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Filtered Search Results
Medchemexpress LLC Thalidomide-4-Br | 2093536-12-8 | MFCD31730866 | 99.6% | 337.13 g·mol⁻¹ | C13H9BrN2O4 | 200 MG
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Thalidomide-4-Br is a brominated thalidomide derivative used as a research compound that engages bromodomains and cereblon-related E3 ligase biology. It is applied in studies of inflammation, tumor biology, and neurology and is supplied as a high-purity solid with recommended cold storage for powder and solutions.
- Engages bromodomains and E3 ligase pathways.
- Used in inflammation, tumor, and neurology research.
- Reported purity approximately 99.6% (COA/product listings).
- Solid, off-white to gray physical form.
- Storage: powder at -20°C (long term) or 4°C (short term); solutions at -80°C or -20°C.
- Available in small-scale amounts and DMSO solution formats.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000664830 THALIDOMIDE-O-AMIDO- 250MG
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Ambeed AMBEED
5000871026 THALIDOMIDE-PIPERAZINE 5-F 1GR
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000596813 THALIDOMIDE-5-NH-PEG 25MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000724078 4-TERT-BUTYLDIMETH 250MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000383115 THALIDOMIDE-O-C3-ACI 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000596790 THALIDOMIDE-5-NH-PEG 50MG
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eMolecules 17557-84-5 | 3-Azetidinone HCl | Ambeed | MFCD01861742 | 107.540 | C3H6ClNO | 97.000 | Cl.O=C1CNC1 | 1g | 525113614
3-Azetidinone HCl | Ambeed | 17557-84-5 | MFCD01861742 | 107.540 | C3H6ClNO | 97.000 | Cl.O=C1CNC1 | 1g | 525113614
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eMolecules 2245697-88-3 | Medchem Express | Thalidomide-4-O-C6-NH2 (hydrochloride) | 5mg | 599150703 | HY-135250B | 409.87 | C19H24ClN3O5
Medchem Express | Canthaxanthin | 5mg | 446274074 | HY-B1960 | 514-78-3 | MFCD00016364 | 564.854 | C40H52O2
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Apexbio Technology LLC Sulbactam 68373-14-8 100mg
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Sulbactam (CAS 68373-14-8) is a small-molecule inhibitor targeting bacterial -lactamase enzymes It is designed to inhibit -lactamase-mediated hydrolytic inactivation of -lactam antibiotics thereby enhancing antibiotic stability and efficacy Sulbactam exerts its biological activity primarily through competitive irreversible inhibition by covalently binding to the -lactamase active site Experimental studies report an IC50 value in the low micromolar range for inhibition of various bacterial -lactamase enzymes Based on these pharmacological properties Sulbactam holds research potential in investigating resistance mechanisms to -lactam antibiotics assessing combined therapeutic regimens and exploring novel clinical strategies for infections caused by -lactamase-producing pathogens
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000380392 THALIDOMIDE-PEG2-NH2 10MM 1ML
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Medchemexpress LLC Thalidomide-5-O-C14-NH2 hydrochloride | 97.7% | 522.08 | 25 MG
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Thalidomide-5-O-C14-NH2 hydrochloride is a thalidomide-based cereblon ligand used in the recruitment of CRBN protein. It can be connected to a ligand for protein by a linker to form PROTACs.
- Thalidomide-based cereblon ligand
- Used in the recruitment of CRBN protein
- Can be connected to a ligand for protein by a linker
- Forms PROTACs
- Targets cereblon
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Medchemexpress LLC Thalidomide-5-O-C12- | 5MG
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Thalidomide-5-O-C12- | 5MG
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Medchemexpress LLC Thalidomide-4-O-C14-NH2 hydrochloride | 99.85% | 522.08 | 25 MG
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Thalidomide-4-O-C14-NH2 hydrochloride is a Thalidomide (HY-10984)-based cereblon ligand that is used in the recruitment of CRBN protein. It can be linked to a protein ligand to create PROTACs. It is for research use only.
- Functions as a ligand for E3 Ligase.
- Involved in the recruitment of CRBN protein.
- Can be connected via a linker to a protein ligand to form PROTACs.
- Intended for research use only.
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Medchemexpress LLC Thalidomide-O-amido-PEG2-C2-NH2 hydrochloride | 2376990-30-4 | 498.91 | 25 MG
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Thalidomide-O-amido-PEG2-C2-NH2 hydrochloride incorporates an E3 ligase ligand and a linker, and can act as an immunomodulator for the treatment of cancer. It is for research use only and not sold to patients.
- PROTACs contain two different ligands connected by a linker: one for an E3 ubiquitin ligase and the other for the target protein.
- PROTACs utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
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