ID: ALA2151285

Max Phase: Preclinical

Molecular Formula: C17H18N6

Molecular Weight: 306.37

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(/N=N/c2c(=N)[nH]n3cc4c(nc23)CCCC4)cc1

Standard InChI:  InChI=1S/C17H18N6/c1-11-6-8-13(9-7-11)20-21-15-16(18)22-23-10-12-4-2-3-5-14(12)19-17(15)23/h6-10H,2-5H2,1H3,(H2,18,22)/b21-20+

Standard InChI Key:  BIOBOUAUSSZFBX-QZQOTICOSA-N

Associated Targets(Human)

c-Jun N-terminal kinase 2 4655 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MAP kinase p38 alpha 12866 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mitogen-activated protein kinase 1 40 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 306.37Molecular Weight (Monoisotopic): 306.1593AlogP: 3.74#Rotatable Bonds: 2
Polar Surface Area: 81.66Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.57CX Basic pKa: 6.92CX LogP: 3.02CX LogD: 3.06
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.69Np Likeness Score: -1.05

References

1. Kaoud TS, Yan C, Mitra S, Tseng CC, Jose J, Taliaferro JM, Tuohetahuntila M, Devkota A, Sammons R, Park J, Park H, Shi Y, Hong J, Ren P, Dalby KN..  (2012)  From in Silico Discovery to intra-Cellular Activity: Targeting JNK-Protein Interactions with Small Molecules.,  (9): [PMID:23002419] [10.1021/ml300129b]

Source