NP-MRD: Showing NP-Card for (2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol (NP0253499)

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Record Information

Version

2.0

Created at

2022-09-07 17:23:02 UTC

Updated at

2022-09-07 17:23:03 UTC

NP-MRD ID

NP0253499

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Description

Lobetyolin, also known as isolobetyol, 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. (2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol is found in Campanula glomerata, Campanula medium, Hippobroma longiflora, Lobelia cardinalis, Lobelia chinensis, Lobelia inflata, Lobelia sessilifolia, Platycodon grandiflorus, Pratia nummularia and Wahlenbergia marginata. (2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol was first documented in 2022 (PMID: 35378415). Based on a literature review a small amount of articles have been published on Lobetyolin (PMID: 35785916) (PMID: 35718519) (PMID: 35598432) (PMID: 35432308).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072219232D          

 28 28  0  0  1  0            999 V2000
   -2.8579    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    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
   -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
    0.0000    4.1250    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  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
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    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  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    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
    0.0000    0.0000    0.0000 C   0  0  1  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
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  3  0  0  0  0
  5  6  1  0  0  0  0
  6  7  3  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 17  1  0  0  0  0
 18 17  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  1  0  0  0
M  END

     RDKit          3D

 56 56  0  0  0  0  0  0  0  0999 V2000
    7.5406   -2.1449    0.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1296   -1.0038    1.1769 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4018   -0.1256    1.8300 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9785   -0.2361    1.8449 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7688   -0.3107    1.8670 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3534   -0.3832    1.9134 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1452   -0.4261    1.9438 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6602   -0.4533    1.9878 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1819    0.4517    2.9255 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1858   -0.0896    0.6200 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8253    1.1784    0.1909 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3446    2.3925    0.2968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9425    2.7733    0.8680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8426    3.4389   -0.1245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2884    4.6897   -0.6722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1134    4.5225   -1.3800 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1364   -0.0483    0.3872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6438   -0.9094   -0.5557 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3080   -0.2180   -1.5066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2521   -0.8246   -2.2425 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5542   -0.0205   -2.0714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5910   -0.5690   -2.7945 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5116   -2.2604   -2.0541 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0527   -3.0231   -3.1549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9821   -2.8929   -0.8241 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7861   -3.5705   -1.1395 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6210   -1.8214    0.1651 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0182   -2.3718    1.2939 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6187   -2.4547    0.9471 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2612   -2.9581    0.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2311   -1.7549   -0.5706 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2131   -0.9313    1.1574 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8764    0.6742    2.3520 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4076   -1.5059    2.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9556    0.7462    3.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6307   -0.8880   -0.0650 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8427    1.1110   -0.2804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9939    3.2077   -0.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7912    3.5079    1.7328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4602    1.9197    1.3646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8517    3.6576    0.3293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    2.7497   -0.9905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0430    5.1014   -1.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1420    5.4858    0.1241 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3756    5.3870   -1.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8903   -1.5588   -1.0309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9939   -0.6666   -3.3346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8083    0.0842   -0.9912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3456    0.9957   -2.4794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2468   -1.1593   -3.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6294   -2.4348   -2.0589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2085   -3.9801   -3.0158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6663   -3.6533   -0.3718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4598   -3.3123   -2.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5147   -1.2761    0.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1899   -1.8373    2.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  3  0
  5  6  1  0
  6  7  3  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 27 18  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  3 33  1  0
  8 34  1  1
  9 35  1  0
 10 36  1  6
 18 46  1  6
 20 47  1  6
 21 48  1  0
 21 49  1  0
 22 50  1  0
 23 51  1  1
 24 52  1  0
 25 53  1  1
 26 54  1  0
 27 55  1  1
 28 56  1  0
 11 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
M  END


  Mrv1652309072219232D          

 28 28  0  0  1  0            999 V2000
   -2.8579    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    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
   -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
    0.0000    4.1250    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  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
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    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  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    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
    0.0000    0.0000    0.0000 C   0  0  1  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
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  3  0  0  0  0
  5  6  1  0  0  0  0
  6  7  3  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 17  1  0  0  0  0
 18 17  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0253499

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=CC#CC#CC(O)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@@H](O)[C@H]1O)C=CCCCO

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O8/c1-2-3-4-5-7-10-14(23)15(11-8-6-9-12-21)27-20-19(26)18(25)17(24)16(13-22)28-20/h2-3,8,11,14-26H,6,9,12-13H2,1H3/t14?,15?,16-,17-,18-,19-,20-/m1/s1

> <INCHI_KEY>
MMMUDYVKKPDZHS-XZOXWEMDSA-N

> <FORMULA>
C20H28O8

> <MOLECULAR_WEIGHT>
396.436

> <EXACT_MASS>
396.178417862

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.456535423930134

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3R,4R,5S,6R)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
-0.22406424766666738

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.526965964114549

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.971078036970571

> <JCHEM_PKA_STRONGEST_BASIC>
-1.939407773355895

> <JCHEM_POLAR_SURFACE_AREA>
139.84

> <JCHEM_REFRACTIVITY>
104.23720000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4R,5S,6R)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.335  12.320   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001  11.550   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001  10.010   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   7.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.001   6.930   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.334  -0.770   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
HETATM   25  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   28  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                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   10   18                                                       
CONECT   18   17   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   18   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   56    0
END

View in JSmol

Synonyms

Value	Source
Isolobetyol	MeSH

Chemical Formula

C₂₀H₂₈O₈

Average Mass

396.4360 Da

Monoisotopic Mass

396.17842 Da

IUPAC Name

(2R,3R,4R,5S,6R)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2R,3R,4R,5S,6R)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CC=CC#CC#CC(O)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@@H](O)[C@H]1O)C=CCCCO

InChI Identifier

InChI=1S/C20H28O8/c1-2-3-4-5-7-10-14(23)15(11-8-6-9-12-21)27-20-19(26)18(25)17(24)16(13-22)28-20/h2-3,8,11,14-26H,6,9,12-13H2,1H3/t14?,15?,16-,17-,18-,19-,20-/m1/s1

InChI Key

MMMUDYVKKPDZHS-XZOXWEMDSA-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
Campanula glomerata	LOTUS Database	35616633
Campanula medium	LOTUS Database	35616633
Hippobroma longiflora	LOTUS Database	35616633
Lobelia cardinalis	LOTUS Database	35616633
Lobelia chinensis	LOTUS Database	35616633
Lobelia inflata	LOTUS Database	35616633
Lobelia sessilifolia	LOTUS Database	35616633
Platycodon grandiflorus	LOTUS Database	35616633
Pratia nummularia	LOTUS Database	35616633
Wahlenbergia marginata	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
Long chain fatty alcohol
Hexose monosaccharide
Alkyl glycoside
O-glycosyl compound
Glycosyl compound
Fatty alcohol
Oxane
Monosaccharide
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
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	-0.22	ChemAxon
pKa (Strongest Acidic)	11.97	ChemAxon
pKa (Strongest Basic)	-1.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	139.84 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	104.24 m³·mol⁻¹	ChemAxon
Polarizability	42.46 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

C00030684

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

126968964

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chen Z, Zhou L, Ge Y, Chen J, Du W, Xiao L, Tong P, Huang J, Shan L, Efferth T: Fuzi decoction ameliorates pain and cartilage degeneration of osteoarthritic rats through PI3K-Akt signaling pathway and its clinical retrospective evidence. Phytomedicine. 2022 Jun;100:154071. doi: 10.1016/j.phymed.2022.154071. Epub 2022 Mar 20. [PubMed:35378415 ]
Liu L, Liu Z, Yang L, Wu X, Zhu J, Liu L, Liu Y: Lobetyolin suppressed lung cancer in a mouse model by inhibiting epithelial-mesenchymal transition. Eur J Histochem. 2022 Jul 4;66(3):3423. doi: 10.4081/ejh.2022.3423. [PubMed:35785916 ]
Tang YN, Han XT, Liu ZQ, Bao LY, Wang HY, Liu KY, Han S, Li WF, Hu FD, DU H: [Influence of processing factors on honey-fried Codonopsis Radix]. Zhongguo Zhong Yao Za Zhi. 2022 Jun;47(11):2975-2981. doi: 10.19540/j.cnki.cjcmm.20211119.302. [PubMed:35718519 ]
Zhu N, Meng T, Li S, Yu C, Tang D, Wang Y, Leng F, Ma J: Improved growth and metabolite accumulation in Codonopsis pilosula (Franch.) Nannf. by inoculation with the endophytic Geobacillu sp. RHBA19 and Pseudomonas fluorescens RHBA17. J Plant Physiol. 2022 Jul;274:153718. doi: 10.1016/j.jplph.2022.153718. Epub 2022 May 13. [PubMed:35598432 ]
Liu C, Zhou M, Jiang W, Ye S, Tian S, Jiang C, Hao K, Li H, Hu Q: GPR105-Targeted Therapy Promotes Gout Resolution as a Switch Between NETosis and Apoptosis of Neutrophils. Front Immunol. 2022 Mar 30;13:870183. doi: 10.3389/fimmu.2022.870183. eCollection 2022. [PubMed:35432308 ]
LOTUS database [Link]

Showing NP-Card for (2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol (NP0253499)

MOL for NP0253499 ((2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0253499 ((2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0253499 ((2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0253499 ((2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0253499 ((2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0253499 ((2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0253499 ((2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0253499 ((2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0253499 ((2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0253499 ((2r,3r,4r,5s,6r)-2-[(1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)