterase 2 (hCES2A), one of the major serine hydrolases distributed in the small intestine, plays a crucial role in hydrolysis of ester-bearing drugs. Accumulating evidence has indicated that hCES2A inhibitor therapy can modulate the pharmacokinetic and toxicological profiles of some important hCES2A-substrate drugs, such as the anticancer agent CPT-11. Herein, a series of indanone-chalcone hybrids are designed and synthesized to find potent and highly selective hCES2A inhibitors. Inhibition assays demonstrated that most indanone-chalcone hybrids displayed strong to moderate hCES2A inhibition activities. Structure-hCES2A inhibition activity relationship studies showed that introduction of a hydroxyl at the C4′ site and introduction of an N-alkyl group at the C6 site were beneficial for hCES2A inhibition. Particularly, B7 (an N-alkylated 1-indanoneechalcone hybrid) exhibited the most potent inhibition on hCES2A and excellent specificity (this agent could not inhibit other human esterases including hCES1A and butyrylcholinesterase). Inhibition kinetic analyses demonstrated that B7 potently inhibited hCES2A-mediated FD hydrolysis in a mixed inhibition manner, with a calculated K-i value of 0.068 mu M. Furthermore, B7 was capable of inhibiting intracellular hCES2A in living cells and displayed good metabolic stability. Collectively, our findings show that indanone-chalcone hybrids are good choices for the development of hCES2A inhibitors, while B7 is a promising candidate for the development of novel anti-diarrhea agents to ameliorate irinotecan-induced intestinal toxicity. (c) 2020 Elsevier Masson SAS. All rights reserved.

Recommanded Product: 123-11-5. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Huo, PC; Guan, XQ; Liu, P; Song, YQ; Sun, MR; He, RJ; Zou, LW; Xue, LJ; Shi, JH; Zhang, N; Liu, ZG; Ge, GB or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

SDS of cas: 99-93-4. Ersan, G; Apul, OG; Karanfil, T in [Ersan, Gamze; Karanfil, Tanju] Clemson Univ, Dept Environm Engn & Earth Sci, Anderson, SC 29625 USA; [Apul, Onur G.] Univ Massachusetts Lowell, Dept Civil & Environm Engn, Lowell, MA 01854 USA published Predictive models for adsorption of organic compounds by Graphene nanosheets: comparison with carbon nanotubes in 2019.0, Cited 32.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.

The Linear Solvation Energy Relationships (LSER) technique was applied in the present study for predicting models of organic compounds (OCs) adsorption by Graphene and Graphene oxide (GO), and the results were compared with those of multi-walled carbon nanotube (MWCNT) and single-walled carbon nanotube (SWCNT). Adsorption database of 38 OCs (28 aromatic and 10 aliphatic) for Graphene and 69 OCs (59 aromatic and 10 aliphatic) for GO were collected from the literature and our laboratory. The r(2) of the LSER models on the adsorption of aromatic OCs by Graphene and GO at three different equilibrium concentrations gradually increased up to OC molecular weight of 400 g/mol, after which a declining trend was observed for GO, while there was no visible change for Graphene. Among descriptors for all LSER models, V (molecular volume) and B (hydrogen bond accepting) for Graphene nanosheets (GNS) and carbon nanotubes (CNT) were the most significant descriptors (p values <= 0.05). B term had high value and was negatively correlated with adsorption of all OCs by Graphene (-1.24 to -9.45), GO (-0.55 to -9.31), SWCNT (-0.10 to -538) and MWCNT (-124 to -1.85). LSER successfully trained models for adsorption of OCs by GNS, and model coefficients were dependent on adsorbent type and OC properties. (C) 2018 Elsevier B.V. All rights reserved. About 4'-Hydroxyacetophenone, If you have any questions, you can contact Ersan, G; Apul, OG; Karanfil, T or concate me.. SDS of cas: 99-93-4

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

In 2021 CHEM BIOL DRUG DES published article about 3-COMPONENT SYNTHESIS; QUINOLINE; DESIGN; DISCOVERY; HYBRIDS; SULFIDE; JAK2 in [Nafie, Mohamed S.] Suez Canal Univ, Dept Chem, Fac Sci, Ismailia 41522, Egypt; [Mahgoub, Sebaey] Childrens Canc Hosp, Prote & Metabol Unit, Cairo, Egypt; [Amer, Atef M.] Zagazig Univ, Dept Chem, Fac Sci, Zagazig, Egypt in 2021, Cited 54. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5. COA of Formula: C8H8O2

Quinoline derivatives are attracting considerable interest due to their biological importance. In this paper, several 2-amino-4-aryl-6-(quinolin-2-ylthio)pyridine-3,5-dicarbonitrile derivatives are synthesized by adopting a one-pot reaction of quinoline-2-thione, aromatic aldehydes, and malononitrile in the presence of sodium hydroxide in absolute ethanol. The structures of these newly synthesized compounds were determined using different spectroscopic techniques, including elemental analyses, IR,H-1 NMR, and MS. The synthesized derivatives were screened for their antimicrobial and cytotoxic activities. Compounds4a,4b,4d, and4eexhibited promising antimicrobial activity compared to antibacterial and antifungal standard drugs. Additionally,4f,4d, and4gshowed potent cytotoxic activity against both MCF-7 and A549 cells with IC(50)values (6.39-9.3 mu M). Our molecular docking results of compound4fprove good binding affinity toward the three tested proteins as Jak2/STATA3 inhibition and are in accordance with the RT-PCR mRNA expressions of the compound against MCF-7 cells which downregulated the Jak2 and STAT3 genes, and this may be the proposed mode of action for anti-breast cancer activity.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Nafie, MS; Mahgoub, S; Amer, AM or concate me.. COA of Formula: C8H8O2

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles