Aminophenols
Medchemexpress LLC Guvacine hydrochloride | 6027-91-4 | MFCD00055191 | 99.9% | 163.60 g/mol | C6H10ClNO2 | 1 ML
Guvacine hydrochloride is a GABA transporter inhibitor used in neuroscience research to investigate GABAergic signaling and transporter pharmacology. It is supplied with documented purity, molecular data, and recommended storage conditions to support reliable in vitro experiments.
- Inhibits GABA transporter activity with reported IC50 values for multiple transporter subtypes.
- Supplied as a ready-to-use 10 mM solution in DMSO (1 ML) for immediate use in assays.
- Also available as a solid for custom preparation and long-term storage.
- High reported purity supports reproducible experimental results.
- Storage guidance provided to maintain stability of solid and solution forms.
Medchemexpress LLC His-Pro hydrochloride | 2415727-78-3 | 99.8% | 288.73 | 100 MG
His-Pro (Histidyl-proline) hydrochloride is a dipeptide consisting of histidyl and proline. It is for research use only and not sold to patients.
- Appearance: Solid
- Color: White to off-white
- Shipping: Room temperature in continental US
- Storage: Sealed storage, away from moisture and light. Powder: -80°C for 2 years, -20°C for 1 year. In solvent: -80°C for 6 months, -20°C for 1 month.
- Solubility (In Vitro): DMSO: 125 mg/mL (432.93 mM)
Medchemexpress LLC NNC 92-1687 | 1MG
NNC 92-1687 is a non-peptide competitive human glucagon receptor antagonist (IC50 20 M Ki 9 1 M) NNC 92-1687 can be used in the research of type 2 diabetes[1]
Medchemexpress LLC Zzw-115 hydrochloride | 10122-45-9 | 98.1 % | 573.97 | 5 MG
ZZW-115 hydrochloride is a potent NUPR1 inhibitor with a Kd of 2.1 μM. It induces tumor cell death through necroptosis and apoptosis, demonstrating anticancer activity. It is efficient in killing various cancer cells with IC50 values ranging from 0.42 μM to 4.93 μM. This compound also induces a decrease in ATP production and a ROS overproduction.
- Efficient in killing cancer cells with IC50 values ranging from 0.42 μM to 7.75 μM
- Induces tumor cell death via necroptosis and apoptosis
- Decreases ATP production and induces ROS overproduction
- Inhibits the growth of pancreatic xenografted tumors in vivo
- Demonstrates potent anticancer activity
Medchemexpress LLC AM-92016 hydrochloride | 133229-11-5 | MFCD00673947 | 99.3% | 483.84 | C19H25Cl3N2O4S | 1 ML
AM-92016 hydrochloride is a small-molecule blocker of delayed rectifier potassium currents (IK), commonly used in electrophysiology and cardiovascular research to modulate action potential duration. It is supplied both as a solid and as a ready-to-use solution to support in vitro pharmacology and ion-channel assays.
- Blocks delayed rectifier potassium channels (IK) and shortens action potential duration.
- Supplied as a 10 mM solution in DMSO or as a dry solid for custom preparation.
- High purity suitable for research use (reported ~99.3%).
- Molecular weight 483.84 and CAS 133229-11-5 for clear identification.
- Available in small-quantity formats compatible with pharmacological assays.
Medchemexpress LLC CWI1-2 hydrochloride | 2408590-37-2 | C22H18Cl4N6O3 | 5 MG
CWI1-2 hydrochloride is an IGF2BP2 inhibitor that binds IGF2BP2 and inhibits its interaction with m6A-modified target transcripts, induces apoptosis and differentiation, and shows promising anti-leukemic effects.
- IGF2BP2 inhibitor.
- Inhibits IGF2BP2 interaction with m6A-modified target transcripts.
- Induces apoptosis and differentiation.
- Demonstrates anti-leukemic effects.
- Effective in reducing Gln uptake and impairing mitochondrial function in AML cells.
- Inhibits colony-forming ability of leukemic mouse blasts.
- Impairs self-renewal of LSC/LIC.
- Delays leukemia onset and prolongs survival in vivo.
Medchemexpress LLC AM-92016 hydrochloride | 133229-11-5 | 99.3% | 483.84 g/mol | C19H25Cl3N2O4S | 10 MG
AM-92016 hydrochloride is a research-grade small molecule that selectively blocks the rectifier potassium current (IK), delaying IK-mediated repolarization and restricting action potential duration. It is supplied as a high-purity solid intended for use in electrophysiology and ion-channel research.
- Specific blocker of rectifier potassium current (IK).
- Suitable for electrophysiology and ion-channel research.
- High purity (99.3%) for reliable experimental results.
- Solid, light yellow to yellow appearance.
- Storage: sealed at 4°C; in solvent -80°C (6 months) or -20°C (1 month).
- Pack size 10 mg for small-scale studies.
eMolecules Fenretinide | 65646-68-6 | MFCD00792674 | 100mg
Apollo Scientific | Fenretinide | 100mg | 562460510 | BIFK0053 | 99.000 | 65646-68-6 | MFCD00792674 | 391.555 | C26H33NO2
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Selleck Chemical LLC Sodium phytate hydrate
Sodium phytate hydrate (Phytic acid Dodecasodium phytate Myo-inositol hexakis Inositol hexakisphosphate) functions as a storage depot and precursor for other inositol phosphates and pyrophosphates It can be used clinically as a hypocalcemic agent and a complexing agent for removal of traces of heavy metal ions
Medchemexpress LLC BN82002 hydrochloride | 1049740-43-3 | 99.4% | 395.88 | 10 MG
BN82002 hydrochloride is a potent, selective, and irreversible inhibitor of the CDC25 phosphatase family. It demonstrates significant inhibitory activity against various CDC25 isoforms including CDC25A, CDC25B2, CDC25B3, CDC25C, and 25C-cat, with IC50 values ranging from 2.4 to 6.3 μM. This compound also exhibits high selectivity, showing approximately 20-fold greater inhibition over CD45 tyrosine phosphatase.
- Potent and selective CDC25 phosphatase inhibitor
- Inhibits CDC25A, CDC25B2, CDC25B3, CDC25C, and 25C-cat
- Demonstrates approximately 20-fold greater selectivity over CD45 tyrosine phosphatase
- Irreversible inhibitor
Medchemexpress LLC CWI1-2 hydrochloride | 2408590-37-2 | C22H18Cl4N6O3 | 100 MG
CWI1-2 hydrochloride | 2408590-37-2 | C22H18Cl4N6O3 | 100 MG