ID: ALA4779222

Max Phase: Preclinical

Molecular Formula: C30H38N6O3S

Molecular Weight: 562.74

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1cc(Nc2nc(Nc3ccccc3S(=O)(=O)C(C)C)c3cc[nH]c3n2)c(OC(C)C)cc1C1CCNCC1

Standard InChI:  InChI=1S/C30H38N6O3S/c1-18(2)39-26-17-23(21-10-13-31-14-11-21)20(5)16-25(26)34-30-35-28-22(12-15-32-28)29(36-30)33-24-8-6-7-9-27(24)40(37,38)19(3)4/h6-9,12,15-19,21,31H,10-11,13-14H2,1-5H3,(H3,32,33,34,35,36)

Standard InChI Key:  CTZVCMKQQAGWBA-UHFFFAOYSA-N

Associated Targets(Human)

NPM/ALK (Nucleophosmin/ALK tyrosine kinase receptor) 119 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Insulin receptor 5558 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cytochrome P450 3A4 53859 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HERG 29587 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

BaF3 4657 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: 562.74Molecular Weight (Monoisotopic): 562.2726AlogP: 6.19#Rotatable Bonds: 9
Polar Surface Area: 121.03Molecular Species: BASEHBA: 8HBD: 4
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.66CX Basic pKa: 10.02CX LogP: 5.82CX LogD: 3.24
Aromatic Rings: 4Heavy Atoms: 40QED Weighted: 0.19Np Likeness Score: -1.03

References

1. Michellys PY,Chen B,Jiang T,Jin Y,Lu W,Marsilje TH,Pei W,Uno T,Zhu X,Wu B,Nguyen TN,Bursulaya B,Lee C,Li N,Kim S,Tuntland T,Liu B,Sun F,Steffy A,Hood T.  (2016)  Design and synthesis of novel selective anaplastic lymphoma kinase inhibitors.,  26  (3.0): [PMID:26750252] [10.1016/j.bmcl.2015.11.049]

Source