| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA5200426
Max Phase: Preclinical
Molecular Formula: C25H28N6O3S
Molecular Weight: 492.61
Associated Items:
Representations
Canonical SMILES: Cc1ccccc1C1C(=O)N(C)c2cnc(Nc3ccc(S(=O)(=O)NCC4CC4)cc3)nc2N1C
Standard InChI: InChI=1S/C25H28N6O3S/c1-16-6-4-5-7-20(16)22-24(32)30(2)21-15-26-25(29-23(21)31(22)3)28-18-10-12-19(13-11-18)35(33,34)27-14-17-8-9-17/h4-7,10-13,15,17,22,27H,8-9,14H2,1-3H3,(H,26,28,29)
Standard InChI Key: ZETIGJJLCPNAGG-UHFFFAOYSA-N
Associated Targets(Human)
Serine/threonine-protein kinase MST1 2643 Activities
Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: | Topical: No | First In Class: No | Black Box: No |
| Chirality: No | Availability: No | Prodrug: No |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 492.61 | Molecular Weight (Monoisotopic): 492.1944 | AlogP: 3.37 | #Rotatable Bonds: 7 |
| Polar Surface Area: 107.53 | Molecular Species: NEUTRAL | HBA: 7 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 9 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 10.63 | CX Basic pKa: 4.01 | CX LogP: 3.73 | CX LogD: 3.73 |
| Aromatic Rings: 3 | Heavy Atoms: 35 | QED Weighted: 0.52 | Np Likeness Score: -1.31 |
References
| 1. Wu Y, Qi Z, Wang B, Wang J, Liu Q, Wang A, Shi C, Zhou B, Liang Q, Wang W, Zou F, Qi S, Wang Z, Wang L, Wang W, Liu J, Liu Q.. (2022) Discovery of IHMT-MST1-58 as a Novel, Potent, and Selective MST1 Inhibitor for the Treatment of Type 1/2 Diabetes., 65 (17.0): [PMID:36037148] [10.1021/acs.jmedchem.2c00926] |
Source
Source(1):