Fumagillin

cas: 23110-15-8 — see every product listed under this CAS number, including other names

Fumagillin (CAS 23110-15-8) is a chemical reagent available from Chemat. Available pack sizes: on request, 10mg, 1mg, 5mg, 25mg, 50mg, 100mg, 500mg. Offered by: Creative Peptides, TRC, GLPBio, Biosynth.

brandCreative Peptides
catalog numberCP-MFP-010
cas23110-15-8
sizeon request
Need more information?

Ask us about this product — we're happy to help.

Available pack sizes

brand size price
Creative Peptides on request price on request
TRC 10mg price on request
TRC 1mg price on request
TRC 5mg price on request
GLPBio 1mg 704.69 Pln
GLPBio 10mg 2193.09 Pln
GLPBio 25mg 3278.97 Pln
GLPBio 5mg 1411.45 Pln
Biosynth 25mg price on request
Biosynth 50mg price on request
Biosynth 100mg price on request
Biosynth 500mg price on request
Biosynth 250mg price on request
HPC Standards 1x1mg 1136.64 Pln

properties

purityNo data
delivery timeTo be confirmed by Chemat
Structural formula: {0} (CAS {1})

Fumagillin is a meroterpenoid resulting from the formal condensation of the hydroxy group of fumagillol with the carboxylic acid group of (all-E)-deca-2,4,6,8-tetraenedioic acid. Originally isolated from the fungus Aspergillus fumigatus, it is used for the control of Nosema infection in honey bees. It has a role as an antimicrobial agent, an antiprotozoal drug, an antibacterial drug, an angiogenesis inhibitor, a methionine aminopeptidase 2 inhibitor and a fungal metabolite. It is a spiro-epoxide, an organooxygen heterocyclic antibiotic, a carboxylic ester, a dicarboxylic acid monoester, a meroterpenoid and an antibiotic antifungal drug. It is functionally related to a fumagillol and an (all-E)-deca-2,4,6,8-tetraenedioic acid.

Source: ChEBI

Identity
Molecular formulaC26H34O7
Molecular weight458.5 g/mol
IUPAC name(2E,4E,6E,8E)-10-[[(3R,4S,5S,6R)-5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-enyl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-yl]oxy]-10-oxodeca-2,4,6,8-tetraenoic acid
InChIKeyNGGMYCMLYOUNGM-CSDLUJIJSA-N
SMILESCC(=CC[C@@H]1[C@@](O1)(C)[C@H]2[C@@H]([C@@H](CC[C@]23CO3)OC(=O)/C=C/C=C/C=C/C=C/C(=O)O)OC)C

Computed by PubChem (NCBI)

Also listed as