Nemorubicin

ID: ALA5314361

Max Phase: Phase

Molecular Formula: C32H37NO13

Molecular Weight: 643.64

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@@H]1C[C@H](N2CCO[C@H](OC)C2)[C@H](O)[C@H](C)O1

Standard InChI:  InChI=1S/C32H37NO13/c1-14-27(36)17(33-7-8-44-22(12-33)43-3)9-21(45-14)46-19-11-32(41,20(35)13-34)10-16-24(19)31(40)26-25(29(16)38)28(37)15-5-4-6-18(42-2)23(15)30(26)39/h4-6,14,17,19,21-22,27,34,36,38,40-41H,7-13H2,1-3H3/t14-,17-,19-,21+,22-,27+,32-/m0/s1

Standard InChI Key:  CTMCWCONSULRHO-GCKWGGDNSA-N

Molfile:  

     RDKit          2D

 46 51  0  0  1  0  0  0  0  0999 V2000
   -1.5450    1.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5450    0.9152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2606    0.5048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2606    2.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1137    0.9152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1242    1.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9798    0.9082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8293    2.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8293    0.5048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9763    1.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0347   -1.9505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3141    1.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0137   -2.7714    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6020    0.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5984    2.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7471   -1.5345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3141   -0.7166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3182   -1.5416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0265   -0.3006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3071    0.9188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7430   -0.7095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6766    2.4877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6020   -0.3167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2945   -3.1608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2642    2.9780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2606   -0.3202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6919    0.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2770   -3.9887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9821   -4.4097    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2112    3.1689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8293    2.9780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8186   -0.3202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1368    1.6855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4558   -1.9449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7188   -3.1924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6919    2.1501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6942   -4.0098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6919   -0.3272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5578   -4.3816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4997    2.5443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8985    3.2665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4587   -0.2955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4181    1.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4006    0.9082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4022   -0.7469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5578   -5.2131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0
  3  2  1  0
  4  1  1  0
  5  6  2  0
  6  8  1  0
  7 10  1  0
  8  1  2  0
  9  2  2  0
 10  4  1  0
 11 18  1  0
 12 15  1  0
 11 13  1  1
 14  5  1  0
 15  6  1  0
 16 21  1  0
 17 23  1  1
 18 17  1  0
 19 17  1  0
 20 12  1  0
 21 19  1  0
 22 12  1  0
 14 23  1  6
 24 13  1  0
 25  4  2  0
 26  3  2  0
 27  7  2  0
 28 24  1  0
 29 37  1  0
 30 22  2  0
 31  8  1  0
 32  9  1  0
 12 33  1  6
 16 34  1  1
 35 13  1  0
 36 10  2  0
 37 35  1  0
 38 27  1  0
 28 39  1  6
 40 22  1  0
 41 40  1  0
 21 42  1  1
 43 36  1  0
 44 43  2  0
 45 38  1  0
 46 39  1  0
  9  5  1  0
  3  7  1  0
 20 14  1  0
 44 27  1  0
 11 16  1  0
 28 29  1  0
M  END

Alternative Forms

  1. Parent:

    ALA5314361

    NEMORUBICIN

Associated Targets(Human)

HeLa (62764 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: YesOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: YesAvailability: 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: 643.64Molecular Weight (Monoisotopic): 643.2265AlogP: 0.35#Rotatable Bonds: 7
Polar Surface Area: 201.75Molecular Species: NEUTRALHBA: 14HBD: 5
#RO5 Violations: 2HBA (Lipinski): 14HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: 8.02CX Basic pKa: 5.47CX LogP: 2.38CX LogD: 2.28
Aromatic Rings: 2Heavy Atoms: 46QED Weighted: 0.22Np Likeness Score: 1.53

References

1. Mazzini S, Scaglioni L, Animati F, Mondelli R..  (2010)  Interaction between double helix DNA fragments and the new antitumor agent sabarubicin, Men10755.,  18  (4): [PMID:20116264] [10.1016/j.bmc.2010.01.012]
2. USP Dictionary of USAN and International Names (2010 edition) and USAN registrations 2007-date, 
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. Coban, Tomris, Robertson, Cameron, Schwikkard, Sianne, Singer, Richard, LeGresley, Adam.  (2021)  Synthesis and evaluation of bis(imino)anthracene derivatives as G-quadruplex ligands,  12  (5.0): [PMID:34124673] [10.1039/d0md00428f]
7. 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]