Gamithromycin
cas: 145435-72-9 — see every product listed under this CAS number, including other names
Gamithromycin (CAS 145435-72-9) is a chemical reagent available from Chemat. Available pack sizes: on request, 50mg, 2g, 5g, 10g, 25g, 50g, 25MG. Offered by: Chemat Brand, Dr. Ehrenstorfer, Biosynth, Sigma-Aldrich.
| brand | Chemat Brand |
|---|---|
| catalog number | ULG057003 |
| cas | 145435-72-9 |
| size | on request |
| availability | Do potwierdzenia przez Chemat|To be confirmed by Chemat |
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Available pack sizes
| brand | size | price | |
|---|---|---|---|
| Chemat Brand | on request | price on request | |
| Dr. Ehrenstorfer | 50mg | price on request | |
| Biosynth | 2g | price on request | |
| Biosynth | 5g | price on request | |
| Biosynth | 10g | price on request | |
| Biosynth | 25g | price on request | |
| Biosynth | 50g | price on request | |
| Sigma-Aldrich | 25MG | 977.00 Pln | |
| HPC Standards | 1x50mg | 840.05 Pln |
properties
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Gamithromycin is a macrolide antibiotic with formula C40H76N2O12. It is used for the treatment of of bovine respiratory disease caused by Mannheimia haemolytica, Pasteurella multocida, Histophilus somni and Mycoplasma bovis in beef and non-lactating dairy cattle. The compound is also licensed in Europe for the treatment of footrot in sheep caused by Dichelobacter nodosus and Fusobacterium nodosus. It has a role as an antibacterial drug and a protein synthesis inhibitor. It is a macrolide antibiotic and a monosaccharide derivative.
Source: ChEBI
| Molecular formula | C40H76N2O12 |
|---|---|
| Molecular weight | 777.0 g/mol |
| IUPAC name | (2R,3S,4R,5S,8R,10R,11R,12S,13S,14R)-11-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-2-ethyl-3,4,10-trihydroxy-13-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,8,10,12,14-hexamethyl-7-propyl-1-oxa-7-azacyclopentadecan-15-one |
| InChIKey | VWAMTBXLZPEDQO-UZSBJOJWSA-N |
| SMILES | CCCN1C[C@@H]([C@H]([C@]([C@H](OC(=O)[C@@H]([C@H]([C@@H]([C@H]([C@](C[C@H]1C)(C)O)O[C@H]2[C@@H]([C@H](C[C@H](O2)C)N(C)C)O)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)O)(C)OC)C)CC)(C)O)O)C |
Computed by PubChem (NCBI)