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Cat No. | Product Name | Synonyms | Targets |
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T16670 | PS210 | PDK | |
PS210 is a potent and selective activator of PDK1 (Kd: 3 μM), specifically targeting the PIF-binding pocket of PDK1, without acting against other protein kinases such as S6K, PKB/Akt, or GSK3. Its prodrug, PS423, serves ... | |||
T77749 | Upifitamab | Others | |
Upifitamab is a naked antibody to upifitamab rilsodotin, which can be used to synthesize the antibody-coupled active molecule UPRI, which can be used to study cancer. | |||
T6271 | Tipifarnib | R115777,Zarnestra,IND 58359 | Transferase |
Tipifarnib (IND 58359) is a nonpeptidomimetic quinolinone with potential antineoplastic activity. Tipifarnib binds to and inhibits the enzyme farnesyl protein transferase, an enzyme involved in protein processing (farnes... | |||
T12472 | Pifithrin-α, p-Nitro, Cyclic | PFN-α | p53 |
Pifithrin-α, p-Nitro, Cyclic (PFN-α) (PFN-α) is cell-permeable and active-form inhibitor of p53. | |||
T2707 | Pifithrin-α hydrobromide | Pifithrin hydrobromide,Pifithrin-α (PFTα) HBr,Pifithrin-α,PFTα,PFTα hydrobromide | Ferroptosis , Aryl Hydrocarbon Receptor , p53 |
Pifithrin-α hydrobromide (Pifithrin-α hydrobromide) is a p53 inhibitor, inhibiting p53-dependent transactivation of p53-responsive genes. | |||
T17102 | Tipifarnib (S enantiomer) | Tipifarnib S enantiomer,(S)-(-)-R-115777,(S)-Tipifarnib,IND-58359 S enantiomer | Transferase |
Tipifarnib S enantiomer ((S)-(-)-R-115777) is the S-enantiomer of Tipifarnib. Tipifarnib is a potent and specific farnesyltransferase inhibitor (IC50: 0.6 nM). | |||
T6210 | Pifithrin-μ | PFTμ,NSC 303580,2-Phenylethynesulfonamide | HSP , p53 , Autophagy |
Pifithrin-μ (NSC-303580) is an inhibitor of p53 and HSP70, with neuroprotective and antitumor activity. | |||
T3637 | Pifithrin-β hydrobromide | Cyclic PFT-α,PFT-β,Cyclic Pifithrin-α hydrobromide,Pifithrin-β,PFT β (hydrobromide) | Ferroptosis , p53 |
Pifithrin-β hydrobromide (Cyclic PFT-α) is an inhibitor of p53; reversibly blocks p53-dependent transcriptional activation and apoptosis. Protects against neuronal death in models of stroke and neurodegenerative disorder... | |||
T31224 | Piflufolastat | DCFPYL | Epigenetic Reader Domain |
Piflufolastat (DCFPYL) is a PET imaging agent for prostate cancer PSMA. It is a fluorinated prostate-specific membrane antigen (PSMA) preparation. Piflufolastat can be used to prepare piflufolastat F 18 (DCFPyL F-18). | |||
T4379 | Tropifexor | LJN452 | FXR , Autophagy |
Tropifexor (LJN452) is a novel and highly potent agonist of FXR with an EC50 of 0.2 nM. | |||
T21978 | P-nitro-Pifithrin-α | ||
p-nitro-Pifithrin-α is a cell-permeable analog of pifithrin-α, a potent p53 inhibitor. It suppresses p53-mediated TGF-β1 expression in HK-2 cells and inhibits the activation of caspase-3 by Zika virus (ZIKV) strains. Mor... | |||
T38897 | RapiFluor-MS | ||
RapiFluor-MS labeling used for LC-MS/MS analysis of N-glycans. | |||
T23156 | Pifithrin-β | Others | |
potent p53 inhibitor | |||
T71882 | Pifexole | ||
Pifexole is the 1,2,4-oxadiazole derivative. It has a similar profile of muscle-relaxant activity in animals to that of chlorzoxazone. In rats, pifexole is reported to be seven times more potent than chlorzoxazone in inh... | |||
T69473 | Pifoxime | ||
Pifoxime, a non-steroidal anti-inflammatory agent (NSAID) and COX-1/2 inhibitor, exhibits anti-inflammatory properties, making it useful in neuropsychiatric research. | |||
T3163 | PS 48 | PDK | |
PS 48 has been shown to be a PKB Kinase (PDK1) activator (Kd: 10.3 μM). This compound selectively binds to the PIF-binding pocket of PKB Kinase (PDK1). | |||
T24676 | PS423 | PS210AM,PS 210 AM,PS 423,PS210-AM,PS-423 | |
PS423 is a substrate-selective protein kinase PDK1 inhibitor that acts by binding to the PIF-pocket allosteric docking site. | |||
T71939 | PS77 | ||
PS77 is a Pkh inhibitor directed to the PIF-pocket with increased selectivity for C. albicans Pkh2. | |||
T28458 | PS432 | PS-432,PS 432 | |
PS432 is an allosteric inhibitor of atypical PKCs. PS432 targets the PIF-pocket resulting in significantly reduce tumor growth without side effects in mouse xenograft model. | |||
T16671 | PS315 | PKC | |
PS315 inhibits the full-length and catalytic domain constructs of PKCζ (IC50=10 μM) and PKCη (IC50=30 μM). PS315 has anti-cancer activity. PS315 is a derivative of PS48 and is an allosteric PKC inhibitor by binding to th... |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T3768 | Epifriedelanol | Epifriedelinol | Others |
Epifriedelanol (Epifriedelinol) suppresses adriamycin-induced cellular senescence, replicative senescence in human fibroblasts (HDFs) and HUVECs. Because of Epifriedelanol can reduce cellular senescence in human primary ... | |||
TN4443 | Lipiferolide | Telomerase , Antifection | |
Lipiferolide is an inhibitor of farnesyl protein transferase(FPTase), it inhibits the FPTase activity in a dose-dependent manner, and shows cell growth inhibitory activity against several tumor cells, it possesses cytoto... | |||
TN2572 | 10-O-Caffeoyl-6-epiferetoside | Others | |
10-O-Caffeoyl-6-epiferetoside is a natural product for research related to life sciences. The catalog number is TN2572 and the CAS number is 83348-22-5. | |||
TN3968 | Epifriedelanol acetate | Others | |
Epifriedelanol exhibits antibacterial activities. It also can reduce cellular senescence in human primary cells and may be used to develop dietary supplements or cosmetics that modulate tissue aging or aging-associated d... |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-00545 | Dermcidin Protein, Human, Recombinant (hFc) | Human | HEK293 Cells |
Hepatocellular carcinoma (HCC) is a major contributor to cancer-related deaths due to its often late stage diagnosis, and dermcidin (DCD) may have the potential to be used as a serum biomarker for HCC for more timely dia... | |||
TMPY-03886 | MPIF-1/CCL23 Protein, Human, Recombinant | Human | E. coli |
MPIF-1/CCL23 Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 11.4 kDa and the accession number is P55773-1. | |||
TMPK-01201 | BPIFA1/LUNX Protein, Human, Recombinant | Human | E. coli |
Bactericidal/permeability-increasing fold containing family A, member 1 (BPIFA1) is a secretory protein found in human upper aerodigestive tract mucosa. This innate material is secreted in mucosal fluid or found in submu... | |||
TMPY-02966 | BPIFA2 Protein, Human, Recombinant (hFc) | Human | HEK293 Cells |
BPIFA2 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 51.8 kDa and the accession number is Q96DR5. | |||
TMPY-03121 | BPIFA2 Protein, Human, Recombinant (His) | Human | HEK293 Cells |
BPIFA2 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 26.5 kDa and the accession number is Q96DR5. | |||
TMPY-03851 | BPIFB1 Protein, Human, Recombinant (His) | Human | HEK293 Cells |
BPIFB1, also known as LPLUNC1, belongs to the BPI/LBP/Plunc superfamily, plunc family. BPIFB1 may be involved in the innate immune response to bacterial exposure in the mouth, nasal cavities, and lungs. BPIFB1 is express... | |||
TMPY-00168 | MPIF-1/CCL23 Protein, Human, Recombinant (His) | Human | P. pastoris (Yeast) |
MPIF-1/CCL23 Protein, Human, Recombinant (His) is expressed in yeast with His tag. The predicted molecular weight is 9.9 kDa and the accession number is P55773.3. |