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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T40412L | BAD (103-127) (human) acetate | BAD (103-127) (human) acetate (331762-68-6 Free base) | Others |
BAD (103-127) (human) acetate is a 25-mer Bad polypeptide from the BAD BH3 domain that antagonizes the effects of Bcl-xl. | |||
T40412 | BAD (103-127) (human) | ||
BAD (103-127) (human) is a 25-mer peptide obtained from the BH3 domain of BAD. It effectively counteracts the activity of Bcl-xL. Notably, BAD (103-127) (human) exhibits an approximately 800-fold greater binding affinity... | |||
T80223 | Bad BH3 (mouse) | ||
Bad BH3 (mouse) is a bioactive peptide derived from the BH3 domain (a death domain) of Bad, encompassing amino acid residues 140 to 165, and functions by binding to bcl-2. | |||
T76082 | BAD (103-127) (human), FAM-labeled | ||
BAD (103-127) (human), FAM-labeled, is a FAM-labeled 25-mer peptide derived from the BH3 domain of human BAD. This peptide can antagonize the function of Bcl-xL [1]. | |||
T1834 | CX-6258 | CX 6258 | Pim |
CX-6258 is an orally valid Pim 1/2/3 kinase(IC50=5 nM/25 nM/16 nM) inhibitor. It has good biological activity and kinase specificity. | |||
T6148 | CX-6258 hydrochloride | CX-6258 HCl,Pim-Kinase Inhibitor X | Pim |
CX-6258 hydrochloride (Pim-Kinase Inhibitor X) is an effective, orally efficacious Pim1/2/3 kinase inhibitor (IC50: 5/25/16 nM). | |||
T8978 | DD1 | 3,3'-Diamino-4'-methoxyflavone,HUN85111 | Proteasome |
DD1 (HUN85111) is a proteasome inhibitor that induces human myeloid tumor-selective apoptosis. | |||
T22596 | BADGE | PPAR | |
PPARγ antagonist | |||
T0770 | Carbadox | Getroxel,Mecadox | Antibacterial , Antibiotic |
Carbadox (Mecadox) is an antibacterial agent that has been used in veterinary practice for treating swine dysentery and enteritis and for promoting growth. However, its use has been prohibited in the UK following reports... | |||
T35760 | Carnaubadiol | ||
Carnaubadiol is a triterpene that has been found in E. corollata and has antiprotozoal activities.1,2 It is active against L. infantum promastigotes and amastigotes, as well as T. cruzi trypomastigotes (IC50s = 46.2, 7.8... | |||
T15258 | Euphorbadienol | alpha-Euphorbol | Others |
Euphorbadienol is a triterpenic compound isolated from the latex of Euphorbia resinifera. It has antileishmanial and antitrypanosomal activity. | |||
T33404 | MitoBADY | Mito-BADY,Mito BADY | |
Mitobady is a sensitive and specific Raman probe, which can be used for living cell imaging of mitochondria. | |||
T40635 | Desoxycarbadox | ||
Desoxycarbadox, derived from Carbadox, is a quinoxaline-di-N-oxide antibiotic compound. | |||
T78067 | Stobadine | (-)-Stobadine | Reactive Oxygen Species |
Stobadine, a potent antioxidant, safeguards endoplasmic reticulum (ER) membrane fluidity against free radical-induced changes. It shows promise in the development of cardio- and neuroprotective agents owing to its mechan... | |||
T14498 | Barbadin | Arrestin | |
Barbadin is a novel and specific inhibitor of β-arrestin/β2-adaptin interaction with an IC50 value of 19.1 μM for β-arestin1 and 15.6 μM for β-arestin2. Barbadin potentiates the long term effects of lorcaserin on POMC ne... | |||
T12249 | NPB | Alpha-NPB | Others |
NPB (Alpha-NPB) is a potent BAD phosphorylation inhibitor(at Ser99,IC50 of 0.41 μM.) | |||
T4S0498 | Glaucocalyxin A | Wangzaozin B,Leukamenin F | Apoptosis , Akt , Caspase , PI3K |
1. Glaucocalyxin A (Leukamenin F)-SBE-β-CD could be useful with a better solubility and sustained function in drug delivery. 2. Glaucocalyxin A activates caspase-3, decreases BAD phosphorylation, and reduces the expressi... | |||
T4827 | Trimethylammonium chloride | Trimethylamine hydrochloride | Others , Endogenous Metabolite |
Trimethylammonium chloride (Trimethylamine hydrochloride) is a product of decomposition of plants and animals. It is the substance mainly responsible for the fishy odor often associated with fouling fish, bacterial vagin... | |||
TP2127 | R18 | ||
Antagonist of 14.3.3 proteins (KD ≈80 nM). Competitively inhibits 14.3.3-ligand interactions without requiring phosphorylation. Blocks the ability of 14.3.3 to bind to target proteins such as Raf-1, Bad, ASK1 and exoenzy... | |||
TN6419 | Chamaejasmine | ||
Chamaejasmine could be a candidate drug for osteosarcoma and breast cancer chemoprevention, induces apoptosis in MG63 and HEp-2 cells by Akt inactivation and dephosphorylation of BAD. It inhibits Bcl-2 expression and ind... |