ChemicalBook > CAS DataBase List > AST-1306

AST-1306

Product Name
AST-1306
CAS No.
1050500-29-2
Chemical Name
AST-1306
Synonyms
AST-6;CS-249;AST-130;AST-1306 (TsOH);AST1306 tosilate;AST-1306 mesylate;AST 1306 tosylate;AST1306; AST 1306;Allitinib tosylate;AST-1306 USP/EP/BP
CBNumber
CB22646572
Molecular Formula
C31H26ClFN4O5S
Formula Weight
621.0783432
MOL File
1050500-29-2.mol
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AST-1306 Property

storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
form 
Powder
color 
Light yellow to yellow
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

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

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N-Bromosuccinimide Price

Cayman Chemical
Product number
29708
Product name
AST-1306 (tosylate)
Packaging
1mg
Price
$57
Updated
2024/03/01
Cayman Chemical
Product number
29708
Product name
AST-1306 (tosylate)
Packaging
25mg
Price
$616
Updated
2024/03/01
Cayman Chemical
Product number
29708
Product name
AST-1306 (tosylate)
Packaging
5mg
Price
$262
Updated
2024/03/01
Cayman Chemical
Product number
29708
Product name
AST-1306 (tosylate)
Packaging
10mg
Price
$412
Updated
2024/03/01
ChemScene
Product number
CS-1209
Product name
Allitinibtosylate
Purity
99.23%
Packaging
5mg
Price
$180
Updated
2021/12/16
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AST-1306 Chemical Properties,Usage,Production

Uses

Alitinib (AST-1306) is a structural analog of lapatinib, a new quinazoline anti-tumor drug, and a small molecule epidermal growth factor receptor tyrosine kinase inhibitor, which selectively acts on EGFR/ErbB2 /ErbB4 receptor.

Biological Activity

ast-1306 is a selective, irreversible inhibitor of erbb2 and egfr with ic50 values of 0.5nm and 3nm, respectively [1].ast-1306 is designed and synthesized based on the chemical structure of lapatinib. the molecular docking method shows ast-1306 binds to the atp-binding pocket of the kinases and form covalent bind with certain amino acids. ast-1306 can inhibit egfr and erbb2 in a cell-free assay with more than 3000-fold selectivity to other kinases. besides the wild-type egfr, ast-1306 also inhibits egfr mutant t790m/l858r both in a cell-free assay and in hih3t3 cells. the growth of the cells is suppressed by ast-1306 due to the inhibition of the phosphorylation of egfr. it also occurs in some human cancer cells. experiments have proved that ast-1306 notly inhibits the phosphorylation of egfr and erbb2 and subsequently decreases the downstream pathways of these kinases in a549 cells, calu-3 cells and sk-ov-3 cells. moreover, ast-1306 potently inhibits the tumor growth both in erbb2-overexpressing xenograft models and fvb-2/nneu transgenic mouse model [1].

target

ErbB2

References

[1] xie h, lin l, tong l, jiang y, zheng m, chen z, jiang x, zhang x, ren x, qu w, yang y, wan h, chen y, zuo j, jiang h, geng m, ding j. ast1306, a novel irreversible inhibitor of the epidermal growth factor receptor 1 and 2, exhibits antitumor activity both in vitro and in vivo. plos one. 2011;6(7):e21487.

AST-1306 Preparation Products And Raw materials

Raw materials

Preparation Products

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AST-1306 Suppliers

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1050500-29-2, AST-1306Related Search:


  • AST-6
  • N-[4-[[3-Chloro-4-[(3-fluorophenyl)methoxy]phenyl]amino]-6-quinazolinyl]-2-propenamide 4-methylbenzenesulfonate
  • AST 1306 (p-Toluenesulfonic acid)
  • AST-1306 (p-Toluenesulfonic acid)
  • AST1306 (p-Toluenesulfonic acid)
  • AST-1306 (TsOH)
  • AST1306 tosilate
  • AST 1306 tosylate
  • AST-1306 mesylate
  • Allitinib tosylate
  • 2-Propenamide, N-[4-[[3-chloro-4-[(3-fluorophenyl)methoxy]phenyl]amino]-6-quinazolinyl]-, 4-methylbenzenesulfonate (1:1)
  • AST1306; AST 1306
  • CS-249
  • AST-130
  • AST-1306 USP/EP/BP
  • Allitinib tosylate AST-1306
  • N-(4-((3-Chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)quinazolin-6-yl)acrylamide 4-methylbenzenesulfonate
  • 1050500-29-2
  • C31H26ClFN4O5S
  • C24H18ClFN4O2C7H8O3S
  • Inhibitors
  • Anti-cancer&immunity