ID: ALA2386483

Max Phase: Preclinical

Molecular Formula: C28H20N4O2S

Molecular Weight: 476.56

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(CSc1nc2c([nH]c3ccccc32)c(=O)n1-c1ccccc1)Nc1ccc2ccccc2c1

Standard InChI:  InChI=1S/C28H20N4O2S/c33-24(29-20-15-14-18-8-4-5-9-19(18)16-20)17-35-28-31-25-22-12-6-7-13-23(22)30-26(25)27(34)32(28)21-10-2-1-3-11-21/h1-16,30H,17H2,(H,29,33)

Standard InChI Key:  ZATQATFITAAENI-UHFFFAOYSA-N

Associated Targets(Human)

Toll-like receptor 4 970 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Toll-like receptor 4 808 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

Properties

Molecular Weight: 476.56Molecular Weight (Monoisotopic): 476.1307AlogP: 5.75#Rotatable Bonds: 5
Polar Surface Area: 79.78Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 9.34CX Basic pKa: 1.84CX LogP: 5.64CX LogD: 5.63
Aromatic Rings: 6Heavy Atoms: 35QED Weighted: 0.25Np Likeness Score: -1.62

References

1. Chan M, Hayashi T, Mathewson RD, Nour A, Hayashi Y, Yao S, Tawatao RI, Crain B, Tsigelny IF, Kouznetsova VL, Messer K, Pu M, Corr M, Carson DA, Cottam HB..  (2013)  Identification of substituted pyrimido[5,4-b]indoles as selective Toll-like receptor 4 ligands.,  56  (11): [PMID:23656327] [10.1021/jm301694x]

Source