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Phenoxy compounds

Organic compounds that have one or more phenyl groups that are bonded to an oxygen with a radical electron; includes compounds with additional substitutions.
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1

1-(4-Methylphenoxy)-2-propanol 90.0+%, TCI America™

CAS: 4369-08-8 Molecular Formula: C10H14O2 Molecular Weight (g/mol): 166.22 MDL Number: MFCD00191544 InChI Key: VTOVIJQMFYQNSX-UHFFFAOYNA-N Synonym: 1-(p-Tolyloxy)-2-propanol PubChem CID: 12384823 IUPAC Name: 1-(4-methylphenoxy)propan-2-ol SMILES: CC1=CC=C(C=C1)OCC(C)O

PubChem CID 12384823
CAS 4369-08-8
Molecular Weight (g/mol) 166.22
MDL Number MFCD00191544
SMILES CC1=CC=C(C=C1)OCC(C)O
Synonym 1-(p-Tolyloxy)-2-propanol
IUPAC Name 1-(4-methylphenoxy)propan-2-ol
InChI Key VTOVIJQMFYQNSX-UHFFFAOYNA-N
Molecular Formula C10H14O2
2

Medchemexpress LLC Bragsin2 | 342795-08-8 | 99.9% | 289.16 | 1 ML
SDP

Bragsin2 is a potent, selective, and noncompetitive inhibitor of the nucleotide exchange factor BRAG2. It functions by binding at the interface between the PH domain of BRAG2 and the lipid bilayer, which prevents BRAG2 from activating lipidated Arf GTPase. Bragsin2 has been shown to affect breast cancer stem cells.

  • Potent, selective, and noncompetitive BRAG2 inhibitor
  • Binds at the interface between the PH domain of BRAG2 and the lipid bilayer
  • Prevents BRAG2 from activating lipidated Arf GTPase
  • Affects breast cancer stem cells
  • Inhibits Arf GTPase activation in HeLa cells at 50 μM
  • Inhibits growth of SUM149 and S68 cells at 50 μM

ENCOMPASS_PREFERRED
3

Medchemexpress LLC HY-15708 5mg Medchemexpress, LY2795050 CAS:1346133-08-1 Purity:>98%
SDP

Medchemexpress, HY-15708 5mg LY2795050 CAS:1346133-08-1 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
4

Medchemexpress LLC HY-112316 10mg Medchemexpress, BAY1238097 CAS:1564268-08-1 Purity:>98%
SDP

Medchemexpress, HY-112316 10mg BAY1238097 CAS:1564268-08-1 BAY1238097 is a potent and selective inhibitor of BET binding to histones and has strong anti-proliferative activity in different AML (acute myeloid leukemia) and MM (multiple myeloma) models through down-regulation of c-Myc levels and its downstream transcriptome (IC50 <100 nM). 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
5

Medchemexpress LLC Bragsin2 | 342795-08-8 | 99.9% | 289.16 | 10 MM * 1 ML
SDP

Bragsin2 is a potent, selective, and noncompetitive nucleotide exchange factor BRAG2 inhibitor, with an IC50 of 3 μM. It functions by binding at the interface between the PH domain of BRAG2 and the lipid bilayer, which prevents BRAG2 from activating lipidated Arf GTPase. Bragsin2 has been observed to affect breast cancer stem cells.

  • Potent, selective, and noncompetitive BRAG2 inhibitor.
  • IC50 of 3 μM against BRAG2.
  • Inhibits Arf GTPase activation in HeLa cells.
  • Inhibits the growth of SUM149 and S68 cells.
  • Affects breast cancer stem cells.

ENCOMPASS_PREFERRED
6

Medchemexpress LLC N-Demethyl Ivabradine hydrochloride | 1246638-08-3 | 99.6% | 1 MG
SDP

N-Demethyl Ivabradine HCl is a metabolite of Ivabradine, which is a specific inhibitor of the funny channel. It is for research use only.

  • Specific inhibitor of the funny channel
  • White to off-white solid appearance
  • Soluble in DMSO
  • Store at 4°C, sealed, away from moisture
  • In solvent, store at -80°C for 6 months or -20°C for 1 month

ENCOMPASS_PREFERRED
7

eMolecules​ Medchem Express / BAY1238097 / 5mg / 448039036 / HY-112316 / / 1564268-08-1 / [null] / 451.571 / C25H33N5O3

Medchem Express / BAY1238097 / 5mg / 448039036 / HY-112316 / / 1564268-08-1 / [null] / 451.571 / C25H33N5O3

ENCOMPASS_PREFERRED
8

Medchemexpress LLC 4H-1-Benzopyran-4-one, 6-methoxy-5-nitro-2-(trifluoromethyl)- | 342795-08-8 | 99.85% | 289.16 | 50 MG
SDP

Bragsin2 is a potent, selective, and noncompetitive nucleotide exchange factor BRAG2 inhibitor with an IC50 of 3 μM. It binds at the interface between the PH domain of BRAG2 and the lipid bilayer, preventing activation of lipidated Arf GTPase. This compound affects breast cancer stem cells.

  • Potent, selective, and noncompetitive nucleotide exchange factor BRAG2 inhibitor with an IC50 of 3 μM.
  • Binds at the interface between the PH domain of BRAG2 and the lipid bilayer.
  • Leads to BRAG2 being unable to activate lipidated Arf GTPase.
  • Affects breast cancer stem cells.
  • Inhibits Arf GTPase activation in HeLa cells at 50 μM.
  • Inhibits the growth of SUM149 and S68 cells at 50 μM.

ENCOMPASS_PREFERRED