1-(3-((4-amino-6-((2,5-dichlorophenethyl)amino)-1,3,5-triazin-2-yl)methoxy)-5-methylphenyl)pyrrolidin-2-one

ID: ALA5285139

Chembl Id: CHEMBL5285139

Max Phase: Preclinical

Molecular Formula: C23H24Cl2N6O2

Molecular Weight: 487.39

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1cc(OCc2nc(N)nc(NCCc3cc(Cl)ccc3Cl)n2)cc(N2CCCC2=O)c1

Standard InChI:  InChI=1S/C23H24Cl2N6O2/c1-14-9-17(31-8-2-3-21(31)32)12-18(10-14)33-13-20-28-22(26)30-23(29-20)27-7-6-15-11-16(24)4-5-19(15)25/h4-5,9-12H,2-3,6-8,13H2,1H3,(H3,26,27,28,29,30)

Standard InChI Key:  AIIZGUNRDJPXHF-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5285139

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Associated Targets(Human)

FFAR1 Tchem Free fatty acid receptor 1 (4763 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FFAR4 Tchem G-protein coupled receptor 120 (2999 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: 487.39Molecular Weight (Monoisotopic): 486.1338AlogP: 4.43#Rotatable Bonds: 8
Polar Surface Area: 106.26Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: HBA (Lipinski): 8HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 5.18CX LogP: 4.81CX LogD: 4.80
Aromatic Rings: 3Heavy Atoms: 33QED Weighted: 0.48Np Likeness Score: -1.81

References

1. Lückmann M, Shenol A, Nissen TAD, Petersen JE, Kouvchinov D, Schwartz TW, Frimurer TM..  (2022)  Optimization of First-in-Class Dual-Acting FFAR1/FFAR4 Allosteric Modulators with Novel Mode of Action.,  13  (12.0): [PMID:36518697] [10.1021/acsmedchemlett.2c00160]

Source