Anagrelide
CAS No. 68475-42-3
Anagrelide( Agrelin | Agrylin | Anagrelide | Anagrelide | BL 4162A | Xagrid | Shire | Thromboreductin )
Catalog No. M15616 CAS No. 68475-42-3
Anagrelide is a Platelet-reducing Agent. The mechanism of action of anagrelide is as a Phosphodiesterase 3 Inhibitor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 140 | In Stock |
|
| 10MG | 199 | In Stock |
|
| 25MG | 311 | In Stock |
|
| 50MG | 480 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameAnagrelide
-
NoteResearch use only, not for human use.
-
Brief DescriptionAnagrelide is a Platelet-reducing Agent. The mechanism of action of anagrelide is as a Phosphodiesterase 3 Inhibitor.
-
DescriptionAnagrelide is a Platelet-reducing Agent. The mechanism of action of anagrelide is as a Phosphodiesterase 3 Inhibitor.
-
In VitroCell Proliferation Assay Cell Line:Megakaryocytic and non-megakaryocytic cellsConcentration:0.05, 0.3, 1 μM Incubation Time:12-day Result:Inhibited only megakaryocytic cell growth at every concentration testedCell Cytotoxicity Assay Cell Line:GIST882 and GIST48 cell line Concentration:0.1, 1, 10, 100, 1000, 10000 nM Incubation Time:Result:Induced a cytotoxic effect in the GIST882 cell line (IC50= 16 nM), but was only weakly active in the GIST48 cell line.
-
In VivoAnimal Model:Adult female athymic mice bearing GIST2B, GIST3, GIST9, GIST882 model Dosage:5 mg/kg Administration:Twice daily; for 10 days Result:Inhibited or reduced tumor growth in three (GIST2B, GIST9, GIST882) of these four models.
-
SynonymsAgrelin | Agrylin | Anagrelide | Anagrelide | BL 4162A | Xagrid | Shire | Thromboreductin
-
PathwayAngiogenesis
-
TargetPDE
-
RecptorPDE
-
Research AreaCardiovascular Disease
-
Indication——
Chemical Information
-
CAS Number68475-42-3
-
Formula Weight256.09
-
Molecular FormulaC10H7Cl2N3O
-
Purity>98% (HPLC)
-
SolubilityDMSO: 10 mM
-
SMILESC1C2=C(C=CC(=C2Cl)Cl)NC3=NC(=O)CN31
-
Chemical Name6,7-dichloro-5,10-dihydro-3H-imidazo[2,1-b]quinazolin-2-one
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Venuti MC, et al. J Med Chem. 1988 Nov; 31(11): 2136-45.
molnova catalog
related products
-
EMD57439
EMD57439 is a selective PDE-III inhibitor, showing no significant increase in c-AMP concentration and producing little change in Ca(50).
-
Udenafil
A potent and selective phosphodiesterase 5 (PDE5) inhibitor for treat erectile dysfunction.
-
PF-8380
Potent autotaxin inhibitor (IC50?= 2.8 nM in isolated enzyme assay; 101 nM in human whole blood).
Cart
sales@molnova.com