MiMeDB: Showing metabocard for 2'-Deoxyguanosine 5'-diphosphate (MMDBc0057194)

Microbial

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2022-11-09 20:24:52 UTC

Update Date

2025-10-07 16:09:55 UTC

Metabolite ID

MMDBc0057194

Metabolite Identification

Common Name

2'-Deoxyguanosine 5'-diphosphate

Description

2'-Deoxyguanosine 5'-diphosphate is a nucleotide metabolite belonging to the class of deoxynucleotides, which are the building blocks of DNA. Its chemical structure consists of a deoxyribose sugar, a guanine base, and two phosphate groups, making it a crucial component in various biochemical pathways. In cellular metabolism, 2'-deoxyguanosine 5'-diphosphate serves as a substrate for the enzyme deoxynucleoside diphosphate kinase, facilitating the conversion to 2'-deoxyguanosine triphosphate (dGTP), which is essential for DNA synthesis and repair. Additionally, it plays a role in nucleotide salvage pathways, contributing to the recycling of nucleotides within the cell. Notably, studies have shown that 2'-deoxyguanosine 5'-diphosphate exhibits an IC50 value of 12.5 μM, indicating it is two times more effective than guanosine-5'-diphosphate sodium in certain biochemical contexts (PMID:26616453 ). This highlights its significance in nucleotide metabolism and potential implications in therapeutic applications targeting nucleic acid synthesis.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1652309042000142D          

 27 29  0  0  1  0            999 V2000
    2.3016    0.0890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6737    0.5296    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0335    0.6302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3814   -0.7574    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9069    0.2799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9512    1.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8115    1.3518    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7760    0.2972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1688   -1.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2305    0.7864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6503   -0.4660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8731   -0.5839    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4351    0.7898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2590   -1.9230    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4251    0.3146    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1684   -0.4660    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2091    0.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4355   -1.2465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8301    0.0162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6591    0.0162    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4884    0.0162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6627   -0.8129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6627    0.8487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3174    0.0232    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3243   -0.8095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1501    0.0232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3243    0.8521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  2  0  0  0  0
  1  4  1  0  0  0  0
  5  2  1  1  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  3  8  1  0  0  0  0
  4  9  2  0  0  0  0
  5 10  1  0  0  0  0
  5 11  1  0  0  0  0
  8 12  1  0  0  0  0
  8 13  2  0  0  0  0
  9 14  1  0  0  0  0
 10 15  1  0  0  0  0
 11 16  1  0  0  0  0
 15 17  1  1  0  0  0
 16 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 24 27  2  0  0  0  0
  6  7  2  0  0  0  0
  9 12  1  0  0  0  0
 15 16  1  0  0  0  0
M  END

HMDB0000960
     RDKit          3D
dGDP
 42 44  0  0  0  0  0  0  0  0999 V2000
   -4.1919    3.0542   -0.1746 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2979    1.6654    0.0623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2103    0.8604    0.1651 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4333   -0.4454    0.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7046   -0.9626    0.5168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5770   -2.2728    0.7335 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2741   -2.5780    0.7457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5608   -1.4567    0.5356 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1216   -1.4347    0.4887 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5908   -1.7624   -0.8972 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8554   -1.2813   -0.7696 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6213   -2.4413   -0.5292 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7720   -0.4065    0.4479 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5324    0.8890    0.2775 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8711    0.5968    0.0214 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7906    1.9927   -0.1816 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.3538    2.3793    1.1618 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8595    3.2486   -0.7671 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1075    1.6520   -1.1967 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2127    0.6452   -0.4526 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.6279    0.8943   -0.9571 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2161    0.8171    1.2327 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8892   -1.0007   -0.7755 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5789   -0.1820    0.7071 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7979   -0.1288    0.4093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9811   -0.5849    0.5216 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5602    1.1716    0.1833 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7036    3.6444    0.5209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5859    3.5016   -1.0197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8773   -3.5876    0.9037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6575   -2.1299    1.2308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6358   -2.8408   -1.1254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1160   -1.1342   -1.6420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1945   -0.7515   -1.6703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2233   -3.2226   -1.0298 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1941   -0.9626    1.3053 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5150    1.4995    1.1982 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1333    1.4209   -0.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1375    3.5680   -1.6610 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5068   -0.0366    1.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2471   -1.2914   -0.0858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4043    1.7956    0.1037 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 20 23  1  0
 13 24  1  0
  5 25  1  0
 25 26  2  0
 25 27  1  0
 27  2  1  0
  8  4  1  0
 24  9  1  0
  1 28  1  0
  1 29  1  0
  7 30  1  0
  9 31  1  1
 10 32  1  0
 10 33  1  0
 11 34  1  6
 12 35  1  0
 13 36  1  1
 14 37  1  0
 14 38  1  0
 18 39  1  0
 22 40  1  0
 23 41  1  0
 27 42  1  0
M  END


  Mrv1652309042000142D          

 27 29  0  0  1  0            999 V2000
    2.3016    0.0890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6737    0.5296    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0335    0.6302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3814   -0.7574    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9069    0.2799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9512    1.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8115    1.3518    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7760    0.2972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1688   -1.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2305    0.7864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6503   -0.4660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8731   -0.5839    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4351    0.7898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2590   -1.9230    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4251    0.3146    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1684   -0.4660    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2091    0.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4355   -1.2465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8301    0.0162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6591    0.0162    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4884    0.0162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6627   -0.8129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6627    0.8487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3174    0.0232    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3243   -0.8095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1501    0.0232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3243    0.8521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  2  0  0  0  0
  1  4  1  0  0  0  0
  5  2  1  1  0  0  0
  2  6  1  0  0  0  0
  3  7  1  0  0  0  0
  3  8  1  0  0  0  0
  4  9  2  0  0  0  0
  5 10  1  0  0  0  0
  5 11  1  0  0  0  0
  8 12  1  0  0  0  0
  8 13  2  0  0  0  0
  9 14  1  0  0  0  0
 10 15  1  0  0  0  0
 11 16  1  0  0  0  0
 15 17  1  1  0  0  0
 16 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 24 27  2  0  0  0  0
  6  7  2  0  0  0  0
  9 12  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0057194

> <DATABASE_NAME>
MIME

> <SMILES>
NC1=NC2=C(N=CN2[C@H]2C[C@H](O)[C@@H](COP(O)(=O)OP(O)(O)=O)O2)C(=O)N1

> <INCHI_IDENTIFIER>
InChI=1S/C10H15N5O10P2/c11-10-13-8-7(9(17)14-10)12-3-15(8)6-1-4(16)5(24-6)2-23-27(21,22)25-26(18,19)20/h3-6,16H,1-2H2,(H,21,22)(H2,18,19,20)(H3,11,13,14,17)/t4-,5+,6+/m0/s1

> <INCHI_KEY>
CIKGWCTVFSRMJU-KVQBGUIXSA-N

> <FORMULA>
C10H15N5O10P2

> <MOLECULAR_WEIGHT>
427.2011

> <EXACT_MASS>
427.029414749

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
34.98723478823068

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[({[(2R,3S,5R)-5-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]phosphonic acid

> <ALOGPS_LOGP>
-1.45

> <JCHEM_LOGP>
-2.518337817879012

> <ALOGPS_LOGS>
-2.07

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.211180454774107

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.791789653298578

> <JCHEM_PKA_STRONGEST_BASIC>
0.44204991344968037

> <JCHEM_POLAR_SURFACE_AREA>
228.04999999999995

> <JCHEM_REFRACTIVITY>
84.85619999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.60e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
dGDP

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0000960
     RDKit          3D
dGDP
 42 44  0  0  0  0  0  0  0  0999 V2000
   -4.1919    3.0542   -0.1746 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2979    1.6654    0.0623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2103    0.8604    0.1651 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4333   -0.4454    0.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7046   -0.9626    0.5168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5770   -2.2728    0.7335 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2741   -2.5780    0.7457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5608   -1.4567    0.5356 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1216   -1.4347    0.4887 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5908   -1.7624   -0.8972 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8554   -1.2813   -0.7696 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6213   -2.4413   -0.5292 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7720   -0.4065    0.4479 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5324    0.8890    0.2775 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8711    0.5968    0.0214 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7906    1.9927   -0.1816 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.3538    2.3793    1.1618 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8595    3.2486   -0.7671 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1075    1.6520   -1.1967 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2127    0.6452   -0.4526 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.6279    0.8943   -0.9571 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2161    0.8171    1.2327 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8892   -1.0007   -0.7755 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5789   -0.1820    0.7071 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7979   -0.1288    0.4093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9811   -0.5849    0.5216 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5602    1.1716    0.1833 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7036    3.6444    0.5209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5859    3.5016   -1.0197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8773   -3.5876    0.9037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6575   -2.1299    1.2308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6358   -2.8408   -1.1254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1160   -1.1342   -1.6420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1945   -0.7515   -1.6703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2233   -3.2226   -1.0298 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1941   -0.9626    1.3053 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5150    1.4995    1.1982 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1333    1.4209   -0.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1375    3.5680   -1.6610 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5068   -0.0366    1.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2471   -1.2914   -0.0858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4043    1.7956    0.1037 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 20 23  1  0
 13 24  1  0
  5 25  1  0
 25 26  2  0
 25 27  1  0
 27  2  1  0
  8  4  1  0
 24  9  1  0
  1 28  1  0
  1 29  1  0
  7 30  1  0
  9 31  1  1
 10 32  1  0
 10 33  1  0
 11 34  1  6
 12 35  1  0
 13 36  1  1
 14 37  1  0
 14 38  1  0
 18 39  1  0
 22 40  1  0
 23 41  1  0
 27 42  1  0
M  END

HEADER    PROTEIN                                 04-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-20         0                                  
HETATM    1  C   UNK     0       4.296   0.166   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       3.124   0.989   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       5.663   1.176   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       4.445  -1.414   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       1.693   0.522   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.642   2.536   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       5.248   2.523   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       7.048   0.555   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.915  -2.055   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.430   1.468   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.214  -0.870   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       7.230  -1.090   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0       8.279   1.474   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0       6.083  -3.590   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      -0.793   0.587   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.314  -0.870   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.257   1.066   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.813  -2.327   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -3.416   0.030   0.000  0.00  0.00           O+0
HETATM   20  P   UNK     0      -4.964   0.030   0.000  0.00  0.00           P+0
HETATM   21  O   UNK     0      -6.512   0.030   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -4.970  -1.517   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -4.970   1.584   0.000  0.00  0.00           O+0
HETATM   24  P   UNK     0      -8.059   0.043   0.000  0.00  0.00           P+0
HETATM   25  O   UNK     0      -8.072  -1.511   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -9.613   0.043   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -8.072   1.591   0.000  0.00  0.00           O+0
CONECT    1    2    3    4                                                  
CONECT    2    1    5    6                                                  
CONECT    3    1    7    8                                                  
CONECT    4    1    9                                                       
CONECT    5    2   10   11                                                  
CONECT    6    2    7                                                       
CONECT    7    3    6                                                       
CONECT    8    3   12   13                                                  
CONECT    9    4   14   12                                                  
CONECT   10    5   15                                                       
CONECT   11    5   16                                                       
CONECT   12    8    9                                                       
CONECT   13    8                                                            
CONECT   14    9                                                            
CONECT   15   10   17   16                                                  
CONECT   16   11   18   15                                                  
CONECT   17   15   19                                                       
CONECT   18   16                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22   23                                             
CONECT   21   20   24                                                       
CONECT   22   20                                                            
CONECT   23   20                                                            
CONECT   24   21   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   24                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

COMPND    HMDB0000960
HETATM    1  N1  UNL     1      -4.192   3.054  -0.175  1.00  0.00           N  
HETATM    2  C1  UNL     1      -4.298   1.665   0.062  1.00  0.00           C  
HETATM    3  N2  UNL     1      -3.210   0.860   0.165  1.00  0.00           N  
HETATM    4  C2  UNL     1      -3.433  -0.445   0.392  1.00  0.00           C  
HETATM    5  C3  UNL     1      -4.705  -0.963   0.517  1.00  0.00           C  
HETATM    6  N3  UNL     1      -4.577  -2.273   0.733  1.00  0.00           N  
HETATM    7  C4  UNL     1      -3.274  -2.578   0.746  1.00  0.00           C  
HETATM    8  N4  UNL     1      -2.561  -1.457   0.536  1.00  0.00           N  
HETATM    9  C5  UNL     1      -1.122  -1.435   0.489  1.00  0.00           C  
HETATM   10  C6  UNL     1      -0.591  -1.762  -0.897  1.00  0.00           C  
HETATM   11  C7  UNL     1       0.855  -1.281  -0.770  1.00  0.00           C  
HETATM   12  O1  UNL     1       1.621  -2.441  -0.529  1.00  0.00           O  
HETATM   13  C8  UNL     1       0.772  -0.407   0.448  1.00  0.00           C  
HETATM   14  C9  UNL     1       1.532   0.889   0.277  1.00  0.00           C  
HETATM   15  O2  UNL     1       2.871   0.597   0.021  1.00  0.00           O  
HETATM   16  P1  UNL     1       3.791   1.993  -0.182  1.00  0.00           P  
HETATM   17  O3  UNL     1       4.354   2.379   1.162  1.00  0.00           O  
HETATM   18  O4  UNL     1       2.860   3.249  -0.767  1.00  0.00           O  
HETATM   19  O5  UNL     1       5.107   1.652  -1.197  1.00  0.00           O  
HETATM   20  P2  UNL     1       6.213   0.645  -0.453  1.00  0.00           P  
HETATM   21  O6  UNL     1       7.628   0.894  -0.957  1.00  0.00           O  
HETATM   22  O7  UNL     1       6.216   0.817   1.233  1.00  0.00           O  
HETATM   23  O8  UNL     1       5.889  -1.001  -0.776  1.00  0.00           O  
HETATM   24  O9  UNL     1      -0.579  -0.182   0.707  1.00  0.00           O  
HETATM   25  C10 UNL     1      -5.798  -0.129   0.409  1.00  0.00           C  
HETATM   26  O10 UNL     1      -6.981  -0.585   0.522  1.00  0.00           O  
HETATM   27  N5  UNL     1      -5.560   1.172   0.183  1.00  0.00           N  
HETATM   28  H1  UNL     1      -3.704   3.644   0.521  1.00  0.00           H  
HETATM   29  H2  UNL     1      -4.586   3.502  -1.020  1.00  0.00           H  
HETATM   30  H3  UNL     1      -2.877  -3.588   0.904  1.00  0.00           H  
HETATM   31  H4  UNL     1      -0.658  -2.130   1.231  1.00  0.00           H  
HETATM   32  H5  UNL     1      -0.636  -2.841  -1.125  1.00  0.00           H  
HETATM   33  H6  UNL     1      -1.116  -1.134  -1.642  1.00  0.00           H  
HETATM   34  H7  UNL     1       1.195  -0.751  -1.670  1.00  0.00           H  
HETATM   35  H8  UNL     1       1.223  -3.223  -1.030  1.00  0.00           H  
HETATM   36  H9  UNL     1       1.194  -0.963   1.305  1.00  0.00           H  
HETATM   37  H10 UNL     1       1.515   1.499   1.198  1.00  0.00           H  
HETATM   38  H11 UNL     1       1.133   1.421  -0.606  1.00  0.00           H  
HETATM   39  H12 UNL     1       3.137   3.568  -1.661  1.00  0.00           H  
HETATM   40  H13 UNL     1       6.507  -0.037   1.677  1.00  0.00           H  
HETATM   41  H14 UNL     1       5.247  -1.291  -0.086  1.00  0.00           H  
HETATM   42  H15 UNL     1      -6.404   1.796   0.104  1.00  0.00           H  
CONECT    1    2   28   29
CONECT    2    3    3   27
CONECT    3    4
CONECT    4    5    5    8
CONECT    5    6   25
CONECT    6    7    7
CONECT    7    8   30
CONECT    8    9
CONECT    9   10   24   31
CONECT   10   11   32   33
CONECT   11   12   13   34
CONECT   12   35
CONECT   13   14   24   36
CONECT   14   15   37   38
CONECT   15   16
CONECT   16   17   17   18   19
CONECT   18   39
CONECT   19   20
CONECT   20   21   21   22   23
CONECT   22   40
CONECT   23   41
CONECT   25   26   26   27
CONECT   27   42
END

HMDB0000960
     RDKit          3D
dGDP
 42 44  0  0  0  0  0  0  0  0999 V2000
   -4.1919    3.0542   -0.1746 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2979    1.6654    0.0623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2103    0.8604    0.1651 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4333   -0.4454    0.3916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7046   -0.9626    0.5168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5770   -2.2728    0.7335 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2741   -2.5780    0.7457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5608   -1.4567    0.5356 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1216   -1.4347    0.4887 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5908   -1.7624   -0.8972 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8554   -1.2813   -0.7696 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6213   -2.4413   -0.5292 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7720   -0.4065    0.4479 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5324    0.8890    0.2775 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8711    0.5968    0.0214 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7906    1.9927   -0.1816 P   0  0  0  0  0  5  0  0  0  0  0  0
    4.3538    2.3793    1.1618 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8595    3.2486   -0.7671 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1075    1.6520   -1.1967 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2127    0.6452   -0.4526 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.6279    0.8943   -0.9571 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2161    0.8171    1.2327 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8892   -1.0007   -0.7755 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5789   -0.1820    0.7071 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7979   -0.1288    0.4093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9811   -0.5849    0.5216 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5602    1.1716    0.1833 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7036    3.6444    0.5209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5859    3.5016   -1.0197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8773   -3.5876    0.9037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6575   -2.1299    1.2308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6358   -2.8408   -1.1254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1160   -1.1342   -1.6420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1945   -0.7515   -1.6703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2233   -3.2226   -1.0298 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1941   -0.9626    1.3053 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5150    1.4995    1.1982 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1333    1.4209   -0.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1375    3.5680   -1.6610 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5068   -0.0366    1.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2471   -1.2914   -0.0858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4043    1.7956    0.1037 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 20 23  1  0
 13 24  1  0
  5 25  1  0
 25 26  2  0
 25 27  1  0
 27  2  1  0
  8  4  1  0
 24  9  1  0
  1 28  1  0
  1 29  1  0
  7 30  1  0
  9 31  1  1
 10 32  1  0
 10 33  1  0
 11 34  1  6
 12 35  1  0
 13 36  1  1
 14 37  1  0
 14 38  1  0
 18 39  1  0
 22 40  1  0
 23 41  1  0
 27 42  1  0
M  END

Synonyms

Value	Source
2'-Deoxyguanosine 5'-diphosphate	ChEBI
Deoxyguanosine diphosphate	ChEBI
2'-Deoxyguanosine 5'-diphosphoric acid	Generator
Deoxyguanosine diphosphoric acid	Generator
2'-Deoxy-GDP	HMDB
2'-Deoxyguanosine-5'-diphosphate	HMDB
5'-dGDP	HMDB
Deoxyguanosine 5'-diphosphate	HMDB
Deoxyguanosine-diphosphate	HMDB

Molecular Formula

C₁₀H₁₅N₅O₁₀P₂

Average Mass

427.2011

Monoisotopic Mass

427.029414749

IUPAC Name

[({[(2R,3S,5R)-5-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]phosphonic acid

Traditional Name

dGDP

CAS Registry Number

Not Available

SMILES

NC1=NC2=C(N=CN2[C@H]2C[C@H](O)[C@@H](COP(O)(=O)OP(O)(O)=O)O2)C(=O)N1

InChI Identifier

InChI=1S/C10H15N5O10P2/c11-10-13-8-7(9(17)14-10)12-3-15(8)6-1-4(16)5(24-6)2-23-27(21,22)25-26(18,19)20/h3-6,16H,1-2H2,(H,21,22)(H2,18,19,20)(H3,11,13,14,17)/t4-,5+,6+/m0/s1

InChI Key

CIKGWCTVFSRMJU-KVQBGUIXSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxycinnamic acids. Hydroxycinnamic acids are compounds containing an cinnamic acid where the benzene ring is hydroxylated.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Hydroxycinnamic acids

Alternative Parents

Substituents

Cinnamic acid
Coumaric acid or derivatives
Hydroxycinnamic acid
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Styrene
Phenol ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Ether
Organic oxygen compound
Carbonyl group
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

ferulic acids (CHEBI:27794 )

Functional Ontology

Not Available

Physical Properties

State

Not Available

Predicted Properties

Property	Value	Source
Water Solubility	3.6 g/L	ALOGPS
logP	-1.4	ALOGPS
logP	-2.5	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	1.79	ChemAxon
pKa (Strongest Basic)	0.44	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	228.05 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	84.86 m³·mol⁻¹	ChemAxon
Polarizability	34.99 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-056v-8931100000-80ef9c9f635e7c791ca3	2017-09-01	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (1 TMS) - 70eV, Positive	splash10-006w-9273200000-8578b4069f91a1e37a93	2017-10-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_1_4) - 70eV, Positive	Not Available	2021-11-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_1_5) - 70eV, Positive	Not Available	2021-11-06	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - LC-ESI-QTOF , negative	splash10-004i-9600800000-36eca5667f3968858676	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - , positive	splash10-0udi-2910000000-7d78949fd021bc9a3e84	2017-09-14	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 20V, Negative	splash10-056r-5921800000-485a79c4e3311f328cf1	2021-09-20	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9200000000-6e2fd4ae48d17fdbe9ae	2021-09-20	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 10V, Negative	splash10-004i-0000900000-f578c8db6d6baa91f146	2021-09-20	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 35V, Positive	splash10-0udi-1900000000-eada75fb37d52199dc57	2021-09-20	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0udi-0901100000-8f9213d3d0d12989aa4e	2016-09-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0udi-0900000000-fe32d673485e026f7ffd	2016-09-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0udi-0900000000-f9d9c2d10a52b1295c20	2016-09-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-004i-0500900000-f643b08ebfbee486ac88	2016-09-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-056r-4900000000-614b7240ac447b1cf302	2016-09-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9100000000-ebc82fc4fdc1243cf001	2016-09-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-004i-0000900000-2f685e4ebf6e3f21813b	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-004i-9221200000-d3ab4261ce93db5c0d8f	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9000000000-a5e502a2627af2048a1f	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0udi-0900100000-b27de50984aa34aec15e	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0udi-0900000000-361a2474138028086bb3	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0udi-0921000000-ed51ef3ce7f119c2cbc3	2021-09-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)		2021-09-29	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm
Mitochondria
Nucleus

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference
MMDBr0026019	2'-Deoxyguanosine 5'-monophosphate	2'-Deoxyguanosine 5'-diphosphate	Deoxynucleotide monophosphate kinase	Phosphorylation	RHEA	34755880
MMDBr0026060	L-Cystine	L-Cysteine	Vitamin B12-dependent ribonucleoside-diphosphate reductase	Reduction	RHEA	34755880
MMDBr0026088	2'-Deoxyguanosine 5'-diphosphate	2'-Deoxyguanosine 5'-triphosphate	Nucleoside diphosphate kinase	Phosphorylation	RHEA	34755880

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

HMDB0000960

DrugBank ID

DB03491

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Wikipedia Link

Deoxyguanosine_diphosphate

METLIN ID

5906

PubChem Compound

439220

PDB ID

Not Available

ChEBI ID

28862

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for 2'-Deoxyguanosine 5'-diphosphate (MMDBc0057194)

MOL for #<Metabolite:0x00007f8d90025088>

3D MOL for #<Metabolite:0x00007f8d90025088>

3D SDF for #<Metabolite:0x00007f8d90025088>

3D-SDF for #<Metabolite:0x00007f8d90025088>

PDB for #<Metabolite:0x00007f8d90025088>

3D PDB for #<Metabolite:0x00007f8d90025088>

SMILES for #<Metabolite:0x00007f8d90025088>

INCHI for #<Metabolite:0x00007f8d90025088>

Structure for #<Metabolite:0x00007f8d90025088>

3D Structure for #<Metabolite:0x00007f8d90025088>