ID: ALA4641619

Max Phase: Preclinical

Molecular Formula: C22H28N6O9

Molecular Weight: 520.50

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COCCOc1nc(N)c2nc(O)n(Cc3ccc(C(=O)NC4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)cc3)c2n1

Standard InChI:  InChI=1S/C22H28N6O9/c1-35-6-7-36-21-25-17(23)13-18(26-21)28(22(34)24-13)8-10-2-4-11(5-3-10)19(33)27-20-16(32)15(31)14(30)12(9-29)37-20/h2-5,12,14-16,20,29-32H,6-9H2,1H3,(H,24,34)(H,27,33)(H2,23,25,26)/t12-,14-,15+,16-,20?/m1/s1

Standard InChI Key:  QKAXNCJSCUTXKM-MLTXWXQLSA-N

Associated Targets(non-human)

Toll-like receptor 7 174 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

Properties

Molecular Weight: 520.50Molecular Weight (Monoisotopic): 520.1918AlogP: -2.28#Rotatable Bonds: 9
Polar Surface Area: 227.56Molecular Species: NEUTRALHBA: 14HBD: 7
#RO5 Violations: 3HBA (Lipinski): 15HBD (Lipinski): 8#RO5 Violations (Lipinski): 3
CX Acidic pKa: 11.45CX Basic pKa: 3.37CX LogP: -1.07CX LogD: -1.07
Aromatic Rings: 3Heavy Atoms: 37QED Weighted: 0.15Np Likeness Score: -0.14

References

1. Baba A, Wakao M, Shinchi H, Chan M, Hayashi T, Yao S, Cottam HB, Carson DA, Suda Y..  (2020)  Synthesis and immunostimulatory activity of sugar-conjugated TLR7 ligands.,  30  (3): [PMID:31864800] [10.1016/j.bmcl.2019.126840]

Source