Sunitinib
- CAS No.
- 557795-19-4
- Chemical Name:
- Sunitinib
- Synonyms
- SUNITINIB BASE;SUNITINIB MALEATE;SNTI;Suniti;Sutini;SU-11248;sunitinib;Sutent-d4;SU-11248-d4;SUNITINIB-D4
- CBNumber:
- CB9728174
- Molecular Formula:
- C22H27FN4O2
- Molecular Weight:
- 398.47
- MOL File:
- 557795-19-4.mol
- Modify Date:
- 2024/7/17 18:13:28
Melting point | 189-191°C |
---|---|
Boiling point | 572.1±50.0 °C(Predicted) |
Density | 1.2 |
Flash point | 299.8℃ |
storage temp. | 2-8°C |
solubility | Chloroform (Slightly), Methanol (Slightly) |
pka | 8.5(at 25℃) |
form | Solid |
color | Yellow to Dark Orange |
CAS DataBase Reference | 557795-19-4(CAS DataBase Reference) |
SAFETY
Risk and Safety Statements
Symbol(GHS) | GHS07 |
---|---|
Signal word | Warning |
Hazard statements | H302-H315-H319-H332-H335 |
Precautionary statements | P280-P305+P351+P338-P310 |
Safety Statements | 24/25 |
HS Code | 29337900 |
Sunitinib Chemical Properties,Uses,Production
Description
Sunitinib is an inhibitor of multiple receptor tyrosine kinases (RTKs) involved in tumor proliferation and angiogenesis, including platelet-derived growth factor receptors (PDGFR), vascular endothelial growth factor receptors (VEGFR), and stem cell factor receptor (KIT). It was launched as an oral treatment for gastrointestinal stromal tumors (GIST) and advanced renal-cell carcinoma (RCC). In vitro, sunitib inhibits VEGFR2, PDGFRα, PDGFRβ, KIT, and FLT3 receptors with IC50 values in the 4–14nM range, and the ligand-dependent autophosphorylation of VEGFR2 and PDGFRb with IC50s of approximately 10 nM. In addition, it inhibits the growth of tumor cells expressing dysregulated target RTKs in vitro and inhibits PDGFRb- and VEGFR2-dependent tumor angiogenesis in vivo. Sunitinib exhibits broad and potent antitumor activity, causing regression in murine models of human epidermal (A431), colon (Colo205 and HT-29), lung (NCI-H226 and H460), breast (MDA-MB-435), prostate (PC3-3M-luc), and renal (786-O) cancers, and suppressing or delaying the growth of many others, including the C6 rat and SF763 T human glioma xenografts and B16 melanoma lung cancer.
Chemical Properties
Yellow Solid
Uses
Sunitinib Malate (Sutent, SU11248) is a multi-targeted RTK inhibitor targeting VEGFR2 (Flk-1) and PDGFRβ with IC50 of 80 nM and 2 nM, and also inhibits c-Kit.
Characteristics
Class: receptor tyrosine kinase
Treatment: RCC, GIST
Elimination half-life = 70 h
Protein binding = 95%
Sunitinib Preparation Products And Raw materials
Raw materials
Preparation Products
Supplier | Tel | Country | ProdList | Advantage | Inquiry |
---|---|---|---|---|---|
J S LABS | +91-7330612784 +91-7330612784 | Tamil Nadu, India | 160 | 58 | Inquiry |
Humble Healthcare Limited | +91-9720093000 +91-8006400378 | Uttar Pradesh, India | 141 | 58 | Inquiry |
Beta Drugs | +91-9316590666 +91-7015991921 | Haryana, India | 34 | 58 | Inquiry |
Shreyaa Medilife Private Limited | +91-6354474696 +91-9879513108 | Ahmedabad, India | 67 | 58 | Inquiry |
Laurus Labs Ltd | +91-4066594333 +91-4039804333 | Telangana, India | 50 | 58 | Inquiry |
Sakar Healthcare | +91-8976292690 +91-9967572302 | Gujarat, India | 47 | 58 | Inquiry |
AKASH PHARMA EXPORTS | +91-9388123451 +91-9846039283 | Kerela, India | 470 | 58 | Inquiry |
Hardik Onco Care | 08047642620 | Ahmedabad, India | 7 | 58 | Inquiry |
Medicare Remedies Private Limited | 08048957356 | Mumbai, India | 8 | 58 | Inquiry |
Pharmaffiliates Analytics and Synthetics P. Ltd | +91-172-5066494 | Haryana, India | 6773 | 58 | Inquiry |
Supplier | Advantage |
---|---|
J S LABS | 58 |
Humble Healthcare Limited | 58 |
Beta Drugs | 58 |
Shreyaa Medilife Private Limited | 58 |
Laurus Labs Ltd | 58 |
Sakar Healthcare | 58 |
AKASH PHARMA EXPORTS | 58 |
Hardik Onco Care | 58 |
Medicare Remedies Private Limited | 58 |
Pharmaffiliates Analytics and Synthetics P. Ltd | 58 |
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