Lactams
Sigma Aldrich Fine Chemicals Biosciences Strychnine hydrochloride | 1421-86-9 | MFCD00058174 | 25g
Strychnine hydrochloride | Mol Wt: 370.87 | 1421-86-9 | MFCD00058174 | 25g
eMolecules 17557-84-5 | 3-Azetidinone HCl | Ambeed | MFCD01861742 | 107.540 | C3H6ClNO | 97.000 | Cl.O=C1CNC1 | 100g | 525113619
3-Azetidinone HCl | Ambeed | 17557-84-5 | MFCD01861742 | 107.540 | C3H6ClNO | 97.000 | Cl.O=C1CNC1 | 100g | 525113619
Medchemexpress LLC 1H-Isoindole-1,3(2H)-dione, 4-[(6-azidohexyl)oxy]-2-(2,6-dioxo-3-piperidinyl)- | 2411389-65-4 | 99.10% | 399.40 | 25 MG
Thalidomide-O-C6-azide is a synthesized E3 ligase ligand-linker conjugate that incorporates a Thalidomide-based cereblon ligand and a linker used in PROTAC technology. It functions as a click chemistry reagent, containing an Azide group, which allows it to undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules that have Alkyne groups. It can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- Synthesized E3 ligase ligand-linker conjugate
- Incorporates a cereblon ligand
- Functions as a click chemistry reagent
- Contains an azide group
- Undergoes copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc)
- Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
- Exploits intracellular ubiquitin-proteasome system for selective target protein degradation
Medchemexpress LLC Thalidomide-O-C6-azide | 2411389-65-4 | 99.1% | 399.40 | 100 MG
Thalidomide-O-C6-azide is a synthesized E3 ligase ligand-linker conjugate, incorporating the Thalidomide based cereblon ligand and a linker used in PROTAC technology. This click chemistry reagent contains an Azide group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules or strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups. It is designed for research applications related to PROTACs, which utilize the ubiquitin-proteasome system to degrade target proteins.
- Incorporates cereblon ligand and a linker for PROTAC technology
- Click chemistry reagent with an Azide group
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Facilitates strain-promoted alkyne-azide cycloaddition (SPAAC)
- Designed for research in protein degradation via PROTACs
Apexbio Technology LLC Aztreonam 78110-38-0 100mg
Aztreonam (CAS 78110-38-0) is a synthetic monocyclic -lactam antibiotic targeting penicillin-binding protein 3 (PBP3) It is designed to bind to PBP3 thereby disrupting bacterial cell wall synthesis and inhibiting bacterial growth Aztreonam exerts its biological activity primarily through inhibition of cell wall synthesis in aerobic Gram-negative bacteria In in vitro studies Aztreonam demonstrates selective antibacterial activity with reported IC50 values ranging from 0 05 8 g/mL against sensitive Gram-negative bacterial strains depending on species and experimental conditions Based on these pharmacological properties Aztreonam holds research potential in studies of bacterial resistance mechanisms -lactamase susceptibility profiles and evaluation of antibiotic permeability
Cayman Chemical Aztreonam-d6 500ug
An internal standard for the quantification of aztreonam by GC- or LC-MS
Medchemexpress LLC Thalidomide-Piperazine 5-fluoride | 2222114-22-7 | 96.5% | 360.34 | 1 G
Thalidomide-Piperazine 5-fluoride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
- Synthesized E3 ligase ligand-linker conjugate
- Incorporates Thalidomide based cereblon ligand
- Utilizes linker in PROTAC technology
- For research use only
- Recommended storage at 4°C, protected from light
- Targets E3 Ligase Ligand-Linker Conjugates, Apoptosis, and Autophagy pathways
- Appears as a light yellow to green yellow solid
Medchemexpress LLC Thalidomide-O-C6-azide | 2411389-65-4 | 99.1% | 399.40 | 50 MG
Thalidomide-O-C6-azide is a synthesized E3 ligase ligand-linker conjugate that incorporates a thalidomide-based cereblon ligand and a linker used in PROTAC technology. This product is also a click chemistry reagent, containing an azide group that can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- Synthesized E3 ligase ligand-linker conjugate
- Incorporates a thalidomide-based cereblon ligand
- Features a linker used in PROTAC technology
- Functions as a click chemistry reagent with an azide group
- Enables copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc)
- Allows strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
- Supports selective degradation of target proteins through PROTACs
Medchemexpress LLC Thalidomide-Piperazine 5-fluoride | 2222114-22-7 | 96.47% | 360.34 | 250 MG
Thalidomide-Piperazine 5-fluoride is a synthesized E3 ligase ligand-linker conjugate. It incorporates a cereblon ligand and a linker utilized in PROTAC technology, designed for research purposes.
- Synthesized E3 ligase ligand-linker conjugate
- Incorporates cereblon ligand
- Linker utilized in PROTAC technology
- Intended for research use only
- Purity: 96.47%
- Molecular weight: 360.34
- Solid appearance
- Color: Light yellow to green yellow
- Soluble in DMSO
Research Products International Corp Aztreonam 25 MG
Aztreonam is a synthetic monocyclic beta-lactam antibiotic, with the nucleus based on a simpler monobactam isolated from Chromobacterium violaceum.