NP-MRD: Showing NP-Card for (2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol (NP0203020)

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Record Information

Version

2.0

Created at

2022-09-04 22:22:51 UTC

Updated at

2022-09-04 22:22:51 UTC

NP-MRD ID

NP0203020

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol

Description

(2R,3R,4S,5R)-2-({[(1R)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol belongs to the class of organic compounds known as aralkylamines. (2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol is found in Garcinia kola. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group (2R,3R,4S,5R)-2-({[(1R)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 42  0  0  0  0  0  0  0  0999 V2000
   -4.2295   -0.2091   -1.3576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9968   -0.5896    0.0842 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9255   -1.5675    0.1639 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7545   -0.7606   -0.0780 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5107   -1.3171    0.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5636   -0.4291    0.2786 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8802   -0.9214    0.5743 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2152   -2.0450   -0.3680 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1589   -1.5572   -1.6924 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8240    0.1862    0.3927 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6307    1.0876   -0.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4810    2.1591   -0.8455 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5594    2.2975    0.0219 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7967    1.4268    1.0545 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9130    0.3799    1.2178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0008    0.6297    0.3519 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8475    1.4646   -0.7586 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4470    0.5890    0.8098 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0211    1.7955    0.4101 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9707   -0.9153   -1.8200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3176   -0.2023   -1.9579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7115    0.7872   -1.3646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9216   -0.9956    0.5155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9038   -2.0377    1.0961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5415   -0.8241   -1.2010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7106   -1.2779    1.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3112   -2.3686    0.3071 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4111    0.5420    0.5526 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9628   -1.2877    1.6323 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5061   -2.8876   -0.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2439   -2.4106   -0.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0071   -1.1301   -1.8918 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7824    0.9890   -1.3131 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3508    2.8686   -1.6253 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2486    3.1086   -0.1020 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6202    1.5010    1.7437 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0469   -0.3461    2.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3972    1.0382    1.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2396    0.9962   -1.4052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4450    0.4434    1.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9994    1.7901    0.4065 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  8  1  0
  8  9  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  2 18  1  0
 18 19  1  0
 18 16  1  0
 16 17  1  0
  7 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 16  4  1  0
 15 10  1  0
  7 29  1  1
  8 30  1  0
  8 31  1  0
  9 32  1  0
  6 28  1  0
  5 26  1  0
  5 27  1  0
  4 25  1  6
  3 24  1  0
  2 23  1  1
  1 20  1  0
  1 21  1  0
  1 22  1  0
 18 40  1  1
 19 41  1  0
 16 38  1  1
 17 39  1  0
 11 33  1  0
 12 34  1  0
 13 35  1  0
 14 36  1  0
 15 37  1  0
M  END


  Mrv0541 05041404272D          

 24 25  0  0  1  0            999 V2000
    0.2002    5.0457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5357    4.2920    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1232    3.5775    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6753    2.9644    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3427    4.1205    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6972    3.4913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5037    2.1575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2532    4.0508    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6701    2.5110    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5356    4.0740    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1002    2.2573    0.0000 H   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
  9  1  1  1  0  0  0
 10  5  2  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  6  0  0  0
 12  8  1  0  0  0  0
 12 10  1  0  0  0  0
 13  9  1  0  0  0  0
 14 11  1  0  0  0  0
 14 13  1  0  0  0  0
 15  7  1  0  0  0  0
 12 15  1  6  0  0  0
 16  9  1  0  0  0  0
 16 11  1  0  0  0  0
 17  8  1  0  0  0  0
 13 18  1  1  0  0  0
 14 19  1  1  0  0  0
  9 20  1  6  0  0  0
 11 21  1  1  0  0  0
 12 22  1  6  0  0  0
 13 23  1  6  0  0  0
 14 24  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0203020

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@](CO)(NC[C@@]1([H])N[C@]([H])(C)[C@]([H])(O)[C@]1([H])O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C14H22N2O3/c1-9-13(18)14(19)11(16-9)7-15-12(8-17)10-5-3-2-4-6-10/h2-6,9,11-19H,7-8H2,1H3/t9-,11-,12+,13+,14-/m1/s1

> <INCHI_KEY>
KHLOMLBNZUMIHX-QKGWFMCXSA-N

> <FORMULA>
C14H22N2O3

> <MOLECULAR_WEIGHT>
266.3361

> <EXACT_MASS>
266.16304258

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
29.22669239434905

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,5R)-2-({[(1R)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol

> <ALOGPS_LOGP>
-0.51

> <JCHEM_LOGP>
-0.418996443999999

> <ALOGPS_LOGS>
-1.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.525594994880244

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.24663456360635

> <JCHEM_PKA_STRONGEST_BASIC>
9.232173979709273

> <JCHEM_POLAR_SURFACE_AREA>
84.75

> <JCHEM_REFRACTIVITY>
72.0379

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.01e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5R)-2-({[(1R)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-MAY-14   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-MAY-14         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  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   16  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   17  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   20  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   21  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   22  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+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    9                                                            
CONECT    2    3    4                                                       
CONECT    3    2    5                                                       
CONECT    4    2    6                                                       
CONECT    5    3   10                                                       
CONECT    6    4   10                                                       
CONECT    7   11   15                                                       
CONECT    8   12   17                                                       
CONECT    9    1   13   16   20                                             
CONECT   10    5    6   12                                                  
CONECT   11    7   14   16   21                                             
CONECT   12    8   10   15   22                                             
CONECT   13    9   14   18   23                                             
CONECT   14   11   13   19   24                                             
CONECT   15    7   12                                                       
CONECT   16    9   11                                                       
CONECT   17    8                                                            
CONECT   18   13                                                            
CONECT   19   14                                                            
CONECT   20    9                                                            
CONECT   21   11                                                            
CONECT   22   12                                                            
CONECT   23   13                                                            
CONECT   24   14                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₂₂N₂O₃

Average Mass

266.3361 Da

Monoisotopic Mass

266.16304 Da

IUPAC Name

(2R,3R,4S,5R)-2-({[(1R)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol

Traditional Name

(2R,3R,4S,5R)-2-({[(1R)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol

CAS Registry Number

Not Available

SMILES

[H][C@@](CO)(NC[C@@]1([H])N[C@]([H])(C)[C@]([H])(O)[C@]1([H])O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C14H22N2O3/c1-9-13(18)14(19)11(16-9)7-15-12(8-17)10-5-3-2-4-6-10/h2-6,9,11-19H,7-8H2,1H3/t9-,11-,12+,13+,14-/m1/s1

InChI Key

KHLOMLBNZUMIHX-QKGWFMCXSA-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
Garcinia kola	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group.

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

Amines

Direct Parent

Aralkylamines

Alternative Parents

Substituents

Aralkylamine
Monocyclic benzene moiety
Benzenoid
Pyrrolidine
1,2-aminoalcohol
Secondary alcohol
Secondary amine
Secondary aliphatic amine
Organoheterocyclic compound
Azacycle
Hydrocarbon derivative
Alcohol
Organopnictogen compound
Primary alcohol
Organooxygen compound
Organic oxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

dihydroxypyrrolidine (CHEBI:42683 )

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	-0.51	ALOGPS
logP	-0.42	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	13.25	ChemAxon
pKa (Strongest Basic)	9.23	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	84.75 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	72.04 m³·mol⁻¹	ChemAxon
Polarizability	29.23 Å³	ChemAxon
Number of Rings	2	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

Not Available

DrugBank ID

Not Available

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

11963508

PDB ID

GB3

ChEBI ID

42683

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol (NP0203020)

MOL for NP0203020 ((2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol)

3D MOL for NP0203020 ((2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol)

3D SDF for NP0203020 ((2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol)

3D-SDF for NP0203020 ((2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol)

PDB for NP0203020 ((2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol)

3D PDB for NP0203020 ((2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol)

SMILES for NP0203020 ((2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol)

INCHI for NP0203020 ((2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol)

Structure for NP0203020 ((2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol)

3D Structure for NP0203020 ((2r,3r,4s,5r)-2-({[(1r)-2-hydroxy-1-phenylethyl]amino}methyl)-5-methylpyrrolidine-3,4-diol)