Heteroaromatic compounds

eMolecules​ Copper(ii) hexafluoroacetylacetonate hydrate | 14781-45-4 | MFCD00151019 | 5g

Combi-Blocks, Inc. | Copper(ii) hexafluoroacetylacetonate hydrate | 5g | 603152935 | QF-5164 | 95.000 | 14781-45-4 | MFCD00151019 | 495.664 | C10H4CuF12O5

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Medchemexpress LLC (2R)-3-(1H-indol-3-yl)-2-[[5-[2-(4-methylphenyl)ethynyl]thiophen-2-yl]sulfonylamino]propanoic acid | 203640-27-1 | MFCD22200275 | 99.8% | 464.56 g/mol | C24H20N2O4S2 | 25 MG

S 3304 is a matrix metalloproteinase inhibitor selective for MMP-2 and MMP-9 that contains an alkyne functional group enabling copper-catalyzed azide-alkyne cycloaddition (CuAAC) for bioorthogonal labeling. It is supplied as a light yellow solid with high purity for research use.

• Selective inhibitor of MMP-2 and MMP-9
• Contains an alkyne for copper-catalyzed azide-alkyne cycloaddition
• High purity (99.8%) suitable for biochemical studies
• Light yellow solid form for convenient handling
• Stable under recommended storage conditions
• Available in small research pack sizes and solution form

Medchemexpress LLC (R)-3-(1H-indol-3-yl)-2-(5-(p-tolylethynyl)thiophene-2-sulfonamido)propanoic acid | 203640-27-1 | MFCD22200275 | 99.8% | 464.56 g/mol | C24H20N2O4S2 | 1 ML

S 3304 is a small-molecule matrix metalloproteinase (MMP) inhibitor selective for MMP-2 and MMP-9. It is a D-tryptophan-derived compound that contains an alkyne handle for copper-catalyzed azide-alkyne cycloaddition (CuAAC). Reported to be orally active and non-cytotoxic in preclinical studies, it has been used to investigate angiogenesis and metastatic colonization.

• Selective inhibitor of MMP-2 and MMP-9.
• Contains an alkyne group for click chemistry (CuAAC).
• Reported oral activity and low cytotoxicity in preclinical models.
• High reported purity suitable for research applications.

Medchemexpress LLC (R)-3-(1H-indol-3-yl)-2-(5-(p-tolylethynyl)thiophene-2-sulfonamido)propanoic acid | 203640-27-1 | MFCD22200275 | 99.8% | 464.56 | C24H20N2O4S2 | 100 MG

S 3304 is a research-grade small-molecule inhibitor of matrix metalloproteinases with demonstrated selectivity for MMP-2 and MMP-9. The compound contains an alkyne functional group enabling click-chemistry applications and is formulated as a high-purity solid for use in in vitro and in vivo studies.

• Selective inhibition of MMP-2 and MMP-9.
• Contains an alkyne moiety compatible with copper-catalyzed azide-alkyne cycloaddition.
• Supplied as a light yellow solid with high purity.
• High solubility in DMSO for in vitro applications.
• Protocols available for in vivo formulation and dosing.
• Stable under frozen storage to preserve activity.
• Provided in a 100 mg research package.