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Sulfaguanidine

Catalog No. S8751 Name Sigma Aldrich
CAS Number 57-67-0 Website http://www.sigmaaldrich.com
M. F. C7H10N4O2S Telephone 1-800-521-8956
M. W. 214.2449 Fax
Purity Email
Storage Chembase ID: 23546

SYNONYMS

Title
磺胺脒
IUPAC name
1-(4-aminobenzenesulfonyl)guanidine
IUPAC Traditional name
aterian
Synonyms
4-氨基-N-脒基苯磺酰胺
4-Amino-N-guanylbenzenesulfonamide
4-氨基-N-(氨基亚氨基甲基)苯磺酰胺
4-Amino-N-(aminoiminomethyl)benzenesulfonamide

DATABASE IDS

PubChem SID 24899810
Beilstein Number 2695326
CAS Number 57-67-0
MDL Number MFCD00038136
EC Number 200-345-9

PROPERTIES

Empirical Formula (Hill Notation) C7H10N4O2S
Gene Information human ... F2(2147), PRSS1(5644)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
RTECS WO8575000
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Application
Sulfaguanidine is used to block the synthesis of folic acid. It is used to study its effect on microsporidial growth and host cell viability2.
Biochem/physiol Actions
Sulfaguanidine is a sulfonamide antibiotic. Sulfonamides block the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase. Sulfonamides are competitive inhibitors of bacterial para-aminobenzoic acid (PABA), which is required for bacterial synthesis of folic acid1. Sulfaguanidine is a dihydrofolate reductase (DHFR) inhibitor. Sulfonamides are active against Gram positive bacteria and Gram negative bacteria. Mode of resistance is via the alteration of dihydropteroate synthase or alternative pathway for folic acid synthesis.
Description (简体中文)
Application
Sulfaguanidine is used to block the synthesis of folic acid. It is used to study its effect on microsporidial growth and host cell viability2.
Biochem/physiol Actions
Sulfaguanidine is a sulfonamide antibiotic. Sulfonamides block the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase. Sulfonamides are competitive inhibitors of bacterial para-aminobenzoic acid (PABA), which is required for bacterial synthesis of folic acid1. Sulfaguanidine is a dihydrofolate reductase (DHFR) inhibitor. Sulfonamides are active against Gram positive bacteria and Gram negative bacteria. Mode of resistance is via the alteration of dihydropteroate synthase or alternative pathway for folic acid synthesis.

REFERENCES