NP-MRD: Showing NP-Card for (+)-Pipeloside A (NP0073134)

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Record Information

Version

2.0

Created at

2022-04-28 18:23:48 UTC

Updated at

2022-04-28 18:23:48 UTC

NP-MRD ID

NP0073134

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Pipeloside A

Description

(4R)-4-[(3S)-3-{[(2R,3R,4S,5S,6R)-5-{[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3,5,5-trimethylcyclohex-2-en-1-one belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. (+)-Pipeloside A is found in Piper aduncum and Piper elongatum VAHL. . Based on a literature review very few articles have been published on (4R)-4-[(3S)-3-{[(2R,3R,4S,5S,6R)-5-{[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3,5,5-trimethylcyclohex-2-en-1-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282220232D          

 48 51  0  0  1  0            999 V2000
   10.7171   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.4315   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.8605    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.7184   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.7184    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.2894    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.1473   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.5762   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.5762    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.8618    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.8618    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   20.0052   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   19.2907   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.5762   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   20.7197   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6153    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3899    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 C   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
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 13 14  1  0  0  0  0
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 13 18  1  0  0  0  0
 17 19  1  6  0  0  0
 19 20  1  0  0  0  0
 16 21  1  1  0  0  0
 22 21  1  1  0  0  0
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 24 25  1  0  0  0  0
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 26 27  1  0  0  0  0
 22 27  1  0  0  0  0
 27 28  1  6  0  0  0
 26 29  1  1  0  0  0
 25 30  1  6  0  0  0
 31 30  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 31 36  1  0  0  0  0
 35 37  1  1  0  0  0
 37 38  1  0  0  0  0
 34 39  1  6  0  0  0
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 32 41  1  6  0  0  0
 24 42  1  1  0  0  0
 42 43  1  0  0  0  0
 15 44  1  1  0  0  0
 14 45  1  1  0  0  0
  6 46  1  0  0  0  0
  6 47  1  0  0  0  0
  1 48  1  0  0  0  0
M  END

     RDKit          3D

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  1 49  1  0
  1 50  1  0
  1 51  1  0
  3 52  1  0
  6 53  1  0
  6 54  1  0
  8 55  1  0
  8 56  1  0
  8 57  1  0
  9 58  1  0
  9 59  1  0
  9 60  1  0
 16 70  1  1
 18 71  1  6
 19 72  1  0
 19 73  1  0
 20 74  1  0
 21 75  1  1
 23 76  1  6
 25 77  1  1
 26 78  1  0
 26 79  1  0
 27 80  1  0
 28 81  1  1
 30 82  1  6
 32 83  1  1
 33 84  1  0
 33 85  1  0
 34 86  1  0
 35 87  1  6
 36 88  1  0
 37 89  1  1
 38 90  1  0
 39 91  1  6
 40 92  1  0
 41 93  1  1
 42 94  1  0
 43 95  1  1
 44 96  1  0
 45 97  1  6
 46 98  1  0
 47 99  1  6
 48100  1  0
M  END


  Mrv1652304282220232D          

 48 51  0  0  1  0            999 V2000
   10.7171   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.4315   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.8605    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.7184   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.7184    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.2894    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.1473   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.5762   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.5762    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.8618    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.8618    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.0052   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.0052   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.2907   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.5762   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.5762   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6153    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3899    0.7284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 C   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 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
 13 18  1  0  0  0  0
 17 19  1  6  0  0  0
 19 20  1  0  0  0  0
 16 21  1  1  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 27  1  0  0  0  0
 27 28  1  6  0  0  0
 26 29  1  1  0  0  0
 25 30  1  6  0  0  0
 31 30  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 31 36  1  0  0  0  0
 35 37  1  1  0  0  0
 37 38  1  0  0  0  0
 34 39  1  6  0  0  0
 33 40  1  1  0  0  0
 32 41  1  6  0  0  0
 24 42  1  1  0  0  0
 42 43  1  0  0  0  0
 15 44  1  1  0  0  0
 14 45  1  1  0  0  0
  6 46  1  0  0  0  0
  6 47  1  0  0  0  0
  1 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0073134

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](CC[C@H]1C(C)=CC(=O)CC1(C)C)O[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C31H52O17/c1-12-7-14(35)8-31(3,4)15(12)6-5-13(2)43-28-24(41)21(38)26(17(10-33)45-28)48-30-25(42)22(39)27(18(11-34)46-30)47-29-23(40)20(37)19(36)16(9-32)44-29/h7,13,15-30,32-34,36-42H,5-6,8-11H2,1-4H3/t13-,15-,16+,17+,18+,19+,20-,21-,22+,23+,24+,25+,26+,27+,28+,29-,30-/m0/s1

> <INCHI_KEY>
FCWUARFDJBCDGC-VNLHNVGESA-N

> <FORMULA>
C31H52O17

> <MOLECULAR_WEIGHT>
696.74

> <EXACT_MASS>
696.320450214

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
70.41400639543092

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4R)-4-[(3S)-3-{[(2R,3R,4S,5S,6R)-5-{[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3,5,5-trimethylcyclohex-2-en-1-one

> <ALOGPS_LOGP>
-1.14

> <JCHEM_LOGP>
-2.8400088603333336

> <ALOGPS_LOGS>
-1.84

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.23014174819364

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.775575663156772

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9813780813790727

> <JCHEM_POLAR_SURFACE_AREA>
274.74999999999994

> <JCHEM_REFRACTIVITY>
159.98440000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.01e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R)-4-[(3S)-3-{[(2R,3R,4S,5S,6R)-5-{[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butyl]-3,5,5-trimethylcyclohex-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      20.005  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      18.672  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      17.338  -2.310   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      16.004  -3.080   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      17.338  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.672  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.005  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.339  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      22.673  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      24.006  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      24.006   1.540   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      25.340  -0.770   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      26.674  -0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      28.007  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      29.341  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      29.341   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      28.007   2.310   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      26.674   1.540   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      28.007   3.850   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      26.674   4.620   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      30.675   2.310   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      32.008   1.540   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      32.008  -0.000   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      33.342  -0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      34.676  -0.000   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      34.676   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      33.342   2.310   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      33.342   3.850   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      36.009   2.310   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      36.009  -0.770   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      36.009  -2.310   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      37.343  -3.080   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      37.343  -4.620   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      36.009  -5.390   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      34.676  -4.620   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      34.676  -3.080   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      33.342  -5.390   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      33.342  -6.930   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      36.009  -6.930   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      38.677  -5.390   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      38.677  -2.310   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      33.342  -2.310   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      32.008  -3.080   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      30.675  -0.770   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      28.007  -2.310   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      17.949   1.360   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      19.394   1.360   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      21.339  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2    7   48                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   46   47                                             
CONECT    7    6    1    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15   45                                                  
CONECT   15   14   16   44                                                  
CONECT   16   15   17   21                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   13                                                       
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   16   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   42                                                  
CONECT   25   24   26   30                                                  
CONECT   26   25   27   29                                                  
CONECT   27   26   22   28                                                  
CONECT   28   27                                                            
CONECT   29   26                                                            
CONECT   30   25   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33   41                                                  
CONECT   33   32   34   40                                                  
CONECT   34   33   35   39                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35   31                                                       
CONECT   37   35   38                                                       
CONECT   38   37                                                            
CONECT   39   34                                                            
CONECT   40   33                                                            
CONECT   41   32                                                            
CONECT   42   24   43                                                       
CONECT   43   42                                                            
CONECT   44   15                                                            
CONECT   45   14                                                            
CONECT   46    6                                                            
CONECT   47    6                                                            
CONECT   48    1                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₅₂O₁₇

Average Mass

696.7400 Da

Monoisotopic Mass

696.32045 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H](CC[C@H]1C(C)=CC(=O)CC1(C)C)O[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@@H](O)[C@H]1O

InChI Identifier

InChI=1S/C31H52O17/c1-12-7-14(35)8-31(3,4)15(12)6-5-13(2)43-28-24(41)21(38)26(17(10-33)45-28)48-30-25(42)22(39)27(18(11-34)46-30)47-29-23(40)20(37)19(36)16(9-32)44-29/h7,13,15-30,32-34,36-42H,5-6,8-11H2,1-4H3/t13-,15-,16+,17+,18+,19+,20-,21-,22+,23+,24+,25+,26+,27+,28+,29-,30-/m0/s1

InChI Key

FCWUARFDJBCDGC-VNLHNVGESA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Piper aduncum	LOTUS Database	35616633
Piper elongatum VAHL.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
Megastigmane sesquiterpenoid
Sesquiterpenoid
Fatty acyl glycoside
Alkyl glycoside
O-glycosyl compound
Glycosyl compound
Cyclohexenone
Fatty acyl
Oxane
Cyclic ketone
Secondary alcohol
Ketone
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Organic oxide
Hydrocarbon derivative
Primary alcohol
Carbonyl group
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	-1.1	ALOGPS
logP	-2.8	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	11.78	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	274.75 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	159.98 m³·mol⁻¹	ChemAxon
Polarizability	70.41 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

154497223

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Pipeloside A (NP0073134)

MOL for NP0073134 ((+)-Pipeloside A)

3D MOL for NP0073134 ((+)-Pipeloside A)

3D SDF for NP0073134 ((+)-Pipeloside A)

3D-SDF for NP0073134 ((+)-Pipeloside A)

PDB for NP0073134 ((+)-Pipeloside A)

3D PDB for NP0073134 ((+)-Pipeloside A)

SMILES for NP0073134 ((+)-Pipeloside A)

INCHI for NP0073134 ((+)-Pipeloside A)

Structure for NP0073134 ((+)-Pipeloside A)

3D Structure for NP0073134 ((+)-Pipeloside A)