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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T23371 | SMER3 | SMER 3 | Others , Ligand for E3 Ligase |
SMER3 is an inhibitor of the Skp1-Cullin-F-box (SCF)(Met30) ubiquitin ligase, a member of the SCF E3-ligase family, which regulates diverse cellular processes including transcription, cell-cycle control and immune respon... | |||
T2850 | Bicuculline | (+)-Bicuculline,d-Bicuculline | GABA Receptor |
Bicuculline ((+)-Bicuculline) is a light-sensitive competitive antagonist of GABAA receptors. It was originally identified in 1932 in plant alkaloid extracts and has been isolated from Dicentra cucullaria, Adlumia fungos... | |||
T22604 | (-)-Bicuculline methiodide | Others | |
(-)-Bicuculline methiodide is a GABAA receptor antagonist. | |||
T12043 | (-)-Bicuculline methobromide | l-Bicuculline methobromide | GABA Receptor |
(-)-Bicuculline methobromide is a potent antagonist of GABAA receptor . | |||
T72246 | Bicuculline methobromide | (+)-Bicuculline methobromide,d-Bicuculline methobromide,(+)-Bicuculline methobromide ; d-Bicuculline methobromide | |
Bicuculline methobromide, a selective GABAA Receptor antagonist with an IC50 value of 3 μM, induces tonic-clonic convulsions in mammals and blocks Ca2+ activated potassium channels. It is applicable in researching epilep... | |||
T74112 | Bicuculline methochloride | ||
Bicuculline methochloride ((+)-Bicuculline; d-Bicuculline), a selective GABAA receptor antagonist, exhibits an IC50 of 3 μM. It induces tonic-clonic convulsions in mammals and blocks Ca2+ activated potassium channels, ma... | |||
T12044 | (-)-Bicuculline methochloride | l-Bicuculline methochloride | GABA Receptor |
(-)-Bicuculline methochloride is a potent antagonist of GABAA receptor. | |||
T77525 | EN450 | NF-κB | |
EN450 is a cysteine-responsive covalent molecular gel degrader of targeted NF-κB with antiproliferative and potentially anticancer activity, which acts through a dependence on Cullin E3 ligase and protease, and can be us... | |||
T9140 | NAcM-OPT HCl(2089293-61-6 free base) | NEDD8 | |
NAcM-OPT HCL is an orally bioavailable cullin neddylation 1 (DCN1) inhibitor that targets N-Acetyl-UBE2M (E2 conjugating enzyme, UBC12) interaction with DCN1 with IC50 of 79 nM. | |||
T5374 | NAcM-OPT | E1/E2/E3 Enzyme , NEDD8 | |
NAcM-OPT is a specific, reversible inhibitor targeting N-Acetyl-UBE2M interaction with DCN1 (IC50: 79 nM). | |||
T0213 | Thalidomide | Thalomid,Sedoval | Apoptosis , TNF , Autophagy , Ligand for E3 Ligase , Molecular Glues |
Thalidomide (Thalomid) is a synthetic derivative of glutamic acid (alpha-phthalimido-glutarimide) with teratogenic, immunomodulatory, anti-inflammatory and anti-angiogenic properties. | |||
T23989 | DI-404 | ||
DI-404 is a high-Affinity Peptidomimetic the DCN1-UBC12 Protein-Protein Interaction inhibitor (Kd= 6.9 nM). DI-404 effectively and selectively inhibits the neddylation of cullin 3 over other cullin members. | |||
T71830 | DT204 | ||
DT204 is a SCFSkp2 inhibitor which blocks Skp2 binding to Cullin-1 and Commd1, thereby synergistically enhancing BTZ-induced apoptosis and stabilization. DT204 also increases p27 levels. | |||
T63930 | DI-1859 | ||
DI-1859 is a selective, potent and covalent inhibitor of DCN1. At low nanomolar concentrations, DI-1859 inhibits the neddylation of cullin 3 in cells. DI-1859 induces a significant increase in NRF2 protein, a CRL3 substr... | |||
T78194 | Skp2 inhibitor 2 | E1/E2/E3 Enzyme | |
Skp2 inhibitor 2 (14f) impedes the F-box protein S-phase kinase-associated protein 2 (Skp2), demonstrating an IC50 of 10.2 μM against Skp2-Cks1. This compound targets Skp2, a component of cullin-RING ligases that recruit... | |||
T18598 | PROTAC BRD2/BRD4 degrader-1 | Others | |
PROTAC BRD2/BRD4 degrader-1 (compound 15) serves as a potent, selective degrader of BET proteins BRD4 and BRD2, achieving rapid, reversible, and unexpectedly selective elimination of BRD4 and BRD2 compared to BRD3. Its e... |