ID: ALA5190943

Max Phase: Preclinical

Molecular Formula: C13H13N5

Molecular Weight: 239.28

Associated Items:

Representations

Canonical SMILES:  CCc1ccc2ncn(-c3ccnc(N)n3)c2c1

Standard InChI:  InChI=1S/C13H13N5/c1-2-9-3-4-10-11(7-9)18(8-16-10)12-5-6-15-13(14)17-12/h3-8H,2H2,1H3,(H2,14,15,17)

Standard InChI Key:  GRNOVSIBVQFUCY-UHFFFAOYSA-N

Associated Targets(Human)

Mitogen-activated protein kinase kinase kinase 14 1412 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

Properties

Molecular Weight: 239.28Molecular Weight (Monoisotopic): 239.1171AlogP: 1.96#Rotatable Bonds: 2
Polar Surface Area: 69.62Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 5.99CX LogP: 2.62CX LogD: 2.60
Aromatic Rings: 3Heavy Atoms: 18QED Weighted: 0.74Np Likeness Score: -1.35

References

1. Al-Khawaldeh I, Al Yasiri MJ, Aldred GG, Basmadjian C, Bordoni C, Harnor SJ, Heptinstall AB, Hobson SJ, Jennings CE, Khalifa S, Lebraud H, Martin MP, Miller DC, Shrives HJ, de Souza JV, Stewart HL, Temple M, Thomas HD, Totobenazara J, Tucker JA, Tudhope SJ, Wang LZ, Bronowska AK, Cano C, Endicott JA, Golding BT, Hardcastle IR, Hickson I, Wedge SR, Willmore E, Noble MEM, Waring MJ..  (2021)  An Alkynylpyrimidine-Based Covalent Inhibitor That Targets a Unique Cysteine in NF-κB-Inducing Kinase.,  64  (14.0): [PMID:34212719] [10.1021/acs.jmedchem.0c01249]

Source