CAS 56092-82-1: Ácido docosadienoico 10,16, 11,19,21-trihidroxi-4,6,8,12,14,18,20-heptametil-22-[(2S,2′R,5S,5′S)-octahidro-5′-[(1R)-1-hidroxietil]-2,5′-dimetil[2,2′-bifurano]-5-il]-9-oxo-, sal de calcio (1:1), (4R,6S,8S,10Z,12R,14R,16E,18R,19R,20S,21S)-
Descripción:
El ácido 10,16-docosadienoico, 11,19,21-trihidroxi-4,6,8,12,14,18,20-heptametilo-22-[(2S,2′R,5S,5′S)-octahidro-5′-[(1R)-1-hidroxietilo]-2,5′-dimetil[2,2′-bifurano]-5-il]-9-oxo-, sal de calcio (1:1) es un compuesto orgánico complejo caracterizado por su larga cadena de carbono y múltiples grupos funcionales, incluidos grupos hidroxilo y ceto. Este compuesto presenta una estructura única con múltiples grupos metilo y una porción de bifurano, lo que contribuye a su potencial actividad biológica. La presencia de calcio como sal indica su naturaleza iónica, lo que puede influir en su solubilidad y estabilidad en diversos entornos. La estereoquímica de la molécula, denotada por configuraciones específicas en varios centros quirales, sugiere que puede exhibir interacciones específicas en sistemas biológicos, lo que podría impactar sus propiedades farmacológicas. En general, la intrincada estructura y diversidad funcional de este compuesto lo convierten en un tema de interés en campos como la química medicinal y la bioquímica, donde comprender sus propiedades podría llevar a aplicaciones en el desarrollo de fármacos o intervenciones terapéuticas.
Fórmula: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
Clave InChI: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]
Sinónimos:- 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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Encontrado 7 productos.
Ionomycin calcium
CAS:Ionomycin calcium (SQ23377 calcium) is an effective and selective calcium ionophore, exhibiting high specificity for calcium ions. Cost-effective and quality-assured.Fórmula:C41H70CaO9Pureza:98% - 98.11%Forma y color:SolidPeso molecular:747.07Ionomycin calcium salt
CAS:Fórmula:C41H70CaO9Pureza:≥ 98%Forma y color:White or almost white powderPeso molecular:747.08Ionomycin calcium
CAS: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. Ionomycin calcium is widely employed in scientific research to study calcium-dependent cellular processes. It serves as a valuable tool in immunology for the activation of T cells and in neuroscience for exploring calcium signaling pathways. Additionally, it is utilized to investigate the role of calcium in apoptosis, cell proliferation, and various other physiological responses. By enabling precise manipulation of calcium dynamics, ionomycin calcium aids scientists in dissecting the intricate roles of calcium in cellular functions.Fórmula:C41H70O9•CaPureza:Min. 95%Peso molecular:747.07 g/molIonomycin Calcium
CAS:Producto controladoStability Light Sensitive, Moisture Sensitive 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. References Liu, W., et al.: J. Antibio., 31, 815 (1978); Liu, C., et al.: J. Biol. Chem., 253, 5892 (1978);Fórmula:C41CaH70O9Forma y color:NeatPeso molecular:747.07Ionomycin calcium salt, 1 mg/ml in methanol, sterile-filtered
CAS: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 Scientific Chemicals.Ionomycin calcium salt
CAS:Ionomycin calcium saltFórmula:C41H70O9·CaPureza:By hplc: 98.05% (Typical Value in Batch COA)Forma y color: slight yellow powderPeso molecular:747.07g/mol
