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Search Results for " br-1 "

20

Compounds

Cat No. Product Name Synonyms Targets
T22136 PRL-3 Inhibitor I PRL-3 Inhibitor,BR-1 Phosphatase , Others
PRL-3 Inhibitor I (BR-1) is a phosphatase of regenerating liver 3 (PRL-3) inhibitor which blocks the migration and invasion of metastatic cancer cells.
TP1549L NY-BR-1 p904 A2 acetate(347142-73-8 free base) Others
T-cell clones specific for this NY-BR-1 epitope (p904) can recognize breast tumor cells expressing NY-BR-1.
TP1549 NY-BR-1 p904 (A2) NY-BR-1 p904 A2
T-cell clones specific for this NY-BR-1 epitope (p904) can recognize breast tumor cells expressing NY-BR-1.
T18161 M-PEG2-Br Others , PROTAC Linker
m-PEG2-Br is a PEG-based PROTAC linker. m-PEG2-Br can be used in the synthesis of PROTACs.
T9855 BR10291 4-Thiazolecarboxamide, N-[2-[(2S)-2-cyano-4,4-difluoro-1-pyrrolidinyl]-2-oxoethyl]-2-[(3,4-dichlorophenyl)methyl]- Others
BR102910 (4-Thiazolecarboxamide, N-[2-[(2S)-2-cyano-4,4-difluoro-1-pyrrolidinyl]-2-oxoethyl]-2-[(3,4-dichlorophenyl)methyl]-) is a selective inhibitor of fibroblast activated protein (FAP).
T38717 Cyclohexane-PEG1-Br Cyclohexane-PEG1-Br
Cyclohexane-PEG1-Br 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...
T18552 Pomalidomide-amido-C1-Br Others
Pomalidomide-amido-C1-Br is a synthesized conjugate consisting of the Pomalidomide-based cereblon ligand and a linker, functioning as an E3 ligase ligand-linker. This compound serves as a tool for designing a B-Raf PROTA...
T39021 N-Ethylpropionamide-PEG1-Br N-Ethylpropionamide-PEG1-Br
N-Ethylpropionamide-PEG1-Br is a polyethylene glycol (PEG) derived PROTAC linker utilized for the synthesis of Proteolysis Targeting Chimeras (PROTACs).
T39160 N-Ethyl-N-methylpropionamide-PEG1-Br N-Ethyl-N-methylpropionamide-PEG1-Br
N-Ethyl-N-methylpropionamide-PEG1-Br is a PEG-derived PROTAC linker suitable for the synthesis of PROTACs.
T75130 Glucocorticoid receptor agonist-1 phosphate Ala-Ala-Br
Glucocorticoid Receptor Agonist-1 Phosphate Ala-Ala-Br is a drug-linker conjugate for antibody-drug conjugates (ADCs), serving as a reaction reagent in the creation of anti-CD40 antibody agent conjugates [1].
T77835 Glucocorticoid receptor agonist-1 phosphate Gly-Glu-Br
Glucocorticoid Receptor Agonist-1 Phosphate (Gly-Glu-Br) is an antibody-drug conjugate (ADC) linker utilized in the synthesis of ABBV-154, ABBV-927, ABBV-368, and related analogs [1].
T17654 Boc-NH-C6-Br Others
Boc-NH-C6-Br is a cleavable linker used for antibody-drug conjugates (ADC)[1].
T14771 Br-PEG4-C2-Boc Others
Br-PEG4-C2-Boc is a cleavable 4-unit PEG ADC linker employed for the synthesis of antibody-drug conjugates (ADCs)[1].
TN5012 Shizukaol C HIV Protease , Antifection
1. Shizukaol C shows anti-HIV-1 replication activities in both wild-type HIV-1 and two NNRTIs-resistant strains. <br/> 2. Shizukaol C has significant cytotoxicities against C8166 cells. <br/>
TN2760 2-Hydroxy-1,8-cineole Antifection
1. 2-endo-Hydroxy-1,8-cineole shows antimicrobial and bactericidal activities against against test bacteria (Staphylococcus aureus, Escherichia coli, and Pseudomonas fluorescens) .<BR/>
T40574 Br-C3-methyl ester Br-C3-methyl ester
Br-C3-methyl ester is an alkyl/ether-based PROTAC linker utilized for the synthesis of PROTAC PD-1/PD-L1 degrader-1.
TN2934 3''-Galloylquercitrin Others
1. 3''-Galloylquercitrin possesses the activity for PTK inhibition. <br/>
TN4411 Lappaol F CDK , P-gp , JNK
1. Lappaol F has antioxidant and antiaging properties, it may promote the C. elegans longevity and stress resistance through a JNK-1-DAF-16 cascade. <br/> 2. Lappaol F has potential chemosensitizing activity, it may be c...
T16619 Propargyl-PEG4-Br Others
Propargyl-PEG4-Br is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
T14772 Br-PEG4-CH2-Boc Others
Br-PEG4-CH2-Boc, a PEG- and Alkyl/ether-based PROTAC linker, serves as a valuable component for the synthesis of PROTACs[1].
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TargetMol