NP-MRD: Showing NP-Card for methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate (NP0326318)

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Record Information

Version

2.0

Created at

2022-09-12 07:46:04 UTC

Updated at

2022-09-12 07:46:04 UTC

NP-MRD ID

NP0326318

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate

Description

11-Hydroxy aclacinomycin A belongs to the class of organic compounds known as anthracyclines. These are polyketides containing a tetracenequinone ring structure with a sugar attached by glycosidic linkage. methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate is found in Streptomyces galilaeus and Streptomyces violaceus. Based on a literature review very few articles have been published on 11-Hydroxy aclacinomycin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122209462D          

 59 65  0  0  0  0            999 V2000
    6.8104    0.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5282    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9979   -0.7752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   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
    5.0013    2.0625    0.0000 O   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
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   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
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    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
    3.5724   -0.4125    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
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   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
    4.2868   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   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
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   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
    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
    0.0000    0.8250    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    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    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
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  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
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 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
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 22 29  1  0  0  0  0
 20 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 16 32  1  0  0  0  0
 14 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
  8 35  1  0  0  0  0
  6 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
 36 43  1  0  0  0  0
 43 44  1  0  0  0  0
  3 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 45 47  1  0  0  0  0
 47 48  1  0  0  0  0
 40 49  1  0  0  0  0
 49 50  2  0  0  0  0
 49 51  1  0  0  0  0
 51 52  2  0  0  0  0
 52 53  1  0  0  0  0
 53 54  2  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 55 57  2  0  0  0  0
 51 57  1  0  0  0  0
 57 58  1  0  0  0  0
 39 58  1  0  0  0  0
 58 59  2  0  0  0  0
M  END

     RDKit          3D

112118  0  0  0  0  0  0  0  0999 V2000
   -6.6170    0.2571   -4.9500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6943    0.7308   -3.8941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7364   -0.1988   -3.2667 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8953   -0.7379   -4.3004 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7839    0.7095   -2.4596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1679   -0.1139   -1.2652 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1614    0.6961   -0.7430 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9451    0.5886   -1.3390 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3821    1.9761   -1.5219 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6162    2.3328   -0.4724 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4373    2.2838    0.8512 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2954    1.2657    1.7510 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3263    3.5739    1.5113 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8479    1.3638   -0.9332 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8698    1.5362   -0.2213 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8758    1.7305    0.4637 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1236    1.5894   -0.6126 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3451    1.6885    0.2990 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9913    2.3478    1.4444 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5024    0.1560    0.6605 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5351   -0.0831    1.4973 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6389   -0.5707    0.7841 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.9839   -1.9979    1.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0061   -2.4187   -0.0430 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8184   -1.1855   -0.3412 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3180   -0.9764   -1.4065 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9499   -0.2408    0.8004 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.0167    0.8074    0.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6963    0.2647    1.0520 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1184   -0.1738    1.1042 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2733   -1.0006    2.3958 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3383    0.9305    1.4833 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2638    0.0378   -1.2392 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1389   -1.1454   -0.8934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0078   -0.1616   -0.6114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3292   -0.3198   -0.4134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3785    0.0835    0.9306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2673    0.6227    1.4537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5433   -0.1034    1.5921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6525   -0.6545    1.0159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6162   -1.0595   -0.3308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7505   -1.5897   -0.8296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4493   -0.8907   -1.0324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1842   -1.3095   -2.4245 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9643   -2.3967   -2.9574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6386   -2.3351   -3.9817 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9695   -3.6278   -2.2713 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7566   -4.6766   -2.8266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8907   -0.8709    1.7569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9226   -1.3880    1.2057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9924   -0.5024    3.1606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2082   -0.7452    3.8159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2616   -0.3909    5.1459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1913    0.1679    5.8029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9769    0.4050    5.1281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9654    0.9565    5.8221 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9041    0.0543    3.7870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6653    0.2580    3.0044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6716    0.7579    3.5646 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8445    1.1176   -5.7049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6412    0.0180   -4.5963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1634   -0.4885   -5.6455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3195    1.2970   -3.1570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0988    1.5894   -4.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3681    0.0489   -4.6535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0286    1.0805   -3.1212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3430    1.5056   -1.9740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7045   -0.9276   -1.8212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1073    0.0338   -2.3088 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1361    1.9007   -2.5431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1910    2.6837   -1.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0600    3.3304   -0.7823 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2126    0.6219    1.9092 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2330    1.7431    2.8066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6129    0.6532    1.7560 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1337    3.5382    2.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6382    3.7343    2.0438 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6034    4.4121    0.8534 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9517    1.9351   -1.9127 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2148    2.8093    0.6928 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9992    2.3734   -1.3243 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0310    0.6056   -1.0277 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2111    2.0401   -0.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4656    2.1202    2.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6759   -0.2627   -0.3774 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4194   -0.5063   -0.3293 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4843   -2.1532    1.9938 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1130   -2.6931    0.8566 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6939   -3.1864    0.3243 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5061   -2.7626   -0.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3096   -0.8458    1.6753 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7110    1.3137   -0.3921 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9669    0.3125    0.3448 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1355    1.4929    1.3982 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5928   -0.8513    0.4206 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7390   -0.3662    3.1778 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3167   -1.3333    2.7769 H   0  0  0  0  0  0  0  0  0  0  0  0
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 56112  1  0
M  END


  Mrv1652309122209462D          

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 36 43  1  0  0  0  0
 43 44  1  0  0  0  0
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 57 58  1  0  0  0  0
 39 58  1  0  0  0  0
 58 59  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0326318

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1(O)CC(OC2CC(C(OC3CC(O)C(OC4CCC(=O)C(C)O4)C(C)O3)C(C)O2)N(C)C)C2=C(O)C3=C(C(O)=C2C1C(=O)OC)C(=O)C1=CC=CC(O)=C1C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C42H53NO16/c1-8-42(52)16-25(30-31(34(42)41(51)53-7)38(50)32-33(37(30)49)36(48)29-20(35(32)47)10-9-11-23(29)45)57-27-14-21(43(5)6)39(18(3)55-27)59-28-15-24(46)40(19(4)56-28)58-26-13-12-22(44)17(2)54-26/h9-11,17-19,21,24-28,34,39-40,45-46,49-50,52H,8,12-16H2,1-7H3

> <INCHI_KEY>
DGBFPZUOWZFVHF-UHFFFAOYSA-N

> <FORMULA>
C42H53NO16

> <MOLECULAR_WEIGHT>
827.877

> <EXACT_MASS>
827.336434631

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
112

> <JCHEM_AVERAGE_POLARIZABILITY>
87.58991158522355

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracene-1-carboxylate

> <JCHEM_LOGP>
4.443433418466026

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
8.16398874186738

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.647061153247476

> <JCHEM_PKA_STRONGEST_BASIC>
9.797698625335343

> <JCHEM_POLAR_SURFACE_AREA>
237.27999999999997

> <JCHEM_REFRACTIVITY>
205.84670000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1H-tetracene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      12.713   1.715   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.186   0.267   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.669  -0.000   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      11.196  -1.447   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.336   3.850   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.669   6.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.003   6.930   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      12.003   8.470   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      13.337   9.240   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.669   9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.337   6.160   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      14.670   6.930   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      16.004   6.160   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.338   6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      18.672   6.160   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      20.005   6.930   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      18.672   4.620   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      20.005   3.850   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      20.005   2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.339   1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      21.339  -0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      20.005  -0.770   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      20.005  -2.310   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      18.672  -0.000   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      17.338  -0.770   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      18.672   1.540   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      17.338   3.850   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      17.338   2.310   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      16.004   4.620   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      13.337   4.620   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      14.670   3.850   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      12.003   3.850   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   44                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   36                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   35                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   14                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   10   15   33                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   32                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   30                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   29                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   22                                                       
CONECT   30   20   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   16                                                       
CONECT   33   14   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33    8                                                       
CONECT   36    6   37   43                                                  
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   58                                                  
CONECT   40   39   41   49                                                  
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   36   44                                                  
CONECT   44   43    3   45                                                  
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   48                                                       
CONECT   48   47                                                            
CONECT   49   40   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   52   57                                                  
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55   51   58                                                  
CONECT   58   57   39   59                                                  
CONECT   59   58                                                            
MASTER        0    0    0    0    0    0    0    0   59    0  130    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₅₃NO₁₆

Average Mass

827.8770 Da

Monoisotopic Mass

827.33643 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CCC1(O)CC(OC2CC(C(OC3CC(O)C(OC4CCC(=O)C(C)O4)C(C)O3)C(C)O2)N(C)C)C2=C(O)C3=C(C(O)=C2C1C(=O)OC)C(=O)C1=CC=CC(O)=C1C3=O

InChI Identifier

InChI=1S/C42H53NO16/c1-8-42(52)16-25(30-31(34(42)41(51)53-7)38(50)32-33(37(30)49)36(48)29-20(35(32)47)10-9-11-23(29)45)57-27-14-21(43(5)6)39(18(3)55-27)59-28-15-24(46)40(19(4)56-28)58-26-13-12-22(44)17(2)54-26/h9-11,17-19,21,24-28,34,39-40,45-46,49-50,52H,8,12-16H2,1-7H3

InChI Key

DGBFPZUOWZFVHF-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Streptomyces galilaeus	LOTUS Database	35616633
Streptomyces violaceus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracyclines. These are polyketides containing a tetracenequinone ring structure with a sugar attached by glycosidic linkage.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Anthracyclines

Sub Class

Not Available

Direct Parent

Anthracyclines

Alternative Parents

Substituents

Anthracyclinone-skeleton
Anthracycline
Tetracenequinone
Aminoglycoside core
Anthracene carboxylic acid or derivatives
Anthracene carboxylic acid
9,10-anthraquinone
1,4-anthraquinone
Anthracene
1-naphthalenecarboxylic acid or derivatives
O-glycosyl compound
Disaccharide
Glycosyl compound
Tetralin
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Amino saccharide
Benzenoid
Oxane
Tertiary alcohol
Methyl ester
Vinylogous acid
Amino acid or derivatives
Cyclic ketone
Carboxylic acid ester
Tertiary aliphatic amine
Tertiary amine
Ketone
Secondary alcohol
Acetal
Polyol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
Organopnictogen compound
Amine
Organonitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	4.44	ChemAxon
pKa (Strongest Acidic)	7.65	ChemAxon
pKa (Strongest Basic)	9.8	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	237.28 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	205.85 m³·mol⁻¹	ChemAxon
Polarizability	87.59 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

388012

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

438788

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate (NP0326318)

MOL for NP0326318 (methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate)

3D MOL for NP0326318 (methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate)

3D SDF for NP0326318 (methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate)

3D-SDF for NP0326318 (methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate)

PDB for NP0326318 (methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate)

3D PDB for NP0326318 (methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate)

SMILES for NP0326318 (methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate)

INCHI for NP0326318 (methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate)

Structure for NP0326318 (methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate)

3D Structure for NP0326318 (methyl 4-{[4-(dimethylamino)-5-({4-hydroxy-6-methyl-5-[(6-methyl-5-oxooxan-2-yl)oxy]oxan-2-yl}oxy)-6-methyloxan-2-yl]oxy}-2-ethyl-2,5,7,12-tetrahydroxy-6,11-dioxo-3,4-dihydro-1h-tetracene-1-carboxylate)