Sulfalene
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Sulfalene
structure -
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CAS No:
152-47-6
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Formula:
C11H12N4O3S
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Chemical Name:
Sulfalene
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Synonyms:
Benzenesulfonamide,4-amino-N-(3-methoxy-2-pyrazinyl)-;Sulfanilamide,N1-(3-methoxypyrazinyl)-;Benzenesulfonamide,4-amino-N-(3-methoxypyrazinyl)-;4-Amino-N-(3-methoxy-2-pyrazinyl)benzenesulfonamide;F.I. 5978;AS 18908;Kelfizin;Kelfizina;3-Methoxypyrazine sulfanilamide;N1-(3-Methoxy-2-pyrazinyl)sulfanilamide;3-Methoxy-2-sulfapyrazine;SMP2;Sulfalene;Sulfamethopyrazine;Sulfamethoxypyrazine;Sulfametopyrazine;2-Sulfanilamido-3-methoxypyrazine;Sulfapyrazinemethoxine;Sulfapyrazinemethoxyne;Polycidal;3-Methoxy-2-sulfanilamidopyrazine;Sulfapyrazinemethoxyine;2-Methoxy-3-sulfanilamidopyrazine;Kelfizine W;Longum;Farmitalia 204/122;Policydal;Dalysep;NSC 110433;Vetkelfizina
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CAS No:
Description
White to Yellow Solid
Solid
Sulfamethopyrazine is a member of pyrazines, a sulfonamide and a sulfonamide antibiotic.|Long-acting plasma-bound sulfonamide used for respiratory and urinary tract infections and also for malaria.|Sulfalene is a long-acting sulfonamide antibiotic used for the treatment of chronic bronchitis, urinary tract infections and malaria.
Sulfalene Basic Attributes
280.3
280.30
205-804-7
T6BL4ZC15G
110433
DTXSID2046179
C80793
J - Antiinfectives for systemic use
2935009090
Characteristics
116
0.7
Solid
1.3936 (rough estimate)
176 °C
488.6±55.0 °C(Predicted)
249.3±31.5 °C
1.6200 (estimate)
>42 [ug/mL]
1.07E-09mmHg at 25°C
LD50 in mice (g/kg): 2.164 orally; 1.41 i.v. ( US 3098069 )
Safety Information
IRRITANT
3
R36/37/38:Irritating to eyes, respiratory system and skin .
S26-S36
WP0175000
Xi
P201, P202, P260, P263, P264, P270, P280, P281, P301+P312, P302+P352, P305+P351+P338, P308+P313, P321, P330, P332+P313, P337+P313, P362, P405, P501
H302
Drug Information
For the treatment of urinary tract infection and chronic bronchitis.
Sulfametopyrazine is a sulfonamide antibiotic. The sulfonamides are synthetic bacteriostatic antibiotics with a wide spectrum against most gram-positive and many gram-negative organisms. However, many strains of an individual species may be resistant. Sulfonamides inhibit multiplication of bacteria by acting as competitive inhibitors of p-aminobenzoic acid in the folic acid metabolism cycle. Bacterial sensitivity is the same for the various sulfonamides, and resistance to one sulfonamide indicates resistance to all. Most sulfonamides are readily absorbed orally. However, parenteral administration is difficult, since the soluble sulfonamide salts are highly alkaline and irritating to the tissues. The sulfonamides are widely distributed throughout all tissues. High levels are achieved in pleural, peritoneal, synovial, and ocular fluids. Although these drugs are no longer used to treat meningitis, CSF levels are high in meningeal infections. Their antibacterial action is inhibited by pus.
Substances that prevent infectious agents or organisms from spreading or kill infectious agents in order to prevent the spread of infection. (See all compounds classified as Anti-Infective Agents.)|Substances capable of killing agents causing urinary tract infections or of preventing them from spreading. (See all compounds classified as Anti-Infective Agents, Urinary.)|Agents used in the treatment of malaria. They are usually classified on the basis of their action against plasmodia at different stages in their life cycle in the human. (From AMA, Drug Evaluations Annual, 1992, p1585) (See all compounds classified as Antimalarials.)
Sulfametopyrazine is a competitive inhibitor of the bacterial enzyme dihydropteroate synthetase. Para-aminobenzoic acid (PABA), a substrate of the enzyme is prevented from binding. The inhibited reaction is necessary in these organisms for the synthesis of folic acid.
Kelfizine
Computed Properties
Molecular Weight:280.31
XLogP3:0.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:4
Exact Mass:280.06301143
Monoisotopic Mass:280.06301143
Topological Polar Surface Area:116
Heavy Atom Count:19
Complexity:376
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Not yet clear
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