ID: ALA3731851

Max Phase: Preclinical

Molecular Formula: C21H28BrN3O3S

Molecular Weight: 482.44

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(N[C@H]1CC[C@H](CO)CC1)[C@H]1[C@H](C(=O)Nc2ncc(Br)s2)[C@@H]2CC[C@H]1C21CC1

Standard InChI:  InChI=1S/C21H28BrN3O3S/c22-15-9-23-20(29-15)25-19(28)17-14-6-5-13(21(14)7-8-21)16(17)18(27)24-12-3-1-11(10-26)2-4-12/h9,11-14,16-17,26H,1-8,10H2,(H,24,27)(H,23,25,28)/t11-,12-,13-,14+,16-,17-/m1/s1

Standard InChI Key:  LOMUBZUTIQZRBB-ATZWAVOESA-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: 482.44Molecular Weight (Monoisotopic): 481.1035AlogP: 3.56#Rotatable Bonds: 5
Polar Surface Area: 91.32Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.88CX Basic pKa: 0.42CX LogP: 2.76CX LogD: 2.64
Aromatic Rings: 1Heavy Atoms: 29QED Weighted: 0.60Np Likeness Score: -0.53

References

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

Source