Pyrrolidines
2-Pyrrolidone 98.0+%, TCI America™
CAS: 616-45-5 Molecular Formula: C4H7NO Molecular Weight (g/mol): 85.106 MDL Number: MFCD00005270 InChI Key: HNJBEVLQSNELDL-UHFFFAOYSA-N Synonym: 2-pyrrolidinone,pyrrolidone,butyrolactam,2-pyrrolidone,2-oxopyrrolidine,pyrrolidon,2-ketopyrrolidine,2-pyrol,pyrrolidinone,gamma-butyrolactam PubChem CID: 12025 ChEBI: CHEBI:36592 IUPAC Name: pyrrolidin-2-one SMILES: C1CC(=O)NC1
Sigma Aldrich Fine Chemicals Biosciences 2-Pyrrolidinone 99% | 616-45-5 | MFCD00005270 | 500G
2-Pyrrolidinone 99% | Purity: 99% | Mol Wt: 85.1 | 616-45-5 | MFCD00005270 | 500G
Medchemexpress LLC (R)-Pyrrolidine-2-carboxamide | 62937-45-5 | 98.0% | 114.15 | 100 G
(R)-Pyrrolidine-2-carboxamide is a proline derivative intended for research use only. Amino acids and amino acid derivatives, such as this product, are commercially used as ergogenic supplements.
- Influences the secretion of anabolic hormones
- Supplies fuel during exercise
- Enhances mental performance during stress-related tasks
- Prevents exercise-induced muscle damage
- Recognized as a beneficial ergogenic dietary substance
eMolecules Methyl 1-cbz-5-hydroxypiperidine-3-carboxylate | 1095010-45-9 | MFCD11656768 | 1g
Combi-Blocks | Methyl 1-cbz-5-hydroxypiperidine-3-carboxylate | 1g | 205411708 | ST-0760 | 95.000 | 1095010-45-9 | MFCD11656768 | 293.319 | C15H19NO5
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Medchemexpress LLC Bisindolylmaleimide II | 137592-45-1 | MFCD00236430 | 99.8% | 438.52 | C27H26N4O2 | 5 MG
Bisindolylmaleimide II is a small-molecule inhibitor used to block protein kinase C (PKC) activity in biochemical and cellular research. Supplied as a solid with high stated purity and DMSO solubility, it is commonly used to probe PKC-dependent signaling and to evaluate kinase-related pathways in vitro.
- General inhibitor of protein kinase C subtypes.
- High purity for research applications.
- Solid form facilitates accurate weighing and storage.
- Soluble in DMSO for solution preparation.
- Suitable for biochemical and cellular PKC assays.
eMolecules 2-Pyrrolidinone | Oakwood Chemicals | 616-45-5 | MFCD00005270 | 85.106 | C4H7NO | 98.000 | O=C1CCCN1 | 500g | 480147992
2-Pyrrolidinone | Oakwood Chemicals | 616-45-5 | MFCD00005270 | 85.106 | C4H7NO | 98.000 | O=C1CCCN1 | 500g | 480147992
Echelon Biosciences Research Labs Endothelin Receptor Antagonist BQ 3020; Acetyl-[Ala11,15]-ET 1 (6-21) - 0.5 mg, CAS#: 143113-45-5
Endothelin Receptor Antagonist BQ 3020; Acetyl-[Ala11,15]-ET 1 (6-21) - 0.5mg , Ac-Leu-Met-Asp-Lys-Glu-Ala-Val-Tyr-Phe-Ala-His-Leu-Asp-Ile-Ile-Trp-OH This item is non returnable
Sigma Aldrich 2-Pyrrolidinone
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich 2-Pyrrolidinone
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich 2-(Piperidin-3-ylmethyl)-1H-benzimidazole
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Apexbio Technology LLC Z-FY-CHO 167498-29-5 1mg
Z-FY-CHO (CAS 167498-29-5) is a potent and selective inhibitor of cathepsin L exhibiting an IC50 of 0 85 nM It demonstrates significantly higher selectivity for cathepsin L over cathepsin B (IC50 85 1 nM) and cathepsin K (IC50 184 nM) In cellular assays Z-FY-CHO shows cytotoxic activity against Trypanosoma brucei (ED50 45 nM) with markedly reduced effects on human HL-60 cells (ED50 21 500 nM) The compound completely inhibits osteoclast-mediated bone resorption at 1 g/ml In murine osteoporosis models Z-FY-CHO produces dose-dependent inhibition of bone loss at 2 5 10 mg/kg This inhibitor serves as a valuable tool for investigating cathepsin L function in proteolysis parasitic infection and bone resorption studies