2-Amino-4-(3-fluoro-4-methylthiophenyl)-4H-naphtho(1,2-b)pyran-3-carbonitrile

ID: ALA5187002

Chembl Id: CHEMBL5187002

PubChem CID: 168281076

Max Phase: Preclinical

Molecular Formula: C21H15FN2OS

Molecular Weight: 362.43

Associated Items:

Names and Identifiers

Canonical SMILES:  CSc1ccc(C2C(C#N)=C(N)Oc3c2ccc2ccccc32)cc1F

Standard InChI:  InChI=1S/C21H15FN2OS/c1-26-18-9-7-13(10-17(18)22)19-15-8-6-12-4-2-3-5-14(12)20(15)25-21(24)16(19)11-23/h2-10,19H,24H2,1H3

Standard InChI Key:  XJMQALOATOUFRV-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5187002

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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: 362.43Molecular Weight (Monoisotopic): 362.0889AlogP: 4.92#Rotatable Bonds: 2
Polar Surface Area: 59.04Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 1.68CX LogP: 4.79CX LogD: 4.79
Aromatic Rings: 3Heavy Atoms: 26QED Weighted: 0.66Np Likeness Score: -1.25

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