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Filtered Search Results
Chemscene CHEMSCENE
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5000576177 1-BENZYLPIPERIDIN-3-OL 100G
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Chemscene CHEMSCENE
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5000578985 R-1-BENZYLPIPERIDIN-3-AMINE 1G
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Chemscene CHEMSCENE
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5000579394 S-1-BOC-3-HYDROXYPIPERIDIN 25G
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Chemscene CHEMSCENE
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5000579341 S-1-BOC-3-HYDROXYPIPERIDINE 5G
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Ambeed AMBEED
5000866773 5-HYDROXYPIPERIDIN-2-ONE 1GR
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Chemscene ChemScene | 6-Chlorobenzo[d]isoxazol-3(2H)-one | 1G | CS-0063922 | 0.98 | 61977-29-5| MFCD00125033 | 169.57
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ChemScene | 6-Chlorobenzo[d]isoxazol-3(2H)-one | 1G | CS-0063922 | 0.98 | 61977-29-5| MFCD00125033 | 169.57
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Medchemexpress LLC (R,R)-GSK321 | 1816272-19-1 | 99.4% | 10 MG
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(R,R)-GSK321 is an inhibitor of wild-type isocitrate dehydrogenase 1 (WT IDH1) with an IC50 value of 120 nM. This compound also acts as a mutant R132H IDH1 inhibitor and is an isomer of GSK321 with some wild-type cross-reactivity. It has a molecular weight of 501.55 and a chemical formula of C28H28FN5O3. This product appears as a white to off-white solid.
- Inhibits wild-type isocitrate dehydrogenase 1 (WT IDH1)
- IC50 value of 120 nM for WT IDH1
- Acts as a mutant R132H IDH1 inhibitor
- Isomer of GSK321 with some wild-type cross-reactivity
- Dose-dependently decreases reductive glutaminolysis in A-498 cells (0.1-3 μM for 5 hours)
- For research use only, not for patient use
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Ambeed Dibenzo b d thiophene 5oxide
Dibenzo[b,d]thiophene 5-oxide, 1013-23-6, 95%
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eMolecules 4783-65-7 | 1-Benzylpiperidin-2-one | Oakwood Chemicals | MFCD00464162 | 189.258 | C12H15NO | 98.000 | O=C1CCCCN1Cc1ccccc1 | 1g | 480163888
1-Benzylpiperidin-2-one | Oakwood Chemicals | 4783-65-7 | MFCD00464162 | 189.258 | C12H15NO | 98.000 | O=C1CCCCN1Cc1ccccc1 | 1g | 480163888
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Medchemexpress LLC (S,R)-GSK321 | 1816272-18-0 | 98.6% | 501.55 g/mol | C28H28FN5O3 | 5 MG
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(S,R)-GSK321 is the (S,R)-enantiomer of GSK321, a potent and selective mutant isocitrate dehydrogenase 1 (IDH1) inhibitor used as a research tool to study IDH1-driven oncogenic metabolism and differentiation. It reduces intracellular 2-hydroxyglutarate (2-HG) levels and promotes granulocytic differentiation in leukemic cells, supporting studies in acute myeloid leukemia and related cancers.
- Potent mutant IDH1 inhibitor with nanomolar activity.
- Reduces intracellular 2-hydroxyglutarate (2-HG) levels.
- Promotes granulocytic differentiation in leukemic cells.
- High purity suitable for research applications (98.6%).
- Molecular weight 501.55 g/mol; molecular formula C28H28FN5O3.
- Available in small research pack sizes, including 5 mg.
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eMolecules 704869-38-5 | Medchem Express | SUN11602 | 5mg | 446256931 | HY-101493 | MFCD28133375 | 451.615 | C26H37N5O2
Medchem Express | SUN11602 | 5mg | 446256931 | HY-101493 | 704869-38-5 | MFCD28133375 | 451.615 | C26H37N5O2
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eMolecules 1443138-53-1 | Medchem Express | GSK2200150A | 5mg | 446260130 | HY-112091 | 357.47 | C20H23NO3S
AstaTech | 1-(2-NITROBENZYL)-4-METHYLPIPERAZINE | 1g | 448262464 | AB9834 | 95.000 | 19577-82-3 | MFCD00810565 | 235.287 | C12H17N3O2
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Medchemexpress LLC Revefenacin | 864750-70-9 | MFCD28386316 | 99.1% | 597.75 g·mol⁻¹ | C35H43N5O4 | 10 MG
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Revefenacin is a long-acting muscarinic acetylcholine receptor antagonist (LAMA) with high affinity for the M3 receptor (Ki = 0.18 nM). This research-grade compound is supplied as a solid (white to off-white powder) for in vitro and preclinical studies; it is for research use only and not for clinical or human use.
- Potent M3 receptor antagonist (Ki = 0.18 nM).
- High chemical purity (99.09%).
- Solid, white to off-white appearance suitable for formulation or assay preparation.
- Soluble in DMSO (≈100 mg/mL); ultrasonic agitation recommended.
- Storage: powder at -20°C (long term) or 4°C (short term); in solvent at -80°C or -20°C.
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Aobchem AOBCHEM
5001072828 METHANONE 3-CHLOROPHENYL 3-
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Aobchem AOBCHEM
5001075966 1-PIPERIDINECARBOXYLIC ACID 4
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