Catalogue Number
BN-O1243
Analysis Method
Specification
99%(HPLC)
Storage
2-8°C
Molecular Weight
214.25
Appearance
Botanical Source
Structure Type
Category
SMILES
C1=CC(=CC=C1N)S(=O)(=O)N=C(N)N
Synonyms
Suganyl/Ruocid/Ganidan/Sulgin/sulfanilylguanidine/A-307/sulphaguanidine/Diacta/Sulfaguanidin/rp2275/4-aminobenzene-sulfonyl-guanidine/Aterian
IUPAC Name
2-(4-aminophenyl)sulfonylguanidine
Density
1.6±0.1 g/cm3
Solubility
Flash Point
211.5±29.3 °C
Boiling Point
426.1±47.0 °C at 760 mmHg
Melting Point
190-193°C
InChl
InChl Key
BRBKOPJOKNSWSG-UHFFFAOYSA-N
WGK Germany
RID/ADR
HS Code Reference
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:57-67-0) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
29437626
The high acquisition rate of drug resistance by Mycobacterium tuberculosis necessitates the ongoing search for new drugs to be incorporated in the tuberculosis (TB) regimen. Compounds used for the treatment of other diseases have the potential to be repurposed for the treatment of TB. In this study, a high-throughput screening of compounds against thiol-deficient Mycobacterium smegmatis strains and subsequent validation with thiol-deficient M. tuberculosis strains revealed that ΔegtA and ΔmshA mutants had increased susceptibility to azaguanine (Aza) and sulfaguanidine (Su); ΔegtB and ΔegtE mutants had increased susceptibility to bacitracin (Ba); and ΔegtA, ΔmshA, and ΔegtB mutants had increased susceptibility to fusaric acid (Fu). Further analyses revealed that some of these compounds were able to modulate the levels of thiols and oxidative stress in M. tuberculosis This study reports the activities of Aza, Su, Fu, and Ba against M. tuberculosis and provides a rationale for further investigations.
antimicrobial agents; oxidative stress; susceptibility testing; thiols.
Compounds With Potential Activity Against Mycobacterium Tuberculosis
C Sao Emani 1 2, M J Williams 3, I J Wiid 3, B Baker # 1, C Carolis # 4
2018 Mar 27
29145096
Sulfaguanidine (SG), belongs to the class of sulfonamide drug used as an effective antibiotic. In the present work, using crystal engineering approach two novel cocrystals of SG were synthesized (SG-TBA and SG-PT) with thiobarbutaric acid (TBA) and 1,10-phenanthroline (PT), characterized by solid state techniques viz., powder X-ray diffraction (PXRD), fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC) and the crystal structures were determined by single crystal X-ray diffraction studies. A comparative antibacterial activity and hemolytic potential was done on SG drug, coformers and their cocrystals. The tested cocrystals formulations showed almost two fold higher antibacterial activity against the tested strains of bacteria Gram-positive bacteria (S. mutans and E. faecalis) and Gram-negative bacteria (E. coli, K. pneumonia and E. clocae) over SG alone and their coformers. Cocrystal SG-TBA showed better antibacterial activity and reduced hemolysis, thereby, reduced cytotoxicity than SG-PT.
Antibacterial; Cocrystals; Hemolytic potential; Sulfaguanidine.
Sulfaguanidine Cocrystals: Synthesis, Structural Characterization and Their Antibacterial and Hemolytic Analysis
Syed Sibte Asghar Abidi 1, Yasser Azim 2, Shahper Nazeer Khan 3, Asad U Khan 3
2018 Feb 5
4594511
[Dysentery]
F Mihaljević
Feb-74
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