Lactams
Medchemexpress LLC Aztreonam-d6 | 1127452-94-1 | 99.3% | 1 MG
Aztreonam-d6 is deuterium labeled Aztreonam. Aztreonam (SQ-26,776) is a synthetic monocyclic beta-lactam antibiotic that has a very high affinity for penicillin-binding protein 3 (PBP-3). It is for research use only. This compound can be used as a tracer and as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Deuterium labeled aztreonam
- Synthetic monocyclic beta-lactam antibiotic
- High affinity for penicillin-binding protein 3 (PBP-3)
- Useful as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- For research use only
Medchemexpress LLC Aztreonam (Standard) | 78110-38-0 | 99.6% | 5 MG
Aztreonam (Standard) is the analytical standard of Aztreonam, intended for research and analytical applications. This synthetic monocyclic beta-lactam antibiotic has a very high affinity for penicillin-binding protein 3 (PBP-3).
- Reference standard supplied assay
- Used in qualitative research experiments
- Used in quantitative research experiments
- Used in methodological research experiments
- Suitable for HPLC
- Suitable for GC
- Suitable for MS
eMolecules AstaTech / (S)-3-((TERT-BUTYLDIMETHYLSILYL)OXY)PYRROLIDIN-2-ONE / 0.25g / 296387864 / W11603 / 95.000 / 130403-91-7 / MFCD26394938 / 215.368 / C10H21NO2Si
AstaTech / (S)-3-((TERT-BUTYLDIMETHYLSILYL)OXY)PYRROLIDIN-2-ONE / 0.25g / 296387864 / W11603 / 95.000 / 130403-91-7 / MFCD26394938 / 215.368 / C10H21NO2Si
eMolecules (R)-1-(3-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYL)-3-(3,4-DIMETHOXYPHENYL)PROPAN-1-OL | 1013621-67-4 | MFCD17170917 | 1g
AstaTech | (R)-1-(3-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYL)-3-(3,4-DIMETHOXYPHENYL)PROPAN-1-OL | 1g | 248480807 | 32403 | 97.000 | 1013621-67-4 | MFCD17170917 | 402.606 | C23H34O4Si
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Medchemexpress LLC Aztreonam (Standard) | 78110-38-0 | 72145 | 99.6% | 25 MG
Aztreonam (Standard) is an analytical standard and synthetic monocyclic beta-lactam antibiotic. It is intended for research and analytical applications, serving as a reference standard for assays.
- Used in qualitative, quantitative, and methodological research experiments
- Utilized with techniques such as HPLC, GC, and MS
- Possesses a very high affinity for penicillin-binding protein 3 (PBP-3)
Apexbio Technology LLC Sulbactam 68373-14-8 10mM (in 1mL DMSO)
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
Selleck Chemical LLC Sulbactam S1958-10mg
Sulbactam(CP45899) is a beta-lactamase inhibitor with an average IC50 of 0 8 M
![eMolecules Medchem Express / Sulbactam / 100mg / 446272524 / HY-B0334 / / 68373-14-8 / [null] / 233.240 / C8H11NO5S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502445100.PNG-250.jpg)
eMolecules Medchem Express / Sulbactam / 100mg / 446272524 / HY-B0334 / / 68373-14-8 / [null] / 233.240 / C8H11NO5S
Medchem Express / Sulbactam / 100mg / 446272524 / HY-B0334 / / 68373-14-8 / [null] / 233.240 / C8H11NO5S
Apexbio Technology LLC Tazobactam (sodium salt) 89785-84-2 250mg
Tazobactam sodium salt (CAS 89785-84-2) is a small-molecule inhibitor targeting -lactamases It is designed to irreversibly bind to -lactamases thereby preventing the enzyme-mediated hydrolysis of -lactam antibiotics Tazobactam sodium salt exerts its biological activity primarily through -lactamase inhibition In microbiological assays tazobactam demonstrates intrinsic antibacterial activity against several Acinetobacter strains typically with MIC values of 8 mg/L (range 2 32 mg/L) Based on these pharmacological properties tazobactam sodium salt holds research potential in microbiological assessments and efficacy evaluations of -lactam antibiotic combinations
Medchemexpress LLC Thalidomide-5-NH2-C8-NH2 (TFA) | 2097509-49-2 | 514.49 g/mol | C23H29F3N4O6 | 10 MG
Thalidomide-5-NH2-C8-NH2 (TFA) is a thalidomide-derived intermediate provided as the trifluoroacetic acid salt for research use and compound synthesis. It is intended for laboratory applications only and should be handled using appropriate safety procedures; store sealed at -20°C away from moisture and light. In solvent, recommended storage is -80°C for up to 6 months or -20°C for up to 1 month.
- Salt form: trifluoroacetic acid (TFA) salt.
- Suitable for compound synthesis and as a building block.
- Molecular formula: C23H29F3N4O6.
- Molecular weight: 514.49 g/mol.
- Storage: sealed at -20°C; in solvent -80°C (6 months) or -20°C (1 month).
- Intended for research use only; not for human or clinical use.
Medchemexpress LLC Thalidomide-NH-CBP/p300 ligand 2 | 2484739-21-9 | 98.6% | 922.03 | 25 MG
Thalidomide-NH-CBP/p300 ligand 2 (P-007) is a PROTAC-based CBP and p300 degrader, as extracted from patent WO2020173440. This compound is intended for research use only.
- Protac-based CBP and p300 degrader
- Extracted from patent WO2020173440
- For research use only
Medchemexpress LLC Thalidomide-O-PEG4-azide | 2380318-57-8 | 98.0% | C23H29N5O9 | 100 MG
Thalidomide-O-PEG4-azide is a synthesized E3 ligase ligand-linker conjugate that incorporates the thalidomide based cereblon ligand and a linker used in PROTAC technology. It is a click chemistry reagent, containing an azide group that can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing alkyne groups, and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- Synthesized E3 ligase ligand-linker conjugate
- Incorporates thalidomide based cereblon ligand
- Used in PROTAC technology
- Click chemistry reagent containing an azide group
- Undergoes copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc)
- Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC)
- Molecular weight of 519.50
- Appears as a colorless to light yellow oil
Medchemexpress LLC Thalidomide-O-PEG4-amine hydrochloride | 2820929-03-9 | C23H32ClN3O9 | 250MG
Thalidomide-O-PEG4-amine hydrochloride is a synthesized E3 ligase ligand-linker conjugate. It incorporates a Thalidomide-based cereblon ligand and a linker used in PROTAC technology. This compound is designed to exploit the intracellular ubiquitin-proteasome system for selective degradation of target proteins.
- Synthesized E3 ligase ligand-linker conjugate
- Incorporates Thalidomide-based cereblon ligand
- Used in PROTAC technology
- Designed for selective degradation of target proteins
Medchemexpress LLC Thalidomide-NH-PEG2-COOH | 2412056-45-0 | 99.0% | 433.41 | 25 MG
Thalidomide-NH-PEG2-COOH is a synthesized E3 ligase ligand-linker conjugate. It incorporates the Thalidomide based cereblon ligand and a linker that is utilized in PROTAC technology. This product is intended for research use only.
- Synthesized E3 ligase ligand-linker conjugate
- Utilizes PROTAC technology
- Incorporates Thalidomide based cereblon ligand
- Intended for research use only
Medchemexpress LLC Thalidomide-Propargyne-PEG2-COOH | 2797619-65-7 | 98.7% | 428.39 | 25 MG
Thalidomide-Propargyne-PEG2-COOH is a synthesized E3 ligase ligand-linker conjugate that incorporates the thalidomide based cereblon ligand and a linker used in PROTAC technology. It is a click chemistry reagent, containing an alkyne group, and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing azide groups.
- Synthesized E3 ligase ligand-linker conjugate.
- Incorporates thalidomide based cereblon ligand.
- Uses a linker in PROTAC technology.
- Click chemistry reagent.
- Contains an alkyne group.
- Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc).