Benzamides
Medchemexpress LLC BMS-986224 | 2055200-88-7 | 99.4% | 498.92 | 100 MG
BMS-986224 is a potent, selective, and orally active APJ receptor agonist with potential for research into heart failure. It exhibits a similar receptor binding and signaling profile to (Pyr1) apelin-13.
- Potent and selective APJ receptor agonist
- Orally active
- Exhibits similar receptor binding and signaling profile to (Pyr1) apelin-13
- Potential for heart failure research
TARGETMOL CHEMICALS INC MOPIDAMOL 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. Mopidamol (RA 233) is a phosphodiesterase inhibitor a dipyridamole derivative with anticancer activity that prevents retinal vascular defects in experimental diabetes. purity: 99%
TARGETMOL CHEMICALS INC TAFAMIDIS 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Tafamidis (Fx-1006A) is a kinetic stabilizer of transthyretin (TTR) that prevents amyloidogenesis by wild-type and mutant TTRs. It binds to TTR with negative cooperativity (Kd1 3 nM; Kd2 278 nM) to stabilize the TTR dimer-dimer interface and inhibit tetrameric dissociation. Tafamidis stabilizes wild-type and clinically significant V30M and V122I mutant TTR amyloidogenic homotetramers (EC50s 2.7-3.2 uM) under fibril-promoting denaturing and physiological conditions in vitro. It stabilizes TTR heterotetramers containing wild-type and mutant subunits ex vivo in human plasma derived from patients carrying V30M or V1221 mutations when used at a concentration of 7.2 uM. Formulations containing tafamidis have been used for the treatment of familial amyloid polyneuropathy. purity: 99%
Medchemexpress LLC Benzamide | 55-21-0 | MFCD00007968 | 1mL
Benzamide (Benzenecarboxamide) is a potent poly(ADP-ribose) polymerase (PARP) inhibitor Benzamide has protective activity against both glutamate- and methamphetamine (METH)-induced neurotoxicity in vitro Benzamide can attenuate the METH-induced dopamine depletions and exhibits neuroprotective activity in mice also has no acute effect on striatal dopamine metabolism and does not reduce body temperature[1]
Chem-Impex International, Inc. Hippuric acid | 495-69-2 | MFCD00002692 | 100G
Hippuric acid, 495-69-2, MFCD00002692, 100G
Medchemexpress LLC 4-Aminohippuric acid-d4 | 1219805-41-0 | 98.0% | 1 MG
4-Aminohippuric acid-d4 is a deuterium-labeled version of 4-Aminohippuric acid, which acts as a coordination ligand for various metal ions and a functionalization reagent for nanomaterials. It can form stable complexes with metal ions or function as a reducing agent/stabilizer in nanomaterial synthesis. This compound is useful for constructing highly sensitive electrochemical or colorimetric sensors for detecting and quantifying heavy metal ions in environmental water and biological samples. It may also serve as a biomarker for attention-deficit/hyperactivity disorder (ADHD).
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis through techniques like NMR, GC-MS, or LC-MS.
Sigma Aldrich Fine Chemicals Biosciences Methotrexate meets USP testing specifications | 133073-73-1 | MFCD00150847 | 25MG
Methotrexate meets USP testing specifications | 133073-73-1 | MFCD00150847 | 25MG
Ambeed Sodium tetrakis 3 5bis trifluo
Sodium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, 79060-88-1, 97%
Ambeed Sodium tetrakis 3 5bis trifluo
Sodium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, 79060-88-1, 97%
Cayman Chemical 4-AmInohIppurIc AcId 5g
A substrate for OAT1 (Km = 14.3 µM), NPT1 (Km = 2.66 mM), and MDR2 (Km = 880 µM); a glycine amide form of 4-aminobenzoic acid