(E)-5-methoxy-3-((6-methoxy-2-methylimidazo[2,1-b]thiazol-5-yl)methylene)-6-methylindolin-2-one

ID: ALA4476696

Chembl Id: CHEMBL4476696

PubChem CID: 155538657

Max Phase: Preclinical

Molecular Formula: C18H17N3O3S

Molecular Weight: 355.42

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc2c(cc1C)NC(=O)/C2=C/c1c(OC)nc2sc(C)cn12

Standard InChI:  InChI=1S/C18H17N3O3S/c1-9-5-13-11(7-15(9)23-3)12(16(22)19-13)6-14-17(24-4)20-18-21(14)8-10(2)25-18/h5-8H,1-4H3,(H,19,22)/b12-6+

Standard InChI Key:  OPZIKHMAPIOJEF-WUXMJOGZSA-N

Alternative Forms

  1. Parent:

    ALA4476696

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Associated Targets(Human)

NSCLC (640 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CNS carcinoma cell (76 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Melanoma cell line (83 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ovarian carcinoma cell (138 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Renal cancer cell line (72 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Prostatic carcinoma cell (85 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Breast carcinoma cell (217 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 355.42Molecular Weight (Monoisotopic): 355.0991AlogP: 3.52#Rotatable Bonds: 3
Polar Surface Area: 64.86Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 11.69CX Basic pKa: 1.25CX LogP: 3.44CX LogD: 3.44
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.73Np Likeness Score: -0.98

References

1. Morigi R, Locatelli A, Leoni A, Rambaldi M, Bortolozzi R, Mattiuzzo E, Ronca R, Maccarinelli F, Hamel E, Bai R, Brancale A, Viola G..  (2019)  Synthesis, in vitro and in vivo biological evaluation of substituted 3-(5-imidazo[2,1-b]thiazolylmethylene)-2-indolinones as new potent anticancer agents.,  166  [PMID:30784885] [10.1016/j.ejmech.2019.01.049]

Source