Entry |
|
Name |
Sulfamethoxypyridazine (INN); Lederkyn (TN) |
Formula |
C11H12N4O3S
|
Exact mass |
280.063
|
Mol weight |
280.303
|
Structure |
|
Simcomp |
|
Class |
Antibacterial
DG01787 Sulfonamide antibacterial
DG01786 Long-acting sulfonamide
|
Remark |
|
Efficacy |
Antibacterial, Folic acid biosynthesis inhibitor |
Target |
dihydropteroate synthase [KO: K00796] |
Pathway |
|
Interaction |
|
Structure map |
map07016 | Sulfonamide derivatives - sulfa drugs |
|
Brite |
Anatomical Therapeutic Chemical (ATC) classification [BR:br08303]
J ANTIINFECTIVES FOR SYSTEMIC USE
J01 ANTIBACTERIALS FOR SYSTEMIC USE
J01E SULFONAMIDES AND TRIMETHOPRIM
J01ED Long-acting sulfonamides
J01ED05 Sulfamethoxypyridazine
D02439 Sulfamethoxypyridazine (INN)
Drug groups [BR:br08330]
Antibacterial
DG01787 Sulfonamide antibacterial
DG01786 Long-acting sulfonamide
DG00601 Sulfamethoxypyridazine
D02439 Sulfamethoxypyridazine
Antimicrobials [BR:br08307]
Antibacterials
Folic acid biosynthesis inhibitor
Long-acting sulfonamide
D02439 Sulfamethoxypyridazine (INN)
Drug groups [BR:br08330]
Antibacterial
DG01787 Sulfonamide antibacterial
DG01786 Long-acting sulfonamide
DG00601 Sulfamethoxypyridazine
|
Other DBs |
|
KCF data |
ATOM 19
1 C8y C 23.8623 -17.0620
2 S4a S 25.0724 -16.3639
3 C8x C 23.8623 -18.4583
4 C8x C 22.6987 -16.3639
5 N1b N 26.2825 -17.0620
6 O3c O 26.0498 -15.3865
7 O3c O 24.0950 -15.3865
8 C8x C 22.6987 -19.2030
9 C8x C 21.4886 -17.0620
10 C8y C 27.4927 -16.3639
11 C8y C 21.4886 -18.4583
12 N1a N 20.2320 -19.2030
13 C8x C 28.7016 -17.0624
14 C8x C 29.9110 -16.3647
15 C8y C 29.9115 -14.9684
16 N5x N 28.6326 -14.2699
17 N5x N 27.4932 -14.9676
18 O2a O 31.1222 -14.2699
19 C1a C 32.3315 -14.9686
BOND 20
1 1 2 1
2 1 3 2
3 1 4 1
4 2 5 1
5 2 6 2
6 2 7 2
7 3 8 1
8 4 9 2
9 5 10 1
10 8 11 2
11 11 12 1
12 9 11 1
13 10 13 2
14 13 14 1
15 14 15 2
16 15 16 1
17 16 17 2
18 10 17 1
19 15 18 1
20 18 19 1
|