(4aR,7aR)-7a-(5-Chlorothiophen-2-yl)-6-(4-ethyl-5-fluoro-6-methoxypyrimidin-2-yl)-2-imino-3-methylhexahydro-1H-pyrrolo[3,4-d]pyrimidin-4(4aH)-one

ID: ALA3797321

Chembl Id: CHEMBL3797321

PubChem CID: 44478997

Max Phase: Preclinical

Molecular Formula: C18H20ClFN6O2S

Molecular Weight: 438.92

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCc1nc(N2C[C@H]3C(=O)N(C)C(=N)N[C@@]3(c3ccc(Cl)s3)C2)nc(OC)c1F

Standard InChI:  InChI=1S/C18H20ClFN6O2S/c1-4-10-13(20)14(28-3)23-17(22-10)26-7-9-15(27)25(2)16(21)24-18(9,8-26)11-5-6-12(19)29-11/h5-6,9H,4,7-8H2,1-3H3,(H2,21,24)/t9-,18-/m0/s1

Standard InChI Key:  ZTDGQYJGQFFPJD-YYSFKGJASA-N

Associated Targets(Human)

BACE1 Tchem Beta-secretase 1 (15641 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

Calculated Properties

Molecular Weight: 438.92Molecular Weight (Monoisotopic): 438.1041AlogP: 2.23#Rotatable Bonds: 4
Polar Surface Area: 94.44Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 4.51CX LogP: 3.38CX LogD: 3.38
Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.76Np Likeness Score: -0.98

References

1. Mandal M, Wu Y, Misiaszek J, Li G, Buevich A, Caldwell JP, Liu X, Mazzola RD, Orth P, Strickland C, Voigt J, Wang H, Zhu Z, Chen X, Grzelak M, Hyde LA, Kuvelkar R, Leach PT, Terracina G, Zhang L, Zhang Q, Michener MS, Smith B, Cox K, Grotz D, Favreau L, Mitra K, Kazakevich I, McKittrick BA, Greenlee W, Kennedy ME, Parker EM, Cumming JN, Stamford AW..  (2016)  Structure-Based Design of an Iminoheterocyclic β-Site Amyloid Precursor Protein Cleaving Enzyme (BACE) Inhibitor that Lowers Central Aβ in Nonhuman Primates.,  59  (7): [PMID:26937601] [10.1021/acs.jmedchem.5b01995]

Source