(N''-{[2-(2-adamantyl)-5-phenyl-1H-pyrrol-1-yl]acetyl}guanidine)

ID: ALA402330

Chembl Id: CHEMBL402330

PubChem CID: 16090342

Max Phase: Preclinical

Molecular Formula: C23H28N4O

Molecular Weight: 376.50

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  NC(N)=NC(=O)Cn1c(-c2ccccc2)ccc1C12CC3CC(CC(C3)C1)C2

Standard InChI:  InChI=1S/C23H28N4O/c24-22(25)26-21(28)14-27-19(18-4-2-1-3-5-18)6-7-20(27)23-11-15-8-16(12-23)10-17(9-15)13-23/h1-7,15-17H,8-14H2,(H4,24,25,26,28)

Standard InChI Key:  FJIMRIOSHHZOSF-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA402330

   N-[2-(2-adamantan-1-yl-5-phenyl-pyrrol-1-yl)-acetyl]-guanidine

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 376.50

Molecular Weight (Monoisotopic): 376.2263

AlogP: 3.42

#Rotatable Bonds: 4

Polar Surface Area: 86.40

Molecular Species: NEUTRAL

HBA: 2

HBD: 2

#RO5 Violations: ┄

HBA (Lipinski): 5

HBD (Lipinski): 4

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: ┄

CX Basic pKa: 8.31

CX LogP: 3.11

CX LogD: 2.19

Aromatic Rings: 2

Heavy Atoms: 28

QED Weighted: 0.63

Np Likeness Score: -0.40

References

1. Cole DC, Manas ES, Stock JR, Condon JS, Jennings LD, Aulabaugh A, Chopra R, Cowling R, Ellingboe JW, Fan KY, Harrison BL, Hu Y, Jacobsen S, Jin G, Lin L, Lovering FE, Malamas MS, Stahl ML, Strand J, Sukhdeo MN, Svenson K, Turner MJ, Wagner E, Wu J, Zhou P, Bard J..  (2006)  Acylguanidines as small-molecule beta-secretase inhibitors.,  49  (21): [PMID:17034121] [10.1021/jm0607451]

2. Jennings LD, Cole DC, Stock JR, Sukhdeo MN, Ellingboe JW, Cowling R, Jin G, Manas ES, Fan KY, Malamas MS, Harrison BL, Jacobsen S, Chopra R, Lohse PA, Moore WJ, O'Donnell MM, Hu Y, Robichaud AJ, Turner MJ, Wagner E, Bard J..  (2008)  Acylguanidine inhibitors of beta-secretase: optimization of the pyrrole ring substituents extending into the S1' substrate binding pocket.,  18  (2): [PMID:18068983] [10.1016/j.bmcl.2007.11.043]

Source

Source(1):

• Scientific Literature