NP-MRD: Showing NP-Card for (2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid (NP0177800)

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Record Information

Version

2.0

Created at

2022-09-03 15:41:31 UTC

Updated at

2022-09-03 15:41:31 UTC

NP-MRD ID

NP0177800

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid

Description

(2R,3S,4E,6S,7S,8E,10S,11R,12E,14S,15R,16E,18S,19S,20S)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. (2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid is found in Xylaria berteroi. Based on a literature review very few articles have been published on (2R,3S,4E,6S,7S,8E,10S,11R,12E,14S,15R,16E,18S,19S,20S)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032217412D          

 37 36  0  0  1  0            999 V2000
   -0.1914    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2375   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9520    1.9520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6664    0.7145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6664   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0954   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    7.6677    1.9520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   11.2401    0.7145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.2401   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9546    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6690    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3835    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.0980    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3835    1.9520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.6690    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0980    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0980    3.1895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.8124    1.9520    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
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
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 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
M  END

     RDKit          3D

 89 88  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309032217412D          

 37 36  0  0  1  0            999 V2000
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    6.9533    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9533   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6677    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6677    1.9520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3822    0.7145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3822   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0967    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8112    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5256    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.5256    1.9520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2401    0.7145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.2401   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9546    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6690    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3835    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.0980    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3835    1.9520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.6690    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0980    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0980    3.1895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.8124    1.9520    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
  3  4  1  1  0  0  0
  3  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0177800

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)[C@H](O)[C@@H](C)\C=C(/C)[C@H](O)[C@@H](C)\C=C(/C)[C@H](O)[C@@H](C)\C=C\[C@H](O)[C@@H](C)\C=C\[C@H](O)[C@@H](C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H52O7/c1-10-17(2)27(33)20(5)15-22(7)29(35)23(8)16-21(6)28(34)19(4)12-13-25(31)18(3)11-14-26(32)24(9)30(36)37/h11-20,23-29,31-35H,10H2,1-9H3,(H,36,37)/b13-12+,14-11+,21-16+,22-15+/t17-,18-,19-,20-,23-,24+,25-,26-,27-,28+,29-/m0/s1

> <INCHI_KEY>
IYZMEJBPKJHYRJ-FJDPVDFZSA-N

> <FORMULA>
C30H52O7

> <MOLECULAR_WEIGHT>
524.739

> <EXACT_MASS>
524.371304014

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
59.77372079187377

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3S,4E,6S,7S,8E,10S,11R,12E,14S,15R,16E,18S,19S,20S)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid

> <JCHEM_LOGP>
4.176825759333331

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.613566597851474

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.457252715753996

> <JCHEM_PKA_STRONGEST_BASIC>
-0.4656052343235001

> <JCHEM_POLAR_SURFACE_AREA>
138.45

> <JCHEM_REFRACTIVITY>
152.23000000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4E,6S,7S,8E,10S,11R,12E,14S,15R,16E,18S,19S,20S)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.357   1.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.976   2.104   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.310  -0.206   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.644   3.644   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.977   1.334   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.977  -0.206   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.311   2.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.645   1.334   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.645  -0.206   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.978   2.104   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.978   3.644   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.312   1.334   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.312  -0.206   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.646   2.104   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.979   1.334   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.979  -0.206   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.313   2.104   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      14.313   3.644   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      15.647   1.334   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.647  -0.206   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.980   2.104   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      18.314   1.334   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      19.648   2.104   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      19.648   3.644   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      20.982   1.334   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      20.982  -0.206   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      22.315   2.104   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      23.649   1.334   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      24.983   2.104   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      26.316   1.334   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      24.983   3.644   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      23.649   4.414   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      26.316   4.414   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      26.316   5.954   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      27.650   3.644   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   72    0
END

View in JSmol

Synonyms

Value	Source
(2R,3S,4E,6S,7S,8E,10S,11R,12E,14S,15R,16E,18S,19S,20S)-3,7,11,15,19-Pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoate	Generator

Chemical Formula

C₃₀H₅₂O₇

Average Mass

524.7390 Da

Monoisotopic Mass

524.37130 Da

IUPAC Name

(2R,3S,4E,6S,7S,8E,10S,11R,12E,14S,15R,16E,18S,19S,20S)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid

Traditional Name

(2R,3S,4E,6S,7S,8E,10S,11R,12E,14S,15R,16E,18S,19S,20S)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid

CAS Registry Number

Not Available

SMILES

CC[C@H](C)[C@H](O)[C@@H](C)\C=C(/C)[C@H](O)[C@@H](C)\C=C(/C)[C@H](O)[C@@H](C)\C=C\[C@H](O)[C@@H](C)\C=C\[C@H](O)[C@@H](C)C(O)=O

InChI Identifier

InChI=1S/C30H52O7/c1-10-17(2)27(33)20(5)15-22(7)29(35)23(8)16-21(6)28(34)19(4)12-13-25(31)18(3)11-14-26(32)24(9)30(36)37/h11-20,23-29,31-35H,10H2,1-9H3,(H,36,37)/b13-12+,14-11+,21-16+,22-15+/t17-,18-,19-,20-,23-,24+,25-,26-,27-,28+,29-/m0/s1

InChI Key

IYZMEJBPKJHYRJ-FJDPVDFZSA-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
Xylaria berteroi	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Sesterterpenoids

Alternative Parents

Substituents

Sesterterpenoid
Very long-chain fatty acid
Beta-hydroxy acid
Branched fatty acid
Methyl-branched fatty acid
Hydroxy fatty acid
Hydroxy acid
Fatty acyl
Fatty acid
Unsaturated fatty acid
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Polyol
Monocarboxylic acid or derivatives
Alcohol
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organooxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	4.18	ChemAxon
pKa (Strongest Acidic)	4.46	ChemAxon
pKa (Strongest Basic)	-0.47	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	138.45 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	152.23 m³·mol⁻¹	ChemAxon
Polarizability	59.77 Å³	ChemAxon
Number of Rings	0	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

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

162916231

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid (NP0177800)

MOL for NP0177800 ((2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid)

3D MOL for NP0177800 ((2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid)

3D SDF for NP0177800 ((2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid)

3D-SDF for NP0177800 ((2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid)

PDB for NP0177800 ((2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid)

3D PDB for NP0177800 ((2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid)

SMILES for NP0177800 ((2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid)

INCHI for NP0177800 ((2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid)

Structure for NP0177800 ((2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid)

3D Structure for NP0177800 ((2r,3s,4e,6s,7s,8e,10s,11r,12e,14s,15r,16e,18s,19s,20s)-3,7,11,15,19-pentahydroxy-2,6,10,12,14,16,18,20-octamethyldocosa-4,8,12,16-tetraenoic acid)