(S)-N1-((2S,3S)-4-((R)-4-(tert-butylcarbamoyl)-5,5-dimethylthiazolidin-3-yl)-3-hydroxy-4-oxo-1-phenylbutan-2-yl)-2-(2-(naphthalen-1-yloxy)acetamido)succinamide

ID: ALA5280289

Max Phase: Preclinical

Molecular Formula: C36H45N5O7S

Molecular Weight: 691.85

Names and Identifiers

Canonical SMILES:  CC(C)(C)NC(=O)[C@H]1N(C(=O)[C@@H](O)[C@H](Cc2ccccc2)NC(=O)[C@H](CC(N)=O)NC(=O)COc2cccc3ccccc23)CSC1(C)C

Standard InChI:  InChI=1S/C36H45N5O7S/c1-35(2,3)40-33(46)31-36(4,5)49-21-41(31)34(47)30(44)25(18-22-12-7-6-8-13-22)39-32(45)26(19-28(37)42)38-29(43)20-48-27-17-11-15-23-14-9-10-16-24(23)27/h6-17,25-26,30-31,44H,18-21H2,1-5H3,(H2,37,42)(H,38,43)(H,39,45)(H,40,46)/t25-,26-,30-,31+/m0/s1

Standard InChI Key:  UFSMRNQSQSGJII-QYRZKEDASA-N

Molfile:  

 
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M  END

Alternative Forms

1. Parent:

   

   ALA5280289

   ---

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

Calculated Properties

Molecular Weight: 691.85

Molecular Weight (Monoisotopic): 691.3040

AlogP: 2.26

#Rotatable Bonds: 13

Polar Surface Area: 180.16

Molecular Species: NEUTRAL

HBA: 8

HBD: 5

#RO5 Violations: 1

HBA (Lipinski): 12

HBD (Lipinski): 6

#RO5 Violations (Lipinski): 3

CX Acidic pKa: 11.87

CX Basic pKa: ┄

CX LogP: 1.50

CX LogD: 1.50

Aromatic Rings: 3

Heavy Atoms: 49

QED Weighted: 0.18

Np Likeness Score: 0.03

References

1. Kashif Khan R, Meanwell NA, Hager HH..  (2022)  Pseudoprolines as stereoelectronically tunable proline isosteres.,  75  [PMID:36096342] [10.1016/j.bmcl.2022.128983]

Source

Source(1):

• Scientific Literature