CAS 56092-82-1
:10,16-Docosadienoic acid, 11,19,21-trihydroxy-4,6,8,12,14,18,20-heptamethyl-22-[(2S,2′R,5S,5′S)-octahydro-5′-[(1R)-1-hydroxyethyl]-2,5′-dimethyl[2,2′-bifuran]-5-yl]-9-oxo-, calcium salt (1:1), (4R,6S,8S,10Z,12R,14R,16E,18R,19R,20S,21S)-
Description:
10,16-Docosadienoic acid, 11,19,21-trihydroxy-4,6,8,12,14,18,20-heptamethyl-22-[(2S,2′R,5S,5′S)-octahydro-5′-[(1R)-1-hydroxyethyl]-2,5′-dimethyl[2,2′-bifuran]-5-yl]-9-oxo-, calcium salt (1:1) is a complex organic compound characterized by its long carbon chain and multiple functional groups, including hydroxyl and keto groups. This compound features a unique structure with multiple methyl groups and a bifuran moiety, contributing to its potential biological activity. The presence of calcium as a salt indicates its ionic nature, which may influence its solubility and stability in various environments. The stereochemistry of the molecule, denoted by specific configurations at various chiral centers, suggests that it may exhibit specific interactions in biological systems, potentially impacting its pharmacological properties. Overall, this compound's intricate structure and functional diversity make it a subject of interest in fields such as medicinal chemistry and biochemistry, where understanding its properties could lead to applications in drug development or therapeutic interventions.
Formula:C41H72O9·Ca
InChI:InChI=1S/C41H72O9.Ca/c1-25(21-29(5)34(43)24-35(44)30(6)22-27(3)20-26(2)14-15-38(46)47)12-11-13-28(4)39(48)31(7)36(45)23-33-16-18-41(10,49-33)37-17-19-40(9,50-37)32(8)42;/h11,13,24-33,36-37,39,42-43,45,48H,12,14-23H2,1-10H3,(H,46,47);/b13-11+,34-24-;/t25-,26-,27+,28-,29-,30+,31+,32-,33+,36+,37-,39-,40+,41+;/m1./s1
InChI key:InChIKey=MERVBOMMKAULKQ-WYGBAUISSA-N
SMILES:C[C@@]1(O[C@H](C[C@@H]([C@@H]([C@@H]([C@@H](/C=C/C[C@H](C[C@H](/C(=C/C([C@H](C[C@H](C[C@@H](CCC(O)=O)C)C)C)=O)/O)C)C)C)O)C)O)CC1)[C@@]2(O[C@@]([C@@H](C)O)(C)CC2)[H].[Ca]
Synonyms:- 10,16-Docosadienoic acid, 11,19,21-trihydroxy-4,6,8,12,14,18,20-heptamethyl-22-[(2S,2′R,5S,5′S)-octahydro-5′-[(1R)-1-hydroxyethyl]-2,5′-dimethyl[2,2′-bifuran]-5-yl]-9-oxo-, calcium salt (1:1), (4R,6S,8S,10Z,12R,14R,16E,18R,19R,20S,21S)-
- Calcium ionomycin
- Ionomycin calcium salt
- Ionomycin, calcium salt (1:1)
- calcium (4R,6S,8S,10Z,12R,14R,16E,18R,19R,20S,21S)-19,21-dihydroxy-22-{(2S,2'R,5S,5'S)-5'-[(1R)-1-hydroxyethyl]-2,5'-dimethyloctahydro-2,2'-bifuran-5-yl}-4,6,8,12,14,18,20-heptamethyl-11-oxido-9-oxodocosa-10,16-dienoate
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Found 7 products.
Ionomycin calcium salt, 1 mg/ml in methanol, sterile-filtered
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Ionomycin calcium salt
CAS:Formula:C41H70CaO9Purity:≥ 98%Color and Shape:White or almost white powderMolecular weight:747.08Ionomycin calcium salt
CAS:<p>Ionomycin calcium salt</p>Formula:C41H70O9·CaPurity:By hplc: 98.05% (Typical Value in Batch COA)Color and Shape: slight yellow powderMolecular weight:747.0671g/molIonomycin Calcium
CAS:Controlled Product<p>Stability Light Sensitive, Moisture Sensitive<br>Applications Ionomycin Calcium is a polyether antibiotic obtained from Streptomyces conglobatus by solvent extraction. It is different from other antibiotics of its class as it absorbs UV light at 300nm maximum. Gram-positive antibiotic.<br>References Liu, W., et al.: J. Antibio., 31, 815 (1978); Liu, C., et al.: J. Biol. Chem., 253, 5892 (1978);<br></p>Formula:C41CaH70O9Color and Shape:NeatMolecular weight:747.07Ionomycin calcium
CAS:<p>Ionomycin calcium (SQ23377 calcium) is an effective and selective calcium ionophore, exhibiting high specificity for calcium ions. Cost-effective and quality-assured.</p>Formula:C41H70CaO9Purity:98% - 98.11%Color and Shape:SolidMolecular weight:747.07Ionomycin calcium
CAS:<p>Ionomycin calcium is a potent calcium ionophore, which is derived from natural sources such as certain Streptomyces species. Its primary mode of action involves facilitating the translocation of calcium ions (Ca^2+) across biological membranes, specifically transporting them from external environments or intracellular stores into the cytoplasm. This action significantly elevates intracellular calcium levels.</p>Formula:C41H70O9•CaPurity:Min. 95%Molecular weight:747.07 g/mol







