NP-MRD: Showing NP-Card for chrysobrevione J (NP0333766)

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Record Information

Version

2.0

Created at

2024-08-26 15:28:47 UTC

Updated at

2025-06-11 03:36:40 UTC

NP-MRD ID

NP0333766

Natural Product DOI

https://doi.org/10.57994/3245

Secondary Accession Numbers

None

Natural Product Identification

Common Name

chrysobrevione J

Description

Chrysobrevione J belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. Based on a literature review very few articles have been published on chrysobrevione J.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 05102318012D          

 35 39  0  0  1  0            999 V2000
    0.4047   -2.6882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9116   -3.3391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4646   -2.7269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1825   -3.7253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1524   -4.5498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -4.9880    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8213   -5.8125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5804   -4.6019    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5503   -5.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6105   -3.7774    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6406   -2.9530    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3396   -3.3913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0385   -3.8295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0084   -4.6540    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7074   -5.0923    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8235   -4.2755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6362   -4.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0744   -3.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8989   -3.4646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2851   -4.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1095   -4.2238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8468   -4.8926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2330   -5.6217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6883   -2.7055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0223   -4.8625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4483   -5.4551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6773   -5.9167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3762   -6.3550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9482   -6.3029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5824   -4.0614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2794   -5.0402    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9783   -5.4784    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2493   -5.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5203   -6.2508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5164   -3.2870    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  6  7  1  6  0  0  0
  8  6  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10  2  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 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
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 18 24  2  0  0  0  0
 17 25  2  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 15 26  1  1  0  0  0
 15 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 14 30  1  6  0  0  0
 31 14  1  0  0  0  0
  8 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 29 33  1  0  0  0  0
 33 34  2  0  0  0  0
  4 35  2  0  0  0  0
M  END


  Mrv2104 05102318012D          

 35 39  0  0  1  0            999 V2000
    0.4047   -2.6882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9116   -3.3391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4646   -2.7269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1825   -3.7253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1524   -4.5498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -4.9880    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8213   -5.8125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5804   -4.6019    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5503   -5.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6105   -3.7774    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6406   -2.9530    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3396   -3.3913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0385   -3.8295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0084   -4.6540    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7074   -5.0923    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8235   -4.2755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6362   -4.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0744   -3.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8989   -3.4646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2851   -4.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1095   -4.2238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8468   -4.8926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2330   -5.6217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6883   -2.7055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0223   -4.8625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4483   -5.4551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6773   -5.9167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3762   -6.3550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9482   -6.3029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5824   -4.0614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2794   -5.0402    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9783   -5.4784    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2493   -5.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5203   -6.2508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5164   -3.2870    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  0  0  0  0
  6  7  1  6  0  0  0
  8  6  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10  2  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 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
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 18 24  2  0  0  0  0
 17 25  2  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 15 26  1  1  0  0  0
 15 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 14 30  1  6  0  0  0
 31 14  1  0  0  0  0
  8 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 29 33  1  0  0  0  0
 33 34  2  0  0  0  0
  4 35  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0333766

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12CC[C@]3(C)[C@]([H])(C(=O)C=C(C)[C@@]33CC4=C(O3)C(C)=C(C)OC4=O)[C@@]1(C)[C@H](O)CC(=O)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C27H34O6/c1-13-10-17(28)22-25(6,9-8-18-24(4,5)19(29)11-20(30)26(18,22)7)27(13)12-16-21(33-27)14(2)15(3)32-23(16)31/h10,18,20,22,30H,8-9,11-12H2,1-7H3/t18-,20+,22-,25+,26+,27-/m0/s1

> <INCHI_KEY>
UMIZNJIXFGGNGB-RELCSYLQSA-N

> <FORMULA>
C27H34O6

> <MOLECULAR_WEIGHT>
454.563

> <EXACT_MASS>
454.235538815

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
49.61085343112143

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,4'aR,4'bS,5'R,8'aR,10'aR)-5'-hydroxy-2',4'b,6,7,8',8',10'a-heptamethyl-3,4,4'a,4'b,5',6',7',8',8'a,9',10',10'a-dodecahydro-4'H-spiro[furo[3,2-c]pyran-2,1'-phenanthrene]-4,4',7'-trione

> <JCHEM_LOGP>
3.623949028333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.981672616250684

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.490448293691045

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0216701798881473

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
125.12659999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4'aR,4'bS,5'R,8'aR,10'aR)-5'-hydroxy-2',4'b,6,7,8',8',10'a-heptamethyl-4'a,5',6',8'a,9',10'-hexahydro-3H-spiro[furo[3,2-c]pyran-2,1'-phenanthrene]-4,4',7'-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-MAY-23         0                                  
HETATM    1  C   UNK     0       0.755  -5.018   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.702  -6.233   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.734  -5.090   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.341  -6.954   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.285  -8.493   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.589  -9.311   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.533 -10.850   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.950  -8.590   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.894 -10.129   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.006  -7.051   0.000  0.00  0.00           C+0
HETATM   11  H   UNK     0       3.062  -5.512   0.000  0.00  0.00           H+0
HETATM   12  C   UNK     0       4.367  -6.330   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.672  -7.148   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.616  -8.687   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.920  -9.506   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.137  -7.981   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.654  -7.716   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.472  -6.411   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.011  -6.467   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      11.732  -7.828   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.271  -7.884   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.914  -9.133   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.635 -10.494   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.751  -5.050   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.375  -9.077   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.304 -10.183   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.864 -11.045   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.169 -11.863   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.503 -11.765   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.687  -7.581   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.255  -9.408   0.000  0.00  0.00           C+0
HETATM   32  H   UNK     0       5.560 -10.226   0.000  0.00  0.00           H+0
HETATM   33  C   UNK     0       4.199 -10.947   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       2.838 -11.668   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      -0.964  -6.136   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   10                                             
CONECT    3    2                                                            
CONECT    4    2    5   35                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   31                                             
CONECT    9    8                                                            
CONECT   10    8    2   11   12                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   30   31                                             
CONECT   15   14   16   26   27                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   25                                                  
CONECT   23   22                                                            
CONECT   24   18                                                            
CONECT   25   17   22   26                                                  
CONECT   26   25   15                                                       
CONECT   27   15   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   33                                                       
CONECT   30   14                                                            
CONECT   31   14    8   32   33                                             
CONECT   32   31                                                            
CONECT   33   31   29   34                                                  
CONECT   34   33                                                            
CONECT   35    4                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₄O₆

Average Mass

454.5630 Da

Monoisotopic Mass

454.23554 Da

IUPAC Name

(2S,4'aR,4'bS,5'R,8'aR,10'aR)-5'-hydroxy-2',4'b,6,7,8',8',10'a-heptamethyl-3,4,4'a,4'b,5',6',7',8',8'a,9',10',10'a-dodecahydro-4'H-spiro[furo[3,2-c]pyran-2,1'-phenanthrene]-4,4',7'-trione

Traditional Name

(2S,4'aR,4'bS,5'R,8'aR,10'aR)-5'-hydroxy-2',4'b,6,7,8',8',10'a-heptamethyl-4'a,5',6',8'a,9',10'-hexahydro-3H-spiro[furo[3,2-c]pyran-2,1'-phenanthrene]-4,4',7'-trione

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC[C@]3(C)[C@]([H])(C(=O)C=C(C)[C@@]33CC4=C(O3)C(C)=C(C)OC4=O)[C@@]1(C)[C@H](O)CC(=O)C2(C)C

InChI Identifier

InChI=1S/C27H34O6/c1-13-10-17(28)22-25(6,9-8-18-24(4,5)19(29)11-20(30)26(18,22)7)27(13)12-16-21(33-27)14(2)15(3)32-23(16)31/h10,18,20,22,30H,8-9,11-12H2,1-7H3/t18-,20+,22-,25+,26+,27-/m0/s1

InChI Key

UMIZNJIXFGGNGB-RELCSYLQSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, CDCl3, experimental)	niusiwen@tio.org.cn	Third Institute of Oceanography, Ministry of Natural Resources	Siwen Niu	2024-08-26	View Spectrum
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, CD3OD, experimental)	niusiwen@tio.org.cn	Third Institute of Oceanography, Ministry of Natural Resources	Siwen Niu	2024-08-26	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	niusiwen@tio.org.cn	Third Institute of Oceanography, Ministry of Natural Resources	Siwen Niu	2024-08-26	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, C2D6OS, experimental)	niusiwen@tio.org.cn	Third Institute of Oceanography, Ministry of Natural Resources	Siwen Niu	2024-08-26	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, C2D6OS, experimental)	niusiwen@tio.org.cn	Third Institute of Oceanography, Ministry of Natural Resources	Siwen Niu	2024-08-26	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C2D6OS, experimental)	niusiwen@tio.org.cn	Third Institute of Oceanography, Ministry of Natural Resources	Siwen Niu	2024-08-26	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Spongiane diterpenoid
Diterpenoid
Diterpene lactone
Cyclohexenone
Pyranone
Fatty acid ester
Alkyl aryl ether
Fatty acyl
Pyran
Beta-hydroxy ketone
Heteroaromatic compound
Vinylogous ester
Alpha,beta-unsaturated ketone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Enone
Enol ester
Dihydrofuran
Cyclic alcohol
Acryloyl-group
Cyclic ketone
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.62	ChemAxon
pKa (Strongest Acidic)	14.49	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	125.13 m³·mol⁻¹	ChemAxon
Polarizability	49.61 Å³	ChemAxon
Number of Rings	5	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for chrysobrevione J (NP0333766)

MOL for NP0333766 (chrysobrevione J)

3D MOL for NP0333766 (chrysobrevione J)

3D SDF for NP0333766 (chrysobrevione J)

3D-SDF for NP0333766 (chrysobrevione J)

PDB for NP0333766 (chrysobrevione J)

3D PDB for NP0333766 (chrysobrevione J)

SMILES for NP0333766 (chrysobrevione J)

INCHI for NP0333766 (chrysobrevione J)

Structure for NP0333766 (chrysobrevione J)

3D Structure for NP0333766 (chrysobrevione J)