ID: ALA4872465

Max Phase: Preclinical

Molecular Formula: C15H15ClN4O2S

Molecular Weight: 350.83

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  NC[C@@H](NC(=O)c1cc2ccc(Cl)cc2[nH]1)c1ncc(CO)s1

Standard InChI:  InChI=1S/C15H15ClN4O2S/c16-9-2-1-8-3-12(19-11(8)4-9)14(22)20-13(5-17)15-18-6-10(7-21)23-15/h1-4,6,13,19,21H,5,7,17H2,(H,20,22)/t13-/m1/s1

Standard InChI Key:  WCAHCXMCMAIQLR-CYBMUJFWSA-N

Associated Targets(Human)

TZM 838 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Envelope glycoprotein gp160 755 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Human immunodeficiency virus type 1 reverse transcriptase 18245 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: 350.83Molecular Weight (Monoisotopic): 350.0604AlogP: 2.20#Rotatable Bonds: 5
Polar Surface Area: 104.03Molecular Species: NEUTRALHBA: 5HBD: 4
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.50CX Basic pKa: 8.36CX LogP: 0.91CX LogD: -0.09
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.57Np Likeness Score: -1.05

References

1. Iusupov IR, Curreli F, Spiridonov EA, Markov PO, Ahmed S, Belov DS, Manasova EV, Altieri A, Kurkin AV, Debnath AK..  (2021)  Design of gp120 HIV-1 entry inhibitors by scaffold hopping via isosteric replacements.,  224  [PMID:34246921] [10.1016/j.ejmech.2021.113681]

Source