Imidazopyridines
eMolecules AstaTech / OLPRINONE HYDROCHLORIDE HYDRATE / 0.25g / 721754863 / E85868 / 95.000 / 2072803-95-1 / MFCD00946577 / 304.730 / C14H13ClN4O2
AstaTech / OLPRINONE HYDROCHLORIDE HYDRATE / 0.25g / 721754863 / E85868 / 95.000 / 2072803-95-1 / MFCD00946577 / 304.730 / C14H13ClN4O2
![eMolecules 6-(TRIFLUOROMETHYL)IMIDAZO[1,2-A]PYRIDIN-2-AMINE | 1005785-87-4 | MFCD11846602 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502181191.JPG-250.jpg)
eMolecules 6-(TRIFLUOROMETHYL)IMIDAZO[1,2-A]PYRIDIN-2-AMINE | 1005785-87-4 | MFCD11846602 | 1g
AstaTech | 6-(TRIFLUOROMETHYL)IMIDAZO[1,2-A]PYRIDIN-2-AMINE | 1g | 233632112 | 86061 | 95.000 | 1005785-87-4 | MFCD11846602 | 201.152 | C8H6F3N3
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![eMolecules Ethyl 6-bromoimidazo[1,2-a]pyrazine-2-carboxylate | 1208085-94-2 | MFCD11044908 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502189643.JPG-250.jpg)
eMolecules Ethyl 6-bromoimidazo[1,2-a]pyrazine-2-carboxylate | 1208085-94-2 | MFCD11044908 | 1g
Combi-Blocks | Ethyl 6-bromoimidazo[1,2-a]pyrazine-2-carboxylate | 1g | 267181887 | QC-4526 | 97.000 | 1208085-94-2 | MFCD11044908 | 270.086 | C9H8BrN3O2
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Medchemexpress LLC Cxcr7 modulator 1 | 2231812-31-8 | 99.5% | 914.07 | C48H57F2N7O7S | 50 MG
CXCR7 modulator 1 is a potent, orally bioavailable peptoid-hybrid modulator of the chemokine receptor CXCR7 with an in vitro Ki of 9 nM. It is supplied for preclinical biochemical and pharmacological research into CXCR7 signaling and ligand-receptor interactions.
- Potent CXCR7 affinity (Ki = 9 nM)
- Orally bioavailable chemical scaffold suitable for in vivo dosing studies
- High reported purity for reliable experimental results
- Supplied as a solid suitable for formulation and analytical work
- Available in multiple small research sizes for dose-ranging studies
![Medchemexpress LLC 4-Oxazolecarboxamide, N-[6-[(2-methoxyethyl)methylamino]-3-pyridinyl]-2-phenyl-5-(trifluorom | 939375-07-2 | 99.9% | 420.39 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000393984.png-250.jpg)
Medchemexpress LLC 4-Oxazolecarboxamide, N-[6-[(2-methoxyethyl)methylamino]-3-pyridinyl]-2-phenyl-5-(trifluorom | 939375-07-2 | 99.9% | 420.39 | 100 MG
DGAT1-IN-3 is a potent, selective, and orally bioavailable inhibitor of DGAT-1. It can be used for research on obesity, dyslipidemia, and metabolic syndrome.
- Potent, selective, and orally bioavailable inhibitor of DGAT-1.
- Inhibits human DGAT-1 with an IC50 of 38 nM.
- Inhibits rat DGAT-1 with an IC50 of 120 nM.
- Supports research into obesity.
- Supports research into dyslipidemia.
- Supports research into metabolic syndrome.
- Reduces cumulative body weight gain in DIO rats.
- Reduces weight gain and plasma triglycerides.
- Improves lipid profiles.
Chembridge Corporation 3H-IMIDAZO 4,5-B PYRIDINE-2-TH
3H-imidazo[4,5-b]pyridine-2-thiol; CAS: 29448-81-5
Medchemexpress LLC Samatasvir | 1312547-19-5 | 99.4% | 885.06 | 5 MG
Samatasvir is a potent, orally active NS5A inhibitor of HCV replication. It is effective and selective against infectious HCV and replicons, with EC50s ranging from 2 to 24 pM in genotype 1 through 5 replicons.
- Potent, orally active NS5A inhibitor of HCV replication.
- Effective and selective against infectious HCV and replicons.
- Retains full activity in the presence of HIV and hepatitis B virus (HBV) antivirals.
- Not cross-resistant with HCV protease, nucleotide, and nonnucleoside polymerase inhibitor classes.
Medchemexpress LLC 3-Cl-Pyridine-amide-acrylaldehyde-piperazine | 99.3% | 294.74 | 50 MG
3-Cl-Pyridine-amide-acrylaldehyde-piperazine is a synthetic intermediate of LO-4-25. LO-4-25 is an androgen receptor (AR) DNA binding domain ligand linked via a linker to the truncated fumaramide handle. This product shows robust degradation of both AR and AR-V7 in 22Rv1 cells.
- Synthetic intermediate.
- Degrades androgen receptor (AR) and AR-V7 in 22Rv1 cells.
- For research use only.
- Relevant to cancer research.
Medchemexpress LLC CXCR7 antagonist-1 | 2990472-61-0 | 99.4% | C21H20ClFN6O | 10MG
CXCR7 antagonist-1 hydrochloride is a small-molecule antagonist of the chemokine receptor CXCR7 that inhibits binding of the chemokines SDF-1 (CXCL12) and I-TAC (CXCL11). It is supplied as the hydrochloride salt for research use in studies of tumor cell proliferation, tumor formation, and inflammatory disease pathways.
- Antagonist of the CXCR7 chemokine receptor.
- Inhibits SDF-1 (CXCL12) and I-TAC (CXCL11) binding to CXCR7.
- Provided as the hydrochloride salt in a solid form.
- High purity (99.4%).
- Supplied in small research-scale quantities suitable for in vitro assays.
Medchemexpress LLC HY-100414 1mg Medchemexpress, Soraprazan CAS:261944-46-1 Purity:>98%
Medchemexpress, HY-100414 1mg Soraprazan CAS:261944-46-1 Soraprazan (BYK61359) is a reversible, and fast-acting inhibitor of gastric H + /K + ATPase . 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.
Medchemexpress LLC Az084 | 929300-19-6 | 99.7% | 10 MG
AZ084 is a potent, selective, orally active CCR8 allosteric antagonist provided for preclinical research. The compound is characterized with manufacturer-reported purity, molecular data, solubility protocols for in vitro and in vivo use, and recommended storage conditions to support pharmacology and immunology studies.
- Potent CCR8 allosteric antagonist with reported Ki ≈ 0.9 nM.
- High purity reported at 99.65%.
- Molecular weight 434.57 g/mol; formula C26H34N4O2.
- Soluble in DMSO (250 mg/mL) and formulatable for in vivo dosing protocols.
- Appearance: light yellow to yellow solid.
- Storage recommendations: powder at -20°C (long term) and in solvent at -80°C for best stability.
- Intended for research use only; not for human or clinical use.