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Filtered Search Results
Medchemexpress LLC Azido-PEG23-C2-azide | 95.0% | 1125.30 | 25 MG
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Azido-PEG23-C2-azide is a PEG-based PROTAC linker used in the synthesis of PROTACs. It is a click chemistry reagent containing an Azide group.
- Can participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with Alkyne groups
- Can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups
- Exploits the intracellular ubiquitin-proteasome system to selectively degrade target proteins
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Aobchem AOBCHEM
5001081648 5-NITRO-2- 2- PYRROLIDIN-1-YL
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C(O)=O)[C@@H]1CCCN1C(=O)OC(C)(C)C | 0.25g | 553648859](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000490630.jpg-250.jpg)
eMolecules 120205-50-7 | N-BOC-DOLAPROINE | AstaTech | MFCD18157735 | 287.356 | C14H25NO5 | 95.000 | CO[C@H]([C@@H](C)C(O)=O)[C@@H]1CCCN1C(=O)OC(C)(C)C | 0.25g | 553648859
N-BOC-DOLAPROINE | AstaTech | 120205-50-7 | MFCD18157735 | 287.356 | C14H25NO5 | 95.000 | CO[C@H]([C@@H](C)C(O)=O)[C@@H]1CCCN1C(=O)OC(C)(C)C | 0.25g | 553648859
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000760022 1-BOC-4-4-CARBOXYBE 1G
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Aobchem AOBCHEM
5001082306 2-FLUORO-3- HYDROXYMETHYL -4-
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Medchemexpress LLC Hydroxymethyl dasatinib | 910297-58-4 | MFCD18252610 | 98.0% | 504.00 g/mol | C22H26ClN7O3S | 5 MG
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Hydroxymethyl dasatinib is the M24 benzylhydroxy metabolite of dasatinib and is supplied as a small-molecule research reagent for in vitro studies. It has been reported to inhibit proliferation of K562 chronic myeloid leukemia cells with an IC50 of 46.7 nM. This compound is intended for research use only and not for human or clinical applications.
- Benzylhydroxy metabolite of dasatinib.
- Reported IC50 of 46.7 nM in K562 cells.
- Small-molecule research reagent for in vitro studies.
- Molecular weight 504.00 g/mol.
- Chemical formula C22H26ClN7O3S.
- CAS number 910297-58-4.
- Available as 5 MG package.
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Medchemexpress LLC Rac-beraprost (sodium) | 88475-69-8 | MFCD00911570 | 5mg
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(Rac)-Beraprost ((Rac)-ML 1129) sodium is a racemic isomer of Beraprost sodium (HY-13569A) Beraprost sodium is an orally active prostacyclin analog that inhibits the release of Ca2 from intracellular storage sites by binding to prostacyclin membrane receptors (Prostaglandin Receptor) leading to relaxation of smooth muscle cells and vasodilation Beraprost sodium has vasodilatory antiplatelet and cytoprotective effects making it promising for research in the field of cardiovascular diseases such as thromboangiitis obliterans and atherosclerosis[1][2]
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Aobchem AOBCHEM
5000903895 ETHYL 6- PYRROLIDIN-1-YL NICOT
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Sigma Aldrich Fine Chemicals Biosciences RI-1 >=98% (HPLC) | 415713-60-9 | MFCD00814248 | 5MG
RI-1 >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 361.61 | 415713-60-9 | MFCD00814248 | 5MG
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Accela Chembio Inc 1-benzyl-5-oxo-3-pyrrolidinecarboxylic Acid | 25g | 5733-86-8 | MFCD00085749 | 97+% | Shelf Life: 2160 Days | Moisture Sensitive
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1-benzyl-5-oxo-3-pyrrolidinecarboxylic Acid | 25g | 5733-86-8 | MFCD00085749 | 97+% | Shelf Life: 2160 Days | Moisture Sensitive
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Aobchem AOBCHEM
5001081681 4-BROMO-3- PYRROLIDINE-1-CARB
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Aobchem AOBCHEM
5000977279 2-FLUORO-6-PYRROLIDIN-1-YLPYRI
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Medchemexpress LLC (Rac)-Idroxioleic acid (2-Hydroxyoleic acid) | 56472-29-8 | 99.9% | 1 MG
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(Rac)-Idroxioleic acid (2-Hydroxyoleic acid) is a synthetic oleic acid (OA) derivative that binds to the plasma membrane and alters lipid organization. It has an anti-tumor effect. It is for research use only.
- Binds to the plasma membrane and alters lipid organization
- Has an anti-tumor effect
- Impairs Jurkat cell growth in a time- and concentration-dependent manner
- Induces a marked and concentration-dependent increase in the proteolytic cleavage of PARP
- Inhibits tumor growth in nude mice
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eMolecules 108787-91-3 | (S)-2-((tert-Butoxycarbonyl)amino)-5-((2,2,10,10-tetramethyl-4,8-dioxo-3,9-dioxa-5,7-diazaundecan-6-ylidene)amino)pentanoic acid | 250mg
Ambeed | 2-(Furan-2-yl)pyridin-4-amine | 100mg | 603088356 | A1077284 | 1159817-12-5 | MFCD12032854 | 160.176 | C9H8N2O
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Medchemexpress LLC (E/Z)-SIS3 free base | 1009104-85-1 | MFCD24368989 | 99.5% | 453.53 | C28H27N3O3 | 100mg
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E/Z-SIS3 free base exhibits an inhibitory efficacy against smad3 exhibits an anti-fibrotic and anti-inflammatory effect through a TGF- /smad3 signaling pathway[1]
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