NP-MRD: Showing NP-Card for (1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone (NP0324810)

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Record Information

Version

2.0

Created at

2022-09-12 05:06:47 UTC

Updated at

2022-09-12 05:06:47 UTC

NP-MRD ID

NP0324810

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone

Description

(1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone is found in Talaromyces purpureogenus.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309122207062D          

 40 46  0  0  1  0            999 V2000
   -2.2104   -3.1673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5170   -2.7204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5573   -1.8963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8639   -1.4494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9042   -0.6254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1301   -1.8265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0898   -2.6505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7832   -3.0974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6641   -3.0112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6744   -3.8361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4497   -2.6111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5155   -3.5072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3095   -3.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5260   -4.6020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8519   -3.1349    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6075   -2.7005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6019   -1.8755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3136   -1.4582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3080   -0.6332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0308   -1.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7425   -1.4484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7369   -0.6235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4597   -1.8561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4654   -2.6810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1826   -3.0887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7537   -3.0984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7593   -3.9234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0364   -2.6908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3248   -3.1081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3304   -3.9331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8480   -1.3065    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9655   -1.1146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7455   -0.3195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3090   -1.7313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5585   -1.3701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5022   -0.5470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5925   -1.8672    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8413   -1.5262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2629   -2.5960    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9713   -3.3678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 15 13  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  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
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 20 28  1  0  0  0  0
 28 29  1  0  0  0  0
 16 29  1  0  0  0  0
 29 30  2  0  0  0  0
 31 17  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 11 34  1  0  0  0  0
 34 35  1  0  0  0  0
  6 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 37  1  0  0  0  0
 37 38  1  6  0  0  0
 37 39  1  0  0  0  0
 15 39  1  0  0  0  0
 11 39  1  0  0  0  0
 39 40  1  1  0  0  0
M  END


  Mrv1652309122207062D          

 40 46  0  0  1  0            999 V2000
   -2.2104   -3.1673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5170   -2.7204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5573   -1.8963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8639   -1.4494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9042   -0.6254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1301   -1.8265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0898   -2.6505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7832   -3.0974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6641   -3.0112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6744   -3.8361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4497   -2.6111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5155   -3.5072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3095   -3.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5260   -4.6020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8519   -3.1349    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6075   -2.7005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6019   -1.8755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3136   -1.4582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3080   -0.6332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0308   -1.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7425   -1.4484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7369   -0.6235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4597   -1.8561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4654   -2.6810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1826   -3.0887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7537   -3.0984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7593   -3.9234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0364   -2.6908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3248   -3.1081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3304   -3.9331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8480   -1.3065    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9655   -1.1146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7455   -0.3195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3090   -1.7313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5585   -1.3701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5022   -0.5470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5925   -1.8672    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8413   -1.5262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2629   -2.5960    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9713   -3.3678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 15 13  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  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
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 20 28  1  0  0  0  0
 28 29  1  0  0  0  0
 16 29  1  0  0  0  0
 29 30  2  0  0  0  0
 31 17  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 11 34  1  0  0  0  0
 34 35  1  0  0  0  0
  6 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 37  1  0  0  0  0
 37 38  1  6  0  0  0
 37 39  1  0  0  0  0
 15 39  1  0  0  0  0
 11 39  1  0  0  0  0
 39 40  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0324810

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(O)=C2C(=O)C3=C(O)[C@H]4[C@@H](O)[C@]5(O)[C@H](C(=O)C[C@]35C(=O)C2=C1)C1=C4C(=O)C2=C(O)C=C(C)C(O)=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C29H20O11/c1-7-3-9-13(10(30)4-7)24(36)20-25(37)18-15-16(19-12(32)6-28(20,26(9)38)29(19,40)27(18)39)23(35)17-14(22(15)34)11(31)5-8(2)21(17)33/h3-5,18-19,27,30-31,33,37,39-40H,6H2,1-2H3/t18-,19+,27+,28+,29+/m0/s1

> <INCHI_KEY>
PKFZUNQTCZISSQ-VCUJTUNOSA-N

> <FORMULA>
C29H20O11

> <MOLECULAR_WEIGHT>
544.468

> <EXACT_MASS>
544.100561464

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
0.0

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4R,15R,26S,27R)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0^{1,17}.0^{4,26}.0^{5,14}.0^{7,12}.0^{19,24}]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone

> <JCHEM_LOGP>
1.8334842730000007

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.130474577133779

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.5518444043460242

> <JCHEM_PKA_STRONGEST_BASIC>
-3.805580281083331

> <JCHEM_POLAR_SURFACE_AREA>
206.72999999999996

> <JCHEM_REFRACTIVITY>
137.67099999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4R,15R,26S,27R)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0^{1,17}.0^{4,26}.0^{5,14}.0^{7,12}.0^{19,24}]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.126  -5.912   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.832  -5.078   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.907  -3.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.613  -2.706   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -1.688  -1.167   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.243  -3.409   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.168  -4.948   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.462  -5.782   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.240  -5.621   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.259  -7.161   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.706  -4.874   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.829  -6.547   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.311  -7.104   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.715  -8.590   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.323  -5.852   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.734  -5.041   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.724  -3.501   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.052  -2.722   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.042  -1.182   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.391  -3.483   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.719  -2.704   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.709  -1.164   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.058  -3.465   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.069  -5.005   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.408  -5.766   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.740  -5.784   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.751  -7.324   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.401  -5.023   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.073  -5.802   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.083  -7.342   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.316  -2.439   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.669  -2.081   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       3.258  -0.596   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       2.444  -3.232   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.043  -2.558   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       0.937  -1.021   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       4.839  -3.485   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       3.437  -2.849   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       4.224  -4.846   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       3.680  -6.287   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   35                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7    2                                                       
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   34   39                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   39                                                  
CONECT   16   15   17   29                                                  
CONECT   17   16   18   31                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   28                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   20   29                                                  
CONECT   29   28   16   30                                                  
CONECT   30   29                                                            
CONECT   31   17   32   37                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   11   35                                                  
CONECT   35   34    6   36                                                  
CONECT   36   35                                                            
CONECT   37   31   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   15   11   40                                             
CONECT   40   39                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₂₀O₁₁

Average Mass

544.4680 Da

Monoisotopic Mass

544.10056 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1=CC(O)=C2C(=O)C3=C(O)[C@H]4[C@@H](O)[C@]5(O)[C@H](C(=O)C[C@]35C(=O)C2=C1)C1=C4C(=O)C2=C(O)C=C(C)C(O)=C2C1=O

InChI Identifier

InChI=1S/C29H20O11/c1-7-3-9-13(10(30)4-7)24(36)20-25(37)18-15-16(19-12(32)6-28(20,26(9)38)29(19,40)27(18)39)23(35)17-14(22(15)34)11(31)5-8(2)21(17)33/h3-5,18-19,27,30-31,33,37,39-40H,6H2,1-2H3/t18-,19+,27+,28+,29+/m0/s1

InChI Key

PKFZUNQTCZISSQ-VCUJTUNOSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Penicillium purpurogenum	LOTUS Database	35616633

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

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone (NP0324810)

MOL for NP0324810 ((1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone)

3D MOL for NP0324810 ((1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone)

3D SDF for NP0324810 ((1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone)

3D-SDF for NP0324810 ((1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone)

PDB for NP0324810 ((1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone)

3D PDB for NP0324810 ((1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone)

SMILES for NP0324810 ((1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone)

INCHI for NP0324810 ((1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone)

Structure for NP0324810 ((1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone)

3D Structure for NP0324810 ((1s,4r,15r,26s,27r)-8,11,16,20,26,27-hexahydroxy-9,22-dimethylheptacyclo[13.10.2.0¹,¹⁷.0⁴,²⁶.0⁵,¹⁴.0⁷,¹².0¹⁹,²⁴]heptacosa-5(14),7,9,11,16,19,21,23-octaene-3,6,13,18,25-pentone)