cas: 21411-53-0 — see every product listed under this CAS number, including other names
Virginiamycin M1 (CAS 21411-53-0) is a chemical reagent available from Chemat. Available pack sizes: on request, 1mg, 10mg, 5mg, 10mM (in 1ml dmso), 2mg, 25MG. Offered by: Chemat Brand, GLPBio, Biosynth, Thermo Scientific (Acros).
| brand | Chemat Brand |
|---|---|
| catalog number | ULV171 |
| cas | 21411-53-0 |
| size | on request |
| availability | Do potwierdzenia przez Chemat|To be confirmed by Chemat |
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| brand | size | price | |
|---|---|---|---|
| Chemat Brand | on request | price on request | |
| GLPBio | 1mg | 1224.23 Pln | |
| GLPBio | 10mg | 2647.10 Pln | |
| GLPBio | 5mg | 1930.98 Pln | |
| GLPBio | 10mM (in 1ml dmso) | 2169.69 Pln | |
| Biosynth | 2mg | price on request | |
| Biosynth | 1mg | price on request | |
| Thermo Scientific (Acros) | 25MG | 1309.61 Pln | |
| Biosynth | 5mg | price on request | |
| Biosynth | 25mg | price on request | |
| Biosynth | 10mg | price on request |
| purity | No data |
|---|---|
| category | Chemicals |
| delivery time | To be confirmed by Chemat |
Pristinamycin IIA is a macrolide that is (together with pristinamycin IA) a component of pristinamycin, an oral streptogramin antibiotic produced by Streptomyces pristinaespiralis. Pristinamycin exhibits bactericidal activity against Gram positive organisms including methicillin-resistant Staphylococcus aureus. It has a role as a Mycoplasma genitalium metabolite and an antibacterial drug. It is a secondary carboxamide, a tertiary carboxamide, a pyrroline, a lactam, a macrolide antibiotic, a macrolide, a secondary alcohol, a cyclic ketone, a member of 1,3-oxazoles and an enamide.
Source: ChEBI
| Molecular formula | C28H35N3O7 |
|---|---|
| Molecular weight | 525.6 g/mol |
| IUPAC name | (10R,11R,12E,17E,19E,21S)-21-hydroxy-11,19-dimethyl-10-propan-2-yl-9,26-dioxa-3,15,28-triazatricyclo[23.2.1.03,7]octacosa-1(27),6,12,17,19,25(28)-hexaene-2,8,14,23-tetrone |
| InChIKey | DAIKHDNSXMZDCU-FQTGFAPKSA-N |
| SMILES | C[C@@H]1/C=C/C(=O)NC/C=C/C(=C/[C@H](CC(=O)CC2=NC(=CO2)C(=O)N3CCC=C3C(=O)O[C@@H]1C(C)C)O)/C |
Computed by PubChem (NCBI)