NP-MRD: Showing NP-Card for ()-hyoscyamine (NP0185035)

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Record Information

Version

1.0

Created at

2022-09-04 00:19:39 UTC

Updated at

2022-09-04 00:19:39 UTC

NP-MRD ID

NP0185035

Secondary Accession Numbers

None

Natural Product Identification

Common Name

()-hyoscyamine

Description

()-hyoscyamine is found in Agrobacterium rhizogenes, Anisodus luridus, Anisodus tanguticus, Anthocercis ilicifolia, Atropa belladonna, Brugmansia arborea, Brugmansia aurea, Brugmansia sanguinea, Brugmansia suaveolens, Brugmansia candida, Datura inoxia, Datura metel, Datura stramonium, Duboisia hopwoodii, Duboisia leichhardtii, Duboisia myoporoides, Hyoscyamus desertorum, Hyoscyamus muticus, Hyoscyamus niger, Hyoscyamus pusillus, Hyoscyamus reticulatus, Mandragora officinarum, Mandragora turcomanica, Sclerotinia minor, Scopolia carniolica, Scopolia japonica, Scopolia parviflora and Solandra grandiflora.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 46  0  0  0  0  0  0  0  0999 V2000
   -4.3130   -0.8606   -0.7370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6314    0.1804   -0.2084 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9144    1.1138   -0.9484 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2883    2.4089   -0.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2221    1.9186    1.2268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4187    0.3963    1.1478 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0538   -0.2145    1.5007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2180   -0.2812    0.2661 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1371   -0.4647    0.4894 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8960   -1.5216    0.0702 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3370   -2.4342   -0.5857 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3459   -1.6186    0.3661 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9286   -2.8927   -0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2844   -2.9405    0.1214 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1112   -0.4887   -0.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1527   -0.2069   -1.5347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8795    0.8603   -2.0289 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5918    1.6826   -1.1839 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5604    1.4140    0.1612 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8254    0.3373    0.6466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4260    0.9132   -0.6580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3911   -0.6965   -1.0307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8364   -1.2516   -1.6767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3473   -1.7349   -0.0438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1267    1.1823   -2.0107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5700    3.2073   -0.4221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3436    2.6774   -0.4230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2506    2.1921    1.6364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0060    2.3764    1.8607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1929    0.0787    1.8435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5809    0.3317    2.3372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2802   -1.2354    1.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5813   -1.1697   -0.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4620   -1.6484    1.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7868   -2.9177   -1.2813 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4420   -3.7757    0.2617 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4919   -2.4106    0.9401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6146   -0.8164   -2.2419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8971    1.0642   -3.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1698    2.5301   -1.5710 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1194    2.0588    0.8279 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8532    0.1953    1.7152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9424    1.8215   -0.3014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9518    0.6400   -1.6243 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3 21  1  0
 21  8  1  0
  8  7  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
  3  2  1  0
 20 15  1  0
  7  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  6 30  1  1
  5 28  1  0
  5 29  1  0
  4 26  1  0
  4 27  1  0
  3 25  1  6
 21 43  1  0
 21 44  1  0
  8 33  1  6
  7 31  1  0
  7 32  1  0
 12 34  1  1
 13 35  1  0
 13 36  1  0
 14 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
 20 42  1  0
M  END


  Mrv0541 09061400162D          

 21 23  0  0  0  0            999 V2000
    7.3590    3.8449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1505    3.5604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1505    2.7354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8649    3.9729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8649    2.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5794    3.5604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7962    3.9962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2087    3.2818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3756    3.5581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1189    2.2706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2939    1.4979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5794    2.7354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9804    4.1192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9073    2.5138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4373    2.7354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2939    2.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0083    2.7354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6445    3.4324    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5794    1.0854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0083    3.5604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7228    2.3229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  2  0  0  0  0
  8  7  1  0  0  0  0
 12  5  2  0  0  0  0
 12  6  1  0  0  0  0
 13  7  1  0  0  0  0
 13  9  1  0  0  0  0
 14  8  1  0  0  0  0
 14 10  1  0  0  0  0
 15  9  1  0  0  0  0
 15 10  1  0  0  0  0
 16 11  1  0  0  0  0
 16 12  1  0  0  0  0
 17 16  1  0  0  0  0
 18  1  1  0  0  0  0
 18 13  1  0  0  0  0
 18 14  1  0  0  0  0
 19 11  1  0  0  0  0
 20 17  2  0  0  0  0
 21 15  1  0  0  0  0
 21 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0185035

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C2CCC1CC(C2)OC(=O)C(CO)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3

> <INCHI_KEY>
RKUNBYITZUJHSG-UHFFFAOYSA-N

> <FORMULA>
C17H23NO3

> <MOLECULAR_WEIGHT>
289.3694

> <EXACT_MASS>
289.167793607

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
31.967119658304433

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-phenylpropanoate

> <ALOGPS_LOGP>
2.19

> <JCHEM_LOGP>
1.571241016666666

> <ALOGPS_LOGS>
-2.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.145740617562414

> <JCHEM_PKA_STRONGEST_BASIC>
9.385561870758496

> <JCHEM_POLAR_SURFACE_AREA>
49.769999999999996

> <JCHEM_REFRACTIVITY>
80.8164

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.52e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
()-hyoscyamine

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-14   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-14         0                                  
HETATM    1  C   UNK     0      13.737   7.177   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.148   6.646   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.148   5.106   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.481   7.416   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.481   4.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.815   6.646   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.686   7.460   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.456   6.126   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.035   6.642   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.422   4.238   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.149   2.796   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.815   5.106   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.163   7.689   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.894   4.692   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.150   5.106   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.149   4.336   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.482   5.106   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      12.403   6.407   0.000  0.00  0.00           N+0
HETATM   19  O   UNK     0       4.815   2.026   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       7.482   6.646   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       8.816   4.336   0.000  0.00  0.00           O+0
CONECT    1   18                                                            
CONECT    2    3    4                                                       
CONECT    3    2    5                                                       
CONECT    4    2    6                                                       
CONECT    5    3   12                                                       
CONECT    6    4   12                                                       
CONECT    7    8   13                                                       
CONECT    8    7   14                                                       
CONECT    9   13   15                                                       
CONECT   10   14   15                                                       
CONECT   11   16   19                                                       
CONECT   12    5    6   16                                                  
CONECT   13    7    9   18                                                  
CONECT   14    8   10   18                                                  
CONECT   15    9   10   21                                                  
CONECT   16   11   12   17                                                  
CONECT   17   16   20   21                                                  
CONECT   18    1   13   14                                                  
CONECT   19   11                                                            
CONECT   20   17                                                            
CONECT   21   15   17                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Value	Source
Anaspaz	MeSH
Cytospaz	MeSH
Atropine sulfate, 3(S)-endo-isomer	MeSH
Hyoscyamine	MeSH
Hyoscyamine hydrobromide	MeSH
Hyoscyamine hydrochloride	MeSH
Atropine, 3(S)-endo-isomer	MeSH
Hyoscyamine sulfate	MeSH
Hyoscyamine sulfate anhydrous	MeSH

Chemical Formula

C₁₇H₂₃NO₃

Average Mass

289.3694 Da

Monoisotopic Mass

289.16779 Da

IUPAC Name

8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-phenylpropanoate

Traditional Name

()-hyoscyamine

CAS Registry Number

Not Available

SMILES

CN1C2CCC1CC(C2)OC(=O)C(CO)C1=CC=CC=C1

InChI Identifier

InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3

InChI Key

RKUNBYITZUJHSG-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
Agrobacterium rhizogenes	LOTUS Database	35616633
Anisodus luridus	LOTUS Database	35616633
Anisodus tanguticus	LOTUS Database	35616633
Anthocercis ilicifolia	LOTUS Database	35616633
Atropa belladonna	LOTUS Database	35616633
Brugmansia arborea	LOTUS Database	35616633
Brugmansia aurea	LOTUS Database	35616633
Brugmansia sanguinea	LOTUS Database	35616633
Brugmansia suaveolens	LOTUS Database	35616633
Brugmansia x candida	LOTUS Database	35616633
Datura inoxia	LOTUS Database	35616633
Datura metel	LOTUS Database	35616633
Datura stramonium	LOTUS Database	35616633
Duboisia hopwoodii	LOTUS Database	35616633
Duboisia leichhardtii	LOTUS Database	35616633
Duboisia myoporoides	LOTUS Database	35616633
Hyoscyamus desertorum	LOTUS Database	35616633
Hyoscyamus muticus	LOTUS Database	35616633
Hyoscyamus niger	LOTUS Database	35616633
Hyoscyamus pusillus	LOTUS Database	35616633
Hyoscyamus reticulatus	LOTUS Database	35616633
Mandragora officinarum	LOTUS Database	35616633
Mandragora turcomanica	LOTUS Database	35616633
Sclerotinia minor	LOTUS Database	35616633
Scopolia carniolica	LOTUS Database	35616633
Scopolia japonica	LOTUS Database	35616633
Scopolia parviflora	LOTUS Database	35616633
Solandra grandiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tropane alkaloids. These are organic compounds containing the nitrogenous bicyclic alkaloid parent N-Methyl-8-azabicyclo[3.2.1]Octane.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Tropane alkaloids

Sub Class

Not Available

Direct Parent

Tropane alkaloids

Alternative Parents

Substituents

Tropane alkaloid
Beta-hydroxy acid
Monocyclic benzene moiety
Hydroxy acid
Piperidine
Benzenoid
N-alkylpyrrolidine
Pyrrolidine
Amino acid or derivatives
Carboxylic acid ester
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Azacycle
Organoheterocyclic compound
Organonitrogen compound
Amine
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organic nitrogen compound
Primary alcohol
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	2.19	ALOGPS
logP	1.57	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	15.15	ChemAxon
pKa (Strongest Basic)	9.39	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	49.77 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	80.82 m³·mol⁻¹	ChemAxon
Polarizability	31.97 Å³	ChemAxon
Number of Rings	3	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

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB004090

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Atropine

METLIN ID

Not Available

PubChem Compound

3661

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for ()-hyoscyamine (NP0185035)

MOL for NP0185035 (()-hyoscyamine)

3D MOL for NP0185035 (()-hyoscyamine)

3D SDF for NP0185035 (()-hyoscyamine)

3D-SDF for NP0185035 (()-hyoscyamine)

PDB for NP0185035 (()-hyoscyamine)

3D PDB for NP0185035 (()-hyoscyamine)

SMILES for NP0185035 (()-hyoscyamine)

INCHI for NP0185035 (()-hyoscyamine)

Structure for NP0185035 (()-hyoscyamine)

3D Structure for NP0185035 (()-hyoscyamine)