N-phenylureas
eMolecules Medchem Express / SB-265610 / 5mg / 713705019 / HY-50688 / / 211096-49-0 / MFCD09971124 / 357.171 / C14H9BrN6O
Medchem Express / SB-265610 / 5mg / 713705019 / HY-50688 / / 211096-49-0 / MFCD09971124 / 357.171 / C14H9BrN6O
AA BLOCKS LLC 922925-46-0 | 6-(4-fluorophenyl)-2-[(pyridin-4-yl)methyl]-2,3-dihydropyridazin-3-one
6-(4-fluorophenyl)-2-[(pyridin-4-yl)methyl]-2,3-dihydropyridazin-3-one. 5 mg. CAS Number: 922925-46-0; Molecular Formula: C16H12FN3O
Medchemexpress LLC SB 452533 | 459429-39-1 | 99.1% | 376.29 g/mol | C18H22BrN3O | 5 MG
SB 452533 is a potent, selective TRPV1 antagonist supplied for research use. It is provided with analytical documentation and safety data suitable for pharmacological and preclinical studies of TRPV1-mediated signaling.
- Selective TRPV1 antagonist for receptor pharmacology studies.
- Purity 99.11%.
- Molecular weight 376.29 g/mol.
- Chemical formula C18H22BrN3O.
- White to off-white solid physical form.
- Supplied with COA, LCMS data, and SDS documentation.
- Soluble in DMSO for assay preparation.
Medchemexpress LLC 1-Phenylurea | 64-10-8 | MFCD00007944 | 99.9% | 136.15 g/mol | C7H8N2O | 500 G
1-Phenylurea is an organic small molecule (C7H8N2O, CAS 64-10-8) supplied as a high-purity solid for laboratory research and biochemical assays. It has a molecular weight of 136.15 g/mol and is used as a reagent or reference compound in analytical and life-science workflows.
- High purity (~99.9%) suitable for research-grade applications.
- Solid form with defined molecular weight (136.15 g/mol) for accurate dosing.
- CAS-registered substance (CAS 64-10-8) for unambiguous identification.
- Available in larger pack sizes for bulk laboratory use.
- Applicable as a reagent, control, or reference in biochemical assays.
- Stable under typical storage conditions for solid organics.
Selleck Chemical LLC A939572-5mg
A939572 is a potent and orally bioavailable stearoyl-CoA desaturase1 (SCD1) inhibitor with IC50 of <4 nM and 37 nM for mSCD1 and hSCD1, respectively.
eMolecules Ambeed / 4-Phenylsemicarbazide / 1g / 575774817 / A368588 / / 537-47-3 / MFCD00007590 / 151.169 / C7H9N3O
Ambeed / 4-Phenylsemicarbazide / 1g / 575774817 / A368588 / / 537-47-3 / MFCD00007590 / 151.169 / C7H9N3O
eMolecules Medchem Express / SB 452533 / 5mg / 686240126 / HY-108458 / / 459429-39-1 / MFCD19690909 / 376.298 / C18H22BrN3O
Medchem Express / SB 452533 / 5mg / 686240126 / HY-108458 / / 459429-39-1 / MFCD19690909 / 376.298 / C18H22BrN3O
Medchemexpress LLC 1-phenylurea | 64-10-8 | MFCD00007944 | 99.9% | 136.15 g/mol | C7H8N2O | 1 KG
1-Phenylurea is an organic phenylurea compound used as a research reagent and building block in synthetic chemistry and biochemical assays. It is provided in research-grade purity for laboratory applications.
- High purity suitable for research-grade applications (reported 99.85%).
- Chemical formula C7H8N2O; molecular weight 136.15 g/mol.
- Commonly used as a building block in organic synthesis and as a reagent in biochemical assays.
- Identified by CAS number 64-10-8 for unambiguous reference.
- Supplied in formats appropriate for routine laboratory handling and storage.
Medchemexpress LLC SB 452533 | 459429-39-1 | 99.11% | 376.29 | 50 MG
SB 452533 is a potent and selective TRPV1 antagonist with a pKb of 7.8. It functions by acting as a potent antagonist at the cloned recombinant rat TRPV1 receptor in HEK293 cells. This compound has been shown to reduce phosphorylation of CAMKK2 and AMPK, and to abolish the effects of Capsaicin in reducing Bleomycin-induced pulmonary fibrosis in mice.
- Potent and selective TRPV1 antagonist
- Reduces phosphorylation of CAMKK2 and AMPK
- Abolishes the effects of capsaicin in reducing bleomycin-induced pulmonary fibrosis in mice
Medchemexpress LLC SB-265610 | 211096-49-0 | 98.98% | C14H9BrN6O | 50 MG
SB-265610 is a selective, competitive, nonpeptide, and allosteric CXCR2 antagonist. It blocks rat CINC-1-induced calcium mobilization (IC50 of 3.7 nM) and neutrophil chemotaxis (IC50 of 70 nM). In animal models, it significantly inhibits Gr-1+CD11b+ cell recruitment to mammary adenocarcinoma.
- Selective, competitive, nonpeptide, and allosteric CXCR2 antagonist.
- Blocks rat CINC-1-induced calcium mobilization (IC50 of 3.7 nM).
- Blocks neutrophil chemotaxis (IC50 of 70 nM).
- Reduces CINC-1's antiapoptotic effect.
- Inhibits Gr-1+CD11b+ cell recruitment to mammary adenocarcinoma in animal models.
Medchemexpress LLC 1-(2-bromophenyl)-3-(7-cyano-2H-benzotriazol-4-yl)urea | 211096-49-0 | MFCD09971124 | 699.0% | 357.16 g·mol⁻¹ | C14H9BrN6O | 10 MG
SB-265610 is a selective, competitive, nonpeptide, allosteric antagonist of the CXCR2 chemokine receptor used as a research reagent to study neutrophil chemotaxis and CXCR2-mediated signaling. It inhibits CINC-1-induced calcium mobilization (IC50 3.7 nM) and neutrophil chemotaxis (IC50 70 nM).
- Selective CXCR2 antagonist for receptor pharmacology studies.
- Reported low-nanomolar potency for calcium mobilization assays.
- Suitable for in vitro chemotaxis and signaling experiments.
- Supplied as a small-molecule solid for formulation or dosing control.
- Characterized by published analytical data and CAS registration for traceability.
Medchemexpress LLC SB 452533 | 459429-39-1 | 99.1% | 376.29 | 1 ML
SB 452533 is a potent and selective TRPV1 antagonist with a pKb of 7.8. It is for research use only and not sold to patients.
- Potent antagonist at the cloned recombinant rat TRPV1 receptor in HEK293 cells.
- Reduces phosphorylation of CAMKK2 and AMPK.
- Abolishes the effects of small dose Capsaicin in reducing Bleomycin-induced pulmonary fibrosis in mice.