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Sulfacetamide

产品号 DB00634 公司名称 DrugBank
CAS号 144-80-9 公司网站 http://www.ualberta.ca/
分子式 C8H10N2O3S 电 话 (780) 492-3111
分子量 214.2416 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 516

产品价格信息

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产品别名

标题
Sulfacetamide
IUPAC标准名
N-(4-aminobenzenesulfonyl)acetamide
IUPAC传统名
N-(4-aminobenzenesulfonyl)acetamide
商标名
P-Aminobenzenesulfonoacetamide
Acetosulfamine
Steri-Units Sulfacetamide
Albucid
Sebizon
Bleph-10
Formosulfacetamide
Isopto Cetamide
N-Acetylsulfanilamide
N-Acetylsulfanilamine
Oclucid
P-Aminobenzenesulfonacetamide
Sulamyd
Sulfacet
Sulfacetamide Sodium
Urosulfon
Acetosulfamin
Albamine
Alesten
Gyne-Sulf
Klaron
N-Sulfanilylacetamide
N-Sulphanilylacetamide
Ocusulf-10
Op-Sulfa 30
Ophthacet
Ophthel-S
Region
Sodium Sulfacetamide
Steramide
Sulf-15
Sulfacyl
Sulfair
Sulfair 10
Sulfair 15
Sulfamide
Sulfanilacetamide
Sulfex
Sulphacetamide Sodium
Trysul
Acetocid
Ak-Sulf
Bleph-10 Liquifilm
Cetamide
I-Sulfacet
Isopto-Cetamide
N'-Acetylsulfanilamide
Sodium Sulamyd
Sulf-10
Sulfacel-15
Sulfacetamide Sodium Anhydrous
Sulfacetamide Sodium Usp
Sulfacetimide
Sulfair Forte
Sulfair-15
Sulfanilazetamid
Sulphacetamide
Sulphasil
Sulten-10
Sultrin
Urosulfone

产品登记号

CAS号 144-80-9
PubChem SID 46504544
PubChem CID 5320

产品性质

疏水性(logP) -0.6
溶解度 1.25E+004 mg/L

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description An anti-infective agent that is used topically to treat skin infections and orally for urinary tract infections. [PubChem]
Indication For the treatment of bacterial vaginitis, keratitis, acute conjunctivitis, and blepharitis.
Pharmacology Sulfacetamide 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.
Toxicity Oral LD50 Mouse : 16500 mg/kg. Side effects include moderate to severe erythema (redness) and moderate edema (raised kin), nausea, vomiting, headache, dizziness, and tiredness. Higher exposure causes unconsciousness.
Affected Organisms
Enteric bacteria and other eubacteria
Half Life 7-12.8 hours
References
Hull CA, Johnson SM: A double-blind comparative study of sodium sulfacetamide lotion 10% versus selenium sulfide lotion 2.5% in the treatment of pityriasis (tinea) versicolor. Cutis. 2004 Jun;73(6):425-9. [Pubmed]
Del Rosso JQ: Evaluating the role of topical therapies in the management of rosacea: focus on combination sodium sulfacetamide and sulfur formulations. Cutis. 2004 Jan;73(1 Suppl):29-33. [Pubmed]
Roth HW, Leimbeck R, Sonnenschein B, Anger CB, Weber S: [The effective antibacterial spectrum of sulfacetamide] Klin Monatsbl Augenheilkd. 1992 Mar;200(3):182-6. [Pubmed]
External Links
Wikipedia
RxList
PDRhealth
Drugs.com

参考文献

  • Hull CA, Johnson SM: A double-blind comparative study of sodium sulfacetamide lotion 10% versus selenium sulfide lotion 2.5% in the treatment of pityriasis (tinea) versicolor. Cutis. 2004 Jun;73(6):425-9. Pubmed
  • Del Rosso JQ: Evaluating the role of topical therapies in the management of rosacea: focus on combination sodium sulfacetamide and sulfur formulations. Cutis. 2004 Jan;73(1 Suppl):29-33. Pubmed
  • Roth HW, Leimbeck R, Sonnenschein B, Anger CB, Weber S: [The effective antibacterial spectrum of sulfacetamide] Klin Monatsbl Augenheilkd. 1992 Mar;200(3):182-6. Pubmed