(R)-2-(3-(2-(3,4-dimethoxyphenyl)acetyl)guanidino)-N-(2-fluoro-3-(1H-tetrazol-5-yl)benzyl)-4-methylpentanamide

ID: ALA3321936

Chembl Id: CHEMBL3321936

PubChem CID: 118709831

Max Phase: Preclinical

Molecular Formula: C25H31FN8O4

Molecular Weight: 526.57

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  COc1ccc(CC(=O)NC(=N)N[C@H](CC(C)C)C(=O)NCc2cccc(-c3nnn[nH]3)c2F)cc1OC

Standard InChI:  InChI=1S/C25H31FN8O4/c1-14(2)10-18(24(36)28-13-16-6-5-7-17(22(16)26)23-31-33-34-32-23)29-25(27)30-21(35)12-15-8-9-19(37-3)20(11-15)38-4/h5-9,11,14,18H,10,12-13H2,1-4H3,(H,28,36)(H3,27,29,30,35)(H,31,32,33,34)/t18-/m1/s1

Standard InChI Key:  CVPVXVCBSKJOPK-GOSISDBHSA-N

Alternative Forms

1. Parent:

   

   ALA3321936

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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: 526.57

Molecular Weight (Monoisotopic): 526.2452

AlogP: 1.94

#Rotatable Bonds: 11

Polar Surface Area: 167.00

Molecular Species: ACID

HBA: 8

HBD: 5

#RO5 Violations: 1

HBA (Lipinski): 12

HBD (Lipinski): 5

#RO5 Violations (Lipinski): 2

CX Acidic pKa: 4.00

CX Basic pKa: 8.10

CX LogP: 1.42

CX LogD: 1.37

Aromatic Rings: 3

Heavy Atoms: 38

QED Weighted: 0.19

Np Likeness Score: -1.00

References

1. Grädler U, Czodrowski P, Tsaklakidis C, Klein M, Werkmann D, Lindemann S, Maskos K, Leuthner B..  (2014)  Structure-based optimization of non-peptidic Cathepsin D inhibitors.,  24  (17): [PMID:25086681] [10.1016/j.bmcl.2014.07.054]

Source

Source(1):

• Scientific Literature