Calcimycin hemimagnesium

For research use only. Not for therapeutic Use.

  • CAT Number: I015171
  • CAS Number: 72124-77-7
  • Molecular Formula: C₅₈H₇₂MgN₆O₁₂
  • Molecular Weight: 1069.53
  • Purity: ≥95%
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Calcimycin hemimagnesium(Cat No.:I015171)is a calcium ionophore that facilitates the transport of calcium ions across biological membranes. This compound, a derivative of calcimycin, is particularly useful in cell biology and biochemistry for studies involving calcium signaling and intracellular calcium dynamics. Calcimycin hemimagnesium acts by forming complexes with calcium ions, allowing them to traverse lipid bilayers. Its applications extend to exploring cellular processes like muscle contraction, neurotransmitter release, and signal transduction. It serves as an important tool in research on ion channel function and cellular responses to calcium modulation.


Catalog Number I015171
CAS Number 72124-77-7
Molecular Formula C₅₈H₇₂MgN₆O₁₂
Purity ≥95%
Target Anti-infection
IUPAC Name magnesium;5-(methylamino)-2-[[(2S,3R,5R,6S,8R,9R)-3,5,9-trimethyl-2-[(2S)-1-oxo-1-(1H-pyrrol-2-yl)propan-2-yl]-1,7-dioxaspiro[5.5]undecan-8-yl]methyl]-1,3-benzoxazole-4-carboxylate
InChI InChI=1S/2C29H37N3O6.Mg/c2*1-15-10-11-29(17(3)13-16(2)27(38-29)18(4)26(33)20-7-6-12-31-20)37-22(15)14-23-32-25-21(36-23)9-8-19(30-5)24(25)28(34)35;/h2*6-9,12,15-18,22,27,30-31H,10-11,13-14H2,1-5H3,(H,34,35);/q;;+2/p-2/t2*15-,16-,17-,18-,22-,27+,29+;/m11./s1
InChIKey XBWKBTZDBYFEMH-UIOMRPQBSA-L
SMILES C[C@@H]1CC[C@]2([C@@H](C[C@H]([C@H](O2)[C@H](C)C(=O)C3=CC=CN3)C)C)O[C@@H]1CC4=NC5=C(O4)C=CC(=C5C(=O)[O-])NC.C[C@@H]1CC[C@]2([C@@H](C[C@H]([C@H](O2)[C@H](C)C(=O)C3=CC=CN3)C)C)O[C@@H]1CC4=NC5=C(O4)C=CC(=C5C(=O)[O-])NC.[Mg+2]
Reference

[1]. Wu Q, et al. Characterization of the biosynthesis gene cluster for the pyrrole polyether antibiotic calcimycin(A23187) in Streptomyces chartreusis NRRL 3882. Antimicrob Agents Chemother. 2011 Mar;55(3):974-82.<br>[2]. Elliott JI, et al. IKCa1 activity is required for cell shrinkage, phosphatidylserine translocation and death in Tlymphocyte apoptosis. EMBO Rep. 2003 Feb;4(2):189-94.<br>[3]. Engedal N, et al. Modulation of intracellular calcium homeostasis blocks autophagosome formation. Autophagy. 2013 Oct;9(10):1475-90.<br>[4]. Mawatwal S, et al. Calcimycin mediates mycobacterial killing by inducing intracellular calcium-regulated autophagy in a P2RX7 dependent manner. Biochim Biophys Acta Gen Subj. 2017 Dec;1861(12):3190-3200.<br>[5]. Wang JP, et al. Effect of norathyriol, isolated from Tripterospermum lanceolatum, on A23187-induced pleurisy and analgesia in mice. Naunyn Schmiedebergs Arch Pharmacol. 1994 Jul;350(1):90-5.

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