About 9 results found for searched term "IDO-IN-2" (0.052 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M2568 | IDO-IN-2 (NLG-919 Analogue) | IDO |
| GDC-0919 analogue | ||
| NLG919 is a potent IDO (indoleamine-(2,3)-dioxygenase) pathway inhibitor with Ki/EC50 of 7 nM/75 nM. | ||
| M6309 | IDO-IN-2 | IDO |
| IDO-IN-2 is an IDO inhibitor, with IC50 values of 0.068 μM in HeLa cell and 0.16 μM in HEK293 cell. | ||
| M9180 | Pyridostatin Trifluoroacetate Salt | DNA/RNA Synthesis |
| Pyridostatin TFA salt; PDS; CAS# 1085412-37-8(free base) | ||
| Pyridostatin Trifluoroacetate Salt is a G-quadruplexe stabilizer, with a Kd of 490 nM. | ||
| M9668 | 6-chloropyrido[3,2-d]pyrimidine-2,4-diamine | Others |
| 6-chloropyrido[3,2-d]pyrimidine-2,4-diamine | ||
| M10377 | Golidocitinib (AZD4205) | JAK |
| AZD-4205; Golidocitinib | ||
| Golidocitinib (AZD4205) is a novel potent and selective janus kinase 1 (JAK1) inhibitor, with IC50 value of 73 nM. | ||
| M42449 | IDO1-IN-22 | IDO |
| IDO1-IN-22 is a IDO1 inhibitor (biochemical hIDO1 IC50: 67.4 nM, HeLa hIDO1 IC50: 17.6 nM). | ||
| M42450 | IDO1-IN-21 | IDO |
| IDO1-IN-21 is an IDO1 inhibitor (IC50 = 0.64 μM). | ||
| M57096 | Thalidomide-Piperazine-PEG1-NH2 | E3 Ligase Ligand-Linker Conjugates |
| Thalidomide-Piperazine-PEG1-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology. | ||
| M57549 | 2-[(Azidoacety)amino]-2-deoxy-D-mannose | Others |
| 2-[(Azidoacety)amino]-2-deoxy-D-mannose | ||
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