2-phenyl-3-(tetrahydro-1H-1-pyrrolylmethyl)benzo[d]imidazo[2,1-b][1,3]thiazole

ID: ALA2171977

Chembl Id: CHEMBL2171977

PubChem CID: 54770912

Max Phase: Preclinical

Molecular Formula: C20H19N3S

Molecular Weight: 333.46

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  c1ccc(-c2nc3sc4ccccc4n3c2CN2CCCC2)cc1

Standard InChI:  InChI=1S/C20H19N3S/c1-2-8-15(9-3-1)19-17(14-22-12-6-7-13-22)23-16-10-4-5-11-18(16)24-20(23)21-19/h1-5,8-11H,6-7,12-14H2

Standard InChI Key:  QJPBAWJEAJFWEX-UHFFFAOYSA-N

Associated Targets(Human)

COLO 205 (50209 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Drosophila melanogaster (359 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

Calculated Properties

Molecular Weight: 333.46Molecular Weight (Monoisotopic): 333.1300AlogP: 4.81#Rotatable Bonds: 3
Polar Surface Area: 20.54Molecular Species: BASEHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.58CX LogP: 4.22CX LogD: 3.01
Aromatic Rings: 4Heavy Atoms: 24QED Weighted: 0.54Np Likeness Score: -1.70

References

1. Pushpavalli SN, Ramaiah MJ, Lavanya A, Ganesh AR, Kumbhare RM, Bhadra K, Bhadra U, Pal-Bhadra M..  (2012)  Imidazo-benzothiazoles a potent microRNA modulator involved in cell proliferation.,  22  (20): [PMID:22981648] [10.1016/j.bmcl.2012.08.058]

Source