About 9 results found for searched term "61-33-6" (0.058 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M2608 | Kobe0065 | Ras |
| Kobe0065 is a novel and effective small-molecule compound inhibiting Ras–Raf interaction by SBDD, exhibits potent activity to competitively inhibit the binding of H-Ras·GTP to c-Raf-1 RBD with a Ki value of 46 ± 13 μM. | ||
| M11397 | D[LEU4,LYS8]-VP TFA | Vasopressin Receptor |
| D[LEU4,LYS8]-VP TFA is a selective agonist of vasopressin V1b receptors, with Ki values of 0.16 nM, 0.52 nM and 1.38 nM for rat, human and mouse V1b receptors, respectively. D[LEU4,LYS8]-VP TFA showed weak antidiuretic, vasopressor and oxytocin activity in vitro. | ||
| M18067 | 6-Methoxykaempferol 3-O-rutinoside | Others |
| 6-Methoxykaempferol 3-O-rutinoside | ||
| M19906 | Amoxicillin trihydrate | Antibiotic |
| Amoxil trihydrate; Amoxipen trihydrate; Moxaline trihydrate | ||
| Amoxicillin is a broad-spectrum, semisynthetic aminopenicillin antibiotic with bactericidal activity. | ||
| M27732 | Lefamulin | Antibiotic |
| BC-3781 | ||
| Lefamulin (BC-3781) is an orally active antibiotic. Lefamulin inhibits protein synthesis by binding to the peptidyl transferase center of the 50S bacterial ribosome. Lefamulin has anti-inflammatory activity. Lefamulin can be used in the research of bacterial infections, such as bacterial pneumonia. | ||
| M28209 | LY2444296 | Opioid Receptor |
| FP3FBZ | ||
| LY2444296 is an orally bioavailable, high-affinity and selective short-acting kappa opioid receptor (KOPR) antagonist, with a Ki value of ∼1 nM. LY2444296 exhibits anti-anxiety like effects. | ||
| M30369 | Penicillin G | Antibiotic |
| Benzylpenicillin | ||
| Penicillin G is a potent penicillinantibiotic. Penicillin G can be used for bacterial infection. | ||
| M49513 | CDK8-IN-12 | CDK |
| CDK8-IN-12 is an orally active, potent CDK8 inhibitor with a Ki of 14 nM. | ||
| M52876 | D[LEU4, LYS8]-VP | Vasopressin Receptor |
| D[LEU4,LYS8]-VP is a selective agonist of vasopressin V1b receptor, with the Kis of 0.16 nM, 0.52 nM, and 0.1.38 nM for rat, human and mouse V1b receptor, respectively. | ||
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