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Filtered Search Results
Medchemexpress LLC Ripk1-In-10 10Mg | HY-143728-10MG
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Ripk1-In-10 10Mg
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Medchemexpress LLC HY-18314 10mg Medchemexpress, GW 441756 CAS:504433-23-2 Purity:>98%
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Medchemexpress, HY-18314 10mg GW 441756 CAS:504433-23-2 0 Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-12809 5mg Medchemexpress, Optovin CAS:348575-88-2 Purity:>98%
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Medchemexpress, HY-12809 5mg Optovin CAS:348575-88-2 Optovin is a reversible photoactivated TRPA1 ligand that enables light-mediated neuronal excitation. Optovin activates TRPA1 via structure-dependent photochemical reactions with redox-sensitive cysteine residues. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Ripk1-in-10 | 2682889-51-4 | 98.25% | C30H28F2N6O4 | 100 MG
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RIPK1-IN-10 is a potent RIPK1 inhibitor, identified as example 37, extracted from patent WO2021160109. This product is intended for research use only and is not sold to patients. It is available as a solid, with a color ranging from white to light yellow.
- Potent RIPK1 inhibitor
- Intended for research use only
- Available as a solid
- Color ranges from white to light yellow
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000307894 JNJ-63576253 5MG
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Medchemexpress LLC BI-2852 | 2375482-51-0 | MFCD32197229 | 10 mg
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BI-2852 | Purity: 98.74% | Mol Wt: 516.60 | 2375482-51-0 | MFCD32197229 | 10 mg
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000378942 JNJ-42226314 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000378202 ADH-503 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000382773 TLR7 8 9-IN-1 100MG
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Medchemexpress LLC BML-111 (lipoxin A4 analog) | 78606-80-1 | ≥98.0% | 192.21 g/mol | C8H16O5 | 5 MG
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BML-111 is a lipoxin A4 analog and FPR2 (lipoxin A4 receptor) agonist used in research to study inflammatory, angiogenic, and tumor-related pathways. It is supplied as a high-purity compound in powder or solution formats for laboratory applications.
- High purity ≥98.0%.
- Molecular weight 192.21 g/mol.
- Molecular formula C8H16O5.
- Available in small pack sizes and solution formats (e.g., 5 mg, 1 mL 10 mM in DMSO).
- Intended for research use only, not for human or veterinary use.
- Suitable for in vitro and in vivo experimental studies.
- CAS number 78606-80-1.
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Medchemexpress LLC HY-18668 5mg Medchemexpress, Integrin Antagonists 27 CAS:593274-97-6 Purity:>98%
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Medchemexpress, HY-18668 5mg Integrin Antagonists 27 CAS:593274-97-6 Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 163769-88-8 | Medchem Express | YM-90709 | 5mg | 446270633 | HY-19969 | MFCD00354370 | 359.429 | C22H21N3O2
AstaTech | 2-(4-CHLOROPHENYL)-134-OXADIAZOLE | 1g | 449735187 | 57414 | 97.000 | 23289-10-3 | MFCD08361748 | 180.590 | C8H5ClN2O
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Medchemexpress LLC Jnj-18038683 | 851376-05-1 | 99.8% | 529.97 g/mol | C26H28ClN3O7 | 10 MG
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This small-molecule research compound is a selective antagonist of the 5-hydroxytryptamine type 7 (5-HT7) receptor used in pharmacology and neuroscience studies. It shows high affinity in binding assays (pKi ≈ 8.19-8.20 for rat and human 5-HT7 in HEK293 cells), produces concentration-dependent inhibition of 5-HT-stimulated adenylyl cyclase, and alters REM sleep in rodent models. Supplied as a solid or as a DMSO solution for in vitro and in vivo research.
- Selective 5-HT7 receptor antagonist with high binding affinity.
- Demonstrated functional antagonism in adenylyl cyclase assays.
- Modulates REM sleep parameters in rodent studies.
- High purity suitable for research applications.
- Available as solid and ready-to-use DMSO solution.
- Store sealed and protect from moisture; follow supplier storage guidelines.
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Medchemexpress LLC TLR7 agonist 3 | 1229024-78-5 | 99.9% | 312.41 | C18H24N4O | 10 MG
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TLR7 agonist 3 is a small-molecule agonist of Toll-like receptor 7 used for preclinical in-vitro and in-vivo research. It is supplied as a white to off-white solid with high reported purity, defined solubility, and recommended storage to support formulation and dosing.
- Potent TLR7 agonist for immune activation studies.
- White to off-white solid appearance.
- High purity (99.9%).
- Molecular formula C18H24N4O; molecular weight 312.41 g/mol.
- Soluble in DMSO and ethanol; compatible with co-solvent in vivo formulations.
- Recommended storage: powder at -20°C for long term, 4°C for shorter storage.
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Medchemexpress LLC TLR7 agonist 3 | 1229024-78-5 | 99.9% | 312.41 g/mol | C18H24N4O | 100 MG
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TLR7 agonist 3 is a small-molecule agonist of Toll-like receptor 7 used as a research reagent to stimulate innate immune responses and evaluate anticancer immunomodulatory strategies. It is supplied as a high-purity solid suitable for in vitro and in vivo studies.
- Potent agonist of Toll-like receptor 7 (TLR7) for immune activation studies.
- Applicable for conjugation to targeting ligands to direct activity to specific cell types.
- High purity solid suitable for analytical and biological assays.
- Soluble in DMSO (100 mg/mL) and ethanol (≥50 mg/mL); compatible with common in vivo formulations at ≥2.5 mg/mL.
- Offered in multiple pack sizes including 100 mg for dosing flexibility.
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