NP-MRD: Showing NP-Card for [2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid (NP0270130)

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Record Information

Version

2.0

Created at

2022-09-08 15:51:27 UTC

Updated at

2022-09-08 15:51:27 UTC

NP-MRD ID

NP0270130

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid

Description

CHEBI:181771 Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. [2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid is found in Perilla frutescens. Based on a literature review very few articles have been published on CHEBI:181771.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082217512D          

 26 27  0  0  0  0            999 V2000
    4.1801    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5846   -1.5291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4131   -0.7221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3715   -0.4672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0262   -0.1701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7041   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4888   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1019   -2.0811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8865   -1.8262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4996   -2.3782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2842   -2.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4557   -1.3163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3281   -3.1852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9411   -3.7372    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5434   -3.4401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3719   -4.2471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9303   -2.8881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1457   -3.1430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  4  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  6 14  1  0  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  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 56 57  0  0  0  0  0  0  0  0999 V2000
    4.5137   -3.3056   -2.6818 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3254   -2.3518   -1.5012 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9509   -1.8329   -1.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7109   -0.5291   -1.5356 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3620    0.0023   -1.4853 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9961    0.9385   -0.3800 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7360    2.1968   -0.2698 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0688    2.1972    0.4015 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1075    1.7502    1.7879 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0815    1.3895    2.4001 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2951    1.7026    2.5024 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7718    3.1429    0.4292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5002    2.8323   -0.3237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4564    1.3845   -0.6414 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2478    0.5989    0.1736 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0844   -0.2745   -0.4426 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3896    0.1906   -0.2384 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7949    0.0475    1.0775 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1683    0.5721    1.3329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2497    1.9240    1.0360 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7382   -1.3928    1.5398 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4610   -2.1781    0.6184 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2892   -1.8265    1.4208 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4364   -1.0065    2.1291 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9361   -1.7007   -0.0686 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8257   -2.5152   -0.7603 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5203   -3.1738   -3.1346 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7863   -3.0558   -3.4909 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3208   -4.3281   -2.3221 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5807   -2.9326   -0.5657 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0942   -1.5734   -1.5944 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1109   -2.4966   -1.3362 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5912    0.0834   -1.6730 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.8688   -1.4502 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0797    0.5597   -2.4405 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0289    0.4157    0.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8901    2.6238   -1.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8259    1.7516   -0.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3660    3.3008    0.4388 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4809    2.4223    3.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6019    2.8832    1.4751 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0844    4.2061    0.3005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4053    3.1383    0.2419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4948    3.5076   -1.2283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6303    1.1746   -1.7242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9356   -0.1789   -1.5570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0769    0.6140    1.7036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3854    0.4595    2.4157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9538   -0.0039    0.8060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2705    2.5045    1.8393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1169   -1.5269    2.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1894   -2.6805    1.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1776   -2.9087    1.6567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7391   -1.5756    2.5484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9420   -2.1208   -0.1671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0272   -2.1773   -1.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 11  1  0
  9 10  2  0
  7 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14  6  1  0
 25 16  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  1
  7 37  1  6
  8 38  1  0
  8 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  6
 16 46  1  6
 18 47  1  1
 19 48  1  0
 19 49  1  0
 20 50  1  0
 21 51  1  1
 22 52  1  0
 23 53  1  1
 24 54  1  0
 25 55  1  1
 26 56  1  0
M  END


  Mrv1652309082217512D          

 26 27  0  0  0  0            999 V2000
    4.1801    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5846   -1.5291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4131   -0.7221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3715   -0.4672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0262   -0.1701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7041   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4888   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1019   -2.0811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8865   -1.8262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4996   -2.3782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2842   -2.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4557   -1.3163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3281   -3.1852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9411   -3.7372    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5434   -3.4401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3719   -4.2471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9303   -2.8881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1457   -3.1430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  4  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  6 14  1  0  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  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0270130

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC=CCC1C(CC(O)=O)CCC1OC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C18H30O8/c1-2-3-4-5-11-10(8-14(20)21)6-7-12(11)25-18-17(24)16(23)15(22)13(9-19)26-18/h3-4,10-13,15-19,22-24H,2,5-9H2,1H3,(H,20,21)

> <INCHI_KEY>
GJZJZRWFRZFTEE-UHFFFAOYSA-N

> <FORMULA>
C18H30O8

> <MOLECULAR_WEIGHT>
374.43

> <EXACT_MASS>
374.194067926

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
39.71123900285225

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid

> <JCHEM_LOGP>
0.2579609783333329

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.210562120705257

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.280248551143153

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835427865827

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
91.89500000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       7.803   1.425   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.803  -0.115   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.469  -0.885   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.136  -0.115   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.802  -0.885   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.802  -2.425   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.556  -3.330   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.091  -2.854   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.771  -1.348   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.693  -0.872   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       1.916  -0.317   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.032  -4.795   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.572  -4.795   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.048  -3.330   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.512  -2.854   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.657  -3.885   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.121  -3.409   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.266  -4.439   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.731  -3.963   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.051  -2.457   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.946  -5.946   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      11.090  -6.976   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.481  -6.422   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.161  -7.928   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.337  -5.391   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.872  -5.867   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    6   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   16   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₃₀O₈

Average Mass

374.4300 Da

Monoisotopic Mass

374.19407 Da

IUPAC Name

2-[2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid

Traditional Name

[2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid

CAS Registry Number

Not Available

SMILES

CCC=CCC1C(CC(O)=O)CCC1OC1OC(CO)C(O)C(O)C1O

InChI Identifier

InChI=1S/C18H30O8/c1-2-3-4-5-11-10(8-14(20)21)6-7-12(11)25-18-17(24)16(23)15(22)13(9-19)26-18/h3-4,10-13,15-19,22-24H,2,5-9H2,1H3,(H,20,21)

InChI Key

GJZJZRWFRZFTEE-UHFFFAOYSA-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
Perilla frutescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Jasmonic acid
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Monosaccharide
Oxane
Secondary alcohol
Acetal
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Polyol
Organic oxide
Hydrocarbon derivative
Carbonyl group
Alcohol
Primary alcohol
Organooxygen compound
Organic oxygen compound
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	0.26	ChemAxon
pKa (Strongest Acidic)	4.28	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	91.9 m³·mol⁻¹	ChemAxon
Polarizability	39.71 Å³	ChemAxon
Number of Rings	2	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

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

74817087

PDB ID

Not Available

ChEBI ID

181771

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid (NP0270130)

MOL for NP0270130 ([2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid)

3D MOL for NP0270130 ([2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid)

3D SDF for NP0270130 ([2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid)

3D-SDF for NP0270130 ([2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid)

PDB for NP0270130 ([2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid)

3D PDB for NP0270130 ([2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid)

SMILES for NP0270130 ([2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid)

INCHI for NP0270130 ([2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid)

Structure for NP0270130 ([2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid)

3D Structure for NP0270130 ([2-(pent-2-en-1-yl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclopentyl]acetic acid)