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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T10860 | Col003 | HSP | |
Col003 is a selective and potent inhibitor of Hsp47 and competitively binds to the collagen-binding site on Hsp47 (IC50: 1.8 μM). It can be used for the investigation of fibrosis. | |||
T4470 | Pyridostatin TFA | DNA/RNA Synthesis | |
Pyridostatin Trifluoroacetate Salt is a G-quadruplexe stabilizer with Kd of 490 nM in a cell-free assay, which targets a series of proto-oncogenes including c-kit, K-ras and Bcl-2. | |||
T1899 | Pyridostatin | RR82,Pyridostatin Trifluoroacetate Salt | DNA/RNA Synthesis |
Pyridostatin (RR82) is a synthetic small-molecule stabilizer of G-quadruplexes, a secondary structure of DNA that usually exists in the end of the chromosome or the telomeres. | |||
T3279 | Silver sulfadiazine | Silvadene,Dermazin,Flamazine | DNA/RNA Synthesis , Antibacterial , Antibiotic |
Silver sulfadiazine (Dermazin) is a sulfonamide-based topical agent with antibacterial and antifungal activity. | |||
T5189 | Omadacycline | PTK 0796,Amadacycline | ribosome , Antibacterial , Antibiotic |
Omadacycline (Amadacycline), a new tetracycline antibiotic, can inhibit the 30s subunit of bacterial ribosome. | |||
T60106 | 2,5-Morpholinedione, 4-methyl-6-(1-methylethyl)-3-(phenylmethyl)- | Others | |
2,5-Morpholinedione, 4-methyl-6-(1-methylethyl)-3-(phenylmethyl)- is the trans structure of Lateritin. | |||
T20456 | 5-Chlorovaleronitrile | AI3 20151,AI3-20151,AI320151 | Others |
5-Chlorovaleronitrile (AI320151) can be used as a quantitative structure-toxicity model to predict the aquatic toxicity. | |||
T8854 | PTEROIC ACID | Others | |
Pteroic acid is part of the structure of folic acid | |||
T39359 | γ-Glu-Gly | gamma-Glutamylglycine | Amino Acids and Derivatives |
γ-Glu-Gly (gamma-Glutamylglycine), a γ-glutamyl dipeptide, is a human lipid metabolite with a structure resembling that of GABA (γ-aminobutyric acid). It functions as an antagonist of excitatory amino acids. | |||
T14594 | Biotin-PEG3-NHS ester | Others | |
Biotin-PEG3-NHS ester is a PROTAC linker based on the PEG structure and can be used to prepare PROTAC. | |||
T3S2152 | 23-Hydroxybetulinic acid | Anemosapogenin | Others |
23-Hydroxybetulinic acid (Anemosapogenin) shows potent anti-tumor effect in vivo, but it has some toxicity, structure modification should be needed. | |||
T22981 | Tetradecyltrimethylammonium bromide | MitMAB,Cetrimide,tetradecyl trimethyl ammonium bromide | Dynamin |
Tetradecyltrimethylammonium bromide (MitMAB) is a Dynamin GTPase activity inhibitor and a cationic surfactant with asymmetrical structure. | |||
T1365 | Thioisonicotinamide | Pyridine-4-carbothioamide,Isothionicotinamide,4-Pyridylthiocarboxamide | Antibiotic |
Thioisonicotinamide (Isothionicotinamide) is a chemical based on the nicotinamide structure, but in which the amide is in the 4-position and not the 3-position. | |||
T69564 | YK-2-69 | ||
YK-2-69 is a highly selective DYRK2 inhibitor which specifically interacts with Lys-231 and Lys-234 in the co-crystal structure. Especially, YK-2-69 exhibits more potent anti-PCa efficacy than the first-line drug enzalut... | |||
T1068 | Dithranol | 1,8,9-trihydroxyanthracene,cignoline,Anthralin | Others , DNA/RNA Synthesis |
Dithranol (cignoline) is an anthracene derivative that disrupts MITOCHONDRIA function and structure and is used for the treatment of DERMATOSES, especially PSORIASIS. It may cause FOLLICULITIS. | |||
T9981 | RDR03785 | Others | |
The MIF Antagonist IV, RDR 03785 controls the biological activity of MIF. This small molecule/inhibitor is primarily used for Cell Structure applications. | |||
TQ0064 | Peretinoin | NIK333 | HCV Protease , Retinoid Receptor , S1P Receptor , Autophagy |
Peretinoin (NIK333) is an oral acyclic retinoid with a vitamin A-like structure that targets retinoid nuclear receptors such as RXR and RAR. | |||
TN1248 | 3-Epioleanolic acid | AChR | |
3-Epioleanolic acid and oleanonic acid possess varying degrees of agonist activity on uterine smooth muscle with minor changes in the molecular structure affecting its intrinsic activity on uterine muscle. | |||
T21743L | Beta-Lipotropin (1-10), porcine Acetate | Beta-Lipotropin (1-10), porcine Acetate(77875-68-4 Free base) | Others |
Beta-Lipotropin (1-10), porcine Acetate (Beta-Lipotropin ) (beta-LPH) was found to contain within its C-terminal sequence the primary structure of these peptides. | |||
T16674 | Pseudouridine | Endogenous Metabolite | |
Pseudouridine is the most abundant modified nucleoside in non-coding RNAs. It enhances the function of transfer RNA and ribosomal RNA by stabilizing RNA structure. |