NP-MRD: Showing NP-Card for 10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione (NP0010561)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-01-05 20:02:16 UTC

Updated at

2021-07-15 17:06:26 UTC

NP-MRD ID

NP0010561

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione

Provided By

NPAtlas

Description

10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione is found in Micromonospora sp. Based on a literature review very few articles have been published on 10beta-carbomethoxy-7,8,9,10-tetrahydro-4,6,7alpha,9alpha,11-pentahydroxy-9-propyltetracene-5,12-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107393D          

 54 57  0  0  0  0            999 V2000
    4.1479   -4.7077    1.0867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7509   -4.1233    1.3649 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7897   -2.7083    0.7969 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4801   -1.9888    0.9888 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1933   -1.9136    2.3450 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3455   -2.6807    0.2937 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9545   -2.1128    0.8890 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9519   -2.2109    2.2562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9374   -0.6171    0.5600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1565   -0.0283    0.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3811   -0.6307    0.6605 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2004    1.3158    0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0450    1.9965   -0.1909 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1840    1.3815   -0.0548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3425    2.0277   -0.2739 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2577    0.0012    0.3392 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6039   -0.5763    0.4713 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3570   -0.4808   -0.8188 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7331   -0.1051   -1.8660 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6977   -0.7724   -0.9622 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3896   -0.6756   -2.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1585    3.4164   -0.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0585    3.9800   -0.8616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4212    4.0572   -0.8427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5354    5.3254   -1.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7267    5.9626   -1.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9011    5.3190   -1.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8270    3.9871   -0.8129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0344    3.3224   -0.5580 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6199    3.3611   -0.5925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5022    1.9569   -0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5361    1.3213    0.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1836   -5.1623    0.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4059   -5.5141    1.8116 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9169   -3.9038    1.2300 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0048   -4.7627    0.9035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6751   -4.0811    2.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5745   -2.1606    1.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0808   -2.7971   -0.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1964   -2.7837    2.8146 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2821   -2.3921   -0.7873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3466   -3.7550    0.3428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8107   -2.6191    0.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2575   -3.0890    2.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4196   -1.6464    0.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7064    2.8601   -0.5178 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2520   -0.0576    1.2289 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2766   -1.3430   -2.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8057    0.3751   -2.1945 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7704   -0.7859   -3.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5702    5.8419   -1.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7534    7.0028   -1.8901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8488    5.8171   -1.4462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1423    2.5570   -0.0139 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  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 17  4  1  0  0  0  0
 30 24  1  0  0  0  0
 16  9  1  0  0  0  0
 31 12  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
  1 35  1  0  0  0  0
  2 36  1  0  0  0  0
  2 37  1  0  0  0  0
  3 38  1  0  0  0  0
  3 39  1  0  0  0  0
  5 40  1  0  0  0  0
  6 41  1  0  0  0  0
  6 42  1  0  0  0  0
  7 43  1  6  0  0  0
  8 44  1  0  0  0  0
 11 45  1  0  0  0  0
 15 46  1  0  0  0  0
 17 47  1  1  0  0  0
 21 48  1  0  0  0  0
 21 49  1  0  0  0  0
 21 50  1  0  0  0  0
 25 51  1  0  0  0  0
 26 52  1  0  0  0  0
 27 53  1  0  0  0  0
 29 54  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
    4.1479   -4.7077    1.0867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7509   -4.1233    1.3649 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7897   -2.7083    0.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4801   -1.9888    0.9888 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1933   -1.9136    2.3450 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3455   -2.6807    0.2937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9545   -2.1128    0.8890 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9519   -2.2109    2.2562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9374   -0.6171    0.5600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1565   -0.0283    0.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3811   -0.6307    0.6605 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2004    1.3158    0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0450    1.9965   -0.1909 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1840    1.3815   -0.0548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3425    2.0277   -0.2739 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2577    0.0012    0.3392 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6039   -0.5763    0.4713 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3570   -0.4808   -0.8188 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7331   -0.1051   -1.8660 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6977   -0.7724   -0.9622 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3896   -0.6756   -2.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1585    3.4164   -0.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0585    3.9800   -0.8616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4212    4.0572   -0.8427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5354    5.3254   -1.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7267    5.9626   -1.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9011    5.3190   -1.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8270    3.9871   -0.8129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0344    3.3224   -0.5580 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6199    3.3611   -0.5925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5022    1.9569   -0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5361    1.3213    0.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1836   -5.1623    0.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4059   -5.5141    1.8116 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9169   -3.9038    1.2300 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0048   -4.7627    0.9035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6751   -4.0811    2.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5745   -2.1606    1.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0808   -2.7971   -0.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1964   -2.7837    2.8146 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2821   -2.3921   -0.7873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3466   -3.7550    0.3428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8107   -2.6191    0.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2575   -3.0890    2.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4196   -1.6464    0.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7064    2.8601   -0.5178 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2520   -0.0576    1.2289 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2766   -1.3430   -2.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8057    0.3751   -2.1945 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7704   -0.7859   -3.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5702    5.8419   -1.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7534    7.0028   -1.8901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8488    5.8171   -1.4462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1423    2.5570   -0.0139 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  1
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 13 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  1  0
 28 30  2  0
 30 31  1  0
 31 32  2  0
 17  4  1  0
 30 24  1  0
 16  9  1  0
 31 12  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  3 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  6
  8 44  1  0
 11 45  1  0
 15 46  1  0
 17 47  1  1
 21 48  1  0
 21 49  1  0
 21 50  1  0
 25 51  1  0
 26 52  1  0
 27 53  1  0
 29 54  1  0
M  END


  Mrv1652306242107393D          

 54 57  0  0  0  0            999 V2000
    4.1479   -4.7077    1.0867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7509   -4.1233    1.3649 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7897   -2.7083    0.7969 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4801   -1.9888    0.9888 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1933   -1.9136    2.3450 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3455   -2.6807    0.2937 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9545   -2.1128    0.8890 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9519   -2.2109    2.2562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9374   -0.6171    0.5600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1565   -0.0283    0.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3811   -0.6307    0.6605 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2004    1.3158    0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0450    1.9965   -0.1909 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1840    1.3815   -0.0548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3425    2.0277   -0.2739 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2577    0.0012    0.3392 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6039   -0.5763    0.4713 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3570   -0.4808   -0.8188 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7331   -0.1051   -1.8660 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6977   -0.7724   -0.9622 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3896   -0.6756   -2.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1585    3.4164   -0.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0585    3.9800   -0.8616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4212    4.0572   -0.8427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5354    5.3254   -1.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7267    5.9626   -1.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9011    5.3190   -1.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8270    3.9871   -0.8129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0344    3.3224   -0.5580 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6199    3.3611   -0.5925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5022    1.9569   -0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5361    1.3213    0.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1836   -5.1623    0.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4059   -5.5141    1.8116 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9169   -3.9038    1.2300 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0048   -4.7627    0.9035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6751   -4.0811    2.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5745   -2.1606    1.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0808   -2.7971   -0.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1964   -2.7837    2.8146 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2821   -2.3921   -0.7873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3466   -3.7550    0.3428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8107   -2.6191    0.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2575   -3.0890    2.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4196   -1.6464    0.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7064    2.8601   -0.5178 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2520   -0.0576    1.2289 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2766   -1.3430   -2.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8057    0.3751   -2.1945 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7704   -0.7859   -3.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5702    5.8419   -1.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7534    7.0028   -1.8901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8488    5.8171   -1.4462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1423    2.5570   -0.0139 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  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 17  4  1  0  0  0  0
 30 24  1  0  0  0  0
 16  9  1  0  0  0  0
 31 12  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
  1 35  1  0  0  0  0
  2 36  1  0  0  0  0
  2 37  1  0  0  0  0
  3 38  1  0  0  0  0
  3 39  1  0  0  0  0
  5 40  1  0  0  0  0
  6 41  1  0  0  0  0
  6 42  1  0  0  0  0
  7 43  1  6  0  0  0
  8 44  1  0  0  0  0
 11 45  1  0  0  0  0
 15 46  1  0  0  0  0
 17 47  1  1  0  0  0
 21 48  1  0  0  0  0
 21 49  1  0  0  0  0
 21 50  1  0  0  0  0
 25 51  1  0  0  0  0
 26 52  1  0  0  0  0
 27 53  1  0  0  0  0
 29 54  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0010561

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)C3=C(C(=O)C2=C([H])C([H])=C1[H])C(O[H])=C1C(=C3O[H])[C@]([H])(O[H])C([H])([H])[C@@](O[H])(C([H])([H])C([H])([H])C([H])([H])[H])[C@@]1([H])C(=O)OC([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H22O9/c1-3-7-23(31)8-11(25)13-14(17(23)22(30)32-2)21(29)15-16(20(13)28)19(27)12-9(18(15)26)5-4-6-10(12)24/h4-6,11,17,24-25,28-29,31H,3,7-8H2,1-2H3/t11-,17-,23+/m1/s1

> <INCHI_KEY>
RBVRMUUHLBHOCG-WEDCLBQXSA-N

> <FORMULA>
C23H22O9

> <MOLECULAR_WEIGHT>
442.42

> <EXACT_MASS>
442.126382288

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
44.9226444773469

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,2S,4R)-2,4,5,7,12-pentahydroxy-6,11-dioxo-2-propyl-1,2,3,4,6,11-hexahydrotetracene-1-carboxylate

> <ALOGPS_LOGP>
2.61

> <JCHEM_LOGP>
3.492154473333333

> <ALOGPS_LOGS>
-2.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.520702587486282

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.899911161069634

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2364433748261554

> <JCHEM_POLAR_SURFACE_AREA>
161.59

> <JCHEM_REFRACTIVITY>
112.33549999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.10e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,2S,4R)-2,4,5,7,12-pentahydroxy-6,11-dioxo-2-propyl-3,4-dihydro-1H-tetracene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
    4.1479   -4.7077    1.0867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7509   -4.1233    1.3649 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7897   -2.7083    0.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4801   -1.9888    0.9888 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1933   -1.9136    2.3450 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3455   -2.6807    0.2937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9545   -2.1128    0.8890 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9519   -2.2109    2.2562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9374   -0.6171    0.5600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1565   -0.0283    0.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3811   -0.6307    0.6605 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2004    1.3158    0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0450    1.9965   -0.1909 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1840    1.3815   -0.0548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3425    2.0277   -0.2739 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2577    0.0012    0.3392 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6039   -0.5763    0.4713 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3570   -0.4808   -0.8188 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7331   -0.1051   -1.8660 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6977   -0.7724   -0.9622 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3896   -0.6756   -2.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1585    3.4164   -0.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0585    3.9800   -0.8616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4212    4.0572   -0.8427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5354    5.3254   -1.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7267    5.9626   -1.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9011    5.3190   -1.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8270    3.9871   -0.8129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0344    3.3224   -0.5580 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6199    3.3611   -0.5925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5022    1.9569   -0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5361    1.3213    0.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1836   -5.1623    0.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4059   -5.5141    1.8116 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9169   -3.9038    1.2300 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0048   -4.7627    0.9035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6751   -4.0811    2.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5745   -2.1606    1.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0808   -2.7971   -0.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1964   -2.7837    2.8146 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2821   -2.3921   -0.7873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3466   -3.7550    0.3428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8107   -2.6191    0.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2575   -3.0890    2.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4196   -1.6464    0.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7064    2.8601   -0.5178 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2520   -0.0576    1.2289 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2766   -1.3430   -2.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8057    0.3751   -2.1945 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7704   -0.7859   -3.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5702    5.8419   -1.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7534    7.0028   -1.8901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8488    5.8171   -1.4462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1423    2.5570   -0.0139 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  1
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 13 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  1  0
 28 30  2  0
 30 31  1  0
 31 32  2  0
 17  4  1  0
 30 24  1  0
 16  9  1  0
 31 12  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  3 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  6
  8 44  1  0
 11 45  1  0
 15 46  1  0
 17 47  1  1
 21 48  1  0
 21 49  1  0
 21 50  1  0
 25 51  1  0
 26 52  1  0
 27 53  1  0
 29 54  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       4.148  -4.708   1.087  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.751  -4.123   1.365  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.790  -2.708   0.797  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.480  -1.989   0.989  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.193  -1.914   2.345  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.346  -2.681   0.294  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.955  -2.113   0.889  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.952  -2.211   2.256  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.937  -0.617   0.560  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.156  -0.028   0.437  0.00  0.00           C+0
HETATM   11  O   UNK     0      -3.381  -0.631   0.661  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.200   1.316   0.048  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.045   1.996  -0.191  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.184   1.381  -0.055  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.343   2.028  -0.274  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.258   0.001   0.339  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.604  -0.576   0.471  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.357  -0.481  -0.819  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.733  -0.105  -1.866  0.00  0.00           O+0
HETATM   20  O   UNK     0       3.698  -0.772  -0.962  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.390  -0.676  -2.186  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.159   3.416  -0.654  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.059   3.980  -0.862  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.421   4.057  -0.843  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.535   5.325  -1.301  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.727   5.963  -1.525  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.901   5.319  -1.289  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.827   3.987  -0.813  0.00  0.00           C+0
HETATM   29  O   UNK     0      -6.034   3.322  -0.558  0.00  0.00           O+0
HETATM   30  C   UNK     0      -3.620   3.361  -0.593  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.502   1.957  -0.138  0.00  0.00           C+0
HETATM   32  O   UNK     0      -4.536   1.321   0.089  0.00  0.00           O+0
HETATM   33  H   UNK     0       4.184  -5.162   0.082  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.406  -5.514   1.812  0.00  0.00           H+0
HETATM   35  H   UNK     0       4.917  -3.904   1.230  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.005  -4.763   0.904  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.675  -4.081   2.467  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.575  -2.161   1.335  0.00  0.00           H+0
HETATM   39  H   UNK     0       3.081  -2.797  -0.266  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.196  -2.784   2.815  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.282  -2.392  -0.787  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.347  -3.755   0.343  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.811  -2.619   0.455  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.258  -3.089   2.605  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.420  -1.646   0.926  0.00  0.00           H+0
HETATM   46  H   UNK     0       1.706   2.860  -0.518  0.00  0.00           H+0
HETATM   47  H   UNK     0       2.252  -0.058   1.229  0.00  0.00           H+0
HETATM   48  H   UNK     0       5.277  -1.343  -2.212  0.00  0.00           H+0
HETATM   49  H   UNK     0       4.806   0.375  -2.195  0.00  0.00           H+0
HETATM   50  H   UNK     0       3.770  -0.786  -3.073  0.00  0.00           H+0
HETATM   51  H   UNK     0      -1.570   5.842  -1.498  0.00  0.00           H+0
HETATM   52  H   UNK     0      -3.753   7.003  -1.890  0.00  0.00           H+0
HETATM   53  H   UNK     0      -5.849   5.817  -1.446  0.00  0.00           H+0
HETATM   54  H   UNK     0      -6.142   2.557  -0.014  0.00  0.00           H+0
CONECT    1    2   33   34   35                                             
CONECT    2    1    3   36   37                                             
CONECT    3    2    4   38   39                                             
CONECT    4    3    5    6   17                                             
CONECT    5    4   40                                                       
CONECT    6    4    7   41   42                                             
CONECT    7    6    8    9   43                                             
CONECT    8    7   44                                                       
CONECT    9    7   10   16                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10   45                                                       
CONECT   12   10   13   31                                                  
CONECT   13   12   14   22                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14   46                                                       
CONECT   16   14   17    9                                                  
CONECT   17   16   18    4   47                                             
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   48   49   50                                             
CONECT   22   13   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   30                                                  
CONECT   25   24   26   51                                                  
CONECT   26   25   27   52                                                  
CONECT   27   26   28   53                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28   54                                                       
CONECT   30   28   31   24                                                  
CONECT   31   30   32   12                                                  
CONECT   32   31                                                            
CONECT   33    1                                                            
CONECT   34    1                                                            
CONECT   35    1                                                            
CONECT   36    2                                                            
CONECT   37    2                                                            
CONECT   38    3                                                            
CONECT   39    3                                                            
CONECT   40    5                                                            
CONECT   41    6                                                            
CONECT   42    6                                                            
CONECT   43    7                                                            
CONECT   44    8                                                            
CONECT   45   11                                                            
CONECT   46   15                                                            
CONECT   47   17                                                            
CONECT   48   21                                                            
CONECT   49   21                                                            
CONECT   50   21                                                            
CONECT   51   25                                                            
CONECT   52   26                                                            
CONECT   53   27                                                            
CONECT   54   29                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  114    0
END

RDKit          3D

54 57  0  0  0  0  0  0  0  0999 V2000
    4.1479   -4.7077    1.0867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7509   -4.1233    1.3649 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7897   -2.7083    0.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4801   -1.9888    0.9888 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1933   -1.9136    2.3450 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3455   -2.6807    0.2937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9545   -2.1128    0.8890 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9519   -2.2109    2.2562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9374   -0.6171    0.5600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1565   -0.0283    0.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3811   -0.6307    0.6605 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2004    1.3158    0.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0450    1.9965   -0.1909 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1840    1.3815   -0.0548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3425    2.0277   -0.2739 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2577    0.0012    0.3392 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6039   -0.5763    0.4713 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3570   -0.4808   -0.8188 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7331   -0.1051   -1.8660 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6977   -0.7724   -0.9622 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3896   -0.6756   -2.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1585    3.4164   -0.6543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0585    3.9800   -0.8616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4212    4.0572   -0.8427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5354    5.3254   -1.3013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7267    5.9626   -1.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9011    5.3190   -1.2888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8270    3.9871   -0.8129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0344    3.3224   -0.5580 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6199    3.3611   -0.5925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5022    1.9569   -0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5361    1.3213    0.0886 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1836   -5.1623    0.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4059   -5.5141    1.8116 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9169   -3.9038    1.2300 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0048   -4.7627    0.9035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6751   -4.0811    2.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5745   -2.1606    1.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0808   -2.7971   -0.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1964   -2.7837    2.8146 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2821   -2.3921   -0.7873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3466   -3.7550    0.3428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8107   -2.6191    0.4550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2575   -3.0890    2.6047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4196   -1.6464    0.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7064    2.8601   -0.5178 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2520   -0.0576    1.2289 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2766   -1.3430   -2.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8057    0.3751   -2.1945 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7704   -0.7859   -3.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5702    5.8419   -1.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7534    7.0028   -1.8901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8488    5.8171   -1.4462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1423    2.5570   -0.0139 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  1
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 13 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  1  0
 28 30  2  0
 30 31  1  0
 31 32  2  0
 17  4  1  0
 30 24  1  0
 16  9  1  0
 31 12  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  3 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  6
  8 44  1  0
 11 45  1  0
 15 46  1  0
 17 47  1  1
 21 48  1  0
 21 49  1  0
 21 50  1  0
 25 51  1  0
 26 52  1  0
 27 53  1  0
 29 54  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
10b-Carbomethoxy-7,8,9,10-tetrahydro-4,6,7a,9a,11-pentahydroxy-9-propyltetracene-5,12-dione	Generator
10Β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione	Generator
Methyl (1S,2S,4R)-2,4,5,7,12-pentahydroxy-6,11-dioxo-2-propyl-1,2,3,4,6,11-hexahydrotetracene-1-carboxylic acid	Generator

Chemical Formula

C₂₃H₂₂O₉

Average Mass

442.4200 Da

Monoisotopic Mass

442.12638 Da

IUPAC Name

methyl (1S,2S,4R)-2,4,5,7,12-pentahydroxy-6,11-dioxo-2-propyl-1,2,3,4,6,11-hexahydrotetracene-1-carboxylate

Traditional Name

methyl (1S,2S,4R)-2,4,5,7,12-pentahydroxy-6,11-dioxo-2-propyl-3,4-dihydro-1H-tetracene-1-carboxylate

CAS Registry Number

Not Available

SMILES

CCC[C@]1(O)C[C@@H](O)C2=C(O)C3=C(C(O)=C2[C@@H]1C(=O)OC)C(=O)C1=C(C(O)=CC=C1)C3=O

InChI Identifier

InChI=1S/C23H22O9/c1-3-7-23(31)8-11(25)13-14(17(23)22(30)32-2)21(29)15-16(20(13)28)19(27)12-9(18(15)26)5-4-6-10(12)24/h4-6,11,17,24-25,28-29,31H,3,7-8H2,1-2H3/t11-,17-,23+/m1/s1

InChI Key

RBVRMUUHLBHOCG-WEDCLBQXSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

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
Micromonospora sp.	NPAtlas	22250891

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	2.61	ALOGPS
logP	3.49	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	7.9	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	161.59 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	112.34 m³·mol⁻¹	ChemAxon
Polarizability	44.92 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

NPA018868

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78442771

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139588362

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione (NP0010561)

MOL for NP0010561 (10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione)

3D MOL for NP0010561 (10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione)

3D SDF for NP0010561 (10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione)

3D-SDF for NP0010561 (10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione)

PDB for NP0010561 (10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione)

3D PDB for NP0010561 (10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione)

SMILES for NP0010561 (10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione)

INCHI for NP0010561 (10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione)

Structure for NP0010561 (10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione)

3D Structure for NP0010561 (10β-carbomethoxy-7,8,9,10-tetrahydro-4,6,7α,9α,11-pentahydroxy-9-propyltetracene-5,12-dione)