
Aripiprazole Lauroxil
CAS No. 1259305-29-7
Aripiprazole Lauroxil( —— )
Catalog No. M26609 CAS No. 1259305-29-7
Aripiprazole lauroxil, the N-acyloxymethyl prodrug form of aripiprazole, a long-acting injectable (LAI) antipsychotic.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
10MG | 37 | Get Quote |
![]() ![]() |
25MG | 59 | Get Quote |
![]() ![]() |
50MG | 87 | Get Quote |
![]() ![]() |
100MG | 119 | Get Quote |
![]() ![]() |
200MG | 178 | Get Quote |
![]() ![]() |
500MG | 301 | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameAripiprazole Lauroxil
-
NoteResearch use only, not for human use.
-
Brief DescriptionAripiprazole lauroxil, the N-acyloxymethyl prodrug form of aripiprazole, a long-acting injectable (LAI) antipsychotic.
-
DescriptionAripiprazole lauroxil, the N-acyloxymethyl prodrug form of aripiprazole, a long-acting injectable (LAI) antipsychotic. Aripiprazole lauroxil is cleaved by esterases in vivo to N-hydroxymethyl aripiprazole (lauric acid), which is then cleaved to aripiprazole, which is non-toxic.(In Vivo):Intravenous administration of 1.87?mg/ml Aripiprazole lauroxil bioconversion in vivo involves the formation of an intermediate,?N-hydroxymethyl aripiprazole. The?in vitro?data indicates a high bioconversion of aripiprazole lauroxil, thus, the concentration of?N-hydroxymethyl aripiprazole observed in the animals dosed with aripiprazole lauroxil is surprisingly high.
-
In Vitro——
-
In VivoAnimal Model:Female Sprague Dawley ratsDosage:1.87?mg/ml?Administration:Blood samples is taken at 5, 15, 30?min and 1, 2, 4, 6, 8 and 24?h after administration Result:Exhibits an clearance: 0.32?±?0.11?L/h/kg.?
-
Synonyms——
-
PathwayGPCR/G Protein
-
TargetDopamine Receptor
-
RecptorMycobacterium tuberculosis
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1259305-29-7
-
Formula Weight660.72
-
Molecular FormulaC36H51Cl2N3O4
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 8.33 mg/mL (12.61 mM)
-
SMILESCCCCCCCCCCCC(=O)OCN1C(=O)CCc2ccc(OCCCCN3CCN(CC3)c3cccc(Cl)c3Cl)cc12
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Korycka-Machala M, et al. Naphthalimides Selectively Inhibit the Activity of Bacterial, Replicative DNA Ligases and Display Bactericidal Effects against Tubercle Bacilli. Molecules. 2017 Jan 17;22(1). pii: E154.
molnova catalog



related products
-
NMI 8739
NMI 8739 is an agonist of D2 autoreceptor. NMI 8739 reduces NO production and elicits concentration-dependent suppression of CCL-20, MCP-1 and IL-6 release.
-
Thiethylperazine dim...
Thiethylperazine dimaleate is an antagonist of the D2 receptor and H1 receptor.
-
Cariprazine HCl
Cariprazine HCl is an antipsychotic drug is a D3 and D2?receptor partial agonist((Ki of 0.085 nM and 0.49 nM respectively).