2-amino-4-(4-methoxy-3-methylphenyl)-4H-benzo[h]chromene-3-carbonitrile

ID: ALA5188662

Chembl Id: CHEMBL5188662

PubChem CID: 3261465

Max Phase: Preclinical

Molecular Formula: C22H18N2O2

Molecular Weight: 342.40

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1ccc(C2C(C#N)=C(N)Oc3c2ccc2ccccc32)cc1C

Standard InChI:  InChI=1S/C22H18N2O2/c1-13-11-15(8-10-19(13)25-2)20-17-9-7-14-5-3-4-6-16(14)21(17)26-22(24)18(20)12-23/h3-11,20H,24H2,1-2H3

Standard InChI Key:  JXHGDGRUSQPSFC-UHFFFAOYSA-N

Associated Targets(Human)

MYB Tbio Transcriptional activator Myb (26 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 342.40Molecular Weight (Monoisotopic): 342.1368AlogP: 4.38#Rotatable Bonds: 2
Polar Surface Area: 68.27Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 1.68CX LogP: 4.38CX LogD: 4.38
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.75Np Likeness Score: -0.84

References

1. Köhler LHF, Reich S, Yusenko M, Klempnauer KH, Shaikh AH, Ahmed K, Begemann G, Schobert R, Biersack B..  (2022)  A New Naphthopyran Derivative Combines c-Myb Inhibition, Microtubule-Targeting Effects, and Antiangiogenic Properties.,  13  (11.0): [PMID:36385941] [10.1021/acsmedchemlett.2c00403]

Source