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Filtered Search Results
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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Across International Ai WaterVac 0.7 cfm 2-Head Water Aspirator Vacuum Pump
Ai WaterVac 0.7 cfm is an oil-free, portable, chemical resistant, 2-head recirculating water aspirator pump, with simplified maintenance, and no frequent and costly oil change. All major parts are made of PTFE, these economical vacuum pumps are perfect for tough lab applications.
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Medchemexpress LLC HY-10977 50mg Medchemexpress, Tivozanib CAS:475108-18-0 Purity:>98%
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Medchemexpress, HY-10977 50mg Tivozanib CAS:475108-18-0 Tivozanib (AV-951; KRN951) is a highly potent and selective VEGFR 1/2/3 inhibitor with IC50s of 0.21, 0.16, and 0.24 nM in cell assay, respectively. 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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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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Sigma Aldrich Fine Chemicals Biosciences Neostigmine methyl sulfate | 51-60-5 | MFCD00011796 | 5G
Neostigmine methyl sulfate | Mol Wt: 334.39 | 51-60-5 | MFCD00011796 | 5G
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Medchemexpress LLC HG-7-85-01-NH2 | 1258391-29-5 | 98.1% | 50 MG
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HG-7-85-01-NH2 is a small-molecule ligand derived from an ABL inhibitor. It serves as a target protein ligand for synthesizing the heterobifunctional molecule SNIPER and can bind to an IAP ligand via a linker to form SNIPER(ABL)-033. The resulting SNIPER(ABL)-033 effectively degrades BCR-ABL protein.
- Derived from an ABL inhibitor.
- Functions as a target protein ligand for SNIPER synthesis.
- Forms a heterobifunctional molecule when linked to an IAP ligand.
- Used in the formation of SNIPER(ABL)-033, which degrades BCR-ABL protein.
- Intended for research use only.
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Medchemexpress LLC Trifarotene | 895542-09-3 | 99.1% | 459.58 g/mol | C29H33NO4 | 100 MG
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Trifarotene is a selective retinoic acid receptor γ (RARγ) agonist supplied as a white to off-white solid for research use. It is intended for in vitro and in vivo studies of RAR/RXR signaling and related pathways and is not for human therapeutic use.
- High purity (≈99.1% by LCMS)
- Chemical formula C29H33NO4, molecular weight 459.58 g/mol
- Soluble in DMSO (≈250 mg/mL) and formulatable for in vivo dosing
- Stable under recommended powder and solution storage conditions
- Suitable for receptor pharmacology and preclinical studies
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Apexbio Technology LLC Clofibrate 637-07-0 5g
Clofibrate (CAS 637-07-0) is a small-molecule agonist targeting peroxisome proliferator-activated receptor alpha (PPAR-alpha) It is designed to activate PPAR-alpha thereby regulating lipid and lipoprotein metabolism pathways Clofibrate exerts its biological activity primarily through PPAR-alpha activation leading to enhanced peroxisome proliferation and fatty acid oxidation In both human and mouse models Clofibrate demonstrates agonist activity with EC50 values of 55 M and 500 M respectively Based on these pharmacological properties Clofibrate holds research potential in investigating lipid metabolism triglyceride regulation and the roles of PPAR-alpha signaling in hyperlipidemia and related metabolic disorders
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Medchemexpress LLC HY-114330A 10mg Medchemexpress, ZK824859 hydrochloride CAS: Purity:>98%
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Medchemexpress, HY-114330A 10mg ZK824859 HCl CAS: ZK824859 hydrochloride is an oral available and selective urokinase plasminogen activator (uPA) inhibitor with IC50s of 79 nM, 1580 nM and 1330 nM for human uPA, tPA, and plasmin, respectively. 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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Medchemexpress LLC HY-14144 5mg Medchemexpress, Aclidinium (Bromide) CAS:320345-99-1 Purity:>98%
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Medchemexpress, HY-14144 5mg Aclidinium (Bromide) CAS:320345-99-1 Aclidinium Bromide (LAS 34273; LAS-W 330) is a long-acting, inhaled muscarinic antagonist. Aclidinium Bromide has the potential for chronic obstructive pulmonary disease (COPD) research[4]. 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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Chemie Tek PF-06821497 5MG
PF-06821497 5mg
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eMolecules 1018678-50-6 | 2-(Difluoromethyl)benzaldehyde | ChemScene | MFCD16875639 | 156.132 | C8H6F2O | 96.000 | FC(F)c1ccccc1C=O | 100mg | 801476742
2-(Difluoromethyl)benzaldehyde | ChemScene | 1018678-50-6 | MFCD16875639 | 156.132 | C8H6F2O | 96.000 | FC(F)c1ccccc1C=O | 100mg | 801476742
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Medchemexpress LLC PRMT5-IN-1 hydrochloride | 99.5% | 455.29 | 10 MG
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PRMT5 IN-1 hydrochloride (compound 9), a hemiaminal, is a potent, selective protein arginine methyltransferase 5 (PRMT5) inhibitor with an IC50 of 11 nM for PRMT5/MEP50. It can be converted to aldehydes and react with C449 to form covalent adducts under physiological conditions. It is for research use only and not sold to patients.
- Potent, selective protein arginine methyltransferase 5 (PRMT5) inhibitor
- IC50 of 11 nM for PRMT5/MEP50
- Inhibits the PRMT5/MEP50 complex very rapidly with a Kinact of 0.068 min-1 and a good binding affinity (KI=55 nM)
- Inhibits the expression of cellular sDMA with an IC50 value of 0.012 μM in Granta-519 cells
- Inhibits cell proliferation in a dose-dependent manner with an IC50 value of 0.06 μM in Granta-519 cells
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Medchemexpress LLC Nutlin carboxylic acid | 2249750-27-2 | 98.6% | 100 MG
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Nutlin carboxylic acid is a Nutlin 3-based MDM2 ligand designed to form PROTACs (Proteolysis-Targeting Chimeras). These PROTACs operate by harnessing the intracellular ubiquitin-proteasome system to achieve selective degradation of target proteins. It has a molecular weight of 639.53 and a chemical formula of C32H32Cl2N4O6, appearing as a white to yellow solid.
- Nutlin 3-based MDM2 ligand
- Forms PROTACs via a linker
- Exploits ubiquitin-proteasome system
- Selectively degrades target proteins
- For research use only
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