ID: ALA4582511

Max Phase: Preclinical

Molecular Formula: C15H15N3O2S

Molecular Weight: 301.37

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1cnc(NC(=O)CCCOc2cccc(C#N)c2)s1

Standard InChI:  InChI=1S/C15H15N3O2S/c1-11-10-17-15(21-11)18-14(19)6-3-7-20-13-5-2-4-12(8-13)9-16/h2,4-5,8,10H,3,6-7H2,1H3,(H,17,18,19)

Standard InChI Key:  AGGFXGBQARTACI-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: 301.37Molecular Weight (Monoisotopic): 301.0885AlogP: 3.12#Rotatable Bonds: 6
Polar Surface Area: 75.01Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.08CX Basic pKa: 0.52CX LogP: 3.10CX LogD: 3.02
Aromatic Rings: 2Heavy Atoms: 21QED Weighted: 0.83Np Likeness Score: -2.46

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