NP-MRD: Showing NP-Card for n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid (NP0195480)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 13:21:16 UTC

Updated at

2022-09-04 13:21:17 UTC

NP-MRD ID

NP0195480

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid

Description

N-{5-[6-(dimethylamino)-9H-purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. Purine 3'-deoxyribonucleosides are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3. Based on a literature review very few articles have been published on N-{5-[6-(dimethylamino)-9H-purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 46  0  0  0  0  0  0  0  0999 V2000
    4.6562    1.9862    0.3371 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9753    1.2463    1.4044 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2601    1.5830    2.7338 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1441    0.3194    1.1678 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7581   -0.1292   -0.1300 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0207   -1.4663   -0.0345 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9936   -2.6121    0.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9242   -2.5790   -0.9146 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3521   -1.5242   -1.2271 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8627   -0.2438   -1.4974 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5461   -0.2444   -1.2542 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4649   -0.5407   -2.1920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7040   -0.4588   -1.6731 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6047   -0.1101   -0.3983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5362    0.1152    0.5983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9240   -0.0228    0.3290 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4987   -1.2491   -0.1138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7477    1.1646    0.5288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0474    0.4629    1.8016 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7308    0.5919    2.0503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8417    0.3681    1.0665 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2383    0.0224   -0.1454 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6653    0.7284   -0.7391 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2409    1.7274   -1.5400 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0804    2.9190    0.1143 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6573    2.3479    0.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7988    1.4139   -0.5829 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0911    1.1817    3.1382 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5794   -0.1824   -0.8714 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3135   -1.3975    0.7888 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3945   -3.5431    0.0925 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5325   -2.5362    1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5997   -2.1864   -1.7519 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0771   -0.0770   -2.5932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3128   -0.8167   -3.2412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8024   -1.9124   -0.6564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3569   -1.0659   -0.7954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9291   -1.7683    0.7756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7723    0.8149    0.7985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8639    1.7389   -0.4138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3972    1.7864    1.3655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3775    0.8793    3.0538 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1630    1.2343    0.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5559    2.0346   -2.1787 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 18  1  0
 16 15  1  0
 15 14  2  0
 14 13  1  0
 13 12  2  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  6  1  0
  6  7  1  0
  7  8  1  0
  6  5  1  0
  5  4  1  0
  4  2  2  0
  2  1  1  0
  2  3  1  0
  5 23  1  0
 23 24  1  0
 11 22  1  0
 22 21  2  0
 21 20  1  0
 20 19  2  0
 19 15  1  0
 22 14  1  0
 23 10  1  0
 17 36  1  0
 17 37  1  0
 17 38  1  0
 18 39  1  0
 18 40  1  0
 18 41  1  0
 12 35  1  0
 10 34  1  6
  6 30  1  1
  7 31  1  0
  7 32  1  0
  8 33  1  0
  5 29  1  6
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
 23 43  1  1
 24 44  1  0
 20 42  1  0
M  END


  Mrv1652309042215212D          

 24 26  0  0  0  0            999 V2000
    0.8416   -5.6672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5867   -4.8826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2203   -4.7111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -4.2695    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -3.4849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0992   -3.2299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5683   -3.7149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3220   -3.3793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0992   -2.4049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3687   -2.8174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1937   -2.8174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  4  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 14 22  1  0  0  0  0
 11 22  1  0  0  0  0
 10 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0195480

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN(C)C1=C2N=CN(C3OC(CO)C(N=C(C)O)C3O)C2=NC=N1

> <INCHI_IDENTIFIER>
InChI=1S/C14H20N6O4/c1-7(22)18-9-8(4-21)24-14(11(9)23)20-6-17-10-12(19(2)3)15-5-16-13(10)20/h5-6,8-9,11,14,21,23H,4H2,1-3H3,(H,18,22)

> <INCHI_KEY>
YUNXLSKYACXNRM-UHFFFAOYSA-N

> <FORMULA>
C14H20N6O4

> <MOLECULAR_WEIGHT>
336.352

> <EXACT_MASS>
336.154603148

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
34.05136901144799

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-{5-[6-(dimethylamino)-9H-purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid

> <JCHEM_LOGP>
-0.7641119564668755

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.974095611771688

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.52610002054569

> <JCHEM_PKA_STRONGEST_BASIC>
3.633130863132771

> <JCHEM_POLAR_SURFACE_AREA>
129.12

> <JCHEM_REFRACTIVITY>
84.54679999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
N-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       1.571 -10.579   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.095  -9.114   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.411  -8.794   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0       2.126  -7.970   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       1.650  -6.505   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.185  -6.029   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.061  -6.934   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.468  -6.308   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       0.185  -4.489   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       2.126  -2.549   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       2.126  -0.057   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       4.924   1.777   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       3.590   2.547   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.258   2.547   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       6.258  -0.533   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       4.924  -2.843   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.555  -5.259   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.095  -5.259   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10                                                       
CONECT   10    9   11   23                                                  
CONECT   11   10   12   22                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   22                                                  
CONECT   15   14   16   19                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   15   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   14   11                                                  
CONECT   23   10    5   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
N-{5-[6-(dimethylamino)-9H-purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidate	Generator

Chemical Formula

C₁₄H₂₀N₆O₄

Average Mass

336.3520 Da

Monoisotopic Mass

336.15460 Da

IUPAC Name

N-{5-[6-(dimethylamino)-9H-purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid

Traditional Name

N-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid

CAS Registry Number

Not Available

SMILES

CN(C)C1=C2N=CN(C3OC(CO)C(N=C(C)O)C3O)C2=NC=N1

InChI Identifier

InChI=1S/C14H20N6O4/c1-7(22)18-9-8(4-21)24-14(11(9)23)20-6-17-10-12(19(2)3)15-5-16-13(10)20/h5-6,8-9,11,14,21,23H,4H2,1-3H3,(H,18,22)

InChI Key

YUNXLSKYACXNRM-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. Purine 3'-deoxyribonucleosides are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Sub Class

Purine 3'-deoxyribonucleosides

Direct Parent

Purine 3'-deoxyribonucleosides

Alternative Parents

Substituents

Purine 3'-deoxyribonucleoside
6-alkylaminopurine
N-glycosyl compound
Glycosyl compound
Pentose monosaccharide
6-aminopurine
Purine
Imidazopyrimidine
Dialkylarylamine
Aminopyrimidine
Imidolactam
Pyrimidine
N-substituted imidazole
Monosaccharide
Heteroaromatic compound
Acetamide
Tetrahydrofuran
Imidazole
Azole
Secondary carboxylic acid amide
Secondary alcohol
Carboxamide group
Oxacycle
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	-0.76	ChemAxon
pKa (Strongest Acidic)	5.53	ChemAxon
pKa (Strongest Basic)	3.63	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	129.12 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	84.55 m³·mol⁻¹	ChemAxon
Polarizability	34.05 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

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

85982704

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid (NP0195480)

MOL for NP0195480 (n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid)

3D MOL for NP0195480 (n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid)

3D SDF for NP0195480 (n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid)

3D-SDF for NP0195480 (n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid)

PDB for NP0195480 (n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid)

3D PDB for NP0195480 (n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid)

SMILES for NP0195480 (n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid)

INCHI for NP0195480 (n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid)

Structure for NP0195480 (n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid)

3D Structure for NP0195480 (n-{5-[6-(dimethylamino)purin-9-yl]-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl}ethanimidic acid)