NP-MRD: Showing NP-Card for (1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone (NP0147755)

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Record Information

Version

2.0

Created at

2022-09-02 03:25:11 UTC

Updated at

2022-09-02 03:25:11 UTC

NP-MRD ID

NP0147755

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone

Description

(1R,2S,5R,8R,9R,14R,15R,17S,18R,21S,24R,26S,27S)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]Nonacos-11-ene-4,10,22,29-tetrone belongs to the class of organic compounds known as physalins and derivatives. These are steroidal constituents of Physalis plants which possess an unusual 13,14-seco-16,24-cyclo-steroidal ring skeleton (where the bond that is normally present between the 13 and 14 positions in other steroids is broken while a new bond between positions 16 and 24 is formed). (1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone is found in Physalis lagascae. Based on a literature review very few articles have been published on (1R,2S,5R,8R,9R,14R,15R,17S,18R,21S,24R,26S,27S)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]Nonacos-11-ene-4,10,22,29-tetrone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022205252D          

 39 46  0  0  1  0            999 V2000
    0.9993   -1.0538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3455   -0.5507    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2048    0.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4623    0.5900    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.7574   -1.0422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3181   -1.6473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1092   -1.2562    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8024   -1.8226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6645   -1.7286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0491   -0.9503    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3141   -0.6152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448    0.4535    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9914   -0.1255    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9441   -0.1740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5026    0.4332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  2  1  1  6  0  0  0
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  4  3  1  6  0  0  0
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  5  6  1  0  0  0  0
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  2 14  1  0  0  0  0
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 36 38  1  0  0  0  0
 26 38  1  0  0  0  0
 31 38  1  0  0  0  0
 38 39  1  6  0  0  0
M  END

     RDKit          3D

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  9 48  1  0
M  END


  Mrv1652309022205252D          

 39 46  0  0  1  0            999 V2000
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    3.2848    0.6302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3951   -0.1878    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8973   -0.8457    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2182   -1.6058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0369   -1.7079    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3578   -2.4679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5346   -1.0500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8555   -1.8100    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3533   -1.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8510   -0.4941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5301    0.2659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7115    0.3680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3906    1.1280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2137   -0.2899    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8928    0.4701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  8  6  1  1  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  1  0  0  0
 11 15  1  0  0  0  0
 15 16  2  0  0  0  0
 13 17  1  0  0  0  0
  4 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 26 25  1  1  0  0  0
 26 27  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 26 38  1  0  0  0  0
 31 38  1  0  0  0  0
 38 39  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0147755

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]12OC(=O)[C@@]3(O)CC[C@@H]4[C@H](C[C@@H](O)[C@@]5(O)CC=CC(=O)[C@]45C)[C@@]45O[C@@]13[C@@H](C4=O)[C@]1(C)C[C@H]2OC(=O)[C@@H]1CO5

> <INCHI_IDENTIFIER>
InChI=1S/C28H32O11/c1-22-10-17-24(3)28-18(22)19(31)27(39-28,36-11-14(22)20(32)37-17)13-9-16(30)25(34)7-4-5-15(29)23(25,2)12(13)6-8-26(28,35)21(33)38-24/h4-5,12-14,16-18,30,34-35H,6-11H2,1-3H3/t12-,13+,14+,16-,17-,18+,22-,23+,24+,25+,26+,27-,28+/m1/s1

> <INCHI_KEY>
DUGJJSWZRHBJJK-VUYURAFHSA-N

> <FORMULA>
C28H32O11

> <MOLECULAR_WEIGHT>
544.553

> <EXACT_MASS>
544.19446185

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
52.506371596695416

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,5R,8R,9R,14R,15R,17S,18R,21S,24R,26S,27S)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1^{18,27}.0^{1,5}.0^{2,24}.0^{8,17}.0^{9,14}.0^{21,26}]nonacos-11-ene-4,10,22,29-tetrone

> <ALOGPS_LOGP>
0.48

> <JCHEM_LOGP>
0.7562966020000005

> <ALOGPS_LOGS>
-2.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.519556331035956

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.676356900585038

> <JCHEM_PKA_STRONGEST_BASIC>
-3.262514362510035

> <JCHEM_POLAR_SURFACE_AREA>
165.89

> <JCHEM_REFRACTIVITY>
127.74119999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.72e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,5R,8R,9R,14R,15R,17S,18R,21S,24R,26S,27S)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1^{18,27}.0^{1,5}.0^{2,24}.0^{8,17}.0^{9,14}.0^{21,26}]nonacos-11-ene-4,10,22,29-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       1.865  -1.967   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.645  -1.028   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.382   0.135   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.863   1.101   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -1.953  -0.309   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.414  -1.945   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.461  -3.075   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.204  -2.345   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.498  -3.402   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.107  -3.227   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.825  -1.774   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.453  -1.148   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.324   0.847   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.851  -0.234   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.629  -0.325   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.672   0.809   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.785   1.772   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.387   2.771   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.132   3.267   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.667   3.421   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.413   4.769   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.365   2.006   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.128   3.344   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.923   2.126   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.132   1.176   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.337  -0.351   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.408  -1.579   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.007  -2.997   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.535  -3.188   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.134  -4.607   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.465  -1.960   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.064  -3.379   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       9.993  -2.151   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.922  -0.922   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.323   0.496   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.795   0.687   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       8.196   2.106   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       7.866  -0.541   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.267   0.878   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8   14                                             
CONECT    3    2    4                                                       
CONECT    4    3    5   17                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    2    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   15   27                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   17   22                                             
CONECT   14   13    2   15                                                  
CONECT   15   14   11   16                                                  
CONECT   16   15                                                            
CONECT   17   13    4   18   19                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   13   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   38                                                  
CONECT   27   26   11   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33   38                                             
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   26   31   39                                             
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₂O₁₁

Average Mass

544.5530 Da

Monoisotopic Mass

544.19446 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@]12OC(=O)[C@@]3(O)CC[C@@H]4[C@H](C[C@@H](O)[C@@]5(O)CC=CC(=O)[C@]45C)[C@@]45O[C@@]13[C@@H](C4=O)[C@]1(C)C[C@H]2OC(=O)[C@@H]1CO5

InChI Identifier

InChI=1S/C28H32O11/c1-22-10-17-24(3)28-18(22)19(31)27(39-28,36-11-14(22)20(32)37-17)13-9-16(30)25(34)7-4-5-15(29)23(25,2)12(13)6-8-26(28,35)21(33)38-24/h4-5,12-14,16-18,30,34-35H,6-11H2,1-3H3/t12-,13+,14+,16-,17-,18+,22-,23+,24+,25+,26+,27-,28+/m1/s1

InChI Key

DUGJJSWZRHBJJK-VUYURAFHSA-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
Physalis lagascae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as physalins and derivatives. These are steroidal constituents of Physalis plants which possess an unusual 13,14-seco-16,24-cyclo-steroidal ring skeleton (where the bond that is normally present between the 13 and 14 positions in other steroids is broken while a new bond between positions 16 and 24 is formed).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Physalins and derivatives

Direct Parent

Physalins and derivatives

Alternative Parents

Substituents

Physalin skeleton
Delta valerolactone
Ketal
Cyclohexenone
Delta_valerolactone
Oxepane
Dicarboxylic acid or derivatives
3-furanone
Gamma butyrolactone
Oxane
Cyclic alcohol
Tetrahydrofuran
Tertiary alcohol
Lactone
Ketone
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid derivative
Polyol
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen 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	0.48	ALOGPS
logS	-2.2	ALOGPS

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

163056514

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone (NP0147755)

MOL for NP0147755 ((1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

3D MOL for NP0147755 ((1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

3D SDF for NP0147755 ((1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

3D-SDF for NP0147755 ((1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

PDB for NP0147755 ((1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

3D PDB for NP0147755 ((1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

SMILES for NP0147755 ((1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

INCHI for NP0147755 ((1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

Structure for NP0147755 ((1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)

3D Structure for NP0147755 ((1r,2s,5r,8r,9r,14r,15r,17s,18r,21s,24r,26s,27s)-5,14,15-trihydroxy-2,9,26-trimethyl-3,19,23,28-tetraoxaoctacyclo[16.9.1.1¹⁸,²⁷.0¹,⁵.0²,²⁴.0⁸,¹⁷.0⁹,¹⁴.0²¹,²⁶]nonacos-11-ene-4,10,22,29-tetrone)