ID: ALA4470066

Max Phase: Preclinical

Molecular Formula: C16H20N6OS

Molecular Weight: 344.44

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(C)c1nc(N2CCOC[C@H]2C)c2nc(-c3cc[nH]n3)sc2n1

Standard InChI:  InChI=1S/C16H20N6OS/c1-9(2)13-19-14(22-6-7-23-8-10(22)3)12-16(20-13)24-15(18-12)11-4-5-17-21-11/h4-5,9-10H,6-8H2,1-3H3,(H,17,21)/t10-/m1/s1

Standard InChI Key:  BLXNMTGPAKSAQI-SNVBAGLBSA-N

Associated Targets(Human)

Cytochrome P450 3A4 53859 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Serine/threonine-protein kinase mTOR 114 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: 344.44Molecular Weight (Monoisotopic): 344.1419AlogP: 2.82#Rotatable Bonds: 3
Polar Surface Area: 79.82Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.61CX Basic pKa: 2.90CX LogP: 3.88CX LogD: 3.88
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.79Np Likeness Score: -1.54

References

1. Bonazzi S, Goold CP, Gray A, Thomsen NM, Nunez J, Karki RG, Gorde A, Biag JD, Malik HA, Sun Y, Liang G, Lubicka D, Salas S, Labbe-Giguere N, Keaney EP, McTighe S, Liu S, Deng L, Piizzi G, Lombardo F, Burdette D, Dodart JC, Wilson CJ, Peukert S, Curtis D, Hamann LG, Murphy LO..  (2020)  Discovery of a Brain-Penetrant ATP-Competitive Inhibitor of the Mechanistic Target of Rapamycin (mTOR) for CNS Disorders.,  63  (3): [PMID:31955578] [10.1021/acs.jmedchem.9b01398]

Source