NP-MRD: Showing NP-Card for n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid (NP0241165)

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Record Information

Version

2.0

Created at

2022-09-07 01:10:40 UTC

Updated at

2022-09-07 01:10:40 UTC

NP-MRD ID

NP0241165

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid

Description

N-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropteridine-6-carboximidic acid 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. n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid is found in Limnatis nilotica. N-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropteridine-6-carboximidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241513412D          

 31 33  0  0  0  0            999 V2000
   -5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    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    3.3000    0.0000 C   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
   -2.1434    2.0625    0.0000 N   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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   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
    2.1434    2.0625    0.0000 C   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    2.0625    0.0000 N   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
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   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  2  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  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
  2 13  1  0  0  0  0
 13 14  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 25 31  1  0  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
   -8.5084   -1.6307   -0.9588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5707   -0.7059   -0.3248 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2374   -0.8378   -0.4438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7794   -1.7815   -1.1183 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3372    0.0308    0.1513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0003   -0.1126    0.0242 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1124    0.7184    0.5930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6719    0.5604    0.4534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8977    1.3708    1.0100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1540   -0.5074   -0.3099 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2665   -0.6856   -0.4598 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0008   -0.9117    0.8224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4709   -1.0965    0.6507 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1453    0.0943    0.0126 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5775   -0.1485   -0.1260 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4439    0.7996   -0.6904 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9277    1.8976   -1.0830 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8503    0.5591   -0.8262 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6575    1.5824   -1.2734 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0153    1.3890   -1.4198 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5959    0.1689   -1.1226 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9544   -0.0262   -1.2685 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7878   -0.8398   -0.6800 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4220   -0.6471   -0.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6267    1.7693    1.3442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9666    1.9249    1.4801 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8380    1.0731    0.8963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1701    1.1966    1.0093 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7128    2.2864    1.7886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0226    0.3265    0.4123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2811    0.4452    0.5205 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5209   -1.1883   -0.8887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2906   -1.7648   -2.0385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4506   -2.6393   -0.5041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8190   -1.1843   -0.7771 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4284   -1.6040   -1.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7388    0.1565   -1.0110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6173   -1.8777    1.2665 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7499   -0.1384    1.5568 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484   -1.9737    0.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9152   -1.3129    1.6430 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9826    0.9633    0.6892 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7686    0.3190   -0.9828 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9469   -1.0533    0.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2654    2.5645   -1.5241 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6305    2.2047   -1.7719 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5735    0.1682   -0.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1960   -1.7960   -0.4400 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8206   -1.5034   -0.1714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9427    2.4451    1.8075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4581    1.9522    2.5341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1209    3.0443    1.0787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9079    2.7929    2.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2 30  1  0
 30 31  2  0
 30 28  1  0
 28 29  1  0
 28 27  1  0
 27 26  2  0
 26 25  1  0
 25  7  2  0
  7  6  1  0
  6  5  2  0
  5  3  1  0
  3  4  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
  3  2  1  0
 24 18  1  0
  5 27  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
 29 51  1  0
 29 52  1  0
 29 53  1  0
 25 50  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 19 45  1  0
 20 46  1  0
 22 47  1  0
 23 48  1  0
 24 49  1  0
M  END


  Mrv1533004241513412D          

 31 33  0  0  0  0            999 V2000
   -5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    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    3.3000    0.0000 C   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
   -2.1434    2.0625    0.0000 N   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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   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
    2.1434    2.0625    0.0000 C   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    2.0625    0.0000 N   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
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   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  2  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  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
  2 13  1  0  0  0  0
 13 14  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 25 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0241165

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C(=O)N(C)C2=NC=C(N=C2C1=O)C(=O)NCCCCNC(=O)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H22N6O5/c1-25-16-15(19(30)26(2)20(25)31)24-14(11-23-16)18(29)22-10-4-3-9-21-17(28)12-5-7-13(27)8-6-12/h5-8,11,27H,3-4,9-10H2,1-2H3,(H,21,28)(H,22,29)

> <INCHI_KEY>
QXOKPMKQWBHORG-UHFFFAOYSA-N

> <FORMULA>
C20H22N6O5

> <MOLECULAR_WEIGHT>
426.433

> <EXACT_MASS>
426.165167832

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
44.33657897101858

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-{4-[(1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropteridin-6-yl)formamido]butyl}-4-hydroxybenzamide

> <ALOGPS_LOGP>
0.50

> <JCHEM_LOGP>
-0.010386279666665887

> <ALOGPS_LOGS>
-3.79

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.282034830642093

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.478350197265994

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6334565202390284

> <JCHEM_POLAR_SURFACE_AREA>
144.82999999999998

> <JCHEM_REFRACTIVITY>
110.57449999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.95e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-{4-[(1,3-dimethyl-2,4-dioxopteridin-6-yl)formamido]butyl}-4-hydroxybenzamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -9.336   3.850   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0      -8.002   4.620   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0      -8.002   6.160   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -9.336   6.930   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0      -6.668   6.930   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -6.668   8.470   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.335   6.160   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      -4.001   6.930   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -4.001   3.850   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.668   3.850   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -6.668   2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0       0.000   4.620   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       6.668   3.850   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.002   6.160   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.003   3.850   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.003   2.310   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      13.337   1.540   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11    7   13                                                  
CONECT   13   12    2   14                                                  
CONECT   14   13                                                            
CONECT   15   10   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   25                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
N-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropteridine-6-carboximidate	Generator

Chemical Formula

C₂₀H₂₂N₆O₅

Average Mass

426.4330 Da

Monoisotopic Mass

426.16517 Da

IUPAC Name

N-{4-[(1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropteridin-6-yl)formamido]butyl}-4-hydroxybenzamide

Traditional Name

N-{4-[(1,3-dimethyl-2,4-dioxopteridin-6-yl)formamido]butyl}-4-hydroxybenzamide

CAS Registry Number

Not Available

SMILES

CN1C(=O)N(C)C2=NC=C(N=C2C1=O)C(=O)NCCCCNC(=O)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C20H22N6O5/c1-25-16-15(19(30)26(2)20(25)31)24-14(11-23-16)18(29)22-10-4-3-9-21-17(28)12-5-7-13(27)8-6-12/h5-8,11,27H,3-4,9-10H2,1-2H3,(H,21,28)(H,22,29)

InChI Key

QXOKPMKQWBHORG-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
Limnatis nilotica	LOTUS Database	35616633

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
Benzamide
Benzoic acid or derivatives
Pyrazine carboxylic acid or derivatives
Pyrazinecarboxamide
2-heteroaryl carboxamide
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyrimidone
Monocyclic benzene moiety
Benzenoid
Pyrimidine
Pyrazine
Heteroaromatic compound
Vinylogous amide
Carboxamide group
Lactam
Urea
Secondary carboxylic acid amide
Carboxylic acid derivative
Azacycle
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Organic oxide
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	0.5	ALOGPS
logP	-0.01	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	8.48	ChemAxon
pKa (Strongest Basic)	-0.63	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	144.83 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	110.57 m³·mol⁻¹	ChemAxon
Polarizability	44.34 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	Yes	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

11362323

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid (NP0241165)

MOL for NP0241165 (n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid)

3D MOL for NP0241165 (n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid)

3D SDF for NP0241165 (n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid)

3D-SDF for NP0241165 (n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid)

PDB for NP0241165 (n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid)

3D PDB for NP0241165 (n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid)

SMILES for NP0241165 (n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid)

INCHI for NP0241165 (n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid)

Structure for NP0241165 (n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid)

3D Structure for NP0241165 (n-{4-[(4-hydroxyphenyl)formamido]butyl}-1,3-dimethyl-2,4-dioxopteridine-6-carboximidic acid)