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Filtered Search Results
Medchemexpress LLC UCM-13369 dihydrochloride | 99.87% | 462.46 | 5 MG
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UCM-13369 (Compound 4b) is a NPM1 inhibitor. It downregulates the pathway associated with mutant NPM1 C+, and specifically recognizes the C-end DNA-binding domain of NPM1 C+. It induces apoptosis in AML cell lines and primary cells and can be used for leukemia research.
- Downregulates the pathway associated with mutant NPM1 C+.
- Specifically recognizes the C-end DNA-binding domain of NPM1 C+.
- Induces apoptosis in AML cell lines and primary cells.
- Can be used for leukemia research.
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Aobchem AOBCHEM
5000862659 2-BROMO-4-CHLORO-5-FLUOROBENZO
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Aobchem AOBCHEM
5000873325 4-FLUORO-3-METHYL-5- METHYLTHI
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eMolecules 61200-60-0 | Ambeed | 25-Dichlorothiophene-3-carbaldehyde | 1g | 552719466 | A374719 | MFCD01571097 | 181.03 | C5H2Cl2OS
Ambeed | 25-Dichlorothiophene-3-carbaldehyde | 1g | 552719466 | A374719 | 61200-60-0 | MFCD01571097 | 181.030 | C5H2Cl2OS
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Aobchem AOBCHEM
5000873809 2-FLUORO-4-FORMYL-3- METHYLTHI
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Ambeed AMBEED
5000885846 TERT-BUTYL THIOPHEN-2-YL 5G
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Medchemexpress LLC Benzo[b]thiophene-3-carbaldehyde | 5381-20-4 | 162.21 | 1 G
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Benzo[b]thiophene-3-carbaldehyde is a 3-formyl-substituted benzo[b]thiophene derivative that functions as an oxidizable substrate. It converts to benzo[b]thiophene-3-carboxylic acid under liquid-phase conditions and exhibits lower oxidation difficulty compared to similar compounds. This compound can significantly increase reaction rates in the presence of initiators and is a key starting material for synthesizing compounds such as heteroaryl chalcones.
- Acts as an oxidizable substrate
- Converts to benzo[b]thiophene-3-carboxylic acid
- Exhibits lower oxidation difficulty
- Increases reaction rates with initiators
- Key starting material for heteroaryl chalcones synthesis
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Aobchem AOBCHEM
5000875186 2 3-DIBROMO-6-METHOXYBENZALDEH
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Aobchem AOBCHEM
5000875396 4 4-DIMETHYL-1- 5-METHYLTHIOPH
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Apexbio Technology LLC Pramipexole dihydrochloride 104632-25-9 10mM (in 1mL DMSO)
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Pramipexole dihydrochloride is a small-molecule agonist targeting dopamine receptors exhibiting selective affinity toward the D3 dopamine receptor subtype and lower affinity for the D2L D2S and D4 subtypes It is designed to stimulate dopamine receptor-mediated signaling thereby modulating dopaminergic pathways involved in motor function Pramipexole dihydrochloride exerts its biological activity primarily through dopamine receptor agonism and also demonstrates receptor-independent neuroprotective effects by attenuating mitochondrial reactive oxygen species (ROS) production and decreasing apoptosis-related signaling cascades Based on these pharmacological properties pramipexole dihydrochloride holds research potential in exploring dopaminergic system involvement and neuroprotective mechanisms relevant to neurodegenerative conditions such as Parkinson s disease and restless legs syndrome
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eMolecules 75815-46-2 | 2-Bromo-1-(2-thienyl)-1-propanone | Combi-Blocks, Inc. | MFCD08443970 | 219.100 | C7H7BrOS | 95.000 | CC(Br)C(=O)c1cccs1 | 1g | 569296515
2-Bromo-1-(2-thienyl)-1-propanone | Combi-Blocks, Inc. | 75815-46-2 | MFCD08443970 | 219.100 | C7H7BrOS | 95.000 | CC(Br)C(=O)c1cccs1 | 1g | 569296515
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O | 10g | 779539165](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000158672.jpg-250.jpg)
eMolecules 3976-69-0 | (R)-Methyl 3-hydroxybutanoate | Synthonix | MFCD00063289 | 118.132 | C5H10O3 | 95.000 | COC(=O)C[C@@H](C)O | 10g | 779539165
(R)-Methyl 3-hydroxybutanoate | Synthonix | 3976-69-0 | MFCD00063289 | 118.132 | C5H10O3 | 95.000 | COC(=O)C[C@@H](C)O | 10g | 779539165
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Medchemexpress LLC Bisantrene dihydrochloride | 71439-68-4 | 98.9% | 471.39 g/mol | C22H24Cl2N8 | 5 MG
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Bisantrene dihydrochloride is an anthracycline-class antitumor compound used in preclinical research. It intercalates into DNA, inhibits eukaryotic type II topoisomerases, and has demonstrated cytotoxic activity across multiple experimental tumor models. The material is provided as a solid for laboratory use with manufacturer storage and solubility guidance for solution preparations.
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![eMolecules 7312-10-9 | 5-Bromo-benzo[b]thiophene-2-carboxylic acid | Advanced Chemical Intermediates | MFCD01929338 | 257.100 | C9H5BrO2SOC(=O)c1cc2cc(Br)ccc2s1 | 10g | 164700649](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000162823.jpg-250.jpg)
eMolecules 7312-10-9 | 5-Bromo-benzo[b]thiophene-2-carboxylic acid | Advanced Chemical Intermediates | MFCD01929338 | 257.100 | C9H5BrO2SOC(=O)c1cc2cc(Br)ccc2s1 | 10g | 164700649
5-Bromo-benzo[b]thiophene-2-carboxylic acid | Advanced Chemical Intermediates | 7312-10-9 | MFCD01929338 | 257.100 | C9H5BrO2SOC(=O)c1cc2cc(Br)ccc2s1 | 10g | 164700649
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Aobchem AOBCHEM
5000861499 5-BROMO-4-METHYLTHIOPHENE-2-CA
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