ID: ALA5094390

Max Phase: Preclinical

Molecular Formula: C25H23FN4O4S2

Molecular Weight: 526.62

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(=O)N1CCc2c(sc3nc(SCC(=O)Nc4ccc(C)c(F)c4)n(Cc4ccco4)c(=O)c23)C1

Standard InChI:  InChI=1S/C25H23FN4O4S2/c1-14-5-6-16(10-19(14)26)27-21(32)13-35-25-28-23-22(24(33)30(25)11-17-4-3-9-34-17)18-7-8-29(15(2)31)12-20(18)36-23/h3-6,9-10H,7-8,11-13H2,1-2H3,(H,27,32)

Standard InChI Key:  YBCGQGIOGAAFJH-UHFFFAOYSA-N

Associated Targets(Human)

Bromodomain-containing protein 3 1086 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: 526.62Molecular Weight (Monoisotopic): 526.1145AlogP: 4.18#Rotatable Bonds: 6
Polar Surface Area: 97.44Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.48CX Basic pKa: 2.08CX LogP: 3.70CX LogD: 3.70
Aromatic Rings: 4Heavy Atoms: 36QED Weighted: 0.30Np Likeness Score: -2.92

References

1. Carrasco K, Montersino C, Derviaux C, Saez-Ayala M, Hoffer L, Restouin A, Castellano R, Casassa J, Roche P, Pasquier E, Combes S, Morelli X, Collette Y, Betzi S..  (2022)  CRCM5484: A BET-BDII Selective Compound with Differential Anti-leukemic Drug Modulation.,  65  (7.0): [PMID:35348328] [10.1021/acs.jmedchem.1c02168]

Source