NP-MRD: Showing NP-Card for Galantamine hydrobromide (NP0138829)

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Record Information

Version

1.0

Created at

2022-06-29 19:19:02 UTC

Updated at

2022-06-29 19:19:02 UTC

NP-MRD ID

NP0138829

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Galantamine hydrobromide

Description

(1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]Heptadeca-6(17),7,9,15-tetraen-14-ol hydrobromide, also known as razadyne or reminyl, belongs to the class of organic compounds known as galanthamine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids with a structure characterized a tetracyclic skeleton with two ortho aromatic protons in ring A (1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]Heptadeca-6(17),7,9,15-tetraen-14-ol hydrobromide is a drug (1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]Heptadeca-6(17),7,9,15-tetraen-14-ol hydrobromide is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 46  0  0  0  0  0  0  0  0999 V2000
    0.7662    0.0000    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -3.4268   -4.1438   -0.1520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1872   -3.5174   -0.0337 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0165   -2.1335   -0.0638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0658   -1.2516   -0.2145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8390    0.1222   -0.2379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5659    0.6349   -0.1117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5405   -0.2719    0.0372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7198   -1.6347    0.0656 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5160   -2.2938    0.2297 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4313   -1.3247    0.7458 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8005   -1.7263    0.3592 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6276   -0.6020   -0.2226 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7696   -1.1976   -0.7812 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8310    0.0796   -1.3010 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5489    0.3564   -1.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9423   -0.0139    0.1937 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0666    1.1206    1.1572 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6874    2.3942    0.4401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6848    2.7716    0.6671 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7843    4.2040    0.3767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6216    2.1012   -0.1711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7662    0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2312   -5.1942   -0.5025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8945   -4.1778    0.8602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0937   -3.6170   -0.8558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0732   -1.6503   -0.3147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6913    0.7876   -0.3585 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2506   -1.3033    1.8398 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3429   -2.0443    1.2976 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7908   -2.6024   -0.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9925    0.1000    0.5437 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5982   -1.5507   -1.6880 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2966    0.3460   -2.2451 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9532    0.8555   -1.8872 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3832    1.0052    2.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1070    1.1700    1.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2989    3.2020    0.9460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9361    2.4255   -0.6175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7700    4.5270    0.7727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0206    4.7896    0.8933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8090    4.3869   -0.7255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4984    2.3837   -1.2575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6372    2.4873    0.1008 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 17 16  1  6
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9  4  1  0
  4  3  1  0
  3  2  1  0
  4  5  2  0
  5  6  1  0
 17 11  1  0
  8 17  1  0
 10 11  1  0
  6  7  2  0
  1 23  1  0
 11 29  1  1
 12 30  1  0
 12 31  1  0
 13 32  1  1
 14 33  1  0
 15 34  1  0
 16 35  1  0
 18 36  1  0
 18 37  1  0
 19 38  1  0
 19 39  1  0
 21 40  1  0
 21 41  1  0
 21 42  1  0
 22 43  1  0
 22 44  1  0
  2 24  1  0
  2 25  1  0
  2 26  1  0
  5 27  1  0
  6 28  1  0
M  END


  Mrv0541 08221314192D          

 24 26  0  0  1  0            999 V2000
    0.6262   -2.9295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763    2.3488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8766   -0.4453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1298    0.3399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6664   -0.4530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8590   -0.6228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2917   -0.8681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2546   -1.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3723    0.9453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9798   -1.4613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0324   -0.6506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9230    0.3310    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5765    0.9518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5650    0.7756    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5167   -0.0067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7699    0.7785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3083   -0.0085    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4676   -2.1199    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7304    0.5008    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8297    1.7369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1014    1.2619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3691    0.0000    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -2.4737   -0.2833    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7383    1.5822    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  2  0  0  0  0
  6  5  2  0  0  0  0
  8  7  1  0  0  0  0
 11  3  1  0  0  0  0
 11 10  1  0  0  0  0
 12  5  1  0  0  0  0
 12  9  1  0  0  0  0
 13  4  1  0  0  0  0
 14  9  1  0  0  0  0
 15 11  2  0  0  0  0
 16 13  2  0  0  0  0
 16 15  1  0  0  0  0
 17  6  1  0  0  0  0
 17  7  1  0  0  0  0
 17 14  1  0  0  0  0
 17 15  1  6  0  0  0
 18  1  1  0  0  0  0
 18  8  1  0  0  0  0
 18 10  1  0  0  0  0
 12 19  1  6  0  0  0
 20  2  1  0  0  0  0
 20 13  1  0  0  0  0
 21 14  1  0  0  0  0
 21 16  1  0  0  0  0
 12 23  1  1  0  0  0
 14 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0138829

> <DATABASE_NAME>
NP-MRD

> <SMILES>
Br.[H][C@]12C[C@@]([H])(O)C=C[C@]11CCN(C)CC3=C1C(O2)=C(OC)C=C3

> <INCHI_IDENTIFIER>
InChI=1S/C17H21NO3.BrH/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17;/h3-6,12,14,19H,7-10H2,1-2H3;1H/t12-,14-,17-;/m0./s1

> <INCHI_KEY>
QORVDGQLPPAFRS-XPSHAMGMSA-N

> <FORMULA>
C17H22BrNO3

> <MOLECULAR_WEIGHT>
368.265

> <EXACT_MASS>
367.078306222

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
31.42318522209436

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6(17),7,9,15-tetraen-14-ol hydrobromide

> <ALOGPS_LOGP>
1.39

> <JCHEM_LOGP>
1.163042803666667

> <ALOGPS_LOGS>
-2.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.810376678600381

> <JCHEM_PKA_STRONGEST_BASIC>
8.90951741506554

> <JCHEM_POLAR_SURFACE_AREA>
41.93000000000001

> <JCHEM_REFRACTIVITY>
82.30490000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.70e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
galantamine hydrobromide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 22-AUG-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-AUG-13         0                                  
HETATM    1  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   19  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   22 Br   UNK     0       0.000   0.000   0.000  0.00  0.00          Br+0
HETATM   23  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   24  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
CONECT    1   18                                                            
CONECT    2   20                                                            
CONECT    3    4   11                                                       
CONECT    4    3   13                                                       
CONECT    5    6   12                                                       
CONECT    6    5   17                                                       
CONECT    7    8   17                                                       
CONECT    8    7   18                                                       
CONECT    9   12   14                                                       
CONECT   10   11   18                                                       
CONECT   11    3   10   15                                                  
CONECT   12    5    9   19   23                                             
CONECT   13    4   16   20                                                  
CONECT   14    9   17   21   24                                             
CONECT   15   11   16   17                                                  
CONECT   16   13   15   21                                                  
CONECT   17    6    7   14   15                                             
CONECT   18    1    8   10                                                  
CONECT   19   12                                                            
CONECT   20    2   13                                                       
CONECT   21   14   16                                                       
CONECT   23   12                                                            
CONECT   24   14                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
Razadyne	Kegg
Reminyl	Kegg
ortho-McNeil neurologics brand OF galantamine	MeSH
Galantamine	MeSH
ortho McNeil neurologics brand OF galantamine	MeSH
Galanthamine	MeSH
Lycoremine	MeSH
Nivalin	MeSH
Nivaline	MeSH
Galantamin	MeSH

Chemical Formula

C₁₇H₂₂BrNO₃

Average Mass

368.2650 Da

Monoisotopic Mass

367.07831 Da

IUPAC Name

(1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.0¹,¹².0⁶,¹⁷]heptadeca-6(17),7,9,15-tetraen-14-ol hydrobromide

Traditional Name

galantamine hydrobromide

CAS Registry Number

1953-04-4

SMILES

Br.[H][C@]12C[C@@]([H])(O)C=C[C@]11CCN(C)CC3=C1C(O2)=C(OC)C=C3

InChI Identifier

InChI=1S/C17H21NO3.BrH/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17;/h3-6,12,14,19H,7-10H2,1-2H3;1H/t12-,14-,17-;/m0./s1

InChI Key

QORVDGQLPPAFRS-XPSHAMGMSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as galanthamine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids with a structure characterized a tetracyclic skeleton with two ortho aromatic protons in ring A.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Amaryllidaceae alkaloids

Sub Class

Galanthamine-type amaryllidaceae alkaloids

Direct Parent

Galanthamine-type amaryllidaceae alkaloids

Alternative Parents

Substituents

Galanthamine-type amaryllidaceae alkaloid
Benzazepine
Coumaran
Anisole
Alkyl aryl ether
Azepine
Aralkylamine
Benzenoid
Secondary alcohol
Tertiary amine
Tertiary aliphatic amine
Oxacycle
Ether
Organoheterocyclic compound
Azacycle
Amine
Organic nitrogen compound
Alcohol
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Hydrobromide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	1.39	ALOGPS
logP	1.16	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	14.81	ChemAxon
pKa (Strongest Basic)	8.91	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	41.93 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	82.3 m³·mol⁻¹	ChemAxon
Polarizability	31.42 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

DBSALT000316

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

121587

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Galantamine hydrobromide (NP0138829)

MOL for NP0138829 (Galantamine hydrobromide)

3D MOL for NP0138829 (Galantamine hydrobromide)

3D SDF for NP0138829 (Galantamine hydrobromide)

3D-SDF for NP0138829 (Galantamine hydrobromide)

PDB for NP0138829 (Galantamine hydrobromide)

3D PDB for NP0138829 (Galantamine hydrobromide)

SMILES for NP0138829 (Galantamine hydrobromide)

INCHI for NP0138829 (Galantamine hydrobromide)

Structure for NP0138829 (Galantamine hydrobromide)

3D Structure for NP0138829 (Galantamine hydrobromide)