ID: ALA3906647

Max Phase: Preclinical

Molecular Formula: C21H24O5

Molecular Weight: 356.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C/C=C/c1cc(OC)c2c(c1)[C@@H](C)[C@H](c1cc(OC)c(O)c(OC)c1)O2

Standard InChI:  InChI=1S/C21H24O5/c1-6-7-13-8-15-12(2)20(26-21(15)18(9-13)25-5)14-10-16(23-3)19(22)17(11-14)24-4/h6-12,20,22H,1-5H3/b7-6+/t12-,20-/m1/s1

Standard InChI Key:  LYZVPGMCGPXCQO-FVFSBHJXSA-N

Associated Targets(Human)

C-C chemokine receptor type 3 1666 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus 284745 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: 356.42Molecular Weight (Monoisotopic): 356.1624AlogP: 4.69#Rotatable Bonds: 5
Polar Surface Area: 57.15Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.30CX Basic pKa: CX LogP: 4.35CX LogD: 4.35
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.84Np Likeness Score: 1.62

References

1. Morikawa T, Hachiman I, Matsuo K, Nishida E, Ninomiya K, Hayakawa T, Yoshie O, Muraoka O, Nakayama T..  (2016)  Neolignans from the Arils of Myristica fragrans as Potent Antagonists of CC Chemokine Receptor 3.,  79  (8): [PMID:27419473] [10.1021/acs.jnatprod.6b00262]

Source