ID: ALA5199671

Max Phase: Preclinical

Molecular Formula: C26H29N5O5

Molecular Weight: 491.55

Associated Items:

Representations

Canonical SMILES:  CC(C)(C)OC(=O)NCCCCn1c(NC(=O)c2cc3ccccc3o2)nc2cc(C(N)=O)ccc21

Standard InChI:  InChI=1S/C26H29N5O5/c1-26(2,3)36-25(34)28-12-6-7-13-31-19-11-10-17(22(27)32)14-18(19)29-24(31)30-23(33)21-15-16-8-4-5-9-20(16)35-21/h4-5,8-11,14-15H,6-7,12-13H2,1-3H3,(H2,27,32)(H,28,34)(H,29,30,33)

Standard InChI Key:  WZNKYSBMFPLHAI-UHFFFAOYSA-N

Associated Targets(Human)

STING1 Tchem Stimulator of interferon genes protein (1885 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THP1-Dual (100 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

Properties

Molecular Weight: 491.55Molecular Weight (Monoisotopic): 491.2169AlogP: 4.44#Rotatable Bonds: 8
Polar Surface Area: 141.48Molecular Species: NEUTRALHBA: 7HBD: 3
#RO5 Violations: 0HBA (Lipinski): 10HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.71CX Basic pKa: 1.31CX LogP: 3.46CX LogD: 3.46
Aromatic Rings: 4Heavy Atoms: 36QED Weighted: 0.31Np Likeness Score: -1.47

References

1. Jeon MJ, Lee H, Lee J, Baek SY, Lee D, Jo S, Lee JY, Kang M, Jung HR, Han SB, Kim NJ, Lee S, Kim H..  (2022)  Development of Potent Immune Modulators Targeting Stimulator of Interferon Genes Receptor.,  65  (7.0): [PMID:35315650] [10.1021/acs.jmedchem.1c01795]

Source