NP-MRD: Showing NP-Card for Picconioside I (NP0071629)

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Record Information

Version

2.0

Created at

2022-04-28 16:58:50 UTC

Updated at

2022-04-28 16:58:51 UTC

NP-MRD ID

NP0071629

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Picconioside I

Description

Methyl (1S,4aS,6S,7R,7aR)-6-[(1S,4aS,7S,7aR)-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbonyloxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton. Picconioside I is found in Strychnos lucida. Based on a literature review very few articles have been published on methyl (1S,4aS,6S,7R,7aR)-6-[(1S,4aS,7S,7aR)-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbonyloxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282218582D          

 51 56  0  0  1  0            999 V2000
   -3.9284    0.7310    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1034    0.7310    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6909    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1034   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9284   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3409    0.0165    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1659    0.0165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5784   -0.6979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1659   -1.4124    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.5784   -2.1269    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4034   -2.1269    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8159   -1.4124    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4034   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6409   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0534   -2.1269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8159   -2.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1659   -2.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3409   -1.4124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8659    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4534    0.7310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4534   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -2.7604    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7845   -2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4990   -2.7604    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4990   -3.5854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    2.7845   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -5.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7845   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8485    1.5156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5159    2.0005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1834    1.5156    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9680    1.7706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 12 14  1  1  0  0  0
 14 15  1  0  0  0  0
 11 16  1  6  0  0  0
 10 17  1  1  0  0  0
  9 18  1  6  0  0  0
  3 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 24 23  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  1  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
 26 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 25 46  1  6  0  0  0
 22 46  1  0  0  0  0
 23 47  1  1  0  0  0
  2 48  1  6  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
  1 50  1  0  0  0  0
 50 51  1  1  0  0  0
M  END

     RDKit          3D

 99104  0  0  0  0  0  0  0  0999 V2000
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   -7.9487    4.3007    0.0648 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1679   -2.6524    0.8563 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2013   -3.1279   -0.2242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8998   -1.8636   -0.9826 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5911   -1.4284   -0.8917 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
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  8 21  1  0
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M  END


  Mrv1652304282218582D          

 51 56  0  0  1  0            999 V2000
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    2.0701   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -2.7604    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7845   -2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4990   -2.7604    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4990   -3.5854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7845   -3.9979    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0701   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -5.2354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -3.9979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8485    1.5156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5159    2.0005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1834    1.5156    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9680    1.7706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 12 14  1  1  0  0  0
 14 15  1  0  0  0  0
 11 16  1  6  0  0  0
 10 17  1  1  0  0  0
  9 18  1  6  0  0  0
  3 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
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 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  1  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
 26 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 25 46  1  6  0  0  0
 22 46  1  0  0  0  0
 23 47  1  1  0  0  0
  2 48  1  6  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
  1 50  1  0  0  0  0
 50 51  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0071629

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]2[C@@H](C)[C@H](C[C@H]12)OC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]2[C@@H](C)CC[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C33H48O18/c1-11-4-5-13-15(9-45-30(20(11)13)50-32-26(40)24(38)22(36)18(7-34)48-32)29(43)47-17-6-14-16(28(42)44-3)10-46-31(21(14)12(17)2)51-33-27(41)25(39)23(37)19(8-35)49-33/h9-14,17-27,30-41H,4-8H2,1-3H3/t11-,12-,13+,14+,17-,18+,19+,20+,21-,22+,23+,24-,25-,26+,27+,30-,31-,32-,33-/m0/s1

> <INCHI_KEY>
XRBMYCJLBGGMOM-DBFWXXPNSA-N

> <FORMULA>
C33H48O18

> <MOLECULAR_WEIGHT>
732.729

> <EXACT_MASS>
732.284064706

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
74.34450816735804

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1S,4aS,6S,7R,7aR)-6-[(1S,4aS,7S,7aR)-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbonyloxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate

> <ALOGPS_LOGP>
-1.14

> <JCHEM_LOGP>
-1.8469490630000007

> <ALOGPS_LOGS>
-2.36

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.427484931953746

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.906001720855174

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847601512

> <JCHEM_POLAR_SURFACE_AREA>
269.81999999999994

> <JCHEM_REFRACTIVITY>
165.095

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.23e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,4aS,6S,7R,7aR)-6-[(1S,4aS,7S,7aR)-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbonyloxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate

> <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      -7.333   1.365   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.793   1.365   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.023   0.031   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.793  -1.303   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -7.333  -1.303   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -8.103   0.031   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -9.643   0.031   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0     -10.413  -1.303   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -9.643  -2.637   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -10.413  -3.970   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -11.953  -3.970   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -12.723  -2.637   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0     -11.953  -1.303   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0     -14.263  -2.637   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0     -15.033  -3.970   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0     -12.723  -5.304   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -9.643  -5.304   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -8.103  -2.637   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -3.483   0.031   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -2.713   1.365   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -2.713  -1.303   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.268  -2.549   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.530   0.237   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.864  -0.533   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.864  -2.073   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.530  -4.383   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       3.864  -5.153   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.198  -4.383   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.531  -5.153   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.531  -6.693   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.198  -7.463   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.864  -6.693   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       5.198  -9.003   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       6.531  -9.773   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       7.865  -7.463   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       7.865  -4.383   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       5.198  -2.843   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       2.530   1.777   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       3.864   2.547   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0       1.197   2.547   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       1.197   4.087   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -0.268  -0.057   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -0.744  -4.013   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -5.317   2.829   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -6.563   3.734   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -7.809   2.829   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -9.274   3.305   0.000  0.00  0.00           C+0
CONECT    1    2    6   50                                                  
CONECT    2    1    3   48                                                  
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10   18                                                  
CONECT   10    9   11   17                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12    8                                                       
CONECT   14   12   15                                                       
CONECT   15   14                                                            
CONECT   16   11                                                            
CONECT   17   10                                                            
CONECT   18    9                                                            
CONECT   19    3   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   46                                                  
CONECT   23   22   24   47                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26   46                                                  
CONECT   26   25   27   42                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   24   30                                                  
CONECT   30   29   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   26   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44                                                            
CONECT   46   25   22                                                       
CONECT   47   23                                                            
CONECT   48    2   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49    1   51                                                  
CONECT   51   50                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  112    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1S,4as,6S,7R,7ar)-6-[(1S,4as,7S,7ar)-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4ah,5H,6H,7H,7ah-cyclopenta[c]pyran-4-carbonyloxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4ah,5H,6H,7H,7ah-cyclopenta[c]pyran-4-carboxylic acid	Generator

Chemical Formula

C₃₃H₄₈O₁₈

Average Mass

732.7290 Da

Monoisotopic Mass

732.28406 Da

IUPAC Name

methyl (1S,4aS,6S,7R,7aR)-6-[(1S,4aS,7S,7aR)-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbonyloxy]-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H]2[C@@H](C)[C@H](C[C@H]12)OC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]2[C@@H](C)CC[C@H]12

InChI Identifier

InChI=1S/C33H48O18/c1-11-4-5-13-15(9-45-30(20(11)13)50-32-26(40)24(38)22(36)18(7-34)48-32)29(43)47-17-6-14-16(28(42)44-3)10-46-31(21(14)12(17)2)51-33-27(41)25(39)23(37)19(8-35)49-33/h9-14,17-27,30-41H,4-8H2,1-3H3/t11-,12-,13+,14+,17-,18+,19+,20+,21-,22+,23+,24-,25-,26+,27+,30-,31-,32-,33-/m0/s1

InChI Key

XRBMYCJLBGGMOM-DBFWXXPNSA-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
Strychnos lucida	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Iridoid O-glycosides

Alternative Parents

Substituents

Iridoid o-glycoside
O-glycosyl compound
Iridoid-skeleton
Glycosyl compound
Monoterpenoid
Oxane
Monosaccharide
Dicarboxylic acid or derivatives
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	-1.8	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	11.91	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	269.82 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	165.1 m³·mol⁻¹	ChemAxon
Polarizability	74.34 Å³	ChemAxon
Number of Rings	6	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

163013906

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Picconioside I (NP0071629)

MOL for NP0071629 (Picconioside I)

3D MOL for NP0071629 (Picconioside I)

3D SDF for NP0071629 (Picconioside I)

3D-SDF for NP0071629 (Picconioside I)

PDB for NP0071629 (Picconioside I)

3D PDB for NP0071629 (Picconioside I)

SMILES for NP0071629 (Picconioside I)

INCHI for NP0071629 (Picconioside I)

Structure for NP0071629 (Picconioside I)

3D Structure for NP0071629 (Picconioside I)