Relevant bibliographies by topics / Sulfonamido Dithiocarbamates

Contents

  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Sulfonamido Dithiocarbamates'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 September 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Sulfonamido Dithiocarbamates.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Sulfonamido Dithiocarbamates"

1

Alagiri, Kaliyamoorthy, та Kandikere Ramaiah Prabhu. "Catalyst-Free Regio- and Stereospecific Synthesis of β-Sulfonamido Dithiocarbamates: Efficient Ring-Opening Reactions of N-Tosyl Aziridines by Dialkyldithiocarbamates". Chemistry - A European Journal 17, № 25 (2011): 6922–25. http://dx.doi.org/10.1002/chem.201100817.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Alagiri, Kaliyamoorthy, та Kandikere Ramaiah Prabhu. "ChemInform Abstract: Catalyst-Free Regio- and Stereospecific Synthesis of β-Sulfonamido Dithiocarbamates: Efficient Ring-Opening Reactions of N-Tosyl Aziridines by Dialkyldithiocarbamates." ChemInform 42, № 41 (2011): no. http://dx.doi.org/10.1002/chin.201141045.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Fu, Dong-Jun, Ying-Chao Liu, Jia-Jia Yang, et al. "Design and Synthesis of Sulfonamide-1,2,3-Triazole Derivatives Bearing a Dithiocarbamate Moiety as Antiproliferative Agents." Journal of Chemical Research 41, no. 9 (2017): 523–25. http://dx.doi.org/10.3184/174751917x15027935057950.

Full text
Abstract:
A series of nine novel 1-(4′-sulfamoylphenyl)-1,2,3-triazole derivatives bearing a 4-dithiocarbamylmethyl moiety were designed using the molecular hybridisation approach and synthesised by alkyne/azide click chemistry. Most of the synthesised compounds exhibited moderate to good antiproliferative activity against oesophagus, gastric and prostate cancer cell lines, but a compound containing a 4-( t-butoxycarbonyl)piperazinylthiocarbonyl moiety showed the highest activity. Against a prostate cancer cell line, it had an IC50 value of 2.4 μM, about 10-fold more active than 5-flurouracil. This work
APA, Harvard, Vancouver, ISO, and other styles
4

D'Ambrosio, Katia, Claudiu T. Supuran, and Giuseppina De Simone. "Are Carbonic Anhydrases Suitable Targets to Fight Protozoan Parasitic Diseases?" Current Medicinal Chemistry 25, no. 39 (2019): 5266–78. http://dx.doi.org/10.2174/0929867325666180326160121.

Full text
Abstract:
Protozoans belonging to Plasmodium, Leishmania and Trypanosoma genera provoke widespread parasitic diseases with few treatment options and many of the clinically used drugs experiencing an extensive drug resistance phenomenon. In the last several years, the metalloenzyme Carbonic Anhydrase (CA, EC 4.2.1.1) was cloned and characterized in the genome of these protozoa, with the aim to search for a new drug target for fighting malaria, leishmaniasis and Chagas disease. P. falciparum encodes for a CA (PfCA) belonging to a novel genetic family, the η-CA class, L. donovani chagasi for a β-CA (LdcCA)
APA, Harvard, Vancouver, ISO, and other styles
5

Supuran, Claudiu T. "Emerging role of carbonic anhydrase inhibitors." Clinical Science 135, no. 10 (2021): 1233–49. http://dx.doi.org/10.1042/cs20210040.

Full text
Abstract:
Abstract Inhibition of carbonic anhydrase (CA, EC 4.2.1.1) was clinically exploited for decades, as most modern diuretics were obtained considering as lead molecule acetazolamide, the prototypical CA inhibitor (CAI). The discovery and characterization of multiple human CA (hCA) isoforms, 15 of which being known today, led to new applications of their inhibitors. They include widely clinically used antiglaucoma, antiepileptic and antiobesity agents, antitumor drugs in clinical development, as well as drugs for the management of acute mountain sickness and idiopathic intracranial hypertension (I
APA, Harvard, Vancouver, ISO, and other styles
6

Zoppi, Carlotta, Alessio Nocentini, Claudiu T. Supuran, Alessandro Pratesi, and Luigi Messori. "Native mass spectrometry of human carbonic anhydrase I and its inhibitor complexes." JBIC Journal of Biological Inorganic Chemistry 25, no. 7 (2020): 979–93. http://dx.doi.org/10.1007/s00775-020-01818-8.

Full text
Abstract:
Abstract Native mass spectrometry is a potent technique to study and characterize biomacromolecules in their native state. Here, we have applied this method to explore the solution chemistry of human carbonic anhydrase I (hCA I) and its interactions with four different inhibitors, namely three sulfonamide inhibitors (AAZ, MZA, SLC-0111) and the dithiocarbamate derivative of morpholine (DTC). Through high-resolution ESI-Q-TOF measurements, the native state of hCA I and the binding of the above inhibitors were characterized in the molecular detail. Native mass spectrometry was also exploited to
APA, Harvard, Vancouver, ISO, and other styles
7

Sağlık, Begüm Nurpelin, Derya Osmaniye, Ulviye Acar Çevik, et al. "Synthesis, characterization and carbonic anhydrase I and II inhibitory evaluation of new sulfonamide derivatives bearing dithiocarbamate." European Journal of Medicinal Chemistry 198 (July 2020): 112392. http://dx.doi.org/10.1016/j.ejmech.2020.112392.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Quero, Javier, José Carlos Royo, Beatrice Fodor, et al. "Sulfonamide-Derived Dithiocarbamate Gold(I) Complexes Induce the Apoptosis of Colon Cancer Cells by the Activation of Caspase 3 and Redox Imbalance." Biomedicines 10, no. 6 (2022): 1437. http://dx.doi.org/10.3390/biomedicines10061437.

Full text
Abstract:
Two new families of dithiocarbamate gold(I) complexes derived from benzenesulfonamide with phosphine or carbene as ancillary ligands have been synthesized and characterized. In the screening of their in vitro activity on human colon carcinoma cells (Caco-2), we found that the more lipophilic complexes—those with the phosphine PPh3—exhibited the highest anticancer activity whilst also displaying significant cancer cell selectivity. [Au(S2CNHSO2C6H5)(PPh3)] (1) and [Au(S2CNHSO2-p-Me-C6H4)(IMePropargyl)] (8) produce cell death, probably by intrinsic apoptosis (mitochondrial membrane potential mod
APA, Harvard, Vancouver, ISO, and other styles
9

Iwakawa, Tsuneo, Tomohiro Sato, and Akira Murabayashi. "Cycloaddition in Synthesis of Sulfonamide Derivatives. VI Unexpected Products from the Reaction of Dithiocarbamate with Chlorosulfonyl Isocyanate a Novel Synthetic Route to 5-Amino-1,2,4-dithiazol-3-one and N,N-Disubstituted N'-Chlorosulfonylcarbamimidoyl Chloride." HETEROCYCLES 38, no. 5 (1994): 1015. http://dx.doi.org/10.3987/com-93-6641.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

IWAKAWA, T., T. SATO, and A. MURABAYASHI. "ChemInform Abstract: Cycloaddition in Synthesis of Sulfonamide Derivatives. Part 6. Unexpected Products from the Reaction of Dithiocarbamate with Chlorosulfonyl Isocyanate. A Novel Synthetic Route to 5-Amino-1,2,4- dithiazol-3-one and N,N-Disubstituted N′." ChemInform 25, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.199432163.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Dissertations / Theses on the topic "Sulfonamido Dithiocarbamates"

1

Rodriguez-Garcia, Valerie. "Efficient methodology for the synthesis of 2,4-benzodiazepin-1-ones, sulfonylbenzotriazoles, sulfonamides, ethylene sulfonamides, thiocarbamates, dithiocarbamates and thioamides." [Gainesville, Fla.] : University of Florida, 2004. http://purl.fcla.edu/fcla/etd/UFE0006303.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Alagiri, K. "Metal-Mediated And Metal-Free Organic Transformations : C-H Functionalization Of Tertiary Amines, Synthesis Of Carbonyl Compounds And Ring-Opening Of Aziridines." Thesis, 2011. https://etd.iisc.ac.in/handle/2005/2061.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Alagiri, K. "Metal-Mediated And Metal-Free Organic Transformations : C-H Functionalization Of Tertiary Amines, Synthesis Of Carbonyl Compounds And Ring-Opening Of Aziridines." Thesis, 2011. http://hdl.handle.net/2005/2061.

Full text
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography