NP-MRD: Showing NP-Card for (2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate (NP0297311)

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Record Information

Version

2.0

Created at

2022-09-10 07:31:35 UTC

Updated at

2022-09-10 07:31:36 UTC

NP-MRD ID

NP0297311

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate

Description

(2R,3S,4R,5R)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity. (2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate is found in Acacia concinna. Based on a literature review very few articles have been published on (2R,3S,4R,5R)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 50 50  0  0  0  0  0  0  0  0999 V2000
    5.2045   -0.9268    2.1807 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3541   -0.6526    0.8843 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2459   -0.1253    0.0522 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3142    1.3634   -0.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0580   -0.4509    0.7394 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2175   -0.8384   -1.2592 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0109   -0.4386   -2.1010 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7518   -0.7279   -1.4530 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7801    0.0538   -1.1150 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7255    1.5076   -1.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8077    2.0660   -1.9403 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4276   -0.5470   -0.4409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4580   -1.7657   -0.2295 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4818    0.2267   -0.0622 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6465   -0.2260    0.5669 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8915    0.0463   -0.2473 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6854   -0.2492   -1.7105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9797   -0.5603    0.2909 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2552   -0.3129    1.5928 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2149   -1.2433    2.0587 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0945   -0.2065    2.5133 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4335    0.4258    3.7268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8780    0.4168    1.9154 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7641    0.3373    2.7330 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0094   -1.3098    2.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2479   -0.7609    2.6393 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3085   -0.8120    0.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5716    1.7540   -1.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1060    1.7281    0.6567 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3726    1.8558    0.3183 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6326    0.3447    1.1343 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1429   -0.6061   -1.8120 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1650   -1.9133   -1.0715 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2098    0.5386   -2.5014 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0777   -1.1368   -3.0014 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6070   -1.8175   -1.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6141    2.0262   -0.3176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2462    1.7990   -1.8339 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0201    2.9598   -1.5643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5392   -1.3297    0.6946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0570    1.1619   -0.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2840    0.4706   -2.3157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6194   -0.1385   -2.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9813   -1.2872   -1.9730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8026    0.6770    1.6403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5875   -1.7664    1.3006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8064   -1.2566    2.8142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4097    0.6446    3.6604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1411    1.4928    1.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8703   -0.4907    3.2743 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 15  1  0
 15 14  1  0
 14 12  1  0
 12 13  2  0
 12  9  1  0
  9 10  1  0
 10 11  1  0
  9  8  2  0
  8  7  1  0
  7  6  1  0
  6  3  1  0
  3  4  1  0
  3  5  1  1
  3  2  1  0
  2  1  2  3
 15 16  1  0
 17 42  1  0
 17 43  1  0
 17 44  1  0
 16 41  1  6
 19 45  1  6
 20 46  1  0
 21 47  1  1
 22 48  1  0
 23 49  1  6
 24 50  1  0
 15 40  1  1
 10 37  1  0
 10 38  1  0
 11 39  1  0
  8 36  1  0
  7 34  1  0
  7 35  1  0
  6 32  1  0
  6 33  1  0
  4 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  2 27  1  0
  1 25  1  0
  1 26  1  0
M  END


  Mrv1652309102209312D          

 24 24  0  0  1  0            999 V2000
    2.1434    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    5.7750    0.0000 O   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    4.5375    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
    0.0000    3.3000    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    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   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    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 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  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  0  0  0  0
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0297311

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1OC(=O)C(CO)=CCCC(C)(O)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C16H26O8/c1-4-16(3,22)7-5-6-10(8-17)14(20)24-13-9(2)23-15(21)12(19)11(13)18/h4,6,9,11-13,15,17-19,21-22H,1,5,7-8H2,2-3H3/t9-,11-,12-,13-,15?,16?/m1/s1

> <INCHI_KEY>
FFLUVDOEJBDSSD-CGVPGNNDSA-N

> <FORMULA>
C16H26O8

> <MOLECULAR_WEIGHT>
346.376

> <EXACT_MASS>
346.162767797

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
35.27160000457466

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3S,4R,5R)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate

> <JCHEM_LOGP>
-0.4294108983333339

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.882988232648273

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.307483763683532

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2853115113873996

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
84.586

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4R,5R)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate

> <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       4.001  13.090   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  12.320   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  10.780   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.127  10.780   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.207  10.780   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.667   9.240   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   8.470   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.667   6.160   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.334   3.850   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   24  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    6                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    3    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   23                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   15   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Value	Source
(2R,3S,4R,5R)-4,5,6-Trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoic acid	Generator

Chemical Formula

C₁₆H₂₆O₈

Average Mass

346.3760 Da

Monoisotopic Mass

346.16277 Da

IUPAC Name

(2R,3S,4R,5R)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate

Traditional Name

(2R,3S,4R,5R)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate

CAS Registry Number

Not Available

SMILES

C[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1OC(=O)C(CO)=CCCC(C)(O)C=C

InChI Identifier

InChI=1S/C16H26O8/c1-4-16(3,22)7-5-6-10(8-17)14(20)24-13-9(2)23-15(21)12(19)11(13)18/h4,6,9,11-13,15,17-19,21-22H,1,5,7-8H2,2-3H3/t9-,11-,12-,13-,15?,16?/m1/s1

InChI Key

FFLUVDOEJBDSSD-CGVPGNNDSA-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
Acacia concinna	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Hexoses

Alternative Parents

Substituents

Hexose monosaccharide
Monocyclic monoterpenoid
Monoterpenoid
Fatty alcohol
Beta-hydroxy acid
Fatty acid ester
Hydroxy acid
Fatty acyl
Oxane
Enoate ester
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Carboxylic acid ester
Hemiacetal
Organoheterocyclic compound
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Polyol
Primary alcohol
Hydrocarbon derivative
Alcohol
Organic oxide
Carbonyl group
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	-0.43	ChemAxon
pKa (Strongest Acidic)	11.31	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	84.59 m³·mol⁻¹	ChemAxon
Polarizability	35.27 Å³	ChemAxon
Number of Rings	1	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

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

53796628

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,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate (NP0297311)

MOL for NP0297311 ((2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate)

3D MOL for NP0297311 ((2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate)

3D SDF for NP0297311 ((2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate)

3D-SDF for NP0297311 ((2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate)

PDB for NP0297311 ((2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate)

3D PDB for NP0297311 ((2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate)

SMILES for NP0297311 ((2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate)

INCHI for NP0297311 ((2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate)

Structure for NP0297311 ((2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate)

3D Structure for NP0297311 ((2r,3s,4r,5r)-4,5,6-trihydroxy-2-methyloxan-3-yl 6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoate)