2-Amino-4-(3-bromo-4-methoxyphenyl)-4H-naphtho(1,2-b)pyran-3-carbonitrile

ID: ALA5203497

Chembl Id: CHEMBL5203497

PubChem CID: 2844733

Max Phase: Preclinical

Molecular Formula: C21H15BrN2O2

Molecular Weight: 407.27

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1ccc(C2C(C#N)=C(N)Oc3c2ccc2ccccc32)cc1Br

Standard InChI:  InChI=1S/C21H15BrN2O2/c1-25-18-9-7-13(10-17(18)22)19-15-8-6-12-4-2-3-5-14(12)20(15)26-21(24)16(19)11-23/h2-10,19H,24H2,1H3

Standard InChI Key:  OXCYLZAOKAPGPF-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: 407.27Molecular Weight (Monoisotopic): 406.0317AlogP: 4.83#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: 4.63CX LogD: 4.63
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.66Np Likeness Score: -0.82

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