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Filtered Search Results
Selleck Chemical LLC N-(Hytroxymethy)micotinamide S5390-25mg
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N-(Hydroxymethyl)nicotinamide (Nikomethamide Bilamid N-hydroxymethylnicotinamide) is an antimicrobial agent
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Medchemexpress LLC HY-108022 10mg Medchemexpress, MSDC-0602 CAS:1133819-87-0 Purity:>98%
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Medchemexpress, HY-108022 10mg MSDC-0602 CAS:1133819-87-0 MSDC-0602, a PPARγ-sparing thiazolidinedione (TZD), interacts with the mitochondrial pyruvate carrier (MPC) and inhibits its activity and are effective for treatment of type 2 diabetes with reducing risk of PPARγ-mediated side effects. 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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![Strem, An Ascensus Company CAS 1372719-93-1. 100mg. (11aR)-10111213-Tetrahydro-5-hydroxy-37-di-9-phenanthrenyl-5-oxide-diindeno[71-de17-fg][132]dioxaphosphocin min. 98%.](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00009818-15-1363.JPG-250.jpg)
Strem, An Ascensus Company CAS 1372719-93-1. 100mg. (11aR)-10111213-Tetrahydro-5-hydroxy-37-di-9-phenanthrenyl-5-oxide-diindeno[71-de17-fg][132]dioxaphosphocin min. 98%.
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CAS 1372719-93-1. 100mg. (11aR)-10111213-Tetrahydro-5-hydroxy-37-di-9-phenanthrenyl-5-oxide-diindeno[71-de17-fg][132]dioxaphosphocin min. 98%. . Molecular Weight 666.70. Molecular Formula C45H31O4P. Color/form white to light-yellow pwdr. Strem 15-1363. http//www.strem.com/catalog/v/15-1363/
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eMolecules 4371-31-7 | 2,2',4,4'-Tetrahydroxybiphenyl | Oakwood Chemical | MFCD00053302 | 218.208 | C12H10O4 | 98.000 | Oc1ccc(c(O)c1)-c1ccc(O)cc1O | 100mg | 537709579
2,2',4,4'-Tetrahydroxybiphenyl | Oakwood Chemical | 4371-31-7 | MFCD00053302 | 218.208 | C12H10O4 | 98.000 | Oc1ccc(c(O)c1)-c1ccc(O)cc1O | 100mg | 537709579
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Medchemexpress LLC TFMB-(R)-2-HG | 1445700-01-5 | 98.3% | 10 MG
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TFMB-(R)-2-HG is a cell membrane-permeable (R)-2-HG and an acute myeloid leukemia (AML) oncogenic factor. It functions by competitively inhibiting α-ketoglutarate-dependent dioxygenases, such as KDM2B and FTO. This compound impairs cell differentiation when there is estrogen withdrawal and is utilized in research concerning acute myeloid leukemia and glioma.
- Promotes growth factor-independent growth of TF-1 cells and inhibits their response to erythropoietin (EPO) in a dose- and passage-dependent manner.
- Significantly enhances anchorage-independent growth of N::TVA;Cdkn2alox/lox;Atrxlox/lox;Ptenlox/lox astrocytes.
- Significantly suppresses global 5hmC levels in TF-1 cells and transforms TF-1 cells.
- Inhibits the differentiation of SCF ER-Hoxb8 cells after estrogen withdrawal in mice.
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eMolecules 1926986-36-8 | Medchem Express | GNE-371 | 5mg | 559839461 | HY-112803 | 431.496 | C24H25N5O3
Ambeed | 2-Fluoronaphthalene | 100mg | 521448198 | A832635 | 323-09-1 | MFCD00082618 | 146.164 | C10H7F
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eMolecules 95094-00-1 | Medchem Express | (S)-Carvedilol | 5mg | 572596951 | HY-B0006B | MFCD00869664 | 406.482 | C24H26N2O4
Medchem Express | (S)-Carvedilol | 5mg | 572596951 | HY-B0006B | 95094-00-1 | MFCD00869664 | 406.482 | C24H26N2O4
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Medchemexpress LLC HY-108415 10mg Medchemexpress, Cloprostenol sodium salt CAS:55028-72-3 Purity:>98%
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Medchemexpress, HY-108415 10mg Cloprostenol sodium salt CAS:55028-72-3 Cloprostenol sodium salt (ICI 80996 sodium salt) is a potent synthetic prostaglandin analogue, acts as a luteolytic agent, and is a PGF2α receptor agonist. 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 101526-62-9 | Medchem Express | Sematilide (hydrochloride) | 5mg | 713704199 | HY-101436A | MFCD01667315 | 349.87 | C14H24ClN3O3S
Pharmablock | methyl 2-bromo-13-benzothiazole-6-carboxylate | 25mg | 784547251 | PBT8584 | 1024583-33-2 | MFCD16660646 | 272.120 | C9H6BrNO2S
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eMolecules 947914-18-3 | Medchem Express | ML365 | 5mg | 446261098 | HY-12345 | MFCD09204310 | 360.413 | C22H20N2O3
Medchem Express | ML365 | 5mg | 446261098 | HY-12345 | 947914-18-3 | MFCD09204310 | 360.413 | C22H20N2O3
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Medchemexpress LLC DSM705 hydrochloride | 2989908-08-7 | 99.6% | C19H20ClF3N6O | 10MG
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DSM705 hydrochloride is the hydrochloride salt of DSM705, a pyrrole-based dihydroorotate dehydrogenase (DHODH) inhibitor with oral antimalarial activity. It shows nanomolar potency against Plasmodium DHODH (IC50 ≈95 nM for P. falciparum and ≈52 nM for P. vivax) and activity against Plasmodium parasites, with minimal inhibition of mammalian DHODHs.
- Pyrrole-based DHODH inhibitor with nanomolar potency.
- Orally active antimalarial compound.
- Selective for Plasmodium DHODH over mammalian DHODHs.
- Hydrochloride salt form for improved solubility and handling.
- Available in multiple solid and solution pack sizes for research use.
- Reported purity approximately 99.6%.
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eMolecules 1141777-14-1 | Medchem Express | Emixustat | 2mg | 446270154 | HY-19720 | MFCD26961089 | 263.381 | C16H25NO2
ChemScene | 4-Chloro-7-fluoro-2-methylquinazoline | 250mg | 572191314 | CS-0102599 | 1206694-32-7 | MFCD12024899 | 196.610 | C9H6ClFN2
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Medchemexpress LLC Esamisulpride (S)-amisulpride | 71675-92-8 | 99.0% | 369.48 g/mol | C17H27N3O4S | 50MG
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Esamisulpride is the S-enantiomer of amisulpride and acts as a potent dopamine D2/D3 receptor antagonist with additional 5-HT7 activity. It is supplied as a research chemical for in vitro and in vivo studies related to schizophrenia and depression, offered in multiple pack sizes and accompanied by analytical documentation.
- Potent dopamine D2/D3 receptor antagonist with 5-HT7 activity.
- High purity suitable for research use.
- Available in multiple pack sizes, including 50 mg.
- Provided with analytical documents such as COA, SDS, HNMR, and LCMS.
- Stable under recommended storage conditions for powder and solutions.
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eMolecules 396094-85-2 | Ambeed | (S)-4-Phenyl-2-(2-((R)-p-tolylsulfinyl)phenyl)-45-dihydrooxazole | 100mg | 633660209 | A1281561 | 361.46 | C22H19NO2S
Medchem Express | MGH-CP1 | 5mg | 736630859 | HY-139330 | 896657-58-2 | 368.500 | C20H24N4OS
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Medchemexpress LLC (E)-5-(4-propoxybenzylidene)thiazolidine-2,4-dione | 587852-28-6 | MFCD31382191 | 98.0% | 263.31 g·mol⁻¹ | C13H13NO3S | 100 MG
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SMI-16a (CAS 587852-28-6) is a selective, ATP-competitive Pim kinase inhibitor used as a research tool to probe Pim kinase signaling and downstream cellular effects. It shows potent biochemical inhibition of Pim isoforms and measurable activity in cellular assays, and is supplied with analytical data for use in preclinical studies.
- Selective Pim1 and Pim2 inhibitor.
- Biochemical IC50: Pim1 0.15 μM, Pim2 0.02 μM; cellular activity in PC3 cells 48 μM.
- Chemical formula C13H13NO3S and molecular weight 263.31 g·mol⁻¹.
- Purity 98.0% as specified by the supplier.
- High solubility in DMSO (≥ 100 mg/mL) and defined in vivo formulation options.
- Powder storage stability: -20°C for 3 years, 4°C for 2 years.
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