NP-MRD: Showing NP-Card for (1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid (NP0235301)

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Record Information

Version

2.0

Created at

2022-09-06 17:50:54 UTC

Updated at

2022-09-06 17:50:54 UTC

NP-MRD ID

NP0235301

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid

Description

(1S,2R,4R,5S,8R,9S,13R,14S,17S,18S,20S)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]Tetracosane-9-carboxylic acid belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. (1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid is found in Petrosaspongia nigra. Based on a literature review very few articles have been published on (1S,2R,4R,5S,8R,9S,13R,14S,17S,18S,20S)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]Tetracosane-9-carboxylic acid.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062219502D          

 35 40  0  0  1  0            999 V2000
    0.4011    3.9102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7474    3.1614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2720    2.4871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5690    3.0869    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9153    2.3381    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7741    2.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2806    1.6822    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0262    0.8974    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5787    0.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3855    0.4567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6399    1.2415    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0875    1.8542    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5350    2.4669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3419    2.6390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1487    2.8111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7012    2.1984    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5080    2.3705    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1985    3.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2074    2.8081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9361    2.4213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1780    3.6326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0605    1.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8061    0.9730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9992    0.8009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4468    1.4136    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1924    0.6288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2011    0.5007    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3549    0.2371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8325    0.9394    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0097    1.1132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0859    1.9390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7984    2.3548    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6822    2.2628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3145    1.6740    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8498    1.1383    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
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 11 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  1  0  0  0
  8 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 28  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 29 34  1  0  0  0  0
  5 34  1  0  0  0  0
 34 35  1  1  0  0  0
 27 35  1  1  0  0  0
M  END


  Mrv1652309062219502D          

 35 40  0  0  1  0            999 V2000
    0.4011    3.9102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7474    3.1614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2720    2.4871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5690    3.0869    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9153    2.3381    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7741    2.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2806    1.6822    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0262    0.8974    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5787    0.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3855    0.4567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6399    1.2415    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0875    1.8542    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5350    2.4669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3419    2.6390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1487    2.8111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7012    2.1984    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5080    2.3705    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1985    3.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2074    2.8081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9361    2.4213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1780    3.6326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0605    1.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8061    0.9730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9992    0.8009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4468    1.4136    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1924    0.6288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2011    0.5007    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3549    0.2371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8325    0.9394    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0097    1.1132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0859    1.9390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7984    2.3548    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6822    2.2628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3145    1.6740    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8498    1.1383    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
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 11 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  1  0  0  0
  8 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 28  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 29 34  1  0  0  0  0
  5 34  1  0  0  0  0
 34 35  1  1  0  0  0
 27 35  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0235301

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1C[C@@H]2[C@H](CC[C@H]3[C@@]2(C)CC[C@@H]2[C@]3(C)CCC[C@]2(C)C(O)=O)[C@@H]2O[C@H]3OC(=O)C[C@]13O2

> <INCHI_IDENTIFIER>
InChI=1S/C27H38O8/c1-14(28)32-19-12-16-15(21-34-23-27(19,35-21)13-20(29)33-23)6-7-17-24(16,2)11-8-18-25(17,3)9-5-10-26(18,4)22(30)31/h15-19,21,23H,5-13H2,1-4H3,(H,30,31)/t15-,16+,17-,18+,19+,21+,23+,24-,25+,26-,27-/m0/s1

> <INCHI_KEY>
RABBRGJJXRWNML-LUOQHXBRSA-N

> <FORMULA>
C27H38O8

> <MOLECULAR_WEIGHT>
490.593

> <EXACT_MASS>
490.256668184

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
52.44441920573494

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,4R,5S,8R,9S,13R,14S,17S,18S,20S)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0^{1,20}.0^{4,17}.0^{5,14}.0^{8,13}]tetracosane-9-carboxylic acid

> <JCHEM_LOGP>
4.2326675773333315

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
17.436081701681047

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.405598630116925

> <JCHEM_PKA_STRONGEST_BASIC>
-4.174307340653315

> <JCHEM_POLAR_SURFACE_AREA>
108.36000000000003

> <JCHEM_REFRACTIVITY>
121.12239999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4R,5S,8R,9S,13R,14S,17S,18S,20S)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0^{1,20}.0^{4,17}.0^{5,14}.0^{8,13}]tetracosane-9-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       0.749   7.299   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.395   5.901   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.508   4.643   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       2.929   5.762   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.575   4.364   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.178   4.414   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.124   3.140   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.649   1.675   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.680   0.531   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.186   0.853   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.661   2.317   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.630   3.461   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.599   4.605   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.105   4.926   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.611   5.247   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.642   4.104   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.148   4.425   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.570   5.852   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.454   5.242   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      14.814   4.520   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      13.399   6.781   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      13.180   3.281   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.705   1.816   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.199   1.495   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.167   2.639   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.692   1.174   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.109   0.935   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.529   0.443   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.554   1.753   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.018   2.078   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -0.160   3.619   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -1.490   4.396   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.273   4.224   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.454   3.125   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.453   2.125   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   34                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9   27                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   25                                                  
CONECT   12   11    7   13   14                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18   19   22                                             
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   11   16   26                                             
CONECT   26   25                                                            
CONECT   27    8   28   35                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   29    5   35                                             
CONECT   35   34   27                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   80    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,4R,5S,8R,9S,13R,14S,17S,18S,20S)-2-(Acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0,.0,.0,.0,]tetracosane-9-carboxylate	Generator

Chemical Formula

C₂₇H₃₈O₈

Average Mass

490.5930 Da

Monoisotopic Mass

490.25667 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C[C@@H]2[C@H](CC[C@H]3[C@@]2(C)CC[C@@H]2[C@]3(C)CCC[C@]2(C)C(O)=O)[C@@H]2O[C@H]3OC(=O)C[C@]13O2

InChI Identifier

InChI=1S/C27H38O8/c1-14(28)32-19-12-16-15(21-34-23-27(19,35-21)13-20(29)33-23)6-7-17-24(16,2)11-8-18-25(17,3)9-5-10-26(18,4)22(30)31/h15-19,21,23H,5-13H2,1-4H3,(H,30,31)/t15-,16+,17-,18+,19+,21+,23+,24-,25+,26-,27-/m0/s1

InChI Key

RABBRGJJXRWNML-LUOQHXBRSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Petrosaspongia nigra	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Oxepane
Gamma butyrolactone
Meta-dioxolane
Tetrahydrofuran
Carboxylic acid ester
Lactone
Acetal
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

29216932

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163060617

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid (NP0235301)

MOL for NP0235301 ((1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

3D MOL for NP0235301 ((1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

3D SDF for NP0235301 ((1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

3D-SDF for NP0235301 ((1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

PDB for NP0235301 ((1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

3D PDB for NP0235301 ((1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

SMILES for NP0235301 ((1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

INCHI for NP0235301 ((1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

Structure for NP0235301 ((1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)

3D Structure for NP0235301 ((1s,2r,4r,5s,8r,9s,13r,14s,17s,18s,20s)-2-(acetyloxy)-5,9,13-trimethyl-22-oxo-19,21,24-trioxahexacyclo[16.5.1.0¹,²⁰.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-9-carboxylic acid)