maxdazol

Also known as spiramycin I

Spiramycin is a macrolide antibiotic and antiparasitic. It is used to treat toxoplasmosis and various other infections of soft tissues.

In the Vinony graph

Vinony's link graph records 125 inbound references to maxdazol, and connects out to neomycin, antibiotic and digital object identifier.

Vinony links it to 24 Wikipedia language editions.

Formula: C43H74N2O14
Molecular weight: 843.1 g/mol
IUPAC name: 2-[(4R,5S,6S,7R,9R,10R,11E,13E,16R)-6-[(2S,3R,4R,5S,6R)-5-[(2S,4R,5S,6S)-4,5-dihydroxy-4,6-dimethyloxan-2-yl]oxy-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-10-[(2R,5S,6S)-5-(dimethylamino)-6-methyloxan-2-yl]oxy-4-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-1-oxacyclohexadeca-11,13-dien-7-yl]acetaldehyde
SMILES: C[C@@H]1C/C=C/C=C/[C@@H]([C@@H](C[C@@H]([C@@H]([C@H]([C@@H](CC(=O)O1)O)OC)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)O)(C)O)N(C)C)O)CC=O)C)O[C@H]4CC[C@@H]([C@@H](O4)C)N(C)C
InChIKey: ACTOXUHEUCPTEW-KWBWCIJSSA-N
XLogP: 2.1
Polar surface area: 195 Å²
H-bond donors: 4
H-bond acceptors: 16
Formal charge: 0

via PubChem

1,735 papers

Spiramycin renaissance.The Journal of antimicrobial chemotherapy · 1998
[Spiramycin].Casopis lekaru ceskych · 1994
SPIRAMYCIN.Canadian Medical Association journal · 1958
SPIRAMYCIN.British medical journal · 1956
Pharmacodynamics and pharmacokinetics of spiramycin and their clinical significance.Clinical pharmacokinetics · 1998

Show 4 more facts

chemical formula: C₄₃H₇₄N₂O₁₄
canonical SMILES: CC1CC=CC=CC(C(CC(C(C(C(CC(=O)O1)O)OC)OC2C(C(C(C(O2)C)OC3CC(C(C(O3)C)O)(C)O)N(C)C)O)CC=O)C)OC4CCC(C(O4)C)N(C)C
isomeric SMILES: CC1C/C=C/C=C/C(C(CC(C(C(C(CC(=O)O1)O)OC)OC2C(C(C(C(O2)C)OC3CC(C(C(O3)C)O)(C)O)N(C)C)O)CC=O)C)OC4CCC(C(O4)C)N(C)C
Commons category: Spiramycin

Sources (2)

via Wikidata · CC0