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IONOMYCIN

CAS No.
56092-81-0
Chemical Name:
IONOMYCIN
Synonyms
Ionomycin from Streptomyces conglobatus;EM 94;SQ-23377;IONOMYCIN;SQ 23377, EM 94;Ionomycinefreeacid;IONOMYCIN (SQ23377);IONOMYCIN USP/EP/BP;Ionomycin, Free Base;Ionomycin Free Acid (85%)
CBNumber:
CB5380046
Molecular Formula:
C41H72O9
Molecular Weight:
709.01
MDL Number:
MFCD06798385
MOL File:
56092-81-0.mol
MSDS File:
SDS
Last updated:2023-06-30 15:45:59

IONOMYCIN Properties

Boiling point 817.2±65.0 °C(Predicted)
Density 1.072±0.06 g/cm3(Predicted)
storage temp. −20°C
solubility Soluble to 10 mM in Ethanol and to 10 mM in DMSO.
form Waxy solid
pka 4.77±0.10(Predicted)
color Yellow
BRN 3642126
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months.
EWG's Food Scores 1
NCI Dictionary of Cancer Terms ionomycin
FDA UNII 54V905V6AT

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS02
Signal word  Warning
Hazard statements  H225
Precautionary statements  P210-P240-P241-P280a-P303+P361+P353-P501a
Hazard Codes  Xn,Xi
Risk Statements  22-36/37/38
Safety Statements  36-36/37/39-27-26-24/25
WGK Germany  3
RTECS  NO0650000
8-10
HazardClass  3
HS Code  29419090
NFPA 704
3
2 0

IONOMYCIN price More Price(24)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich I9657 Ionomycin from Streptomyces conglobatus ≥98% (HPLC) 56092-81-0 1mg $197 2024-03-01 Buy
Sigma-Aldrich 407950 Ionomycin, Free Acid, Streptomyces conglobatus - CAS 56092-81-0 - Calbiochem Ionomycin, Free Acid, Streptomyces conglobatus, CAS 56092-81-0, is a highly specific for divalent cations and more effective than A23187 (Cat. No. 100105) as a mobile ion carrier for Ca2+. 56092-81-0 1mg $155 2024-03-01 Buy
Sigma-Aldrich 407951 Ionomycin, Free Acid, 56092-81-0 1mg $190 2024-03-01 Buy
Sigma-Aldrich 407950 Ionomycin, Free Acid, Streptomyces conglobatus - CAS 56092-81-0 - Calbiochem Ionomycin, Free Acid, Streptomyces conglobatus, CAS 56092-81-0, is a highly specific for divalent cations and more effective than A23187 (Cat. No. 100105) as a mobile ion carrier for Ca2+. 56092-81-0 5mg $572 2024-03-01 Buy
Alfa Aesar J62448 Ionomycin, 98% 56092-81-0 1mg $87.8 2023-06-20 Buy
Product number Packaging Price Buy
I9657 1mg $197 Buy
407950 1mg $155 Buy
407951 1mg $190 Buy
407950 5mg $572 Buy
J62448 1mg $87.8 Buy

IONOMYCIN Chemical Properties,Uses,Production

Description

Ionomycin (56092-81-0) is a highly selective nonfluorescent calcium (Ca2+) ionophore.1 Induces a rapid rise in cytosolic Ca2+ in human neutrophils which is due to both release from cytosolic Ca2+ stores as well as Ca2+ influx.2 It activates (2 μM) and primes (20-200 nM) neutrophil NADPH oxidase2. Down regulates beta-catenin/Tcf signaling in a colon cancer cell line via suppressing the binding of Tcf to its specific DNA-binding site.3 In rat hepatoma cells, sub-lethal ionomycin activates the stress response by activating SAPK/JNK and HSF/HSE interaction leading to upregulation of HSP70 biosynthesis.4

Chemical Properties

White powder

Uses

Ionomycin was isolated from Streptomyces conglobatus as a potent Gram positive antibiotic . During isolation, it was recognised that ionomycin exhibits a very high affinity and selectivity for calcium ions, suggesting the metabolite acts as a calcium ionophore. More recently, ionomycin has been used in cell biology as a universal calcium ionophore to explore the role of calcium regulation in the cell.

Uses

Ionomycin free acid is a beneficial tool in research to raise intracellular calcium levels. Also this antibiotic can be used to study the calcium transport across the plasma membrane. It has been shown to induce central demyelination , inhibit adrenal bovine TREK-1 channels , and to regulate cell division of mature human B cells . It is used to study the effects of calcium flux on endoplasmic reticulum (ER) stress, mitochondrial stress and intrinsic apoptosis mechanisms. It is also used to stimulate the intracellular production of the cytokines, interferon, perforin, IL-2, and IL-4 usually in conjunction with PMA.

Uses

Ionomycin is more effective than A23187 as a Ca++ionophore. Ionomycin is used in research on Ca++ transport across biological membranes; Ionomycin induces apoptotic degeneration of embryonic cortical neurons

Definition

ChEBI: 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 osition 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 memb anes.

General Description

Highly specific for divalent cations (Ca2+ > Mg2+ >> Sr2+ = Ba2+). More effective than antibiotic A23187 as a mobile ion carrier for Ca2+. Complexes with Ca2+ between pH 7 and 9.5, causing significant absorption in the UV range; however, in contrast to A23187 (Cat. No. 100105), it is not fluorescent. Useful for studies of Ca2+ transport across biological membranes and measurement of cytoplasmic free Ca2+. Induces apoptotic neuronal degeneration in embryonic cortical neurons. Also induces cell cycle arrest in the G1 interval of mature Burkitt lymphoma cell lines.

Biological Activity

Calcium ionophore; more specific than A23187 (5-(Methylamino)-2-[[2R,3R,6S,8S,9R,11R)-3,9,11-trimethyl-8-[(1S)-1-methyl-2-oxo-2-(1H-pyrrol-2-yl)-ethyl]-1,7-dioxaspiro[5.5]undec-2-yl]methyl]-4-benzoxazolecarboxylic acid ).

Biochem/physiol Actions

Cell permeable: yes

in vitro

calcium ion can be extracted by ionomycin fom the queous phase into the organic phase. ionomycin also acts as a mobile ion carrier, which transports the cation across a solvent barrier [1].

in vivo

efficiency of ionomycin on oocyte activation and subsequent development was evaluated, which identified ionomycin as an efficient activator at the concentation of 10 μmol/l. with a second exposure to 5 μmol/l ionomycin on blastocyst development, an improved effect was found. no adverse effects of ionomycin on mouse embryo development were identified [2].

storage

-20°C

References

1) Kaufmann et al., (1980), Cation transport and specificity of ionomycin. Comparison with ionophore A23187 in rat liver mitochondria; J. Biol. Chem. 255 2735 2) Elzi et al., (2001), Ionomycin causes activation of p38 and p42/44 mitogen-activated protein kinases in human neutrophils; Am. J. Physiol. Cell Physiol. 281 C350 3) Park et al., (2005), Ionomycin downregulates beta-catenin/tcf signaling in colon cancer cell line; Carcinogenesis, 26 1929 4) Sreedhar and Srinivas (2002), Activation of stress response by ionomycin in rat hepatoma cells; J. Cell Biochem., 86 154

IONOMYCIN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 138)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Dideu Medichem Co. Ltd
18192627656 1012@dideu.com China 3422 58
Hubei Ipure Biology Co., Ltd
+8613367258412 ada@ipurechemical.com China 10326 58
HONG KONG IPURE BIOLOGY CO.,LIMITED
86 18062405514 18062405514 ada@ipurechemical.com CHINA 3465 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29271 58
BOC Sciences
+16314854226 inquiry@bocsci.com United States 19743 58
LEAP CHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 24738 58
ZHEJIANG JIUZHOU CHEM CO., LTD
+86-0576225566889 +86-13454675544 admin@jiuzhou-chem.com;jamie@jiuzhou-chem.com;alice@jiuzhou-chem.com China 20000 58
Wuhan Topule Biopharmaceutical Co., Ltd
+8618327326525 masar@topule.com China 8474 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43348 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+undefined18621343501 product@acmec-e.com China 33349 58

View Lastest Price from IONOMYCIN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
IONOMYCIN USP/EP/BP pictures 2021-07-17 IONOMYCIN USP/EP/BP
56092-81-0
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
Ionomycin pictures 2020-05-12 Ionomycin
56092-81-0
US $0.01-1.00 / KG 1KG 99% 50 tons Shaanxi Dideu Medichem Co. Ltd
  • Ionomycin pictures
  • Ionomycin
    56092-81-0
  • US $0.01-1.00 / KG
  • 99%
  • Shaanxi Dideu Medichem Co. Ltd
(4R,6S,8R,12R,14S,18S,19R,20R,21R)-19,21-Dihydroxy-22-[(2R,5R)-5-[(2R,5S)-5-(1-hydroxyethyl)-5-methyl-oxolan-2-yl]-5-methyl-oxolan-2-yl]-4,6,8,12,14,18,20-heptamethyl-11-oxido-9-oxo-docosa-10,16-dienoate calcium salt SQ-23377 Ionomycin,Free Acid,from Streptomyces conglbatus (4R,6S,8S,10Z,12R,14R,16E,18R,19R,20S,21S)-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-10,16-docosadienoicacid SQ 23377, EM 94 Ionomycin, free acid, from Streptomyces conglobatus (4R,6S,8S,10Z,12R,14R,16E,18S,19S,20R,21S)-11,19,21-Trihydroxy-22-{(2S,2'S,5S,5'R)-5'-[(1S)-1-hydroxyethyl]-2,5'-dimethyloctahydro-2,2'-bifuran-5-yl}-4,6,8,12,14,18,20-heptamethyl-9-oxo-10,16-docosadi enoic acid ionomycin calcium salt from streptomyces conglobatus Ionomycin, Free Acid, Streptomyces conglobatus (4R,6S,8S,10Z,12R,14R,16E,18R,19R,20S,21S)-11,19,21-Trihydroxy-4,6,8,12,14,18,20-heptamethyl-22-((2S,2'R,5S,5'S)-octahyd Ionomycinefreeacid IONOMYCIN IONOMYCIN, STREPTOMYCES CONGLOBATUS IONOMYCIN (SQ23377) Ionomycin, Free Acid, Streptomyces conglobatus - CAS 56092-81-0 - Calbiochem Ionomycin, Free Acid, Streptomyces conglobatus in Solution - CAS 56092-81-0 - Calbiochem EM 94 Ionomycin, 98.5%, from Streptomyces conglobatus 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-, (4R,6S,8S,10Z,12R,14R,16E,18R,19R,20S,21S)- IONOMYCIN USP/EP/BP Ionomycin Free Acid (85%) Ionomycin from Streptomyces conglobatus (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 Ionomycin, Free Base 56092-81-0 C41H72O9 BioChemical Antibiotics Antibiotics G-M Antibiotics A to Z antibiotic Ion Channels MiscellaneousMore...Close... A - KResearch Essentials Antibacterial Antibiotics A to Antibiotics by Application Antibiotics G-MAntibiotics AntibioticsAntibiotics Calcium channel Spectrum of Activity Chemical Structure Class Core Bioreagents Interferes with Cell Membrane Permeability (Ionophores)Antibiotics Mechanism of Action Antineoplastic and Immunosuppressive AntibioticsAntibiotics