Non-Mammalian cDNA
Medchemexpress LLC Umibecestat | 1387560-01-1 | 99.8% | 50 MG
Umibecestat is a small-molecule beta-secretase (BACE-1) inhibitor used for research into Alzheimer's disease. Provided as a research-grade solid for in vitro and preclinical studies, it has formula C19H15ClF7N5O2 and a molecular weight of 513.8 g/mol.
- Beta-secretase (BACE-1) inhibitor for Alzheimer's disease research.
- High purity suitable for biochemical and cellular assays.
- Available in multiple pack sizes, including 50 MG solid vials.
- Also available as a 10 mM solution in DMSO for ready-to-use experiments.
Cayman Chemical 9 SHODEd4 MaxSpecStndar 10ug
A quantitative analytical standard guaranteed to meet MaxSpec identity, purity, stability, and concentration specifications
Cayman Chemical LPA2 ntagonIst 1 5mg
An LPA2 antagonist (IC50 = 17 nM); selective for LPA2 over LPA1 and LPA3 (IC50s = >50 μM); inhibits HGF-induced phosphorylation of ERK and proliferation of HCT116 colon cancer cells
ABclonal Technology CD64 Rabbit pAb
This gene encodes a protein that plays an important role in the immune response. This protein is a high-affinity Fc-gamma receptor. The gene is one of three related gene family members located on chromosome 1.
Biolegend Brilliant Violet 605TM anti-mo
Brilliant Violet 605™ anti-mouse CD134 (OX-40) [OX-86]; Isotype: Rat IgG1, κ; Reactivity: Mouse; Apps: FC; Size: 50 μg
Abcam SB 204741, 5-HT2B receptor antagonist, 10MG
MW 286.35 g/mol, Purity >99%. Selective 5-HT₂B receptor antagonist. High affinity for 5-HT₂B receptors (pKi = 7.85), some activity at 5-HT₂C receptors (pKi = 5.8).
The product is subject to the following: Abcam Restricted Use Statement
MOLECULAR DEPOT LLC Neuromedin U - 100 ug
Neuromedin U (Human) is a synthetic peptide consisting of the sequence Phe-Arg-Val-Asp-Glu-Glu-Phe-Gln-Ser-Pro-Phe-Ala-Ser-Gln-Ser-Arg-Gly-Tyr-Phe-Leu-Phe-Arg-Pro-Arg-Asn-NH2 The molecular weight of this peptide is 3080 4 g/mol and the CAS number is 312306-89-1 This product is for in vitro research use only This product is not for human or animal use
Medchemexpress LLC Rimonabant | 168273-06-1 | 99.5% | C22H21Cl3N4O | 50 MG
Rimonabant (SR141716) is a highly potent, brain-penetrated, and selective central cannabinoid receptor (CB1) antagonist with a Ki of 1.8 nM. It also inhibits Mycobacterial membrane protein Large 3 (MMPL3).
- Highly potent, brain-penetrated, and selective central cannabinoid receptor (CB1) antagonist
- Inhibits mycobacterial membrane protein Large 3 (MMPL3)
- Exhibits Ki of 1.8 nM for CB1
- Inhibits LPS-induced NO production in BV-2 cells (IC50 = 16.17 μM)
- Can inhibit the growth of Mtb with an MIC of 54 μM
- Reduced RANTES and MCP-1 serum levels in obese Zucker rats
- Slowed weight gain and reduced platelet-bound fibrinogen in obese Zucker rats
- Significantly reduced many cardiometabolic risk factors
