N-((S)-1-((S,E)-1-fluoro-5-phenyl-1-(phenylsulfonyl)pent-1-en-3-ylamino)-1-oxo-3-phenylpropan-2-yl)-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxamide

ID: ALA4871417

PubChem CID: 164621156

Max Phase: Preclinical

Molecular Formula: C35H33FN2O6S

Molecular Weight: 628.72

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  O=C(N[C@@H](Cc1ccccc1)C(=O)N[C@H](/C=C(\F)S(=O)(=O)c1ccccc1)CCc1ccccc1)c1ccc2c(c1)OCCO2

Standard InChI:  InChI=1S/C35H33FN2O6S/c36-33(45(41,42)29-14-8-3-9-15-29)24-28(18-16-25-10-4-1-5-11-25)37-35(40)30(22-26-12-6-2-7-13-26)38-34(39)27-17-19-31-32(23-27)44-21-20-43-31/h1-15,17,19,23-24,28,30H,16,18,20-22H2,(H,37,40)(H,38,39)/b33-24+/t28-,30-/m0/s1

Standard InChI Key:  NPJYBJKLELDEDD-SARUODQOSA-N

Molfile:  

 
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M  END

Alternative Forms

1. Parent:

   

   ALA4871417

   ---

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: 628.72

Molecular Weight (Monoisotopic): 628.2043

AlogP: 5.20

#Rotatable Bonds: 12

Polar Surface Area: 110.80

Molecular Species: NEUTRAL

HBA: 6

HBD: 2

#RO5 Violations: 2

HBA (Lipinski): 8

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 2

CX Acidic pKa: 13.51

CX Basic pKa: ┄

CX LogP: 6.32

CX LogD: 6.32

Aromatic Rings: 4

Heavy Atoms: 45

QED Weighted: 0.22

Np Likeness Score: -0.39

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