AA-UTP tetrasodium is an amine-modified nucleotide that can be directly incorporated into labeled-UTP. DG013B has weak affinity for ERAP1 and ERAP2 and is often used as a negative control to study the binding properties of DG013A and its analogues to ERAP1 and ERAP2.

8-Nitro-2'3'cAMP is composed of 8-nitro-AMP, ribose and phosphate, and is a cyclic nucleotide derivative.

7-Methylguanosine 5′-monophosphate (7-Methylguanylic acid) is a building block of nucleic acid.

5-Hydroxycytidine is the RNA modified nucleoside that can be found in the 23S rRNA of bacteria E. coli. 5-Hydroxycytidine modifies at the C2501 site, exhibits a higher modification level in stationary cells. 5-Hydroxycytidine exhibits a higher modification level in radiation resistant Radius than in E. coli.

3'-Deoxy-3'-amino-ATP tetrasodium is an ATP substitute created by inserting an amino acid at the C3 position of ATP. 3'-Deoxy-3'-amino-ATP tetrasodium catalyzes RNA synthesis in the presence of RNA polymerase.

3'-Amino-3'-dGTP tetrasodium is a substitute for GTP, produced by inserting an amino acid into the C3 position of GTP.

2'-O-MOE-UTP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2'-O-MOE-GTP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2'-F-UMP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2'-F-CMP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2'-F-CDP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2'-F-AMP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2'-F-ADP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2-Amino-ATP tetrasodium is an ATP substitute produced by inserting an amino acid at the C2 position of ATP.

2′-O-MOE-CMP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2′-O-MOE-AMP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2′-OMe-UMP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2′-OMe-UDP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2′-OMe-GDP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2′-OMe-ADP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

2′-F-UDP is a nucleotide analog that can be used in the synthesis of oligonucleotides.

MDI-114215 (compound 85) is an allosteric LIMK1/2 dual inhibitor with good in vivo tolerance. MDI-114215 can inhibit cofilin phosphorylation in mouse brain region-induced pluripotent stem cells (iPSCs), which can be used for Fragile X Syndrome (FXS) research.

LIJTF500025 is a potent and selective LIMK inhibitor, with pIC50 values of 6.77 and 7.03 for LIMK1 and LIMK2, respectively, as determined by NanoBRET. LIJTF500025 can be used for the research of cancer.

α,β-MTDP trisodium, a thymidylate analog, is a thymidine kinase inhibitor with a Ki of 23 µM.

Xanthosine-5'-Triphosphate (5'-XTP) trisodium, a nucleotide, is produced by deamination of purine bases. Xanthosine-5'-Triphosphate trisodium is a substrate of inosine triphosphate pyrophosphatase (ITPase).

VPC-80051 is an inhibitor of hnRNP A1 splicing activity. VPC-80051 directly interacts with hnRNP A1 RBD and reduces AR-V7 messenger levels in 22Rv1 CRPC cell line. VPC-80051 can be used in prostate cancer research.

Uridylyl-(3′→5′)-adenosine (UpA) is a dinucleotide, which is composed of a unrail base and an adenosine suger molecule through a 3'-5' phosphodiester bond. Uridylyl-(3′→5′)-adenosine participates in the biological processes, such as gene expression regulation, signal transduction, and protein synthesis.

Teloxantrone (CI-937; DUP 937) is a DNA synthesis inhibitor (IC50: 0.33 μM). Teloxantrone has antitumor activity and can be used in colorectal cancer research.

RNA recruiter 2 is a QSOX1 mRNA ligand. RNA recruiter 2 can serve as a ligand for target RNA (Ligands for Target RNA for RIBOTAC) for the development of RIBOTAC RNA degraders with antitumor activity. RNA recruiter 2 can be used for the synthesis of F1-RIBOTAC.

RNA binder 1 (Compound 4b) is a blood-brain permeable RNA binder. RNA binder 1 can selectively bind to the G-quadruplex structure of the G4C2 repeat sequence RNA of the C9orf72 gene. RNA binder 1 significantly reduces the levels of toxic polypeptides poly(GA) and poly(GP) produced by the G4C2 repeat sequence in amyotrophic lateral sclerosis (ALS) patient-derived cells. RNA binder 1 has no significant effect on the antisense polypeptide poly(PR), showing selectivity for sense RNA. RNA binder 1 can be used in the study of ALS and frontotemporal dementia (FTD).