SID85268800

ID: ALA1603529

Cas Number: 953807-04-0

PubChem CID: 4832445

Max Phase: Preclinical

Molecular Formula: C13H23N5OS

Molecular Weight: 297.43

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  Cc1nnc(SCC(=O)NC2CCCC(C)C2C)n1N

Standard InChI:  InChI=1S/C13H23N5OS/c1-8-5-4-6-11(9(8)2)15-12(19)7-20-13-17-16-10(3)18(13)14/h8-9,11H,4-7,14H2,1-3H3,(H,15,19)

Standard InChI Key:  WHJAUBYNWWGLFF-UHFFFAOYSA-N

Molfile:  

     RDKit          2D

 20 21  0  0  0  0  0  0  0  0999 V2000
   -3.6853   -0.9026    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2563   -1.7276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4860    0.3304    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1534   -0.8257    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7055   -0.2126    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5419   -0.4901    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8729    0.8824    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3998   -0.4901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2930    0.5019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8274   -0.9026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1129   -0.4901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2563   -0.9026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9708   -0.4901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6015   -0.9026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8274   -1.7276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6285    1.2556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6015   -1.7276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1129   -2.1401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1129    0.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3160   -0.4901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  8  1  0
  1 13  1  0
  2 12  2  0
  3  7  1  0
  3  8  1  0
  3  9  1  0
  4  5  1  0
  4  8  2  0
  5  9  2  0
  6 10  1  0
  6 12  1  0
  9 16  1  0
 10 11  1  0
 10 15  1  0
 11 14  1  0
 11 19  1  0
 12 13  1  0
 14 17  1  0
 14 20  1  0
 15 18  1  0
 17 18  1  0
M  END

Associated Targets(Human)

L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KPNB1 Tbio Importin subunit beta-1/Snurportin-1 (25097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

rep Replicase polyprotein 1ab (11336 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: 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: 297.43Molecular Weight (Monoisotopic): 297.1623AlogP: 1.33#Rotatable Bonds: 4
Polar Surface Area: 85.83Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 2.07CX LogP: 0.40CX LogD: 0.40
Aromatic Rings: 1Heavy Atoms: 20QED Weighted: 0.65Np Likeness Score: -2.11

References

1. PubChem BioAssay data set, 
2. 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]
3. 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]