N-((1S,4S)-4-(2-Methoxyethoxy)cyclohexyl)-6-(thlazol-5-yl)-1H-indole-4-carboxamide

ID: ALA5202189

Chembl Id: CHEMBL5202189

PubChem CID: 156339372

Max Phase: Preclinical

Molecular Formula: C21H25N3O3S

Molecular Weight: 399.52

Associated Items:

Names and Identifiers

Canonical SMILES:  COCCO[C@H]1CC[C@@H](NC(=O)c2cc(-c3cncs3)cc3[nH]ccc23)CC1

Standard InChI:  InChI=1S/C21H25N3O3S/c1-26-8-9-27-16-4-2-15(3-5-16)24-21(25)18-10-14(20-12-22-13-28-20)11-19-17(18)6-7-23-19/h6-7,10-13,15-16,23H,2-5,8-9H2,1H3,(H,24,25)/t15-,16+

Standard InChI Key:  JKVDPAQLSFMJRS-IYBDPMFKSA-N

Alternative Forms

  1. Parent:

    ALA5202189

    ---

Associated Targets(Human)

CD38 Tclin Lymphocyte differentiation antigen CD38 (364 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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

Calculated Properties

Molecular Weight: 399.52Molecular Weight (Monoisotopic): 399.1617AlogP: 4.00#Rotatable Bonds: 7
Polar Surface Area: 76.24Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 2.78CX LogP: 2.46CX LogD: 2.46
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.59Np Likeness Score: -0.82

References

1. Lagu B, Wu X, Kulkarni S, Paul R, Becherer JD, Olson L, Ravani S, Chatzianastasiou A, Papapetropoulos A, Andrzejewski S..  (2022)  Orally Bioavailable Enzymatic Inhibitor of CD38, MK-0159, Protects against Ischemia/Reperfusion Injury in the Murine Heart.,  65  (13.0): [PMID:35762533] [10.1021/acs.jmedchem.2c00688]

Source