ID: ALA4570111

Max Phase: Preclinical

Molecular Formula: C15H18N2O2S

Molecular Weight: 290.39

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(OCCCC(=O)Nc2ncc(C)s2)cc1

Standard InChI:  InChI=1S/C15H18N2O2S/c1-11-5-7-13(8-6-11)19-9-3-4-14(18)17-15-16-10-12(2)20-15/h5-8,10H,3-4,9H2,1-2H3,(H,16,17,18)

Standard InChI Key:  AIAZHHRCIAZXGH-UHFFFAOYSA-N

Associated Targets(Human)

HEK293 82097 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Human immunodeficiency virus type 1 Tat protein 1183 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: 290.39Molecular Weight (Monoisotopic): 290.1089AlogP: 3.56#Rotatable Bonds: 6
Polar Surface Area: 51.22Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.08CX Basic pKa: 0.52CX LogP: 3.76CX LogD: 3.68
Aromatic Rings: 2Heavy Atoms: 20QED Weighted: 0.83Np Likeness Score: -1.99

References

1. Nguyen W, Jacobson J, Jarman KE, Jousset Sabroux H, Harty L, McMahon J, Lewin SR, Purcell DF, Sleebs BE..  (2019)  Identification of 5-Substituted 2-Acylaminothiazoles That Activate Tat-Mediated Transcription in HIV-1 Latency Models.,  62  (10): [PMID:30973727] [10.1021/acs.jmedchem.9b00462]

Source