(E)-3-((6-methoxy-2-methylimidazo[2,1-b]thiazol-5-yl)methylene)-1,3-dihydro-2H-benzo[g]indol-2-one

ID: ALA4566972

Chembl Id: CHEMBL4566972

PubChem CID: 155543924

Max Phase: Preclinical

Molecular Formula: C20H15N3O2S

Molecular Weight: 361.43

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1nc2sc(C)cn2c1/C=C1/C(=O)Nc2c1ccc1ccccc21

Standard InChI:  InChI=1S/C20H15N3O2S/c1-11-10-23-16(19(25-2)22-20(23)26-11)9-15-14-8-7-12-5-3-4-6-13(12)17(14)21-18(15)24/h3-10H,1-2H3,(H,21,24)/b15-9+

Standard InChI Key:  ZZWBPDMKIRAWQA-OQLLNIDSSA-N

Alternative Forms

  1. Parent:

    ALA4566972

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Associated Targets(Human)

Leukemia cell (223 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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: 361.43Molecular Weight (Monoisotopic): 361.0885AlogP: 4.36#Rotatable Bonds: 2
Polar Surface Area: 55.63Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 10.79CX Basic pKa: 1.25CX LogP: 4.08CX LogD: 4.08
Aromatic Rings: 4Heavy Atoms: 26QED Weighted: 0.54Np Likeness Score: -0.93

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