Alcohols and polyols
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- (1)
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- (399)
- (6)
- (102)
- (22)
- (50)
- (31)
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- (13)
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- (1)
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- (1)
- (25)
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- (1)
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- (1)
- (463)
- (9)
- (46)
- (10)
- (46)
- (6)
- (1)
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- (13)
- (148)
- (114)
- (9)
- (5)
- (1)
- (1)
- (1)
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- (1)
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- (1)
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- (1)
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- (1)
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- (1)
- (20)
- (10)
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- (15)
- (1)
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- (6)
- (2)
- (1)
- (2)
- (2)
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- (1)
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- (1)
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- (7)
- (3)
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- (1)
- (36)
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- (4)
- (2)
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- (4)
- (17)
- (14)
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- (1)
- (2)
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- (1)
- (4)
- (37)
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- (2)
- (6)
- (8)
- (2)
- (2)
- (9)
- (7)
- (7)
- (2)
- (1)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (2)
- (1)
- (14)
- (12)
- (1)
- (3)
- (2)
- (7)
- (12)
- (1)
- (1)
- (14)
- (24)
- (1)
- (8)
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- (1)
- (2)
- (1)
- (22)
- (2)
- (6)
- (5)
- (2)
- (1)
- (5)
- (3)
- (4)
- (24)
- (5)
- (3)
- (5)
- (14)
- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
- (4)
- (11)
- (2)
- (6)
- (4)
- (1)
- (3)
- (6)
- (11)
- (5)
- (4)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
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- (1)
- (3)
- (1)
- (2)
- (1)
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- (1)
- (2)
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- (4)
- (1)
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- (1)
- (3)
- (5)
- (1)
- (1)
- (2)
- (1)
- (1)
- (10)
- (2)
- (2)
- (3)
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- (1)
- (1)
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- (1)
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- (1)
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- (1)
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- (60)
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- (1)
- (1)
- (30)
- (2)
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- (11)
- (81)
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- (5)
- (1)
- (81)
- (3)
- (378)
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- (1)
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- (1)
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- (25)
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- (21)
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- (8)
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- (731)
- (11)
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Filtered Search Results
Medchemexpress LLC AR-R17779 hydrochloride | 178419-42-6 | 99.0% | C9H15ClN2O2 | 10MG
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AR-R17779 hydrochloride is a research-grade, potent and selective full agonist of the α7 subtype of neuronal nicotinic acetylcholine receptors, provided as the hydrochloride salt for preclinical pharmacology studies. It is intended for in vitro and in vivo research to probe receptor signaling, cognitive effects, and neuroprotective mechanisms.
- Potent, selective α7 nicotinic acetylcholine receptor agonist.
- High purity (99.0%) suitable for research applications.
- Supplied as a white to off-white solid for ease of handling.
- Stable under recommended storage conditions to preserve activity.
- Suitable for in vitro assays and in vivo pharmacology studies.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC SB-269970 hydrochloride | 261901-57-9 | MFCD03788020 | C18H29ClN2O3S | 10 MM * 1 ML
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SB-269970 hydrochloride is a potent, selective, and brain-penetrant antagonist of the 5-HT7 receptor. It demonstrates over 50-fold selectivity against other 5-HT receptors with a pKi of 8.3.
- Potent and selective 5-HT7 receptor antagonist
- Brain-penetrant
- Exhibits over 50-fold selectivity against other 5-HT receptors
- Significantly blocks amphetamine and ketamine-induced hyperactivity in animal models
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC SB-612111 hydrochloride | 99.6% | 454.86 | 100 MG
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SB-612111 hydrochloride is a novel and potent opiate receptor-like orphan receptor (ORL-1) antagonist with a high affinity for hORL-1 (Ki=0.33 nM). It exhibits selectivity for μ-, κ- and δ-receptors with Ki values of 57.6 nM, 160.5 nM, and 2109 nM, respectively. SB-612111 hydrochloride effectively antagonizes the pronociceptive action of Nociceptin in an acute pain model.
- Novel and potent ORL-1 antagonist
- High affinity for hORL-1 (Ki=0.33 nM)
- Selectivity for μ-, κ- and δ-receptors
- Effectively antagonizes pronociceptive action of Nociceptin in an acute pain model
- Purity: 99.64%
- Available in solid form (white to off-white)
- In-stock for 100 mg quantity
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Czc-54252 hydrochloride | 1784253-05-9 | 98.4% | 1 ML
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CZC-54252 hydrochloride is a potent and selective LRRK2 inhibitor with IC50 values of 1.28 nM for wild-type LRRK2 and 1.85 nM for G2019S LRRK2. It attenuates G2019S LRRK2-induced human neuronal injury with an EC50 of approximately 1 nM and demonstrates neuroprotective activity. This compound is intended for research use only.
- Potent and selective LRRK2 inhibitor
- Attenuates G2019S LRRK2-induced human neuronal injury
- Demonstrates neuroprotective activity
- For research use only
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Medchemexpress LLC Clorgyline hydrochloride | 17780-75-5 | MFCD00052012 | 99.9% | 308.63 g/mol | C13H16Cl3NO | 5 MG
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Clorgyline hydrochloride is an irreversible, selective monoamine oxidase A (MAO-A) inhibitor used in biochemical and pharmacological research. Supplied as the hydrochloride salt with high reported purity, it is used to probe MAO-A activity, neurotransmitter metabolism, and related signaling pathways. The molecule's alkyne functionality also enables copper-catalyzed azide-alkyne cycloaddition (CuAAC) applications.
- Selective irreversible MAO-A inhibitor.
- High purity suitable for research applications.
- Available in small, precise quantities for laboratory use.
- Contains an alkyne group compatible with CuAAC click chemistry.
- Useful for studies of neurotransmitter metabolism and MAO-A function.
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Medchemexpress LLC BMT-090605 hydrochloride | 2231664-45-0 | 98.8% | 400.90 g/mol | C21H25ClN4O2 | 25 MG
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BMT-090605 hydrochloride is the hydrochloride salt of a potent kinase inhibitor selective for adaptor protein-2 associated kinase 1 (AAK1). It is supplied for preclinical research use, including studies of neuropathic pain, and shows activity versus related kinases in addition to AAK1.
- Potent AAK1 inhibitor (IC50 0.6 nM).
- Activity against BIKE and GAK (IC50 45 nM and 60 nM).
- High purity (98.8%).
- Molecular weight 400.90 g/mol; formula C21H25ClN4O2.
- Available as a solid in multiple sizes, including 25 mg.
- 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; not for human or clinical use.
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Medchemexpress LLC Bmt-090605 hydrochloride | 2231664-45-0 | 98.8% | 400.90 g/mol | C21H25ClN4O2 | 50 MG
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BMT-090605 hydrochloride is the hydrochloride salt of a potent, selective adapter protein-2 associated kinase 1 (AAK1) inhibitor for biochemical and cellular research. Supplied as a light-yellow solid with high reported purity, it is intended for in vitro and early-stage preclinical studies to probe AAK1-mediated pathways and mechanism-of-action experiments.
- High reported purity suitable for research-grade assays.
- Supplied as a solid with consistent physical characterization.
- Available in small research pack sizes, enabling dose-range studies.
- Used to interrogate AAK1-related signaling in biochemical and cellular assays.
- Stable under typical frozen and refrigerated storage conditions (refer to SDS).
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Medchemexpress LLC Bmt-090605 (hydrochloride) | 2231664-45-0 | 98.8% | 400.90 g·mol⁻¹ | C21H25ClN4O2 | 5 MG
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BMT-090605 hydrochloride is a potent, selective small-molecule inhibitor of adaptor protein-2 associated kinase 1 (AAK1) with additional activity against BIKE and GAK. Supplied as the hydrochloride salt for research use, it is provided as a solid with specified purity and storage recommendations, making it suitable for kinase profiling and target validation studies.
- Potent AAK1 inhibition with low-nanomolar IC50 (0.6 nM).
- Selective activity against related kinases BIKE and GAK.
- High purity (98.8%) suitable for biochemical assays.
- Molecular weight 400.90 g·mol⁻¹.
- Available in small pre-weighed sizes for research, including 5 mg.
- Stable as a powder when stored at recommended temperatures.
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Medchemexpress LLC Simufilam hydrochloride | 2480226-07-9 | 99.9% | 295.81 | 10 MG
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Simufilam hydrochloride (PTI-125 hydrochloride) is an orally active FLNA modulator. It restores NMDAR signaling and Arc expression, inhibits overactive mTOR signaling by restoring the normal conformation of FLNA, improves insulin sensitivity, and reduces Aβ42-induced neuroinflammation and tau protein hyperphosphorylation. It can be used for research of Alzheimer's disease.
- Acts as an orally active FLNA modulator
- Restores NMDAR signaling and Arc expression
- Inhibits overactive mTOR signaling by restoring normal FLNA conformation
- Improves insulin sensitivity
- Reduces Aβ42-induced neuroinflammation and tau protein hyperphosphorylation
- Useful for Alzheimer's disease research
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Medchemexpress LLC Acotiamide hydrochloride | 185104-11-4 | 99.6% | 50MG
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Acotiamide hydrochloride | 185104-11-4 | 99.6% | 50MG
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Medchemexpress LLC DC-BPi-11 (hydrochloride) | 2758411-61-7 | 97.0% | C20H24ClN5O2S | 25 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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DC-BPi-11 hydrochloride is an inhibitor of bromodomain PHD finger transcription factor (BPTF) with an IC50 value of 698 nM. It shows remarkable inhibition against leukemia cell proliferation.
- Inhibitor of bromodomain PHD finger transcription factor (BPTF)
- Shows remarkable inhibition against leukemia cell proliferation
- Decreases downstream oncogene expression
- Dose-dependently decreases c-Myc protein level
- Induces cell apoptosis by arresting the cell cycle at G1 phase
- Minimal effects on normal cells
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Ambeed AMBEED
5000950417 5-NITROBENZENE-123-TRIOL 50MG
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Sigma Aldrich Fine Chemicals Biosciences N-Acetyl-2,3-dehydro-2-deoxyneuraminic acid >=93% | 24967-27-9 | MFCD00135810 | 25MG
N-Acetyl-2,3-dehydro-2-deoxyneuraminic acid >=93% | Purity: >=93% | Mol Wt: 291.25 | 24967-27-9 | MFCD00135810 | 25MG
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eMolecules 32638-88-3 | Pyrogallol red | Oakwood Chemicals | MFCD00005046 | 400.360 | C19H12O8S | 0.000 | Oc1ccc2c(Oc3c(O)c(O)ccc3C22OS(=O)(=O)c3ccccc23)c1O | 1g | 532150587
Pyrogallol red | Oakwood Chemicals | 32638-88-3 | MFCD00005046 | 400.360 | C19H12O8S | 0.000 | Oc1ccc2c(Oc3c(O)c(O)ccc3C22OS(=O)(=O)c3ccccc23)c1O | 1g | 532150587
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Chem-Impex International, Inc. Pyrogallol | 87-66-1 | MFCD00002192 | 25G
Pyrogallol , 87-66-1, MFCD00002192, 25G
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