NP-MRD: Showing NP-Card for 9α-hydroxydihydrodesoxybostrycin (NP0008123)

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Record Information

Version

2.0

Created at

2020-12-09 05:46:29 UTC

Updated at

2021-07-15 16:59:29 UTC

NP-MRD ID

NP0008123

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9α-hydroxydihydrodesoxybostrycin

Provided By

NPAtlas

Description

9Alpha-Hydroxydihydrodesoxybostrycin belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings. 9α-hydroxydihydrodesoxybostrycin is found in Aspergillus sp. and Unknown-fungus sp.. 9α-hydroxydihydrodesoxybostrycin was first documented in 2014 (PMID: 24840716). Based on a literature review very few articles have been published on 9Alpha-Hydroxydihydrodesoxybostrycin.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106073D          

 43 45  0  0  0  0            999 V2000
    6.0825    0.5560    0.8284 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8621    1.2199    0.5882 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7380    0.4940    0.1946 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7402   -0.8581    0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875   -1.5024   -0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5824   -2.8991   -0.5518 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4254   -0.8167   -0.5914 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4098    0.5659   -0.4175 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5366    1.2109   -0.0337 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5758    2.5738    0.1520 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0816    1.1999   -0.6962 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0265    2.5278   -0.5016 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9251    0.3901    0.1062 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2261    1.1171    0.1035 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1561    0.2924    1.0043 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4694    0.9986    1.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5393    0.2224    2.2456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3153   -1.0507    0.3680 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1163   -1.8301    1.2145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0128   -1.7807    0.1272 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0988   -0.9123   -0.6688 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1925   -1.5030   -1.0064 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2794   -2.5601   -1.6287 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9729   -0.3788    1.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7340    1.2504    1.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6212    0.3000   -0.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6758   -1.4109    0.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3968   -3.4562   -0.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8527    3.1942    0.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1394    0.9461   -1.7860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5192    2.9438   -1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5264    0.1939    1.1105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0950    2.1386    0.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6086    1.1531   -0.9333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9503    0.8244    2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3208    2.0941    0.9675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1199    0.6764    0.2054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9856   -0.4415    2.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7957   -0.9005   -0.6223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9678   -1.3298    1.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2617   -2.6708   -0.4942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5536   -2.1323    1.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6177   -0.6495   -1.6206 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  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
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  1  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
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 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
  9  3  1  0  0  0  0
 21 13  1  0  0  0  0
 22  7  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  4 27  1  0  0  0  0
  6 28  1  0  0  0  0
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 12 31  1  0  0  0  0
 13 32  1  1  0  0  0
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 16 35  1  0  0  0  0
 16 36  1  0  0  0  0
 16 37  1  0  0  0  0
 17 38  1  0  0  0  0
 18 39  1  6  0  0  0
 19 40  1  0  0  0  0
 20 41  1  0  0  0  0
 20 42  1  0  0  0  0
 21 43  1  6  0  0  0
M  END

     RDKit          3D

 43 45  0  0  0  0  0  0  0  0999 V2000
    6.0825    0.5560    0.8284 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8621    1.2199    0.5882 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7380    0.4940    0.1946 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7402   -0.8581    0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875   -1.5024   -0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5824   -2.8991   -0.5518 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4254   -0.8167   -0.5914 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4098    0.5659   -0.4175 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5366    1.2109   -0.0337 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5758    2.5738    0.1520 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0816    1.1999   -0.6962 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0265    2.5278   -0.5016 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9251    0.3901    0.1062 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2261    1.1171    0.1035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1561    0.2924    1.0043 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4694    0.9986    1.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5393    0.2224    2.2456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3153   -1.0507    0.3680 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1163   -1.8301    1.2145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0128   -1.7807    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0988   -0.9123   -0.6688 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1925   -1.5030   -1.0064 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2794   -2.5601   -1.6287 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9729   -0.3788    1.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7340    1.2504    1.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6212    0.3000   -0.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6758   -1.4109    0.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3968   -3.4562   -0.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8527    3.1942    0.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1394    0.9461   -1.7860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5192    2.9438   -1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5264    0.1939    1.1105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0950    2.1386    0.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6086    1.1531   -0.9333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9503    0.8244    2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3208    2.0941    0.9675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1199    0.6764    0.2054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9856   -0.4415    2.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7957   -0.9005   -0.6223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9678   -1.3298    1.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2617   -2.6708   -0.4942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5536   -2.1323    1.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6177   -0.6495   -1.6206 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  8 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  1
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
  9  3  1  0
 21 13  1  0
 22  7  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  6 28  1  0
 10 29  1  0
 11 30  1  6
 12 31  1  0
 13 32  1  1
 14 33  1  0
 14 34  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  6
 19 40  1  0
 20 41  1  0
 20 42  1  0
 21 43  1  6
M  END


  Mrv1652306242106073D          

 43 45  0  0  0  0            999 V2000
    6.0825    0.5560    0.8284 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8621    1.2199    0.5882 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7380    0.4940    0.1946 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7402   -0.8581    0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875   -1.5024   -0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5824   -2.8991   -0.5518 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4254   -0.8167   -0.5914 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4098    0.5659   -0.4175 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5366    1.2109   -0.0337 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5758    2.5738    0.1520 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0816    1.1999   -0.6962 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0265    2.5278   -0.5016 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9251    0.3901    0.1062 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2261    1.1171    0.1035 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1561    0.2924    1.0043 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4694    0.9986    1.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5393    0.2224    2.2456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3153   -1.0507    0.3680 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1163   -1.8301    1.2145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0128   -1.7807    0.1272 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0988   -0.9123   -0.6688 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1925   -1.5030   -1.0064 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2794   -2.5601   -1.6287 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9729   -0.3788    1.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7340    1.2504    1.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6212    0.3000   -0.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6758   -1.4109    0.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3968   -3.4562   -0.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8527    3.1942    0.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1394    0.9461   -1.7860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5192    2.9438   -1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5264    0.1939    1.1105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0950    2.1386    0.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6086    1.1531   -0.9333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9503    0.8244    2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3208    2.0941    0.9675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1199    0.6764    0.2054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9856   -0.4415    2.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7957   -0.9005   -0.6223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9678   -1.3298    1.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2617   -2.6708   -0.4942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5536   -2.1323    1.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6177   -0.6495   -1.6206 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  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
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  1  0  0  0
 15 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  2  0  0  0  0
  9  3  1  0  0  0  0
 21 13  1  0  0  0  0
 22  7  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  4 27  1  0  0  0  0
  6 28  1  0  0  0  0
 10 29  1  0  0  0  0
 11 30  1  6  0  0  0
 12 31  1  0  0  0  0
 13 32  1  1  0  0  0
 14 33  1  0  0  0  0
 14 34  1  0  0  0  0
 16 35  1  0  0  0  0
 16 36  1  0  0  0  0
 16 37  1  0  0  0  0
 17 38  1  0  0  0  0
 18 39  1  6  0  0  0
 19 40  1  0  0  0  0
 20 41  1  0  0  0  0
 20 42  1  0  0  0  0
 21 43  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0008123

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)[C@@]3([H])C([H])([H])[C@@]([H])(O[H])[C@](O[H])(C([H])([H])[H])C([H])([H])[C@]3([H])[C@@]([H])(O[H])C2=C(O[H])C(OC([H])([H])[H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H20O7/c1-16(22)5-7-6(3-10(16)18)13(19)11-8(17)4-9(23-2)15(21)12(11)14(7)20/h4,6-7,10,14,17-18,20-22H,3,5H2,1-2H3/t6-,7-,10+,14+,16-/m0/s1

> <INCHI_KEY>
LNMXRONIHUOFQM-HVRKRCABSA-N

> <FORMULA>
C16H20O7

> <MOLECULAR_WEIGHT>
324.329

> <EXACT_MASS>
324.120902984

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
32.81174643714532

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3S,4aS,9aS,10R)-2,3,5,8,10-pentahydroxy-6-methoxy-3-methyl-1,2,3,4,4a,9,9a,10-octahydroanthracen-9-one

> <ALOGPS_LOGP>
-0.30

> <JCHEM_LOGP>
0.08783675866666665

> <ALOGPS_LOGS>
-1.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.52828986254971

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.976588607732024

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2141345718231067

> <JCHEM_POLAR_SURFACE_AREA>
127.45000000000002

> <JCHEM_REFRACTIVITY>
80.38229999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.95e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6S,7R,8aS,10R,10aS)-1,4,6,7,10-pentahydroxy-3-methoxy-6-methyl-5,7,8,8a,10,10a-hexahydroanthracen-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 43 45  0  0  0  0  0  0  0  0999 V2000
    6.0825    0.5560    0.8284 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8621    1.2199    0.5882 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7380    0.4940    0.1946 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7402   -0.8581    0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875   -1.5024   -0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5824   -2.8991   -0.5518 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4254   -0.8167   -0.5914 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4098    0.5659   -0.4175 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5366    1.2109   -0.0337 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5758    2.5738    0.1520 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0816    1.1999   -0.6962 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0265    2.5278   -0.5016 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9251    0.3901    0.1062 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2261    1.1171    0.1035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1561    0.2924    1.0043 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4694    0.9986    1.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5393    0.2224    2.2456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3153   -1.0507    0.3680 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1163   -1.8301    1.2145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0128   -1.7807    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0988   -0.9123   -0.6688 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1925   -1.5030   -1.0064 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2794   -2.5601   -1.6287 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9729   -0.3788    1.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7340    1.2504    1.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6212    0.3000   -0.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6758   -1.4109    0.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3968   -3.4562   -0.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8527    3.1942    0.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1394    0.9461   -1.7860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5192    2.9438   -1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5264    0.1939    1.1105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0950    2.1386    0.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6086    1.1531   -0.9333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9503    0.8244    2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3208    2.0941    0.9675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1199    0.6764    0.2054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9856   -0.4415    2.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7957   -0.9005   -0.6223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9678   -1.3298    1.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2617   -2.6708   -0.4942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5536   -2.1323    1.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6177   -0.6495   -1.6206 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  8 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  1
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
  9  3  1  0
 21 13  1  0
 22  7  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  6 28  1  0
 10 29  1  0
 11 30  1  6
 12 31  1  0
 13 32  1  1
 14 33  1  0
 14 34  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  6
 19 40  1  0
 20 41  1  0
 20 42  1  0
 21 43  1  6
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       6.082   0.556   0.828  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.862   1.220   0.588  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.738   0.494   0.195  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.740  -0.858   0.021  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.587  -1.502  -0.370  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.582  -2.899  -0.552  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.425  -0.817  -0.591  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.410   0.566  -0.418  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.537   1.211  -0.034  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.576   2.574   0.152  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.082   1.200  -0.696  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.027   2.528  -0.502  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.925   0.390   0.106  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.226   1.117   0.104  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.156   0.292   1.004  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.469   0.999   1.036  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.539   0.222   2.246  0.00  0.00           O+0
HETATM   18  C   UNK     0      -3.315  -1.051   0.368  0.00  0.00           C+0
HETATM   19  O   UNK     0      -4.116  -1.830   1.214  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.013  -1.781   0.127  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.099  -0.912  -0.669  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.193  -1.503  -1.006  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.279  -2.560  -1.629  0.00  0.00           O+0
HETATM   24  H   UNK     0       5.973  -0.379   1.394  0.00  0.00           H+0
HETATM   25  H   UNK     0       6.734   1.250   1.435  0.00  0.00           H+0
HETATM   26  H   UNK     0       6.621   0.300  -0.117  0.00  0.00           H+0
HETATM   27  H   UNK     0       4.676  -1.411   0.199  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.397  -3.456  -0.406  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.853   3.194   0.037  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.139   0.946  -1.786  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.519   2.944  -1.255  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.526   0.194   1.111  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.095   2.139   0.517  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.609   1.153  -0.933  0.00  0.00           H+0
HETATM   35  H   UNK     0      -4.950   0.824   2.040  0.00  0.00           H+0
HETATM   36  H   UNK     0      -4.321   2.094   0.968  0.00  0.00           H+0
HETATM   37  H   UNK     0      -5.120   0.676   0.205  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.986  -0.442   2.795  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.796  -0.901  -0.622  0.00  0.00           H+0
HETATM   40  H   UNK     0      -4.968  -1.330   1.392  0.00  0.00           H+0
HETATM   41  H   UNK     0      -2.262  -2.671  -0.494  0.00  0.00           H+0
HETATM   42  H   UNK     0      -1.554  -2.132   1.061  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.618  -0.650  -1.621  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5   27                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   28                                                       
CONECT    7    5    8   22                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8   10    3                                                  
CONECT   10    9   29                                                       
CONECT   11    8   12   13   30                                             
CONECT   12   11   31                                                       
CONECT   13   11   14   21   32                                             
CONECT   14   13   15   33   34                                             
CONECT   15   14   16   17   18                                             
CONECT   16   15   35   36   37                                             
CONECT   17   15   38                                                       
CONECT   18   15   19   20   39                                             
CONECT   19   18   40                                                       
CONECT   20   18   21   41   42                                             
CONECT   21   20   22   13   43                                             
CONECT   22   21   23    7                                                  
CONECT   23   22                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    4                                                            
CONECT   28    6                                                            
CONECT   29   10                                                            
CONECT   30   11                                                            
CONECT   31   12                                                            
CONECT   32   13                                                            
CONECT   33   14                                                            
CONECT   34   14                                                            
CONECT   35   16                                                            
CONECT   36   16                                                            
CONECT   37   16                                                            
CONECT   38   17                                                            
CONECT   39   18                                                            
CONECT   40   19                                                            
CONECT   41   20                                                            
CONECT   42   20                                                            
CONECT   43   21                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   90    0
END

RDKit          3D

43 45  0  0  0  0  0  0  0  0999 V2000
    6.0825    0.5560    0.8284 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8621    1.2199    0.5882 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7380    0.4940    0.1946 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7402   -0.8581    0.0209 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875   -1.5024   -0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5824   -2.8991   -0.5518 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4254   -0.8167   -0.5914 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4098    0.5659   -0.4175 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5366    1.2109   -0.0337 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5758    2.5738    0.1520 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0816    1.1999   -0.6962 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0265    2.5278   -0.5016 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9251    0.3901    0.1062 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2261    1.1171    0.1035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1561    0.2924    1.0043 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4694    0.9986    1.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5393    0.2224    2.2456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3153   -1.0507    0.3680 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1163   -1.8301    1.2145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0128   -1.7807    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0988   -0.9123   -0.6688 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1925   -1.5030   -1.0064 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2794   -2.5601   -1.6287 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9729   -0.3788    1.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7340    1.2504    1.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6212    0.3000   -0.1171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6758   -1.4109    0.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3968   -3.4562   -0.4064 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8527    3.1942    0.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1394    0.9461   -1.7860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5192    2.9438   -1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5264    0.1939    1.1105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0950    2.1386    0.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6086    1.1531   -0.9333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9503    0.8244    2.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3208    2.0941    0.9675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1199    0.6764    0.2054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9856   -0.4415    2.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7957   -0.9005   -0.6223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9678   -1.3298    1.3917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2617   -2.6708   -0.4942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5536   -2.1323    1.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6177   -0.6495   -1.6206 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  8 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  1
 15 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
  9  3  1  0
 21 13  1  0
 22  7  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  6 28  1  0
 10 29  1  0
 11 30  1  6
 12 31  1  0
 13 32  1  1
 14 33  1  0
 14 34  1  0
 16 35  1  0
 16 36  1  0
 16 37  1  0
 17 38  1  0
 18 39  1  6
 19 40  1  0
 20 41  1  0
 20 42  1  0
 21 43  1  6
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
9a-Hydroxydihydrodesoxybostrycin	Generator
9Α-hydroxydihydrodesoxybostrycin	Generator

Chemical Formula

C₁₆H₂₀O₇

Average Mass

324.3290 Da

Monoisotopic Mass

324.12090 Da

IUPAC Name

(2R,3S,4aS,9aS,10R)-2,3,5,8,10-pentahydroxy-6-methoxy-3-methyl-1,2,3,4,4a,9,9a,10-octahydroanthracen-9-one

Traditional Name

(6S,7R,8aS,10R,10aS)-1,4,6,7,10-pentahydroxy-3-methoxy-6-methyl-5,7,8,8a,10,10a-hexahydroanthracen-9-one

CAS Registry Number

Not Available

SMILES

COC1=C(O)C2=C(C(O)=C1)C(=O)[C@H]1C[C@@H](O)[C@@](C)(O)C[C@@H]1[C@H]2O

InChI Identifier

InChI=1S/C16H20O7/c1-16(22)5-7-6(3-10(16)18)13(19)11-8(17)4-9(23-2)15(21)12(11)14(7)20/h4,6-7,10,14,17-18,20-22H,3,5H2,1-2H3/t6-,7-,10+,14+,16-/m0/s1

InChI Key

LNMXRONIHUOFQM-HVRKRCABSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Aspergillus sp.	Fungi	KNApSAcK
Unknown-fungus sp.	NPAtlas	19043240

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Anthracenes

Sub Class

Not Available

Direct Parent

Anthracenes

Alternative Parents

Substituents

Anthracene
Tetralin
Anisole
Aryl alkyl ketone
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Cyclic alcohol
Tertiary alcohol
Vinylogous acid
Ketone
Secondary alcohol
Polyol
Ether
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	-0.3	ALOGPS
logP	0.088	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	8.98	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	127.45 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	80.38 m³·mol⁻¹	ChemAxon
Polarizability	32.81 Å³	ChemAxon
Number of Rings	3	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

NPAtlas ID

NPA000835

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

25054966

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25015070

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Xia G, Li J, Li H, Long Y, Lin S, Lu Y, He L, Lin Y, Liu L, She Z: Alterporriol-type dimers from the mangrove endophytic fungus, Alternaria sp. (SK11), and their MptpB inhibitions. Mar Drugs. 2014 May 16;12(5):2953-69. doi: 10.3390/md12052953. [PubMed:24840716 ]

Showing NP-Card for 9α-hydroxydihydrodesoxybostrycin (NP0008123)

MOL for NP0008123 (9α-hydroxydihydrodesoxybostrycin)

3D MOL for NP0008123 (9α-hydroxydihydrodesoxybostrycin)

3D SDF for NP0008123 (9α-hydroxydihydrodesoxybostrycin)

3D-SDF for NP0008123 (9α-hydroxydihydrodesoxybostrycin)

PDB for NP0008123 (9α-hydroxydihydrodesoxybostrycin)

3D PDB for NP0008123 (9α-hydroxydihydrodesoxybostrycin)

SMILES for NP0008123 (9α-hydroxydihydrodesoxybostrycin)

INCHI for NP0008123 (9α-hydroxydihydrodesoxybostrycin)

Structure for NP0008123 (9α-hydroxydihydrodesoxybostrycin)

3D Structure for NP0008123 (9α-hydroxydihydrodesoxybostrycin)