NP-MRD: Showing NP-Card for (1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate (NP0284557)

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Record Information

Version

2.0

Created at

2022-09-09 12:18:33 UTC

Updated at

2022-09-09 12:18:33 UTC

NP-MRD ID

NP0284557

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate

Description

Lancifodilactone J belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid. (1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate is found in Schisandra lancifolia. Based on a literature review very few articles have been published on Lancifodilactone J.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092214182D          

 42 48  0  0  1  0            999 V2000
    4.2044   -5.8605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 42 40  1  6  0  0  0
  5 42  1  0  0  0  0
 19 42  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309092214182D          

 42 48  0  0  1  0            999 V2000
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    3.3493   -1.7763    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1303   -2.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6991   -2.6760    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7562   -1.8786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3398   -1.2880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1428   -1.5492    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9827   -0.7399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7710   -1.0145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7077   -0.1919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4738   -1.4467    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2365   -1.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2799   -2.2486    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.8146   -2.8768    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.6372   -2.8134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9517   -3.5761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7535   -3.7700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3234   -4.1109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3868   -4.9334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6207   -3.6787    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4573   -2.3119    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0819   -3.1164    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7631   -3.5818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4914   -2.7779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434   -3.7852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6540   -4.5829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5815   -3.5258    0.0000 C   0  0  2  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  1  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  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 17 16  1  6  0  0  0
  7 17  1  0  0  0  0
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 29 35  1  6  0  0  0
 36 28  1  6  0  0  0
 22 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  6  0  0  0
 37 39  1  0  0  0  0
 19 39  1  6  0  0  0
 37 40  1  0  0  0  0
 40 41  2  0  0  0  0
 42 40  1  6  0  0  0
  5 42  1  0  0  0  0
 19 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0284557

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@H]([C@H]2OC(=O)C(C)=C2)[C@H]2[C@](C)(CC[C@]34C[C@]56OC(=O)C[C@H]5OC(C)(C)[C@@H]6C[C@H](OC(C)=O)[C@H]3C(=O)[C@@]2(O)O4)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H38O11/c1-13-9-16(39-26(13)36)21-14(2)24(34)28(6)7-8-29-12-30-18(27(4,5)40-19(30)11-20(33)41-30)10-17(38-15(3)32)22(29)25(35)31(37,42-29)23(21)28/h9,14,16-19,21-23,37H,7-8,10-12H2,1-6H3/t14-,16-,17-,18-,19+,21+,22-,23-,28-,29-,30+,31-/m0/s1

> <INCHI_KEY>
RXNQFRVLPNMCHU-VJZLCUFQSA-N

> <FORMULA>
C31H38O11

> <MOLECULAR_WEIGHT>
586.634

> <EXACT_MASS>
586.241412044

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
59.73601479603057

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,7R,10S,12S,13R,15S,16S,17S,18S,20S)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2R)-4-methyl-5-oxo-2,5-dihydrofuran-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0^{1,13}.0^{3,7}.0^{3,10}.0^{16,20}]tricosan-12-yl acetate

> <JCHEM_LOGP>
2.556607493000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.932845184149556

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.079088329319463

> <JCHEM_PKA_STRONGEST_BASIC>
-4.005032437423924

> <JCHEM_POLAR_SURFACE_AREA>
151.73

> <JCHEM_REFRACTIVITY>
141.94180000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,7R,10S,12S,13R,15S,16S,17S,18S,20S)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0^{1,13}.0^{3,7}.0^{3,10}.0^{16,20}]tricosan-12-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       7.848 -10.940   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.056  -9.414   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.481  -8.831   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.838  -8.471   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.046  -6.945   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.631  -6.158   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.204  -4.572   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.728  -3.847   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.277  -5.320   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.203  -3.635   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.695  -2.284   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.236  -1.980   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.010  -0.584   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.490  -0.913   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.679   0.066   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       7.529  -2.428   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.252  -3.316   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.710  -3.766   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.772  -4.995   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.878  -3.507   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.968  -2.404   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.467  -2.892   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.168  -1.381   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.639  -1.894   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      12.521  -0.358   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      13.951  -2.700   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.375  -2.113   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.589  -4.197   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.587  -5.370   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      16.123  -5.252   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      16.710  -6.675   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      18.207  -7.037   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      15.537  -7.674   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      15.655  -9.209   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      14.225  -6.867   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      12.054  -4.316   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      11.353  -5.817   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      12.624  -6.686   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      10.251  -5.185   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      10.161  -7.066   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      10.554  -8.555   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       8.552  -6.581   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   42                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   17                                                  
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16    7   12   18                                             
CONECT   18   17   19                                                       
CONECT   19   18   20   39   42                                             
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   36                                             
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   36                                                  
CONECT   29   28   30   35                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   29                                                       
CONECT   36   28   22   37                                                  
CONECT   37   36   38   39   40                                             
CONECT   38   37                                                            
CONECT   39   37   19                                                       
CONECT   40   37   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40    5   19                                                  
MASTER        0    0    0    0    0    0    0    0   42    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₃₈O₁₁

Average Mass

586.6340 Da

Monoisotopic Mass

586.24141 Da

IUPAC Name

(1S,3R,7R,10S,12S,13R,15S,16S,17S,18S,20S)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2R)-4-methyl-5-oxo-2,5-dihydrofuran-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0^{1,13}.0^{3,7}.0^{3,10}.0^{16,20}]tricosan-12-yl acetate

Traditional Name

(1S,3R,7R,10S,12S,13R,15S,16S,17S,18S,20S)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0^{1,13}.0^{3,7}.0^{3,10}.0^{16,20}]tricosan-12-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@H]([C@H]2OC(=O)C(C)=C2)[C@H]2[C@](C)(CC[C@]34C[C@]56OC(=O)C[C@H]5OC(C)(C)[C@@H]6C[C@H](OC(C)=O)[C@H]3C(=O)[C@@]2(O)O4)C1=O

InChI Identifier

InChI=1S/C31H38O11/c1-13-9-16(39-26(13)36)21-14(2)24(34)28(6)7-8-29-12-30-18(27(4,5)40-19(30)11-20(33)41-30)10-17(38-15(3)32)22(29)25(35)31(37,42-29)23(21)28/h9,14,16-19,21-23,37H,7-8,10-12H2,1-6H3/t14-,16-,17-,18-,19+,21+,22-,23-,28-,29-,30+,31-/m0/s1

InChI Key

RXNQFRVLPNMCHU-VJZLCUFQSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Schisandra lancifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Prostaglandins and related compounds

Alternative Parents

Substituents

Prostaglandin skeleton
Terpene lactone
11-noriridane monoterpenoid
Monoterpenoid
Tricarboxylic acid or derivatives
Furofuran
Oxepane
2-furanone
3-furanone
Gamma butyrolactone
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Hemiacetal
Ketone
Lactone
Organoheterocyclic compound
Oxacycle
Ether
Dialkyl ether
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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
logP	2.56	ChemAxon
pKa (Strongest Acidic)	10.08	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	151.73 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	141.94 m³·mol⁻¹	ChemAxon
Polarizability	59.74 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00041618

Chemspider ID

9831924

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11657186

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate (NP0284557)

MOL for NP0284557 ((1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate)

3D MOL for NP0284557 ((1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate)

3D SDF for NP0284557 ((1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate)

3D-SDF for NP0284557 ((1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate)

PDB for NP0284557 ((1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate)

3D PDB for NP0284557 ((1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate)

SMILES for NP0284557 ((1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate)

INCHI for NP0284557 ((1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate)

Structure for NP0284557 ((1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate)

3D Structure for NP0284557 ((1s,3r,7r,10s,12s,13r,15s,16s,17s,18s,20s)-15-hydroxy-9,9,18,20-tetramethyl-17-[(2r)-4-methyl-5-oxo-2h-furan-2-yl]-5,14,19-trioxo-4,8,23-trioxahexacyclo[13.7.1.0¹,¹³.0³,⁷.0³,¹⁰.0¹⁶,²⁰]tricosan-12-yl acetate)