Cresols
Aobchem 2-Hydroxy-3-(trifluoromethyl)pyridine | ≥97% | CAS 22245-83-6 | C6H4F3NO | 100g
2-Hydroxy-3-(trifluoromethyl)pyridine | ≥97% | CAS 22245-83-6 | C6H4F3NO | 100g
Medchemexpress LLC P-CAB agent 2 hydrochloride | 2209911-80-6 | C22H26ClFN2O4S | 1 ML
P-CAB agent 2 hydrochloride is a potent and orally active potassium-competitive acid blocker and a gastric acid secretion inhibitor. It inhibits H+/K+-ATPase activity with an IC50 value of <100 nM. It also inhibits the hERG potassium channel with an IC50 value of 18.69 μM. This agent shows no acute toxicity and inhibits histamine-induced gastric acid secretion.
- Potent and orally active potassium-competitive acid blocker.
- Inhibits gastric acid secretion.
- Inhibits H+/K+-ATPase activity with an IC50 value of <100 nM.
- Inhibits hERG potassium channel with an IC50 value of 18.69 μM.
- Shows no acute toxicity.
- Effectively inhibits histamine-induced gastric acid secretion.
Aobchem (5-Fluoro-2-formyl-4-methylphenyl)boronic acid | 97% | C8H8BFO3 | 250mg
(5-Fluoro-2-formyl-4-methylphenyl)boronic acid | 97% | C8H8BFO3 | 250mg
Aobchem (3-Bromo-2-methoxy-5-methylphenyl)(phenyl)methanone | 95% | CAS 6723-10-0 | C15H13BrO2 | 500mg
(3-Bromo-2-methoxy-5-methylphenyl)(phenyl)methanone | 95% | CAS 6723-10-0 | C15H13BrO2 | 500mg
Medchemexpress LLC Potassium p-nitrophenyl sulfate | 6217-68-1 | 99.9% | 257.26 | 1 G
p-Nitrophenyl Sulfate Potassium is a chromogenic substrate for arylsulfatase. It is released by arylsulfonase cleavage, and the activity of arylsulfonase can be quantitatively determined by colorimetric detection at 400 nm.
- Chromogenic substrate for arylsulfatase
- Useful for quantitative determination of arylsulfonase activity
- Colorimetric detection at 400 nm
eMolecules 113535-00-5 | Di-1-indanylamine hydrochloride | Combi-Blocks | MFCD00054293 | 285.820 | C18H20ClN | 97.000 | Cl.C1Cc2ccccc2C1NC1CCc2ccccc12 | 1g | 448009107
Di-1-indanylamine hydrochloride | Combi-Blocks | 113535-00-5 | MFCD00054293 | 285.820 | C18H20ClN | 97.000 | Cl.C1Cc2ccccc2C1NC1CCc2ccccc12 | 1g | 448009107
Medchemexpress LLC P,p'-DDE; p,p'-dichlorodiphenyldichloroethylene | 72-55-9 | 99.9% | 250 MG
p,p'-DDE (4,4'-DDE) is the major and persistent metabolite of DDT. This orally active androgen receptor antagonist can affect the development and function of the male reproductive system by inhibiting androgen binding and transcriptional activity. High serum concentrations of p,p'-DDE may also be a risk factor for type 2 diabetes in women.
- Major and persistent metabolite of DDT
- Orally active androgen receptor antagonist
- Affects development and function of male reproductive system
- Inhibits androgen binding to the androgen receptor
- Inhibits androgen-induced transcriptional activity
- May be a risk factor for type 2 diabetes in women
Medchemexpress LLC Amyloid P-IN-1 | 1819986-22-5 | 99.59% | 656.68 | 5 MG
amyloid P-IN-1 is utilized in the research of diseases or disorders characterized by the depletion of serum amyloid P component (SAP). These conditions include amyloidosis, Alzheimer's disease, type 2 diabetes mellitus, and osteoarthritis. It is intended for research use only and not for sale to patients.
- Used in research for diseases involving serum amyloid P component (SAP) depletion.
- Has a purity of 99.59%.
- Available in various quantities as solid or in DMSO solution.
Aobchem (2-Ethoxy-3-fluoro-5-methylphenyl)(methyl)sulfane | 97% | CAS 2709871-05-4 | C10H13FOS | 500mg
(2-Ethoxy-3-fluoro-5-methylphenyl)(methyl)sulfane | 97% | CAS 2709871-05-4 | C10H13FOS | 500mg
Medchemexpress LLC L-p-boronophenylalanine | 76410-58-7 | MFCD01075172 | 99.8% | 209.01 | C9H12BNO4 | 250 MG
L-p-Boronophenylalanine is a boron-containing amino acid used as a substrate for L-type amino acid transporters (LAT1 and LAT2). It selectively accumulates in tumor cells and is used in boron neutron capture therapy (BNCT) research and studies of amino acid transport in cancer biology.
- High purity suitable for research applications.
- Available as a white to off-white solid powder for storage stability.
- Molecular formula C9H12BNO4 and molecular weight 209.01 g/mol.
- Stable under recommended storage conditions (powder: -20°C for long-term storage).
Medchemexpress LLC Fibrinogen-binding peptide | 137235-80-4 | 96.32% | 565.62 | 10 MG
Fibrinogen-Binding Peptide is a presumptive peptide mimic of the vitronectin binding site on the fibrinogen receptor. It binds fibrinogen and inhibits both the adhesion of platelets to fibrinogen and platelet aggregation, and also inhibits the adhesion of platelets to vitronectin.
- Shipping at room temperature in continental US; may vary elsewhere.
- For solid storage, keep sealed, away from moisture.
- Solid storage stability: 2 years at -80°C, 1 year at -20°C.
- For in-solvent storage, keep sealed, away from moisture.
- In-solvent storage stability: 6 months at -80°C, 1 month at -20°C.
Medchemexpress LLC STO-609 | 52029-86-4 | 98.20% | 314.29 | 5 MG
STO-609 is a selective and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK). It inhibits AMP-activated protein kinase kinase (AMPKK) activity in HeLa cell lysates with an IC50 ~0.02 g/ml.
- Inhibits activities of recombinant CaM-KKα and CaM-KKβ isoforms with Ki values of 80 and 15 ng/mL, respectively.
- Inhibits their autophosphorylation activities.
- Highly selective for CaM-KK without significant effect on downstream CaM kinases (CaM-KI and -IV).
- Inhibits constitutively active CaM-KKα as well as the wild-type enzyme.
- Suppresses Ca2+-induced activation of CaM-KIV in transfected HeLa cells in a dose-dependent manner.
- Reduces endogenous activity of CaM-KK in SH-SY5Y neuroblastoma cells at 1μg/mL (80% inhibitory rate).