Pyrrolidines
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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000759175 BIOTIN-PEG-MALEIMIDE 100MG
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Aobchem AOBCHEM
5001064239 2 4-DICHLOROPHENYL PYRROLIDI
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5000759711 1-BOC-4-4-CARBOXYBE 5G
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5001069556 4-METHOXYPHENYL PYRROLIDIN-1
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![eMolecules 1363380-83-9 | 1-{[(tert-butoxy)carbonyl]amino}-3,3-difluorocyclobutane-1-carboxylic acid | Pharmablock | MFCD22415254 | 251.230 | C10H15F2NO4 | 97.000 | CC(C)(C)OC(=O)NC1(CC(F)(F)C1)C(O)=O | 50mg | 551133434](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000473896.jpg-250.jpg)
eMolecules 1363380-83-9 | 1-{[(tert-butoxy)carbonyl]amino}-3,3-difluorocyclobutane-1-carboxylic acid | Pharmablock | MFCD22415254 | 251.230 | C10H15F2NO4 | 97.000 | CC(C)(C)OC(=O)NC1(CC(F)(F)C1)C(O)=O | 50mg | 551133434
1-{[(tert-butoxy)carbonyl]amino}-3,3-difluorocyclobutane-1-carboxylic acid | Pharmablock | 1363380-83-9 | MFCD22415254 | 251.230 | C10H15F2NO4 | 97.000 | CC(C)(C)OC(=O)NC1(CC(F)(F)C1)C(O)=O | 50mg | 551133434
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000696506 RAC-IBR120 10MG
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Medchemexpress LLC N-Fmoc-N'-(azido-PEG4)-L-lysine PFP ester | 00-00-0 | 95.0% | C38H42F5N5O9 | 10MG
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N-Fmoc-N'-(azido-PEG4)-L-lysine PFP ester is an Fmoc-protected, PEG-based amino acid derivative featuring an azide functional group and an activated pentafluorophenyl (PFP) ester. It functions as a bifunctional linker and click-chemistry reagent for bioconjugation and PROTAC assembly, enabling selective amine coupling through the PFP ester and subsequent azide-alkyne cycloaddition reactions.
- Fmoc-protected α-amine for orthogonal protection strategies.
- Azide functional group compatible with CuAAC and SPAAC click reactions.
- Activated PFP ester for efficient coupling to primary amines.
- PEG4 spacer improves solubility and reduces steric hindrance.
- High purity suitable for synthetic and bioconjugation applications.
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Medchemexpress LLC (Z)-3-propyl-2-(o-tolylimino)thiazolidin-4-one | 1228116-62-8 | MFCD31560466 | 100mg
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(Z)-3-propyl-2-(o-tolylimino)thiazolidin-4-one is a drug impurity
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Medchemexpress LLC N-(2-hydroxyethyl)iminodiacetic acid | 93-62-9 | MFCD00004293 | >=98.0% | 177.16 g/mol | C6H11NO5 | 100 G
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N-(2-Hydroxyethyl)iminodiacetic acid is an amino acid derivative used as a chelating and buffering reagent in laboratory research. It is supplied as a powder for biochemical and analytical applications where metal ion complexation or buffer formulation is required. Identifiers include CAS 93-62-9, formula C6H11NO5, and molecular weight 177.16 g/mol.
- Chelating agent for metal ions including Fe(III)
- Useful as a buffer component in biochemical assays
- Solid powder form convenient for weighing and storage
- Available in multiple pack sizes for laboratory use
- High purity suitable for research (>=98.0%)
- For research use only; not for human or clinical applications
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![eMolecules 127199-14-8 | (1S,2S)-2-Fluorocyclopropanecarboxylic acid | Apollo Scientific104.080 | C4H5FO2 | 95.000 | OC(=O)[C@@H]1C[C@@H]1F | 1g | 562463109](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000488724.jpg-250.jpg)
eMolecules 127199-14-8 | (1S,2S)-2-Fluorocyclopropanecarboxylic acid | Apollo Scientific104.080 | C4H5FO2 | 95.000 | OC(=O)[C@@H]1C[C@@H]1F | 1g | 562463109
(1S,2S)-2-Fluorocyclopropanecarboxylic acid | Apollo Scientific | 127199-14-8104.080 | C4H5FO2 | 95.000 | OC(=O)[C@@H]1C[C@@H]1F | 1g | 562463109
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Vector Laboratories CY5 5 MALEIMIDE-1MG
NC3877560 CY5 5 MALEIMIDE-1MG
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Medchemexpress LLC HY-17584 10mg , Linaclotide CAS:851199-59-2 Purity:98%
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Medchemexpress, HY-17584 10mg Linaclotide CAS:851199-59-2 Formula:C59H79N15O21S6 Purity:98% Linaclotide is a potent and selective guanylate cyclase C agonist; developed for the treatment of constipation-predominant irritable bowel syndrome (IBS-C) and chronic constipation. 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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Medchemexpress LLC Phenol, 3-[[4-(2-pyridinyl)-2-thiazolyl]amino]- | 315702-75-1 | 99.95% | 50 MG
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KCC-07 is a potent and brain-penetrant MBD2 (methyl-CpG-binding domain protein 2) inhibitor. It prevents binding of MBD2 to methylated DNA and activates brain specific angiogenesis inhibitor 1 (BAI1), inducing anti-proliferative BAI1/p53/p21 signaling. It exhibits anticancer activity.
- Clearly inhibited medulloblastomas (MB) cell growth in vitro.
- Largely abrogated MBD2 binding to the ADGRB1 promoter in BAI1-silent MB cells.
- Treatment inhibited tumor growth and significantly extended the survival of MB xenografts in athymic nude mice.
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Medchemexpress LLC (Rac)-IBT6A | 1412418-47-3 | 50 MG
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(Rac)-IBT6A is a racemate of IBT6A, which is an impurity of Ibrutinib. It can be utilized in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct. Ibrutinib is a selective, irreversible Btk inhibitor.
- Can be used in synthesis of Ibrutinib and Ibrutinib-based activity-based probes (ABPs)
- Racemate form of IBT6A
- Serves as an impurity of Ibrutinib
- Ibrutinib is a selective, irreversible Btk inhibitor with an IC50 of 0.5 nM
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eMolecules 1188405-87-9 | (1-(tert-Butoxycarbonyl)-1H-pyrazol-4-yl)boronic acid | ChemScene | MFCD09951915 | 212.010 | C8H13BN2O4 | 96.000 | CC(C)(C)OC(=O)n1cc(cn1)B(O)O | 25g | 536848341
(1-(tert-Butoxycarbonyl)-1H-pyrazol-4-yl)boronic acid | ChemScene | 1188405-87-9 | MFCD09951915 | 212.010 | C8H13BN2O4 | 96.000 | CC(C)(C)OC(=O)n1cc(cn1)B(O)O | 25g | 536848341
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