(R)-N-(2-Amino-1-(4-(hydroxymethyl)thiazol-2-yl)ethyl)-5-(3-fluoro-4-(trifluoromethyl)phenyl)-3-methyl-1H-pyrrole-2-carboxamide

ID: ALA5277436

Chembl Id: CHEMBL5277436

Max Phase: Preclinical

Molecular Formula: C19H18F4N4O2S

Molecular Weight: 442.44

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1cc(-c2ccc(C(F)(F)F)c(F)c2)[nH]c1C(=O)N[C@H](CN)c1nc(CO)cs1

Standard InChI:  InChI=1S/C19H18F4N4O2S/c1-9-4-14(10-2-3-12(13(20)5-10)19(21,22)23)26-16(9)17(29)27-15(6-24)18-25-11(7-28)8-30-18/h2-5,8,15,26,28H,6-7,24H2,1H3,(H,27,29)/t15-/m1/s1

Standard InChI Key:  DDARDFGMRMQOSP-OAHLLOKOSA-N

Alternative Forms

  1. Parent:

    ALA5277436

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Associated Targets(Human)

TZM (838 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Human immunodeficiency virus 1 (70413 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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

Calculated Properties

Molecular Weight: 442.44Molecular Weight (Monoisotopic): 442.1087AlogP: 3.53#Rotatable Bonds: 6
Polar Surface Area: 104.03Molecular Species: NEUTRALHBA: 5HBD: 4
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 5#RO5 Violations (Lipinski):
CX Acidic pKa: 13.85CX Basic pKa: 8.36CX LogP: 2.33CX LogD: 1.33
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.44Np Likeness Score: -1.11

References

1. Curreli F, Ahmed S, Benedict Victor SM, Iusupov IR, Spiridonov EA, Belov DS, Altieri A, Kurkin AV, Debnath AK..  (2021)  Design, synthesis, and antiviral activity of a series of CD4-mimetic small-molecule HIV-1 entry inhibitors.,  32  [PMID:33461144] [10.1016/j.bmc.2021.116000]

Source