4-(2-(5-fluoro-2-(1-(2-fluorobenzyl)-5-(isoxazol-3-yl)-1H-pyrazol-3-yl)pyrimidin-4-yloxy)ethyl)morpholine

ID: ALA4845811

PubChem CID: 118965719

Max Phase: Preclinical

Molecular Formula: C23H22F2N6O3

Molecular Weight: 468.46

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  Fc1ccccc1Cn1nc(-c2ncc(F)c(OCCN3CCOCC3)n2)cc1-c1ccon1

Standard InChI:  InChI=1S/C23H22F2N6O3/c24-17-4-2-1-3-16(17)15-31-21(19-5-9-34-29-19)13-20(28-31)22-26-14-18(25)23(27-22)33-12-8-30-6-10-32-11-7-30/h1-5,9,13-14H,6-8,10-12,15H2

Standard InChI Key:  XWOZRFODXUXUNL-UHFFFAOYSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA4845811

    ---

Associated Targets(Human)

GUCY1B1 Tclin Soluble guanylate cyclase (679 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: 468.46Molecular Weight (Monoisotopic): 468.1721AlogP: 3.03#Rotatable Bonds: 8
Polar Surface Area: 91.33Molecular Species: NEUTRALHBA: 9HBD:
#RO5 Violations: HBA (Lipinski): 9HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 5.76CX LogP: 3.67CX LogD: 3.66
Aromatic Rings: 4Heavy Atoms: 34QED Weighted: 0.39Np Likeness Score: -2.03

References

1. Rennie GR, Barden TC, Bernier SG, Carvalho A, Deming R, Germano P, Hudson C, Im GJ, Iyengar RR, Jia L, Jung J, Kim E, Lee TW, Mermerian A, Moore J, Nakai T, Perl NR, Tobin J, Zimmer DP, Renhowe PA..  (2021)  Discovery of CYR715: A novel carboxylic acid-containing soluble guanylate cyclase stimulator.,  40  [PMID:33662540] [10.1016/j.bmcl.2021.127886]

Source