Interesting facts
Interesting Facts about 4-amino-N-(6-chloropyridazin-3-yl)benzenesulfonamide
4-amino-N-(6-chloropyridazin-3-yl)benzenesulfonamide is a fascinating compound that stands out due to its unique structure and potential applications. Here are some noteworthy points:
- Antimicrobial Activity: Compounds similar to 4-amino-N-(6-chloropyridazin-3-yl)benzenesulfonamide have been investigated for their ability to inhibit various bacterial strains, highlighting their significance in pharmaceutical research.
- Structural Diversity: The presence of the pyridazin and benzenesulfonamide groups provides an interesting platform for further modifications, allowing chemists to explore a wide range of derivatives with potentially enhanced biological activities.
- Medicinal Chemistry: This compound is a part of a larger class of sulfonamide compounds, which have been widely used in the development of drugs due to their effective therapeutic properties, particularly in treating bacterial infections.
- Mechanism of Action: The sulfonamide moiety acts as a competitive inhibitor of the enzyme dihydropteroate synthase, which is crucial in bacterial folate synthesis. This inhibition leads to the cessation of bacterial growth.
- Research Potential: Ongoing studies continue to explore the potential of this compound in overcoming antibiotic resistance, which is a major concern in modern medicine.
In summary, 4-amino-N-(6-chloropyridazin-3-yl)benzenesulfonamide represents a significant compound within medicinal chemistry, with its diverse functional groups offering myriad avenues for exploration and development in antimicrobial therapies.
Synonyms
Sulfachloropyridazine
sulfachlorpyridazine
80-32-0
4-amino-N-(6-chloropyridazin-3-yl)benzenesulfonamide
Sulphachlorpyridazine
Nefrosul
Sonilyn
N1-(6-Chloro-3-pyridazinyl)sulfanilamide
Sulfachlorpyridazinum
Sulfacloropiridazina
Durasulf
Benzenesulfonamide, 4-amino-N-(6-chloro-3-pyridazinyl)-
4-Amino-N-(6-chloro-3-pyridazinyl)benzenesulfonamide
Sulfachloropyridizine
CHEBI:59057
Sulfaclorpiridazina
Ba 10370
Nefrosul (TN)
NSC-757858
DTXSID9045265
P78D9P90C0
MFCD00057371
N(sup 1)-(6-Chloro-3-pyridazinyl)sulfanilamide
MLS000777734
DTXCID7025265
SULFACHLORPYRIDAZINE [MI]
SULFACHLORPYRIDAZINE [INN]
SULFACHLORPYRIDAZINE [MART.]
SULFACHLORPYRIDAZINE [USP-RS]
SULFACHLORPYRIDAZINE [WHO-DD]
Ba-10370
4-Amino-N-(6-chloropyridazin-3-yl)-benzenesulfonamide
CAS-80-32-0
NCGC00016323-01
NCGC00016323-04
SULFACHLORPYRIDAZINE [GREEN BOOK]
Cluricol
SMR000414174
SULFACHLORPYRIDAZINE [USP MONOGRAPH]
N(1)-(6-Chloro-3-pyridazinyl)sulfanilamide
C10H9ClN4O2S
Sulfachloropyridazine 100 microg/mL in Acetonitrile
4-amino-N-(6-chloro-3-pyridazinyl)-benzenesulfnamide
4-Amino-N-(6-chloro-pyridazin-3-yl)-benzenesulfonamide
Vetisulid (Veterinary)
SULFACHLORPYRIDAZINE (MART.)
SULFACHLORPYRIDAZINE (USP-RS)
Prinzone vet.
Solfaclorpiridazina
Solfaclorpiridazina [DCIT]
SCP
SULFACHLORPYRIDAZINE (USP MONOGRAPH)
EINECS 245-553-0
Sulfachlorpyridazinum [INN-Latin]
SR-01000773478
Sulfacloropiridazina [INN-Spanish]
EINECS 201-269-9
N1-(6-Chlor-3-pyridazinyl)sulfanilamid
Cosulid
UNII-P78D9P90C0
Prestwick_130
Sulfachlorpyridazine [USP:INN:BAN]
Sulfanilamide, N1-(6-chloro-3-pyridazinyl)-, monosodium salt
Cosumix (Salt/Mix)
Benzenesulfonamide, 4-amino-N-(6-chloro-3-pyridazinyl)-, monosodium salt
Spectrum_000127
Prestwick0_000715
Prestwick1_000715
Prestwick2_000715
Prestwick3_000715
Spectrum2_001942
Spectrum3_001221
Spectrum4_000444
Spectrum5_001011
Vetisulid Oral Suspension
Epitope ID:122243
cid_6634
Ciba 10370
Oprea1_485631
SCHEMBL94138
BSPBio_000929
BSPBio_002662
KBioGR_000828
KBioSS_000587
SPECTRUM1501142
SPBio_002003
SPBio_002850
BPBio1_001023
Sulfachloropyridazine (Standard)
Sulfachlorpyridazine (USP/INN)
[(4-aminophenyl)sulfonyl](6-chloropyridazin-3-yl)amine
CHEMBL1443577
BDBM90673
GTPL12634
HY-B1781R
KBio2_000587
KBio2_003155
KBio2_005723
KBio3_002162
4-amino-N-(6-chloropyridazin-3-yl)benzene-1-sulfonamide
MSK4034
HMS1570O11
HMS1921J11
HMS2092F19
HMS2097O11
HMS2766B06
HMS3714O11
Pharmakon1600-01501142
ALBB-011657
HY-B1781
STR03778
Tox21_110372
Tox21_112957
BBL037369
CCG-39459
NSC757858
s3708
STK315422
AKOS000308728
Tox21_110372_1
CS-7970
DB11461
NSC 757858
NCGC00016323-02
NCGC00016323-03
NCGC00016323-09
NCGC00094909-01
NCGC00094909-02
AC-12002
SBI-0051655.P002
AB00052217
NS00000002
C76571
D05948
AB00052217_11
SR-01000773478-2
SR-01000773478-3
BRD-K32021043-001-05-1
BRD-K32021043-001-14-3
Q27126423
Sulfachloropyridazine 1000 microg/mL in Acetonitrile
4-Amino-N-(6-chloro-3-pyridazinyl)benzenesulfonamide #
4-azanyl-N-(6-chloranylpyridazin-3-yl)benzenesulfonamide
Pyridazin-3-amine, N-(4-aminophenylsulfonyl)-6-chloro-
Sulfachloropyridazine, VETRANAL(TM), analytical standard
4-AMINO-N-(6-CHLORO-3-PYRIDAZINYL)-1-BENZENESULFONAMIDE
Sulfachlorpyridazine, United States Pharmacopeia (USP) Reference Standard
201-269-9
Solubility of 4-amino-N-(6-chloropyridazin-3-yl)benzenesulfonamide
The solubility of 4-amino-N-(6-chloropyridazin-3-yl)benzenesulfonamide, often referred to as a sulfonamide derivative, is influenced by several factors related to its molecular structure. This compound exhibits some unique solubility characteristics, which can be summarized as follows:
However, it is noteworthy to mention that solubility can vary significantly depending on environmental conditions such as:
In laboratory settings, the solubility of this compound is often measured to inform dosing and formulation decisions, particularly in pharmacological applications. Thus, understanding its solubility behavior is crucial for effective utilization in various chemical contexts.