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Filtered Search Results
eMolecules EMOLECULES INC
NC3962223 S-PIPERIDINE-2-CARBOXAMIDE
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Chembridge Corporation 4-(BENZYLOXY)PIPERIDINE
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4-(benzyloxy)piperidine. 76716-51-3 MFCD07186358
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eMolecules Medchem Express / TAK-960 / 5mg / 446265042 / HY-15160 / / 1137868-52-0 / MFCD22420821 / 561.610 / C27H34F3N7O3
Medchem Express / TAK-960 / 5mg / 446265042 / HY-15160 / / 1137868-52-0 / MFCD22420821 / 561.610 / C27H34F3N7O3
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Medchemexpress LLC 3-Amino-2,6-piperidinedione | 2353-44-8 | 99.96% | 128.13 | 500 MG
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3-Amino-2,6-piperidinedione is a synthetic intermediate utilized in the design of antitumor compounds. This product is for research use only and is not sold to patients.
- Synthetic intermediate.
- Used in the design of antitumor compounds.
- Purity: 99.96%.
- Available in multiple pack sizes (e.g., 250 mg, 500 mg, 1 g, 5 g, 10 g, 25 g, 50 g).
- Appearance: Solid, off-white to light blue.
- Shipping: Room temperature (continental US).
- Storage: 4°C, protected from light.
- Storage in solvent: -80°C for 6 months; -20°C for 1 month (protected from light).
- For research use only.
- Cited in scientific literature for its use in synthesizing antitumor agents.
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Medchemexpress LLC 3-[1-[(3S)-1-prop-2-enoylpyrrolidin-3-yl]oxyisoquinolin-3-yl]-1,4-dihydro-1,2,4-triazol-5-one | 1627603-21-7 | 99.9% | C18H17N5O3 | 10MG
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TAK-020 is a covalent Bruton's tyrosine kinase (BTK) inhibitor developed by Takeda and advanced as a clinical candidate for hematologic malignancies and autoimmune diseases. It irreversibly binds Cys481 in BTK's ATP-binding site and is provided by research suppliers as a characterized small-molecule reagent (CAS 1627603-21-7).
- Covalent inhibitor that targets Cys481 in BTK.
- Selective BTK inhibition supported by preclinical and clinical data.
- Well-characterized small molecule with published analytical reports.
- Available from vendors in mg-scale quantities for research use.
- Typically supplied as high-purity material for in vitro and in vivo studies.
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eMolecules Combi-Blocks N-Boc-piperidine-4-carboxylic acid 1kg 290684670 AM-1030 98 000 84358-13-4 MFCD00076999 229 276 C11H19NO4
Combi-Blocks N-Boc-piperidine-4-carboxylic acid 1kg 290684670 AM-1030 98 000 84358-13-4 MFCD00076999 229 276 C11H19NO4
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Medchemexpress LLC Piperidine-4-sulfonic acid | 72450-62-5 | MFCD00055097 | C5H11NO3S | 10MG
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Piperidine-4-sulfonic acid is a small-molecule research reagent that acts as a potent GABA receptor agonist used to probe GABAergic binding and function in in vitro neuroscience studies. It is supplied as a high-purity solid with supporting analytical and safety documentation for laboratory research use.
- Potent GABA receptor agonist with reported IC50 = 0.034 μM for inhibition of H-GABA binding.
- High purity (99.95%) suitable for analytical and biological assays.
- Molecular formula C5H11NO3S and molecular weight 165.21 g·mol⁻¹.
- Intended for in vitro research use only.
- Provided with RP-HPLC purity profile and safety data sheet.
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eMolecules Ambeed / 4-Amino-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid / 250mg / 490553782 / A319862 / / 183673-71-4 / MFCD01318728 / 244.291 / C11H20N2O4
Ambeed / 4-Amino-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid / 250mg / 490553782 / A319862 / / 183673-71-4 / MFCD01318728 / 244.291 / C11H20N2O4
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Medchemexpress LLC HY-12882A 50mg Medchemexpress, Ifenprodil (tartrate) CAS:23210-58-4 Purity:>98%
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Medchemexpress, HY-12882A 50mg Ifenprodil (tartrate) CAS:23210-58-4 Ifenprodil tartrate is a typical noncompetitive NMDA receptor antagonist. Ifenprodil tartrate exerts high affinity at NR1A/NR2B receptors (IC50=0.34 μM) over 400-fold than at NR1A/NR2A receptors (IC50=146 μM). Ifenprodil tartrate inhibits GIRK (Kir3), reduces inward currents through the basal GIRK activity. Ifenprodil tartrate has the potential to be a cerebral vasodilator. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Chem-Impex International, Inc. 4-Benzylpiperidine | MFCD00006006 | 25G
4-Benzylpiperidine, MFCD00006006, 25G
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eMolecules Oakwood Chemicals 4-Methoxy-piperidine 250mg 480121256 029227 0 000 4045-24-3 MFCD04115010 115 176 C6H13NO
Oakwood Chemicals 4-Methoxy-piperidine 250mg 480121256 029227 0 000 4045-24-3 MFCD04115010 115 176 C6H13NO
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eMolecules 4-(4-Fluorobenzyl)Piperidine Hydrochloride | 193357-52-7 | MFCD03840140 | 1g
Chem-Impex | 4-(4-Fluorobenzyl)Piperidine Hydrochloride | 1g | 112758133 | 23656 | | 193357-52-7 | MFCD03840140 | 229.720 | C12H17ClFN
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Medchemexpress LLC 3-Amino-2,6-piperidinedione | 2353-44-8 | 100.0% | 128.13 | 5 G
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3-Amino-2,6-piperidinedione is a synthetic intermediate, meaning it serves as a foundational component in the creation of more complex chemical structures. Specifically, this compound has been utilized in the development of antitumor compounds. It presents as a solid, ranging in color from off-white to light blue.
- Solid appearance.
- Off-white to light blue color.
- Used as a synthetic intermediate.
- Applied in the design of antitumor compounds.
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Medchemexpress LLC 3-Amino-2,6-piperidinedione | 2353-44-8 | 100.0% | 128.13 | 10 G
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3-Amino-2,6-piperidinedione is a synthetic intermediate used in the design of antitumor compounds. This product is intended for research use only and has not been fully validated for medical applications.
- Synthetic intermediate for antitumor compound design
- Stable under recommended storage conditions
- Should be stored at 4°C, protected from light
- For research use only
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Medchemexpress LLC Piperidine-4-sulfonic acid | 72450-62-5 | 99.9% | 165.21 | 25 MG
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Piperidine-4-sulfonic acid is a potent GABA agonist with an IC50 of 0.034 μM for the inhibition of H-GABA binding. It is intended for research use only.
- Potent GABA agonist
- IC50 of 0.034 μM for inhibition of H-GABA binding
- Solid appearance, light brown to brown color
- Purity of 99.95%
- Stable in powder form at -20°C for 3 years or 4°C for 2 years
- Stable in solvent at -80°C for 6 months or -20°C for 1 month
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