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カタログ番号 | 製品名 | 別名 | ターゲット |
---|---|---|---|
T9499 | Icenticaftor | QBW251 | CFTR |
Icenticaftor (QBW251) is an orally active potentiator of CFTR channel. | |||
T16681 | Nesolicaftor | PTI-428 | CFTR , Autophagy |
Nesolicaftor (PTI-428) specifically enhances cystic fibrosis transmembrane conductance regulator protein synthesis. | |||
T14935 | Elexacaftor | VX-445 | CFTR , Autophagy |
Elexacaftor (VX-445) is a modulator of cystic fibrosis transmembrane conductance regulator (CFTR) and it also facilitates the processing and trafficking of CFTR to increase the amount of CFTR at the cell surface. | |||
T3135 | KM11060 | CFTR , Autophagy | |
KM11060 is a novel corrector of the F508del-CFTR trafficking defect, Correcting F508del-CFTR trafficking, increasing the amount of functional CFTR at the plasma membrane. | |||
T1634 | Glibenclamide | Glyburide | Potassium Channel , Mitochondrial Metabolism , CFTR , P-gp , Autophagy |
Glibenclamide (Glyburide) is an antidiabetic sulfonylurea derivative with actions similar to those of chlorpropamide. | |||
T1805 | Ataluren | PTC124 | CFTR , Autophagy |
Ataluren (PTC124) is a novel, orally administered drug that targets nonsense mutations. Ataluren is approved for use by the European Medicines Agency to treat Duchenne Muscular Dystrophy in patients aged 5 years and olde... | |||
T5312 | CFTR corrector 2 | FDL169 | CFTR , Autophagy |
CFTR corrector 2 (FDL169) is a novel and potent CFTR (Cystic fibrosis transmembrane conductance regulator) corrector for treating cystic fibrosis (CF) patients who carry the F508del mutation. | |||
T2486 | IOWH-032 | IOWH032,IOWH 032 | CFTR , Autophagy |
IOWH-032 (IOWH032) , a synthetic CFTR inhibitor, has been investigated for the treatment of cholera, diarrhea, and secretory diarrhea. | |||
T2451 | GlyH-101 | GlyH 101 | CFTR , Autophagy |
GlyH-101 is a cell-permeable glycinyl hydrazone compound that blocks CFTR with Ki of 1.4 uM. | |||
T1874 | PPQ-102 | PPQ102,CFTR Inhibitor,PPQ 102 | CFTR , Autophagy |
PPQ-102 (CFTR Inhibitor), an effective CFTR inhibitor, can completely inhibit CFTR chloride current (IC50: 90 nM). | |||
T2588 | Ivacaftor | Ivacaftor (VX-770),VX-770 | CFTR , Autophagy |
Ivacaftor (VX-770) (VX-770) is a potentiator of CFTR targeting G551D-CFTR (EC50: 100 nM) and F508del-CFTR (EC50: 25 nM) in Fisher rat thyroid cells, respectively. | |||
T4503 | Talniflumate | Somalgen | Chloride channel , COX , N-Acetylglucosaminyltransferase , Anion Exchanger |
Talniflumate (Somalgen) is a calcium-activated chloride channel (hCLCA1/mCLCA3) blocker that reduces mucin synthesis and releases in animal models and cell culture. It possesses anti-inflammatory actions via inhibition o... | |||
T7083 | GLPG1837 | ABBV-974 | CFTR , Autophagy |
GLPG1837 (ABBV-974) is an effective CFTR potentiator, with EC50s of 3 nM and 339 nM for F508del and G551D CFTR, respectively. | |||
T10591 | BPO-27 racemate | BPO-27 (racemate) | CFTR , Autophagy |
T2595 | Lumacaftor | VX-809,VRT 826809 | CFTR , Autophagy |
Lumacaftor (VRT 826809) is a CFTR modulator that corrects the folding and trafficking of CFTR protein. It enhances F508del-CFTR protein maturation in FRT cells (EC50: 100 nM). | |||
T1394 | Ibuprofen | Brufen,(±)-Ibuprofe,Motrin,Advil | COX |
Ibuprofen (Advil) is a propionic acid derivate and nonsteroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic, and antipyretic effects. Ibuprofen inhibits the activity of cyclo-oxygenase I and II, resu... | |||
T6540 | Ibuprofen Lysine | Neoprofen | COX |
Ibuprofen Lysine (Neoprofen) is a non-steroidal anti-inflammatory drug. | |||
T2355 | CFTR(inh)-172 | CFTRinh 172,CFTR Inhibitor-172,CFTRinh-172,CFTRinh172 | CFTR , Autophagy |
CFTR(inh)-172 (CFTR Inhibitor-172) is a voltage-independent, selective CFTR inhibitor. | |||
T15543 | IA-Alkyne | N-Hex-5-ynyl-2-iodo-acetamide,Iodoacetamide-alkyne | TRP/TRPV Channel |
IA-Alkyne (Iodoacetamide-alkyne) is a TRP channel (TRPC) agonist. IA-Alkyne can be used to develop an isotopically tagged probe for quantitative cysteine-reactivity profiling. It also has the potential for the study of r... | |||
T2263 | Tezacaftor | VX661 | CFTR , Autophagy |
Tezacaftor (VX661) is a small molecule that can be used as a corrector of the cystic fibrosis transmembrane conductance regulator (CFTR) gene function. | |||
T131553 | Echinocystic acid (Albizziagenin) | ||
Echinocystic acid (Albizziagenin) is a useful organic compound for research related to life sciences and the catalog number is T131553. | |||
T20341 | DNDS | CFTR | |
DNDS is a channel blocker of voltage-dependent cystic fibrosis transmembrane conductance regulator (CFTR). | |||
T29041 | UCCF-853 | UCCF853,UCCF 853 | CFTR |
UCCF-853 is a small-molecule CFTR modulator that can be used to study cystic fibrosis. | |||
T63806 | CFTR corrector 8 | CFTR | |
CFTR corrector 8 is a highly effective modulator of the cystic fibrosis transmembrane conductance regulator (CFTR). This compound is specifically designed for utilization in research related to cystic fibrosis, a genetic... | |||
T26955 | Cavosonstat | N91115,N 91115,N-91115 | GSNOR , CFTR |
Cavosonstat (N91115) is an orally active S-nitrosoglutathione reductase (GSNOR) inhibitor that promotes cystic fibrosis transmembrane conductance regulator (CFTR) maturation and plasma membrane stabilization.Cavosonstat ... | |||
T60653 | CFTR corrector 9 | CFTR | |
CFTR Corrector 9, a cystic fibrosis transmembrane conductance regulator (CFTR) modulator, is employed in the research of cystic fibrosis (CF) and related CFTR-associated disorders [1]. | |||
T10776 | CFTR corrector 4 | CFTR | |
CFTR corrector 4 is a potent and orally available transmembrane conductance regulator (CFTR) for cystic fibrosis and is a potent (R,R) type active enantiomer. CFTR corrector 4 increases CFTR levels on the cell surface a... | |||
T31014 | Corrector C4 | Corr 4a,Corrector C-4,Corr4a,Corrector C 4,Corr-4a | Others |
Corrector C4, a corrector commonly used to study cystic fibrosis mutants, works by alleviating the interaction between CFTR transmembrane domain mutants and protein homeostasis. | |||
T29114 | VRT-532 | CFpot-532,CFpot-532) | CFTR |
VRT-532 (CFpot-532) is an effective modulator of CFTR and is commonly used in studies of cystic fibrosis (CF) caused by CFTR defects. Arylsulfatase B (ARSB), which is necessary to reduce the accumulation of sulphate glyc... | |||
T30293 | Bamocaftor | VX-659 | CFTR |
Bamocaftor is a CFTR channel (DeltaF508-CFTR mutation) corrector for CF transmembrane conductance regulators designed to restore F508del-CFTR protein function. Combined use of tezacaftor and VX-561 for the treatment of c... | |||
T77604 | WAY-326766 | CFTR | |
WAY-326766 increases ion transport through mutant CFTR and can be used to alter the lifespan of eukaryotes.WAY-326766 can be used to treat cystic fibrosis (CF). | |||
T72918 | JNJ-49095397 | RV568 | Antiviral , p38 MAPK |
JNJ-49095397 (RV568) is a selective p38 MAPK-α and p38 MAPK--γ kinase inhibitor with anti-inflammatory activity and potential antiviral activity for chronic obstructive pulmonary disease (COPD), cystic fibrosis, and resp... | |||
T25376 | Ensifentrine | Ensifentrina,Ensifentrinum | PDE |
Ensifentrine (Ensifentrinum) is a PDE3/4 inhibitor, although its affinity for PDE3(IC50: 0.4 nM) is 3,440 times higher than that for PDE4(IC50: 1479 nM), that is under clinical development for the treatment of asthma and... | |||
T37744 | N-octanoyl-L-Homoserine lactone | C8-HSL,N-octanoyl-L-Homoserine lactone,OHL | Antibacterial |
N-octanoyl-L-Homoserine lactone (C8-HSL) is a diffusible exogenous Yersinia pestis population-sensing molecule that modulates LcrV virulence factors, controls gene expression by participating in population sensing, and a... | |||
T111959 | IFB-088 acetate | ||
IFB-088 acetate, a benzyl guanidine derivative, is used to treat diseases and cancers associated with the PPP1R15A pathway and associated with protein misfolding stress, Examples include tau disease, synaptic riboprotein... | |||
T27098 | Ivacaftor-D9 | deutivacaftor,CTP-656 | |
CTP-656, a cystic fibrosis transmembrane conductance regulator (CFTR) channel activator, is used potentially for the treatment of cystic fibrosis. | |||
T27734 | KM-003 (sulfite) | KM 003,P-552,KM003,P552,P 552,KM-003 | |
KM-003, a sodium channel blocker, is used potentially for the treatment of cystic fibrosis. | |||
T22252 | Galicaftor | Others | |
ABBV-2222 is a CFTR corrector which is studied for the treatment of cystic fibrosis (CF). | |||
T13742 | Ivacaftor benzenesulfonate | VX-770 benzenesulfonate | Others |
T25136 | Aztreonam lysine | Corus 1020,Corus1020,Corus-1020,Aztreonam lysinate | |
Aztreonam lysine is an inhaled anti-pseudomonal treatment for people who have pulmonary Pseudomonas aeruginosa infection with cystic fibrosis (CF). | |||
T13704 | GLPG-3221 | Others | |
GLPG-3221 can be uesd for the treatment of cystic fibrosis.GLPG-3221 is a potent, orally active corrector of CFTR (cystic fibrosis transmembrane conductance regulator), with an EC50 of 105 nM. | |||
T29040 | UCCF-029 | UC(CF)-029,UC(CF) 029,UCCF029,UC(CF)029 | |
UCCF-029 is an activator of cystic fibrosis transmembrane conductance regulator (CFTR). | |||
T36519 | Posenacaftor sodium | ||
Posenacaftor (PTI-801) sodium, a cystic fibrosis transmembrane regulator (CFTR) modulator, corrects CFTR protein folding and trafficking. It is utilized in researching cystic fibrosis (CF)[1]. | |||
T13705 | GLPG2451 | Cysteine Protease | |
GLPG2451 is a cystic fibrosis transmembrane conductance regulator (CFTR) potentiator. It effectively potentiates low temperature rescued F508del CFTR (EC50: 11.1 nM). | |||
T27146 | Denufosol tetrasodium | INS37217,INS 37217,INS-37217 | |
Denufosol is a P2Y2 agonist potentially for the treatment of cystic fibrosis. | |||
T23648 | AF-2785 | ||
In epididymal epithelial cells, AF-2785 inhibits cystic fibrosis transmembrane conductance regulator Cl(-) channels. | |||
T13742L | Ivacaftor hydrate | VX-770 hydrate | Others |
Ivacaftor hydrate is an orally bioavailable CFTR potentiator. It also is used for cystic fibrosis treatment. | |||
T74417 | Vanzacaftor | ||
Vanzacaftor is a cystic fibrosis transmembrane conductance regulator (CFTR) modulator researched for cystic fibrosis treatment. | |||
T25898 | Olacaftor | VX 440,VX-440,VX440 | |
Olacaftor, also known as VX-440, is a protein modulator of cystic fibrosis transmembrane regulator (CFTR). | |||
T74748 | Zatonacaftor | ||
Zatonacaftor, a cystic fibrosis transmembrane regulator (CFTR) modulator, is utilized in the research of cystic fibrosis [1] [2]. |
カタログ番号 | 製品名 | 別名 | ターゲット |
---|---|---|---|
T2866 | Echinocystic acid | Apoptosis , Antioxidant , Reactive Oxygen Species | |
Echinocystic acid (EA), a natural triterpone enriched in various herbs, shows a range of pharmacological activities including anti-inflammatory and antioxidant effects. | |||
T41139 | Echinocystic acid 28-O-β-D-glucoside | ||
Echinocystic acid 28-O-β-D-glucoside is a metabolite resulting from the microbial oxidation and glucosidation of Echinocystic acid. It exhibits inhibitory activity towards the tissue factor pathway, with an IC50 value me... | |||
T2532 | Tauroursodeoxycholate | Taurolite,Tauroursodeoxycholic Acid,UR 906,Ursodeoxycholyltaurine,TUDCA | Apoptosis , ERK , P450 , Caspase , Endogenous Metabolite |
Tauroursodeoxycholate (UR 906), also known as ursodoxicoltaurine, is a highly hydrophilic tertiary bile acid that is produced in humans at a low concentration. Tauroursodeoxycholate is the more hydrophilic form of ursode... | |||
T11124 | Duramycin | Lancovutide,Moli1901 | Others |
Duramycin is a cyclic peptide lantibiotic derived from Streptomyces cinnamoneuma. Duramycin interacts with phosphatidylethanolamine (PE) and has antibacterial, antiviral effects. Duramycin stimulates chloride secretion ... |
カタログ番号 | 製品名 | Species | Expression System |
---|---|---|---|
TMPY-03855 | DNase I Protein, Human, Recombinant (His) | Human | HEK293 Cells |
DNase1, also known as deoxyribonuclease I and DNL1, is a member of the DNase family. DNaseI is a nuclease that cleaves DNA preferentially at phosphodiester linkages adjacent to a pyrimidine nucleotide, yielding 5'-phos... | |||
TMPJ-01350 | XPNPEP3 Protein, Human, Recombinant (His) | Human | E. coli |
Probable Xaa-Pro Aminopeptidase 3 (XPNPEP3) is a member of the peptidase M24B family. XPNPEP3 has two isoforms and both are widely expressed. XPNPEP3 is localized in the Mitochondrion. XPNPEP3 catalyzes the release of an... | |||
TMPY-04633 | Frizzled 2 Protein, Mouse, Recombinant (hFc) | Mouse | HEK293 Cells |
FZD2 may be a tumor suppressor gene in salivary adenoid cystic carcinomas (SACCs) that inhibits cell growth and migration. OMOD2 is a rare skeletal dysplasia and characterized by facial dysmorphism and shortness of the u... | |||
TMPY-03629 | Syntaxin 8 Protein, Human, Recombinant (His) | Human | HEK293 Cells |
STX8, also known as syntaxin 8, directly interacts with HECTd3. STX8 forms the SNARE complex with syntaxin 7, vti1b and endobrevin. STX8 belongs to the syntaxin family. Members of this family are key molecules implicated... | |||
TMPJ-00991 | S100A8 Protein, Rat, Recombinant (His) | Rat | E. coli |
Protein S100-A8(Mrp8) contains 2 EF-hand domains and belongs to the S-100 family. Mrp8 binds two calcium ions per molecule with an affinity similar to that of the S-100 proteins. S100 proteins are localized in the cytop... | |||
TMPY-02769 | RNASET2 Protein, Human, Recombinant (His) | Human | Baculovirus Insect Cells |
RNASET2 (ribonuclease T2) is an enzyme that belongs to the RNase T2 family. It is highly expressed in the temporal lobe and fetal brain. RNASET2 gene is a novel member of the Rh/T2/S-glycoprotein class of extracellular r... |