Ionomycin, 99.27%

cas: 56092-81-0 — see every product listed under this CAS number, including other names

Ionomycin, 99.27% (CAS 56092-81-0) is a chemical reagent available from Chemat. Available pack sizes: 1 mg (14.1 mM * 100 μL in Ethanol), 10 mg (14.1 mM * 1 mL in Ethanol), 25 mg (14.1 mM * 2.5 mL in Ethanol), 50 mg (14.1 mM * 5 mL in Ethanol), 5 mg (14.1 mM * 500 μL in Ethanol). Offered by: MedChemExpress.

brandMedChemExpress
catalog numberHY-13434-1 mg (14.1 mM * 100 μL in Ethanol)
cas56092-81-0
size1 mg (14.1 mM * 100 μL in Ethanol)
availability In stock
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Available pack sizes

brand size price
MedChemExpress 1 mg (14.1 mM * 100 μL in Ethanol) 867.68 Pln
MedChemExpress 10 mg (14.1 mM * 1 mL in Ethanol) 2363.05 Pln
MedChemExpress 25 mg (14.1 mM * 2.5 mL in Ethanol) 4350.68 Pln
MedChemExpress 50 mg (14.1 mM * 5 mL in Ethanol) 6890.95 Pln
MedChemExpress 5 mg (14.1 mM * 500 μL in Ethanol) 1615.37 Pln

properties

delivery time 2-3 weeks
purity99.27%
Structural formula: {0} (CAS {1})

Ionomycin is a very long-chain fatty acid that is docosa-10,16-dienoic acid which is substituted by methyl groups at positions 4, 6, 8, 12, 14, 18 and 20, by hydroxy groups at positions 11, 19 and 21, and by a (2',5-dimethyloctahydro-2,2'-bifuran-5-yl)ethanol group at position 21. An ionophore produced by Streptomyces conglobatus, it is used in research to raise the intracellular level of Ca2+ and as a research tool to understand Ca2+ transport across biological membranes. It has a role as a calcium ionophore and a metabolite. It is a polyunsaturated fatty acid, a very long-chain fatty acid, an enol and a cyclic ether.

Source: ChEBI

Identity
Molecular formulaC41H72O9
Molecular weight709.0 g/mol
IUPAC name(4R,6S,8S,10Z,12R,14R,16E,18R,19R,20S,21S)-11,19,21-trihydroxy-22-[(2S,5S)-5-[(2R,5S)-5-[(1R)-1-hydroxyethyl]-5-methyloxolan-2-yl]-5-methyloxolan-2-yl]-4,6,8,12,14,18,20-heptamethyl-9-oxodocosa-10,16-dienoic acid
InChIKeyPGHMRUGBZOYCAA-ADZNBVRBSA-N
SMILESC[C@H](CCC(=O)O)C[C@H](C)C[C@H](C)C(=O)/C=C(/[C@H](C)C[C@H](C)C/C=C/[C@@H](C)[C@H]([C@@H](C)[C@H](C[C@@H]1CC[C@@](O1)(C)[C@H]2CC[C@@](O2)(C)[C@@H](C)O)O)O)\O

Computed by PubChem (NCBI)

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