NP-MRD: Showing NP-Card for [3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate (NP0201894)

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Record Information

Version

2.0

Created at

2022-09-04 21:00:51 UTC

Updated at

2022-09-04 21:00:52 UTC

NP-MRD ID

NP0201894

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate

Description

[3,4-Bis(acetyloxy)-5-[(4-hydroxy-2-oxo-1,2-dihydropyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond. [3,4-Bis(acetyloxy)-5-[(4-hydroxy-2-oxo-1,2-dihydropyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191514162D          

 27 28  0  0  0  0            999 V2000
    3.4656    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367    1.1759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -0.0616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -1.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1393   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3188   -3.1499    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -3.8173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9866   -3.7311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222   -2.9774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1426   -2.8911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8372   -2.3099    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0168   -2.3962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4682   -1.7287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9341   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5986   -3.9898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -4.0760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0835   -4.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7041   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4888   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1019   -2.0811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9303   -2.8881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8865   -1.8262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  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
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
  8 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 18 23  1  0  0  0  0
  6 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

 47 48  0  0  0  0  0  0  0  0999 V2000
   -5.4497   -3.3154    1.2955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8931   -1.9690    0.9219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6050   -0.9396    0.9015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5673   -1.8720    0.5952 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9297   -0.6637    0.2277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4651   -0.9228   -0.0669 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7937   -1.4377    1.0188 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5409   -0.9709    0.9046 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2784   -1.7749   -0.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6491   -1.3474   -0.2634 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9803   -0.4315   -1.1890 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2999   -0.0144   -1.3647 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2874   -0.5558   -0.5691 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5061   -0.2080   -0.6907 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9123   -1.4662    0.3410 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6269   -1.8634    0.5026 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3962   -2.7300    1.3954 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2859    0.4595    0.5895 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3513    1.2835    0.4030 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7476    2.3678    1.1256 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9281    3.2109    0.8478 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0253    2.6452    2.1034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7635    0.3845   -0.4606 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6415    1.4894   -0.3378 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9606    2.2516   -1.4507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8785    3.4252   -1.3822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4368    1.9095   -2.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5314   -3.2541    1.4474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2764   -4.0589    0.4892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0009   -3.6977    2.2258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0006   -0.0001    1.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4322   -0.1293   -0.5831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4183   -1.6719   -0.8824 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9666   -1.0569    1.9072 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3331   -2.8244    0.3205 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7734   -1.8863   -1.0691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2595    0.0254   -1.8427 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5623    0.7275   -2.1156 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6714   -1.8713    0.9406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2535    0.8562    1.5125 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6948    3.1879    1.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5993    4.2740    0.7503 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3264    2.9219   -0.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4258    0.2619   -1.4788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9299    3.1477   -1.2886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7522    4.0080   -2.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5966    4.0959   -0.5333 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  2  0
  8 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 18 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  2  0
 23  6  1  0
 16 10  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  6
  8 34  1  1
  9 35  1  0
  9 36  1  0
 11 37  1  0
 12 38  1  0
 15 39  1  0
 18 40  1  1
 21 41  1  0
 21 42  1  0
 21 43  1  0
 23 44  1  6
 26 45  1  0
 26 46  1  0
 26 47  1  0
M  END


  Mrv1533004191514162D          

 27 28  0  0  0  0            999 V2000
    3.4656    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367    1.1759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -0.0616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -1.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1393   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3188   -3.1499    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -3.8173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9866   -3.7311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222   -2.9774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1426   -2.8911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8372   -2.3099    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0168   -2.3962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4682   -1.7287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9341   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5986   -3.9898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -4.0760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0835   -4.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7041   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4888   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1019   -2.0811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9303   -2.8881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8865   -1.8262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  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
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
  8 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 18 23  1  0  0  0  0
  6 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>
NP0201894

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1OC(CN2C=CC(=O)NC2=O)C(OC(C)=O)C1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H20N2O9/c1-8(19)24-7-12-15(26-10(3)21)14(25-9(2)20)11(27-12)6-18-5-4-13(22)17-16(18)23/h4-5,11-12,14-15H,6-7H2,1-3H3,(H,17,22,23)

> <INCHI_KEY>
LFOHPKKMDYSRLY-UHFFFAOYSA-N

> <FORMULA>
C16H20N2O9

> <MOLECULAR_WEIGHT>
384.341

> <EXACT_MASS>
384.116880232

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
36.56698729579719

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[3,4-bis(acetyloxy)-5-[(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate

> <ALOGPS_LOGP>
-0.15

> <JCHEM_LOGP>
-1.3579769110000002

> <ALOGPS_LOGS>
-1.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.758399254005047

> <JCHEM_PKA_STRONGEST_BASIC>
-4.190948747171333

> <JCHEM_POLAR_SURFACE_AREA>
137.54000000000002

> <JCHEM_REFRACTIVITY>
84.95270000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.25e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[3,4-bis(acetyloxy)-5-[(2,4-dioxo-3H-pyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       6.469   2.195   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.136   1.425   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.802   2.195   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       5.136  -0.115   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.802  -0.885   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.802  -2.425   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.556  -3.330   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.032  -4.795   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.127  -6.041   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       0.595  -5.880   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -0.310  -7.126   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.842  -6.965   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.468  -5.558   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -4.000  -5.397   0.000  0.00  0.00           O+0
HETATM   15  N   UNK     0      -1.563  -4.312   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      -0.031  -4.473   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.874  -3.227   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.572  -4.795   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.477  -6.041   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.851  -7.448   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.319  -7.609   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.756  -8.693   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.048  -3.330   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.512  -2.854   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.657  -3.885   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.337  -5.391   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.121  -3.409   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   18                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16                                                            
CONECT   18    8   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18    6   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

Value	Source
[3,4-Bis(acetyloxy)-5-[(4-hydroxy-2-oxo-1,2-dihydropyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetic acid	Generator

Chemical Formula

C₁₆H₂₀N₂O₉

Average Mass

384.3410 Da

Monoisotopic Mass

384.11688 Da

IUPAC Name

[3,4-bis(acetyloxy)-5-[(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate

Traditional Name

[3,4-bis(acetyloxy)-5-[(2,4-dioxo-3H-pyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1OC(CN2C=CC(=O)NC2=O)C(OC(C)=O)C1OC(C)=O

InChI Identifier

InChI=1S/C16H20N2O9/c1-8(19)24-7-12-15(26-10(3)21)14(25-9(2)20)11(27-12)6-18-5-4-13(22)17-16(18)23/h4-5,11-12,14-15H,6-7H2,1-3H3,(H,17,22,23)

InChI Key

LFOHPKKMDYSRLY-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 c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

C-glycosyl compounds

Alternative Parents

Substituents

C-glycosyl compound
Pentose monosaccharide
Tricarboxylic acid or derivatives
Hydroxypyrimidine
Pyrimidone
Hydropyrimidine
Monosaccharide
Pyrimidine
Heteroaromatic compound
Tetrahydrofuran
Carboxylic acid ester
Oxacycle
Ether
Dialkyl ether
Carboxylic acid derivative
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Hydrocarbon derivative
Organonitrogen compound
Organic oxide
Organopnictogen compound
Carbonyl group
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	-0.15	ALOGPS
logP	-1.4	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	9.76	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	137.54 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	84.95 m³·mol⁻¹	ChemAxon
Polarizability	36.57 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate (NP0201894)

MOL for NP0201894 ([3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate)

3D MOL for NP0201894 ([3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate)

3D SDF for NP0201894 ([3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate)

3D-SDF for NP0201894 ([3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate)

PDB for NP0201894 ([3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate)

3D PDB for NP0201894 ([3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate)

SMILES for NP0201894 ([3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate)

INCHI for NP0201894 ([3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate)

Structure for NP0201894 ([3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate)

3D Structure for NP0201894 ([3,4-bis(acetyloxy)-5-[(4-hydroxy-2-oxopyrimidin-1-yl)methyl]oxolan-2-yl]methyl acetate)