Aminophenols
eMolecules 3,6-Dimethyl-2-nitrophenol | 71608-10-1 | MFCD12198862 | 1g
Combi-Blocks | 3,6-Dimethyl-2-nitrophenol | 1g | 517034738 | ST-4209 | 95.000 | 71608-10-1 | MFCD12198862 | 167.164 | C8H9NO3
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Medchemexpress LLC XMD8-92 | 1234480-50-2 | 99.5% | C26H30N6O3 | 10 MM * 1 ML
XMD8-92 is a potent inhibitor of ERK5 (BMK1) and BRD4, with Kds of 80 nM and 190 nM, respectively. It also inhibits DCAMKL2, PLK4, and TNK1. This compound exhibits anti-cancer activity and is intended for research use only.
- Potent ERK5 (BMK1) and BRD4 inhibitor
- Kds of 80 nM for BMK1 and 190 nM for BRD4
- Inhibits DCAMKL2, PLK4, and TNK1
- Exhibits anti-cancer activity
- For research use only
- Inhibits proliferation of HMEC and cancer cells
- Effectively inhibits BMK1 activation
- Induces PML's downstream effector, p21
- Significantly inhibits bFGF induced angiogenesis
Medchemexpress LLC Mepazine hydrochloride | 2975-36-2 | 99.3% | 10 MG
Mepazine hydrochloride is a small-molecule MALT1 protease inhibitor used in cellular and biochemical research to study apoptosis and signaling pathways.
- High listed purity (99.25%).
- Molecular weight 346.92 g/mol and formula C19H23ClN2S.
- Available in small research pack sizes including 10 MG.
- Suitable for cellular assays probing MALT1 activity and apoptosis.
- Storage: solid at 4°C; solutions at -80°C for long-term, sealed and protected from moisture.
Medchemexpress LLC Acetaminophen | 103-90-2 | 99.97% | C8H9NO2 | 10 G
Acetaminophen (Paracetamol) is a selective cyclooxygenase-2 (COX-2) inhibitor and a widely used antipyretic and analgesic agent. It is also a potent hepatic N-acetyltransferase 2 (NAT2) inhibitor that induces ferroptosis and can lead to acute liver injury in mice models.
- Selective COX-2 inhibitor with an IC50 of 25.8 μM
- Widely used as an antipyretic and analgesic
- Potent hepatic N-acetyltransferase 2 (NAT2) inhibitor
- Induces ferroptosis
- Can lead to acute liver injury in mice models
Medchemexpress LLC SBI-810 hydrochloride | 2772746-58-2 | 99.6% | 483.05 | C27H35ClN4O2 | 10 MG
SBI-810 hydrochloride is a β-arrestin-biased allosteric modulator of the neurotensin receptor 1 (NTSR1) supplied as the hydrochloride salt for research use. Provided as a solid with high analytical purity, it is intended for in vitro pharmacology and preclinical signaling or analgesia studies.
- β-arrestin-biased NTSR1 allosteric modulator for receptor signaling studies.
- High purity; typically ≥99.5% by supplier assay.
- Molecular weight 483.05; formula C27H35ClN4O2.
- Available in small-mass pack sizes suitable for in vitro and preclinical work.
- Option for 10 mM solution in DMSO, ready for reconstitution.
- Store sealed at 4°C; in solution store at -80°C for long-term storage.
Medchemexpress LLC CGP71683 hydrochloride | 192322-50-2 | MFCD07783999 | 99.4% | 512.07 | C26H30ClN5O2S | 10 MG
CGP71683 hydrochloride is the hydrochloride salt of a selective neuropeptide Y Y5 receptor antagonist used as a research tool in neuroscience and endocrinology. It is supplied as a high-purity solid for non-clinical laboratory use, with supporting datasheet and certificate of analysis available.
- Selective antagonist for the neuropeptide Y Y5 receptor (Ki ~1.3 nM).
- High reported purity, 99.4%.
- Molecular weight 512.07 g/mol; chemical formula C26H30ClN5O2S.
- CAS number 192322-50-2 for unambiguous identification.
- Solid powder suitable for dissolution in appropriate solvents for assays.
- Supplied with datasheet and certificate of analysis for quality assurance.
- Available in small milligram pack sizes for screening and mechanistic studies.
Medchemexpress LLC L-742001 hydrochloride | 174605-64-2 | MFCD22587878 | 99.0% | 450.35 g·mol⁻1 | C23H25Cl2NO4 | 10 MG
L-742001 hydrochloride is a research reagent that inhibits the influenza virus PA endonuclease, with an observed EC90 of 4.3 μM for vRNP activity in HEK293T cells. It is supplied as a white to off-white solid with reported high purity and is intended for laboratory research use only.
- CAS number 174605-64-2.
- Molecular formula C23H25Cl2NO4.
- Molecular weight 450.35 g·mol⁻1.
- Purity 99.0%.
- Appearance white to off-white solid.
- Solubility DMSO: 20 mg/mL (44.41 mM); warming and sonication may be required.
- Storage powder: -20°C (3 years) or 4°C (2 years); in solvent: -80°C (6 months) or -20°C (1 month).
- For research use only.
Medchemexpress LLC Cyclohexanecarboxylic acid, 1-phenyl-, 2-(4-morpholinyl)ethyl ester, hydrochloride (1:1) | 75136-54-8 | 99.8% | 353.88 | 10 MG
PRE-084 hydrochloride is a highly selective σ1 receptor (S1R) agonist, with an IC50 of 44 nM. This product is intended for research and analytical applications.
- Highly selective σ1 receptor (S1R) agonist with an IC50 of 44 nM.
- Exhibits good neuroprotective effects.
- Can improve motor function and motor neuron survival in mice.
- Can ameliorate myocardial ischemia-reperfusion injury in rats by activating the Akt-eNOS pathway.
Medchemexpress LLC Benzamide, 4-fluoro-N-[2-[4-(7-methoxy-1-naphthalenyl)-1-piperazinyl] ethyl] HCl | 286369-38-8 | 99.9% | 443.94 | 10 MG
S-14506 hydrochloride is a potent 5-HT1A agonist and a 5-HT2A/2C antagonist. It also demonstrates dopamine antagonist properties by blocking dopamine D2 receptors. This compound effectively inhibits the in vivo binding of [3H]raclopride in the striatum and olfactory bulbs, holding potential for research as an anxiolytic agent.
- Potent 5-HT1A agonist
- 5-HT2A/2C antagonist
- Dopamine D2 receptor blocker
- Inhibits [3H]raclopride binding
- Potential anxiolytic agent
Medchemexpress LLC 4-Piperidinecarboxamide, N-hydroxy-1-(2-methoxyethyl)-4-[[4-[4-(trifluoromethoxy)phenoxy]phenyl]sulfonyl]-, hydrochloride (1:1) | 226395-93-3 | 99.4% | 554.96 | 10 MG
SD-2590 hydrochloride is a potent MMP inhibitor with IC50 values of <0.1, <0.1, 0.18, and 1.7 nM for MMP2, MMP13, MMP9, and MMP8, respectively. It inhibits dilation of the left ventricle in rats. This product is for research use only.
- Potent MMP inhibitor
- Inhibits dilation of the left ventricle in rats
- Solid appearance
- White to off-white color
- Ships at room temperature
- Store at -20°C, sealed, away from moisture
- Soluble in DMSO at 55.5 mg/mL
TARGETMOL CHEMICALS INC K02288 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. K 02288 is a novel small molecule inhibitor of ALK1/2/3/6. purity: 99%
Matrix Scientific 2,4-DICHLORO-6-AMINOPHENOL2-10
2,4-dichloro-6-aminophenol Mf C6h5cl2no Mw 178.02 Cas 527-62-8 Mdl MFCD00035766
TARGETMOL CHEMICALS INC SB-366791 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. SB-366791 is a new and selective cinnamide TRPV1 antagonist. purity: 98%
TARGETMOL CHEMICALS INC FMK 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. FMK is an irreversible inhibitor of RSK2 kinase. purity: 98%
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%
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