Month: February 2022

Application In Synthesis of 1H-1,2,4-Triazol-5-amine. Recently I am researching about DRUG; 5-ENE-4-THIAZOLIDINONES; INHIBITORS; DESIGN; AGENTS; ASSAY, Saw an article supported by the . Published in ACADEMIC PRESS INC ELSEVIER SCIENCE in SAN DIEGO ,Authors: Holota, S; Kryshchyshyn, A; Derkach, H; Trufin, Y; Demchuk, I; Gzella, A; Grellier, P; Lesyk, R. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

A series of novel 2-(5-aminomethylene-4-oxo-2-thioxothiazolidin-3-yl)-3-phenylpropionic acid ethyl esters has been synthesized. Target compounds were evaluated for their trypanocidal activity towards Trypanosoma brucei brucei and Trypanosoma brucei gambiense. Several hit-compounds (8, 10, 12) inhibited growth of the parasites at sub-micromolar concentrations (IC50 0.027-1.936 mu M) and showed significant selectivity indices (SI= 108-1396.2) being non-toxic towards the human primary fibroblasts. The screening of anticancer activity in vitro within NCI DTP protocol allowed to identify active 2-(5-{[5-(2,4-dichlorobenzyl)-thiazol-2-ylamino]methylene}- 4-oxo-2-thioxothiazolidin-3-yl)-3-phenylpropionic acid ethyl ester 14 that demonstrated inhibition against all 59 human tumor cell lines with the average GI(50) value of 2.57 mu M. It was established that the activity type (antitrypanosomal or anticancer) as well as its level depends on the character of enamine fragment in the C5 position of thiazolidinone core.

Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.. Application In Synthesis of 1H-1,2,4-Triazol-5-amine

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Meng, XX; Li, L; De Clercq, I; Narsai, R; Xu, Y; Hartmann, A; Claros, DL; Custovic, E; Lewsey, MG; Whelan, J; Berkowitz, O in [Meng, Xiangxiang; Li, Lu; Narsai, Reena; Xu, Yue; Hartmann, Andreas; Claros, Diego Lozano; Lewsey, Mathew G.; Whelan, James; Berkowitz, Oliver] La Trobe Univ, Australian Res Council, Dept Anim Plant & Soil Sci, Ctr Excellence Plant Energy Biol, Bundoora, Vic 3086, Australia; [De Clercq, Inge] Univ Ghent, Dept Plant Biotechnol & Bioinformat, B-9052 Ghent, Belgium; [De Clercq, Inge] VIB, Ctr Plant Syst Biol, B-9052 Ghent, Belgium; [Custovic, Eddie] La Trobe Univ, Sch Engn & Math Sci, Bundoora, Vic 3086, Australia published ANAC017 Coordinates Organellar Functions and Stress Responses by Reprogramming Retrograde Signaling in 2019.0, Cited 103.0. Formula: C2H4N4. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Mitochondria adjust their activities in response to external and internal stimuli to optimize growth via the mitochondrial retrograde response signaling pathway. The Arabidopsis (Arabidopsis thaliana) NAC domain transcription factor ANAC017 has previously been identified as a regulator of the mitochondrial retrograde response. We show here that overexpression of ANAC017 in Arabidopsis leads to growth retardation, altered leaf development with decreased cell size and viability, and early leaf senescence. RNA sequencing analyses revealed that increased ANAC017 expression leads to higher expression of genes related to mitochondrial stress, cell death/autophagy, and leaf senescence under nonlimiting growth conditions as well as extensive repression of chloroplast function. Gene regulatory network analysis indicated that a complex hierarchy of transcription factors exists downstream of ANAC017. These involve a set of up-regulated ANAC and WRKY transcription factors associated with organellar signaling and senescence. The network also includes a number of ethylene- and gibberellic acid-related transcription factors with established functions in stress responses and growth regulation, which down-regulate their target genes. A number of BASIC LEUCINE-ZIPPER MOTIF transcription factors involved in the endoplasmic reticulum unfolded protein response or balancing of energy homeostasis via the SNF1-RELATED PROTEIN KINASE1 were also down-regulated by ANAC017 overexpression. Our results show that the endoplasmic reticulum membrane tethering of the constitutively expressed ANAC017, and its controlled release, are crucial to fine-tune a fast reactive but potentially harmful signaling cascade. Thus, ANAC017 is a master regulator of cellular responses with mitochondria acting as central sensors.

Welcome to talk about 61-82-5, If you have any questions, you can contact Meng, XX; Li, L; De Clercq, I; Narsai, R; Xu, Y; Hartmann, A; Claros, DL; Custovic, E; Lewsey, MG; Whelan, J; Berkowitz, O or send Email.. Formula: C2H4N4

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Authors Holzel, T; Ganter, C in ELSEVIER SCIENCE SA published article about N-HETEROCYCLIC CARBENE; STABLE CARBENES; COMPLEXES; LIGANDS; CATALYSTS; VERSATILE; ACCESS in [Hoelzel, Torsten; Ganter, Christian] Heinrich Heine Univ Dusseldorf, Inst Anorgan Chem & Strukturchem, Univ Str 1, D-40225 Dusseldorf, Germany in 2020.0, Cited 76.0. COA of Formula: C2H4N4. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Methylation of 3-amino-1,2,4-triazole and 1-methyl-3-nitro-1,2,4-triazole provides access to three NHC-precursors. For the nitro compound only a monomethylation to the triazolium salt 3(OTf) is observed. The aminotriazole could be subsequently converted to mono- and dicationic carbene precursors 1I and 2(OTf)(2), respectively. The nitro group on NHC 3 leads to a decrease of donor strength and a slightly enhanced acceptor character as compared to a related NHC lacking the nitro group. The cationic NHC 2 is the poorest donor within the series and shows a TEP value of 2072 cm(-1). The properties of this species are dominated by its cationic nature while the influence of the NMe2 group is surprisingly small. X-ray diffraction studies suggest a guanidinium-like character for the NMe2 substituted compounds. (C) 2020 Elsevier B.V. All rights reserved.

COA of Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Holzel, T; Ganter, C or concate me.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

An article Synthesis and molecular docking study of new pyrazole derivatives as potent anti-breast cancer agents targeting VEGFR-2 kinase WOS:000552629800008 published article about GROWTH-FACTOR RECEPTOR-2; BIOLOGICAL EVALUATION; ANTICANCER EVALUATION; INHIBITORS; ANGIOGENESIS; RESISTANCE; MECHANISM; DISCOVERY; DESIGN in [Dawood, Dina H.] Natl Res Ctr, Chem Nat & Microbial Prod Dept, Pharmaceut & Drug Ind Res Div, 33 El Bohouth St,POB 12622, Giza, Egypt; [Nossier, Eman S.] Al Azhar Univ, Fac Pharm Girls, Dept Pharmaceut Chem, POB 11754, Cairo, Egypt; [Ali, Mamdouh M.; Mahmoud, Abeer E.] Natl Res Ctr, Biochem Dept, Genet Engn & Biotechnol Res Div, 33 El Bohouth St,POB 12622, Giza, Egypt in 2020.0, Cited 50.0. Safety of 1H-1,2,4-Triazol-5-amine. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Based on the previous studies that revealed the valuable role of pyrazole scaffold in cancer management and VEGFR-2 inhibition, a new set of pyrazole conjugated with pyrazoline, triazolopyrimidine and pyrazolone moieties were synthesized and investigated for their anticancer efficiency against human breast cancer MCF-7. The anticancer screening revealed the significant sensitivity of breast carcinoma towards compounds 4b, 5c, 6c, 7b, 7c and 12c with IC50 values ranging from 16.50 – 26.73 mu M in comparison with tamoxifen (IC50 = 23.31 mu M). Moreover, the new analogues were further examined for their VEGFR-2 inhibitory activity, among the tested derivatives 5c, 6c, 7b, 7c and 12c displayed prominent inhibitory efficiency versus VEGFR-2 kinase with % inhibition ranging from 70 to 79%. Compounds 6c, 7c and 12c revealed inhibitory efficiency in nanomolar level with IC50 (913.51, 225.17 and 828.23 nM, respectively) comparing to sorafenib (IC50 = 186.54 nM). Flow cytometric analysis revealed that the promising compound 12c prompted pre-G1 apoptosis and cell growth cessation at G2/M phase and stimulated apoptosis via activation of caspase-3. Moreover, molecular docking study of the promising derivatives was performed to highlight their binding modes and interactions with the amino acid residues of VEGFR-2 enzyme.

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Dawood, DH; Nossier, ES; Ali, MM; Mahmoud, AE or concate me.. Safety of 1H-1,2,4-Triazol-5-amine

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Authors Salimi, P; Norouzi, O; Pourhoseini, SEM; Bartocci, P; Tavasoli, A; Di Maria, F; Pirbazari, SM; Bidini, G; Fantozzi, F in PERGAMON-ELSEVIER SCIENCE LTD published article about CLADOPHORA-GLOMERATA MACROALGAE; BIO-OIL PRODUCTION; HYDROGEN-RICH GAS; ELECTROCHEMICAL PERFORMANCE; MARINE BIOMASS; FURAN COMPOUNDS; ENERGY-STORAGE; POROUS CARBON; ELECTROLYTE; NANOSHEETS in [Salimi, Pejman] Tarbiat Modares Univ, Fac Sci, Dept Phys Chem, POB 14115-175, Tehran, Iran; [Norouzi, Omid; Pourhoseini, S. E. M.; Tavasoli, Ahmad; Pirbazari, S. M.] Univ Tehran, Sch Chem, Coll Sci, Tehran, Iran; [Norouzi, Omid; Bartocci, Pietro; Bidini, Gianni; Fantozzi, Francesco] Univ Perugia, Dept Engn, Via G Duranti 67, I-06125 Perugia, Italy; [Norouzi, Omid; Di Maria, Francesco] Univ Perugia, Dipartimento Ingn, LAR5 Lab, Via G Duranti 93, I-06125 Perugia, Italy in 2019.0, Cited 67.0. Quality Control of 1H-1,2,4-Triazol-5-amine. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

In this work, Cladophora glomerata, a harmful seaweed, is converted into an olive-shaped magnetic biochar by a slow pyrolysis process catalyzed by iron. The resultant magnetic biochar has a high surface area of 296.4 m(2) g(-1) with a carbon-rich structure that makes it suitable to be used as an electrode in Li ion batteries. The catalytic pyrolysis process showed significant effect on steam reforming, ketonization and deoxygenation and/or denitrogenation reactions. The overall quality of the pyrolysis products increases: the gas contains a higher percentage of hydrogen (up to 22%), while the oil is enriched in furans (with a selectivity of about 14%). The electrochemistry behavior of magnetic biochar has been also evaluated, using galvanostatic charge discharge, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) analyses. The electrochemical results indicated a higher initial specific discharge capacity (740 mAh g(-1)) and great cyclic stability for magnetic electrode as compared to the biochar electrode. (C) 2019 Elsevier Ltd. All rights reserved.

Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.. Quality Control of 1H-1,2,4-Triazol-5-amine

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Name: 1H-1,2,4-Triazol-5-amine. Authors Mu, YZ; Maharjan, Y; Dutta, RK; Wei, XF; Kim, JH; Son, J; Park, C; Park, R in PUBLIC LIBRARY SCIENCE published article about in [Mu, Yizhu; Maharjan, Yunash; Dutta, Raghbendra Kumar; Wei, Xiaofan; Kim, Jin Hwi; Son, Jinbae; Park, Channy; Park, Raekil] Gwangju Inst Sci & Technol, Dept Biomed Sci & Engn, Gwangju, South Korea in 2021.0, Cited 36.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Peroxisomes are metabolically active organelles which are known to exert anti-inflammatory effects especially associated with the synthesis of mediators of inflammation resolution. However, the role of catalase and effects of peroxisome derived reactive oxygen species (ROS) caused by lipid peroxidation through 4-hydroxy-2-nonenal (4-HNE) on lipopolysaccharide (LPS) mediated inflammatory pathway are largely unknown. Here, we show that inhibition of catalase by 3-aminotriazole (3-AT) results in the generation of peroxisomal ROS, which contribute to leaky peroxisomes in RAW264.7 cells. Leaky peroxisomes cause the release of matrix proteins to the cytosol, which are degraded by ubiquitin proteasome system. Furthermore, 3-AT promotes the formation of 4HNE-I kappa B alpha adduct which directly interferes with LPS induced NF-kappa B activation. Even though, a selective degradation of peroxisome matrix proteins and formation of 4HNE- I kappa B alpha adduct are not directly related with each other, both of them are could be the consequences of lipid peroxidation occurring at the peroxisome membrane.

Name: 1H-1,2,4-Triazol-5-amine. Bye, fridends, I hope you can learn more about C2H4N4, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Recently I am researching about NANOSHEETS; G-C3N4; NITROGEN; WATER; PERFORMANCE; EVOLUTION; TRANSFORMATIONS; MELAMINE; C3N4; SOFT, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21771061, 21601055]; University Nursing Program for Young Scholars with Creative Talents in Heilongjiang Province [UNPYSCT-2017118]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Zhao, C; Li, Q; Xie, Y; Zhang, LP; Xiao, XD; Wang, D; Jiao, YQ; Price, CAH; Jiang, BJ; Liu, J. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine. COA of Formula: C2H4N4

The three-dimensional character of carbon nitride can endow it with a larger specific surface area and more catalytic active sites, which are beneficial for charge and mass transfer to enhance photocatalytic hydrogen production reactions. Herein, we reported the direct assembly of three-dimensional structured carbon nitride from the thermal polymerization of 3-amino-1,2,4-triazole (AT) and melamine molecules. The 3D C3N4 consisted of one-dimensional thick tubes with numbers of thin tubes grown uniformly on their surfaces. It was noted that the assembly was decorated with triazole ring groups that generated a special nitrogen-rich structure, further broadening the visible-light response range. Furthermore, the nitrogen-rich carbon nitride had a large surface area of 71 m(2) g(-1), leading to a significant increase in the number of catalytic active sites. Thus, the photocatalytic hydrogen production rate reached 7.1 mmol g(-1) h(-1), 11.2 times higher than that of bulk C3N4. This work may provide a new strategy to controllably synthesize three-dimensional carbon nitride assemblies for photocatalytic applications.

COA of Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhao, C; Li, Q; Xie, Y; Zhang, LP; Xiao, XD; Wang, D; Jiao, YQ; Price, CAH; Jiang, BJ; Liu, J or concate me.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Zhang, L; Zhang, F; Liu, FB; Shen, J; Wang, JX; Jiang, M; Zhang, DS; Yang, PF; Chen, Y; Song, SY in [Zhang, Liang; Liu, Fangbing; Song, Shiyong] Chinese Acad Sci, CAS Key Lab Plant Germplasm Enhancement & Special, Wuhan Bot Garden, Wuhan 430074, Hubei, Peoples R China; [Zhang, Liang; Liu, Fangbing] Univ Chinese Acad Sci, Beijing 100049, Peoples R China; [Zhang, Liang; Liu, Fangbing; Song, Shiyong] Chinese Acad Sci, Ctr Econ Bot, Core Bot Gardens, Wuhan 430074, Peoples R China; [Zhang, Fan; Shen, Jun; Wang, Jiaxuan; Jiang, Meng; Chen, Ying; Song, Shiyong] Zhejiang Univ, Inst Crop Sci, State Key Lab Rice Biol, Zhejiang Prov Key Lab Crop Genet Resources, Hangzhou 310058, Peoples R China; [Zhang, Dasheng] Chinese Acad Sci, Shanghai Chenshan Bot Garden, Shanghai Chenshan Plant Sci Res Ctr, Shanghai 201602, Peoples R China; [Yang, Pingfang] Hubei Univ, Sch Life Sci, State Key Lab Biocatalysis & Enzyme Engn, Wuhan 430062, Peoples R China published The lotus NnFTIP1 and NnFT1 regulate flowering time in Arabidopsis in 2021.0, Cited 40.0. Category: Triazoles. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

In higher plants, floral signals are mainly collected and transduced to FLOWERING LOCUS T (FT) in Arabidopsis and its orthologues. The movement of FT from leaves to the shoot apical meristem (SAM) is partially mediated by FT-INTERACTING PROTEIN1 (FTIP1). Although the functions of OsFTIP1 in rice and DOFTIP1 in orchid in FT transport have also been investigated, the FTIP1 homologue in lotus (Nelumbo nucifera Gaertn.), a type of horticultural plant with high economic and cultural value, has not been isolated, and the mechanism of NnFT1 transport has not been explored. Here, we revealed that NnFTIP1 mediates the transport of NnFT1 in ectopic transgenic lines in Arabidopsis. Overexpression of NnFTIP1 in the ftip1-1 background rescued the late flowering phenotype of ftip1-1, indicating that NnFTIP1 has a conserved function as FTIP1. NnFTIP1 and NnFT1 share similar tissue expression patterns and subcellular localization. NnFTIP1 and NnFT1 interact both in vitro and in vivo. In addition, NnFTIP1 affects NnFT1 transport from leaves to the SAM. Furthermore, we found that NnUOF8, a MYB-like transcription factor, directly regulates the expression of NnFTIP1. Our results suggest that the functions of FTIP1 and FT are conserved during evolution in flowering plants.

Welcome to talk about 61-82-5, If you have any questions, you can contact Zhang, L; Zhang, F; Liu, FB; Shen, J; Wang, JX; Jiang, M; Zhang, DS; Yang, PF; Chen, Y; Song, SY or send Email.. Category: Triazoles

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

In 2020.0 MOL DIVERS published article about FUNCTIONALIZED MCM-41; BIOLOGICAL EVALUATION; DERIVATIVES in [Akrami, Sedigheh; Karami, Bahador; Farahi, Mahnaz] Univ Yasuj, Dept Chem, Yasuj 7591874831, Iran in 2020.0, Cited 36.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. HPLC of Formula: C2H4N4

Herein, an effectual, quick and novel method is described for the synthesis of new triazolo[1,5-a]pyrimidine, triazolo[5,1-b][1,3] thiazine and pyrazolo[1,5-a]pyrimidine derivatives. This series of fused six-member rings to triazole and pyrazole was prepared via the catalyst-free reaction of dialkyl acetylenedicarboxylates and 3-substituted 1H-1,2,4-triazole or 3-amino-1H-pyrazole-4-carbonitrile. The structures of the prepared products were deduced from their Fourier-transform infrared, elemental analysis and proton and carbon-13 nuclear magnetic resonance spectral data. Graphical abstract A novel and green method is described for the synthesis of new triazolo[1,5-a]pyrimidine, triazolo[5,1-b][1,3] thiazine and pyrazolo[1,5-a]pyrimidine derivatives. [GRAPHICS] .

HPLC of Formula: C2H4N4. Welcome to talk about 61-82-5, If you have any questions, you can contact Akrami, S; Karami, B; Farahi, M or send Email.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

Safety of 1H-1,2,4-Triazol-5-amine. In 2021.0 SYNTHETIC COMMUN published article about FAST-ATOM-BOMBARDMENT; BIGINELLI; 3-AMINO-1,2,4-TRIAZOLE; ANTICANCER in [Shvets, Elena H.; Pidvorotnia, Anastasiia, V; Kulyk, Olesia G.; Kolosov, Maksim A.] Kharkov Natl Univ, Sch Chem, UA-61022 Kharkiv, Ukraine; [Mazepa, Alexander, V] NAS Ukraine, AV Bogatsky Physicochem Inst, Odesa, Ukraine in 2021.0, Cited 31.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

4,7-Dihydroazolo[1,5-a]pyrimidin-5-ylmethanesulfonamides are side-products of the three-component Biginelli-like reaction of aminoazoles, aldehydes andN,N-dialkyl-2-ketomethanesulfonamides. Herein, we report a straightforward synthesis of 5-sulfonamidomethyl substituted 4,7-dihydroazolo[1,5-a]pyrimidines by a two-component condensation of aminoazoles andN,N-dialkyl(cinnamoyl)methanesulfonamides in DMF at reflux. The startingN,N-dialkyl-2-ketomethanesulfonamides can be obtained by either lithiation ofN,N-dialkylmethanesulfonamides and reaction with aldehydes followed by oxidation of the resulting alcohols or by Claisen condensation ofN,N-dialkylmethanesulfonamides with the corresponding esters. The chemical structures of all synthesized compounds are supported by(1)H and(13)C NMR-spectroscopy, mass spectrometry and elemental analysis.

Safety of 1H-1,2,4-Triazol-5-amine. Welcome to talk about 61-82-5, If you have any questions, you can contact Shvets, EH; Pidvorotnia, AV; Kulyk, OG; Mazepa, AV; Kolosov, MA or send Email.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics