ID: ALA2377639

Max Phase: Preclinical

Molecular Formula: C14H11Br2NO2

Molecular Weight: 385.06

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cn1c(/C=C/C(=O)c2ccc(O)cc2)cc(Br)c1Br

Standard InChI:  InChI=1S/C14H11Br2NO2/c1-17-10(8-12(15)14(17)16)4-7-13(19)9-2-5-11(18)6-3-9/h2-8,18H,1H3/b7-4+

Standard InChI Key:  XEVLJMNHDCAKAD-QPJJXVBHSA-N

Associated Targets(Human)

Caco-2 12174 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

WRL68 207 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

PA-1 704 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MCF7 126967 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 385.06Molecular Weight (Monoisotopic): 382.9157AlogP: 4.15#Rotatable Bonds: 3
Polar Surface Area: 42.23Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.87CX Basic pKa: CX LogP: 4.05CX LogD: 3.92
Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.64Np Likeness Score: 0.22

References

1. Rane RA, Sahu NU, Gutte SD, Mahajan AA, Shah CP, Bangalore P..  (2013)  Synthesis and evaluation of novel marine bromopyrrole alkaloid-based hybrids as anticancer agents.,  63  [PMID:23584542] [10.1016/j.ejmech.2013.03.029]

Source