NP-MRD: Showing NP-Card for (3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione (NP0206718)

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Record Information

Version

2.0

Created at

2022-09-05 03:04:41 UTC

Updated at

2022-09-05 03:04:41 UTC

NP-MRD ID

NP0206718

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione

Description

Atramycin B 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. (3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione is found in Streptomyces atratus. (3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione was first documented in 1991 (PMID: 1938611). Based on a literature review very few articles have been published on Atramycin B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052205042D          

 33 37  0  0  1  0            999 V2000
    6.1154    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.2566    0.0000 C   0  0  2  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
    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
    3.6850    0.5684    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
    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
    2.6048    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
    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
   -0.6358    2.1275    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9058    2.9071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7159    3.0630    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9860    3.8425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2560    2.4393    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0662    2.5952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9860    1.6598    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5261    1.0361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1758    1.5039    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9058    0.7243    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
    5.0352    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
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 20 28  1  0  0  0  0
 28 29  1  6  0  0  0
 18 30  2  0  0  0  0
 14 30  1  0  0  0  0
 30 31  1  0  0  0  0
 10 31  1  0  0  0  0
 31 32  2  0  0  0  0
  7 33  1  0  0  0  0
  2 33  1  0  0  0  0
M  END

     RDKit          3D

 57 61  0  0  0  0  0  0  0  0999 V2000
    6.8449   -0.3235    1.4972 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7978   -0.5930    0.0079 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3218    0.6367   -0.6869 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0185    0.4614   -1.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6803    0.9510   -2.4705 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0426   -0.3799   -0.6754 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5223   -1.5836   -0.1211 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6332   -2.4407    0.4565 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2667   -2.1130    0.4895 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8094   -0.9324   -0.0535 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7058   -0.0343   -0.6512 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2595    1.2158   -1.2192 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0207    2.0302   -1.7382 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8376    1.5326   -1.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4079    2.7111   -1.7097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9487    3.0575   -1.6881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8404    2.1606   -1.0974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4253    0.9731   -0.5494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2486    0.0456    0.0466 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6265    0.1299    0.2027 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9192    0.0540    1.5633 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1745   -0.4686    1.8047 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7151    0.2083    3.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1585   -0.1708    0.6952 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.3702   -0.7674    1.0498 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7320   -0.7701   -0.6199 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.8526    0.2091   -1.6248 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2474   -1.0835   -0.5025 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7381   -1.1389   -1.7970 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0697    0.6738   -0.5947 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3965   -0.5788   -0.0229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4066   -1.3936    0.5148 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9675   -1.8219   -0.2000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9348    0.1905    1.8543 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7736    0.2465    1.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8979   -1.2881    2.0813 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8474   -0.7874   -0.3039 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2185    1.4637    0.0395 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0403    0.9625   -1.4665 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9563   -3.3589    0.8855 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5492   -2.7686    0.9350 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1110    3.3737   -2.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3108    3.9778   -2.1067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8967    2.3874   -1.0588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1109    1.0231   -0.1860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1686   -1.5516    2.0108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3693   -0.3168    3.9794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4072    1.2828    3.0617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8409    0.2409    3.0330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3027    0.9228    0.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2640   -1.7437    0.8417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3258   -1.6344   -0.9303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0237    1.1017   -1.2535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1134   -2.0058    0.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7567   -1.0405   -1.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2478   -2.6150    0.5225 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2547   -2.2375   -1.2105 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  2  0
  4  6  1  0
  6  7  2  0
  7 33  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
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 21 22  1  0
 22 23  1  0
 22 24  1  0
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 24 26  1  0
 26 27  1  0
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 28 29  1  0
 18 30  2  0
 30 31  1  0
 31 32  2  0
 33  2  1  0
 31 10  1  0
 11  6  1  0
 30 14  1  0
 28 20  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  6
  3 38  1  0
  3 39  1  0
 33 56  1  0
 33 57  1  0
  8 40  1  0
  9 41  1  0
 15 42  1  0
 16 43  1  0
 17 44  1  0
 20 45  1  6
 22 46  1  1
 23 47  1  0
 23 48  1  0
 23 49  1  0
 24 50  1  6
 25 51  1  0
 26 52  1  6
 27 53  1  0
 28 54  1  1
 29 55  1  0
M  END


  Mrv1652309052205042D          

 33 37  0  0  1  0            999 V2000
    6.1154    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.2566    0.0000 C   0  0  2  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
    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
    3.6850    0.5684    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
    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
    2.6048    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
    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
   -0.6358    2.1275    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9058    2.9071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7159    3.0630    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9860    3.8425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2560    2.4393    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0662    2.5952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9860    1.6598    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5261    1.0361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1758    1.5039    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9058    0.7243    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
    5.0352    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
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 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 20 28  1  0  0  0  0
 28 29  1  6  0  0  0
 18 30  2  0  0  0  0
 14 30  1  0  0  0  0
 30 31  1  0  0  0  0
 10 31  1  0  0  0  0
 31 32  2  0  0  0  0
  7 33  1  0  0  0  0
  2 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0206718

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC(=O)C2=C(C1)C=CC1=C2C(=O)C2=CC=CC(O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H24O8/c1-10-8-12-6-7-14-19(17(12)15(26)9-10)22(29)13-4-3-5-16(18(13)21(14)28)33-25-24(31)23(30)20(27)11(2)32-25/h3-7,10-11,20,23-25,27,30-31H,8-9H2,1-2H3/t10-,11-,20-,23+,24+,25-/m0/s1

> <INCHI_KEY>
MOHALZUCHLKMFC-FGEMJCSKSA-N

> <FORMULA>
C25H24O8

> <MOLECULAR_WEIGHT>
452.459

> <EXACT_MASS>
452.147117733

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
46.87206046324642

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S)-3-methyl-8-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-1,2,3,4,7,12-hexahydrotetraphene-1,7,12-trione

> <JCHEM_LOGP>
1.9888805749999996

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.268439687116487

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.213569098916288

> <JCHEM_PKA_STRONGEST_BASIC>
-3.612200363197915

> <JCHEM_POLAR_SURFACE_AREA>
130.36

> <JCHEM_REFRACTIVITY>
116.5499

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S)-3-methyl-8-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2H-tetraphene-1,7,12-trione

> <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      11.415   0.188   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.903   0.479   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.895  -0.685   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.383  -0.394   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.375  -1.558   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.879   1.061   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.887   2.225   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  C   UNK     0       4.862   2.807   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.366   1.352   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.358   0.188   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.862  -1.267   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.846   0.479   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.838  -0.685   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.326  -0.394   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.179   1.061   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.830   2.225   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.326   3.680   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.187   3.971   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.691   5.427   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -3.203   5.718   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.707   7.173   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.211   4.553   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -5.723   4.844   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -3.707   3.098   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -4.715   1.934   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -2.195   2.807   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.691   1.352   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.342   1.934   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.350   3.098   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.846   4.553   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       9.399   1.934   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   33                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   11                                                  
CONECT    7    6    8   33                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   31                                                  
CONECT   11   10    6   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   30                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   30                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   20   29                                                  
CONECT   29   28                                                            
CONECT   30   18   14   31                                                  
CONECT   31   30   10   32                                                  
CONECT   32   31                                                            
CONECT   33    7    2                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₄O₈

Average Mass

452.4590 Da

Monoisotopic Mass

452.14712 Da

IUPAC Name

(3S)-3-methyl-8-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-1,2,3,4,7,12-hexahydrotetraphene-1,7,12-trione

Traditional Name

(3S)-3-methyl-8-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2H-tetraphene-1,7,12-trione

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC(=O)C2=C(C1)C=CC1=C2C(=O)C2=CC=CC(O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)=C2C1=O

InChI Identifier

InChI=1S/C25H24O8/c1-10-8-12-6-7-14-19(17(12)15(26)9-10)22(29)13-4-3-5-16(18(13)21(14)28)33-25-24(31)23(30)20(27)11(2)32-25/h3-7,10-11,20,23-25,27,30-31H,8-9H2,1-2H3/t10-,11-,20-,23+,24+,25-/m0/s1

InChI Key

MOHALZUCHLKMFC-FGEMJCSKSA-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 atratus	LOTUS Database	35616633

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
9,10-anthraquinone
Anthraquinone
Phenolic glycoside
Anthracene
Phenanthrene
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Tetralin
Aryl alkyl ketone
Aryl ketone
Benzenoid
Oxane
Monosaccharide
Secondary alcohol
Ketone
Polyol
Organoheterocyclic compound
Acetal
Oxacycle
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organooxygen compound
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	1.99	ChemAxon
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	130.36 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	116.55 m³·mol⁻¹	ChemAxon
Polarizability	46.87 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

C00017161

Chemspider ID

116633

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

132030

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Fujioka K, Furihata K, Shimazu A, Hayakawa Y, Seto H: Isolation and characterization of atramycin A and atramycin B, new isotetracenone type antitumor antibiotics. J Antibiot (Tokyo). 1991 Sep;44(9):1025-8. doi: 10.7164/antibiotics.44.1025. [PubMed:1938611 ]
LOTUS database [Link]

Showing NP-Card for (3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione (NP0206718)

MOL for NP0206718 ((3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione)

3D MOL for NP0206718 ((3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione)

3D SDF for NP0206718 ((3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione)

3D-SDF for NP0206718 ((3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione)

PDB for NP0206718 ((3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione)

3D PDB for NP0206718 ((3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione)

SMILES for NP0206718 ((3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione)

INCHI for NP0206718 ((3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione)

Structure for NP0206718 ((3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione)

3D Structure for NP0206718 ((3s)-3-methyl-8-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-3,4-dihydro-2h-tetraphene-1,7,12-trione)