ID: ALA4204909

Max Phase: Preclinical

Molecular Formula: C23H31N5O4S

Molecular Weight: 473.60

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCO/N=C1\CCc2cc(OCCCCCN3CCN(c4ccnc(N)c4)S3(=O)=O)ccc21

Standard InChI:  InChI=1S/C23H31N5O4S/c1-2-32-26-22-9-6-18-16-20(7-8-21(18)22)31-15-5-3-4-12-27-13-14-28(33(27,29)30)19-10-11-25-23(24)17-19/h7-8,10-11,16-17H,2-6,9,12-15H2,1H3,(H2,24,25)/b26-22+

Standard InChI Key:  RPOJRJQAEGPSHW-XTCLZLMSSA-N

Associated Targets(Human)

RD 1212 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HERG 29587 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Genome polyprotein 22 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mus musculus 284745 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Enterovirus A71 1246 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: 473.60Molecular Weight (Monoisotopic): 473.2097AlogP: 2.97#Rotatable Bonds: 10
Polar Surface Area: 110.35Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.16CX LogP: 2.21CX LogD: 1.45
Aromatic Rings: 2Heavy Atoms: 33QED Weighted: 0.42Np Likeness Score: -0.52

References

1. Li P, Yu J, Hao F, He H, Shi X, Hu J, Wang L, Du C, Zhang X, Sun Y, Lin F, Gu Z, Xu D, Chen X, Shen L, Hu G, Li J, Chen S, Xiao W, Wang Z, Guo Q, Chang X, Tian X, Lin T..  (2017)  Discovery of Potent EV71 Capsid Inhibitors for Treatment of HFMD.,  (8): [PMID:28835799] [10.1021/acsmedchemlett.7b00188]

Source