Chemical Structure : AMD-070
CAS No.: 558447-26-0
货号: PC-45823Not For Human Use, Lab Use Only.
Mavorixafor (AMD-070, AMD-11070) is a potent and selective antagonist of CXCR4 with IC50 of 13 nM in a CXCR4 125I-SDF inhibition binding assay.
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---|---|---|---|
5 mg | ¥1280 | In stock | |
10 mg | ¥1980 | In stock | |
25 mg | ¥3580 | In stock | |
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100 mg | Get quote |
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Mavorixafor (AMD-070, AMD-11070) is a potent and selective antagonist of CXCR4 with IC50 of 13 nM in a CXCR4 125I-SDF inhibition binding assay.
AMD-070 displays no significant activity (IC50>10 uM) for a series of other closely GPCRs (CCR1, CCR2b, CCR4, CCR5, CXCR1, and CXCR2).
AMD-070 inhibits the replication of T-tropic HIV-1 (NL4.3 strain) in MT-4 cells and PBMCs with IC50 of 2 nM and 26 nM, respectively, with noncytotoxic to cells (>23 uM).
AMD-070 exhibits good PK profiles and excellent oral bioavailability.
AMD-070 also inhibits CXCR4/SDF-1-mediated events in ALL cancer cells and transplant models.
分子量 | 349.4726 | |
分子式 | C21H27N5 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
1,4-Butanediamine, N1-(1H-benzimidazol-2-ylmethyl)-N1-[(8S)-5,6,7,8-tetrahydro-8-quinolinyl]- |
1. Skerlj RT, et al. J Med Chem. 2010 Apr 22;53(8):3376-88.
2. Stone ND, et al. Antimicrob Agents Chemother. 2007 Jul;51(7):2351-8.
3. Parameswaran R, et al. Leukemia. 2011 Aug;25(8):1314-23.
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