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Home > Products
| Cat.No. | Product name | Product Description |
| R11190 | HUHS015 | HUHS015 is a potent PCA-1/ALKBH3 inhibitor both in vitro and in vivo. The bioava |
| R11191 | Ixazomib citrate;MLN9708 | Ixazomib citrate (MLN9708) is a reversible inhibitor of the chymotrypsin-like pr |
| R11192 | Ilomastat (Synonyms: GM6001; Galardin) | Ilomastat (GM6001) is a potent and broad spectrum matrix metalloprotease (MMP) i |
| R11194 | SCH23390 | N/A |
| R11195 | RSL3 | (1S,3R)-RSL3 is an inhibitor of glutathione peroxidase 4 (GPX4), reduces the exp |
| R11196 | AG-120 Ivosidenib | Ivosidenib (AG-120) is an orally active inhibitor of isocitrate dehydrogenase 1 |
| R11060 | elagolix intermediate 3 | N/A |
| R11061 | elagolix intermediate 4 | N/A |
| R11062 | elagolix intermediate 6 | N/A |
| R11074 | elagolix intermediate 2 | N/A |
| R11076 | elagolix intermediate 7 | N/A |
| R11077 | elagolix intermediate 9 | N/A |
| R11124 | GSK1059615 | GSK1059615 is a dual inhibitor of PI3Kα/β/δ/γ (reversible) and mTOR with IC50 of |
| R11125 | KRN-633;KRN633;KRN 633 | KRN-633 is a potent VEGFR inhibitor with IC50s of 170, 160 and 125 nM for VEGFR1 |
| R11198 | Deoxynivalenol | Vomitoxin, also known as deoxynivalenol (DON), is a type B trichothecene, an epo |
| R11199 | T-2 Toxin (Synonyms: T-2 Mycotoxin) | T-2 Toxin (T-2 Mycotoxin) is a toxic trichothecene mycotoxin produced by various |
| R11202 | Fludarabine; NSC 118218 | N/A |
| R11208 | 4-Piperazinobenzonitrile | N/A |
| R11211 | Isavuconazole; BAL-4815; RO-0094815 | N/A |
| R11213 | Romidepsin (Synonyms: FK 228; FR 901228; NSC 630176) | Romidepsin (FK 228) is a Histone deacetylase (HDAC) inhibitor with anti-tumor ac |
| R11214 | Oritavancin diphosphate (Synonyms: LY333328 diphosphate) | Oritavancin diphosphate is a novel semisynthetic glycopeptide antibiotic being d |
| R11215 | (1S-cis)-Milnacipran Hydrochloride | N/A |
| R11216 | A-1155463 | A-1155463, a chemical probe, is a highly potent and selective BCL-XL inhibitor w |
| R11217 | Furanylfentanyl | N/A |
| R11219 | TA 01 | TA-01 is a potent CK1 and p38 MAPK inhibitor, with IC50s of 6.4 nM, 6.8 nM, 6.7 |
