Azobenzenes

eMolecules​ 4'-Aminoazobenzene-4-sulphonic acid | 104-23-4 | MFCD00035778 | 1g

Combi-Blocks | 4'-Aminoazobenzene-4-sulphonic acid | 1g | 205402053 | QA-5157 | 97.000 | 104-23-4 | MFCD00035778 | 277.300 | C12H11N3O3S

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Medchemexpress LLC 2-pyridinecarboxamide, 5-[[(6-chloro-2-pyridinyl)methyl](1-oxo-2-propen-1-yl)amino]-N-phenyl | 2305052-86-0 | MFCD06761688 | 99.9% | C21H17ClN4O2 | 10MG

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BPK-25 is an acrylamide-containing small-molecule research reagent that promotes degradation of nucleosome remodeling and deacetylation (NuRD) complex proteins and inhibits TMEM173 (STING) activation, resulting in modulation of NF-κB signaling. Supplied as a high-purity solid for in vitro and biochemical research; not intended for human use.

• Promotes NuRD complex protein degradation by covalent protein engagement.
• Inhibits STING (TMEM173) activation by the cyclic dinucleotide cGAMP.
• High purity suitable for biochemical assays and in vitro studies.
• Supplied as an off-white to light yellow solid for convenient handling.
• Recommended storage: 4°C under nitrogen; in solvent: -80°C (6 months) or -20°C (1 month).
• For research use only; not for clinical or human use.

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Medchemexpress LLC MEDCHEMEXPRESS LLC

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5000361194 MIND4-19 5MG

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Medchemexpress LLC MEDCHEMEXPRESS LLC

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5000400167 EPQPYEEIPIYL 1MG

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eMolecules​ Medchem Express / FzM1.8 / 10mg / 533802341 / HY-117163 / / 2204290-85-5 / [null] / 322.320 / C18H14N2O4

Medchem Express / FzM1.8 / 10mg / 533802341 / HY-117163 / / 2204290-85-5 / [null] / 322.320 / C18H14N2O4

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Chemscene ChemScene | Methyl 6-formylnicotinate | 5G | CS-D0517 | 0.98 | 10165-86-3| MFCD08275010 | 165.15

ChemScene | Methyl 6-formylnicotinate | 5G | CS-D0517 | 0.98 | 10165-86-3| MFCD08275010 | 165.15

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Medchemexpress LLC 5-hydroxy-2-methyl-7-(thiiran-2-ylmethoxy)-4H-chromen-4-one | 2133499-85-9 | MFCD32201069 | 99.7% | 264.30 g/mol | C13H12O4S | 10MG

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HSP27 inhibitor J2 is a small-molecule research reagent that targets heat shock protein 27 (HSP27), inducing abnormal HSP27 dimer formation and disrupting polymer assembly. It is provided as a solid and as a 10 mM solution in DMSO for biochemical and cellular studies; not for clinical use.

• Selective inhibitor of HSP27 for in vitro research.
• High purity: 99.7%.
• Molecular weight: 264.30 g/mol.
• Chemical formula: C13H12O4S.
• Available as solid and 10 mM solution in DMSO.
• Physical form: off-white to light yellow solid.
• Recommended storage: powder at -20°C or 4°C; in solvent at -80°C or -20°C.

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eMolecules​ Ambeed / 2-(5-(Dimethylamino)naphthalene-1-sulfonamido)acetic acid / 250mg / 586458002 / A836722 / / 1091-85-6 / MFCD00037734 / 308.350 / C14H16N2O4S

Ambeed / 2-(5-(Dimethylamino)naphthalene-1-sulfonamido)acetic acid / 250mg / 586458002 / A836722 / / 1091-85-6 / MFCD00037734 / 308.350 / C14H16N2O4S

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eMolecules​ Medchem Express / Nacubactam / 5mg / 628192271 / HY-109008 / / 1452458-86-4 / [null] / 324.310 / C9H16N4O7S

Medchem Express / Nacubactam / 5mg / 628192271 / HY-109008 / / 1452458-86-4 / [null] / 324.310 / C9H16N4O7S

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eMolecules​ ChemScene / Irondisulfide(Ironpyrite) / 5g / 601109816 / CS-0111192 / 0.000 / 12068-85-8 / [null] / 119.970 / FeS2

ChemScene / Irondisulfide(Ironpyrite) / 5g / 601109816 / CS-0111192 / 0.000 / 12068-85-8 / [null] / 119.970 / FeS2

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Medchemexpress LLC 1-(3,4-dihydroxy-5-nitrophenyl)-2-phenylethanone | 274925-86-9 | MFCD09954136 | 99.9% | 273.24 | C14H11NO5 | 100 MG

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Nebicapone is a reversible catechol-O-methyltransferase (COMT) inhibitor provided as a high-purity research reagent for biochemical and pharmacological studies. It is characterized by known identifiers and physical properties, and is intended for laboratory research use only (not for human use).

• Reversible COMT inhibitor suitable for enzyme assays and pharmacology studies.
• High purity for analytical and experimental consistency.
• Well-characterized identifiers available (CAS, MFCD, InChIKey).
• Soluble in DMSO for preparation of concentrated stock solutions.
• Supplied in a measured 100 mg amount for small-scale experiments.

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Medchemexpress LLC 4-N,6-N-bis[(4-fluoro-3-methylphenyl)methyl]pyrimidine-4,6-dicarboxamide | 544678-85-5 | MFCD09878513 | 99.2% | 410.42 g/mol | C22H20F2N4O2 | 5MG

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DB04760 is a potent, highly selective, non-zinc-chelating inhibitor of matrix metalloproteinase-13 (MMP-13) with a reported IC50 of 8 nM. In preclinical studies it reduced paclitaxel-induced neurotoxicity and exhibited anticancer activity. The compound is supplied for research use in multiple solid and solution formats and is provided with high purity.

• Potent MMP-13 inhibitor (IC50 = 8 nM).
• Non-zinc-chelating mechanism reduces off-target zinc interaction risk.
• Shown to reduce paclitaxel-induced neurotoxicity in studies.
• Exhibits anticancer activity in reported preclinical work.
• High purity (≈99.2%) with molecular weight 410.42 and formula C22H20F2N4O2.
• Available in solid and DMSO solution formats for research applications.

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Medchemexpress LLC MEDCHEMEXPRESS LLC

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5000355068 VALATEGRAST 50MG

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eMolecules​ Ambeed / (4S5S)-2-(2-(Diphenylphosphanyl)phenyl)-45-diphenyl-45-dihydrooxazole / 100mg / 633660447 / A1352088 / / 1918125-85-5 / [null] / 483.551 / C33H26NOP

Ambeed / (4S5S)-2-(2-(Diphenylphosphanyl)phenyl)-45-diphenyl-45-dihydrooxazole / 100mg / 633660447 / A1352088 / / 1918125-85-5 / [null] / 483.551 / C33H26NOP

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eMolecules​ AstaTech / (4-ETHYLTHIAZOL-2-YL)METHANAMINE DIHYDROCHLORIDE / 1g / 718080323 / AT34437 / 95.000 / 1262771-85-6 / MFCD09864312 / 215.140 / C6H12Cl2N2S

AstaTech / (4-ETHYLTHIAZOL-2-YL)METHANAMINE DIHYDROCHLORIDE / 1g / 718080323 / AT34437 / 95.000 / 1262771-85-6 / MFCD09864312 / 215.140 / C6H12Cl2N2S

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