Benzothiadiazine
Appearance
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Preferred IUPAC name
2H-1,2,4-Benzothiadiazine | |
Identifiers | |
3D model (JSmol)
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C7H6N2S | |
Molar mass | 150.20 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Benzothiadiazine is a bicyclic heterocyclic benzene derivative with the heterocycle containing two nitrogens and one sulfur.[1]
Some benzothiadiazine derivatives are used as pharmaceutical drugs, including:
![](http://upload.wikimedia.org/wikipedia/commons/thumb/b/bc/Hydrochlorothiazide.png/150px-Hydrochlorothiazide.png)
References
[edit]- ^ Hu Z, Martí J, Lu H (October 2021). "Structure of benzothiadiazine at zwitterionic phospholipid cell membranes". The Journal of Chemical Physics. 155 (15): 154303. arXiv:2107.14565. Bibcode:2021JChPh.155o4303H. doi:10.1063/5.0065163. PMID 34686044. S2CID 239471390.
- ^ a b Hu Z, Marti J (March 2022). "In Silico Drug Design of Benzothiadiazine Derivatives Interacting with Phospholipid Cell Membranes". Membranes. 12 (3): 331. doi:10.3390/membranes12030331. PMC 8949146. PMID 35323806.
- ^ Huwaimel BI, Bhakta M, Kulkarni CA, Milliken AS, Wang F, Peng A, et al. (April 2021). "Discovery of Halogenated Benzothiadiazine Derivatives with Anticancer Activity*". ChemMedChem. 16 (7): 1143–1162. doi:10.1002/cmdc.202000729. PMC 8035258. PMID 33331124.
- ^ Varano F, Catarzi D, Colotta V, Squarcialupi L, Matucci R (November 2014). "1,2,4-Benzothiadiazine-1,1-dioxide derivatives as ionotropic glutamate receptor ligands: synthesis and structure-activity relationships". Archiv der Pharmazie. 347 (11): 777–785. doi:10.1002/ardp.201400192. PMID 25204434. S2CID 1765795.
- ^ Ganeshpurkar A, Gutti G, Singh SK (2019-01-01). "Chapter 1 - RNA-Dependent RNA Polymerases and Their Emerging Roles in Antiviral Therapy". In SP (ed.). Viral Polymerases. Academic Press. pp. 1–42. doi:10.1016/B978-0-12-815422-9.00001-2. ISBN 978-0-12-815422-9. S2CID 92095885.