NP-MRD: Showing NP-Card for (1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one (NP0325156)

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Record Information

Version

2.0

Created at

2022-09-12 05:41:46 UTC

Updated at

2022-09-12 05:41:46 UTC

NP-MRD ID

NP0325156

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one

Description

Acnistin E belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton. (1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one is found in Dunalia solanacea. Based on a literature review very few articles have been published on Acnistin E.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309122207412D          

 35 41  0  0  1  0            999 V2000
    5.7518    1.7357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3919    0.9934    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8601    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0480    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7677    0.7029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2995    0.0722    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0192   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2071   -0.8489    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3949   -0.9941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6752   -0.2182    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8631   -0.3634    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5828   -1.1393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3313    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6116    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4237    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7040    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9555    0.5577    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2358    1.3336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1116    0.2174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7629   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4458    0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2165    0.9666    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9773    1.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3379    1.7826    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1257    2.0273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4257    2.7958    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2483    2.8590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4718    2.7422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6553    2.2460    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5921    3.0686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1958    3.6309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9511    4.4188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0118    3.5095    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1149    4.3280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7346    3.9072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  5 17  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  1  0  0  0
  6 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  6  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 29 28  1  1  0  0  0
 24 29  1  0  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
 26 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  6  0  0  0
M  END


  Mrv1652309122207412D          

 35 41  0  0  1  0            999 V2000
    5.7518    1.7357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3919    0.9934    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8601    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0480    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7677    0.7029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2995    0.0722    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0192   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2071   -0.8489    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3949   -0.9941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6752   -0.2182    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8631   -0.3634    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5828   -1.1393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3313    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6116    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4237    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7040    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9555    0.5577    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2358    1.3336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1116    0.2174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7629   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4458    0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2165    0.9666    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9773    1.2854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3379    1.7826    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1257    2.0273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4257    2.7958    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2483    2.8590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4718    2.7422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6553    2.2460    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5921    3.0686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1958    3.6309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9511    4.4188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0118    3.5095    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1149    4.3280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7346    3.9072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  5 17  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  1  0  0  0
  6 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  6  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 29 28  1  1  0  0  0
 24 29  1  0  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
 26 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0325156

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]12C[C@@H](OC(=O)[C@]1(C)O)[C@H](C2)[C@]1(O)CC[C@H]2[C@@H]3C[C@H]4O[C@]44[C@@H](O)C=CC(=O)[C@]4(C)[C@H]3CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C28H38O7/c1-23-12-17(18(13-23)34-22(31)26(23,4)32)27(33)10-8-15-14-11-21-28(35-21)20(30)6-5-19(29)25(28,3)16(14)7-9-24(15,27)2/h5-6,14-18,20-21,30,32-33H,7-13H2,1-4H3/t14-,15-,16-,17-,18+,20-,21+,23+,24-,25-,26-,27+,28+/m0/s1

> <INCHI_KEY>
FKQUQCYOBZEPTK-QTLUSXIASA-N

> <FORMULA>
C28H38O7

> <MOLECULAR_WEIGHT>
486.605

> <EXACT_MASS>
486.261753564

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
52.11763974551542

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,6S,7R,9R,11S,12S,15R,16S)-6,15-dihydroxy-15-[(1R,4R,5R,7S)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-4-en-3-one

> <JCHEM_LOGP>
2.271312723

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.38203855977347

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.169410664491348

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1923739033384972

> <JCHEM_POLAR_SURFACE_AREA>
116.59000000000002

> <JCHEM_REFRACTIVITY>
125.7889

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,6S,7R,9R,11S,12S,15R,16S)-6,15-dihydroxy-15-[(1R,4R,5R,7S)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-4-en-3-one

> <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      10.737   3.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.065   1.854   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.072   3.032   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.556   2.761   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.033   1.312   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.026   0.135   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.502  -1.314   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.986  -1.585   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.471  -1.856   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.994  -0.407   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.478  -0.678   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.955  -2.127   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.485   0.499   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.008   1.947   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.524   2.218   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.047   3.667   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.517   1.041   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.040   2.489   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.542   0.406   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.757  -0.539   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.032   0.325   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.604   1.804   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      13.024   2.399   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      11.831   3.327   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.301   3.784   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.861   5.219   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.397   5.337   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.081   5.119   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.557   4.193   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      10.439   5.728   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      11.565   6.778   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      11.109   8.248   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      13.089   6.551   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.281   8.079   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      14.438   7.293   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   19   22                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   17                                                  
CONECT    6    5    7   19                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8   10                                                       
CONECT   10    9    8   11   17                                             
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    5   10   18                                             
CONECT   18   17                                                            
CONECT   19    6    2   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    2   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28   33                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   24   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   26   34   35                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₈O₇

Average Mass

486.6050 Da

Monoisotopic Mass

486.26175 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@]12C[C@@H](OC(=O)[C@]1(C)O)[C@H](C2)[C@]1(O)CC[C@H]2[C@@H]3C[C@H]4O[C@]44[C@@H](O)C=CC(=O)[C@]4(C)[C@H]3CC[C@]12C

InChI Identifier

InChI=1S/C28H38O7/c1-23-12-17(18(13-23)34-22(31)26(23,4)32)27(33)10-8-15-14-11-21-28(35-21)20(30)6-5-19(29)25(28,3)16(14)7-9-24(15,27)2/h5-6,14-18,20-21,30,32-33H,7-13H2,1-4H3/t14-,15-,16-,17-,18+,20-,21+,23+,24-,25-,26-,27+,28+/m0/s1

InChI Key

FKQUQCYOBZEPTK-QTLUSXIASA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Saracha nigribaccata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Steroid lactones

Alternative Parents

Substituents

Steroid lactone
Estrane-skeleton
5,6-epoxysteroid
Caprolactone
Delta valerolactone
Cyclohexenone
Delta_valerolactone
Oxepane
Oxane
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
Ketone
Lactone
Organoheterocyclic compound
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organic oxide
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Alcohol
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

8633538

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10458124

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,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one (NP0325156)

MOL for NP0325156 ((1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one)

3D MOL for NP0325156 ((1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one)

3D SDF for NP0325156 ((1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one)

3D-SDF for NP0325156 ((1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one)

PDB for NP0325156 ((1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one)

3D PDB for NP0325156 ((1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one)

SMILES for NP0325156 ((1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one)

INCHI for NP0325156 ((1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one)

Structure for NP0325156 ((1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one)

3D Structure for NP0325156 ((1s,2r,6s,7r,9r,11s,12s,15r,16s)-6,15-dihydroxy-15-[(1r,4r,5r,7s)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-3-one)