Identification of isobaric amino-sulfonamides without prior separation.[Clinical and experimental studies on the chemotherapeutic effectiveness of sulfadiazines substituted in position 5 and the combination of 5-methylsulfadiazine with a derivative of penicillin.][Antibacterial properties of 5-methylsulfadiazine and phenoxymethylpenicillin in combined use and in the presence of penicillinase.]
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
Sulfaperin
@sh
Sulfaperin
@sr
sulfaperin
@en
سلفابيرين
@ar
سولفاپرین
@fa
ซัลฟาเพอริน
@th
磺胺培林
@zh
type
label
Sulfaperin
@sh
Sulfaperin
@sr
sulfaperin
@en
سلفابيرين
@ar
سولفاپرین
@fa
ซัลฟาเพอริน
@th
磺胺培林
@zh
altLabel
2-(p-aminobenzenesulfonamido)-5-methylpyrimidine
@en
2-(sulfanilamido)-5-methylpyrimidine
@en
4-amino-N-(5-methyl-2-pyrimidinyl)benzenesulfonamide
@en
5-methylsulfadiazine
@en
N(1)-(5-methyl-2-pyrimidinyl)sulfanilamide
@en
Sulfaperin
@ar
isosulfamerazine
@en
methylsulfadiazine
@en
السلفابيرين
@ar
prefLabel
Sulfaperin
@sh
Sulfaperin
@sr
sulfaperin
@en
سلفابيرين
@ar
سولفاپرین
@fa
ซัลฟาเพอริน
@th
磺胺培林
@zh
P592
P661
P662
P665
P683
P1579
P2067
P2275
sulfaperin
@en
P231
P232
P233
CC1=CN=C(N=C1)NS(=O)(=O)C2=CC=C(C=C2)N
P234
1S/C11H12N4O2S/c1-8-6-13-11(14 ...... 10/h2-7H,12H2,1H3,(H,13,14,15)
P235
DZQVFHSCSRACSX-UHFFFAOYSA-N
P2566
100.009.071
P267
P274
C₁₁H₁₂N₄O₂S
P3117
DTXSID2057782
P592
CHEMBL2105499
P652
W5E840UV9P