ID: ALA4849327

Max Phase: Preclinical

Molecular Formula: C47H47FN8O5

Molecular Weight: 822.94

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C=C(C)C(=O)N(CC)c1cc(-c2ccc(N3CCN(C(=O)c4cc(Cc5n[nH]c(=O)c6ccccc56)ccc4F)CC3)nc2)cc(C(=O)NCc2c(C)cc(C)[nH]c2=O)c1C

Standard InChI:  InChI=1S/C47H47FN8O5/c1-7-56(46(60)27(2)3)41-24-33(23-36(30(41)6)43(57)50-26-38-28(4)20-29(5)51-44(38)58)32-13-15-42(49-25-32)54-16-18-55(19-17-54)47(61)37-21-31(12-14-39(37)48)22-40-34-10-8-9-11-35(34)45(59)53-52-40/h8-15,20-21,23-25H,2,7,16-19,22,26H2,1,3-6H3,(H,50,57)(H,51,58)(H,53,59)

Standard InChI Key:  LPDOHGNBHJLAJC-UHFFFAOYSA-N

Associated Targets(Human)

MDA-MB-231 (73002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-468 (9477 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF-10A (2462 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PRAP1 Tchem Proline-rich acidic protein 1 (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EZH2 Tclin Histone-lysine N-methyltransferase EZH2 (2012 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: 822.94Molecular Weight (Monoisotopic): 822.3653AlogP: 6.15#Rotatable Bonds: 11
Polar Surface Area: 164.46Molecular Species: NEUTRALHBA: 8HBD: 3
#RO5 Violations: 2HBA (Lipinski): 13HBD (Lipinski): 3#RO5 Violations (Lipinski): 3
CX Acidic pKa: 9.95CX Basic pKa: 6.91CX LogP: 5.17CX LogD: 5.15
Aromatic Rings: 6Heavy Atoms: 61QED Weighted: 0.13Np Likeness Score: -1.58

References

1. Wang C, Qu L, Li S, Yin F, Ji L, Peng W, Luo H, Lu D, Liu X, Chen X, Kong L, Wang X..  (2021)  Discovery of First-in-Class Dual PARP and EZH2 Inhibitors for Triple-Negative Breast Cancer with Wild-Type BRCA.,  64  (17.0): [PMID:34455779] [10.1021/acs.jmedchem.1c00567]

Source