Cat. No. | 製品名 | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
TP1364L | ALX 40-4C acetate | TP1364L | 98% |
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ALX 40-4C acetate is a CXCR4 inhibitor of the chemokine receptor (Ki = 1 μM) and suppresses the replication of X4 strains of HIV-1. ALX 40-4C acetate is an antag... | ||||
TP2051L | CTCE 9908 acetate | 98% |
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CTCE 9908 acetate is an antagonist of CXCR4 and inhibits migration in CXCR4-expressing ovarian cancer cells. | ||||
T76794 | Ulocuplumab | 1375830-34-4 | 98% |
Ulocuplumab
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Ulocuplumab (BMS-936564) is a fully human anti-CXCR4 IgG4 antibody.Ulocplumab exhibits antitumor activity in acute myeloid leukemia (AML), non-Hodgkin's lymphoma... | ||||
T76782 | Mogamulizumab | 1159266-37-1 | 98% |
Mogamulizumab
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Mogamulizumab (KW-0761) is a monoclonal antibody against T cell CC chemokine receptor 4. Mogamulizumab has anticancer activity, eliminating tumor cells through a... | ||||
T76741 | Eldelumab | 946414-98-8 | 98% |
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Eldelumab (BMS-936557) is a humanized anti-IP-10 IgG type 1 monoclonal antibody with inhibitory activity against CXCL10.Eldelumab has anti-inflammatory activity ... | ||||
TQ0174 | Mavorixafor | 558447-26-0 | 98% |
|
Mavorixafor (AMD-070) is an effective and selective antagonist of CXCR4, with an IC50 value of 13 nM against CXCR4 125I-SDF binding. Mavorixafor inhibits the rep... | ||||
T9721 | ML339 | 2579689-83-9 | 98% |
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ML339 a selective inhibitor of CXCR6(IC50 = 140 nM) with no response when screened against CXCR5 and CXCR4. | ||||
T5849 | JMS-17-2 | 1380392-05-1 |
|
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JMS-17-2 is a potent and selective antagonist of CX3CR1( IC50 : 0.32 nM). | ||||
T1776L | Plerixafor octahydrochloride | 155148-31-5 |
|
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Plerixafor octahydrochloride (JM3100 octahydrochloride) blocks the binding of stromal cell-derived factor (SDF-1alpha) to the cellular receptor CXCR4, resulting ... | ||||
TP2112L | TC14012 acetate | TP2112L |
|
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TC14012 acetate is a serum-stable derivative of T140 which is a selective and peptidomimetic CXCR4 antagonist with an IC50 of 19.3 nM. TC14012 is also a potent C... | ||||
T1776 | Plerixafor | 110078-46-1 | 100% |
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Plerixafor (AMD-3329), a chemokine receptor antagonist, blocks the binding of stromal cell-derived factor (SDF-1alpha) to the cellular receptor CXCR4. | ||||
T14665L | Motixafortide TFA(664334-36-5,Free) | T14665L | 100% |
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Motixafortide TFA(664334-36-5,Free) (BKT140 TFA) is an antagonist of CXCR4 with IC50 of ~1 nM. It induces the apoptosis of AML blasts by down-regulating ERK, BCL... | ||||
T11179 | Elubrixin | 688763-64-6 | 100.00% |
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Elubrixin (SB-656933) inhibits neutrophil CD11b upregulation (IC50 of 260.7 nM) and shape change (IC50 of 310.5 nM). Elubrixin can be used for inflammatory disea... | ||||
T1955 | SB225002 | 182498-32-4 | 96.86% |
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SB225002 is a potent and selective CXCR2 antagonist inhibiting interleukin IL-8 binding to CXCR2. | ||||
T3992 | MSX-122 | 897657-95-3 | 97.02% |
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MSX-122 is a novel small molecule and partial CXCR4 antagonist, with potent inhibition of CXCR4/CXCL12 actions(IC50 = 10 nM). | ||||
T6764L | ATI-2341 acetate(1337878-62-2 free base) | T6764L | 97.14% |
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ATI-2341 acetate is an effective allosteric agonist of CXCR4, it activates Gα1 instead of Gα13. ATI-2341 acetate activates inhibitory heterotrimeric G protein (G... | ||||
T12705 | Reparixin L-lysine salt | 266359-93-7 | 97.31% |
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Reparixin L-lysine salt (Repertaxin L-lysine salt) is an allosteric chemokine receptor 1/2 (CXCR1/2) activation inhibitor. | ||||
T15805L | LY2510924 acetate(1088715-84-7 free base) | T15805L | 97.32% |
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Ly2510924 acetate is an potent and selective CXCR4 antagonist. It prevents the binding of SDF-1 to CXCR4 with an IC50 of 0.079 nM. | ||||
T16850 | SB-265610 | 211096-49-0 | 97.67% |
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SB-265610 (GSK-CXCR2) is a nonpeptide and allosteric CXCR2 antagonist. SB-265610 blocks rat cytokine-induced neutrophil chemoattractant-1 (CINC-1)-induced calciu... | ||||
T26035 | Rac-NBI-74330 | 473722-68-8 | 97.85% |
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rac-NBI-74330 is an effective and selective CXCR3 antagonist. |