MedChem Express
Bmpr1a Mouse Pre-designed siRNA Set A contains three designed siRNAs for Bmpr1a gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Bmpr1a Rat Pre-designed siRNA Set A contains three designed siRNAs for Bmpr1a gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BMPR1B Human Pre-designed siRNA Set A contains three designed siRNAs for BMPR1B gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Bmpr1b Mouse Pre-designed siRNA Set A contains three designed siRNAs for Bmpr1b gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Bmpr1b Rat Pre-designed siRNA Set A contains three designed siRNAs for Bmpr1b gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BMPR2 Human Pre-designed siRNA Set A contains three designed siRNAs for BMPR2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Bmpr2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Bmpr2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Bmpr2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Bmpr2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BMPR2-IN-1 (Compound 8a) is a BMPR2 inhibitor with an IC50 of 506 nM and a KD of 83.5 nM. BMPR2-IN-1 can be used for research of pulmonary arterial hypertension, Alzheimer’s disease and cancer[1].
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MedChem Express
BMPR2-IN-1 (Compound 8a) is a BMPR2 inhibitor with an IC50 of 506 nM and a KD of 83.5 nM. BMPR2-IN-1 can be used for research of pulmonary arterial hypertension, Alzheimer’s disease and cancer[1].
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BMS-932481 is an orally active modulator for γ-secretase, selectively reduce Aβ1-42 and Aβ1-40 production, with IC50s of 6.6 and 25.3 nM, respectively[1].
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BMS-960 is a potent and selective S1P1 receptor agonist containing isoxazole, which can be used in the research of immune diseases and vascular diseases[1].
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BMS-960 free base is a potent and selective S1P1 receptor agonist containing isoxazole, which can be used in the research of immune diseases and vascular diseases[1].
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BMS-986365 is a selective heterobifunctional ligand-directed degrader (LDD) targeting the androgen receptor (AR). BMS-986365 demonstrated significant in vivo potency, degrading AR, inhibiting AR signaling, and inhibiting tumor growth in animal models of advanced prostate cancer.
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BMS-986365 is a selective heterobifunctional ligand-directed degrader (LDD) targeting the androgen receptor (AR). BMS-986365 demonstrated significant in vivo potency, degrading AR, inhibiting AR signaling, and inhibiting tumor growth in animal models of advanced prostate cancer.
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MedChem Express
BMS-986365 is a selective heterobifunctional ligand-directed degrader (LDD) targeting the androgen receptor (AR). BMS-986365 demonstrated significant in vivo potency, degrading AR, inhibiting AR signaling, and inhibiting tumor growth in animal models of advanced prostate cancer.
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MedChem Express
BMS-986365 is a selective heterobifunctional ligand-directed degrader (LDD) targeting the androgen receptor (AR). BMS-986365 demonstrated significant in vivo potency, degrading AR, inhibiting AR signaling, and inhibiting tumor growth in animal models of advanced prostate cancer.
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MedChem Express
BMS-986365 is a selective heterobifunctional ligand-directed degrader (LDD) targeting the androgen receptor (AR). BMS-986365 demonstrated significant in vivo potency, degrading AR, inhibiting AR signaling, and inhibiting tumor growth in animal models of advanced prostate cancer.
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MedChem Express
BMS1 Human Pre-designed siRNA Set A contains three designed siRNAs for BMS1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BMT2 Human Pre-designed siRNA Set A contains three designed siRNAs for BMT2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BMX Human Pre-designed siRNA Set A contains three designed siRNAs for BMX gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Bmx Mouse Pre-designed siRNA Set A contains three designed siRNAs for Bmx gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Bmx Rat Pre-designed siRNA Set A contains three designed siRNAs for Bmx gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BN-82685 is a a quinone-based CDC25 inhibitor with IC50 of 201 nM, 117 nM, 109 nM, 160 nM, 249 nM, for CDC25C, CDC25C-cat, CDC25A, CDC25B2, CDC25B3, respectively. BN-82685 plays an important role in cancer research[1].
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BN-82685 is a a quinone-based CDC25 inhibitor with IC50 of 201 nM, 117 nM, 109 nM, 160 nM, 249 nM, for CDC25C, CDC25C-cat, CDC25A, CDC25B2, CDC25B3, respectively. BN-82685 plays an important role in cancer research[1].
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MedChem Express
BN-82685 is a a quinone-based CDC25 inhibitor with IC50 of 201 nM, 117 nM, 109 nM, 160 nM, 249 nM, for CDC25C, CDC25C-cat, CDC25A, CDC25B2, CDC25B3, respectively. BN-82685 plays an important role in cancer research[1].
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MedChem Express
BN-82685 is a a quinone-based CDC25 inhibitor with IC50 of 201 nM, 117 nM, 109 nM, 160 nM, 249 nM, for CDC25C, CDC25C-cat, CDC25A, CDC25B2, CDC25B3, respectively. BN-82685 plays an important role in cancer research[1].
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MedChem Express
BN-82685 is a a quinone-based CDC25 inhibitor with IC50 of 201 nM, 117 nM, 109 nM, 160 nM, 249 nM, for CDC25C, CDC25C-cat, CDC25A, CDC25B2, CDC25B3, respectively. BN-82685 plays an important role in cancer research[1].
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BNC1 Human Pre-designed siRNA Set A contains three designed siRNAs for BNC1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BNC2 Human Pre-designed siRNA Set A contains three designed siRNAs for BNC2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BNIP1 Human Pre-designed siRNA Set A contains three designed siRNAs for BNIP1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BNIP2 Human Pre-designed siRNA Set A contains three designed siRNAs for BNIP2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BNIP3 Human Pre-designed siRNA Set A contains three designed siRNAs for BNIP3 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BNIP3L Human Pre-designed siRNA Set A contains three designed siRNAs for BNIP3L gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BNIPL Human Pre-designed siRNA Set A contains three designed siRNAs for BNIPL gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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BNT411 is a selective TLR7 agonist that can induce the release of IFNa both in vivo and in vitro. BNT411 has anticancer activity and can be used in cancer research, including non-small cell lung cancer, pancreatic cancer, and untreated extensive-stage small cell lung cancer (ES-SCLC)[1].
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BOC Human Pre-designed siRNA Set A contains three designed siRNAs for BOC gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Boc-Asp(OBzl)-CMK is an inhibitor for IL-1 converting enzyme (ICE, caspase1). Boc-Asp(OBzl)-CMK prevents death of CHP100 neuroblastoma cell, and IL-1β release elicited by the viral coat protein[1].
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Boc-Orn(Z)-OH (Nα-Boc-Nδ-Cbz-L-ornithine) is a biochemical reagent that can be used as a biological material or organic compound for life science related research[1].
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BOD1 Human Pre-designed siRNA Set A contains three designed siRNAs for BOD1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
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