NP-MRD: Showing NP-Card for Tetarimycin B (NP0011264)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2021-01-05 21:01:02 UTC

Updated at

2021-07-15 17:08:26 UTC

NP-MRD ID

NP0011264

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Tetarimycin B

Provided By

NPAtlas

Description

Tetarimycin B is found in eDNA sp. It was first documented in 2012 (PMID: 23157252). Based on a literature review very few articles have been published on 2,4,6,7,9-pentahydroxy-7,12,12-trimethyl-5,7,8,9,10,12-hexahydrotetracen-5-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242116553D          

 49 52  0  0  0  0            999 V2000
   -3.9761    1.5081   -0.6908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4757    0.7802    0.5399 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5277    1.7171    1.5922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4780   -0.2885    0.8754 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1140   -1.5053    0.0213 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1468   -2.4159   -0.0299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8438   -2.0743    0.5833 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7733   -1.0464    0.3929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4613   -1.4264    0.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5809   -0.4974    0.0525 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2318    0.8288    0.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0879    1.2396    0.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5019    2.5321    0.1980 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1112    0.2731    0.3798 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3044    1.8223   -0.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9701    3.0111   -0.1551 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6676    1.3443   -0.3092 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6740    2.3000   -0.4867 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4300    3.6315   -0.5129 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0066    1.8808   -0.6471 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2983    0.5558   -0.6276 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6190    0.1046   -0.7850 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107   -0.3491   -0.4549 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9577    0.0045   -0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9554   -1.0194   -0.1089 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8872   -2.0195   -1.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3208   -1.7619    1.1943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6457    1.0523   -1.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0845    1.4837   -0.6568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7075    2.6008   -0.6297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0600    1.3596    2.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5197    0.0286    0.6726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3490   -0.6416    1.9378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8834   -1.1102   -0.9884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6332   -2.2669   -0.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9533   -2.3409    1.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5684   -2.9809   -0.0176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2369   -2.4643    0.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0536    3.3621    0.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6393    4.1470   -0.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7819    2.6512   -0.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1782   -0.0046    0.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278   -1.3857   -0.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8661   -2.1692   -1.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0966   -1.7437   -1.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257   -2.9991   -0.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4438   -2.2848    1.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1781   -2.4096    0.9780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6407   -1.0139    1.9432 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  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
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 11 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 14  2  1  0  0  0  0
 24 17  1  0  0  0  0
 14  8  1  0  0  0  0
 25 10  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  3 31  1  0  0  0  0
  4 32  1  0  0  0  0
  4 33  1  0  0  0  0
  5 34  1  6  0  0  0
  6 35  1  0  0  0  0
  7 36  1  0  0  0  0
  7 37  1  0  0  0  0
  9 38  1  0  0  0  0
 13 39  1  0  0  0  0
 19 40  1  0  0  0  0
 20 41  1  0  0  0  0
 22 42  1  0  0  0  0
 23 43  1  0  0  0  0
 26 44  1  0  0  0  0
 26 45  1  0  0  0  0
 26 46  1  0  0  0  0
 27 47  1  0  0  0  0
 27 48  1  0  0  0  0
 27 49  1  0  0  0  0
M  END

     RDKit          3D

 49 52  0  0  0  0  0  0  0  0999 V2000
   -3.9761    1.5081   -0.6908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4757    0.7802    0.5399 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5277    1.7171    1.5922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4780   -0.2885    0.8754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1140   -1.5053    0.0213 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1468   -2.4159   -0.0299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8438   -2.0743    0.5833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7733   -1.0464    0.3929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4613   -1.4264    0.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5809   -0.4974    0.0525 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2318    0.8288    0.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0879    1.2396    0.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5019    2.5321    0.1980 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1112    0.2731    0.3798 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3044    1.8223   -0.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9701    3.0111   -0.1551 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6676    1.3443   -0.3092 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6740    2.3000   -0.4867 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4300    3.6315   -0.5129 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0066    1.8808   -0.6471 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2983    0.5558   -0.6276 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6190    0.1046   -0.7850 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107   -0.3491   -0.4549 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9577    0.0045   -0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9554   -1.0194   -0.1089 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8872   -2.0195   -1.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3208   -1.7619    1.1943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6457    1.0523   -1.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0845    1.4837   -0.6568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7075    2.6008   -0.6297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0600    1.3596    2.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5197    0.0286    0.6726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3490   -0.6416    1.9378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8834   -1.1102   -0.9884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6332   -2.2669   -0.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9533   -2.3409    1.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5684   -2.9809   -0.0176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2369   -2.4643    0.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0536    3.3621    0.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6393    4.1470   -0.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7819    2.6512   -0.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1782   -0.0046    0.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278   -1.3857   -0.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8661   -2.1692   -1.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0966   -1.7437   -1.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257   -2.9991   -0.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4438   -2.2848    1.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1781   -2.4096    0.9780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6407   -1.0139    1.9432 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  1
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 11 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  6
 25 27  1  0
 14  2  1  0
 24 17  1  0
 14  8  1  0
 25 10  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  6
  6 35  1  0
  7 36  1  0
  7 37  1  0
  9 38  1  0
 13 39  1  0
 19 40  1  0
 20 41  1  0
 22 42  1  0
 23 43  1  0
 26 44  1  0
 26 45  1  0
 26 46  1  0
 27 47  1  0
 27 48  1  0
 27 49  1  0
M  END


  Mrv1652306242116553D          

 49 52  0  0  0  0            999 V2000
   -3.9761    1.5081   -0.6908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4757    0.7802    0.5399 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5277    1.7171    1.5922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4780   -0.2885    0.8754 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1140   -1.5053    0.0213 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1468   -2.4159   -0.0299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8438   -2.0743    0.5833 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7733   -1.0464    0.3929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4613   -1.4264    0.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5809   -0.4974    0.0525 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2318    0.8288    0.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0879    1.2396    0.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5019    2.5321    0.1980 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1112    0.2731    0.3798 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3044    1.8223   -0.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9701    3.0111   -0.1551 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6676    1.3443   -0.3092 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6740    2.3000   -0.4867 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4300    3.6315   -0.5129 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0066    1.8808   -0.6471 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2983    0.5558   -0.6276 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6190    0.1046   -0.7850 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107   -0.3491   -0.4549 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9577    0.0045   -0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9554   -1.0194   -0.1089 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8872   -2.0195   -1.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3208   -1.7619    1.1943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6457    1.0523   -1.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0845    1.4837   -0.6568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7075    2.6008   -0.6297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0600    1.3596    2.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5197    0.0286    0.6726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3490   -0.6416    1.9378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8834   -1.1102   -0.9884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6332   -2.2669   -0.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9533   -2.3409    1.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5684   -2.9809   -0.0176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2369   -2.4643    0.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0536    3.3621    0.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6393    4.1470   -0.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7819    2.6512   -0.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1782   -0.0046    0.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278   -1.3857   -0.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8661   -2.1692   -1.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0966   -1.7437   -1.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257   -2.9991   -0.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4438   -2.2848    1.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1781   -2.4096    0.9780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6407   -1.0139    1.9432 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  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
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 11 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 14  2  1  0  0  0  0
 24 17  1  0  0  0  0
 14  8  1  0  0  0  0
 25 10  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  3 31  1  0  0  0  0
  4 32  1  0  0  0  0
  4 33  1  0  0  0  0
  5 34  1  6  0  0  0
  6 35  1  0  0  0  0
  7 36  1  0  0  0  0
  7 37  1  0  0  0  0
  9 38  1  0  0  0  0
 13 39  1  0  0  0  0
 19 40  1  0  0  0  0
 20 41  1  0  0  0  0
 22 42  1  0  0  0  0
 23 43  1  0  0  0  0
 26 44  1  0  0  0  0
 26 45  1  0  0  0  0
 26 46  1  0  0  0  0
 27 47  1  0  0  0  0
 27 48  1  0  0  0  0
 27 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0011264

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(O[H])=C2C(=O)C3=C(C([H])=C4C(=C3O[H])[C@@](O[H])(C([H])([H])[H])C([H])([H])[C@]([H])(O[H])C4([H])[H])C(C2=C1[H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O6/c1-20(2)12-5-9-4-11(23)8-21(3,27)17(9)19(26)16(12)18(25)15-13(20)6-10(22)7-14(15)24/h5-7,11,22-24,26-27H,4,8H2,1-3H3/t11-,21-/m1/s1

> <INCHI_KEY>
NUPKBVWVJRTNCS-UHFFFAOYSA-N

> <FORMULA>
C21H22O6

> <MOLECULAR_WEIGHT>
370.401

> <EXACT_MASS>
370.141638428

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
39.065630071929036

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(7R,9R)-2,4,6,7,9-pentahydroxy-7,12,12-trimethyl-5,7,8,9,10,12-hexahydrotetracen-5-one

> <ALOGPS_LOGP>
2.12

> <JCHEM_LOGP>
3.57002459

> <ALOGPS_LOGS>
-3.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.01768465002341

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.845648228123702

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8095769604184175

> <JCHEM_POLAR_SURFACE_AREA>
118.22

> <JCHEM_REFRACTIVITY>
111.0353

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.10e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(7R,9R)-2,4,6,7,9-pentahydroxy-7,12,12-trimethyl-9,10-dihydro-8H-tetracen-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 49 52  0  0  0  0  0  0  0  0999 V2000
   -3.9761    1.5081   -0.6908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4757    0.7802    0.5399 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5277    1.7171    1.5922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4780   -0.2885    0.8754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1140   -1.5053    0.0213 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1468   -2.4159   -0.0299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8438   -2.0743    0.5833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7733   -1.0464    0.3929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4613   -1.4264    0.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5809   -0.4974    0.0525 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2318    0.8288    0.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0879    1.2396    0.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5019    2.5321    0.1980 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1112    0.2731    0.3798 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3044    1.8223   -0.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9701    3.0111   -0.1551 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6676    1.3443   -0.3092 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6740    2.3000   -0.4867 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4300    3.6315   -0.5129 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0066    1.8808   -0.6471 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2983    0.5558   -0.6276 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6190    0.1046   -0.7850 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107   -0.3491   -0.4549 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9577    0.0045   -0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9554   -1.0194   -0.1089 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8872   -2.0195   -1.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3208   -1.7619    1.1943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6457    1.0523   -1.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0845    1.4837   -0.6568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7075    2.6008   -0.6297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0600    1.3596    2.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5197    0.0286    0.6726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3490   -0.6416    1.9378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8834   -1.1102   -0.9884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6332   -2.2669   -0.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9533   -2.3409    1.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5684   -2.9809   -0.0176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2369   -2.4643    0.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0536    3.3621    0.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6393    4.1470   -0.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7819    2.6512   -0.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1782   -0.0046    0.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278   -1.3857   -0.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8661   -2.1692   -1.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0966   -1.7437   -1.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257   -2.9991   -0.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4438   -2.2848    1.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1781   -2.4096    0.9780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6407   -1.0139    1.9432 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  1
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 11 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  6
 25 27  1  0
 14  2  1  0
 24 17  1  0
 14  8  1  0
 25 10  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  6
  6 35  1  0
  7 36  1  0
  7 37  1  0
  9 38  1  0
 13 39  1  0
 19 40  1  0
 20 41  1  0
 22 42  1  0
 23 43  1  0
 26 44  1  0
 26 45  1  0
 26 46  1  0
 27 47  1  0
 27 48  1  0
 27 49  1  0
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      -3.976   1.508  -0.691  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.476   0.780   0.540  0.00  0.00           C+0
HETATM    3  O   UNK     0      -3.528   1.717   1.592  0.00  0.00           O+0
HETATM    4  C   UNK     0      -4.478  -0.289   0.875  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.114  -1.505   0.021  0.00  0.00           C+0
HETATM    6  O   UNK     0      -5.147  -2.416  -0.030  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.844  -2.074   0.583  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.773  -1.046   0.393  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.461  -1.426   0.234  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.581  -0.497   0.053  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.232   0.829   0.041  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.088   1.240   0.200  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.502   2.532   0.198  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.111   0.273   0.380  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.304   1.822  -0.147  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.970   3.011  -0.155  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.668   1.344  -0.309  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.674   2.300  -0.487  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.430   3.632  -0.513  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.007   1.881  -0.647  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.298   0.556  -0.628  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.619   0.105  -0.785  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.311  -0.349  -0.455  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.958   0.005  -0.289  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.955  -1.019  -0.109  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.887  -2.019  -1.248  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.321  -1.762   1.194  0.00  0.00           C+0
HETATM   28  H   UNK     0      -3.646   1.052  -1.627  0.00  0.00           H+0
HETATM   29  H   UNK     0      -5.085   1.484  -0.657  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.708   2.601  -0.630  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.060   1.360   2.392  0.00  0.00           H+0
HETATM   32  H   UNK     0      -5.520   0.029   0.673  0.00  0.00           H+0
HETATM   33  H   UNK     0      -4.349  -0.642   1.938  0.00  0.00           H+0
HETATM   34  H   UNK     0      -3.883  -1.110  -0.988  0.00  0.00           H+0
HETATM   35  H   UNK     0      -5.633  -2.267  -0.895  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.953  -2.341   1.666  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.568  -2.981  -0.018  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.237  -2.464   0.249  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.054   3.362   0.101  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.639   4.147  -0.430  0.00  0.00           H+0
HETATM   41  H   UNK     0       5.782   2.651  -0.785  0.00  0.00           H+0
HETATM   42  H   UNK     0       7.178  -0.005   0.070  0.00  0.00           H+0
HETATM   43  H   UNK     0       4.528  -1.386  -0.438  0.00  0.00           H+0
HETATM   44  H   UNK     0       2.866  -2.169  -1.738  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.097  -1.744  -1.952  0.00  0.00           H+0
HETATM   46  H   UNK     0       1.626  -2.999  -0.784  0.00  0.00           H+0
HETATM   47  H   UNK     0       1.444  -2.285   1.601  0.00  0.00           H+0
HETATM   48  H   UNK     0       3.178  -2.410   0.978  0.00  0.00           H+0
HETATM   49  H   UNK     0       2.641  -1.014   1.943  0.00  0.00           H+0
CONECT    1    2   28   29   30                                             
CONECT    2    1    3    4   14                                             
CONECT    3    2   31                                                       
CONECT    4    2    5   32   33                                             
CONECT    5    4    6    7   34                                             
CONECT    6    5   35                                                       
CONECT    7    5    8   36   37                                             
CONECT    8    7    9   14                                                  
CONECT    9    8   10   38                                                  
CONECT   10    9   11   25                                                  
CONECT   11   10   12   15                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12   39                                                       
CONECT   14   12    2    8                                                  
CONECT   15   11   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   24                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   40                                                       
CONECT   20   18   21   41                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21   42                                                       
CONECT   23   21   24   43                                                  
CONECT   24   23   25   17                                                  
CONECT   25   24   26   27   10                                             
CONECT   26   25   44   45   46                                             
CONECT   27   25   47   48   49                                             
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    3                                                            
CONECT   32    4                                                            
CONECT   33    4                                                            
CONECT   34    5                                                            
CONECT   35    6                                                            
CONECT   36    7                                                            
CONECT   37    7                                                            
CONECT   38    9                                                            
CONECT   39   13                                                            
CONECT   40   19                                                            
CONECT   41   20                                                            
CONECT   42   22                                                            
CONECT   43   23                                                            
CONECT   44   26                                                            
CONECT   45   26                                                            
CONECT   46   26                                                            
CONECT   47   27                                                            
CONECT   48   27                                                            
CONECT   49   27                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  104    0
END

RDKit          3D

49 52  0  0  0  0  0  0  0  0999 V2000
   -3.9761    1.5081   -0.6908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4757    0.7802    0.5399 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5277    1.7171    1.5922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4780   -0.2885    0.8754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1140   -1.5053    0.0213 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1468   -2.4159   -0.0299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8438   -2.0743    0.5833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7733   -1.0464    0.3929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4613   -1.4264    0.2336 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5809   -0.4974    0.0525 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2318    0.8288    0.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0879    1.2396    0.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5019    2.5321    0.1980 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1112    0.2731    0.3798 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3044    1.8223   -0.1474 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9701    3.0111   -0.1551 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6676    1.3443   -0.3092 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6740    2.3000   -0.4867 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4300    3.6315   -0.5129 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0066    1.8808   -0.6471 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2983    0.5558   -0.6276 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6190    0.1046   -0.7850 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107   -0.3491   -0.4549 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9577    0.0045   -0.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9554   -1.0194   -0.1089 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8872   -2.0195   -1.2483 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3208   -1.7619    1.1943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6457    1.0523   -1.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0845    1.4837   -0.6568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7075    2.6008   -0.6297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0600    1.3596    2.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5197    0.0286    0.6726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3490   -0.6416    1.9378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8834   -1.1102   -0.9884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6332   -2.2669   -0.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9533   -2.3409    1.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5684   -2.9809   -0.0176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2369   -2.4643    0.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0536    3.3621    0.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6393    4.1470   -0.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7819    2.6512   -0.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1782   -0.0046    0.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278   -1.3857   -0.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8661   -2.1692   -1.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0966   -1.7437   -1.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6257   -2.9991   -0.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4438   -2.2848    1.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1781   -2.4096    0.9780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6407   -1.0139    1.9432 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  1
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 11 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  6
 25 27  1  0
 14  2  1  0
 24 17  1  0
 14  8  1  0
 25 10  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  6
  6 35  1  0
  7 36  1  0
  7 37  1  0
  9 38  1  0
 13 39  1  0
 19 40  1  0
 20 41  1  0
 22 42  1  0
 23 43  1  0
 26 44  1  0
 26 45  1  0
 26 46  1  0
 27 47  1  0
 27 48  1  0
 27 49  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₁H₂₂O₆

Average Mass

370.4010 Da

Monoisotopic Mass

370.14164 Da

IUPAC Name

(7R,9R)-2,4,6,7,9-pentahydroxy-7,12,12-trimethyl-5,7,8,9,10,12-hexahydrotetracen-5-one

Traditional Name

(7R,9R)-2,4,6,7,9-pentahydroxy-7,12,12-trimethyl-9,10-dihydro-8H-tetracen-5-one

CAS Registry Number

Not Available

SMILES

CC1(O)CC(O)CC2=C1C(O)=C1C(=O)C3=C(O)C=C(O)C=C3C(C)(C)C1=C2

InChI Identifier

InChI=1S/C21H22O6/c1-20(2)12-5-9-4-11(23)8-21(3,27)17(9)19(26)16(12)18(25)15-13(20)6-10(22)7-14(15)24/h5-7,11,22-24,26-27H,4,8H2,1-3H3

InChI Key

NUPKBVWVJRTNCS-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, 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
eDNA sp.	NPAtlas	23157252

Chemical Taxonomy

Classification

Not classified

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	2.12	ALOGPS
logP	3.57	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	7.85	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	118.22 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	111.04 m³·mol⁻¹	ChemAxon
Polarizability	39.07 Å³	ChemAxon
Number of Rings	4	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

NPA006659

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78435450

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71507686

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Kallifidas D, Kang HS, Brady SF: Tetarimycin A, an MRSA-active antibiotic identified through induced expression of environmental DNA gene clusters. J Am Chem Soc. 2012 Dec 5;134(48):19552-5. doi: 10.1021/ja3093828. Epub 2012 Nov 27. [PubMed:23157252 ]

Showing NP-Card for Tetarimycin B (NP0011264)

MOL for NP0011264 (Tetarimycin B)

3D MOL for NP0011264 (Tetarimycin B)

3D SDF for NP0011264 (Tetarimycin B)

3D-SDF for NP0011264 (Tetarimycin B)

PDB for NP0011264 (Tetarimycin B)

3D PDB for NP0011264 (Tetarimycin B)

SMILES for NP0011264 (Tetarimycin B)

INCHI for NP0011264 (Tetarimycin B)

Structure for NP0011264 (Tetarimycin B)

3D Structure for NP0011264 (Tetarimycin B)