NP-MRD: Showing NP-Card for (2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid (NP0300578)

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Record Information

Version

2.0

Created at

2022-09-10 13:03:03 UTC

Updated at

2022-09-10 13:03:03 UTC

NP-MRD ID

NP0300578

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid

Description

Saliniketal B belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. (2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid is found in Salinispora arenicola. (2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid was first documented in 2009 (PMID: 19722715). Based on a literature review very few articles have been published on saliniketal B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102215032D          

 29 30  0  0  1  0            999 V2000
   -3.5932   -0.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5932   -0.1444    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3077    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    1.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0221    1.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0221    2.3306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7366    2.7431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7366    3.5681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    2.7431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    3.5681    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5932    2.3306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8787    0.2681    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8787    1.0931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1643   -0.1444    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1643   -0.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4498    0.2681    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4498    1.0931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7353   -0.1444    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7353   -0.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0208    0.2681    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6608   -0.1966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4492    0.0465    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0103   -0.5582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7506    0.8145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3381    1.5290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5223    1.6520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1864    0.9651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0825    1.0908    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8505    1.3922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  2 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
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 16 18  1  0  0  0  0
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 26 27  1  6  0  0  0
 22 27  1  0  0  0  0
 26 28  1  0  0  0  0
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 28 29  1  6  0  0  0
M  END

     RDKit          2D

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    9.2851   -7.0572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1766   -0.8355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1766    0.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1595    1.8121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1 32  1  0
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  7 38  1  0
  8 39  1  0
 11 41  1  0
 10 40  1  0
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 26 62  1  1
 28 63  1  6
 29 64  1  0
 29 65  1  0
 29 66  1  0
M  END


  Mrv1652309102215032D          

 29 30  0  0  1  0            999 V2000
   -3.5932   -0.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5932   -0.1444    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3077    0.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    1.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0221    1.5056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0221    2.3306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7366    2.7431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7366    3.5681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    2.7431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077    3.5681    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5932    2.3306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6608   -0.1966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
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M  END
> <DATABASE_ID>
NP0300578

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](\C=C\C=C(\CO)C(O)=N)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@@H]1O[C@@]2(C)CC[C@@H](O2)[C@H]1C

> <INCHI_IDENTIFIER>
InChI=1S/C22H37NO6/c1-12(7-6-8-16(11-24)21(23)27)18(25)14(3)19(26)15(4)20-13(2)17-9-10-22(5,28-17)29-20/h6-8,12-15,17-20,24-26H,9-11H2,1-5H3,(H2,23,27)/b7-6+,16-8-/t12-,13+,14+,15+,17+,18-,19+,20+,22-/m0/s1

> <INCHI_KEY>
QWSYKJZSJYRUSS-XCPHXFLXSA-N

> <FORMULA>
C22H37NO6

> <MOLECULAR_WEIGHT>
411.539

> <EXACT_MASS>
411.262087915

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
31.115414435787137

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2Z,4E,6S,7S,8R,9R,10R)-10-[(1S,3S,4R,5R)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid

> <JCHEM_LOGP>
-1.0453517707366822

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.220074024911018

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.48872998512803223

> <JCHEM_PKA_STRONGEST_BASIC>
12.282421692495562

> <JCHEM_POLAR_SURFACE_AREA>
123.23000000000002

> <JCHEM_REFRACTIVITY>
123.52270000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2Z,4E,6S,7S,8R,9R,10R)-10-[(1S,3S,4R,5R)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.707  -1.810   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.707  -0.270   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.041   0.500   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.041   2.040   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.375   2.810   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.375   4.350   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -10.708   5.120   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0     -10.708   6.660   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -8.041   5.120   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      -8.041   6.660   0.000  0.00  0.00           N+0
HETATM   11  O   UNK     0      -6.707   4.350   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -5.374   0.500   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -5.374   2.040   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -4.040  -0.270   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.040  -1.810   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.706   0.500   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.706   2.040   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.373  -0.270   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.373  -1.810   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.039   0.500   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.234  -0.367   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.705   0.087   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.753  -1.042   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.268   1.520   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.498   2.854   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.975   3.084   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.215   1.802   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -0.154   2.036   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.588   2.599   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    2   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24   27                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26   22                                                       
CONECT   28   26   20   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₇NO₆

Average Mass

411.5390 Da

Monoisotopic Mass

411.26209 Da

IUPAC Name

(2Z,4E,6S,7S,8R,9R,10R)-10-[(1S,3S,4R,5R)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid

Traditional Name

(2Z,4E,6S,7S,8R,9R,10R)-10-[(1S,3S,4R,5R)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid

CAS Registry Number

Not Available

SMILES

C[C@@H](\C=C\C=C(\CO)C(O)=N)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@@H]1O[C@@]2(C)CC[C@@H](O2)[C@H]1C

InChI Identifier

InChI=1S/C22H37NO6/c1-12(7-6-8-16(11-24)21(23)27)18(25)14(3)19(26)15(4)20-13(2)17-9-10-22(5,28-17)29-20/h6-8,12-15,17-20,24-26H,9-11H2,1-5H3,(H2,23,27)/b7-6+,16-8-/t12-,13+,14+,15+,17+,18-,19+,20+,22-/m0/s1

InChI Key

QWSYKJZSJYRUSS-XCPHXFLXSA-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
Salinispora arenicola	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Oxepane
Ketal
Meta-dioxane
Oxolane
Carboxamide group
Primary carboxylic acid amide
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organic oxide
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
Primary alcohol
Hydrocarbon derivative
Alcohol
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	-1	ChemAxon
pKa (Strongest Acidic)	0.49	ChemAxon
pKa (Strongest Basic)	12.28	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	123.23 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	123.52 m³·mol⁻¹	ChemAxon
Polarizability	31.12 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

C00040187

Chemspider ID

23278450

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44418843

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Liu J, De Brabander JK: A concise total synthesis of saliniketal B. J Am Chem Soc. 2009 Sep 9;131(35):12562-3. doi: 10.1021/ja9061757. [PubMed:19722715 ]
LOTUS database [Link]

Showing NP-Card for (2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid (NP0300578)

MOL for NP0300578 ((2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

3D MOL for NP0300578 ((2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

3D SDF for NP0300578 ((2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

3D-SDF for NP0300578 ((2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

PDB for NP0300578 ((2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

3D PDB for NP0300578 ((2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

SMILES for NP0300578 ((2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

INCHI for NP0300578 ((2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

Structure for NP0300578 ((2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)

3D Structure for NP0300578 ((2z,4e,6s,7s,8r,9r,10r)-10-[(1s,3s,4r,5r)-1,4-dimethyl-2,8-dioxabicyclo[3.2.1]octan-3-yl]-7,9-dihydroxy-2-(hydroxymethyl)-6,8-dimethylundeca-2,4-dienimidic acid)