ID: ALA5209185

Max Phase: Preclinical

Molecular Formula: C27H28N2O4S

Molecular Weight: 476.60

Representations

Canonical SMILES:  CC(=O)NCc1ccccc1C(=O)N[C@H](/C=C/S(=O)(=O)c1ccccc1)CCc1ccccc1

Standard InChI:  InChI=1S/C27H28N2O4S/c1-21(30)28-20-23-12-8-9-15-26(23)27(31)29-24(17-16-22-10-4-2-5-11-22)18-19-34(32,33)25-13-6-3-7-14-25/h2-15,18-19,24H,16-17,20H2,1H3,(H,28,30)(H,29,31)/b19-18+/t24-/m0/s1

Standard InChI Key:  OZFMVBBSYMTNPH-QYNZQUMISA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type:

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Properties

Molecular Weight: 476.60

Molecular Weight (Monoisotopic): 476.1770

AlogP: 4.04

#Rotatable Bonds: 10

Polar Surface Area: 92.34

Molecular Species: NEUTRAL

HBA: 4

HBD: 2

#RO5 Violations: 0

HBA (Lipinski): 6

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 0

CX Acidic pKa:

CX Basic pKa:

CX LogP: 3.68

CX LogD: 3.68

Aromatic Rings: 3

Heavy Atoms: 34

QED Weighted: 0.46

Np Likeness Score: -0.52

References

1. Jung S, Fuchs N, Grathwol C, Hellmich UA, Wagner A, Diehl E, Willmes T, Sotriffer C, Schirmeister T..  (2022)  New peptidomimetic rhodesain inhibitors with improved selectivity towards human cathepsins.,  238  [PMID:35597010] [10.1016/j.ejmech.2022.114460]

Source

Source(1):

• Scientific Literature