Pyrrolidines
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Filtered Search Results
Medchemexpress LLC C12-200 | 1220890-25-4 | 99.91% | C70H145N5O5 | 25 MG
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C12-200 | 1220890-25-4 | 99.91% | C70H145N5O5 | 25 MG
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AARON CHEMICALS LLC N-METHYLMALEIMIDE 25 GRAM
NC2888137 N-METHYLMALEIMIDE 25 GRAM
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Bioss NSF N-ethylmaleimide sensitive
NSF N-ethylmaleimide sensitive fusion protein Antibody
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Aobchem AOBCHEM
5000918041 2 2 2-TRIFLUORO-1- 2- PYRROLID
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Medchemexpress LLC Biotin-C2-maleimide | 139554-72-6 | MFCD02094223 | 99.5% | 366.44 | C16H22N4O4S | 10 MG
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Biotin-C2-maleimide is a thiol-reactive biotinylation reagent used to label cysteine residues and other thiol-containing biomolecules. The compound pairs a biotin tag with a short C2 spacer and a maleimide reactive group to enable efficient conjugation while minimizing impact on biological activity. Supplied as a solid for research use only.
- Thiol-specific labeling via maleimide chemistry
- Short C2 spacer minimizes steric effects
- High purity for reproducible conjugation
- Suitable for protein, peptide, and small-molecule modification
- Stable as a dry solid; store protected from light
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Medchemexpress LLC Z-LEVD-FMK | 1135688-25-3 | 98.0% | 50 MG
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Z-LEVD-FMK is a cell-permeable caspase-4 inhibitor that blocks ER stress-induced apoptosis in cancer cells. It has a molecular weight of 652.71 and a chemical formula of C31H45FN4O10, appearing as a white to off-white solid. It can be dissolved in DMSO at 125 mg/mL.
- Cell-permeable caspase-4 inhibitor
- Blocks ER stress-induced apoptosis in cancer cells
- Molecular weight of 652.71
- Chemical formula C31H45FN4O10
- Appears as a white to off-white solid
- Dissolves in DMSO at 125 mg/mL
- Blocks IL-1β-induced IL-8 production in hRPE cells
- Inhibits caspase-3 activity in hRPE cells
- Completely blocks E2-induced PARP cleavage in 5C cells
- Reverses E2-inhibited growth and prevents morphologic alterations associated with apoptosis in 5C cells
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C1=O.Cc1ccc(cc1)S(O)(=O)=O | 1g | 529046739](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502148133.JPG-250.jpg)
eMolecules 2449063-37-8 | (S)-3-Amino-1-methyl-pyrrolidin-2-one tosylate | J & W PharmLab LLC286.350 | C12H18N2O4S | 96.000 | CN1CC[C@H](N)C1=O.Cc1ccc(cc1)S(O)(=O)=O | 1g | 529046739
(S)-3-Amino-1-methyl-pyrrolidin-2-one tosylate | J & W PharmLab LLC | 2449063-37-8286.350 | C12H18N2O4S | 96.000 | CN1CC[C@H](N)C1=O.Cc1ccc(cc1)S(O)(=O)=O | 1g | 529046739
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C1=O.Cc1ccc(cc1)S(O)(=O)=O | 1g | 529046733](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502148130.JPG-250.jpg)
eMolecules 2412809-21-1 | (R)-3-Amino-1-methyl-pyrrolidin-2-one tosylate | J & W PharmLab LLC286.350 | C12H18N2O4S | 96.000 | CN1CC[C@@H](N)C1=O.Cc1ccc(cc1)S(O)(=O)=O | 1g | 529046733
(R)-3-Amino-1-methyl-pyrrolidin-2-one tosylate | J & W PharmLab LLC | 2412809-21-1286.350 | C12H18N2O4S | 96.000 | CN1CC[C@@H](N)C1=O.Cc1ccc(cc1)S(O)(=O)=O | 1g | 529046733
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Medchemexpress LLC (Z)-FeCP-oxindole | 1137967-28-2 | 99.62% | 329.17 | 25 MG
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(Z)-FeCP-oxindole is a selective human vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with an IC50 value of 200 nM. It can significantly inhibit VEGFR1 and PDGFRα or β at 10 μM. (Z)-FeCP-oxindole also exhibits anticancer activity, specifically acting on B16 murine melanoma lines with an IC50 less than 1 μM.
- Selective human vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor.
- Inhibits VEGFR1 and PDGFRα or β.
- Has anticancer activity on B16 murine melanoma lines.
- For research use only.
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Medchemexpress LLC AZIDO-PEG4-CH2-BOC 250MG
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5000202883 AZIDO-PEG4-CH2-BOC 250MG
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eMolecules 887922-93-2 | 3-(Pyrrolidin-1-ylmethyl)benzoic acid hydrochloride | Combi-Blocks | MFCD08690301 | 241.720 | C12H16ClNO2 | 97.000 | Cl.OC(=O)c1cccc(CN2CCCC2)c1 | 250mg | 359296751
3-(Pyrrolidin-1-ylmethyl)benzoic acid hydrochloride | Combi-Blocks | 887922-93-2 | MFCD08690301 | 241.720 | C12H16ClNO2 | 97.000 | Cl.OC(=O)c1cccc(CN2CCCC2)c1 | 250mg | 359296751
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eMolecules 887922-93-2 | 3-(Pyrrolidin-1-ylmethyl)benzoic acid hydrochloride | Combi-Blocks | MFCD08690301 | 241.720 | C12H16ClNO2 | 97.000 | Cl.OC(=O)c1cccc(CN2CCCC2)c1 | 1g | 290705235
3-(Pyrrolidin-1-ylmethyl)benzoic acid hydrochloride | Combi-Blocks | 887922-93-2 | MFCD08690301 | 241.720 | C12H16ClNO2 | 97.000 | Cl.OC(=O)c1cccc(CN2CCCC2)c1 | 1g | 290705235
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Medchemexpress LLC 3,6,9,16-Tetraoxaheptadecanoic acid, 17-phenyl-, 1,1-dimethylethyl ester | 2381196-81-0 | 95.8% | 100 MG
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Boc-C1-PEG3-C4-OBn is a PROTAC linker, which refers to the PEG composition. It can be used in the synthesis of various PROTACs. PROTACs consist of two distinct ligands linked by a linker; one ligand targets an E3 ubiquitin ligase, and the other targets the protein of interest. PROTACs leverage the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PROTAC linker with PEG composition
- Can be used in the synthesis of various PROTACs
- Targets an E3 ubiquitin ligase and a protein of interest
- Leverages the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
- For research use only
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Chemscene CHEMSCENE
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5000578085 S-1-BOC-2-AZETIDINEMETHANO 25G
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Sigma Aldrich Fine Chemicals Biosciences N Ethylmaleimide crystalli100G
N Ethylmaleimide crystalli100G
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