NP-MRD: Showing NP-Card for glycopyrrolate (NP0144223)

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Record Information

Version

2.0

Created at

2022-09-01 23:07:28 UTC

Updated at

2022-09-01 23:07:28 UTC

NP-MRD ID

NP0144223

Secondary Accession Numbers

None

Natural Product Identification

Common Name

glycopyrrolate

Description

Glycopyrrolate belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene. Glycopyrrolate is an extremely weak basic (essentially neutral) compound (based on its pKa). Like other anticholinergic (antimuscarinic) agents, it inhibits the action of acetylcholine on structures innervated by postganglionic cholinergic nerves and on smooth muscles that respond to acetylcholine but lack cholinergic innervation. These peripheral cholinergic receptors are present in the autonomic effector cells of smooth muscle, cardiac muscle, the sinoatrial node, the atrioventricular node, exocrine glands and, to a limited degree, in the autonomic ganglia. Thus, it diminishes the volume and free acidity of gastric secretions and controls excessive pharyngeal, tracheal, and bronchial secretions. It is a synthetic anticholinergic agent with a quaternary ammonium structure. A muscarinic competitive antagonist used as an antispasmodic, in some disorders of the gastrointestinal tract, and to reduce salivation with some anesthetics. Glycopyrrolate binds competitively to the muscarinic acetylcholine receptor. glycopyrrolate is found in Rhizoglyphus robini. glycopyrrolate was first documented in 1993 (PMID: 8249551). Glycopyrrolate is only found in individuals that have used or taken this drug.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
    5.2837   -0.6040   -0.2480 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0157    0.0323   -0.6102 N   0  0  0  0  0  4  0  0  0  0  0  0
    4.3190    1.2886   -1.2816 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2966   -0.7896   -1.5561 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5345   -1.7235   -0.6114 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9954   -0.7115    0.3944 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8800   -0.0191   -0.1350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3374   -0.0823    0.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3781   -0.7650    1.5869 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5592    0.5906    0.0807 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1800    1.2877   -1.1043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1298    1.5563    1.0458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5391    2.7996    0.6058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0826    3.7470    1.4525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2283    3.4557    2.7891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8234    2.2111    3.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2806    1.2759    2.3854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5504   -0.4280   -0.3817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0250   -1.2625   -1.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8930   -2.5135   -1.5160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7935   -2.3891   -0.2885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9040   -1.4933    0.5957 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1862    0.2134    0.5404 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1120   -1.2098    0.6688 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0853    0.1178   -0.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5965   -1.3108   -1.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8264    1.0228   -2.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9978    1.9225   -0.6908 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809    1.8095   -1.5426 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9440   -1.3473   -2.2351 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5265   -0.1738   -2.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2187   -2.4003   -0.0968 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7426   -2.1909   -1.1954 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7480   -1.2478    1.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7479    0.6892   -1.7352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4419    3.0687   -0.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4028    4.7295    1.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6504    4.1727    3.4849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9382    1.9802    4.3097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9913    0.3299    2.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4954    0.0244   -0.7551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9713   -1.5746   -1.3823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1114   -0.7191   -2.4943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2717   -3.4325   -1.3918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4635   -2.5229   -2.4542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7116   -1.8397   -0.5621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9589   -3.3449    0.2055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4127   -1.1686    1.4965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0677   -2.1614    0.8823 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9053    1.2531    0.7474 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7463   -0.1527    1.4413 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6 23  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  6
 10 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 23  2  1  0
 22 18  1  0
 17 12  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  6 34  1  1
 23 50  1  0
 23 51  1  0
 11 35  1  0
 18 41  1  0
 19 42  1  0
 19 43  1  0
 20 44  1  0
 20 45  1  0
 21 46  1  0
 21 47  1  0
 22 48  1  0
 22 49  1  0
 13 36  1  0
 14 37  1  0
 15 38  1  0
 16 39  1  0
 17 40  1  0
M  CHG  1   2   1
M  END

986
  Mrv0541 02231215092D          

 23 25  0  0  1  0            999 V2000
    3.9683    0.9047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9058    0.1902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9683   -0.5242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0629    1.3172    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    5.2783    1.5722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7934    0.9047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0629    0.4922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7308    1.0153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2783    0.2373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7308    0.1902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0634    1.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3982    1.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3183    2.2848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1433    2.2848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8879    1.3172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3179    2.1019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5558    0.1902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7308   -0.6348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4453   -1.0473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0163   -1.0473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4453   -1.8723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0163   -1.8723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7308   -2.2848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  6  1  0  0  0  0
  1 17  1  0  0  0  0
  2 10  1  0  0  0  0
  3 17  2  0  0  0  0
  4  5  1  0  0  0  0
  4  7  1  0  0  0  0
  4 15  1  0  0  0  0
  4 16  1  0  0  0  0
  5  6  1  0  0  0  0
  6  9  1  0  0  0  0
  7  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
  8 12  1  0  0  0  0
 10 17  1  0  0  0  0
 10 18  1  0  0  0  0
 11 13  1  0  0  0  0
 12 14  1  0  0  0  0
 13 14  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 19 21  1  0  0  0  0
 20 22  2  0  0  0  0
 21 23  2  0  0  0  0
 22 23  1  0  0  0  0
M  CHG  1   4   1
M  END
> <DATABASE_ID>
NP0144223

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[N+]1(C)CCC(C1)OC(=O)C(O)(C1CCCC1)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H28NO3/c1-20(2)13-12-17(14-20)23-18(21)19(22,16-10-6-7-11-16)15-8-4-3-5-9-15/h3-5,8-9,16-17,22H,6-7,10-14H2,1-2H3/q+1

> <INCHI_KEY>
ANGKOCUUWGHLCE-UHFFFAOYSA-N

> <FORMULA>
C19H28NO3

> <MOLECULAR_WEIGHT>
318.4305

> <EXACT_MASS>
318.206918767

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
35.879872537584205

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[(2-cyclopentyl-2-hydroxy-2-phenylacetyl)oxy]-1,1-dimethylpyrrolidin-1-ium

> <ALOGPS_LOGP>
-1.20

> <JCHEM_LOGP>
-1.4080879931384127

> <ALOGPS_LOGS>
-5.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.533272276219833

> <JCHEM_PKA_STRONGEST_BASIC>
-4.315146706381445

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
101.0809

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.44e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
glycopyrrolate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: 986                                               
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0       7.407   1.689   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0       3.557   0.355   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0       7.407  -0.979   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0      11.317   2.459   0.000  0.00  0.00           N+1
HETATM    5  C   UNK     0       9.853   2.935   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.948   1.689   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.317   0.919   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.097   1.895   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.853   0.443   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.097   0.355   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.852   2.800   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.343   2.800   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.327   4.265   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.867   4.265   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.857   2.459   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.793   3.924   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.637   0.355   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.097  -1.185   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.431  -1.955   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.764  -1.955   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.431  -3.495   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.764  -3.495   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.097  -4.265   0.000  0.00  0.00           C+0
CONECT    1    6   17                                                       
CONECT    2   10                                                            
CONECT    3   17                                                            
CONECT    4    5    7   15   16                                             
CONECT    5    4    6                                                       
CONECT    6    1    5    9                                                  
CONECT    7    4    9                                                       
CONECT    8   10   11   12                                                  
CONECT    9    6    7                                                       
CONECT   10    2    8   17   18                                             
CONECT   11    8   13                                                       
CONECT   12    8   14                                                       
CONECT   13   11   14                                                       
CONECT   14   12   13                                                       
CONECT   15    4                                                            
CONECT   16    4                                                            
CONECT   17    1    3   10                                                  
CONECT   18   10   19   20                                                  
CONECT   19   18   21                                                       
CONECT   20   18   22                                                       
CONECT   21   19   23                                                       
CONECT   22   20   23                                                       
CONECT   23   21   22                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Value	Source
Glycopyrrolic acid	Generator
Glycopyrronium bromide	HMDB
Bromide, glycopyrronium	MeSH
Glycopyrrolate	MeSH
NVA-237	MeSH
NVA 237	MeSH
Pyrrolidinium, 3-((cyclopentylhydroxyphenylacetyl)oxy)-1,1-dimethyl-, bromide	MeSH

Chemical Formula

C₁₉H₂₈NO₃

Average Mass

318.4305 Da

Monoisotopic Mass

318.20692 Da

IUPAC Name

3-[(2-cyclopentyl-2-hydroxy-2-phenylacetyl)oxy]-1,1-dimethylpyrrolidin-1-ium

Traditional Name

glycopyrrolate

CAS Registry Number

Not Available

SMILES

C[N+]1(C)CCC(C1)OC(=O)C(O)(C1CCCC1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C19H28NO3/c1-20(2)13-12-17(14-20)23-18(21)19(22,16-10-6-7-11-16)15-8-4-3-5-9-15/h3-5,8-9,16-17,22H,6-7,10-14H2,1-2H3/q+1

InChI Key

ANGKOCUUWGHLCE-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Rhizoglyphus robini	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Not Available

Direct Parent

Benzene and substituted derivatives

Alternative Parents

Substituents

Monocyclic benzene moiety
N-alkylpyrrolidine
Pyrrolidine
Quaternary ammonium salt
Tertiary alcohol
Tetraalkylammonium salt
Carboxylic acid ester
Organoheterocyclic compound
Azacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organic salt
Amine
Aromatic alcohol
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic nitrogen compound
Organic cation
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-1.2	ALOGPS
logP	-1.4	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	11.53	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	101.08 m³·mol⁻¹	ChemAxon
Polarizability	35.88 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0015121

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

3374

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Glycopyrronium bromide

METLIN ID

Not Available

PubChem Compound

3494

PDB ID

Not Available

ChEBI ID

775286

Good Scents ID

Not Available

References

General References

Ali-Melkkila T, Kanto J, Iisalo E: Pharmacokinetics and related pharmacodynamics of anticholinergic drugs. Acta Anaesthesiol Scand. 1993 Oct;37(7):633-42. doi: 10.1111/j.1399-6576.1993.tb03780.x. [PubMed:8249551 ]
LOTUS database [Link]

Showing NP-Card for glycopyrrolate (NP0144223)

MOL for NP0144223 (glycopyrrolate)

3D MOL for NP0144223 (glycopyrrolate)

3D SDF for NP0144223 (glycopyrrolate)

3D-SDF for NP0144223 (glycopyrrolate)

PDB for NP0144223 (glycopyrrolate)

3D PDB for NP0144223 (glycopyrrolate)

SMILES for NP0144223 (glycopyrrolate)

INCHI for NP0144223 (glycopyrrolate)

Structure for NP0144223 (glycopyrrolate)

3D Structure for NP0144223 (glycopyrrolate)