NP-MRD: Showing NP-Card for 3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione (NP0218402)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 19:03:44 UTC

Updated at

2022-09-05 19:03:44 UTC

NP-MRD ID

NP0218402

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione

Description

AC1NST2T belongs to the class of organic compounds known as naphthoquinones. Naphthoquinones are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone). AC1NST2T is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161503332D          

 58 67  0  0  0  0            999 V2000
   -6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1934   -0.8963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  2  0  0  0  0
  2 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  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
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 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
 19 27  1  0  0  0  0
 27 28  2  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 18 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 34 41  1  0  0  0  0
 41 42  2  0  0  0  0
 30 42  1  0  0  0  0
 42 43  1  0  0  0  0
 37 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 49 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 51 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  2  0  0  0  0
 54 56  1  0  0  0  0
 48 56  1  0  0  0  0
 56 57  2  0  0  0  0
 44 57  1  0  0  0  0
 57 58  1  0  0  0  0
M  END

     RDKit          3D

 84 93  0  0  0  0  0  0  0  0999 V2000
   10.7232   -0.5120   -2.1170 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4407   -1.0847   -1.6570 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2501   -2.4378   -1.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0568   -3.0424   -1.3630 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9115   -4.3981   -1.5056 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1020   -2.1908   -0.8277 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2822   -0.8361   -0.7001 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4722   -0.2585   -1.1198 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2496    0.0604   -0.1269 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4765    1.2747   -0.0483 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9814   -0.4862    0.3315 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8598    0.3548    0.7984 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5387    0.1021    0.5315 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1680   -0.9306   -0.4799 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4948    0.8368    1.1117 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1212    0.5223    0.7939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5121   -0.4068    1.6002 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1818   -1.0539    2.7429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8279   -0.7578    1.3533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012   -0.1620    0.2830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8817    0.7575   -0.5187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5664    1.0952   -0.2557 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0608    2.0152   -1.0538 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6358    1.3367   -1.6128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0616    2.1844   -2.3493 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0406    0.9331   -1.8452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6668    0.0514   -1.0910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0791   -0.2391   -1.2405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6042   -1.5103   -1.1887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6925   -2.6845   -1.2049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9744   -1.7912   -1.2122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8692   -0.7604   -1.2945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3915    0.5157   -1.3496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0109    0.8066   -1.3230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6508    2.1028   -1.3686 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3446    1.6193   -1.4406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8933    2.7420   -1.8019 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7711    1.4527   -1.1299 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.5934    0.9250   -2.1332 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2784    0.1283   -0.9795 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.3184   -0.9750   -1.3260 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7331   -2.1162   -1.6533 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9039   -0.5206    0.0008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3792   -1.3702    0.8077 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7923    1.8484    1.9753 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1207    2.1505    2.2801 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1096    1.4106    1.6979 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4099    1.6955    2.0013 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3571    3.2652    3.2038 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4113    3.9192    3.0446 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3669    3.5723    4.2650 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7025    2.5364    4.9153 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0368    3.3989    3.8984 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7796    2.6663    2.6361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3493    2.7091    2.0518 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8303   -1.7893    0.2011 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261   -2.7084   -0.3622 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6020   -3.9336   -0.4519 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6764   -0.1467   -3.1656 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5122   -1.2671   -1.9512 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9600    0.3410   -1.4384 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0039   -3.0888   -2.1996 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2394   -5.0478   -1.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6085    0.8097   -1.0165 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7690   -1.7949    0.0352 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9602   -1.1647   -1.1919 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2878   -0.4551   -1.0589 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0154   -0.4444    3.1441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5629   -1.1852    3.5549 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6036   -2.0131    2.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3020   -1.4760    1.9849 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9992    2.3290   -0.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5240    1.3871   -2.7201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1530   -3.3783   -2.0057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8372   -3.2549   -0.2841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6861   -2.4692   -1.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3477   -2.7906   -1.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7676    2.4970   -1.3028 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1853    2.2734   -0.4951 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1101   -0.1102   -0.3135 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8524    2.3392    2.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6968    4.3713    4.9605 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1932    3.9628    4.2928 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9129   -2.2566    0.5773 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  1  0
  4  6  2  0
  6 57  1  0
 57 58  2  0
 57 56  1  0
 56 11  2  0
 11  9  1  0
  9 10  2  0
  9  7  1  0
  7  8  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 43  1  0
 43 44  2  0
 43 27  1  0
 27 26  2  0
 26 24  1  0
 24 25  2  0
 24 21  1  0
 21 22  2  0
 22 23  1  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 29 31  1  0
 31 32  2  0
 32 41  1  0
 41 42  2  0
 41 40  1  0
 40 39  1  0
 39 38  1  0
 38 36  1  0
 36 37  2  0
 36 33  1  0
 33 34  2  0
 34 35  1  0
 15 45  2  0
 45 54  1  0
 54 55  2  0
 54 53  1  0
 53 52  1  0
 52 51  1  0
 51 49  1  0
 49 50  2  0
 49 46  1  0
 46 47  2  0
 47 48  1  0
  8  2  1  0
 47 12  1  0
  7  6  1  0
 22 16  1  0
 34 28  1  0
 46 45  1  0
 21 20  1  0
 33 32  1  0
 51 53  1  0
 38 40  1  0
  1 59  1  0
  1 60  1  0
  1 61  1  0
  3 62  1  0
  5 63  1  0
 56 84  1  0
  8 64  1  0
 14 65  1  0
 14 66  1  0
 14 67  1  0
 18 68  1  0
 18 69  1  0
 18 70  1  0
 19 71  1  0
 26 73  1  0
 23 72  1  0
 30 74  1  0
 30 75  1  0
 30 76  1  0
 31 77  1  0
 40 80  1  1
 38 79  1  1
 35 78  1  0
 53 83  1  1
 51 82  1  1
 48 81  1  0
M  END


  Mrv1533004161503332D          

 58 67  0  0  0  0            999 V2000
   -6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1934   -0.8963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  2  0  0  0  0
  2 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  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
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 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
 19 27  1  0  0  0  0
 27 28  2  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 18 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 34 41  1  0  0  0  0
 41 42  2  0  0  0  0
 30 42  1  0  0  0  0
 42 43  1  0  0  0  0
 37 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 49 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 51 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  2  0  0  0  0
 54 56  1  0  0  0  0
 48 56  1  0  0  0  0
 56 57  2  0  0  0  0
 44 57  1  0  0  0  0
 57 58  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0218402

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(O)=C2C(=O)C=C(C(=O)C2=C1)C1=C(C)C(C2=C(C)C=C3C(=O)C(=CC(=O)C3=C2O)C2=C(C)C=C3C(=O)C4OC4C(=O)C3=C2O)=C2C(=O)C3OC3C(=O)C2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C44H26O14/c1-11-5-15-27(20(45)6-11)21(46)10-19(32(15)48)25-14(4)26(30-31(37(25)53)40(56)44-43(58-44)39(30)55)24-13(3)8-16-28(36(24)52)22(47)9-18(33(16)49)23-12(2)7-17-29(35(23)51)38(54)42-41(57-42)34(17)50/h5-10,41-45,51-53H,1-4H3

> <INCHI_KEY>
MAFARFGSWMJHCN-UHFFFAOYSA-N

> <FORMULA>
C44H26O14

> <MOLECULAR_WEIGHT>
778.678

> <EXACT_MASS>
778.132255517

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
78.61247299938259

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1aH,2H,7H,7aH-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxo-5,8-dihydronaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-5-methyl-1aH,2H,7H,7aH-naphtho[2,3-b]oxirene-2,7-dione

> <ALOGPS_LOGP>
4.58

> <JCHEM_LOGP>
7.2279956080000005

> <ALOGPS_LOGS>
-5.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
10

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.693984484616085

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.190554158087671

> <JCHEM_PKA_STRONGEST_BASIC>
-6.041418683586676

> <JCHEM_POLAR_SURFACE_AREA>
242.53999999999996

> <JCHEM_REFRACTIVITY>
204.88020000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.10e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1aH,7aH-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1aH,7aH-naphtho[2,3-b]oxirene-2,7-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0     -12.003 -14.630   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -10.669 -13.860   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.336 -14.630   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.002 -13.860   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -6.668 -14.630   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -8.002 -12.320   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -5.335 -12.320   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0     -10.669  -9.240   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0     -10.669  -1.540   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0     -10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0     -12.003  -5.390   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0     -10.669  -7.700   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -5.961  -1.673   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       8.002  -1.540   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   13                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6   14                                                  
CONECT   14   13    2                                                       
CONECT   15   10   16   28                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   30                                                  
CONECT   19   18   20   27                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22   24                                                       
CONECT   24   23   22   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   19   28                                                  
CONECT   28   27   15   29                                                  
CONECT   29   28                                                            
CONECT   30   18   31   42                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   41                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   44                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   34   42                                                  
CONECT   42   41   30   43                                                  
CONECT   43   42                                                            
CONECT   44   37   45   57                                                  
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   48                                                       
CONECT   48   47   49   56                                                  
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   52   53                                                  
CONECT   52   51   53                                                       
CONECT   53   52   51   54                                                  
CONECT   54   53   55   56                                                  
CONECT   55   54                                                            
CONECT   56   54   48   57                                                  
CONECT   57   56   44   58                                                  
CONECT   58   57                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  134    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₄H₂₆O₁₄

Average Mass

778.6780 Da

Monoisotopic Mass

778.13226 Da

IUPAC Name

3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1aH,2H,7H,7aH-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxo-5,8-dihydronaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-5-methyl-1aH,2H,7H,7aH-naphtho[2,3-b]oxirene-2,7-dione

Traditional Name

3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1aH,7aH-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1aH,7aH-naphtho[2,3-b]oxirene-2,7-dione

CAS Registry Number

Not Available

SMILES

CC1=CC(O)=C2C(=O)C=C(C(=O)C2=C1)C1=C(C)C(C2=C(C)C=C3C(=O)C(=CC(=O)C3=C2O)C2=C(C)C=C3C(=O)C4OC4C(=O)C3=C2O)=C2C(=O)C3OC3C(=O)C2=C1O

InChI Identifier

InChI=1S/C44H26O14/c1-11-5-15-27(20(45)6-11)21(46)10-19(32(15)48)25-14(4)26(30-31(37(25)53)40(56)44-43(58-44)39(30)55)24-13(3)8-16-28(36(24)52)22(47)9-18(33(16)49)23-12(2)7-17-29(35(23)51)38(54)42-41(57-42)34(17)50/h5-10,41-45,51-53H,1-4H3

InChI Key

MAFARFGSWMJHCN-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 naphthoquinones. Naphthoquinones are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone).

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Naphthoquinone
Tetralin
Quinone
Aryl ketone
Aryl alkyl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Vinylogous acid
Ketone
Oxacycle
Ether
Oxirane
Dialkyl ether
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Aldehyde
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	4.58	ALOGPS
logP	7.23	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	6.19	ChemAxon
pKa (Strongest Basic)	-6	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	242.54 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	204.88 m³·mol⁻¹	ChemAxon
Polarizability	78.61 Å³	ChemAxon
Number of Rings	10	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

5315474

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione (NP0218402)

MOL for NP0218402 (3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione)

3D MOL for NP0218402 (3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione)

3D SDF for NP0218402 (3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione)

3D-SDF for NP0218402 (3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione)

PDB for NP0218402 (3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione)

3D PDB for NP0218402 (3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione)

SMILES for NP0218402 (3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione)

INCHI for NP0218402 (3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione)

Structure for NP0218402 (3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione)

3D Structure for NP0218402 (3-hydroxy-6-(1-hydroxy-6-{3-hydroxy-5-methyl-2,7-dioxo-1ah,7ah-naphtho[2,3-b]oxiren-4-yl}-3-methyl-5,8-dioxonaphthalen-2-yl)-4-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-5-methyl-1ah,7ah-naphtho[2,3-b]oxirene-2,7-dione)