NP-MRD: Showing NP-Card for (-)-Premnaodoroside A (NP0077006)

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Record Information

Version

2.0

Created at

2022-04-28 22:10:58 UTC

Updated at

2022-04-28 22:10:58 UTC

NP-MRD ID

NP0077006

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Premnaodoroside A

Description

(2R,7R)-8-[(1S,4aS,7S,7aS)-7-hydroxy-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]-2,7-dimethyloctyl (1S,4aS,7S,7aS)-7-hydroxy-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. (-)-Premnaodoroside A is found in Premna odorata and Premna subscandens. Based on a literature review very few articles have been published on (2R,7R)-8-[(1S,4aS,7S,7aS)-7-hydroxy-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]-2,7-dimethyloctyl (1S,4aS,7S,7aS)-7-hydroxy-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


  Mrv1652304292200102D          

 62 67  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
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0000   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0000   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8158   -7.9770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1514   -8.7307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9719   -8.6445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1970   -7.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0286   -8.2237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -7.8375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -8.6625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.8605   -9.0750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.1460   -8.6625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5329   -9.2145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8685   -9.9682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6890   -9.8820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8689  -10.6871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4709  -10.1451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -8.6625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0039   -7.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.7184   -7.4250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.4328   -7.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.4328   -8.6625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.7184   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -8.6625    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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  6  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
  4 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  3 21  1  1  0  0  0
 19 22  1  1  0  0  0
 19 23  1  6  0  0  0
  2 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  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
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  6  0  0  0
 39 44  1  0  0  0  0
 44 45  1  6  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 43 47  1  0  0  0  0
 47 48  1  6  0  0  0
 47 49  1  1  0  0  0
 42 50  1  1  0  0  0
 51 50  1  1  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 51 56  1  0  0  0  0
 55 57  1  1  0  0  0
 57 58  1  0  0  0  0
 54 59  1  6  0  0  0
 53 60  1  1  0  0  0
 52 61  1  6  0  0  0
 34 62  1  6  0  0  0
M  END

     RDKit          3D

128133  0  0  0  0  0  0  0  0999 V2000
    3.3113   -2.9187   -0.4856 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7274   -3.2415    0.9318 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2605   -3.0718    0.7265 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3465   -3.3270    1.8669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0896   -3.0313    1.3753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2701   -1.5850    1.0854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5734   -1.2099    0.4611 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6898   -1.9289   -0.8943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7369   -1.5908    1.3344 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9556   -1.1864    0.6696 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2381    0.1541    0.4851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3879    0.9517    0.9829 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3737    0.7156   -0.2094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3311    0.0368   -0.8020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3434    0.8055   -1.4260 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9390    1.9016   -0.7741 C   0  0  1  0  0  0  0  0  0  0  0  0
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    7.1273   -1.7347    1.8378 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9854   -0.7947    2.3341 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.1722   -3.6158   -1.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
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 62128  1  0
M  END


  Mrv1652304292200102D          

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 34 62  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0077006

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CCCC[C@@H](C)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]1CC[C@]2(C)O)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]1CC[C@]2(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C42H66O20/c1-19(15-55-35(51)23-17-57-37(27-21(23)9-11-41(27,3)53)61-39-33(49)31(47)29(45)25(13-43)59-39)7-5-6-8-20(2)16-56-36(52)24-18-58-38(28-22(24)10-12-42(28,4)54)62-40-34(50)32(48)30(46)26(14-44)60-40/h17-22,25-34,37-40,43-50,53-54H,5-16H2,1-4H3/t19-,20-,21-,22-,25-,26-,27-,28-,29-,30-,31+,32+,33-,34-,37+,38+,39+,40+,41+,42+/m1/s1

> <INCHI_KEY>
FLSSLHNUZDULJM-QHIBPMJRSA-N

> <FORMULA>
C42H66O20

> <MOLECULAR_WEIGHT>
890.97

> <EXACT_MASS>
890.414744525

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
128

> <JCHEM_AVERAGE_POLARIZABILITY>
92.59550212413106

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,7R)-8-[(1S,4aS,7S,7aS)-7-hydroxy-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]-2,7-dimethyloctyl (1S,4aS,7S,7aS)-7-hydroxy-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>
0.46

> <JCHEM_LOGP>
-0.40690716333333443

> <ALOGPS_LOGS>
-3.03

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.427483172726966

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.905999756797666

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847601927755

> <JCHEM_POLAR_SURFACE_AREA>
310.28

> <JCHEM_REFRACTIVITY>
209.44860000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.35e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,7R)-8-[(1S,4aS,7S,7aS)-7-hydroxy-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7aH-cyclopenta[c]pyran-4-carbonyloxy]-2,7-dimethyloctyl (1S,4aS,7S,7aS)-7-hydroxy-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7aH-cyclopenta[c]pyran-4-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       5.335 -12.320   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001 -14.630   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.001 -11.550   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       1.334 -11.550   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.523 -14.890   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.149 -16.297   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.681 -16.136   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.368 -13.872   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.053 -15.351   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.668 -16.170   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       8.002 -13.860   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.336 -14.630   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      12.003 -14.630   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      13.337 -13.860   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      14.670 -14.630   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      16.004 -13.860   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      17.338 -14.630   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      20.005 -14.630   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      21.339 -12.320   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      22.673 -14.630   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      24.006 -13.860   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      25.340 -14.630   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      25.340 -16.170   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      24.006 -16.940   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      22.673 -16.170   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      21.528 -17.200   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      22.154 -18.607   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      23.686 -18.446   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      24.022 -19.949   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      25.146 -18.938   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      26.674 -16.940   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      28.007 -16.170   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      28.007 -14.630   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      29.341 -13.860   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      30.675 -14.630   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      30.675 -16.170   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      29.341 -16.940   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0      32.008 -16.940   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0      33.342 -16.170   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0      32.008 -13.860   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0      29.341 -12.320   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      26.674 -13.860   0.000  0.00  0.00           O+0
HETATM   62  C   UNK     0      17.338 -16.170   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   24                                                  
CONECT    3    2    4   21                                                  
CONECT    4    3    5   19                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    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    4   20   22   23                                             
CONECT   20   19   21                                                       
CONECT   21   20    3                                                       
CONECT   22   19                                                            
CONECT   23   19                                                            
CONECT   24    2   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   62                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   44                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43   50                                                  
CONECT   43   42   44   47                                                  
CONECT   44   43   39   45                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   43   48   49                                             
CONECT   48   47                                                            
CONECT   49   47                                                            
CONECT   50   42   51                                                       
CONECT   51   50   52   56                                                  
CONECT   52   51   53   61                                                  
CONECT   53   52   54   60                                                  
CONECT   54   53   55   59                                                  
CONECT   55   54   56   57                                                  
CONECT   56   55   51                                                       
CONECT   57   55   58                                                       
CONECT   58   57                                                            
CONECT   59   54                                                            
CONECT   60   53                                                            
CONECT   61   52                                                            
CONECT   62   34                                                            
MASTER        0    0    0    0    0    0    0    0   62    0  134    0
END

View in JSmol

Synonyms

Value	Source
(2R,7R)-8-[(1S,4AS,7S,7as)-7-hydroxy-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]-2,7-dimethyloctyl (1S,4as,7S,7as)-7-hydroxy-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

C₄₂H₆₆O₂₀

Average Mass

890.9700 Da

Monoisotopic Mass

890.41474 Da

IUPAC Name

Traditional Name

(2R,7R)-8-[(1S,4aS,7S,7aS)-7-hydroxy-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7aH-cyclopenta[c]pyran-4-carbonyloxy]-2,7-dimethyloctyl (1S,4aS,7S,7aS)-7-hydroxy-7-methyl-1-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1H,4aH,5H,6H,7aH-cyclopenta[c]pyran-4-carboxylate

CAS Registry Number

Not Available

SMILES

C[C@H](CCCC[C@@H](C)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]1CC[C@]2(C)O)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]1CC[C@]2(C)O

InChI Identifier

InChI=1S/C42H66O20/c1-19(15-55-35(51)23-17-57-37(27-21(23)9-11-41(27,3)53)61-39-33(49)31(47)29(45)25(13-43)59-39)7-5-6-8-20(2)16-56-36(52)24-18-58-38(28-22(24)10-12-42(28,4)54)62-40-34(50)32(48)30(46)26(14-44)60-40/h17-22,25-34,37-40,43-50,53-54H,5-16H2,1-4H3/t19-,20-,21-,22-,25-,26-,27-,28-,29-,30-,31+,32+,33-,34-,37+,38+,39+,40+,41+,42+/m1/s1

InChI Key

FLSSLHNUZDULJM-QHIBPMJRSA-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
Premna odorata	LOTUS Database	35616633
Premna subscandens	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
Fatty alcohol ester
O-glycosyl compound
Iridoid-skeleton
Glycosyl compound
Monoterpenoid
Oxane
Monosaccharide
Dicarboxylic acid or derivatives
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Cyclic alcohol
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	0.46	ALOGPS
logP	-0.41	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	11.91	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	310.28 Å²	ChemAxon
Rotatable Bond Count	19	ChemAxon
Refractivity	209.45 m³·mol⁻¹	ChemAxon
Polarizability	92.6 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

163104001

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Premnaodoroside A (NP0077006)

MOL for NP0077006 ((-)-Premnaodoroside A)

3D MOL for NP0077006 ((-)-Premnaodoroside A)

3D SDF for NP0077006 ((-)-Premnaodoroside A)

3D-SDF for NP0077006 ((-)-Premnaodoroside A)

PDB for NP0077006 ((-)-Premnaodoroside A)

3D PDB for NP0077006 ((-)-Premnaodoroside A)

SMILES for NP0077006 ((-)-Premnaodoroside A)

INCHI for NP0077006 ((-)-Premnaodoroside A)

Structure for NP0077006 ((-)-Premnaodoroside A)

3D Structure for NP0077006 ((-)-Premnaodoroside A)