NP-MRD: Showing NP-Card for (1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate (NP0268532)

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Record Information

Version

2.0

Created at

2022-09-08 13:41:25 UTC

Updated at

2022-09-08 13:41:25 UTC

NP-MRD ID

NP0268532

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate

Description

Pelargoniin C belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. (1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate is found in Pelargonium reniforme. Based on a literature review very few articles have been published on Pelargoniin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082215412D          

 44 49  0  0  1  0            999 V2000
    8.1717   -2.7166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.5854   -1.2291    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    5.7362   -1.1684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309082215412D          

 44 49  0  0  1  0            999 V2000
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    4.3147   -2.8597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4532   -2.0464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0685   -3.2082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6954   -2.6550    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3402   -1.9033    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5626   -1.6277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1249   -4.1448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9495   -4.1718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3383   -4.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1629   -4.9264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9027   -5.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2915   -6.3276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0781   -5.5730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6424   -6.2735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6892   -4.8454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 21 28  1  0  0  0  0
 28 29  1  0  0  0  0
 13 29  1  0  0  0  0
 18 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 33 32  1  6  0  0  0
  4 33  1  0  0  0  0
 33 34  1  0  0  0  0
  9 34  1  0  0  0  0
 34 35  1  1  0  0  0
  2 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  2  0  0  0  0
 36 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0268532

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H]1O[C@@H](OC(=O)C2=CC(O)=C(O)C(O)=C2)[C@@H]2OC(=O)C3=C4C5C(O)(OC4=C(O)C(O)=C3)C(O)CC5(O)C(=O)O[C@H]1[C@@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C26H24O18/c27-5-11-17-16(34)19(23(40-11)43-21(35)6-1-8(28)14(32)9(29)2-6)41-22(36)7-3-10(30)15(33)18-13(7)20-25(38,24(37)42-17)4-12(31)26(20,39)44-18/h1-3,11-12,16-17,19-20,23,27-34,38-39H,4-5H2/t11-,12?,16+,17-,19-,20?,23+,25?,26?/m1/s1

> <INCHI_KEY>
OPDCHSHIPIOYPU-GHUMVCHFSA-N

> <FORMULA>
C26H24O18

> <MOLECULAR_WEIGHT>
624.46

> <EXACT_MASS>
624.096263933

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
54.45498454423786

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,17R,18S,20R,21S)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1^{7,10}.0^{4,8}.0^{9,14}]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate

> <JCHEM_LOGP>
-1.1439747266666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.656991878727217

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.94905320116985

> <JCHEM_PKA_STRONGEST_BASIC>
-3.70900400770594

> <JCHEM_POLAR_SURFACE_AREA>
299.65999999999997

> <JCHEM_REFRACTIVITY>
133.63819999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,17R,18S,20R,21S)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1^{7,10}.0^{4,8}.0^{9,14}]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  O   UNK     0      15.254  -5.071   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      14.441  -6.379   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      12.901  -6.328   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      12.175  -4.970   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      13.031  -3.664   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      12.293  -2.294   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.129  -1.001   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      14.667  -1.078   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.708  -2.181   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.364  -1.331   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.773  -1.337   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.725   0.202   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.197  -1.431   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.818  -0.022   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.211  -0.215   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.755  -0.757   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.479   0.106   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.796  -2.334   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.318  -1.903   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       2.920  -3.635   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.853  -4.895   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.514  -6.450   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.047  -6.918   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.660  -7.493   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.332  -8.998   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.144  -7.019   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.496  -5.487   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.338  -4.389   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.294  -2.763   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.054  -5.338   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.313  -3.820   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       9.461  -5.989   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      10.631  -4.956   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.968  -3.553   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       8.517  -3.038   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      15.166  -7.737   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      16.706  -7.787   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      17.432  -9.146   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      18.971  -9.196   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      16.618 -10.453   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      17.344 -11.811   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      15.079 -10.403   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      14.266 -11.711   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      14.353  -9.045   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   36                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   33                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   34                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   29                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   29                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   28                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   21   29                                                  
CONECT   29   28   13   18                                                  
CONECT   30   27   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32    4   34                                                  
CONECT   34   33    9   35                                                  
CONECT   35   34                                                            
CONECT   36    2   37   44                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   36                                                       
MASTER        0    0    0    0    0    0    0    0   44    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₂₄O₁₈

Average Mass

624.4600 Da

Monoisotopic Mass

624.09626 Da

IUPAC Name

(1S,17R,18S,20R,21S)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1^{7,10}.0^{4,8}.0^{9,14}]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate

Traditional Name

(1S,17R,18S,20R,21S)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1^{7,10}.0^{4,8}.0^{9,14}]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@@H](OC(=O)C2=CC(O)=C(O)C(O)=C2)[C@@H]2OC(=O)C3=C4C5C(O)(OC4=C(O)C(O)=C3)C(O)CC5(O)C(=O)O[C@H]1[C@@H]2O

InChI Identifier

InChI=1S/C26H24O18/c27-5-11-17-16(34)19(23(40-11)43-21(35)6-1-8(28)14(32)9(29)2-6)41-22(36)7-3-10(30)15(33)18-13(7)20-25(38,24(37)42-17)4-12(31)26(20,39)44-18/h1-3,11-12,16-17,19-20,23,27-34,38-39H,4-5H2/t11-,12?,16+,17-,19-,20?,23+,25?,26?/m1/s1

InChI Key

OPDCHSHIPIOYPU-GHUMVCHFSA-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
Pelargonium reniforme	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Hydrolyzable tannins

Direct Parent

Hydrolyzable tannins

Alternative Parents

Substituents

Hydrolyzable tannin
Galloyl ester
Gallic acid or derivatives
P-hydroxybenzoic acid alkyl ester
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
Dihydroxybenzoic acid
Benzoate ester
Coumaran
Tricarboxylic acid or derivatives
Pyrogallol derivative
Benzoic acid or derivatives
Benzenetriol
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Oxane
Monosaccharide
Monocyclic benzene moiety
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Lactone
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
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	-1.1	ChemAxon
pKa (Strongest Acidic)	7.95	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	299.66 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	133.64 m³·mol⁻¹	ChemAxon
Polarizability	54.45 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	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

C00053642

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

102509860

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate (NP0268532)

MOL for NP0268532 ((1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate)

3D MOL for NP0268532 ((1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate)

3D SDF for NP0268532 ((1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate)

3D-SDF for NP0268532 ((1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate)

PDB for NP0268532 ((1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate)

3D PDB for NP0268532 ((1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate)

SMILES for NP0268532 ((1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate)

INCHI for NP0268532 ((1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate)

Structure for NP0268532 ((1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate)

3D Structure for NP0268532 ((1s,17r,18s,20r,21s)-4,6,7,11,12,21-hexahydroxy-20-(hydroxymethyl)-3,15-dioxo-2,16,19,22-tetraoxapentacyclo[15.3.1.1⁷,¹⁰.0⁴,⁸.0⁹,¹⁴]docosa-9(14),10,12-trien-18-yl 3,4,5-trihydroxybenzoate)