1-(2-(5-(4-(4-Ammoniobutyl)-1H-1,2,3-triazol-1-yl)-2-(4-([1,1'-biphenyl]-4-yl)-5-phenylthiazol-2-yl)phenoxy)ethyl)imidazolidin-2-one 2,2,2-Trifluoroacetate

ID: ALA4879027

PubChem CID: 164625859

Max Phase: Preclinical

Molecular Formula: C40H38F3N7O4S

Molecular Weight: 655.83

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  NCCCCc1cn(-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)c(-c4ccccc4)s3)c(OCCN3CCNC3=O)c2)nn1.O=C(O)C(F)(F)F

Standard InChI:  InChI=1S/C38H37N7O2S.C2HF3O2/c39-20-8-7-13-31-26-45(43-42-31)32-18-19-33(34(25-32)47-24-23-44-22-21-40-38(44)46)37-41-35(36(48-37)30-11-5-2-6-12-30)29-16-14-28(15-17-29)27-9-3-1-4-10-27;3-2(4,5)1(6)7/h1-6,9-12,14-19,25-26H,7-8,13,20-24,39H2,(H,40,46);(H,6,7)

Standard InChI Key:  ZFGUUNXZCRFJPM-UHFFFAOYSA-N

Molfile:  

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M  END

Associated Targets(Human)

HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

TRYR Trypanothione reductase (236 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Leishmania infantum (5912 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

Calculated Properties

Molecular Weight: 655.83Molecular Weight (Monoisotopic): 655.2729AlogP: 7.08#Rotatable Bonds: 13
Polar Surface Area: 111.19Molecular Species: BASEHBA: 8HBD: 2
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 13.76CX Basic pKa: 10.21CX LogP: 6.67CX LogD: 4.07
Aromatic Rings: 6Heavy Atoms: 48QED Weighted: 0.13Np Likeness Score: -1.22

References

1. Revuelto A, de Lucio H, García-Soriano JC, Sánchez-Murcia PA, Gago F, Jiménez-Ruiz A, Camarasa MJ, Velázquez S..  (2021)  Efficient Dimerization Disruption of Leishmania infantum Trypanothione Reductase by Triazole-phenyl-thiazoles.,  64  (9.0): [PMID:33945281] [10.1021/acs.jmedchem.1c00206]

Source