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Salinomycin sodium salt - ≥98%, high purity , CAS No.55721-31-8

    Grade & Purity:
  • ≥98%
In stock
Item Number
S303981
Grouped product items
SKU Size
Availability
Price Qty
S303981-25mg
25mg
5
$89.90
S303981-50mg
50mg
4
$143.90
S303981-100mg
100mg
3
$229.90

Cation ionophore. Antibiotic agent.

Basic Description

Synonyms NCGC00095055-01 | (2R)-2-[(2R,5S,6R)-6-[(3S,5S,7R,9S,10S,12R,15R)-3-[(2R,5R,6S)-5-Ethyl-5-hydroxy-6-methyloxan-2-yl]-15-hydroxy-3,10,12-trimethyl-4,6,8-trioxadispiro[4.1.5.3]pentadec-13-en-9-yl]-3-hydroxy-4-methyl-5-oxooctan-2-yl]-5-methyloxan-2-yl]butano
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms Cation ionophore. Antibiotic agent. Salinomycin salt. Shows cancer stems cell selective antiproliferative effects (IC 50 values are 24 and 90 μM for cancer stem cell subpopulation and HMLER breast cancer cells respectively). Shows antitumor e
Storage Temp Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Note Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Salinomycin sodium salt (Salinomycin sodium), an antibiotic potassium ionophore, is a potent inhibitor of Wnt/β-catenin signaling. Salinomycin sodium salt (Salinomycin sodium) acts on the Wnt/Fzd/LRP complex, blocks Wnt-induced LRP6 phosphorylation, and causes degradation of the LRP6 protein. Salinomycin sodium salt (Salinomycin sodium) shows selective activity against human cancer stem cells.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Lipids and lipid-like molecules
Class Prenol lipids
Subclass Terpene glycosides
Intermediate Tree Nodes Not available
Direct Parent Diterpene glycosides
Alternative Parents Diterpenoids  Ketals  Beta-hydroxy ketones  Oxanes  Pyrans  Tertiary alcohols  Tetrahydrofurans  Carboxylic acid salts  Secondary alcohols  Oxacyclic compounds  Monocarboxylic acids and derivatives  Dialkyl ethers  Carboxylic acids  Organic zwitterions  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aliphatic heteropolycyclic compounds
Substituents Diterpene glycoside - Diterpenoid - Ketal - Beta-hydroxy ketone - Oxane - Pyran - Tertiary alcohol - Tetrahydrofuran - Carboxylic acid salt - Ketone - Secondary alcohol - Acetal - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Oxacycle - Ether - Organic alkali metal salt - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Hydrocarbon derivative - Carbonyl group - Alcohol - Organic oxide - Organooxygen compound - Organic sodium salt - Organic oxygen compound - Organic salt - Organic zwitterion - Aliphatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated.
External Descriptors Not available

Associated Targets(Human)

MCF7 (126967 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HepG2 (196354 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Plasmodium berghei (192651 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Bacillus anthracis (2936 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504769704
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504769704
IUPAC Name sodium;(2R)-2-[(2R,5S,6R)-6-[(2S,3S,4S,6R)-6-[(3S,5S,7R,9S,10S,12R,15R)-3-[(2R,5R,6S)-5-ethyl-5-hydroxy-6-methyloxan-2-yl]-15-hydroxy-3,10,12-trimethyl-4,6,8-trioxadispiro[4.1.57.35]pentadec-13-en-9-yl]-3-hydroxy-4-methyl-5-oxooctan-2-yl]-5-methyloxan-2-yl]butanoate
INCHI InChI=1S/C42H70O11.Na/c1-11-29(38(46)47)31-15-14-23(4)36(50-31)27(8)34(44)26(7)35(45)30(12-2)37-24(5)22-25(6)41(51-37)19-16-32(43)42(53-41)21-20-39(10,52-42)33-17-18-40(48,13-3)28(9)49-33;/h16,19,23-34,36-37,43-44,48H,11-15,17-18,20-22H2,1-10H3,(H,46,47);/q;+1/p-1/t23-,24-,25+,26-,27-,28-,29+,30-,31+,32+,33+,34+,36+,37-,39-,40+,41-,42-;/m0./s1
InChIKey YPZYGIQXBGHDBH-UZHRAPRISA-M
Smiles CCC(C1CCC(C(O1)C(C)C(C(C)C(=O)C(CC)C2C(CC(C3(O2)C=CC(C4(O3)CCC(O4)(C)C5CCC(C(O5)C)(CC)O)O)C)C)O)C)C(=O)[O-].[Na+]
Isomeric SMILES CC[C@H]([C@H]1CC[C@@H]([C@@H](O1)[C@@H](C)[C@@H]([C@H](C)C(=O)[C@H](CC)[C@@H]2[C@H](C[C@H]([C@]3(O2)C=C[C@H]([C@@]4(O3)CC[C@@](O4)(C)[C@H]5CC[C@@]([C@@H](O5)C)(CC)O)O)C)C)O)C)C(=O)[O-].[Na+]
PubChem CID 23703990
Molecular Weight 772.98

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot Number Certificate Type Date Item
B2429526 Certificate of Analysis Feb 01, 2024 S303981
B2429527 Certificate of Analysis Feb 01, 2024 S303981
B2429528 Certificate of Analysis Feb 01, 2024 S303981
B2429529 Certificate of Analysis Feb 01, 2024 S303981
F2306645 Certificate of Analysis Apr 12, 2023 S303981
F2306646 Certificate of Analysis Apr 12, 2023 S303981
F2306647 Certificate of Analysis Apr 12, 2023 S303981
F2306648 Certificate of Analysis Apr 12, 2023 S303981
F2306650 Certificate of Analysis Apr 12, 2023 S303981
F2306649 Certificate of Analysis Apr 12, 2023 S303981

Chemical and Physical Properties

Sensitivity Moisture sensitive
Molecular Weight 773.000 g/mol
XLogP3
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 11
Rotatable Bond Count 12
Exact Mass 772.474 Da
Monoisotopic Mass 772.474 Da
Topological Polar Surface Area 164.000 Ų
Heavy Atom Count 54
Formal Charge 0
Complexity 1330.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 18
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 2

Solution Calculators

Reviews

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