NP-MRD: Showing NP-Card for {1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid (NP0220099)

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Record Information

Version

2.0

Created at

2022-09-05 21:18:58 UTC

Updated at

2022-09-05 21:18:59 UTC

NP-MRD ID

NP0220099

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid

Description

2-{1,3,14,19-Tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]Icosa-2,4(13),6(11),9,14-pentaen-9-yl}acetic acid belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone. {1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid is found in Streptomyces thermoviolaceus. 2-{1,3,14,19-Tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]Icosa-2,4(13),6(11),9,14-pentaen-9-yl}acetic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191523032D          

 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
    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
    4.8548    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
    3.4259    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
    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
    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
    3.4259    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
    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
    7.7127    0.8250    0.0000 O   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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 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
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 15 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 10 26  1  0  0  0  0
 26 27  1  0  0  0  0
  6 27  1  0  0  0  0
 27 28  2  0  0  0  0
  4 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END

     RDKit          3D

 52 56  0  0  0  0  0  0  0  0999 V2000
    3.4748   -2.9532    0.6643 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4518   -1.8940   -0.4392 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7193   -1.3368   -0.4876 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9291    0.0532   -0.3759 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3495    0.4583   -0.4475 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6954    1.8396   -0.3472 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9255    2.7898   -0.2012 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0689    2.1940   -0.4197 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9005    0.8405   -0.2249 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5221    0.3181   -0.1672 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3355   -0.9621   -0.2704 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9553   -1.4825   -0.2138 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8131   -2.7156   -0.3161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2058   -0.6103   -0.0462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4883   -1.1260    0.0035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7775   -2.4510   -0.0961 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5227   -0.2009    0.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2842    1.1408    0.2714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9971    1.6843    0.2240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8958    3.0208    0.3388 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0450    0.7680    0.0612 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3934    1.2681    0.0051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6543    2.4870    0.0971 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5061    1.9625    0.4387 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1583    1.4078    1.7185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4204   -0.0608    1.6171 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8248   -0.2254    1.6038 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9583   -0.5686    0.2417 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2421   -1.8745    0.0123 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7175    0.3501   -0.7284 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6544   -0.2051   -2.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3213    1.6569   -0.6554 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4862   -3.4376    0.5890 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4371   -2.4992    1.6662 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7422   -3.7450    0.5060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3274   -2.4993   -1.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9041   -0.1746    0.3158 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8036    0.0573   -1.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4629    2.0394   -1.3607 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9927    1.9063   -0.1340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2357   -3.2164   -0.2072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1163    3.5877    0.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3478    3.0259    0.5146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3885    1.6009    2.5211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0536    2.0041    1.9438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9854   -0.6582    2.4300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0796   -0.9940    2.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4776   -1.9878   -0.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7820    0.2858   -0.4105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4868   -0.9058   -2.3514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7963    0.6646   -2.8208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6656   -0.6271   -2.3747 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  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 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
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 22 23  2  0
 11  2  1  0
 21 14  1  0
 22 10  1  0
 28 17  1  0
 32 24  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  6
  5 37  1  0
  5 38  1  0
  8 39  1  0
  9 40  1  0
 16 41  1  0
 24 43  1  1
 25 44  1  0
 25 45  1  0
 26 46  1  1
 27 47  1  0
 29 48  1  0
 30 49  1  1
 31 50  1  0
 31 51  1  0
 31 52  1  0
 20 42  1  0
M  END


  Mrv1533004191523032D          

 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
    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
    4.8548    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
    3.4259    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
    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
    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
    3.4259    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
    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
    7.7127    0.8250    0.0000 O   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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 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
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 15 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 10 26  1  0  0  0  0
 26 27  1  0  0  0  0
  6 27  1  0  0  0  0
 27 28  2  0  0  0  0
  4 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0220099

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(CC(O)=O)=CC2=C1C(=O)C1=C(O)C3=C(C4CC(O)C3(O)C(C)O4)C(O)=C1C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H20O10/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/h3,6-7,10-11,23,28-30H,4-5H2,1-2H3,(H,24,25)

> <INCHI_KEY>
KXKAQNZWMODXGL-UHFFFAOYSA-N

> <FORMULA>
C22H20O10

> <MOLECULAR_WEIGHT>
444.392

> <EXACT_MASS>
444.105646844

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
43.16611725469437

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid

> <ALOGPS_LOGP>
0.20

> <JCHEM_LOGP>
0.3810720439999997

> <ALOGPS_LOGS>
-2.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.085929410343605

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.082540184833501

> <JCHEM_PKA_STRONGEST_BASIC>
-3.405808516579362

> <JCHEM_POLAR_SURFACE_AREA>
170.82

> <JCHEM_REFRACTIVITY>
108.94159999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.72e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid

> <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      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      10.396  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.062   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.062   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.729   2.310   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.729   3.850   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.395   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.061   2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.061   3.850   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.728   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.728   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.394  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.060  -0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.060   1.540   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.273   2.310   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.394   2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.394   3.850   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.137   1.283   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.625   0.990   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.137   0.257   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.061  -0.770   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.061  -2.310   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.395   0.000   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.729  -0.770   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.729  -2.310   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      13.063  -0.770   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      14.397  -0.000   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      14.397   1.540   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      15.731  -0.770   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   29                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   27                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   26                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   19                                                  
CONECT   14   13   15   24                                                  
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   13   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   15                                                       
CONECT   24   14   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   10   27                                                  
CONECT   27   26    6   28                                                  
CONECT   28   27                                                            
CONECT   29    4   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Value	Source
2-{1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0,.0,.0,]icosa-2,4(13),6(11),9,14-pentaen-9-yl}acetate	Generator
2-{1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2,4(13),6(11),9,14-pentaen-9-yl}acetate	Generator

Chemical Formula

C₂₂H₂₀O₁₀

Average Mass

444.3920 Da

Monoisotopic Mass

444.10565 Da

IUPAC Name

2-{1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid

Traditional Name

{1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid

CAS Registry Number

Not Available

SMILES

CC1OC(CC(O)=O)=CC2=C1C(=O)C1=C(O)C3=C(C4CC(O)C3(O)C(C)O4)C(O)=C1C2=O

InChI Identifier

InChI=1S/C22H20O10/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/h3,6-7,10-11,23,28-30H,4-5H2,1-2H3,(H,24,25)

InChI Key

KXKAQNZWMODXGL-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 thermoviolaceus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Anthraquinone
1,4-anthraquinone
Benzoisochromanequinone
Isochromanequinone
Naphthopyranone
Naphthopyran
Benzopyran
Isochromane
Naphthalene
Tetralin
2-benzopyran
Quinone
Aryl ketone
Pyranone
Pyran
Oxane
Tertiary alcohol
Vinylogous acid
Secondary alcohol
1,2-diol
Ketone
Oxacycle
Ether
Dialkyl ether
Carboxylic acid
Carboxylic acid derivative
Polyol
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Organic oxide
Carbonyl group
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
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	0.2	ALOGPS
logP	0.38	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	3.08	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	170.82 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	108.94 m³·mol⁻¹	ChemAxon
Polarizability	43.17 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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 {1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid (NP0220099)

MOL for NP0220099 ({1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid)

3D MOL for NP0220099 ({1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid)

3D SDF for NP0220099 ({1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid)

3D-SDF for NP0220099 ({1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid)

PDB for NP0220099 ({1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid)

3D PDB for NP0220099 ({1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid)

SMILES for NP0220099 ({1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid)

INCHI for NP0220099 ({1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid)

Structure for NP0220099 ({1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid)

3D Structure for NP0220099 ({1,3,14,19-tetrahydroxy-7,18-dimethyl-5,12-dioxo-8,17-dioxapentacyclo[14.2.2.0²,¹⁵.0⁴,¹³.0⁶,¹¹]icosa-2(15),3,6(11),9,13-pentaen-9-yl}acetic acid)