ID: ALA4643621

Max Phase: Preclinical

Molecular Formula: C21H22N6O2S

Molecular Weight: 422.51

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(O)(C#Cc1ccc(N2CCOCC2)c(Nc2ccnc(N)n2)c1)c1nccs1

Standard InChI:  InChI=1S/C21H22N6O2S/c1-21(28,19-23-8-13-30-19)6-4-15-2-3-17(27-9-11-29-12-10-27)16(14-15)25-18-5-7-24-20(22)26-18/h2-3,5,7-8,13-14,28H,9-12H2,1H3,(H3,22,24,25,26)

Standard InChI Key:  VCUYMRXFDJRYRL-UHFFFAOYSA-N

Associated Targets(Human)

Mitogen-activated protein kinase kinase kinase 14 1412 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

J774 3120 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

Properties

Molecular Weight: 422.51Molecular Weight (Monoisotopic): 422.1525AlogP: 2.35#Rotatable Bonds: 4
Polar Surface Area: 109.42Molecular Species: NEUTRALHBA: 9HBD: 3
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.47CX Basic pKa: 6.54CX LogP: 2.63CX LogD: 2.58
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.55Np Likeness Score: -1.28

References

1. Zhu Y, Ma Y, Zu W, Song J, Wang H, Zhong Y, Li H, Zhang Y, Gao Q, Kong B, Xu J, Jiang F, Wang X, Li S, Liu C, Liu H, Lu T, Chen Y..  (2020)  Identification of N-Phenyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine Derivatives as Novel, Potent, and Selective NF-κB Inducing Kinase (NIK) Inhibitors for the Treatment of Psoriasis.,  63  (13): [PMID:32479083] [10.1021/acs.jmedchem.0c00055]

Source