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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T10545 | BIO-32546 | PDE | |
BIO-32546 (S-isomer) is a highly potent regulator of autotaxin (ATX) with an IC50 value of 1 nM. | |||
T21868 | BIO-1211 | Integrin | |
BIO-1211 is a more potent inhibitor of α4β1 (VLA-4, IC50 = 4 nM) over α4β7(IC50 = 2 μM). | |||
TP1457 | BIO-11006 acetate salt (901117-03-1 free base) | BIO-11006 acetate salt | Others |
BIO-11006 acetate salt (901117-03-1 free base) is a polyglycosylated alanine rich C kinase substrate (MARCKS) inhibitor similar to MANS peptides. | |||
T6787 | BIO-acetoxime | BIA,GSK-3 Inhibitor X | Apoptosis , GSK-3 , HSV |
BIO-acetoxime (GSK-3 Inhibitor X) is a potent dual GSK3α/β inhibitor with IC50 of 10 nM, >240-fold selectivity over CDK5/p25, CDK2/cyclin A and CDK1/cyclin B. | |||
T8330 | BIO-013077-01 | TGF-beta/Smad | |
BIO-013077-01 is a potent TGFbeta family type I receptors antagonist. | |||
T1917 | GSK 3 Inhibitor IX | BIO,GSK 3 IX,6-BIO,6-Bromoindirubin-3'-oxime,MLS 2052,6-bromoindirubin-3-oxime | Apoptosis , GSK-3 , Tyrosine Kinases , CDK |
GSK 3 Inhibitor IX (6-BIO) is a selective reversible, ATP-competitive inhibitor of GSK-3α/β and CDK1-cyclinB complex. It inhibits (GSK-3α/β)/CDK1/CDK5 activity with IC50 values of 5 nM/320 nM/83 nM, respectively. | |||
T10546 | bio-THZ1 | CDK | |
bio-THZ1 is a biotinylated version of THZ1. THZ1 is a selective and irreversibly covalent CDK7 inhibitor (IC50: 3.2 nM). | |||
T23795 | BIO-7662 | BIO7662 | |
BIO-7662 is an effective and highly selective antagonist of α4β1 integrin. | |||
T78122 | Bio-AMS | ||
Bio-AMS is a potent inhibitor of bacterial biotin protein ligase, exhibiting selective activity against Mycobacterium tuberculosis (Mtb) and disrupting fatty acid and lipid biosynthesis [1] [2]. | |||
T23794 | BIO592 | BIO-592,BIO 592 | |
BIO592 is a modulator of RORγt. BIO592 triggers inverse agonism of RORγ. | |||
T83884 | Bio-Ben | Biotin-Benzoboroxole | |
Bio-ben functions as a sulfenic acid probe, utilized for labeling both free sulfenic acid and cysteine sulfenic acid within proteins and peptides. | |||
T23793 | BIO399 | BIO 399 | |
BIO399 is an agonist of the RORγt inverse. | |||
T73821 | Bio-AMS TFA | ||
Bio-AMS (TFA) is a potent inhibitor of bacterial biotin protein ligase, exhibiting selective efficacy against Mycobacterium tuberculosis (Mtb) by inhibiting fatty acid and lipid biosynthesis [1]. | |||
T61890 | (E/Z)-BIO-acetoxime | ||
(E/Z) - BIO-acetoxime is effective and selective GSK-3 α/β Inhibitors. For GSK-3 α/β, CDK5/p25, CDK2/cyclin A and CDK1/cyclin B, IC50 are 10nM, 2.4 μM, 4.3 μ M, 63 μ M, respectively。 | |||
T36296 | BIO5192 hydrate | ||
BIO5192 hydrate is a selective and potent integrin α4β1 (VLA-4) inhibitor (Kd<10 pM). BIO5192 hydrate selectively binds to α4β1 (IC50=1.8 nM) over a range of other integrins. BIO5192 hydrate results in a 30-fold increase... | |||
T2167 | Lutidinic acid | 2,4-Pyridinedicarboxylic acid,2,4-Dicarboxypyridine,2, 4-PDCA,2,4-PDCA | Histone Methyltransferase |
lutidinic acid (2,4-Dicarboxypyridine) is an in vitro and in cell inhibitor, as well as a known inhibitor of the histone lysine demethylases. | |||
T38888 | Azide-PEG3-Desthiobiotin | Azide-PEG3-Desthiobiotin | |
Azide-PEG3-Desthiobiotin is a PROTAC linker belonging to the PEG class and can be used to synthesize PROTAC molecules. | |||
T14577 | Biotin-DADOO | EZ-Link Amine-PEO2-Biotin,Biotinyl-3,6-dioxaoctanediamine | Others |
Biotin-DADOO (Biotinyl-3,6-dioxaoctanediamine) is a biotinylation reagent that can be used to synthesize a biotin-estradiol conjugate(i.e., biotin-DADOO-estradiol) to develop a direct, broad-range enzyme immunoassay to m... | |||
T3S2156 | Chrysin 7-O-beta-gentiobioside | Chrysin 7-O-β-gentiobioside | Others |
Chrysin 7-O-beta-gentiobioside (Chrysin 7-O-β-gentiobioside), a glycosylation product of Chrysin, is from Spartium junceum. | |||
T60017 | 5-Bromo-4-chloro-3-indoxyl-beta-D-cellobioside | Others | |
5-Bromo-4-chloro-3-indoxyl-beta-D-cellobioside is a chromogenic compound used to detect cellobiohydrolases. |