About 7 results found for searched term "67-20-9" (0.074 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M1723 | Crenolanib | VEGFR/PDGFR |
| CP-868596 | ||
| Crenolanib (CP-868596) is an orally bioavailable, selective small molecule inhibitor of PDGFRα and PDGFRβ with IC50 of 0.9 and 1.8 nM respectively. | ||
| M4146 | Sodium-Danshensu | Cytochrome P450 (e.g. CYP17) |
| Sodium Danshensu; (±)-DanShenSu sodium sal | ||
| Danshensu (sodium) is the active component of salvia miltiorrhiza, which can inhibit the formation of reactive oxygen species, inhibit platelet adhesion and aggregation, and protect myocardial ischemia. | ||
| M5818 | Nitrofurantoin | Antibiotic |
| Macrodantin, Furadantine, Furadonine | ||
| Nitrofurantoin is an antibiotic used to treat bladder infections.It inhibits bacterial DNA, RNA, and cell wall protein synthesis. | ||
| M28797 | BMS-8 | PD-1/PD-L1 |
| BMS-8 inhibits the PD-1/PD-L1 interaction with IC50 of 7.2 μM. BMS-8, binds directly to PD-L1 and induces formation of PD-L1 homodimers, which in turn prevents the interaction with PD-1. | ||
| M31421 | Isomyosmine | TNF Receptor |
| Isomyosmine is an orally active inhibitor of TNF-alpha that can be used in studies related to sarcopenia as well as chronic inflammation. | ||
| M43406 | PROTAC BTK Degrader-6 | BTK |
| PROTAC BTK Degrader-6 is a PROTAC BTK degrader (DC50: 3.18 nM. | ||
| M56318 | SCH79797 dihydrochloride | PAR |
| SCH79797 dihydrochloride is a highly potent, selective nonpeptide protease activated receptor 1 (PAR1) antagonist. | ||
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