Lactams
Medchemexpress LLC Thalidomide-O-PEG4-azide | 2380318-57-8 | 98.0% | C23H29N5O9 | 50 MG
Thalidomide-O-PEG4-azide is a synthesized E3 ligase ligand-linker conjugate that integrates a Thalidomide-based cereblon ligand with a linker used in PROTAC technology. This compound is intended for research use only.
- Acts as a click chemistry reagent due to its Azide group
- Participates in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules containing Alkyne groups
- Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups
eMolecules 2341840-99-9 | Medchem Express | Thalidomide-4-O-C2-NH2 (hydrochloride) | 10mg | 761506298 | HY-136162 | 353.76 | C15H16ClN3O5
ChemScene | 5-Methoxyquinolin-6-amine | 100mg | 687357489 | CS-0197274 | 54620-48-3 | MFCD18971257 | 174.203 | C10H10N2O
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Medchemexpress LLC Thalidomide-O-C8-Boc | 2225148-52-5 | MFCD32701934 | 95.1% | C26H34N2O7 | 10MG
Thalidomide-O-C8-Boc is a thalidomide-derived Cereblon (CRBN) ligand intended for use as the E3 ligase-recruiting moiety in PROTAC design. It features an O-linked eight-carbon spacer with a Boc-protected terminus to enable linker attachment. Manufacturer data report molecular formula C26H34N2O7, molecular weight 486.56, and typical purity ~95%.
- Provides an O-linked C8 spacer with a Boc-protected terminus for linker attachment.
- Suitable for recruiting Cereblon (CRBN) as the E3 ligase in degrader strategies.
- Reported purity approximately 95.1%.
- High solubility in DMSO (100 mg/mL); manufacturer lists example in vivo formulations.
- Recommended storage: solid at -20°C under nitrogen; in solution -80°C (6 months) or -20°C (1 month).
Medchemexpress LLC Thalidomide-O-C8-Boc | 2225148-52-5 | 95.1% | 25 MG
Thalidomide-O-C8-Boc is a thalidomide-based Cereblon ligand used for 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 used to form PROTACs when connected to a ligand for protein by a linker
- Appearance: Solid, white to off-white
- For research use only
![eMolecules 1208530-70-4 | tert-butyl N-(9-azabicyclo[3.3.1]nonan-3-yl)carbamate | Pharmablock | MFCD13196387 | 240.347 | C13H24N2O2 | 97.000 | CC(C)(C)OC(=O)NC1CC2CCCC(C1)N2 | 25mg | 721772855](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502451719.PNG-250.jpg)
eMolecules 1208530-70-4 | tert-butyl N-(9-azabicyclo[3.3.1]nonan-3-yl)carbamate | Pharmablock | MFCD13196387 | 240.347 | C13H24N2O2 | 97.000 | CC(C)(C)OC(=O)NC1CC2CCCC(C1)N2 | 25mg | 721772855
tert-butyl N-(9-azabicyclo[3.3.1]nonan-3-yl)carbamate | Pharmablock | 1208530-70-4 | MFCD13196387 | 240.347 | C13H24N2O2 | 97.000 | CC(C)(C)OC(=O)NC1CC2CCCC(C1)N2 | 25mg | 721772855
Medchemexpress LLC Thalidomide-CH2NH2 (hydrochloride) | 444287-40-5 | 98.1% | 323.73 | 25 MG
Thalidomide-CH2NH2 hydrochloride is a Thalidomide analogue featuring a primary amine, which is a versatile group which may participate in many reactions.
- Features a primary amine, which is a versatile group that may participate in many reactions.
eMolecules 68373-14-8 | Medchem Express | Sulbactam | 100mg | 446272524 | HY-B0334 | 233.24 | C8H11NO5S
Medchem Express | Sulbactam | 100mg | 446272524 | HY-B0334 | 68373-14-8 | 233.240 | C8H11NO5S
Selleck Chemical LLC Laurocapram S4841-25mg
Laurocapram (N-Dodecylcaprolactam Azone N-0252 N-Lauryl caprolactam Tranzone) is a skin penetration enhancer that facilitates absorption of cutaneously applied substances
Medchemexpress LLC Thalidomide-pinacolborane | 2229725-98-6 | 97.0% | 384.19 | C19H21BN2O6 | 100 MG
Thalidomide-pinacolborane is a thalidomide analogue that incorporates a boronic pinacol ester (Bpin). It is used as an E3 ligase ligand in PROTAC research and as a boronate building block for cross-coupling chemistry. Intended for research use only.
- Contains a boronic pinacol ester (Bpin) suitable for Suzuki cross-coupling.
- Acts as a ligand for E3 ligase in PROTAC applications.
- Characterized identity with CAS 2229725-98-6 and molecular weight 384.19.
- Purity typically reported as 97.0% by supplier.
- Recommended storage under nitrogen at -20°C; in solvent, store at -80°C for up to 6 months.
TARGETMOL CHEMICALS INC TIGEMONAM 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. Tigemonam is a monobactam. Tigemonam has potent activity against Gram-negative aerobic bacterial pathogens. purity: 99%
Apexbio Technology LLC Laurocapram 59227-89-3 500mg
Laurocapram is an amphiphilic compound primarily applied as a percutaneous absorption enhancer Laurocapram exerts its biological activity by temporarily altering the lipid architecture within the stratum corneum thereby lowering barrier resistance and increasing skin and mucosal permeability to both hydrophilic and lipophilic substances Based on these pharmacological properties Laurocapram holds research potential in the investigation of transdermal drug delivery mechanisms evaluation of pharmacokinetic profiles and the development of topical therapeutic agents and delivery formulations
Medchemexpress LLC Acy-957 | 1609389-52-7 | 99.6% | 429.54 g/mol | C24H23N5OS | 50 MG
ACY-957 is an orally active, selective small-molecule inhibitor of histone deacetylase isoforms HDAC1 and HDAC2, used for research into epigenetic regulation. It shows potent activity against HDAC1 and HDAC2, reduced activity against HDAC3, and no measurable inhibition of several class II HDACs. The compound is supplied as a high-purity solid and is available in solution formats for assay use.
- Potent inhibition of HDAC1 and HDAC2.
- High selectivity over HDAC3 and class II HDACs.
- Suitable for in vitro and in vivo formulation protocols.
- High reported purity for reliable experimental results.
- Provided as a solid and as ready-to-use DMSO solutions.
- Documented storage and stability conditions for sample handling.