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Salinomycin

CAS No.
53003-10-4
Chemical Name:
Salinomycin
Synonyms
SALINOMYCIN SODIUM;SALINOMYCIN SODIUM SALT;coxistac;Procoxacin;Salinomycin;SALINOMYCIN 90%;Antibiotic-61477;Salinomycin, >98%;SalinoMycin 12% 24%;SALINOMYCIN GRANULE
CBNumber:
CB9161784
Molecular Formula:
C42H70O11
Molecular Weight:
751
MDL Number:
MFCD25541652
MOL File:
53003-10-4.mol
MSDS File:
SDS
Last updated:2024-10-31 18:15:48

Salinomycin Properties

Melting point 112.5-113.5 °C(lit.)
Boiling point 839.2±65.0 °C(Predicted)
alpha D25 -63° (c = 1 in ethanol)
Density 1.18±0.1 g/cm3(Predicted)
Flash point >110°(230°F)
storage temp. Sealed in dry,2-8°C
solubility insoluble in H2O; ≥142.2 mg/mL in EtOH; ≥91.8 mg/mL in DMSO
pka 6.4 (DMF)
form White solid
color White to light yellow
optical activity -6325 (cl, ethanol)
Water Solubility Soluble in methanol. Insoluble in water
Merck 13,8415
Stability Stable, but may be heat sensitive - keep cool. Incompatible with strong oxidizing agents.
LogP 5.596 (est)
FDA 21 CFR 558.4
CAS DataBase Reference 53003-10-4(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 62UXS86T64

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Danger
Hazard statements  H300
Precautionary statements  P264-P270-P301+P310-P405-P501
Hazard Codes  T,Xi
Risk Statements  25-36/37/38
Safety Statements  45-36-26
RIDADR  UN 3462 6.1/PG 2
WGK Germany  3
RTECS  VO8620000
10
HazardClass  6.1(a)
PackingGroup  II
Toxicity LD50 in mice (mg/kg): 18 i.p.; 50 orally (Miyazaki)
NFPA 704
0
4 0

Salinomycin price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich S4526 Salinomycin from Streptomyces albus, ≥98% (HPLC) 53003-10-4 5mg $135 2024-03-01 Buy
Cayman Chemical 13579 Salinomycin ≥90% 53003-10-4 5mg $25 2024-03-01 Buy
Cayman Chemical 13579 Salinomycin ≥90% 53003-10-4 10mg $37 2024-03-01 Buy
Cayman Chemical 13579 Salinomycin ≥90% 53003-10-4 50mg $94 2024-03-01 Buy
Cayman Chemical 13579 Salinomycin ≥90% 53003-10-4 100mg $163 2024-03-01 Buy
Product number Packaging Price Buy
S4526 5mg $135 Buy
13579 5mg $25 Buy
13579 10mg $37 Buy
13579 50mg $94 Buy
13579 100mg $163 Buy

Salinomycin Chemical Properties,Uses,Production

Description

Salinomycin was found in the culture mycelium of Streptomyces albus by Otake et al. of the University of Tokyo in 1973. Like other polyether ionophore antibiotics, it shows activity against gram-positive bacteria, fungi, and Coccidium. Salinomycin has been used as a feed additive to protect poultry against coccidial infections.

Chemical Properties

solid

Uses

Salinomycin was used as a standard in the development of LC-MS/MS method for detection of residual coccidiostats in egg and muscle samples. It was used to screen out CD44+CD24- mesenchymal-like subpopulation within breast carcinomas.

Uses

antibacterial

Uses

Salinomycin is a polyether ionophore with broad spectrum Gram positive and anti-coccidial activity. Salinomycin has a high affinity for monovalent cations, particularly potassium. Salinomycin is used to control coccidia in animals and for growth promotion in ruminants. Recently, salinomycin has been shown to inhibit cancer stem cells and is >100 times more potent than taxol. While the mechanism of action is unknown, it was noted that among the 60,000 compounds screened, another monovalent ionophore, nigericin, and a chloride channel inhibitor, avermectin, were also active.

Definition

ChEBI: Salinomycin is a polyketide and a spiroketal. It has a role as an animal growth promotant and a potassium ionophore.

General Description

Chemical structure: polyether

Biological Activity

salinomycin (sal), which is a polyether ionophore antibiotic from streptomyces albus, has been proven to be able to kill different types of human cancer cells, most likely via interfering with abc drug transporters, the wnt/β-catenin signaling pathway, or other pathways.

Biochem/physiol Actions

Salinomycin produced by Streptomyces albus is a carboxylic polyether ionophore with antibiotic and anti-cancer properties. It induces cell death in some types of cancer cells such as breast, lung, gastric cancer, leukemia and osteosarcoma. Salinomycin inhibits multidrug resistance protein 1 and induces apoptosis by the generation of reactive oxygen species that cause DNA damage and inactivation of Stat3. Use of salinomycin as antibiotic results in lowered spermatozoa count and motility and decreased steroidogenesis in mice.

in vitro

several hepatocellular carcinoma (hcc) cell lines were treated with sal. results showed that sal inhibited proliferation and decreased pcna levels. cell cycle analysis showed that sal caused cell cycle arrest in different phases. sal induced apoptosis as characterized by an increase in the bax/bcl-2 ratio. compared to control, β-catenin expression was down-regulated by sal treatment significantly. the ca2+ concentration in hcc cells was examined by flow cytometry and it was found that higher ca2+ concentrations were observed in sal treatment groups [1].

in vivo

the in vivo anti-tumor effect of sal was verified using the hepatoma orthotopic tumor model and results showed that the liver tumor size in sal-treated groups decreased. immunohistochemistry and tunel staining also demonstrated that sal could in vivo inhibit proliferation and induced apoptosis [1].

IC 50

7.7, 13.7 and 10.4 μm for hepg2, smmc-7721 and bel-7402 cell line, respectively (after 24h treatment)

References

[1] wang f,he l,dai wq,xu yp,wu d,lin cl,wu sm,cheng p,zhang y,shen m,wang cf,lu j,zhou yq,xu xf,xu l,guo cy. salinomycin inhibits proliferation and induces apoptosis of human hepatocellular carcinoma cells in vitro and in vivo. plos one.2012;7(12):e50638.

Salinomycin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 259)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Chuanghai Biotechnology Co,.LTD
+86-13131129325 sales1@chuanghaibio.com China 5893 58
shandong perfect biotechnology co.ltd
+86-53169958659; +8618596095638 sales@sdperfect.com China 294 58
Shaanxi TNJONE Pharmaceutical Co., Ltd
+8618092446649 sarah@tnjone.com China 1143 58
Capot Chemical Co.,Ltd.
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Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21639 55
Zhejiang ZETian Fine Chemicals Co. LTD
+8618957127338 stella@zetchem.com China 2136 58
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Xiamen AmoyChem Co., Ltd
+86-86-5926051114 +8618959220845 sales@amoychem.com China 6383 58
CONIER CHEM AND PHARMA LIMITED
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View Lastest Price from Salinomycin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Salinomycin pictures 2024-11-04 Salinomycin
53003-10-4
US $32.00-74.00 / mg 98.00% 10g TargetMol Chemicals Inc.
Salinomycin pictures 2024-11-04 Salinomycin
53003-10-4
US $32.00-74.00 / mg 98.00% 10g TargetMol Chemicals Inc.
Salinomycin pictures 2024-10-25 Salinomycin
53003-10-4
US $0.00 / kg 1kg 0.99 20tons Hebei Yanxi Chemical Co., Ltd.
  • Salinomycin pictures
  • Salinomycin
    53003-10-4
  • US $32.00-74.00 / mg
  • 98.00%
  • TargetMol Chemicals Inc.
  • Salinomycin pictures
  • Salinomycin
    53003-10-4
  • US $32.00-74.00 / mg
  • 98.00%
  • TargetMol Chemicals Inc.
  • Salinomycin pictures
  • Salinomycin
    53003-10-4
  • US $0.00 / kg
  • 0.99
  • Hebei Yanxi Chemical Co., Ltd.
coxistac SALINOMYCIN GRANULE Salinomycin Premix 12% SALINOMYCIN FROM STREPTOMYCES ALBUS SALINOMYCIN 90% SV sodium salt,2,5 salinomycin hydrate (2R)-2-((5S)-6-{5-[(10S,12R)-2-((6S,5R)-5-Ethyl-5-hydroxy-6-methylperhydro-2H-pyran-2-yl)-15-hydroxy-2,10,12-trimethyl-1,6,8-trioxadispiro[4.1.5.3]pentadec-13-en-9-yl](1S,2S,3S,5R)-2-hydroxy-1,3-dimethyl-4-oxoheptyl}-5-methylperhydro-2H-pyran-2-yl)butanoic acid Salinomycin Antibiotic-61477 SalinoMycin(Procoxacin) SalinoMycin 12% 24% Procoxacin Eustin, AHR 3096, K 364, 61477 Salinomycin Solution, 100ppm Salinomycin, >98% Salinomycin USP/EP/BP SALINOMYCIN SODIUM PREMIX (10%, 12%, 45%) 99% purity Salinomycin Salinomycin (10mM in DMSO) (R)-2-((2R,5S,6R)-6-((2S,3S,4S,6R)-6-((2S,5S,7R,9S,10S,12R,15R)-2-((2R,5R,6S)-5-Ethyl-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)-15-hydroxy-2,10,12-trimethyl-1,6,8-trioxadispiro[4.1.57.35]pentadec-13-en-9-yl)-3-hydroxy-4-methyl-5-oxooctan-2-yl)-5-methyltetrahydro-2H-pyran-2-yl)butanoic acid (R)-2-((2R,5S,6R)-6-((2S,3S,4S,6R)-6-((2S,5S,7R,9S,10S,12R,15R)-2-((2R,5R,6S)-5-Ethyl-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)-15-hydroxy-2,10,12-trimethyl-1,6,8-trioxadispiro[4.1.57.35]pentadec-13-en-9-yl)-3-hydroxy-4-methyl-5-oxooctan-2-yl)-5-methylt SalinomycinQ: What is Salinomycin Q: What is the CAS Number of Salinomycin Q: What is the storage condition of Salinomycin Q: What are the applications of Salinomycin SALINOMYCIN SODIUM SALINOMYCIN SODIUM SALT Salinomycin in Methanol Salinomycin in Acetonitrile 53003-10-4 C42H69NaO11 C42H69O11Na C42H70O11 Antibiotics N-S Antibiotics A to Z Antibiotics BioChemical KOKCISAN Antibacterial Antibiotics Antibiotics A to Antibiotics N-SAntibiotics Chemical Structure Class L - ZAntibiotics Mechanism of Action Monovalent Ion Channels Polyethers Inhibitors Interferes with Cell Membrane Permeability (Ionophores)Voltage-gated Ion Channels IonophoresSpectrum of Activity 53003-10-4