ID: ALA4847830

Max Phase: Preclinical

Molecular Formula: C27H35FN4O4S2

Molecular Weight: 562.73

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CSCC[C@@H](/C=C(\F)S(=O)(=O)c1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)N1CCN(C)CC1

Standard InChI:  InChI=1S/C27H35FN4O4S2/c1-31-14-16-32(17-15-31)27(34)30-24(19-21-9-5-3-6-10-21)26(33)29-22(13-18-37-2)20-25(28)38(35,36)23-11-7-4-8-12-23/h3-12,20,22,24H,13-19H2,1-2H3,(H,29,33)(H,30,34)/b25-20+/t22-,24-/m0/s1

Standard InChI Key:  QKRDRRVQRUOUCH-MZBRKLLYSA-N

Associated Targets(Human)

HeLa 62764 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Proteasome Macropain subunit 1025 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Trypanosoma brucei brucei 13300 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

J774.1 238 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: 562.73Molecular Weight (Monoisotopic): 562.2084AlogP: 3.08#Rotatable Bonds: 11
Polar Surface Area: 98.82Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.74CX Basic pKa: 7.02CX LogP: 3.47CX LogD: 3.31
Aromatic Rings: 2Heavy Atoms: 38QED Weighted: 0.44Np Likeness Score: -0.82

References

1. Jung S, Fuchs N, Johe P, Wagner A, Diehl E, Yuliani T, Zimmer C, Barthels F, Zimmermann RA, Klein P, Waigel W, Meyr J, Opatz T, Tenzer S, Distler U, Räder HJ, Kersten C, Engels B, Hellmich UA, Klein J, Schirmeister T..  (2021)  Fluorovinylsulfones and -Sulfonates as Potent Covalent Reversible Inhibitors of the Trypanosomal Cysteine Protease Rhodesain: Structure-Activity Relationship, Inhibition Mechanism, Metabolism, and In Vivo Studies.,  64  (16.0): [PMID:34378914] [10.1021/acs.jmedchem.1c01002]

Source