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Filtered Search Results
Medchemexpress LLC [2-[[5-[(4-fluorophenyl)carbamoyl]pyrimidin-2-yl]sulfanylmethyl]-4-(trifluoromethoxy)phenyl]boronic acid | 1648843-04-2 | 98.7% | 1 ML
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SX-682 is a small-molecule allosteric inhibitor of chemokine receptors CXCR1 and CXCR2. It has been investigated preclinically and in clinical trials for reducing tumor myeloid-derived suppressor cell recruitment and enhancing anti-tumor immune responses.
- Potent CXCR1/2 allosteric inhibitor used in research.
- Investigated in immuno-oncology and tumor microenvironment studies.
- Reported to reduce myeloid-derived suppressor cell recruitment.
- Supplied for laboratory research, often as concentrated solutions or milligram-scale powders.
- Soluble in DMSO at high concentrations for in vitro use.
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Apexbio Technology LLC NVR 3-778 1445790-55-5 10mg
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NVR 3-778 (CAS 1445790-55-5) is a small-molecule modulator targeting the hepatitis B virus (HBV) core protein It is designed to interfere with HBV capsid assembly thereby inhibiting viral genome encapsidation and replication NVR 3-778 exerts its biological activity primarily by disrupting capsid formation and reducing viral replication In in vitro studies NVR 3-778 demonstrates antiviral inhibition with a half-maximal inhibitory concentration (IC50) reported in the low micromolar range Based on these pharmacological properties NVR 3-778 holds research potential in the investigation of HBV biology and the development of alternative therapeutic approaches for chronic hepatitis B infection
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5000338703 THP-PEG5-OH 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000383713 TOS-PEG5-C2-BOC 250MG
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5000380488 BR-PEG3-OH 5G
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eMolecules CYCLOPENT-2-ENONE 1G
5000158806 CYCLOPENT-2-ENONE 1G
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eMolecules 2-(BROMODIFLUOROMETHYL)-BENZOTHIAZOLE | 235781-28-9 | MFCD09264133 | 1g
AstaTech | 2-(BROMODIFLUOROMETHYL)-BENZOTHIAZOLE | 1g | 385237042 | 70315 | 97.000 | 235781-28-9 | MFCD09264133 | 264.090 | C8H4BrF2NS
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Apexbio Technology LLC NVR 3-778 1445790-55-5 5mg
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NVR 3-778 (CAS 1445790-55-5) is a small-molecule modulator targeting the hepatitis B virus (HBV) core protein It is designed to interfere with HBV capsid assembly thereby inhibiting viral genome encapsidation and replication NVR 3-778 exerts its biological activity primarily by disrupting capsid formation and reducing viral replication In in vitro studies NVR 3-778 demonstrates antiviral inhibition with a half-maximal inhibitory concentration (IC50) reported in the low micromolar range Based on these pharmacological properties NVR 3-778 holds research potential in the investigation of HBV biology and the development of alternative therapeutic approaches for chronic hepatitis B infection
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000360144 S R S -AHPC-C2-PEG3 100MG
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eMolecules EMOLECULES INC
5000191410 TERT-BUTYL-2-IODOETHOXY 250MG
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5000352588 NH-BIS C2-PEG1-AZIDE 250MG
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5000352736 N- AZIDO-PEG3 -N-BIO 250MG
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5000352556 N- AZIDO-PEG2 -N-BIS 250MG
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5000352548 M-PEG3-OMS 250MG
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5000342576 POMALIDOMIDE-PEG3-C2 2G
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