Category: 100-83-4

Kumar, GS; Harinath, A; Narvariya, R; Panda, TK in [Kumar, Gobbilla Sai; Harinath, Adimulam; Narvariya, Rajrani; Panda, Tarun K.] Indian Inst Technol, Dept Chem, Sangareddy 502285, Telangana, India published Homoleptic Zinc-Catalyzed Hydroboration of Aldehydes and Ketones in the Presence of HBpin in 2020.0, Cited 85.0. Safety of 3-Hydroxybenzaldehyde. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

Here, we report the reaction between N-phenyl-o-phenylenediamine and pyrrole-2-carboxaldehyde to afford the N-phenyl-o-phenyl-enediiminopyrrole ligand {L-H2} in quantitative yield. A one-pot reaction between {L-H2} and diethylzinc (ZnEt2) in a 2:1 ratio afforded the homoleptic zinc metal complex [{L-H}(2)Zn] (1). The solid-state structures of ligand {L-H2} and zinc complex 1 were confirmed using X-ray crystallography. Further, complex 1 was used for chemoselective hydroboration of aldehydes and ketones in the presence of pinacolborane (HBpin) at ambient temperature to produce the corresponding boronate esters in high yield.

About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Kumar, GS; Harinath, A; Narvariya, R; Panda, TK or concate me.. Safety of 3-Hydroxybenzaldehyde

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

An article Design, Synthesis, Antimalarial Activity and Docking Study of 7-Chloro-4-(2-(substituted benzylidene)hydrazineyl)quinolines WOS:000589443500007 published article about DRUG DISCOVERY; DERIVATIVES; POTENT; SERIES in [Kalita, Jahnabi; Chetia, Dipak; Rudrapal, Mithun] Dibrugarh Univ, Dept Pharmaceut Sci, Dibrugarh 786004, Assam, India in 2020.0, Cited 16.0. Category: indole-building-block. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4

Background: Malaria is a growing infectious disease burden due to the increasing emergence of resistant strains of Plasmodium falciparum. Because of the limited therapeutic efficacy of available antimalarial drugs, the development of potent antimalarial drug agents is therefore an urgent requirement to fight against resistant malaria. Objective: The objective of this work was to develop novel quinoline-baed antimalarial agents that would be active against resistant P. falciparum malaria. Methods: Some 7-chloro-4-(2-(substituted benzylidene)hydrazineyl)quinolines were synthesized for the evaluation of their potential as possible antimalarial agents, particularly against resistant malaria. The antimalarial activity of synthesized compounds was evaluated in vitro against bloodstage parasites of P. falciparum. Further, molecular docking and drug-likeness including ADMET (Absorption, Distribution, Metabolism, Elimination and Toxicity) studies were also carried out using in silico tools. Results: Results reveal the in vitro antimalarial activity of synthesized 7-chloro-4-(2-(substituted benzylidene)hydrazineyl)quinolines against P. falciparum. The docking study investigates the antimalarial effectiveness of synthesized quinolines as novel plasmepsin 2 inhibitors. Drug-likeness prediction exhibits acceptable drug-likeness and ADMET properties. Conclusion: Based upon our findings, it is concluded that the molecular scaffold of 7-chloro-4-(2(substituted benzylidene)hydrazineyl)quinolines may be used as a lead structure for further modifications in the search of more potent antimalarial drug molecules.

Category: indole-building-block. About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Kalita, J; Chetia, D; Rudrapal, M 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

Thanaraj, C; Dharsini, GRP; Ananthan, N; Velladurai, R in [Thanaraj, Clarina; Dharsini, G. R. Priya; Ananthan, Neela; Velladurai, Rama] Manonmaniam Sundaranar Univ, Sarah Tucker Coll, Dept Chem, Tirunelveli 627012, Tamil Nadu, India published Facile route for the synthesis and cytotoxic effect of 2-amino-4H-benzo[b]pyran derivatives in aqueous media using copper oxide nanoparticles decorated on cellulose nanocrystals as heterogeneous catalyst in 2019.0, Cited 58.0. Name: 3-Hydroxybenzaldehyde. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

A simple, facile, green eco-friendly one pot synthesis of 2-amino-4H-benzo[b]pyrans derivatives catalyzed by copper oxide nanoparticles decorated on cellulose nanocrystals (CuO-CNs), a biodegradable matrice in aqueous media at room temperature is reported with excellent yields. The catalyst is recycled six times without significant loss in catalytic activity. Smaller E-factor and higher atom economy makes this protocol a true green and sustainable one. Cytotoxic effects of synthesized 2-amino-4H-benzo[b]pyrans derivatives are assayed with standard MTT colorimetric procedure against the human breast adenocarcinoma cell lines (MCF7) and showed nearly mild to moderate cell line inhibition at 125 mu M tested dose.

Name: 3-Hydroxybenzaldehyde. About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Thanaraj, C; Dharsini, GRP; Ananthan, N; Velladurai, R 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

Recommanded Product: 3-Hydroxybenzaldehyde. Ocak, H; Ozerol, EA; Celikel, FC; Okutan, M; Eran, BB in [Ocak, Hale; Celikel, Fulya Cagla; Eran, Belkiz Bilgin] Yildiz Tech Univ, Dept Chem, TR-34220 Istanbul, Turkey; [Ozerol, Esma Ahlatcioglu] Yildiz Tech Univ, Dept Bioengn, TR-34220 Istanbul, Turkey; [Okutan, Mustafa] Yildiz Tech Univ, Dept Phys, TR-34220 Istanbul, Turkey published The synthesis, mesomorphic and dielectric investigation of new unsymmetrical bent-core mesogens derived from 3-hydroxybenzoic acid in 2020.0, Cited 51.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

The synthesis, mesomorphic and dielectric investigation of new unsymmetrical bent-core mesogens derived from 3-hydroxybenzoic acid central core with linked two rodlike units carrying (S)-3,7-dimethyloctyloxy group and an n-alkyloxy chain at both terminals are presented. The liquid crystalline properties of the new unsymmetrical bent-core materials have been investigated by polarizing optical microscopy and differential scanning calorimetry. New compounds with the reversed ester linking unit exhibit a monotropic or enantiotropic columnar mesophase at lower temperatures as compared to analogs with a straight chain depending on the presence of the branched (S)-3,7-dimethyloctyloxy terminal chain. Dielectric measurements for one of the bent-core mesogens, 3-[[4-[[4-(octyloxy)benzoyl]oxy]benzoyl]oxy]benzoic acid 4-[[4-((S)-3,7-dimethyloctyloxy)phenoxy]carbonyl]phenyl ester (OBDPE), have been carried out on the angular frequency range from 25.12 to 50265k rad/s at different temperatures. Thanks to dielectric measurements, real and imaginary dielectric constant, conductivity mechanism and dielectric relaxation mechanism of OBDPE were obtained. [GRAPHICS] .

Recommanded Product: 3-Hydroxybenzaldehyde. About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Ocak, H; Ozerol, EA; Celikel, FC; Okutan, M; Eran, BB 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

In 2019.0 BIOORG MED CHEM LETT published article about EG5; DISCOVERY; KINESIN-5; PROTEIN; AURORA in [Dumas, Megan E.; Kendrick, Nicole D.] Vanderbilt Univ, Dept Cell & Dev Biol, Nashville, TN 37232 USA; [Chen, Geng-Yuan; Hancock, William] Penn State Univ, Dept Biomed Engn, State Coll, PA USA; [Xu, George; Ohi, Ryoma] Univ Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA; [Larsen, Scott A.] Univ Michigan, Dept Med Chem, Ann Arbor, MI 48109 USA; [Jana, Somnath; Waterson, Alex G.] Vanderbilt Inst Chem Biol, Nashville, TN 37232 USA; [Waterson, Alex G.; Sulikowski, Gary A.] Vanderbilt Univ, Dept Chem, Nashville, TN 37232 USA; [Waterson, Alex G.] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA; [Bauer, Joshua A.] Vanderbilt Univ, Dept Biochem, Nashville, TN 37232 USA; [Ohi, Ryoma] Univ Michigan, Life Sci Inst, Ann Arbor, MI 48109 USA; [Chen, Geng-Yuan] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA in 2019.0, Cited 30.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4. Product Details of 100-83-4

The mitotic spindle is a microtubule-based machine that segregates a replicated set of chromosomes during cell division. Many cancer drugs alter or disrupt the microtubules that form the mitotic spindle. Microtubule-dependent molecular motors that function during mitosis are logical alternative mitotic targets for drug development. Eg5 (Kinesin-5) and Kif15 (Kinesin-12), in particular, are an attractive pair of motor proteins, as they work in concert to drive centrosome separation and promote spindle bipolarity. Furthermore, we hypothesize that the clinical failure of Eg5 inhibitors may be (in part) due to compensation by Kif15. In order to test this idea, we screened a small library of kinase inhibitors and identified GW108X, an oxindole that inhibits Kif15 in vitro. We show that GW108X has a distinct mechanism of action compared with a commercially available Kif15 inhibitor, Kif15-IN-1 and may serve as a lead with which to further develop Kif15 inhibitors as clinically relevant agents.

About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Dumas, ME; Chen, GY; Kendrick, ND; Xu, G; Larsen, SA; Jana, S; Waterson, AG; Bauer, JA; Hancock, W; Sulikowski, GA; Ohi, R or concate me.. Product Details of 100-83-4

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

An article Synthesis and Characterization of Magnetic Functionalized Ni and Cu Nano Catalysts and Their Application in Oxidation, Oxidative Coupling and Various Multi-Component Reactions WOS:000604191500004 published article about ONE-POT SYNTHESIS; RECYCLABLE CATALYST; EFFICIENT CATALYST; 5-SUBSTITUTED 1H-TETRAZOLES; SELECTIVE OXIDATION; HYDROGEN-PEROXIDE; IRON-OXIDE; NANOPARTICLES; SULFIDES; COMPLEX in [Hajjami, Maryam] Bu Ali Sina Univ, Dept Organ Chem, Fac Chem, Hamadan 6517838683, Hamadan, Iran; [Sheikhaei, Shiva; Gholamian, Fatemeh; Yousofvand, Zakieh] Ilam Univ, Fac Sci, Dept Chem, POB 69315516, Ilam, Iran in 2021.0, Cited 47.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4. Recommanded Product: 100-83-4

Two magnetic nano catalysts of nickel and copper, Fe3O4@SiO2@DOP-BenPyr-M(II), (M=Ni and Cu) have been synthesized. These catalysts were applied as recoverable, efficient and new heterogeneous catalysts for the high yielding and room temperature one-pot procedure of selective oxidation of sulfides to sulfoxides and oxidative coupling of thiols to disulfides. In addition, the catalytic activity of Fe3O4@SiO2@DOP-BenPyr-Ni(II) was investigated as heterogeneous nanocatalyst for synthesis of 2,3-dihydroquinazolin-4(1H)-ones, 5-substituted 1H-tetrazoles and polyhydroquinolines. The synthesized catalysts were characterized by FT-IR, TGA, XRD, VSM, EDX, ICP and SEM techniques. These catalysts were recovered by an external magnet and reused several times without significant loss of catalytic efficiency. [GRAPHICS] .

About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Hajjami, M; Sheikhaei, S; Gholamian, F; Yousofvand, Z or concate me.. Recommanded Product: 100-83-4

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

Authors Jlassi, R; Khalladi, A; Naili, H; Ruffer, T; Lang, H; Rekik, W in PERGAMON-ELSEVIER SCIENCE LTD published article about DOUBLE SULFATES; COMPLEXES; SPECTRA; NITRATE; LIGANDS; DESIGN; CU(II) in [Jlassi, Raja; Khalladi, Ahmed; Naili, Houcine; Rekik, Walid] Univ Sfax, Lab Physicochim Etat Solide, Dept Chim, Fac Sci Sfax, BP 1171, Sfax 3000, Tunisia; [Khalladi, Ahmed; Ruffer, Tobias; Lang, Heinrich] Tech Univ Chemnitz, Fak Nat Wissensch, Inst Chem, Anorgan Chem, D-09107 Chemnitz, Germany in 2019.0, Cited 40.0. Category: indole-building-block. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4

The new complex [Zn(im)(4)](NO3)(2) (1) was synthesized and crystallographically characterized. In the solid state, 1 is built up by [Zn(C3H4N2)](2+) cations and NO3- anions interlinked by N-H center dot center dot center dot O hydrogen bonds which give rise to the formation of a 3D network. Complex 1 and [CdNa2(mu-L-2)](n)center dot 6.34H(2)O (2), (L=2-(2-(4,4-dimethyl-2,6-dioxocyclohexylidene) hydrazinyl)terephthalate) were used as catalysts for the Henry reaction, and high yields were obtained under optimum conditions. Both 1 and 2 act as very efficient catalysts for the Henry reaction and convert nitroethane and aldehydes to beta-nitroalcohols in yields of up to 89%. The threo/erythro diastereoselectivity depends on the choice of catalyst and also the selection of the reaction substrate, reaching values up to 89:11. (C) 2018 Elsevier Ltd. All rights reserved.

Category: indole-building-block. About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Jlassi, R; Khalladi, A; Naili, H; Ruffer, T; Lang, H; Rekik, W 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

An article Green synthesis, biological evaluation, molecular docking studies and 3D-QSAR analysis of novel phenylalanine linked quinazoline-4(3H)-one-sulphonamide hybrid entities distorting the malarial reductase activity in folate pathway WOS:000476887000008 published article about MICROWAVE-ASSISTED SYNTHESIS; IONIC-LIQUID; DRUG-RESISTANCE; DIHYDROFOLATE-REDUCTASE; SULFONAMIDE; INHIBITORS; ANTICANCER; EFFICIENT; PARASITE; PREDICT in [Patel, Tarosh S.; Dixit, Bharat C.] Sardar Patel Univ, VP&RPTP Sci Coll, Chem Dept, Vallabh Vidyanagar 388120, Gujarat, India; [Bhatt, Jaimin D.] Sardar Patel Univ, VP&RPTP Sci Coll, Ind Chem Dept, Vallabh Vidyanagar 388120, Gujarat, India; [Dixit, Ritu B.] Ashok & Rita Patel Inst Integrated Studies & Res, New Vallabh Vidyanagar 388121, Gujarat, India; [Chudasama, Chaitanya J.] Sardar Patel Univ, Shree Alpesh N Patel PG Inst, Dept Biochem, Anand 388001, Gujarat, India; [Patel, Bhavesh D.] Sardar Patel Univ, VP&RPTP Sci Coll, Microbiol Dept, Vallabh Vidyanagar 388120, Gujarat, India in 2019.0, Cited 65.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4. Recommanded Product: 3-Hydroxybenzaldehyde

A modified Grimmel’s method for N-heterocyclization of phenylalanine linked sulphonamide side arm at position-2 was optimized leading to 2,3-disustituted-4-quinazolin-(3H)-ones. Further, [Bmim][BF4]-H2O (IL) was used as green solvent as well as catalyst for the synthesis of twenty two hybrid quinazolinone motifs (4a-4v) by N-heterocyclization reaction using microwave irradiation technique. The in vitro screening of the hybrid entities against the malarial species Plasmodium falciparum yielded five potent molecules 4l, 4n, 4r, 4t & 4u owing comparable antimalarial activity to the reference drugs. In continuation, an in silico study was carried out to obtain a pharmacophoric model and quantitative structure activity relationship. We also built a 3D-QSAR model to procure more information that could be applied to design new molecules with more potent Pf-DHFR inhibitory activity. The designed pharmacophore was recognized to be more potent for the selected molecules, exhibiting five pharmacophoric features. The active scaffolds were further evaluated for enzyme inhibition efficacy against alleged receptor Pf-DHFR computationally and in vitro, proving their candidature as lead dihydrofolate reductase inhibitors as well as the selectivity of the test candidates was ascertained by toxicity study against vero cells. The perception of good oral bioavailability was also proved by study of pharmacokinetic properties.

Recommanded Product: 3-Hydroxybenzaldehyde. About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Patel, TS; Bhatt, JD; Dixit, RB; Chudasama, CJ; Patel, BD; Dixit, BC 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

Computed Properties of C7H6O2. In 2020.0 BIOORG CHEM published article about CURCUMIN ANALOGS; KAPPA-B; DERIVATIVES; INFLAMMATION; FLAVONOIDS; SYNTHASE in [Faudzi, Siti Munirah Mohd; Abdullah, Maryam Aisyah; Manap, Mohd Rashidi Abdull; Ismail, Ahmad Zaidi] Univ Putra Malaysia, Fac Sci, Dept Chem, Serdang 43400, Selangor, Malaysia; [Faudzi, Siti Munirah Mohd; Abas, Faridah; Lajis, Nordin H.] Univ Putra Malaysia, Inst Biosci, Lab Nat Prod, Serdang 43400, Selangor, Malaysia; [Rullah, Kamal] Int Islamic Univ Malaysia, Kuliyyah Pharm, Dept Pharmaceut Chem, Kuantan 25200, Pahang, Malaysia; [Aluwi, Mohd Fadhlizil Fasihi Mohd; Ramli, Aizi Nor Mazila] Univ Malaysia Pahang, Fac Ind Sci & Technol, Kuantan 26300, Pahang, Malaysia; [Abas, Faridah] Univ Putra Malaysia, Fac Food Sci & Technol, Dept Food Sci, Serdang 43400, Selangor, Malaysia in 2020.0, Cited 40.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

In search of potent anti-inflammatory agents, twenty-four chalcone derivatives including seven new compounds (13 – 17, 21 and 23) containing pyrrole moiety were designed, synthesized, and assessed for their nitric oxide (NO) and prostaglandin E-2 (PGE(2)) suppression ability on IFN-gamma/LPS-induced RAW 264.7 macrophage cells. Results showed that none of the synthesized compounds were PAINS-associated molecules, with 3-(2,5-dimethoxyphenyl)-1-(1H-pyrrol-2-yl) prop-2-en-1-one (compound 16) exhibiting remarkable inhibition activity towards PGE(2) and NO production with IC50 values of 0.5 +/- 1.5 mu M and 12.1 +/- 1.5 mu M, respectively. Physicochemical and ADMET studies showed that majority of the compounds obey to Lipinski’s rule of five (RO5) having high blood brain barrier (BBB) penetration, human intestinal absorption (HIA), P- glycoprotein (PgP) inhibition and plasma binding protein (PPB) inhibition. The obtained atomic coordinates for the single-crystal XRD of 16 were then applied in a molecular docking simulation, and compound 16 was found to participate in a number of important binding interactions in the binding sites of ERK and mPGES-1. Based on these results, we have observed the potential of compound 16 as a new hit anti-inflammatory agent, and these findings could serve as a basis for further studies on its mechanism of action.

Computed Properties of C7H6O2. About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Faudzi, SMM; Abdullah, MA; Manap, MRA; Ismail, AZ; Rullah, K; Aluwi, MFFM; Ramli, ANM; Abas, F; Lajis, NH 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

Kapoor, G; Pathak, DP; Bhutani, R; Husain, A; Jain, S; Iqbal, MA in [Kapoor, Garima; Pathak, Dharam Pal; Bhutani, Rubina] Delhi Inst Pharmaceut Sci & Res, Dept Pharmaceut Chem, New Delhi 110017, India; [Husain, Asif; Iqbal, Md. Azhar] Hamdard Univ, Jamia Hamdard, Fac Pharm, Dept Pharmaceut Chem, New Delhi, India; [Jain, Sandeep] Guru Jambeshwar Univ Sci & Technol, Dept Pharmaceut Chem, Hisar, Haryana, India published Synthesis, ADME, docking studies and in vivo anti-hyperglycaemic potential estimation of novel Schiff base derivatives from octadec-9-enoic acid in 2019.0, Cited 40.0. COA of Formula: C7H6O2. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

A new series of octadec-9-enoic acid schiff base entities (S1-S30) were designed and synthesized targeting peroxisome proliferator activated receptor-gamma for agonist action. Molinspiration software (online) was used to estimate drug like molecular properties of the metabolites. Docking disquisition on co-crystallized protein of PPAR-gamma (PDB ID 1FM9) was carried out which showed S21, S10 and S7 as best situated in the vital sites of receptor having docking scores – 9.19, – 8.68 and – 8.64 respectively. Free binding energy measured using model of Maestro 9.0 and was in range of from – 40.01 and – 80.54 kcal/mol, significant when compared with pioglitazone (- 51.58 Kcal/mol). Seven best docked derivatives were assessed for in-vivo oral glucose tolerance on normal rats and anti-hyperglycaemic activity by streptozotocin induced diabetes model. S21 unveiled to be the best measured analogue among all the synthesized entities. Encouraging outcomes motivates fatty acids for further development of more effective and safer compounds.

COA of Formula: C7H6O2. About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Kapoor, G; Pathak, DP; Bhutani, R; Husain, A; Jain, S; Iqbal, MA 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