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Filtered Search Results
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%.
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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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 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 Dapoxetine-d7 hydrochloride | 2699607-47-9 | 100.0% | 1 MG
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Dapoxetine-d7 hydrochloride is the deuterium labeled form of Dapoxetine hydrochloride, a short-acting selective serotonin reuptake inhibitor (SSRI). This compound is intended for research use only.
- Utilized as a tracer
- Serves as an internal standard for quantitative analysis through techniques such as NMR, GC-MS, or LC-MS
- Short-acting selective serotonin reuptake inhibitor (SSRI)
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Medchemexpress LLC Esamisulpride (S)-amisulpride | 71675-92-8 | 99.0% | 369.48 g/mol | C17H27N3O4S | 25MG
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Esamisulpride (S-amisulpride) is the S-enantiomer of amisulpride supplied as a research-grade chemical standard for pharmacology and receptor-binding studies. It acts as a dopamine D2/D3 receptor antagonist and is provided as a solid for in vitro receptor and pharmacological assays.
- High purity: 99.0% (as stated by supplier).
- Molecular formula: C17H27N3O4S; molecular weight: 369.48 g/mol.
- CAS number: 71675-92-8.
- Available in a 25 mg quantity suitable for small-scale research use.
- Storage: powder at -20°C (up to 3 years) or 4°C (up to 2 years); in solution at -80°C (up to 6 months) or -20°C (up to 1 month).
- Appearance: solid, white to light yellow.
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*IMAGION BIOSYSTEMS INC PrecisionMRX Carboxylic Acid Functionalized Iron Oxide Nanoparticles -10mg
Water soluble, superparamagnetic iron oxide nanoparticles with a core diameter of 24 – 26 nm and a low size dispersity (≤7%) as measured by Small Angle X-ray Scattering (SAXS). Nanoparticle cores are coated with a monolayer of oleic acid and a monolayer of an amphiphilic polymer with carboxylic acid functional groups displayed on the surface. Carboxylic acid functionality allows conjugation to molecules containing amine groups, such as proteins and peptides. The hydrodynamic diameter of the particles is approximately 30 nm larger than the core size measured by SAXS, and their zeta potential ranges from -60 to -70 mV. These particles are stable in most buffer solutions in the range of pH 4 – 10.
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eMolecules 122-99-6 | 2-Phenoxyethanol | Ambeed | MFCD00002857 | 138.166 | C8H10O2 | 94.000 | OCCOc1ccccc1 | 500g | 591797609
2-Phenoxyethanol | Ambeed | 122-99-6 | MFCD00002857 | 138.166 | C8H10O2 | 94.000 | OCCOc1ccccc1 | 500g | 591797609
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eMolecules 132683-62-6 | 4,6-Dichloropicolinaldehyde | MFCD10698614 | 100mg
Ambeed | 4-Fluorobenzylmercaptan | 1g | 602852436 | A745533 | 15894-04-9 | MFCD00040724 | 142.190 | C7H7FS
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Medchemexpress LLC Mcoppb (trihydrochloride) | 1108147-88-1 | 100.0% | 50 MG
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MCOPPB trihydrochloride is a nonpeptide nociceptin/orphanin FQ peptide (NOP)-receptor agonist, exhibiting a pKi of 10.07 for the human NOP receptor. It shows weaker activity at other opioid receptors. This compound is the trihydrochloride form of MCOPPB, making it suitable for various research applications.
- Acts as a nociceptin receptor agonist
- Demonstrates high purity of 99.98%
- Stable under recommended storage conditions
- Soluble in DMSO (100 mg/mL) for in vitro applications
- Can be formulated for in vivo studies with clear solutions
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Medchemexpress LLC RVX-297 50mg | 1044871-04-6 | 423.50 | C24H29N3O4 | 50 MG
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RVX-297 is a potent, orally active BD2-selective BET bromodomain inhibitor used in preclinical research to study inflammation and autoimmune disease mechanisms. It preferentially binds BD2 domains of BET proteins and suppresses inflammatory gene expression.
- BD2-selective BET bromodomain inhibitor for mechanistic studies.
- Orally active in preclinical models of inflammation and autoimmunity.
- Potent activity: BRD2(BD2) IC50 = 0.08 μM, BRD3(BD2) = 0.05 μM, BRD4(BD2) = 0.02 μM.
- High purity (95.0%) suitable for in vitro and in vivo research.
- Stable solid: powder storage recommended at low temperatures for long-term stability.
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Chemscene CHEMSCENE
5000578138 1 3-DIMETHOXYBENZENE 1KG
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