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Mavorixafor trihydrochloride (C007B-374714)

Catalog No.
C007B-374714
Manufacturer No.
M649127-10mg
Manufacturer Name
Aladdin Scientific
Quantity
1
Unit of Measure
EA

Mavorixafor trihydrochloride (AMD-070 trihydrochloride) is a potent, selective and orally available CXCR4 antagonist, with an IC 50 value of 13 nM against CXCR4 125 I-SDF binding, and also inhibits the replication of T-tropic HIV-1 (NL4.3 strain) in

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Mavorixafor trihydrochloride (AMD-070 trihydrochloride) is a potent, selective and orally available CXCR4 antagonist, with an IC 50 value of 13 nM against CXCR4 125 I-SDF binding, and also inhibits the replication of T-tropic HIV-1 (NL4.3 strain) in MT-4 cells and PBMCs with an IC 50 of 1 and 9 nM, respectively.In VitroMavorixafor (AMD-070) is a potent and orally available CXCR4 antagonist, with an IC 50 value of 13 nM against CXCR4 125 I-SDF binding, and also inhibits the replication of T-tropic HIV-1 (NL4.3 strain) in MT-4 cells and PBMCs with an IC 50 of 1 and 9 nM, respectively. Mavorixafor (AMD-070) shows no effect on other chemokine receptors (CCR1, CCR2b, CCR4, CCR5, CXCR1, and CXCR2). Mavorixafor (AMD-070) (6.6 µM) significantly suppresses the anchorage-dependent growth, the migration and matrigel invasion of the B88-SDF-1 cells. MCE has not independently confirmed the accuracy of these methods. They are for reference only.In VivoMavorixafor (AMD-070) (2 mg/kg, p.o.) significantly reduces the number of metastatic lung nodules in mice, and lowers the expression of human Alu DNA in mice, without body weight loss. MCE has not independently confirmed the accuracy of these methods. They are for reference only.Cell AssayCells are seeded on a 96-well plate at 5 × 10 3 cells/well in DMEM containing 10% FCS. Twenty-four hours later, the cells are treated with or without 2 µM Mavorixafor (AMD-070) or 6.6 µM AMD-070 . After 24 or 48 h , the number of cells is quantified by an assay using MTT. MCE has not independently confirmed the accuracy of these methods. They are for reference only.Animal administrationMice BALB/c nude mice are maintained under pathogen-free conditions. The experiments are initiated when the mice are 8 weeks of age. Briefly, the cells are inoculated into the blood vessels of nude mice ( 1× 10 6 ). These mice are sacrificed at day 49. The presence or absence of distant metastases is confirmed by hematoxylin and eosin (H&E) staining. For experimental chemotherapy, the mice are treated by the daily oral administration of 0.2 mL of saline for a vehicle or the same volume of Mavorixafor (AMD-070) (2 mg/kg) . aladdin has not independently confirmed the accuracy of these methods. They are for reference only.Form:SolidIC50& Target:125 I-SDF-CXCR4 13 nM (IC 50 ) HIV-1 (NL4.3 strain) 1 nM (IC 50 , in MT-4 cells) HIV-1 (NL4.3 strain) 9 nM (IC 50 , in PBMCs) HIV-1 (NL4.3 strain) 3 nM (IC90, in MT-4 cells) HIV-1 (NL4.3 strain) 26 nM (IC90, in PBMCs).

Specifications and Purity: ≥98%

Molecular Formula: C21H30Cl3N5

Molecular Weight: 458.86

PubChem CID: 78357868

Isomeric SMILES: C1C[C@@H](C2=C(C1)C=CC=N2)N(CCCCN)CC3=NC4=CC=CC=C4N3.Cl.Cl.Cl

UPC:
51101616
Condition:
New
HazmatClass:
No
WeightUOM:
LB
MPN:
M649127-10mg
CAS:
2309699-17-8
Product Size:
10mg

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