NP-MRD: Showing NP-Card for (2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid (NP0147123)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 02:39:54 UTC

Updated at

2022-09-02 02:39:54 UTC

NP-MRD ID

NP0147123

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid

Description

Apodoa belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. (2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid is found in Gymnocladus chinensis. Based on a literature review very few articles have been published on Apodoa.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 46  0  0  0  0  0  0  0  0999 V2000
    0.0768    1.4250    2.1640 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1785    0.1085    2.2646 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1495   -0.8458    1.1600 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0187   -2.0807    1.4878 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8326   -0.2033   -0.0284 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2479    0.1839    0.3565 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9715    0.8164   -0.7598 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0778    0.2600   -1.2092 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5926   -1.0104   -0.5832 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8423    0.8215   -2.3010 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8903    0.2574   -2.6960 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3888    2.0077   -2.9083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0485   -1.3221    0.7879 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0271   -0.5563    0.2948 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1666   -0.4710    1.1014 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7905    0.7541    0.9319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6634    1.2684   -0.4849 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8161    2.0029   -0.7606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6416    0.0904   -1.4298 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9045   -0.4962   -1.3759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5551   -0.9203   -1.0751 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6018   -1.0189   -2.0552 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0415    1.9288    1.2131 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1051    2.0862    3.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2960   -0.3020    3.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3566   -2.5046    0.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8394   -1.8121    2.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3641   -2.7978    2.0379 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8444   -0.9163   -0.8832 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2806    0.6937   -0.3709 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2442    0.8908    1.1862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7499   -0.7820    0.6140 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6271    1.7206   -1.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5662   -1.3002   -1.0243 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8341   -1.7949   -0.7798 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7798   -0.8717    0.5023 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6158    2.8573   -2.3862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6683    0.5013    0.2246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4182    1.4726    1.6635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8715    0.5845    1.1180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8133    1.9574   -0.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5447    1.7521   -0.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5107    0.4395   -2.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9154   -1.1909   -0.6644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0689   -1.9201   -0.9945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7029   -1.7632   -2.6774 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3 13  1  6
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
  3  2  1  0
  2  1  2  3
  8 10  1  0
 10 12  1  0
 10 11  2  0
 21 14  1  0
  9 34  1  0
  9 35  1  0
  9 36  1  0
  7 33  1  0
  6 31  1  0
  6 32  1  0
  5 29  1  0
  5 30  1  0
  4 26  1  0
  4 27  1  0
  4 28  1  0
 14 38  1  6
 16 39  1  0
 16 40  1  0
 17 41  1  1
 18 42  1  0
 19 43  1  6
 20 44  1  0
 21 45  1  1
 22 46  1  0
  2 25  1  0
  1 23  1  0
  1 24  1  0
 12 37  1  0
M  END


  Mrv1652309022204392D          

 22 22  0  0  1  0            999 V2000
    1.2375    3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125    3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4125    1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   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
  3  4  1  6  0  0  0
  3  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
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
  3 13  1  1  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0147123

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(=C/CC[C@](C)(O[C@@H]1OC[C@H](O)[C@H](O)[C@H]1O)C=C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O7/c1-4-15(3,7-5-6-9(2)13(19)20)22-14-12(18)11(17)10(16)8-21-14/h4,6,10-12,14,16-18H,1,5,7-8H2,2-3H3,(H,19,20)/b9-6+/t10-,11-,12+,14-,15+/m0/s1

> <INCHI_KEY>
SUXYTSNUWGRMRJ-XTHZRIGOSA-N

> <FORMULA>
C15H24O7

> <MOLECULAR_WEIGHT>
316.35

> <EXACT_MASS>
316.152203113

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
32.26323802482807

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,6S)-2,6-dimethyl-6-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid

> <ALOGPS_LOGP>
0.15

> <JCHEM_LOGP>
0.6986843479999991

> <ALOGPS_LOGS>
-1.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.245287799707453

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.34955300041217

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5265811794955466

> <JCHEM_POLAR_SURFACE_AREA>
116.45000000000002

> <JCHEM_REFRACTIVITY>
78.37460000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.59e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E,6S)-2,6-dimethyl-6-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid

> <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       2.310   5.954   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.770   5.954   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.770   3.286   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334   5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667   7.700   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  10.010   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.001  10.010   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.001  11.550   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      -5.335   9.240   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   13                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    3   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   14   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Value	Source
6 alpha-Arabinosyloxy-2,6-dimethyl-2,7-octadienoic acid	MeSH

Chemical Formula

C₁₅H₂₄O₇

Average Mass

316.3500 Da

Monoisotopic Mass

316.15220 Da

IUPAC Name

(2E,6S)-2,6-dimethyl-6-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid

Traditional Name

(2E,6S)-2,6-dimethyl-6-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid

CAS Registry Number

Not Available

SMILES

C\C(=C/CC[C@](C)(O[C@@H]1OC[C@H](O)[C@H](O)[C@H]1O)C=C)C(O)=O

InChI Identifier

InChI=1S/C15H24O7/c1-4-15(3,7-5-6-9(2)13(19)20)22-14-12(18)11(17)10(16)8-21-14/h4,6,10-12,14,16-18H,1,5,7-8H2,2-3H3,(H,19,20)/b9-6+/t10-,11-,12+,14-,15+/m0/s1

InChI Key

SUXYTSNUWGRMRJ-XTHZRIGOSA-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
Gymnocladus chinensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

O-glycosyl compound
Monocyclic monoterpenoid
Monoterpenoid
Medium-chain fatty acid
Methyl-branched fatty acid
Branched fatty acid
Sugar acid
Heterocyclic fatty acid
Hydroxy fatty acid
Fatty acid
Fatty acyl
Unsaturated fatty acid
Oxane
Monosaccharide
Secondary alcohol
Oxacycle
Monocarboxylic acid or derivatives
Polyol
Organoheterocyclic compound
Carboxylic acid
Carboxylic acid derivative
Acetal
Organic oxide
Carbonyl group
Alcohol
Hydrocarbon derivative
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	0.15	ALOGPS
logP	0.7	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	4.35	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	78.37 m³·mol⁻¹	ChemAxon
Polarizability	32.26 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

4943020

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6438552

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid (NP0147123)

MOL for NP0147123 ((2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid)

3D MOL for NP0147123 ((2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid)

3D SDF for NP0147123 ((2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid)

3D-SDF for NP0147123 ((2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid)

PDB for NP0147123 ((2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid)

3D PDB for NP0147123 ((2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid)

SMILES for NP0147123 ((2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid)

INCHI for NP0147123 ((2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid)

Structure for NP0147123 ((2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid)

3D Structure for NP0147123 ((2e,6s)-2,6-dimethyl-6-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}octa-2,7-dienoic acid)