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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
TP1106L | α-Factor Mating Pheromone, yeast acetate | Mating Factor α acetate,α-Factor Mating Pheromone, yeast acetate(59401-28-4 free base) | Others |
α-Factor Mating Pheromone, yeast acetate (Mating Factor α acetate) is a peptide of 13 amino acids secreted by Saccharomyces cerevisiae α cells. | |||
TP1105 | α-Factor Mating Pheromone, yeast (TFA) | α-Factor Mating Pheromone, yeast (TFA)(59401-28-4,FREE),Mating Factor α (TFA) | |
The alpha factor pheromone arrests yeast in the G1 phase of their cell cycle. Alpha Factor Mating Pheromone induces the expression of mating genes, changes in nuclear architecture, and polarzes growth toward the mating p... | |||
TP1106 | α-Factor Mating Pheromone, yeast | Mating Factor α | |
Alpha factor mating pheromone is a peptide of 13 amino acids secreted by Saccharomyces cerevisiae α cells. | |||
T78500 | α-Factor Mating Pheromone, yeast TFA | Mating Factor α TFA | |
α-Factor Mating Pheromone (yeast TFA) is a tridecapeptide secreted by Saccharomyces cerevisiae α cells and interacts with the Ste2p receptor [1]. | |||
T9423 | Alkyne tyramide | Others | |
Alkyne tyramide is a clickable ascorbate peroxidase 2 (APEX2) probe which enable biotin-independent detection of labeled proteins. | |||
T7846 | Aegeline | Others , Antifungal | |
Aegeline is an alkaloidal-amide, isolated from the leaves of Aegle marmelos and have shown antihyperglycemic as well as antidyslipidemic activities in the validated animal models of type 2 diabetes mellitus. | |||
T8536 | Filastatin | Antifungal | |
Filastatin is a long-lasting inhibitor of Candida albicans filamentation, and has potent antifungal effect. | |||
T19833 | 5-Fluoroorotic acid | DNA/RNA Synthesis , Antifungal | |
5-Fluoroorotic acid is an inhibitor of thymidylate synthase. 5-Fluoroorotic is a selective agent in yeast molecular genetics.5-Fluoroorotic possesses a well-expressed anticandidal effect close to that of 5-fluorocytosine... | |||
T40661 | ML-60218 | DNA/RNA Synthesis | |
ML-60218 is an inhibitor of broad-spectrum RNA pol III with IC50s of 32 and 27 μM for Saccharomyces cerevisiae and human. ML-60218 disrupts already assembled viroplasms and hampers the formation of new viroplasms. | |||
T27617 | Inz-1 | P450 | |
Inz-1 is an effective and fungal-selective inhibitor of mitochondrial cytochrome bc1 with IC50s of 8.092 and 45.320 μM for yeast and human. Inz-1 reverses Fluconazole or other triazole antifungals’ resistance in the path... | |||
T2352 | AMI-1 | Histone Methyltransferase | |
AMI-1 is an effective and selective Histone Methyltransferase (HMT) inhibitor (IC50: 3.0/8.8 μM, for yeast Hmt1p, and human PRMT1). | |||
T8703 | YGsy2p-IN-1 | Others | |
yGsy2p-IN-1 is a potent yeast glycogen synthase 2 (yGsy2p) and human glycogen synthase 1 (hGYS1) inhibitor. yGsy2p-IN-H23 a pyrazole inhibitor,and is used for glycogen storage diseases (GSDs) | |||
T10797 | Chlormidazole hydrochloride | Clomidazole hydrochloride | Antifungal |
Chlormidazole hydrochloride (Clomidazole hydrochloride) has inhibitory activity against many fungi and some gram-positive cocci. It can be applied in fungal and bacterial infections of skin and nails, including interdigi... | |||
T4S1820 | Parishin | Parishin A | Others |
Parishin (Parishin A) A is isolated from the rhizomes of Gastrodia elata. It has good neuroprotective effects against brain disorders. | |||
T0146 | Tioconazole | UK-20349,Vagistat | Antibiotic , Antifection , Antifungal |
Tioconazole (Vagistat) is a synthetic imidazole derivative, inhibits cell wall synthesis by inhibiting the biosynthesis of ergosterol or other sterols, damaging the fungal cell membrane, altering its permeability, and pr... | |||
TN3748 | D-Asparagine | H-D-Asn-OH | Others , Endogenous Metabolite |
D-Asparagine (H-D-Asn-OH) is a source of nitrogen for yeast strains. D-Asparagine is a competitive inhibitor of L-Asparagine hydrolysis (Ki = 0.24 mM). | |||
T19808 | 5-Bromo-5-nitro-1,3-dioxane | Bronidox | Others , Antibacterial , Antifungal |
5-Bromo-5-nitro-1,3-dioxane (Bronidox) is an antimicrobial compound that works by inhibiting enzyme activity in bacteria. | |||
T2028 | NG 52 | NG52,NG-52,Compound 52 | CDK |
NG 52 (NG-52) is a cell-permeable, reversible, and ATP-compatible inhibitor of the cell cycle-regulating kinase Cdc28p and the related Pho85p kinase. | |||
T75163 | GW297361 | VEGFR , CDK , Src | |
GW297361 is a potent inhibitor of the cell cycle protein-dependent kinase Cdk1 and also inhibits the Pho85 signaling pathway.The IC50s of GW297361 on yeast Cdk1 and Pho85 were 20 nM and 400 nM, respectively. | |||
T1820 | CK-636 | CK-0944636,CK 636 | Microtubule Associated |
CK-636 (CK-0944636), an Arp2/3 complex inhibitor, can inhibit actin polymerization induced by the human (IC50: 4 μM), fission yeast (IC50: 24 μM) and bovine (IC50: 32 μM) Arp2/3 complex, respectively. |