ID: ALA5180970

Max Phase: Preclinical

Molecular Formula: C37H46N8O11S

Molecular Weight: 810.89

Associated Items:

Representations

Canonical SMILES:  O=C1c2ccc3c4c(c(NCc5cn(CCS[C@@H]6O[C@H](CO)[C@H](O)[C@H](O)[C@H]6O)nn5)cc(c24)C(=O)N1CCN1CCOCC1)C(=O)N(CCN1CCOCC1)C3=O

Standard InChI:  InChI=1S/C37H46N8O11S/c46-20-26-30(47)31(48)32(49)37(56-26)57-16-11-43-19-21(39-40-43)18-38-25-17-24-27-22(33(50)44(35(24)52)5-3-41-7-12-54-13-8-41)1-2-23-28(27)29(25)36(53)45(34(23)51)6-4-42-9-14-55-15-10-42/h1-2,17,19,26,30-32,37-38,46-49H,3-16,18,20H2/t26-,30+,31+,32-,37+/m1/s1

Standard InChI Key:  FKCPZQOWUXMHKA-SVRKZTCTSA-N

Associated Targets(Human)

HT-29 80576 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MRC5 9203 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

quadruplex DNA 2700 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Trypanosoma brucei 78846 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Leishmania major 2877 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

Properties

Molecular Weight: 810.89Molecular Weight (Monoisotopic): 810.3007AlogP: -1.57#Rotatable Bonds: 14
Polar Surface Area: 232.59Molecular Species: NEUTRALHBA: 18HBD: 5
#RO5 Violations: 2HBA (Lipinski): 19HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.47CX Basic pKa: 6.25CX LogP: -1.58CX LogD: -1.61
Aromatic Rings: 3Heavy Atoms: 57QED Weighted: 0.12Np Likeness Score: -0.51

References

1. Belmonte-Reche E, Benassi A, Peñalver P, Cucchiarini A, Guédin A, Mergny JL, Rosu F, Gabelica V, Freccero M, Doria F, Morales JC..  (2022)  Thiosugar naphthalene diimide conjugates: G-quadruplex ligands with antiparasitic and anticancer activity.,  232  [PMID:35168151] [10.1016/j.ejmech.2022.114183]

Source