NP-MRD: Showing NP-Card for n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid (NP0220159)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 21:23:22 UTC

Updated at

2022-09-05 21:23:22 UTC

NP-MRD ID

NP0220159

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid

Description

N-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxo-7,12-dihydrotetraphen-5-yl)oxan-4-yl]ethanimidic acid belongs to the class of organic compounds known as angucyclines. These are polyketides with a structure based on then benz[a]anthracene skeleton, with the particularity that the central ring of the anthracene moiety is a para-quinone. Based on a literature review very few articles have been published on N-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxo-7,12-dihydrotetraphen-5-yl)oxan-4-yl]ethanimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052223232D          

 36 40  0  0  0  0            999 V2000
    8.0057    3.3748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1955    3.5307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9255    4.3103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6555    2.9071    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8453    3.0630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    2.4393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4951    2.5952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.9716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449    2.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    2.9071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149   -0.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1154    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    2.4393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    3.3748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    3.9984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4951    4.7780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5753    3.8425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1154    4.4662    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
  2  4  2  0  0  0  0
  4  5  1  4  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
  8 20  2  0  0  0  0
 13 20  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 23 29  1  0  0  0  0
 29 30  1  0  0  0  0
 11 30  1  0  0  0  0
 30 31  2  0  0  0  0
  7 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
  5 35  1  0  0  0  0
 35 36  1  0  0  0  0
M  END

     RDKit          3D

 61 65  0  0  0  0  0  0  0  0999 V2000
    6.4383   -0.3238   -0.6299 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7506    0.7507    0.0836 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4675    1.7147    0.7586 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4457    0.8561    0.1211 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6153   -0.1191   -0.5640 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1767    0.2319   -0.6692 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4299    0.1500    0.6435 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0615    0.2385    0.4176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8491   -0.8729    0.2466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2930   -2.0857    0.2664 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2060   -0.6722    0.0697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8245    0.5678    0.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0228    1.6754    0.2374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5470    2.9371    0.1868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8754    3.1975    0.0221 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6764    4.0228    0.3146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3419    3.9084    0.4893 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5646    5.0958    0.5624 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1846    2.6306    0.5454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6262    1.5239    0.4227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2467    0.6855   -0.1875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8781    1.7261   -0.2157 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0290   -0.5384   -0.4287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3708   -0.4115   -0.7076 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1201   -1.5413   -0.9815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5368   -2.7711   -0.9750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1705   -2.9180   -0.6903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6511   -4.1806   -0.6954 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4286   -1.7962   -0.4218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9981   -1.8664   -0.1652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4543   -2.9762   -0.1491 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6788   -1.1494    1.2017 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3513   -1.9401    0.3233 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5439   -3.3887    0.7718 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8073   -1.4185    0.2229 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1898   -1.1390    1.5183 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4877   -0.0147   -0.9182 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9871   -0.5565   -1.6449 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5690   -1.2686   -0.1062 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3903    1.8446    1.7469 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0270   -0.2795   -1.5636 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1841    1.3127   -1.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6381   -0.3031   -1.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7299    0.8358    1.4062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3553   -3.0103    0.2230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2231    4.1728   -0.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1470    5.0106    0.2543 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5818    4.7321    0.7005 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3270    5.7691    1.3969 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4686    5.7083   -0.3677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2385    2.4729    0.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8538    0.5759   -0.7209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1804   -1.3690   -1.2090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1272   -3.6471   -1.1943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8057   -4.5857   -0.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9465   -1.9388   -0.7264 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5766   -3.7462    0.6253 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8318   -3.9938    0.1245 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1784   -3.4562    1.8087 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4135   -2.1573   -0.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6802   -1.9120    1.9067 H   0  0  0  0  0  0  0  0  0  0  0  0
 34 33  1  0
 33 32  1  0
 32  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  2  0
  2  1  1  0
  2  3  1  0
  5 35  1  0
 35 36  1  0
  7  8  1  0
  8 20  1  0
 20 19  2  0
 19 17  1  0
 17 18  1  0
 17 16  2  0
 16 14  1  0
 14 15  1  0
 14 13  2  0
 13 12  1  0
 12 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 27 29  2  0
 29 30  1  0
 30 31  2  0
 30 11  1  0
 11  9  1  0
  9 10  1  0
 35 33  1  0
  9  8  2  0
 13 20  1  0
 11 12  2  0
 29 23  1  0
 34 57  1  0
 34 58  1  0
 34 59  1  0
 33 56  1  6
  7 44  1  1
  6 42  1  0
  6 43  1  0
  5 41  1  6
  1 37  1  0
  1 38  1  0
  1 39  1  0
  3 40  1  0
 35 60  1  6
 36 61  1  0
 19 51  1  0
 18 48  1  0
 18 49  1  0
 18 50  1  0
 16 47  1  0
 15 46  1  0
 24 52  1  0
 25 53  1  0
 26 54  1  0
 28 55  1  0
 10 45  1  0
M  END


  Mrv1652309052223232D          

 36 40  0  0  0  0            999 V2000
    8.0057    3.3748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1955    3.5307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9255    4.3103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6555    2.9071    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8453    3.0630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    2.4393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4951    2.5952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.9716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449    2.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    2.9071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149   -0.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1154    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    2.4393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251    3.3748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    3.9984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4951    4.7780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5753    3.8425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1154    4.4662    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
  2  4  2  0  0  0  0
  4  5  1  4  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
  8 20  2  0  0  0  0
 13 20  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 23 29  1  0  0  0  0
 29 30  1  0  0  0  0
 11 30  1  0  0  0  0
 30 31  2  0  0  0  0
  7 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
  5 35  1  0  0  0  0
 35 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0220159

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(CC(N=C(C)O)C1O)C1=C2C=C(C)C=C(O)C2=C2C(=O)C3=CC=CC(O)=C3C(=O)C2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H25NO8/c1-10-7-14-19(17(31)8-10)22-23(26(34)20-13(25(22)33)5-4-6-16(20)30)27(35)21(14)18-9-15(28-12(3)29)24(32)11(2)36-18/h4-8,11,15,18,24,30-32,35H,9H2,1-3H3,(H,28,29)

> <INCHI_KEY>
CIRRCIZRHRGWRI-UHFFFAOYSA-N

> <FORMULA>
C27H25NO8

> <MOLECULAR_WEIGHT>
491.496

> <EXACT_MASS>
491.158016769

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
51.19352056804452

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxo-7,12-dihydrotetraphen-5-yl)oxan-4-yl]ethanimidic acid

> <JCHEM_LOGP>
4.322360931666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.426303289952927

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.408248723794132

> <JCHEM_PKA_STRONGEST_BASIC>
2.5995467281192726

> <JCHEM_POLAR_SURFACE_AREA>
156.88

> <JCHEM_REFRACTIVITY>
130.6856

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
N-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      14.944   6.300   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.432   6.591   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      12.928   8.046   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0      12.424   5.427   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      10.911   5.718   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.903   4.553   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.391   4.844   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.383   3.680   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.870   3.971   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.366   5.427   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.862   2.807   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.366   1.352   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.879   1.061   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.383  -0.394   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.375  -1.558   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.895  -0.685   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.903   0.479   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.415   0.188   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.399   1.934   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.887   2.225   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.358   0.188   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.862  -1.267   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.846   0.479   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.838  -0.685   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.326  -0.394   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.179   1.061   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.830   2.225   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.326   3.680   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.342   1.934   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.350   3.098   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       2.846   4.553   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       7.887   6.300   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       8.895   7.464   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.391   8.919   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.407   7.173   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      11.415   8.337   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   35                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   32                                                  
CONECT    8    7    9   20                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   30                                                  
CONECT   12   11   13   21                                                  
CONECT   13   12   14   20                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19    8   13                                                  
CONECT   21   12   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   23   30                                                  
CONECT   30   29   11   31                                                  
CONECT   31   30                                                            
CONECT   32    7   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33    5   36                                                  
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   80    0
END

View in JSmol

Synonyms

Value	Source
N-[3-Hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxo-7,12-dihydrotetraphen-5-yl)oxan-4-yl]ethanimidate	Generator

Chemical Formula

C₂₇H₂₅NO₈

Average Mass

491.4960 Da

Monoisotopic Mass

491.15802 Da

IUPAC Name

N-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxo-7,12-dihydrotetraphen-5-yl)oxan-4-yl]ethanimidic acid

Traditional Name

N-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid

CAS Registry Number

Not Available

SMILES

CC1OC(CC(N=C(C)O)C1O)C1=C2C=C(C)C=C(O)C2=C2C(=O)C3=CC=CC(O)=C3C(=O)C2=C1O

InChI Identifier

InChI=1S/C27H25NO8/c1-10-7-14-19(17(31)8-10)22-23(26(34)20-13(25(22)33)5-4-6-16(20)30)27(35)21(14)18-9-15(28-12(3)29)24(32)11(2)36-18/h4-8,11,15,18,24,30-32,35H,9H2,1-3H3,(H,28,29)

InChI Key

CIRRCIZRHRGWRI-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 angucyclines. These are polyketides with a structure based on then benz[a]anthracene skeleton, with the particularity that the central ring of the anthracene moiety is a para-quinone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Angucyclines

Sub Class

Not Available

Direct Parent

Angucyclines

Alternative Parents

Substituents

Angucycline core
Anthraquinone
9,10-anthraquinone
Phenanthrol
Phenanthrene
Anthracene
1-naphthol
2-naphthol
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Oxane
Acetamide
Vinylogous acid
Secondary carboxylic acid amide
Secondary alcohol
Ketone
Carboxamide group
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen 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
logP	4.32	ChemAxon
pKa (Strongest Acidic)	5.41	ChemAxon
pKa (Strongest Basic)	2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	156.88 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	130.69 m³·mol⁻¹	ChemAxon
Polarizability	51.19 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163033816

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid (NP0220159)

MOL for NP0220159 (n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid)

3D MOL for NP0220159 (n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid)

3D SDF for NP0220159 (n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid)

3D-SDF for NP0220159 (n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid)

PDB for NP0220159 (n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid)

3D PDB for NP0220159 (n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid)

SMILES for NP0220159 (n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid)

INCHI for NP0220159 (n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid)

Structure for NP0220159 (n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid)

3D Structure for NP0220159 (n-[3-hydroxy-2-methyl-6-(1,6,8-trihydroxy-3-methyl-7,12-dioxotetraphen-5-yl)oxan-4-yl]ethanimidic acid)