NP-MRD: Showing NP-Card for 3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid (NP0147421)

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Record Information

Version

2.0

Created at

2022-09-02 03:01:18 UTC

Updated at

2022-09-02 03:01:18 UTC

NP-MRD ID

NP0147421

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid

Description

AC1NDLKF belongs to the class of organic compounds known as pteridines and derivatives. These are polycyclic aromatic compounds containing a pteridine moiety, which consists of a pyrimidine fused to a pyrazine ring to form pyrimido(4,5-b)pyrazine. AC1NDLKF is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171502452D          

 27 28  0  0  0  0            999 V2000
   -3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    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
   -2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 O   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
    2.1434    3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.1250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    5.3625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.8875    0.0000 O   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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  2  0  0  0  0
 13 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
    2.7347   -2.0056    1.2237 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7934   -2.1449    0.5613 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9553   -2.4135    1.2688 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7728   -2.0218   -0.9193 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4193   -1.7198   -1.4596 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8808   -0.4261   -0.9264 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6144    0.3134   -0.0905 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1023    1.4682    0.3653 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8389    2.2749    1.2239 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9911    1.8733    1.5653 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3187    3.4305    1.6564 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0969    3.8390    1.2835 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5853    4.9144    1.6711 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3557    3.0582    0.4388 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8521    1.8935   -0.0091 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0707    1.1624   -0.8609 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2188    1.5048   -1.2739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3180    1.0213   -0.3785 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3408    1.5877    0.8905 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4236   -0.4593   -0.1844 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3882   -0.9481    0.5837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7016   -0.8044    0.6000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8170   -0.3392   -0.1115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8489   -2.3087    0.6820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7774   -2.8553    1.3795 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6338    0.0103   -1.2924 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0054   -0.7378   -2.0874 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8667   -2.5179    0.8249 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5590   -1.3187   -1.2812 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0734   -3.0213   -1.3196 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7515   -2.5728   -1.2045 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4945   -1.6319   -2.5563 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8632    4.0503    2.3057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5690    3.3586    0.1274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4426    2.5486   -1.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4070    0.9800   -2.2679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3357    1.3196   -0.8189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2565    1.5351    1.2556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4876   -0.9921   -1.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0544   -1.7912    0.2208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6605   -0.4241    1.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2128    0.3911    0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7727   -2.5332    1.2362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9652   -2.7600   -0.3243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6317   -3.7874    1.0848 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 22  1  0
 22 23  1  0
 22 20  1  0
 20 21  1  0
 20 18  1  0
 18 19  1  0
 18 17  1  0
 17 16  1  0
 16 26  1  0
 26 27  2  0
 26  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  0
  6  7  2  0
  7  8  1  0
  8 15  2  0
 15 14  1  0
 14 12  1  0
 12 13  2  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
 15 16  1  0
  9  8  1  0
 25 45  1  0
 24 43  1  0
 24 44  1  0
 22 41  1  1
 23 42  1  0
 20 39  1  6
 21 40  1  0
 18 37  1  6
 19 38  1  0
 17 35  1  0
 17 36  1  0
  5 31  1  0
  5 32  1  0
  4 29  1  0
  4 30  1  0
  3 28  1  0
 14 34  1  0
 11 33  1  0
M  END


  Mrv1533004171502452D          

 27 28  0  0  0  0            999 V2000
   -3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    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
   -2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 O   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
    2.1434    3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.1250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    5.3625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.8875    0.0000 O   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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  2  0  0  0  0
 13 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0147421

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC(O)C(O)C(O)CN1C(=O)C(CCC(O)=O)=NC2=C1NC(=O)NC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C14H18N4O9/c19-4-7(21)10(24)6(20)3-18-11-9(12(25)17-14(27)16-11)15-5(13(18)26)1-2-8(22)23/h6-7,10,19-21,24H,1-4H2,(H,22,23)(H2,16,17,25,27)

> <INCHI_KEY>
PTYCEIBBGGLADD-UHFFFAOYSA-N

> <FORMULA>
C14H18N4O9

> <MOLECULAR_WEIGHT>
386.317

> <EXACT_MASS>
386.107378176

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
35.50435748271491

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[2,4,7-trioxo-8-(2,3,4,5-tetrahydroxypentyl)-1,2,3,4,7,8-hexahydropteridin-6-yl]propanoic acid

> <ALOGPS_LOGP>
-2.20

> <JCHEM_LOGP>
-4.035367579666667

> <ALOGPS_LOGS>
-2.06

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.65202092064604

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.7276305998093604

> <JCHEM_PKA_STRONGEST_BASIC>
-2.974178810426092

> <JCHEM_POLAR_SURFACE_AREA>
209.08999999999997

> <JCHEM_REFRACTIVITY>
94.32479999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.35e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[2,4,7-trioxo-8-(2,3,4,5-tetrahydroxypentyl)-1,3-dihydropteridin-6-yl]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  O   UNK     0      -6.668   5.390   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001   5.390   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -4.001   6.930   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.667   3.080   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.334   5.390   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.334   6.930   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.000   4.620   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       1.334   5.390   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.667   3.080   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       4.001   6.930   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       2.667   7.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0      -0.000   7.700   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       0.000   9.240   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.334  10.010   0.000  0.00  0.00           O+0
HETATM   20  N   UNK     0       1.334  10.010   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       2.667   9.240   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.001  10.010   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668   5.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.336   5.390   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       8.002   3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   23                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   21                                                  
CONECT   16   15   10   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   15   22                                                  
CONECT   22   21                                                            
CONECT   23   13   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₁₈N₄O₉

Average Mass

386.3170 Da

Monoisotopic Mass

386.10738 Da

IUPAC Name

3-[2,4,7-trioxo-8-(2,3,4,5-tetrahydroxypentyl)-1,2,3,4,7,8-hexahydropteridin-6-yl]propanoic acid

Traditional Name

3-[2,4,7-trioxo-8-(2,3,4,5-tetrahydroxypentyl)-1,3-dihydropteridin-6-yl]propanoic acid

CAS Registry Number

Not Available

SMILES

OCC(O)C(O)C(O)CN1C(=O)C(CCC(O)=O)=NC2=C1NC(=O)NC2=O

InChI Identifier

InChI=1S/C14H18N4O9/c19-4-7(21)10(24)6(20)3-18-11-9(12(25)17-14(27)16-11)15-5(13(18)26)1-2-8(22)23/h6-7,10,19-21,24H,1-4H2,(H,22,23)(H2,16,17,25,27)

InChI Key

PTYCEIBBGGLADD-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 pteridines and derivatives. These are polycyclic aromatic compounds containing a pteridine moiety, which consists of a pyrimidine fused to a pyrazine ring to form pyrimido(4,5-b)pyrazine.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pteridines and derivatives

Sub Class

Not Available

Direct Parent

Pteridines and derivatives

Alternative Parents

Substituents

Pteridine
Pyrimidone
Pyrazine
Pyrimidine
Heteroaromatic compound
Vinylogous amide
Lactam
Urea
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Polyol
Azacycle
Alcohol
Organooxygen compound
Organonitrogen compound
Carbonyl group
Organic nitrogen compound
Primary alcohol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	-2.2	ALOGPS
logP	-4	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	3.73	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	209.09 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	94.32 m³·mol⁻¹	ChemAxon
Polarizability	35.5 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

4627790

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid (NP0147421)

MOL for NP0147421 (3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid)

3D MOL for NP0147421 (3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid)

3D SDF for NP0147421 (3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid)

3D-SDF for NP0147421 (3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid)

PDB for NP0147421 (3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid)

3D PDB for NP0147421 (3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid)

SMILES for NP0147421 (3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid)

INCHI for NP0147421 (3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid)

Structure for NP0147421 (3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid)

3D Structure for NP0147421 (3-[2,4-dihydroxy-7-oxo-8-(2,3,4,5-tetrahydroxypentyl)pteridin-6-yl]propanoic acid)