ID: ALA3732729

Max Phase: Preclinical

Molecular Formula: C19H25BrN4O2S

Molecular Weight: 453.41

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(NC1CCCNC1)[C@H]1[C@H](C(=O)Nc2ncc(Br)s2)[C@@H]2CC[C@H]1C21CC1

Standard InChI:  InChI=1S/C19H25BrN4O2S/c20-13-9-22-18(27-13)24-17(26)15-12-4-3-11(19(12)5-6-19)14(15)16(25)23-10-2-1-7-21-8-10/h9-12,14-15,21H,1-8H2,(H,23,25)(H,22,24,26)/t10?,11-,12+,14-,15-/m1/s1

Standard InChI Key:  BECUZOPGDIDRHF-IHZUMSIISA-N

Associated Targets(Human)

FML2_HUMAN 519 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Lipoxin A4 receptor 3472 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: 453.41Molecular Weight (Monoisotopic): 452.0882AlogP: 2.76#Rotatable Bonds: 4
Polar Surface Area: 83.12Molecular Species: BASEHBA: 5HBD: 3
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.87CX Basic pKa: 9.53CX LogP: 0.85CX LogD: 0.31
Aromatic Rings: 1Heavy Atoms: 27QED Weighted: 0.66Np Likeness Score: -0.62

References

1.  (2012)  Bridged spiro [2.4] heptane derivatives as alx receptor and/or fprl2 agonists, 

Source