About 14 results found for searched term "55-03-8" (0.055 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M1672 | BI 2536 | PLK |
| BI 2536 is a novel, highly selective, potent dual PLK1 and BRD4 inhibitor with IC50s of 0.83 and 25 nM, respectively. | ||
| M1678 | BI 6727 | PLK |
| Volasertib | ||
| BI 6727 (Volasertib) is a small highly potent Polo-like kinase inhibitor (Plk1) with an IC50 of 0 .87 nM. | ||
| M4283 | Usaramine | Anti-infection |
| Usaramine | ||
| M8887 | Btk inhibitor 2 | BTK |
| BGB-3111 | ||
| Btk inhibitor 2 (BGB-3111) is a Brutons tyrosine kinase (BTK) inhibitor. | ||
| M11003 | Benpyrine | Others |
| Benpyrine is a highly specific orally active TNF-α inhibitor.KD The value is 82.1 μM. Benpyrine binds tightly to TNF-α and blocks its interaction with TNFR1,IC50 The value is 0.109 μM. | ||
| M14800 | L-Thyroxine sodium | Animal Modeling |
| Levothyroxine sodium; T4 sodium | ||
| L-Thyroxine sodium (Levothyroxine sodium) is a synthetic hormone for the research of hypothyroidism. DIO enzymes convert biologically active thyroid hormone (Triiodothyronine,T3) from L-Thyroxine (T4). | ||
| M16141 | Guineensine | Alkaloids |
| Guineensine | ||
| M17026 | (+)-Perillaldehyde | Monoterpenoids |
| (+)-Perillaldehyde | ||
| M17303 | Confluentin | Phenols |
| Confluentin | ||
| M28057 | JTE-952 | CSF-1R (c-Fms) |
| JTE-952 is a potent, oral active and selective Type II inhibitor of colony stimulating factor-1 receptor (CSF-1R or cFMS, type III receptor tyrosine kinase), with IC50 values of 13 nM and 261 nM for CSF1R and TrkA , respectively. Effective against a mouse collagen-induced model of arthritis. | ||
| M41269 | GRL-1720 | Anti-infection |
| GRL-1720 is a potent SARS-CoV-2 Mpro inhibitor with an EC50 value of 15 µM. | ||
| M41732 | WAY-181187 hydrochloride | 5-HT Receptor |
| WAY-181187 (SAX-187) hydrochloride is a potent and selective full 5-HT6 receptor agonist with a Ki of 2.2 nM and an EC50 of 6.6 nM. | ||
| M43424 | CRBN ligand-9 | Ligand for E3 Ligase |
| CRBN ligand-9 is a CRBN ligand (Ki: 8.9 μM). | ||
| M44892 | Isatidine | Others |
| Retrorsine N-oxide, an N-oxide of pyrrolizidine alkaloid, is a carcinogen. Retrorsine N-oxide-derived DNA adducts are common toxicological biomarkers of pyrrolizidine alkaloid N-oxides. | ||
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