NP-MRD: Showing NP-Card for {1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid (NP0196329)

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Record Information

Version

2.0

Created at

2022-09-04 14:24:25 UTC

Updated at

2022-09-04 14:24:25 UTC

NP-MRD ID

NP0196329

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid

Description

DTXSID60981902 belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group. {1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid is found in Streptomyces violaceoruber. Based on a literature review very few articles have been published on DTXSID60981902.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042216242D          

 32 36  0  0  0  0            999 V2000
    5.5693    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5693    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2837    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2837    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9982   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7127    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4272   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7127    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5693   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8548   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1403   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1403   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4259   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4259    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1403    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1403    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8548    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7114    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7114    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9969    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9969    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7114   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7114   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2825   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5680   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5680    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1465    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2825    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2825    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1450    0.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3351    0.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1450    0.1375    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  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  1  0  0  0  0
 15 17  2  0  0  0  0
 10 17  1  0  0  0  0
  2 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 20 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 24 32  1  0  0  0  0
M  END

     RDKit          3D

 54 58  0  0  0  0  0  0  0  0999 V2000
   -3.2305    0.2962   -3.2004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9691   -0.8229   -2.2080 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1293   -1.1036   -1.5367 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5398   -0.0642   -0.7036 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9359   -0.3627   -0.2218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9919   -1.6369    0.5360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9298   -2.7084   -0.1150 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1089   -1.6625    1.9168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6401    0.0332    0.5206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2281   -0.0222    0.0575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2590    0.3642    1.0170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6665    0.7448    2.2496 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0664    0.3384    0.6598 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3791   -0.0701   -0.6368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5876   -0.4406   -1.5487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2127   -0.8379   -2.8251 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9247   -0.4201   -1.2050 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7912   -0.0935   -1.0077 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1384   -0.4572   -2.1764 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8111    0.2975   -0.0481 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5135    0.6855    1.1824 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1213    0.7251    1.5986 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8816    1.1015    2.7821 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6770    1.0505    2.0224 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3539    2.2019    1.2577 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7304    1.7401   -0.1185 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0466    2.5054   -1.0861 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2764    0.3031   -0.3325 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5957   -0.1770   -1.5713 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8753   -0.5295    0.7955 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1881   -1.8982    0.7988 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6476    0.0369    2.0198 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2805    0.6421   -3.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0462   -0.0632   -4.2427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5655    1.1652   -3.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6461   -1.7446   -2.7332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5125    0.9281   -1.1914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3236    0.4415    0.4500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6217   -0.4242   -1.0982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0043   -2.5298    2.4245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8432    1.0180    0.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8676   -0.8192    1.1731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1678    1.0339    3.0119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8794   -1.1191   -3.5297 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4147    1.3371    3.0349 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2961    2.4786    1.7795 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6521    3.0586    1.2557 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8044    1.8729   -0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1177    2.0397   -1.9502 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8727   -1.1230   -1.4803 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9588   -0.6389    0.5531 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8810   -2.7172    0.9835 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6075   -2.0124   -0.1410 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4136   -1.9405    1.6184 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  8  1  0
  6  7  2  0
  4  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 14 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  2  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  6
 28 30  1  0
 30 31  1  0
 30 32  1  0
 21 22  1  0
 22 23  2  0
 17  2  1  0
 28 20  1  0
 17 10  1  0
 32 24  1  0
 22 13  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  6
  4 37  1  6
  5 38  1  0
  5 39  1  0
  8 40  1  0
  9 41  1  0
  9 42  1  0
 12 43  1  0
 16 44  1  0
 24 45  1  1
 25 46  1  0
 25 47  1  0
 26 48  1  6
 27 49  1  0
 29 50  1  0
 30 51  1  6
 31 52  1  0
 31 53  1  0
 31 54  1  0
M  END


  Mrv1652309042216242D          

 32 36  0  0  0  0            999 V2000
    5.5693    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5693    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2837    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2837    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9982   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7127    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4272   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7127    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5693   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8548   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1403   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1403   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4259   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4259    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1403    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1403    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8548    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7114    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7114    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9969    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9969    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7114   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7114   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2825   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5680   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5680    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1465    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2825    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2825    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1450    0.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3351    0.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1450    0.1375    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  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  1  0  0  0  0
 15 17  2  0  0  0  0
 10 17  1  0  0  0  0
  2 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 20 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 24 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0196329

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(CC(O)=O)CC2=C(O)C3=C(C(O)=C12)C(=O)C1=C(C2CC(O)C1(O)C(C)O2)C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H22O10/c1-6-13-9(3-8(31-6)4-12(24)25)18(26)15-16(19(13)27)21(29)17-14(20(15)28)10-5-11(23)22(17,30)7(2)32-10/h6-8,10-11,23,26-27,30H,3-5H2,1-2H3,(H,24,25)

> <INCHI_KEY>
GNTIHWMOJLHUNA-UHFFFAOYSA-N

> <FORMULA>
C22H22O10

> <MOLECULAR_WEIGHT>
446.408

> <EXACT_MASS>
446.121296908

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
44.03008865122848

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0^{2,15}.0^{4,13}.0^{6,11}]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid

> <JCHEM_LOGP>
0.7133286469999994

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.034767829310502

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.25484106862393

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3491437001878346

> <JCHEM_POLAR_SURFACE_AREA>
170.81999999999996

> <JCHEM_REFRACTIVITY>
107.44819999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
{1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0^{2,15}.0^{4,13}.0^{6,11}]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      10.396   3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.396   2.310   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      11.730   1.540   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      11.730   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.063  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.397   0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      15.731  -0.770   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      14.397   1.540   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.396  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.062  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.729  -0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.729  -2.310   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.395  -0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.395   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.729   2.310   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.729   3.850   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.062   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.061   2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.061   3.850   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.728   1.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.728   0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.061  -0.770   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.061  -2.310   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.394  -0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.060  -0.000   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.060   1.540   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.273   2.310   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.394   2.310   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       2.394   3.850   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.137   1.283   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.625   0.990   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.137   0.257   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   17                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   22                                                  
CONECT   14   13   15   18                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   10    2                                                  
CONECT   18   14   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   28                                                  
CONECT   21   20   22   24                                                  
CONECT   22   21   13   23                                                  
CONECT   23   22                                                            
CONECT   24   21   25   32                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   20   29   30                                             
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   24                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₂O₁₀

Average Mass

446.4080 Da

Monoisotopic Mass

446.12130 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1OC(CC(O)=O)CC2=C(O)C3=C(C(O)=C12)C(=O)C1=C(C2CC(O)C1(O)C(C)O2)C3=O

InChI Identifier

InChI=1S/C22H22O10/c1-6-13-9(3-8(31-6)4-12(24)25)18(26)15-16(19(13)27)21(29)17-14(20(15)28)10-5-11(23)22(17,30)7(2)32-10/h6-8,10-11,23,26-27,30H,3-5H2,1-2H3,(H,24,25)

InChI Key

GNTIHWMOJLHUNA-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
Streptomyces violaceoruber	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Hydroxyanthraquinones

Alternative Parents

Substituents

Isochromanequinone
Hydroxyanthraquinone
Benzoisochromanequinone
Naphthopyranone
Naphthopyran
2-benzopyran
Naphthalene
Isochromane
Benzopyran
Aryl ketone
Quinone
Pyranone
Pyran
Oxane
Vinylogous acid
Tertiary alcohol
Secondary alcohol
Ketone
1,2-diol
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

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

142434

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162191

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid (NP0196329)

MOL for NP0196329 ({1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid)

3D MOL for NP0196329 ({1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid)

3D SDF for NP0196329 ({1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid)

3D-SDF for NP0196329 ({1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid)

PDB for NP0196329 ({1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid)

3D PDB for NP0196329 ({1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid)

SMILES for NP0196329 ({1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid)

INCHI for NP0196329 ({1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid)

Structure for NP0196329 ({1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid)

3D Structure for NP0196329 ({1,5,12,19-tetrahydroxy-7,18-dimethyl-3,14-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),4(13),5,11-tetraen-9-yl}acetic acid)