Ethanesulfonic acid (R)-((R)-6-cyano-3-hydroxy-2,2-dimethyl-chroman-4-yl)-methyl-amide

ID: ALA434045

Cas Number: 163163-23-3

PubChem CID: 121846

Product Number: C288018, Order Now?

Max Phase: Preclinical

Molecular Formula: C15H20N2O4S

Molecular Weight: 324.40

Molecule Type: Small molecule

Associated Items:

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Names and Identifiers

Canonical SMILES:  CCS(=O)(=O)N(C)[C@H]1c2cc(C#N)ccc2OC(C)(C)[C@@H]1O

Standard InChI:  InChI=1S/C15H20N2O4S/c1-5-22(19,20)17(4)13-11-8-10(9-16)6-7-12(11)21-15(2,3)14(13)18/h6-8,13-14,18H,5H2,1-4H3/t13-,14+/m0/s1

Standard InChI Key:  HVSJHHXUORMCGK-UONOGXRCSA-N

Molfile:  

     RDKit          2D

 22 23  0  0  1  0  0  0  0  0999 V2000
    3.2542   -3.6375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9750   -2.4000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.5417   -4.0542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2542   -2.8125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9750   -4.0542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9750   -4.8792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2542   -5.2917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5417   -4.8792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3208   -3.2292    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8292   -3.6417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9750   -1.5750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6875   -2.8125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4000   -3.6417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8292   -5.2917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1167   -4.0542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6875   -1.9792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6917   -3.6417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1167   -4.8792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9667   -5.7042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6875   -4.4667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5417   -2.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4042   -2.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  4  1  0
  3  1  1  0
  1  4  1  6
  5  1  1  0
  6  5  1  0
  7  6  1  0
  8  3  1  0
  9 13  3  0
 10  3  2  0
 11  2  2  0
 12  2  2  0
 13 15  1  0
 14  8  2  0
 15 10  1  0
 16  2  1  0
  5 17  1  1
 18 15  2  0
 19  6  1  0
 20  6  1  0
 21  4  1  0
 22 16  1  0
  7  8  1  0
 18 14  1  0
M  END

Alternative Forms

  1. Parent:

Associated Targets(Human)

KCNQ1 Tclin Voltage-gated potassium channel, IKs; KCNQ1(Kv7.1)/KCNE1(MinK) (185 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HDAC6 Tclin Histone deacetylase 6 (20808 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

KCNQ1 Voltage-gated potassium channel subunit Kv7.1 (54 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (11336 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 324.40Molecular Weight (Monoisotopic): 324.1144AlogP: 1.41#Rotatable Bonds: 3
Polar Surface Area: 90.63Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 13.23CX Basic pKa: CX LogP: 0.80CX LogD: 0.80
Aromatic Rings: 1Heavy Atoms: 22QED Weighted: 0.91Np Likeness Score: -0.31

References

1. Wermuth CG..  (2004)  Selective optimization of side activities: another way for drug discovery.,  47  (6): [PMID:14998318] [10.1021/jm030480f]
2. Gerlach U, Brendel J, Lang HJ, Paulus EF, Weidmann K, Brüggemann A, Busch AE, Suessbrich H, Bleich M, Greger R..  (2001)  Synthesis and activity of novel and selective I(Ks)-channel blockers.,  44  (23): [PMID:11689069] [10.1021/jm0109255]
3. Bernhard Ellinger, Denisa Bojkova, Andrea Zaliani, Jindrich Cinatl, Carsten Claussen, Sandra Westhaus, Jeanette Reinshagen, Maria Kuzikov, Markus Wolf, Gerd Geisslinger, Philip Gribbon, Sandra Ciesek.  (2020)  Identification of inhibitors of SARS-CoV-2 in-vitro cellular toxicity in human (Caco-2) cells using a large scale drug repurposing collection,  [10.21203/rs.3.rs-23951/v1]
4. Maria Kuzikov, Elisa Costanzi, Jeanette Reinshagen, Francesca Esposito, Laura Vangeel, Markus Wolf, Bernhard Ellinger, Carsten Claussen, Gerd Geisslinger, Angela Corona, Daniela Iaconis, Carmine Talarico, Candida Manelfi, Rolando Cannalire, Giulia Rossetti, Jonas Gossen, Simone Albani, Francesco Musiani, Katja Herzog, Yang Ye, Barbara Giabbai, Nicola Demitri, Dirk Jochmans, Steven De Jonghe, Jasper Rymenants, Vincenzo Summa, Enzo Tramontano, Andrea R. Beccari, Pieter Leyssen, Paola Storici, Johan Neyts, Philip Gribbon, and Andrea Zaliani.  (2020)  Identification of inhibitors of SARS-Cov2 M-Pro enzymatic activity using a small molecule repurposing screen,  [10.6019/CHEMBL4495564]
5. Andrea Zaliani, Laura Vangeel, Jeanette Reinshagen, Daniela Iaconis, Maria Kuzikov, Oliver Keminer, Markus Wolf, Bernhard Ellinger, Francesca Esposito, Angela Corona, Enzo Tramontano, Candida Manelfi, Katja Herzog, Dirk Jochmans, Steven De Jonghe, Winston Chiu, Thibault Francken, Joost Schepers, Caroline Collard, Kayvan Abbasi, Carsten Claussen , Vincenzo Summa, Andrea R. Beccari, Johan Neyts, Philip Gribbon and Pieter Leyssen.  (2020)  Cytopathic SARS-Cov2 screening on VERO-E6 cells in a large repurposing effort,  [10.6019/CHEMBL4495565]
6. Bernhard Ellinger, Justus Dick, Vanessa Lage-Rupprecht, Bruce Schultz, Andrea Zaliani, Marcin Namysl, Stephan Gebel, Ole Pless, Jeanette Reinshagen, Christian Ebeling, Alexander Esser, Marc Jacobs, Carsten Claussen, and Martin Hofmann-Apitius.  (2021)  HDAC6 screening dataset using tau-based substrate in an enzymatic assay yields selective inhibitors and activators,  [10.6019/CHEMBL4808148]