ID: ALA340614

Max Phase: Preclinical

Molecular Formula: C36H74N4O7Si2

Molecular Weight: 731.18

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCC(C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](C)NC(=O)OC(C)(C)C)C(C)O[Si](C)(C)C(C)(C)C)C(C)C)C(N)=O

Standard InChI:  InChI=1S/C36H74N4O7Si2/c1-20-23(4)29(30(37)41)40-32(43)28(22(2)3)39-31(42)26(25(6)46-48(16,17)35(10,11)12)21-27(47-49(18,19)36(13,14)15)24(5)38-33(44)45-34(7,8)9/h22-29H,20-21H2,1-19H3,(H2,37,41)(H,38,44)(H,39,42)(H,40,43)/t23?,24-,25?,26+,27+,28-,29-/m0/s1

Standard InChI Key:  YOISDXAVGVRXOR-WMODMLNLSA-N

Associated Targets(Human)

Gamma-secretase subunit PEN-2 38 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: 731.18Molecular Weight (Monoisotopic): 730.5096AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

References

1. Nadin A, Owens AP, Castro JL, Harrison T, Shearman MS..  (2003)  Synthesis and gamma-secretase activity of APP substrate-based hydroxyethylene dipeptide isosteres.,  13  (1): [PMID:12467612] [10.1016/s0960-894x(02)00840-5]

Source