NP-MRD: Showing NP-Card for Globostellatic acid A (NP0077963)

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Record Information

Version

2.0

Created at

2022-04-28 23:06:58 UTC

Updated at

2022-04-28 23:06:58 UTC

NP-MRD ID

NP0077963

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Globostellatic acid A

Description

Globostellatic acid A, also known as globostellatate a, belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Globostellatic acid A is found in Rhabdastrella globostellata. Based on a literature review very few articles have been published on globostellatic acid A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292201062D          

 39 41  0  0  1  0            999 V2000
    3.9558    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5212    0.4383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9112   -0.2887    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7358   -0.3145    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1704    0.3867    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7804    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9950    0.3610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4296    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2542    1.0365    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0396    1.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7388   -1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4548   -1.5494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0259   -1.5546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4214   -0.7733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6520   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1645   -1.0538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7945   -1.5864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4246   -2.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3271   -0.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2619   -2.2164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8357   -1.8917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9770   -1.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7565   -0.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312    1.1653    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  4 11  1  6  0  0  0
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 11 13  1  0  0  0  0
  4 14  1  1  0  0  0
  3 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  2 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
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 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
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 32 35  1  0  0  0  0
 28 36  1  0  0  0  0
 23 37  1  0  0  0  0
 17 38  1  1  0  0  0
  2 39  1  6  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304292201062D          

 39 41  0  0  1  0            999 V2000
    3.9558    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3882   -1.3331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1645   -1.0538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7945   -1.5864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4246   -2.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3271   -0.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2619   -2.2164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8357   -1.8917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9770   -1.3851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7565   -0.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312    1.1653    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  4 11  1  6  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  4 14  1  1  0  0  0
  3 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  2 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 32 35  1  0  0  0  0
 28 36  1  0  0  0  0
 23 37  1  0  0  0  0
 17 38  1  1  0  0  0
  2 39  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0077963

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1CC[C@]2(C)[C@@H]3CC(=O)\C(=C(\C)C(=O)\C=C\C(\C)=C\C=C\C(C)(C)O)[C@@]3(C)CC[C@H]2[C@@]1(C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H44O7/c1-19(10-9-15-29(4,5)38)11-12-22(34)20(2)27-23(35)18-25-30(6)17-14-26(39-21(3)33)32(8,28(36)37)24(30)13-16-31(25,27)7/h9-12,15,24-26,38H,13-14,16-18H2,1-8H3,(H,36,37)/b12-11+,15-9+,19-10+,27-20+/t24-,25+,26-,30+,31+,32-/m1/s1

> <INCHI_KEY>
FCEBMUDWBVZUAU-JZOYBAOCSA-N

> <FORMULA>
C32H44O7

> <MOLECULAR_WEIGHT>
540.697

> <EXACT_MASS>
540.308703757

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
61.42538925969166

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3Z,3aS,5aR,6R,7R,9aR,9bS)-7-(acetyloxy)-3-[(4E,6E,8E)-10-hydroxy-6,10-dimethyl-3-oxoundeca-4,6,8-trien-2-ylidene]-3a,6,9a-trimethyl-2-oxo-dodecahydro-1H-cyclopenta[a]naphthalene-6-carboxylic acid

> <ALOGPS_LOGP>
4.51

> <JCHEM_LOGP>
5.091415431999999

> <ALOGPS_LOGS>
-5.59

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
17.911529550978646

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.2354248517487285

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5252890233654286

> <JCHEM_POLAR_SURFACE_AREA>
117.97000000000001

> <JCHEM_REFRACTIVITY>
152.67230000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.40e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3Z,3aS,5aR,6R,7R,9aR,9bS)-7-(acetyloxy)-3-[(4E,6E,8E)-10-hydroxy-6,10-dimethyl-3-oxoundeca-4,6,8-trien-2-ylidene]-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalene-6-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       7.384   2.127   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.573   0.818   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.301  -0.539   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.840  -0.587   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.651   0.722   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.923   2.079   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.191   0.674   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      12.002   1.983   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      13.541   1.935   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.274   3.340   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.846  -2.127   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.182  -2.892   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       7.515  -2.902   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.120  -1.444   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.490  -1.848   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.950  -1.800   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.222  -0.443   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.034   0.866   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.039   2.042   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.614   1.460   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.305   2.271   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.727  -0.076   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.551  -1.070   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.102  -0.549   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.171   0.967   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -1.074  -1.543   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.523  -1.021   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.700  -2.016   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -5.149  -1.494   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -6.325  -2.488   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.774  -1.967   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -8.950  -2.961   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -10.126  -3.955   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -9.944  -1.785   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -7.956  -4.137   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -3.427  -3.531   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.824  -2.586   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.279  -1.660   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.845   2.175   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   18   39                                             
CONECT    3    2    4   15                                                  
CONECT    4    3    5   11   14                                             
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    4   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    4                                                            
CONECT   15    3   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22   38                                             
CONECT   18   17    2   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   17   23                                                  
CONECT   23   22   24   37                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   36                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34   35                                             
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   32                                                            
CONECT   36   28                                                            
CONECT   37   23                                                            
CONECT   38   17                                                            
CONECT   39    2                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   82    0
END

View in JSmol

Synonyms

Value	Source
Globostellatate a	Generator

Chemical Formula

C₃₂H₄₄O₇

Average Mass

540.6970 Da

Monoisotopic Mass

540.30870 Da

IUPAC Name

(3Z,3aS,5aR,6R,7R,9aR,9bS)-7-(acetyloxy)-3-[(4E,6E,8E)-10-hydroxy-6,10-dimethyl-3-oxoundeca-4,6,8-trien-2-ylidene]-3a,6,9a-trimethyl-2-oxo-dodecahydro-1H-cyclopenta[a]naphthalene-6-carboxylic acid

Traditional Name

(3Z,3aS,5aR,6R,7R,9aR,9bS)-7-(acetyloxy)-3-[(4E,6E,8E)-10-hydroxy-6,10-dimethyl-3-oxoundeca-4,6,8-trien-2-ylidene]-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalene-6-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1CC[C@]2(C)[C@@H]3CC(=O)\C(=C(\C)C(=O)\C=C\C(\C)=C\C=C\C(C)(C)O)[C@@]3(C)CC[C@H]2[C@@]1(C)C(O)=O

InChI Identifier

InChI=1S/C32H44O7/c1-19(10-9-15-29(4,5)38)11-12-22(34)20(2)27-23(35)18-25-30(6)17-14-26(39-21(3)33)32(8,28(36)37)24(30)13-16-31(25,27)7/h9-12,15,24-26,38H,13-14,16-18H2,1-8H3,(H,36,37)/b12-11+,15-9+,19-10+,27-20+/t24-,25+,26-,30+,31+,32-/m1/s1

InChI Key

FCEBMUDWBVZUAU-JZOYBAOCSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Rhabdastrella globostellata	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Dicarboxylic acid or derivatives
Acryloyl-group
Enone
Alpha,beta-unsaturated ketone
Tertiary alcohol
Carboxylic acid ester
Ketone
Cyclic ketone
Carboxylic acid
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

acetate ester (CHEBI:72301 )
enone (CHEBI:72301 )
dioxo monocarboxylic acid (CHEBI:72301 )
tricyclic triterpenoid (CHEBI:72301 )

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	4.51	ALOGPS
logP	5.09	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	4.24	ChemAxon
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	117.97 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	152.67 m³·mol⁻¹	ChemAxon
Polarizability	61.43 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00041547

Chemspider ID

8705892

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10530497

PDB ID

Not Available

ChEBI ID

72301

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Globostellatic acid A (NP0077963)

MOL for NP0077963 (Globostellatic acid A)

3D MOL for NP0077963 (Globostellatic acid A)

3D SDF for NP0077963 (Globostellatic acid A)

3D-SDF for NP0077963 (Globostellatic acid A)

PDB for NP0077963 (Globostellatic acid A)

3D PDB for NP0077963 (Globostellatic acid A)

SMILES for NP0077963 (Globostellatic acid A)

INCHI for NP0077963 (Globostellatic acid A)

Structure for NP0077963 (Globostellatic acid A)

3D Structure for NP0077963 (Globostellatic acid A)