Metropine

ID: ALA516476

Cas Number: 52-88-0

PubChem CID: 657381

Max Phase: Approved

Molecular Formula: C18H26N2O6

Molecular Weight: 304.41

Molecule Type: Small molecule

Names and Identifiers

Synonyms: 8-methylatropinium nitrate | Atropine methyl nitrate | Atropine methylnitrate | Methylatropine nitrate | N-methylatropine nitrate | NSC-759122 | METHYLATROPINE NITRATE|Atropine methonitrate|52-88-0|Ekomine|Atropine methyl nitrate|Eumydrin|Atropine methylnitrate|N-Methylatropine nitrate|8-Methylatropinium nitrate|Methylatropine nitrate [USAN]|Atropine methonitrate [INN]|MLS000028616|DTXSID0045543|Q48D9J47K2|NSC-759122|Pylostropin|SMR000058663|Methylatropine nitrate (USAN)|DTXCID8025543|HarvatrateShow More⌵

Trade Names(1): Eumydrin

Canonical SMILES:  C[N+]1(C)[C@@H]2CC[C@H]1C[C@@H](OC(=O)C(CO)c1ccccc1)C2.O=[N+]([O-])[O-]

Standard InChI:  InChI=1S/C18H26NO3.NO3/c1-19(2)14-8-9-15(19)11-16(10-14)22-18(21)17(12-20)13-6-4-3-5-7-13;2-1(3)4/h3-7,14-17,20H,8-12H2,1-2H3;/q+1;-1/t14-,15+,16+,17?;

Standard InChI Key:  NEDVJZNVOSNSHF-KUMOIWDRSA-N

Molfile:  

     RDKit          2D

 28 29  0  0  0  0  0  0  0  0999 V2000
    7.7730   -5.7423    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.4907   -5.3287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0598   -5.3287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7730   -6.6165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5603   -2.8735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6382   -3.6870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1187   -3.2503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1313   -3.2503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9873   -2.4257    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.5003   -2.8581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6036   -3.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2314   -3.5940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9000   -1.4332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3026   -3.2503    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9624   -2.1560    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8470   -4.4770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5583   -4.8873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2747   -4.4787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5564   -5.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9890   -4.8908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2767   -3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9892   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7038   -6.1281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4182   -5.7154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4180   -4.8903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7034   -4.4781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1904   -2.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9922   -3.2426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0
  3  1  1  0
  4  1  2  0
  6  7  1  0
  8 14  1  1
  7  8  1  0
  5 15  1  6
  8  9  1  0
  6 16  1  6
  9  5  1  0
 16 17  1  0
  5 10  1  0
 17 18  1  0
 10  6  1  0
 17 19  2  0
  8 11  1  0
 18 20  1  0
  5 12  1  0
 18 21  1  0
 11 12  1  0
  9 13  1  0
 20 22  1  0
 20 26  2  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
  9 27  1  0
 21 28  1  0
M  CHG  4   1   1   2  -1   3  -1   9   1
M  END

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 304.41

Molecular Weight (Monoisotopic): 304.1907

AlogP: 2.08

#Rotatable Bonds: 4

Polar Surface Area: 46.53

Molecular Species: NEUTRAL

HBA: 3

HBD: 1

#RO5 Violations: ┄

HBA (Lipinski): 4

HBD (Lipinski): 1

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: ┄

CX Basic pKa: ┄

CX LogP: -2.59

CX LogD: -2.59

Aromatic Rings: 1

Heavy Atoms: 22

QED Weighted: 0.68

Np Likeness Score: 0.87

References

1. Santana L, González-Díaz H, Quezada E, Uriarte E, Yáñez M, Viña D, Orallo F..  (2008)  Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors.,  51  (21): [PMID:18834112] [10.1021/jm800656v]

2. Diamandis P, Wildenhain J, Clarke ID, Sacher AG, Graham J, Bellows DS, Ling EK, Ward RJ, Jamieson LG, Tyers M, Dirks PB..  (2007)  Chemical genetics reveals a complex functional ground state of neural stem cells.,  3  (5): [PMID:17417631] [10.1038/nchembio873]

3. PubChem BioAssay data set, 

4. PubChem BioAssay data set, 

5. PubChem BioAssay data set, 

6. USP Dictionary of USAN and International Names (2010 edition) and USAN registrations 2007-date, 

7. Honda H, Tomizawa M, Casida JE..  (2007)  Insect muscarinic acetylcholine receptor: pharmacological and toxicological profiles of antagonists and agonists.,  55  (6): [PMID:17319687] [10.1021/jf0631934]

8. PubChem BioAssay data set, 

9. PubChem BioAssay data set, 

10. British National Formulary (72nd edition), 

11. 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]

12. 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]

13. 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]

Source

Source(5):

• Scientific Literature
• PubChem BioAssays
• USP Dictionary of USAN and International Drug Names
• British National Formulary
• SARS-CoV-2 Screening Data 2020-21