ID: ALA3729977

Max Phase: Preclinical

Molecular Formula: C18H24BrN3O4S

Molecular Weight: 458.38

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C18H24BrN3O4S/c19-12-9-21-17(27-12)22-16(25)14-11-2-1-10(18(11)3-4-18)13(14)15(24)20-5-7-26-8-6-23/h9-11,13-14,23H,1-8H2,(H,20,24)(H,21,22,25)/t10-,11+,13-,14-/m1/s1

Standard InChI Key:  LAODHUZQKOBJIN-ZMJPVWNMSA-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: 458.38Molecular Weight (Monoisotopic): 457.0671AlogP: 2.02#Rotatable Bonds: 8
Polar Surface Area: 100.55Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.88CX Basic pKa: CX LogP: 1.29CX LogD: 1.18
Aromatic Rings: 1Heavy Atoms: 27QED Weighted: 0.52Np Likeness Score: -0.66

References

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

Source