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Ionomycin, Free Acid | CAS [56092-81-0] | Calcium Ionophore | A.G. Scientific

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Ionomycin, Free Acid | CAS [56092-81-0] | Calcium Ionophore | A.G. Scientific

品牌：AG Scientific

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規格：1 mg

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CAS:56092-81-0Formula:C41H72O9MW:709Appearance:WaxycolorlesstoyellowmaterialPurity:99.57%

商品詳情參考文獻相關資料

Ionomycin, free acid, is a highly specific ionophore useful in studying Ca2+ transportation. FromStreptomyces conglobatus. Highly specific ionophore useful in studying Ca2+ transportation.The Mitochondrial Permeability Transition Regulates Cytochrome c Release for Apoptosis during Endoplasmic Reticulum Stress by Remodeling the Cristae Junction.HIV-1-Specific Interleukin-21+ CD4+ T Cell Responses Contribute to Durable Viral Control through the Modulation of HIV-Specific CD8+ T Cell Function.Frequent and Strong Antibody-Mediated Natural Killer Cell Activation in Response to HIV-1 Env in Individuals with Chronic HIV-1 Infection.LIME acts as a transmembrane adapter mediating BCR-dependent B-cell activation.Immune-driven recombination and loss of control after HIV superinfection.

Additional Information

Product #	I-1014
CAS #	56092-81-0
Chemical Name	(4R,6S,8S,10Z,12R,14R,16E,18R,19R,20S,21S)-11,19,21-TRIHYDROXY-22-((2S,2'R,5S,5'S)-5'-((R)-1-HYDROXYETHYL)-2,5'-DIMETHYLOCTAHYDRO-[2,2'-BIFURAN]-5-YL)-4,6,8,12,14,18,20-HEPTAMETHYL-9-OXODOCOSA-10,16-DIENOIC ACID
Formula	C₄₁H₇₂O₉
MW	709
Appearance	Waxy colorless to yellow material
Purity	99.57%
Solubility	DMSO/DCM/CH₃OH: clear colorless solution at 10 mg/ml
Storage Temp	Store at room temperature. Protect from light.
Use	A potent and selective calcium ionophore

Additional Information

MDL Number	MFCD06798385
ChemACX	X1098403-1
InChI	InChI=1S/C41H72O9/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
SMILES	C[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

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