8'-(3-chloro-4-fluorobenzyl)-2'-(2-(2,5-dioxopyrrolidin-1-yl)ethyl)-6'-hydroxy-9',10'-dihydro-1'H-spiro[bicyclo[3.1.0]hexane-2,3'-imidazo[5,1-a][2,6]naphthyridine]-1',5',7'(2'H,8'H)-trione

ID: ALA4067020

PubChem CID: 68071774

Max Phase: Preclinical

Molecular Formula: C28H26ClFN4O6

Molecular Weight: 568.99

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C1c2c(c3n(c(=O)c2O)C2(CCC4CC42)N(CCN2C(=O)CCC2=O)C3=O)CCN1Cc1ccc(F)c(Cl)c1

Standard InChI:  InChI=1S/C28H26ClFN4O6/c29-18-11-14(1-2-19(18)30)13-31-8-6-16-22(25(31)38)24(37)27(40)34-23(16)26(39)33(28(34)7-5-15-12-17(15)28)10-9-32-20(35)3-4-21(32)36/h1-2,11,15,17,37H,3-10,12-13H2

Standard InChI Key:  FZIARXBYDXZUIQ-UHFFFAOYSA-N

Molfile:  

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M  END

Associated Targets(non-human)

Plasma (810 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Canis familiaris (36305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pol Human immunodeficiency virus type 1 integrase (9041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 568.99Molecular Weight (Monoisotopic): 568.1525AlogP: 2.23#Rotatable Bonds: 5
Polar Surface Area: 120.23Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 8.02CX Basic pKa: 0.44CX LogP: 0.72CX LogD: 0.63
Aromatic Rings: 2Heavy Atoms: 40QED Weighted: 0.55Np Likeness Score: -0.52

References

1. Schreier JD, Embrey MW, Raheem IT, Barbe G, Campeau LC, Dubost D, McCabe Dunn J, Grobler J, Hartingh TJ, Hazuda DJ, Klein D, Miller MD, Moore KP, Nguyen N, Pajkovic N, Powell DA, Rada V, Sanders JM, Sisko J, Steele TG, Wai J, Walji A, Xu M, Coleman PJ..  (2017)  Discovery and optimization of 2-pyridinone aminal integrase strand transfer inhibitors for the treatment of HIV.,  27  (9): [PMID:28285916] [10.1016/j.bmcl.2017.02.039]

Source