ID: ALA4752106

Max Phase: Preclinical

Molecular Formula: C31H33N3O5S

Molecular Weight: 559.69

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(C)(C)NS(=O)(=O)c1cccc2c(NC(=O)[C@H](Cc3ccccc3)NC(=O)OCc3ccccc3)cccc12

Standard InChI:  InChI=1S/C31H33N3O5S/c1-31(2,3)34-40(37,38)28-19-11-16-24-25(28)17-10-18-26(24)32-29(35)27(20-22-12-6-4-7-13-22)33-30(36)39-21-23-14-8-5-9-15-23/h4-19,27,34H,20-21H2,1-3H3,(H,32,35)(H,33,36)/t27-/m0/s1

Standard InChI Key:  CHDISSRELOSFSF-MHZLTWQESA-N

Associated Targets(Human)

Ubiquitin carboxyl-terminal hydrolase 30 944 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 559.69Molecular Weight (Monoisotopic): 559.2141AlogP: 5.39#Rotatable Bonds: 9
Polar Surface Area: 113.60Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 9.88CX Basic pKa: CX LogP: 5.55CX LogD: 5.55
Aromatic Rings: 4Heavy Atoms: 40QED Weighted: 0.25Np Likeness Score: -0.96

References

1. Kluge AF,Lagu BR,Maiti P,Jaleel M,Webb M,Malhotra J,Mallat A,Srinivas PA,Thompson JE.  (2018)  Novel highly selective inhibitors of ubiquitin specific protease 30 (USP30) accelerate mitophagy.,  28  (15): [PMID:29935771] [10.1016/j.bmcl.2018.05.013]

Source