Mupirocin

cas: 12650-69-0 — see every product listed under this CAS number, including other names

Mupirocin (CAS 12650-69-0) is a chemical reagent available from Chemat. Available pack sizes: on request, 250mg, 10mg, 100mg, 25mg, 10mM (in 1ml dmso), 5g, 10g. Offered by: Chemat Brand, Mikromol, GLPBio, Biosynth.

brandChemat Brand
catalog numberULM1816
cas12650-69-0
sizeon 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
Mikromol 250mg price on request
GLPBio 10mg 587.68 Pln
GLPBio 100mg 1631.43 Pln
GLPBio 25mg 760.86 Pln
GLPBio 10mM (in 1ml dmso) 587.68 Pln
Biosynth 5g price on request
Biosynth 10g price on request
Biosynth 25g price on request
Biosynth 50g price on request
Biosynth 100g price on request

properties

purityNo data
categoryChemicals
delivery timeTo be confirmed by Chemat

Mupirocin is an alpha,beta-unsaturated ester resulting from the formal condensation of the alcoholic hydroxy group of 9-hydroxynonanoic acid with the carboxy group of (2E)-4-[(2S)-tetrahydro-2H-pyran-2-yl]-3-methylbut-2-enoic acid in which the tetrahydropyranyl ring is substituted at positions 3 and 4 by hydroxy groups and at position 5 by a {(2S,3S)-3-[(2S,3S)-3-hydroxybutan-2-yl]oxiran-2-yl}methyl group. Originally isolated from the Gram-negative bacterium Pseudomonas fluorescens, it is used as a topical antibiotic for the treatment of Gram-positive bacterial infections. It has a role as an antibacterial drug, a protein synthesis inhibitor and a bacterial metabolite. It is a monocarboxylic acid, a triol, an epoxide, a secondary alcohol, a member of oxanes and an alpha,beta-unsaturated carboxylic ester. It is a conjugate acid of a mupirocin(1-).

Source: ChEBI

Identity
Molecular formulaC26H44O9
Molecular weight500.6 g/mol
IUPAC name9-[(E)-4-[(2S,3R,4R,5S)-3,4-dihydroxy-5-[[(2S,3S)-3-[(2S,3S)-3-hydroxybutan-2-yl]oxiran-2-yl]methyl]oxan-2-yl]-3-methylbut-2-enoyl]oxynonanoic acid
InChIKeyMINDHVHHQZYEEK-HBBNESRFSA-N
SMILESC[C@H]([C@H]1[C@@H](O1)C[C@H]2CO[C@H]([C@@H]([C@@H]2O)O)C/C(=C/C(=O)OCCCCCCCCC(=O)O)/C)[C@H](C)O

Computed by PubChem (NCBI)

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