Thiophenes

Aobchem AOBCHEM

5000907070 TRIMETHYL 5- METHYLTHIO THIOPH

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Aobchem AOBCHEM

5000907084 ETHYL 2- 3-FLUORO-5- METHYLTHI

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Aobchem AOBCHEM

5000907793 2-FLUORO-4-METHYL-3- METHYLTHI

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eMolecules​ 6164-79-0 | methyl pyrazine-2-carboxylate | Pharmablock | MFCD00014611 | 138.126 | C6H6N2O2 | 97.000 | COC(=O)c1cnccn1 | 5g | 596114927

methyl pyrazine-2-carboxylate | Pharmablock | 6164-79-0 | MFCD00014611 | 138.126 | C6H6N2O2 | 97.000 | COC(=O)c1cnccn1 | 5g | 596114927

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eMolecules​ 1013-23-6 | Dibenzo[b,d]thiophene 5-oxide | ChemScene | MFCD00046902 | 200.260 | C12H8OS | 96.000 | O=s1c2ccccc2c2ccccc12 | 25g | 711937355

Dibenzo[b,d]thiophene 5-oxide | ChemScene | 1013-23-6 | MFCD00046902 | 200.260 | C12H8OS | 96.000 | O=s1c2ccccc2c2ccccc12 | 25g | 711937355

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Selleck Chemical LLC 1400W 2HCl

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1400W (N-(3-(Aminomethyl)benzyl)acetamidine) is a slow tight binding and highly selective inhibitor of inducible nitric-oxide synthase(iNOS)

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Medchemexpress LLC Minaprine dihydrochloride | 25953-17-7 | 99.9% | 1 ML

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Minaprine dihydrochloride | 25953-17-7 | 99.9% | 1 ML

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Apexbio Technology LLC H 89 2HCl 130964-39-5 50mg

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H 89 2HCl (CAS 130964-39-5) is a small-molecule inhibitor targeting cyclic AMP-dependent protein kinase (PKA) It exhibits a Ki of approximately 48 nM toward PKA and demonstrates substantial selectivity compared to related kinases such as PKG (about 10-fold) PKC MLCK calmodulin kinase II and casein kinases (approximately 500-fold) In PC12D cells H 89 at micromolar concentrations suppresses forskolin-induced phosphorylation events and neurite outgrowth without altering intracellular cAMP levels Due to its selective inhibitory profile H 89 is widely utilized in cell signaling studies examining cAMP-dependent pathways

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eMolecules​ 6165-68-0 | (thiophen-2-yl)boronic acid | Key Organics/BIONET | MFCD00151850 | 127.950 | C4H5BO2S | 95.000 | OB(O)c1cccs1 | 50mg | 564105737

(thiophen-2-yl)boronic acid | Key Organics/BIONET | 6165-68-0 | MFCD00151850 | 127.950 | C4H5BO2S | 95.000 | OB(O)c1cccs1 | 50mg | 564105737

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Medchemexpress LLC Lomerizine dihydrochloride | 101477-54-7 | 99.95% | 1 ML

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Lomerizine dihydrochloride, also known as KB-2796, is a potent antagonist of L- and T-type voltage-gated calcium channels. This chemical is supplied at a concentration of 10mM in 1mL of DMSO. It is crucial for researchers studying calcium channel modulation and related neurological processes.

• Antagonist of L-type voltage-gated calcium channels
• Antagonist of T-type voltage-gated calcium channels
• Packaged as a 10mM solution in DMSO
• Recommended storage at 4°C, sealed, away from moisture
• Stable in solvent for 6 months at -80°C or 1 month at -20°C
• Suitable for shipping at room temperature for durations less than 2 weeks

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eMolecules​ 127025-34-7 | THIENO[3,2-B]THIOPHEN-2-YLMETHANOL | AstaTech | MFCD08059495 | 170.240 | C7H6OS2 | 95.000 | OCc1cc2sccc2s1 | 1g | 342445113

THIENO[3,2-B]THIOPHEN-2-YLMETHANOL | AstaTech | 127025-34-7 | MFCD08059495 | 170.240 | C7H6OS2 | 95.000 | OCc1cc2sccc2s1 | 1g | 342445113

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Medchemexpress LLC Alexidine dihydrochloride | 1715-30-6 | ≥98% | 581.71 | 1 ML

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Alexidine dihydrochloride is an anticancer agent that targets a mitochondrial tyrosine phosphatase, PTPMT1, in mammalian cells, leading to mitochondrial apoptosis. It also exhibits broad-spectrum antifungal and antibiofilm activity against various fungal pathogens, including fluconazole-resistant strains and mature biofilms.

• Targets mitochondrial tyrosine phosphatase (PTPMT1).
• Induces mitochondrial apoptosis.
• Shows broad-spectrum antifungal activity against diverse fungal pathogens.
• Effective against fluconazole-resistant Candida isolates.
• Inhibits filamentation and proliferation of fungi.
• Decimates mature biofilms of Candida, Cryptococcus, and Aspergillus species at low concentrations.
• Inhibits lateral yeast formation and biofilm dispersal in C. albicans.
• Reduces fungal biofilm growth and viability by 67% in C. albicans murine models.

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Medchemexpress LLC DDP-38003 dihydrochloride | 1831167-98-6 | 99.3% | 423.38 | 50 MG

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DDP-38003 dihydrochloride is a novel, orally available inhibitor of histone lysine-specific demethylase 1A (KDM1A/LSD1) with an IC50 of 84 nM. It demonstrates significant in vitro and in vivo efficacy, inhibiting KDM1A and reducing colony forming ability in THP-1 cells. In mouse leukemia models, oral administration of DDP-38003 dihydrochloride led to increased survival.

• Inhibits histone lysine-specific demethylase 1A (KDM1A/LSD1)
• Orally available
• IC50 of 84 nM for KDM1A
• Reduces colony forming ability and induces differentiation of THP-1 cells
• Shows in vivo efficacy in mouse leukemia models
• Potential oral anticancer agent

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Medchemexpress LLC 5-Methyl-2-thiophenecarboxaldehyde | 13679-70-4 | 99.9% | 126.18 | 100 G

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5-Methyl-2-thiophenecarboxaldehyde acts as a candidate to microscopic third order non-linear optical (NLO) material. It is also an analytical standard intended for research and analytical applications.

• Acts as a candidate to microscopic third order non-linear optical (NLO) material.
• Analytical standard for research and analytical applications.

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Aobchem AOBCHEM

5000917531 5-BROMO-2-FLUORO-3- METHYLTHI

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