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ChemicalBook >> CAS DataBase List >> Pazopanib-d6

Pazopanib-d6

Pazopanib-d6 price.
  • $290 - $710
  • Product name: Pazopanib-d6
  • CAS: 1219592-01-4
  • MF: C21H23N7O2S
  • MW: 437.52
  • EINECS:
  • MDL Number:
  • Synonyms:Pazopanib-d6;2-methyl-5-[[4-[methyl-d3-[3-methyl-2-(methyl-d3)-2H-indazol-6-yl]amino]-2-pyrimidinyl]amino]-benzenesulfonamide;2H6]-Pazopanib
3 prices
Selected condition:
Brand
  • AK Scientific
  • Cayman Chemical
Package
  • 500μg
  • 1mg
  • ManufacturerAK Scientific
  • Product number3396DH
  • Product description2-Methyl-5-[[4-[[3-methyl-2-(trideuteriomethyl)indazol-6-yl]-(trideuteriomethyl)amino]pyrimidin-2-yl]amino]benzenesulfonamide
  • Packaging1mg
  • Price$710
  • Updated2021-12-16
  • Buy
  • ManufacturerCayman Chemical
  • Product number25446
  • Product descriptionPazopanib-d6 ≥99% deuterated forms (d1-d6)
  • Packaging500μg
  • Price$290
  • Updated2024-03-01
  • Buy
  • ManufacturerCayman Chemical
  • Product number25446
  • Product descriptionPazopanib-d6 ≥99% deuterated forms (d1-d6)
  • Packaging1mg
  • Price$549
  • Updated2024-03-01
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
AK Scientific 3396DH 2-Methyl-5-[[4-[[3-methyl-2-(trideuteriomethyl)indazol-6-yl]-(trideuteriomethyl)amino]pyrimidin-2-yl]amino]benzenesulfonamide 1mg $710 2021-12-16 Buy
Cayman Chemical 25446 Pazopanib-d6 ≥99% deuterated forms (d1-d6) 500μg $290 2024-03-01 Buy
Cayman Chemical 25446 Pazopanib-d6 ≥99% deuterated forms (d1-d6) 1mg $549 2024-03-01 Buy

Properties

storage temp. :Store at -20°C
solubility :DMF: 16 mg/ml; DMSO: 16 mg/ml
form :A solid

Safety Information

Symbol(GHS):
Signal word:
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
Precautionary statements:

Description

Pazopanib-d6 is intended for use as an internal standard for the quantification of pazopanib by GC- or LC-MS. Pazopanib is a multi-kinase inhibitor that inhibits the VEGF receptors VEGFR1, VEGFR2, and VEGFR3 (IC50s = 10, 30, and 47 nM, respectively, in a cell-free enzyme assay).1 It also inhibits PDGFRα, PDGFRβ, and c-Kit (IC50s = 71, 84, and 74 nM, respectively, in a cell-free enzyme assay) as well as additional receptor tyrosine kinases. Pazopanib inhibits upregulation of the surface adhesion proteins ICAM-1 and VCAM-1 induced by VEGF in multiple myeloma cells cocultured with human umbilical vein endothelial cells (HUVECs) and decreases multiple myeloma cell adhesion to HUVECs.2 It also inhibits proliferation of multiple myeloma cells cocultured with HUVECs. Pazopanib (30 and 100 mg/kg) reduces tumor growth, induces apoptosis, decreases angiogenesis, and increases survival in a multiple myeloma mouse xenograft model. Formulations containing pazopanib have been used in the treatment of cancer.