Aryl iodides
eMolecules 598-39-0 | 1,1-Difluoro-2-Iodoethane | AA Blocks LLC | MFCD04038311 | 191.947 | C2H3F2I | 0.000 | FC(F)CI | 5g | 460604635
1,1-Difluoro-2-Iodoethane | AA Blocks LLC | 598-39-0 | MFCD04038311 | 191.947 | C2H3F2I | 0.000 | FC(F)CI | 5g | 460604635
eMolecules 29504-81-2 | 2-Bromo-5-iodothiophene | Accela ChemBio (ASD) | MFCD08695058 | 288.930 | C4H2BrIS | 95.000 | Brc1ccc(I)s1 | 1g | 510409038
2-Bromo-5-iodothiophene | Accela ChemBio (ASD) | 29504-81-2 | MFCD08695058 | 288.930 | C4H2BrIS | 95.000 | Brc1ccc(I)s1 | 1g | 510409038
eMolecules 689260-53-5 | 2-Bromo-5-iodo-1,3-dimethylbenzene | Synthonix - Stock | MFCD07780650 | 310.960 | C8H8BrI | 97.000 | Cc1cc(I)cc(C)c1Br | 1g | 459637399
2-Bromo-5-iodo-1,3-dimethylbenzene | Synthonix - Stock | 689260-53-5 | MFCD07780650 | 310.960 | C8H8BrI | 97.000 | Cc1cc(I)cc(C)c1Br | 1g | 459637399
Medchemexpress LLC 5-Iodo-indirubin-3'-monoxime | 331467-03-9 | 98.1% | 403.17 | 1 ML
5-Iodo-indirubin-3'-monoxime is a potent inhibitor of GSK-3β, CDK5/P25, and CDK1/cyclin B. It competes with ATP for binding to the catalytic site of the kinase, with IC50 values of 9, 20, and 25 nM, respectively. It is intended for research use only.
- Potent GSK-3β, CDK5/P25 and CDK1/cyclin B inhibitor
- Competes with ATP for binding to the catalytic site of the kinase
- IC50s of 9 nM (GSK-3β), 20 nM (Cdk5/p25), and 25 nM (Cdk1/cyclin B)
- For research use only
Chem-Impex International, Inc. 4-Iodo-1H-imidazole | MFCD01632213 | 1G
4-Iodo-1H-imidazole, MFCD01632213, 1G
Medchemexpress LLC Iodo-PEG3-N3 | 936917-36-1 | 97.0% | 100 MG
Iodo-PEG3-N3 is a PEG-based PROTAC linker used in the synthesis of PROTACs. It is also a click chemistry reagent, containing an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. It can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups. PROTACs employ the intracellular ubiquitin-proteasome system to specifically degrade target proteins.
- PEG-based PROTAC linker
- Used in PROTAC synthesis
- Click chemistry reagent
- Contains an azide group
- Facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions
- Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
- Enables specific degradation of target proteins