19
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T3532 | 5S rRNA modificator | FAI,Furoyl Acylimidazole | Others |
5S rRNA modificator (FAI), used in 5S rRNA RNA modification, is a suitable electrophile for 2'-hydroxyl acylation on structured RNA molecules. | |||
T8643 | NAI | 5S rRNA modificator 2 | Others |
NAI (5S rRNA modificator 2) is an RNA SHAPE reagent. | |||
T13499 | 3-Methyluridine | Endogenous Metabolite | |
3-Methyluridine is a modified nucleoside of cellular RNA. | |||
T9726 | 2’-OMe-Guanosine | Apoptosis , Nucleoside Antimetabolite/Analog | |
2'-OMe-Guanosine is a modified nucleoside produced by the action of tRNA guanosine-2'-o-methyltransferase. 2'-OMe-Guanosine has a certain pro-apoptotic effect. | |||
T35648 | 4-Thiouridine | Others | |
4-Thiouridine (4-SU) is a photoactivatable ribonucleoside analog that is widely used for RNA analysis, including short-range RNA-RNA crosslinking and nascent RNA labeling. The crosslinking thio moiety is attached directl... | |||
T16698 | Pyronin Y | C.I. 45005,Pyronine G | Others |
Pyronin Y (Pyronine G) is an intercalating cationic dye that shows specificity towards RNA. | |||
T4S0554 | Theaflavine-3,3'-digallate | TFBG,theaflavin digallate | Others |
1. Theaflavine-3,3'-digallate (theaflavin digallate) and lactic acid together could reduce herpes simplex virus transmission. | |||
T2100 | CX-5461 | DNA/RNA Synthesis | |
CX-5461, a selective inhibitor of rRNA synthesis, suppresses Pol I-driven transcription of rRNA. | |||
TN7106 | 2′-O-Methyluridine | Others | |
2′-O-Methyluridine is a natural product that found in RNA such as rRNA, snRNA, snoRNA and tRNA in Archaea, Bacteria, and Eukaryota. | |||
T22297 | Clindamycin hydrochloride monohydrate | Clindamycin alcoholate | Antibiotic |
Clindamycin hydrochloride monohydrate (Clindamycin alcoholate) is a protein synthesis inhibitor used orally, capable of diminishing virulence factor expression in Staphylococcus aureus at sub-minimum inhibitory concentra... | |||
T1349 | 5-Fluorouridine | Others , DNA/RNA Synthesis | |
5-fluorouridine is also known as FUrd, 5-Fluorouracil 1-beta-D-ribofuranoside, 5-Fur, or 5-Fluoro-uridine. 5-fluorouridine is a solid. This compound belongs to the pyrimidine nucleosides and analogues. These are compound... | |||
T10067 | 2',5-Difluoro-2'-deoxycytidine | HCV Protease | |
2',5-Difluoro-2'-deoxycytidine has potent anti-HCV activity and toxicity to rRNA. | |||
T1707 | EA25 | Others | |
EA25 has been identified in the clone library of the bacterial 16S rRNA gene sequence. | |||
T61121 | NusB-IN-1 | ||
NusB-IN-1 (Compound 22r) is a highly effective bacterial rRNA synthesis inhibitor, administered orally. It exhibits potent antimicrobial activity against MRSA and VRSA [1]. | |||
T64150 | CX-5461 dihydrochloride | ||
CX-5461 dihydrochloride is a potent, orally active inhibitor of Pol I-mediated rRNA synthesis that acts on HCT-116 cells (IC50: 142 nM), A375 cells (IC50: 113 nM) and MIA PaCa-2 cells (IC50: 54 nM), and to a lesser exten... | |||
T27165 | Diazaborine | Diazaborine compound 2b18,Pkf 84.474,Pkf 84474,Pkf-84474,SA-84474 | |
Diazaborine inhibits maturation of rRNAs for the large ribosomal subunit. Diazaborine blocks ribosome biogenesis by inhibiting the AAA-ATPase Drg1. Diazaborine treatment causes, within minutes, a rapid redistribution of ... | |||
T69908 | Pidnarulex HCl | ||
Pidnarulex HCl is the salt form of CX-5461, a first-in-class non-genotoxic small molecule targeted inhibitor of RNA polymerase I (Pol I) that activates the p53 pathway without causing DNA damage. CX-5461 selectively inhi... | |||
T79015 | SEQ-9 | ||
SEQ-9 is an orally active inhibitor targeting the Mycobacterium tuberculosis (Mtb) 23S bacterial ribosome, demonstrating an inhibitory concentration (IC50) around 170 nM against unmethylated Mtb ribosomes and showing pot... | |||
T37154 | 7-Methylguanosine 5'-diphosphate sodium | ||
7-Methylguanosine 5’-diphosphate (7-Methyl-GDP) sodium, a cap analog, is utilized in the synthesis of mRNA cap analogues[1]. |