ChemicalBook > CAS DataBase List > Rosiglitazone maleate

Rosiglitazone maleate

Product Name
Rosiglitazone maleate
CAS No.
155141-29-0
Chemical Name
Rosiglitazone maleate
Synonyms
Avandi;BRL-49653c;RSIGLITAZONEMALEATE;RosiglitazoneTartrate;ROSIGLITAZONE MALEATE;Rosiglitazone-d3 Maleate;Rosiglitazone Maleate forM;β-D-Fructopyranose1-Sulfamate;Rosiglitazone Maleate (200 mg);C16819000 RosiglitazonEMaleate
CBNumber
CB0133276
Molecular Formula
C22H23N3O7S
Formula Weight
473.5
MOL File
155141-29-0.mol
More
Less

Rosiglitazone maleate Property

Melting point:
235-240°C
storage temp. 
2-8°C
solubility 
Soluble in DMSO (up to 50 mg/ml).
pka
6.1; 6.8(at 25℃)
form 
White powder
color 
White
BCS Class
1
Stability:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months
InChIKey
HCDYSWMAMRPMST-NTCAYCPXSA-N
SMILES
C(/C(=O)O)=C/C(=O)O.C(C1C=CC(OCCN(C2N=CC=CC=2)C)=CC=1)C1C(NC(=O)S1)=O
CAS DataBase Reference
155141-29-0(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
20/21/22-36/38
Safety Statements 
24/25-37/39-26
WGK Germany 
3
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
PHR2513
Product name
Rosiglitazone maleate
Purity
Pharmaceutical Secondary Standard; Certified Reference Material
Packaging
300MG
Price
$183
Updated
2025/07/31
Sigma-Aldrich
Product number
557366-M
Product name
Rosiglitazone - CAS 155141-29-0 - Calbiochem
Packaging
10MG
Price
$123
Updated
2025/07/31
Sigma-Aldrich
Product number
1605817
Product name
Rosiglitazone maleate
Packaging
200mg
Price
$467
Updated
2025/07/31
TCI Chemical
Product number
R0271
Product name
Rosiglitazone Maleate
Packaging
1G
Price
$79
Updated
2025/07/31
TCI Chemical
Product number
R0271
Product name
Rosiglitazone Maleate
Packaging
5G
Price
$237
Updated
2025/07/31
More
Less

Rosiglitazone maleate Chemical Properties,Usage,Production

Description

Rosiglitazone maleate, belongs to a novel class of thiazolidine diones launched for the treatment of non-insulin-dependent diabetes mellitus (NIDDM), a disease characterized by a pancreatic β-cell defect and insulin resistance in the liver and peripheral tissues. The racemic base can be obtained by KnSvenagel condensation between 2, 4-thiazolidinedione and the corresponding 4-substituted benzaldehyde (itself prepared in 2 steps from 2-chloropyridine), followed by reduction of the benzylidene. Rosiglitazone was shown to be a potent agonist of peroxisome proliferator activated receptor-gamma (PPARgamma), a nuclear receptor involved in the differentiation of adipose tissue, without activating liver PPAR-alpha receptors. This activation of PPAR-gamma could mediate the down-regulation of leptin gene expression. In animal models, Rosiglitazone has been shown to normalize glucose metabolism and reduce the exogenous dose of insulin needed to achieve glycemic control. In patients with Type II diabetes, daily doses (4 or 8 mg) of Rosiglitazone significantly improved blood sugar control without affecting cardiac structure or function.

Chemical Properties

White To Off-White Solid

Originator

SmithKline Beecham (US)

Uses

Thiazole alkanes antidiabetic drug

Uses

Thiazolidinediones (TZDs) are a group of structurally related peroxisome proliferator-activated receptor γ (PPARγ) agonists with antidiabetic actions in vivo. Rosiglitazone is a prototypical TZD that has served as a reference compound for this class. It is a potent and selective PPARγ ligand that binds to the PPARγ ligand-binding domain with a Kd value of 43 nM. It activates luciferase-based expression constructs PPARγ1 and PPARγ2 with EC50 values of approximately 30 nM and 100 nM, respectively. Rosiglitazone is active in vivo as an antidiabetic agent in the ob/ob mouse model, and has been used as an oral hypoglycemic agent in the treatment of type 2 diabetes in humans for many years.[Cayman Chemical]

Uses

Insulin sensitizer; binds to peroxisome proliferator activated receptor gamma (PPAR- γ).

Indications

Rosiglitazone maleate is an antihyperglycemic agent in the thiazolidinedione class. It is indicated for the treatment of patients with type 2 diabetes mellitus.

brand name

Avandia (GlaxoSmithKline).

General Description

A thiazolidinedione compound that acts as an anti-diabetic agent and serves as a potent and selective agonist of peroxisome proliferator-activated receptor-g (PPARg) (Kd ~40 nM) in fat cells. Shown to reduce fatty acid uptake and ameliorate lipid metabolism and insulin resistance in animal models of type II diabetes. Reported to activate both a1- and a2-containing AMPK complexes. Unlike troglitazone, it does not induce the activity of P4503A4. Significantly improves the differentiation of C3H10T1/2 stem cells into adipocytes. Shown to block estrogen synthesis by interfering with androgen binding to aromatase, but without affecting aromatase mRNA or protein expression.

Synthesis

110-16-7

122320-73-4

155141-29-0

Example 3: Preparation of rosiglitazone maleate 93.3 g (261.0 mmol) of rosiglitazone base prepared in Example 2 and 36.4 g (313.2 mmol) of maleic acid were suspended in 510 mL of isopropanol. The suspension was heated to reflux temperature and held for 1 hour until the initial suspension was transformed into a clarified colorless solution. Subsequently, the solution was cooled to 10 °C and filtered using a Büchner funnel. The filter cake was washed with 200 mL of isopropanol to yield 105.0 g of crude rosiglitazone maleate (85% yield, 99.57% HPLC purity). 41.1 g (86.9 mmol) of the above crude solid was suspended with 1.7 g (14.5 mmol) of maleic acid in 200 mL of ethanol (the ratio of maleic acid to ethanol was about 13.5:1, i.e., 0.17 equivalents of maleic acid per 2.3 L of ethanol). The suspension was heated to reflux temperature and maintained for 20 minutes. After that, the solution was cooled to 65 °C and the crystal seed particles of the desired rosiglitazone maleate polymorph were added. The resulting suspension was further cooled to 0 °C and filtered using a Büchner funnel. The filter cake was washed with 50 mL of ethanol to give a final product of 39.5 g of rosiglitazone maleate (96% yield, 99.89% HPLC purity) with a melting point of 120.6-121.7°C.

storage

+4°C

References

[1] BARRIE C. C. CANTELLO. [[.omega.-(Heterocyclylamino)alkoxy]benzyl]-2,4-thiazolidinediones as potent antihyperglycemic agents[J]. Journal of Medicinal Chemistry, 1994, 37 23: 3977-3985. DOI:10.1021/jm00049a017
[2] J M LEHMANN. An antidiabetic thiazolidinedione is a high affinity ligand for peroxisome proliferator-activated receptor gamma (PPAR gamma).[J]. The Journal of Biological Chemistry, 1995, 270 22: 12953-12956. DOI:10.1074/jbc.270.22.12953
[3] TIMOTHY M. WILLSON. The Structure−Activity Relationship between Peroxisome Proliferator-Activated Receptor γ Agonism and the Antihyperglycemic Activity of Thiazolidinediones[J]. Journal of Medicinal Chemistry, 1996, 39 3: 665-668. DOI:10.1021/jm950395a
[4] HARUYA OHNO. PPARγ agonists induce a white-to-brown fat conversion through stabilization of PRDM16 protein.[J]. Cell metabolism, 2012: 395-404. DOI:10.1016/j.cmet.2012.01.019
[5] FRANCISCO JAVIER RUIZ-OJEDA. Cell Models and Their Application for Studying Adipogenic Differentiation in Relation to Obesity: A Review.[J]. International Journal of Molecular Sciences, 2016, 17 7. DOI:10.3390/ijms17071040

Rosiglitazone maleate Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Rosiglitazone maleate Suppliers

Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10186
Advantage
62
LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
BOC Sciences
Tel
1-631-485-4226; 16314854226
Email
info@bocsci.com
Country
United States
ProdList
12952
Advantage
65
MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4861
Advantage
58
AdooQ BioScience, LLC
Tel
+1 (866) 930-6790
Fax
+1 (866) 333-9607
Email
info@adooq.com
Country
United States
ProdList
2782
Advantage
58
ApexBio Technology LLC
Tel
+1-832-696-8203
Fax
+1-832-641-3177
Email
info@apexbt.com
Country
United States
ProdList
477
Advantage
60
HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
EMMX Biotechnology LLC
Tel
888-539-0666
Fax
888-539-0666
Email
info@emmx.com
Country
United States
ProdList
8447
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354; +17819995354
Email
marketing@targetmol.com
Country
United States
ProdList
32435
Advantage
58
InvivoChem
Tel
+1-708-310-1919 +1-13798911105
Fax
708-557-7486
Email
sales@invivochem.cn
Country
United States
ProdList
6391
Advantage
58
Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
ApexBio Technology
Tel
--
Fax
--
Email
sales@apexbt.com
Country
United States
ProdList
6251
Advantage
58
BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Country
United States
ProdList
9923
Advantage
65
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6962
Advantage
56
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
Focus Biomolecules
Tel
--
Fax
--
Email
sales@focusbiomolecules.com
Country
United States
ProdList
1284
Advantage
58
Abcam Limited
Tel
--
Fax
--
Email
us.orders@abcam.com
Country
United States
ProdList
6001
Advantage
50
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81
Selleck Chemicals LLC
Tel
--
Fax
--
Email
sales@selleckchem.com
Country
United States
ProdList
1848
Advantage
58
SST Corporation
Tel
--
Fax
--
Email
info@sst-corp.com
Country
United States
ProdList
237
Advantage
38
ACIC Fine Chemicals Inc.
Tel
--
Fax
--
Email
sales@acic.com
Country
United States
ProdList
492
Advantage
48
OChem Incorporation
Tel
--
Fax
--
Email
sales@ocheminc.com
Country
United States
ProdList
6501
Advantage
60
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Ivy Fine Chemicals
Tel
--
Fax
--
Email
sales@ivychem.com
Country
United States
ProdList
6493
Advantage
58
LKT Laboratories, Inc.
Tel
--
Fax
--
Email
info@lktlabs.com
Country
United States
ProdList
2164
Advantage
64
Santa Cruz Biotechnology, Inc.
Tel
--
Fax
--
Email
scbt@scbt.com
Country
United States
ProdList
3597
Advantage
60
Medical Isotopes
Tel
--
Fax
--
Email
stohler@medicalisotopes.com
Country
United States
ProdList
6181
Advantage
68
AstaTech, Inc
Tel
--
Fax
--
Email
sales@astatechinc.com
Country
United States
ProdList
6371
Advantage
58
Beta Pharma, Inc.
Tel
--
Fax
--
Email
sales@betapharma.com
Country
United States
ProdList
6226
Advantage
60
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
Altan Corporation
Tel
--
Fax
--
Email
OrderingService@AltanBiochemicals.com
Country
United States
ProdList
1161
Advantage
30
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
APAC Pharmaceutical, LLC
Tel
--
Fax
--
Email
sales@apacpharma.com
Country
United States
ProdList
6322
Advantage
38
Fine Chem Trading LTD
Tel
--
Fax
--
Email
chemfinder@chemfinder.co.uk
Country
United States
ProdList
1609
Advantage
64
Molcan Corporation
Tel
--
Fax
--
Email
info@molcan.com
Country
United States
ProdList
686
Advantage
60
SynFine Research
Tel
--
Fax
--
Email
research@synfine.com
Country
United States
ProdList
1024
Advantage
68
Lab Express
Tel
--
Fax
--
Email
sales@labexpress.com
Country
United States
ProdList
1577
Advantage
67
BOSCHE SCIENTIFIC, LLC
Tel
--
Fax
--
Email
Sales@BoscheSci.com
Country
United States
ProdList
6477
Advantage
55
American Custom Chemicals Corporation
Tel
--
Fax
--
Email
sales@acccorporation.com
Country
United States
ProdList
6820
Advantage
51
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
A.G. Scientific, Inc.
Tel
--
Fax
--
Email
support@agscientific.com
Country
United States
ProdList
1066
Advantage
71
ChemPacific Corporation
Tel
--
Fax
--
Email
sales@chempacific.com
Country
United States
ProdList
6891
Advantage
51
More
Less

View Lastest Price from Rosiglitazone maleate manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Rosiglitazone maleate 155141-29-0
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98.0%
Supply Ability
1kg/month
Release date
2023-02-13
XINGTAI XINGJIU NEW MATERIAL TECHNOLOGY CO., LTD
Product
Rosiglitazone maleate 155141-29-0
Price
US $80.00/KG
Min. Order
1KG
Purity
99.9%
Supply Ability
500MT/month
Release date
2022-02-11
Zhuozhou Wenxi import and Export Co., Ltd
Product
Rosiglitazone maleate 155141-29-0
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-08-10

155141-29-0, Rosiglitazone maleateRelated Search:


  • 5-((4-[2-(METHYL-2-PYRIDINYLAMINO)-ETHOXY]-PHENYL)-METHYLENE)-2,4-THIAZOLIDINEDIONE
  • 5-{p-[2-(methyl-2-pyridylamino)ethoxy]benzyl}-2,4-thiazolidinedione maleate
  • ROSIGLITAZONE MALEATE
  • RosiglitazoneTartrate
  • Avandi
  • BRL-49653c
  • RSIGLITAZONEMALEATE
  • 5-(4-(2-(Methyl(pyridin-2-yl)aMino)ethoxy)benzyl)thiazolidine-2,4-dione Maleate
  • Rosiglitazone Maleate (200 mg)
  • 5-[[4-[2-(Methyl-2-pyridinylaMino)ethoxy]phenyl]Methyl]-2,4-thiazolidinedione (2Z)-2-Butenedioate
  • Rosiglitazone Maleate forM
  • Rosiglitazone-d3 Maleate
  • 5-[[4-[2-(methyl-2-pyridinylamino)ethoxy]phenyl]methyl]-2,4-thiazolidinedione,(2Z)-2-butenedioate (1:1)
  • 5-[[4-[2-(Methyl-2-pyridinylamino)ethoxy]phenyl]methyl]-2,4-thiazolidinedione maleate salt
  • 5-[[4-[2-[methyl(2-pyridinyl)amino]ethoxy]phenyl]methyl]thiazolidine-2,4-dione
  • Rosiglitazone maleate Solution, 1000ppm
  • 2,4-Thiazolidinedione, 5-[[4-[2-(methyl-2-pyridinylamino)ethoxy]phenyl]methyl]-, (2Z)-2-butenedioate (1:1)
  • Rosiglitazone maleate USP/EP/BP
  • Rosiglitazone maleateQ: What is Rosiglitazone maleate Q: What is the CAS Number of Rosiglitazone maleate Q: What is the storage condition of Rosiglitazone maleate Q: What are the applications of Rosiglitazone maleate
  • 2,4-Thiazolidinedione, 5-[[4-[2-(methyl-2-pyridinylamino)ethoxy]phenyl]methyl]-, (2Z)-2-butenedioate (1:1) (9CI, ACI)
  • 5-[[4-[2-(methyl-2-pyridinylamino)ethoxy]phenyl]methyl]-2,4-Thiazolidinedione (2Z)-2-butenedioate (1:1) (9CI ACI)
  • β-D-Fructopyranose1-Sulfamate
  • Rosiglitazone (BRL-49653) maleate
  • C16819000 RosiglitazonEMaleate
  • Rosiglitazone maleate (Avandia), PPARgamma agonist. Maleate salt.
  • Rosiglitazone maleate, 10 mM in DMSO
  • ROSIGLITAZONE MALEATE (NON-STERILE BULK DRUG SUBSTANCE)
  • Rosiglitazone maleate - Bio-X ?
  • 155141-29-0
  • C18H19N3O3SC4H4O4C22H23N3O7S
  • C18H19N3O3SC4H4O4C
  • C18H19N3O3SoC4H4O4
  • C18H19N3O3SC4H4O4
  • C22H23N3O7S
  • API
  • Inhibitor
  • Antidiabetic
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • API's
  • Rosiglitazone
  • Heterocycles
  • Sulfur & Selenium Compounds
  • Active Pharmaceutical Ingredients
  • 155141-29-0