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N-phenylureas

Organic compounds that consist of a urea molecule with a phenyl functional group substitution on one of the two nitrogen atoms on the urea molecule.
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31 – 45 of 60 results
31

Medchemexpress LLC Urea, N-(2-bromophenyl)-N'-[2-[ethyl(3-methylphenyl)amino]ethyl]- | 459429-39-1 | 99.1% | 376.29 | 100 MG
SDP

SB 452533 is a potent and selective TRPV1 antagonist with a pKb of 7.8. It is intended for research use only.

  • Acts as a potent antagonist at the cloned recombinant rat TRPV1 receptor in HEK293 cells, with a pKb of 7.7 and a pIC50 of 7.0.
  • Reduces the phosphorylation of CAMKK2 and AMPK in skeletal muscle (C2C12) cells.
  • Abolishes Capsaicin's effect of reducing Bleomycin-induced pulmonary fibrosis in BALB/c mice.

ENCOMPASS_PREFERRED
32

AMBEED 1 4 FLUOROPHENYL CYCLOBUTANECA

NC2790813 1 4 FLUOROPHENYL CYCLOBUTANECA

ENCOMPASS_PREFERRED
33

AA BLOCKS LLC

NC4037976 2 BROMO 6 FLUOROPHENYL BIS 2

ENCOMPASS
34

Aobchem 1 3-Bis(3 4-difluorophenyl)urea | 95% | CAS 218135-47-8 | C13H8F4N2O | 5g

1 3-Bis(3 4-difluorophenyl)urea | 95% | CAS 218135-47-8 | C13H8F4N2O | 5g

ENCOMPASS_PREFERRED
35

Aobchem 1 3-Bis(3 4-difluorophenyl)urea | 95% | CAS 218135-47-8 | C13H8F4N2O | 500mg

1 3-Bis(3 4-difluorophenyl)urea | 95% | CAS 218135-47-8 | C13H8F4N2O | 500mg

ENCOMPASS_PREFERRED
36

Aobchem 1 3-Bis(3 4-difluorophenyl)urea | 95% | CAS 218135-47-8 | C13H8F4N2O | 1g

1 3-Bis(3 4-difluorophenyl)urea | 95% | CAS 218135-47-8 | C13H8F4N2O | 1g

ENCOMPASS_PREFERRED
37

Aobchem 1 3-Bis(3 4-difluorophenyl)urea | 95% | CAS 218135-47-8 | C13H8F4N2O | 250mg

1 3-Bis(3 4-difluorophenyl)urea | 95% | CAS 218135-47-8 | C13H8F4N2O | 250mg

ENCOMPASS_PREFERRED
38

Medchemexpress LLC SB 452533 | 459429-39-1 | 99.1% | 376.29 | 1 ML
SDP

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.

ENCOMPASS_PREFERRED
39

BLD PHARMATECH CO LIMITED 2 4 FLUOROPHENYL 5 METHOXYP 1G

NC3253461 2 4 FLUOROPHENYL 5 METHOXYP 1G

ENCOMPASS_PREFERRED
40

Medchemexpress LLC SB-265610 | 211096-49-0 | 98.98% | C14H9BrN6O | 50 MG
SDP

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.

ENCOMPASS_PREFERRED
41

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
SDP

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.

ENCOMPASS_PREFERRED
42

Medchemexpress LLC SB 452533 | 459429-39-1 | 99.11% | 376.29 | 50 MG
SDP

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

ENCOMPASS_PREFERRED
43

Medchemexpress LLC SB-265610 | 211096-49-0 | ≥99.0% | C14H9BrN6O | 5 MG
SDP

SB-265610 | 211096-49-0 | ≥99.0% | C14H9BrN6O | 5 MG

ENCOMPASS_PREFERRED
44

Medchemexpress LLC HY-50688 25mg Medchemexpress, SB-265610 CAS:211096-49-0 Purity:>98%
SDP

Medchemexpress, HY-50688 25mg SB-265610 CAS:211096-49-0 SB-265610 is a selective, competitive, nonpeptide and allosteric CXCR2 antagonist. SB-265610 blocks rat cytokine-induced neutrophil chemoattractant-1 (CINC-1)-induced calcium mobilization and neutrophil chemotaxis with IC50s of 3.7 nM and 70 nM, 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.

ENCOMPASS_PREFERRED
45

eMolecules​ 64-10-8 | N-Phenylurea | Ambeed | MFCD19441482 | 136.154 | C7H8N2O | 98.000 | OC(=N)Nc1ccccc1 | 25g | 523728438

N-Phenylurea | Ambeed | 64-10-8 | MFCD19441482 | 136.154 | C7H8N2O | 98.000 | OC(=N)Nc1ccccc1 | 25g | 523728438

ENCOMPASS_PREFERRED