2-(((3S,4R)-4-((3,4-dichlorophenyl)sulfonyl)-1,1-dioxidotetrahydrothiophen-3-yl)amino)ethane-1-sulfonamide

ID: ALA5282987

Max Phase: Preclinical

Molecular Formula: C12H16Cl2N2O6S3

Molecular Weight: 451.38

Names and Identifiers

Canonical SMILES:  NS(=O)(=O)CCN[C@H]1CS(=O)(=O)C[C@@H]1S(=O)(=O)c1ccc(Cl)c(Cl)c1

Standard InChI:  InChI=1S/C12H16Cl2N2O6S3/c13-9-2-1-8(5-10(9)14)25(21,22)12-7-23(17,18)6-11(12)16-3-4-24(15,19)20/h1-2,5,11-12,16H,3-4,6-7H2,(H2,15,19,20)/t11-,12-/m0/s1

Standard InChI Key:  TZYOKZXGKCLYKY-RYUDHWBXSA-N

Molfile:  

 
     RDKit          2D

 25 26  0  0  0  0  0  0  0  0999 V2000
   -0.6729    0.2248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1520    0.2248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4021   -0.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2512   -1.0498    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9187   -0.5578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0852    0.9391    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9100    0.9391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3223    0.2248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1471    0.2248    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.5644    0.9391    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.3891    0.9391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8017    1.6532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6240    1.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0364    0.9380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6275    0.2265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8032    0.2218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8612    0.9380    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.0399   -0.4876    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.5644    1.7653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493    1.3522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6644   -1.7653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1602   -1.7653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5594   -0.4894    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1471    1.0511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8612    0.6387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  1  5  1  0
  5  4  1  0
  1  6  1  6
  6  7  1  0
  7  8  1  0
  8  9  1  0
  2 10  1  1
 10 11  1  0
 12 11  2  0
 13 12  1  0
 14 13  2  0
 15 14  1  0
 16 15  2  0
 11 16  1  0
 14 17  1  0
 15 18  1  0
 10 19  2  0
 10 20  2  0
  4 21  2  0
  4 22  2  0
  9 23  1  0
  9 24  2  0
  9 25  2  0
M  END

Alternative Forms

1. Parent:

   

   ALA5282987

   ---

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: 451.38

Molecular Weight (Monoisotopic): 449.9548

AlogP: -0.19

#Rotatable Bonds: 6

Polar Surface Area: 140.47

Molecular Species: NEUTRAL

HBA: 7

HBD: 2

#RO5 Violations: ┄

HBA (Lipinski): 8

HBD (Lipinski): 3

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: 11.50

CX Basic pKa: 5.87

CX LogP: -0.81

CX LogD: -0.83

Aromatic Rings: 1

Heavy Atoms: 25

QED Weighted: 0.61

Np Likeness Score: -1.67

References

1. Jo J, Kim J, Ibrahim L, Kumar M, Iaconelli J, Tran CS, Moon HR, Jung Y, Wiseman RL, Lairson LL, Chatterjee AK, Bollong MJ, Yun H..  (2023)  Optimization of 3-aminotetrahydrothiophene 1,1-dioxides with improved potency and efficacy as non-electrophilic antioxidant response element (ARE) activators.,  89  [PMID:37116763] [10.1016/j.bmcl.2023.129306]

Source

Source(1):

• Scientific Literature