Aminophenols
Medchemexpress LLC DiAzKs hydrochlorid 10mM 1mL | 2421187-79-1 | 98.0% | 10MM/1ML
DiAzKs (H-L-Photo-lysine) hydrochloride is a diazirine-containing lysine amino acid and a photo-cross-linker. It can be site-selectively incorporated into proteins and is used to crosslink protein-protein interactions in vitro and in living cells. This compound acts as a UV light-activated photo-crosslinking probe.
- Site-selective incorporation into proteins.
- Crosslinks protein-protein interactions.
- UV light-activated photo-crosslinking probe.
- Used in vitro and in living cells.
TARGETMOL CHEMICALS INC TALOTREXIN AMMONIUM 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. Talotrexin ammonium is a non-polyglutamic acid antifolate. Talotrexin ammonium inhibits tumor growth by targeting dihydrofolate reductase (DHFR) thereby improving anti-tumor activity in a wide range of cancer models helping to inhibit tumor growth. purity: 97%
Medchemexpress LLC MRL-494 (hydrochloride) | 2699937-04-5 | 98.6% | 25 MG
MRL-494 hydrochloride is an antibacterial agent that acts as an inhibitor of β-barrel assembly machine A (BamA). It is impervious to efflux and the outer membrane permeability barrier, effectively inhibiting both Gram-positive and Gram-negative bacteria. The agent lethally disrupts the cytoplasmic membrane and inhibits outer membrane protein biogenesis by targeting BamA.
- Impervious to efflux and outer membrane permeability barrier
- Inhibits both Gram-positive and Gram-negative bacteria
- Lethally disrupts cytoplasmic membrane
- Inhibits outer membrane protein biogenesis
Medchemexpress LLC NS8593 (hydrochloride) | 875755-24-1 | 99.8% | 299.80 | 25 MG
NS8593 hydrochloride is a potent and selective inhibitor of small conductance Ca2+-activated K+ channels (SK channels). It reversibly inhibits SK3-mediated currents with a Kd value of 77 nM. It also inhibits SK1-3 subtypes in a Ca2+-dependent manner (Kds of 0.42, 0.60, and 0.73 μM, respectively, at 0.5 μM Ca2+), but it does not affect intermediate and large conductance Ca2+-activated K+ channels (hIK and hBK channels).
- Potent and selective small conductance Ca2+-activated K+ channels (SK channels) inhibitor.
- Reversibly inhibits SK3-mediated currents.
- Active on apamin-insensitive SK3 channels.
- Affects firing rate and pattern of dopaminergic neurons in vivo.
eMolecules Key Organics/BIONET Medetomidine Hydrochloride 10mg 564356419 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Key Organics/BIONET Medetomidine Hydrochloride 10mg 564356419 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Medchemexpress LLC Ethylenediaminetetraacetic acid sodium hydrate | 85715-60-2 | MFCD00149675 | 97.0% | 376.20 g/mol | C10H15N2Na3O9 | 25 G
EDTA sodium hydrate (ethylenediaminetetraacetic acid trisodium salt hydrate) is a sodium salt hydrate of EDTA used as a metal chelating agent and laboratory reagent. It binds divalent and trivalent metal ions to stabilize solutions and remove trace metals during buffer preparation, sample cleanup, and analytical assays. Supplied as a crystalline powder for research use.
- High purity (97.0%).
- Effective chelator of Ca2+ and Mg2+.
- Stable crystalline powder, easy to weigh and dissolve.
- Suitable for buffer preparation and analytical assays.
- Available in multiple pack sizes, including 25 g.
- Identified by CAS number 85715-60-2 for traceability.
Medchemexpress LLC S65487 hydrochloride | 1644543-95-2 | 99.7% | 753.72 | 1 ML
S65487 hydrochloride (VOB560 hydrochloride) is a potent and selective Bcl-2 inhibitor, acting as a proagent of S55746. It is effective against BCL-2 mutations like G101V and D103Y, while showing low affinity for MCL-1, BFL-1, and BCL-XL. This compound is known to induce apoptosis and exhibits anticancer activities.
- Potent and selective Bcl-2 inhibitor.
- Proagent of S55746.
- Active against BCL-2 mutations (G101V and D103Y).
- Low affinity with MCL-1, BFL-1, and BCL-XL.
- Induces apoptosis.
- Exhibits anticancer activities.
- Induces complete regression in BCL-2-dependent RS4;11 tumors in vivo after a single intravenous administration.
- Shows strong and persistent tumor regression in xenograft models of lymphoid malignancies in mouse and rat when combined with the MCL-1-specific inhibitor S64315/MIK665.
Medchemexpress LLC Quercetagetin-7-O-glucoside | 548-75-4 | MFCD09263523 | 480.38 g/mol | C21H20O13 | 10 MG
Quercetagitrin (quercetagetin-7-O-glucoside) is a naturally occurring flavone glycoside supplied as an analytical standard for research and analytical applications. It has reported anti-inflammatory and neuroprotective activities, inhibits Tau accumulation, and shows activity against protein tyrosine phosphatases (PTPN6, PTPN9). Researchers use it in preclinical studies of neuroinflammation, Alzheimer's disease models, and glucose uptake assays.
- Natural flavone glycoside and analytical standard.
- Reported anti-inflammatory and neuroprotective activity.
- Inhibits Tau accumulation and NF-κB activation in preclinical models.
- Shows inhibitory activity vs PTPN6 and PTPN9 and enhances glucose uptake.
- Intended for research use only; refer to Certificate of Analysis for storage and assay details.
Ambeed 2 1HImidazol4yl ethan1amine di
2-(1H-Imidazol-4-yl)ethan-1-amine dihydrochloride, 56-92-8, 98%
Ambeed 2 1HImidazol4yl ethan1amine di
2-(1H-Imidazol-4-yl)ethan-1-amine dihydrochloride, 56-92-8, 98%
U.S. Pharmacopeia 4-Aminophenol, 123-30-8, MFCD00007869, 100mg
Molecular Formula C6H7NO, Molecular Weight 109.127, Melting Point 356 - 374 °F (180 - 190 °C), Boiling Point 543.2 °F (284 °C) (decomposes), Synonyms: p-Aminophenol, 4-Amino-1-hydroxybenzene
TARGETMOL CHEMICALS INC NECROPTOSIS-IN-1 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Necroptosis-IN-1 is a potent necroptosis inhibitor of RIPK1. It is an analog of Necrostatin-1. purity: 99%