N-((S)-1-((S,E)-1-(benzylsulfonyl)-1-fluoro-5-phenylpent-1-en-3-ylamino)-1-oxo-3-p-tolylpropan-2-yl)-3,5-difluorobenzamide

ID: ALA4867613

PubChem CID: 164624605

Max Phase: Preclinical

Molecular Formula: C35H33F3N2O4S

Molecular Weight: 634.72

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  Cc1ccc(C[C@H](NC(=O)c2cc(F)cc(F)c2)C(=O)N[C@H](/C=C(\F)S(=O)(=O)Cc2ccccc2)CCc2ccccc2)cc1

Standard InChI:  InChI=1S/C35H33F3N2O4S/c1-24-12-14-26(15-13-24)18-32(40-34(41)28-19-29(36)21-30(37)20-28)35(42)39-31(17-16-25-8-4-2-5-9-25)22-33(38)45(43,44)23-27-10-6-3-7-11-27/h2-15,19-22,31-32H,16-18,23H2,1H3,(H,39,42)(H,40,41)/b33-22+/t31-,32-/m0/s1

Standard InChI Key:  JYMUZDQLWHGQRH-OYSXGLALSA-N

Molfile:  

 
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M  END

Alternative Forms

1. Parent:

   

   ALA4867613

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Unknown

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 634.72

Molecular Weight (Monoisotopic): 634.2113

AlogP: 6.16

#Rotatable Bonds: 13

Polar Surface Area: 92.34

Molecular Species: NEUTRAL

HBA: 4

HBD: 2

#RO5 Violations: 2

HBA (Lipinski): 6

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 2

CX Acidic pKa: 13.30

CX Basic pKa: ┄

CX LogP: 7.37

CX LogD: 7.37

Aromatic Rings: 4

Heavy Atoms: 45

QED Weighted: 0.18

Np Likeness Score: -0.48

References

1. Jung S, Fuchs N, Johe P, Wagner A, Diehl E, Yuliani T, Zimmer C, Barthels F, Zimmermann RA, Klein P, Waigel W, Meyr J, Opatz T, Tenzer S, Distler U, Räder HJ, Kersten C, Engels B, Hellmich UA, Klein J, Schirmeister T..  (2021)  Fluorovinylsulfones and -Sulfonates as Potent Covalent Reversible Inhibitors of the Trypanosomal Cysteine Protease Rhodesain: Structure-Activity Relationship, Inhibition Mechanism, Metabolism, and In Vivo Studies.,  64  (16.0): [PMID:34378914] [10.1021/acs.jmedchem.1c01002]

Source

Source(1):

• Scientific Literature