ID: ALA281325

Max Phase: Preclinical

Molecular Formula: C11H17NO2S

Molecular Weight: 227.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(CCN)c(SC)c1OC

Standard InChI:  InChI=1S/C11H17NO2S/c1-13-9-5-4-8(6-7-12)11(15-3)10(9)14-2/h4-5H,6-7,12H2,1-3H3

Standard InChI Key:  NJNFCDQQEIAOIF-UHFFFAOYSA-N

Associated Targets(Human)

Homo sapiens 32628 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Monoamine oxidase 74 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: 227.33Molecular Weight (Monoisotopic): 227.0980AlogP: 1.93#Rotatable Bonds: 5
Polar Surface Area: 44.48Molecular Species: BASEHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.75CX LogP: 1.70CX LogD: -0.57
Aromatic Rings: 1Heavy Atoms: 15QED Weighted: 0.78Np Likeness Score: 0.20

References

1. Jacob P, Shulgin AT..  (1981)  Sulfur analogues of psychotomimetic agents. Monothio analogues of mescaline and isomescaline.,  24  (11): [PMID:7310812] [10.1021/jm00143a017]

Source