1-(6'-(2-Hydroxyethoxy)-4-((4-methylpyridin-3-yl)oxy)-[3,3'-bipyridin]-6-yl)-3-methylurea

ID: ALA4566968

PubChem CID: 155543920

Max Phase: Preclinical

Molecular Formula: C20H21N5O4

Molecular Weight: 395.42

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CNC(=O)Nc1cc(Oc2cnccc2C)c(-c2ccc(OCCO)nc2)cn1

Standard InChI:  InChI=1S/C20H21N5O4/c1-13-5-6-22-12-17(13)29-16-9-18(25-20(27)21-2)23-11-15(16)14-3-4-19(24-10-14)28-8-7-26/h3-6,9-12,26H,7-8H2,1-2H3,(H2,21,23,25,27)

Standard InChI Key:  XJJQINAUBRDFIN-UHFFFAOYSA-N

Molfile:  

 
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    7.9294   -9.0319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

Alternative Forms

  1. Parent:

    ALA4566968

    ---

Associated Targets(Human)

GCK Tchem Hexokinase type IV (3191 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: 395.42Molecular Weight (Monoisotopic): 395.1594AlogP: 2.76#Rotatable Bonds: 7
Polar Surface Area: 118.49Molecular Species: NEUTRALHBA: 7HBD: 3
#RO5 Violations: HBA (Lipinski): 9HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 11.75CX Basic pKa: 5.59CX LogP: 1.45CX LogD: 1.44
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.56Np Likeness Score: -1.10

References

1. Dransfield PJ, Pattaropong V, Lai S, Fu Z, Kohn TJ, Du X, Cheng A, Xiong Y, Komorowski R, Jin L, Conn M, Tien E, DeWolf WE, Hinklin RJ, Aicher TD, Kraser CF, Boyd SA, Voegtli WC, Condroski KR, Veniant-Ellison M, Medina JC, Houze J, Coward P..  (2016)  Novel Series of Potent Glucokinase Activators Leading to the Discovery of AM-2394.,  (7): [PMID:27437083] [10.1021/acsmedchemlett.6b00140]

Source