NP-MRD: Showing NP-Card for 28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate (NP0142850)

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Record Information

Version

2.0

Created at

2022-09-01 21:29:28 UTC

Updated at

2022-09-01 21:29:28 UTC

NP-MRD ID

NP0142850

Secondary Accession Numbers

None

Natural Product Identification

Common Name

28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate

Description

28-(Acetyloxy)-8,23,27-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]Octacosa-4(9),5,7,11,19(24),20,22,26-octaen-14-yl acetate belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone. 28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate is found in Cladonia bellidiflora. 28-(Acetyloxy)-8,23,27-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]Octacosa-4(9),5,7,11,19(24),20,22,26-octaen-14-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161506182D          

 45 52  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004161506182D          

 45 52  0  0  0  0            999 V2000
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    1.5221    1.9062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7746    1.5653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4510    2.0434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3460    2.4483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1940    2.1510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4704    3.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3372    4.0166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1974    3.5317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0201    2.9156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2167    3.2691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3943    2.6398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1234    3.0535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2388    3.9156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8348    2.6361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5546    3.0392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7691    3.8762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2636    2.6174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2527    1.7924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9939    1.3555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5329    1.3894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8239    1.8112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0819    1.4165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8925    0.4008    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2749    1.7471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0922    4.1397    0.0000 O   0  0  0  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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  8 21  1  0  0  0  0
 21 22  1  0  0  0  0
  5 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 24 29  1  0  0  0  0
 21 29  1  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  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  2  0  0  0  0
 34 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
  6 44  1  0  0  0  0
 23 44  1  0  0  0  0
 31 44  1  0  0  0  0
 30 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0142850

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1C2C=C3C(=O)C4=C(O)C=C(C)C=C4C(=O)C33C1C1C(OC(C)=O)C3C(O)=C3C(=O)C4=C(O)C=C(C)C=C4C(=O)C213

> <INCHI_IDENTIFIER>
InChI=1S/C34H26O11/c1-10-5-14-20(18(37)7-10)26(39)16-9-17-29(44-12(3)35)22-23-30(45-13(4)36)25(33(16,22)31(14)42)28(41)24-27(40)21-15(32(43)34(17,23)24)6-11(2)8-19(21)38/h5-9,17,22-23,25,29-30,37-38,41H,1-4H3

> <INCHI_KEY>
IUKUFMFGKRXEJD-UHFFFAOYSA-N

> <FORMULA>
C34H26O11

> <MOLECULAR_WEIGHT>
610.571

> <EXACT_MASS>
610.147511657

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
61.070953522401375

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
28-(acetyloxy)-8,23,27-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate

> <ALOGPS_LOGP>
3.04

> <JCHEM_LOGP>
2.55370048

> <ALOGPS_LOGS>
-4.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.348981309431155

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.531064798049914

> <JCHEM_PKA_STRONGEST_BASIC>
-5.4904233063388626

> <JCHEM_POLAR_SURFACE_AREA>
181.57

> <JCHEM_REFRACTIVITY>
156.5853

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.64e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
28-(acetyloxy)-8,23,27-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -0.208   4.210   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.568   3.487   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -2.740   4.254   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -1.718   1.760   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.188   2.064   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.628   1.389   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.208   0.780   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.333   2.010   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.929   1.819   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.380   0.263   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.965   2.997   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.472   2.682   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.273   1.288   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.499   3.831   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.018   5.294   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.381   6.186   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.716   5.536   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.484   4.460   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.987   4.706   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.233   6.253   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.841   3.558   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.446   2.922   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.842   3.814   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.513   4.570   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.095   4.015   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.611   5.809   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.363   7.498   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.968   6.593   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.904   5.443   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.405   6.102   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.736   4.928   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.097   5.700   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -2.312   7.309   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -3.425   4.921   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -4.769   5.673   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -5.169   7.236   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -6.092   4.886   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -6.072   3.346   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -7.455   2.530   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -4.728   2.593   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -3.405   3.381   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -2.019   2.644   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -1.666   0.748   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -0.513   3.261   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       0.172   7.727   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   22                                                  
CONECT    6    5    7   44                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   21                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   18                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   11   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    8   22   29                                             
CONECT   22   21    5   23                                                  
CONECT   23   22   24   44                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   24   21   30                                                  
CONECT   30   29   31   45                                                  
CONECT   31   30   32   44                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   41                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   34   42                                                  
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42    6   23   31                                             
CONECT   45   30                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  104    0
END

View in JSmol

Synonyms

Value	Source
28-(Acetyloxy)-8,23,27-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0,.0,.0,.0,.0,.0,]octacosa-4(9),5,7,11,19(24),20,22,26-octaen-14-yl acetic acid	Generator
28-(Acetyloxy)-8,23,27-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4(9),5,7,11,19(24),20,22,26-octaen-14-yl acetic acid	Generator

Chemical Formula

C₃₄H₂₆O₁₁

Average Mass

610.5710 Da

Monoisotopic Mass

610.14751 Da

IUPAC Name

28-(acetyloxy)-8,23,27-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(=O)OC1C2C=C3C(=O)C4=C(O)C=C(C)C=C4C(=O)C33C1C1C(OC(C)=O)C3C(O)=C3C(=O)C4=C(O)C=C(C)C=C4C(=O)C213

InChI Identifier

InChI=1S/C34H26O11/c1-10-5-14-20(18(37)7-10)26(39)16-9-17-29(44-12(3)35)22-23-30(45-13(4)36)25(33(16,22)31(14)42)28(41)24-27(40)21-15(32(43)34(17,23)24)6-11(2)8-19(21)38/h5-9,17,22-23,25,29-30,37-38,41H,1-4H3

InChI Key

IUKUFMFGKRXEJD-UHFFFAOYSA-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
Cladonia bellidiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

9,10-anthraquinone
Anthraquinone
Tetralin
Naphthalene
Aryl alkyl ketone
Aryl ketone
Quinone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Dicarboxylic acid or derivatives
Vinylogous acid
Carboxylic acid ester
Ketone
Enol
Carboxylic acid derivative
Polyol
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	3.04	ALOGPS
logP	2.55	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	7.53	ChemAxon
pKa (Strongest Basic)	-5.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	181.57 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	156.59 m³·mol⁻¹	ChemAxon
Polarizability	61.07 Å³	ChemAxon
Number of Rings	8	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

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

LOTUS database [Link]

Showing NP-Card for 28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate (NP0142850)

MOL for NP0142850 (28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate)

3D MOL for NP0142850 (28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate)

3D SDF for NP0142850 (28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate)

3D-SDF for NP0142850 (28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate)

PDB for NP0142850 (28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate)

3D PDB for NP0142850 (28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate)

SMILES for NP0142850 (28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate)

INCHI for NP0142850 (28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate)

Structure for NP0142850 (28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate)

3D Structure for NP0142850 (28-(acetyloxy)-8,12,23-trihydroxy-6,21-dimethyl-3,10,18,25-tetraoxooctacyclo[14.11.1.0²,¹¹.0²,¹⁵.0⁴,⁹.0¹³,¹⁷.0¹⁷,²⁶.0¹⁹,²⁴]octacosa-4,6,8,11,19,21,23,26-octaen-14-yl acetate)