tert-butyl 4-(4-(9,10-dioxo-9,10-dihydroanthracen-1-yl)-1H-pyrazol-1-yl)piperidine-1-carboxylate

ID: ALA4441364

PubChem CID: 154697562

Max Phase: Preclinical

Molecular Formula: C27H27N3O4

Molecular Weight: 457.53

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)(C)OC(=O)N1CCC(n2cc(-c3cccc4c3C(=O)c3ccccc3C4=O)cn2)CC1

Standard InChI:  InChI=1S/C27H27N3O4/c1-27(2,3)34-26(33)29-13-11-18(12-14-29)30-16-17(15-28-30)19-9-6-10-22-23(19)25(32)21-8-5-4-7-20(21)24(22)31/h4-10,15-16,18H,11-14H2,1-3H3

Standard InChI Key:  GWORUPZVCQORCU-UHFFFAOYSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA4441364

    ---

Associated Targets(Human)

PDK4 Tchem Pyruvate dehydrogenase kinase isoform 4 (177 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

Calculated Properties

Molecular Weight: 457.53Molecular Weight (Monoisotopic): 457.2002AlogP: 4.90#Rotatable Bonds: 2
Polar Surface Area: 81.50Molecular Species: NEUTRALHBA: 6HBD:
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 2.06CX LogP: 3.92CX LogD: 3.92
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.43Np Likeness Score: -0.58

References

1. Lee D, Pagire HS, Pagire SH, Bae EJ, Dighe M, Kim M, Lee KM, Jang YK, Jaladi AK, Jung KY, Yoo EK, Gim HE, Lee S, Choi WI, Chi YI, Song JS, Bae MA, Jeon YH, Lee GH, Liu KH, Lee T, Park S, Jeon JH, Lee IK, Ahn JH..  (2019)  Discovery of Novel Pyruvate Dehydrogenase Kinase 4 Inhibitors for Potential Oral Treatment of Metabolic Diseases.,  62  (2): [PMID:30623649] [10.1021/acs.jmedchem.8b01168]

Source