2-methyl-7,8-dihydro-1H-thiopyrano[4,3-d]pyrimidin-4(5H)-one

ID: ALA483348

Cas Number: 284028-90-6

PubChem CID: 135522417

Product Number: T120464, Order Now?

Max Phase: Preclinical

Molecular Formula: C8H10N2OS

Molecular Weight: 182.25

Molecule Type: Small molecule

In stock!

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1nc2c(c(=O)[nH]1)CSCC2

Standard InChI:  InChI=1S/C8H10N2OS/c1-5-9-7-2-3-12-4-6(7)8(11)10-5/h2-4H2,1H3,(H,9,10,11)

Standard InChI Key:  HRYKZAKEAVZGJD-UHFFFAOYSA-N

Molfile:  

     RDKit          2D

 12 13  0  0  0  0  0  0  0  0999 V2000
   -1.7507   -0.8712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0362   -0.4587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3217   -0.8713    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3928   -0.4588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1072   -0.8713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8217   -0.4587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8217    0.3663    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.1072    0.7788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3928    0.3662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3217    0.7787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3217    1.6037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0362    0.3663    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2 12  1  0
  4  3  1  0
  5  4  1  0
  4  9  2  0
  6  5  1  0
  6  7  1  0
  8  7  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
M  END

Associated Targets(Human)

PARP3 Tclin Poly [ADP-ribose] polymerase 3 (206 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PARP1 Tclin Poly [ADP-ribose] polymerase-1 (6206 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PARP15 Tchem Poly [ADP-ribose] polymerase 15 (178 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PARP14 Tchem Poly [ADP-ribose] polymerase 14 (380 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)

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: 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: 182.25Molecular Weight (Monoisotopic): 182.0514AlogP: 0.87#Rotatable Bonds:
Polar Surface Area: 45.75Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 8.21CX Basic pKa: 2.27CX LogP: -0.13CX LogD: -0.18
Aromatic Rings: 1Heavy Atoms: 12QED Weighted: 0.65Np Likeness Score: -1.65

References

1. Lehtiö L, Jemth AS, Collins R, Loseva O, Johansson A, Markova N, Hammarström M, Flores A, Holmberg-Schiavone L, Weigelt J, Helleday T, Schüler H, Karlberg T..  (2009)  Structural basis for inhibitor specificity in human poly(ADP-ribose) polymerase-3.,  52  (9): [PMID:19354255] [10.1021/jm900052j]
2. 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]
3. 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]
4. 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]
5.  (2018)  An elisa-like assay for quantifying enzymatic activities of mono-adp-ribosyltransferases, 
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]