missing translation for 'onlineSavingsMsg'
Learn More

Rapamycin, 98+%

Rapamycin, CAS # 53123-88-9, is a macrolide compound showing suppressor activity against the immune system and also exhibits inhibitory activity in tumor growth. | CAS: 53123-88-9 | C51H79NO13 | 914.187 g/mol

$285.99 - $797.92

Chemical Identifiers

CAS 53123-88-9
Molecular Formula C51H79NO13
Molecular Weight (g/mol) 914.187
MDL Number MFCD00867594
InChI Key QFJCIRLUMZQUOT-HPLJOQBZSA-N
Synonym Sirolimus; AY-22989
PubChem CID 5284616
ChEBI CHEBI:9168
SMILES CC1CCC2CC(C(=CC=CC=CC(CC(C(=O)C(C(C(=CC(C(=O)CC(OC(=O)C3CCCCN3C(=O)C(=O)C1(O2)O)C(C)CC4CCC(C(C4)OC)O)C)C)O)OC)C)C)C)OC
View More Specs

Products 2
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAJ62473MF
View Documents
Thermo Scientific Chemicals
J62473MF
50 mg N/A
Only null left
 
AAJ62473EX3
View Documents
Thermo Scientific Chemicals
J62473EX3
200 mg N/A
Only null left
 
Description

Description

Blocks cytokine-mediated signal transduction pathwaysRapamycin is used to inhibit tumor growth by halting tumor cell proliferation and suppressing tumor angiogenesis. It forms a complex with FKBP12 that binds and inhibits the molecular target of rapamycin (mTOR) as well as suppresses the immune system, preventing transplant rejection.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

General Description

  • Rapamycin is a natural macrolide compound showing antiproliferative activities in mammalian cells
  • Rapamycin is a specific inhibitor of rapamycin kinase. It forms a complex with FKBP12 that consequently binds and inhibits rapamycin’s molecular target (rapamycin kinase)

Application

  • Rapamycin inhibits tumor growth by preventing tumor cell proliferation and suppressing tumor angiogenesis
  • This compound also blocks cytokine-mediated signal transduction pathways
  • Rapamycin also promotes the suppression of the immune system
  • It was initially defined as an antifungal metabolite produced by Streptomyces hygroscopicus
  • In vitro studies demonstrated that this compound is an important mediator of PI3 kinase signaling
Specifications

Chemical Identifiers

53123-88-9
914.187
QFJCIRLUMZQUOT-HPLJOQBZSA-N
5284616
CC1CCC2CC(C(=CC=CC=CC(CC(C(=O)C(C(C(=CC(C(=O)CC(OC(=O)C3CCCCN3C(=O)C(=O)C1(O2)O)C(C)CC4CCC(C(C4)OC)O)C)C)O)OC)C)C)C)OC
C51H79NO13
MFCD00867594
Sirolimus; AY-22989
CHEBI:9168

Specifications

Rapamycin
53123-88-9
50 mg
MFCD00867594
Sirolimus; AY-22989
QFJCIRLUMZQUOT-HPLJOQBZSA-N
914.187
CHEBI:9168
≥99%
Powder
White
C51H79NO13
14,8114
Soluble in DMSO at 50mg/ml or methanol at 25mg/mlSoluble in alcohol,dimethyl sulfoxide and dimethyl formamide; Insoluble in water.
CC1CCC2CC(C(=CC=CC=CC(CC(C(=O)C(C(C(=CC(C(=O)CC(OC(=O)C3CCCCN3C(=O)C(=O)C1(O2)O)C(C)CC4CCC(C(C4)OC)O)C)C)O)OC)C)C)C)OC
5284616
914.17
Rapamycin
Videos
Safety and Handling

Safety and Handling

RTECSNumber : VE6250000

TSCA : No

Recommended Storage : Store at -20°C

SDS
missing translation for 'documents'

missing translation for 'documents'

RUO – Research Use Only