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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T8816 | NAE-IN-M22 | NEDD8 inhibitor M22 | Apoptosis , E1/E2/E3 Enzyme |
NAE-IN-M22 (NEDD8 inhibitor M22) is a selective, potent and reversible inhibitor of NEDD8 activating enzyme (NAE). NAE-IN-M22 inhibits multiple cancer cell lines and induces apoptosis in A549 cells. NAE-IN-M22 also can i... | |||
T6332 | Pevonedistat | MLN4924 | E1/E2/E3 Enzyme , NEDD8 |
Pevonedistat (MLN4924) is a potent and selective NEDD8 activating enzyme (NAE) inhibitor (IC50=4.7 nM). Pevonedistat can be used for the treatment of myelodysplastic syndromes (MDS) and also has antitumor activity. | |||
T13090 | TAS4464 hydrochloride | E1/E2/E3 Enzyme , NEDD8 | |
TAS4464 hydrochloride is a highly potent and selective NEDD8 activating enzyme (NAE) inhibitor(IC50 of 0.955 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). | |||
T16335 | Nonaethylene glycol monododecyl ether | Nonaoxyethylene monododecyl ether,Polidocanol | Others |
Nonaethylene glycol monododecyl ether (Polidocanol) is a nonionic surfactant and polyethylene glycol (PEG) detergent. It can be used to form initial coalesced O/W emulsion droplets and for protein separation and purifica... | |||
T76249 | RNAENFDRF | ||
RNAENFDRF (βIIPKC624-632) conjugated to TAT47-57, a cell-permeable peptide, forms SAMβA, a rationally designed peptide that selectively antagonizes Mfn1-βIIPKC association. SAMβA acts as a selective inhibitor of mitofusi... | |||
T16337 | Nonaethylene glycol | Others | |
Nonaethylene glycol is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome syst... | |||
T16336 | Nonaethylene glycol monomethyl ether | Others | |
Nonaethylene glycol monomethyl ether, a PEG-based PROTAC linker, facilitates PROTAC synthesis[1]. | |||
T25847 | NAEPA | ||
NAEPA, an LPA mimetic, is a selective agonist of the lysophosphatidic acid-1 (LPA1) receptor. | |||
T76249L | RNAENFDRF TFA | ||
RNAENFDRF (βIIPKC624-632) TFA is conjugated to the cell permeable peptide TAT47-57, which can be used to form an inhibitory peptide SAMβA. SAMβA, a rationally designed selective antagonist of Mfn1-βIIPKC association. SAM... | |||
T33578 | Naepaine hydrochloride | ||
Naepaine hydrochloride is a biochemical. | |||
T124493 | Senaetnine | ||
Senaetnine is a useful organic compound for research related to life sciences and the catalog number is T124493. | |||
T126132 | Tabernaecorymbosine A | ||
Tabernaecorymbosine A is a useful organic compound for research related to life sciences and the catalog number is T126132. | |||
T13412 | ZM223 | ZM-223 | E1/E2/E3 Enzyme |
ZM223 is an inhibitor of NEDD8 activating enzyme (NAE). | |||
T16102 | ML-792 | E1/E2/E3 Enzyme | |
ML-792 is a specific small ubiquitin-like modifier (SUMO)-activating enzyme (SAE) inhibitor. Compared with NAE/NEDD8 and UAE/ubiquitin (IC50s of 32 μM and >100 μM, respectively), ML-792 is an effective and selective inhi... | |||
T63800 | ZM223 hydrochloride | ||
ZM223 hydrochloride is a potent, non-covalent, orally active inhibitor of NEDD8 activase (NAE). | |||
T68059 | Ebalzotan | ||
NAE-086 is a high-affinity and selective 5-HT(1A) receptor ligand with a K(i) value of 4.5 nM in membranes from rat hippocampus. | |||
T69577 | LEI-301 | ||
LEI-301 is a novel potent inhibitor for the PLAAT family members, reducing the NAE levels, including anandamide, in cells overexpressing PLAAT2 or PLAAT5. | |||
T28007 | MDPD | ||
MDPD is an enhancer of the N-acylethanolamine degrading enzyme, fatty acid amide hydrolase, in Arabidopsis. MDPD alleviates the growth inhibitory effects of NAE 12:0, in part by enhancing the enzymatic activity of Arabid... | |||
T13412L | ZM223 hydrochloride (2031177-48-5 free base) | ZM223 hydrochloride | Serine Protease |
ZM223 hydrochloride is an orally active, potent non-covalent inhibitor of NEDD8 activating enzyme (NAE), and with excellent anticancer activity. |