NP-MRD: Showing NP-Card for (-)-Caryoptosidic acid (NP0077549)

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Record Information

Version

2.0

Created at

2022-04-28 22:40:53 UTC

Updated at

2022-04-28 22:40:53 UTC

NP-MRD ID

NP0077549

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Caryoptosidic acid

Description

(1S)-1alpha-(beta-D-Glucopyranosyloxy)-6alpha,7-dihydroxy-7beta-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylic acid 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. (-)-Caryoptosidic acid is found in Lippia graveolens . Based on a literature review very few articles have been published on (1S)-1alpha-(beta-D-Glucopyranosyloxy)-6alpha,7-dihydroxy-7beta-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292200402D          

 27 29  0  0  1  0            999 V2000
    3.3523    1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.5854    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3523    4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    4.8229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7812    4.4104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7812    3.5854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    3.1729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    4.8229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    5.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    6.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3018    2.9991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5314    2.7488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  8  7  1  6  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
 13 14  1  1  0  0  0
 12 15  1  6  0  0  0
 11 16  1  1  0  0  0
 10 17  1  6  0  0  0
 17 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  4 21  1  1  0  0  0
 20 22  1  6  0  0  0
 19 23  1  1  0  0  0
 19 24  1  6  0  0  0
  3 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
   -1.3664   -1.4800    1.8662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4020   -0.5567    1.3284 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0937    0.0317    2.3682 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3610   -1.1794    0.3748 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3604   -1.9017    1.0269 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9417    0.0076   -0.3595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0790    1.1946   -0.0424 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8159    2.0381   -1.2366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4518    3.3421   -1.3960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2372    3.7689   -0.5143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2207    4.1432   -2.4998 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9817    1.5416   -2.1337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4499    0.2975   -1.8600 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8925    0.0668   -0.5816 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3605    0.6518   -0.5791 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4009   -0.2563   -0.4431 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1039    0.1079    0.6682 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2218   -0.5875    0.9639 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0961    0.3266    1.8377 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3787    1.4805    1.0710 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0627   -1.0458   -0.1621 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7630   -2.2038    0.2490 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3497   -1.3063   -1.4410 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2485   -1.3502   -2.4973 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3547   -0.1591   -1.6384 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7216   -0.3753   -2.8329 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8043    0.5709    0.4884 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4922   -0.8718    2.1994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8014   -1.9721    2.7821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0335   -2.2544    1.1564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7231   -0.6350    2.7348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8963   -1.8620   -0.3525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1216   -2.1035    0.4585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9804    0.1514    0.0044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9823   -0.2154   -1.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5326    1.7842    0.7771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8450    5.0862   -2.3518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7602    2.1320   -3.0310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8448   -1.0400   -0.4731 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0571   -1.2896   -0.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9921   -1.4672    1.6334 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0065   -0.1732    2.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5311    0.6526    2.7406 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2365    1.8925    1.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8741   -0.2944   -0.3749 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6164   -2.3774    1.2247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8178   -2.2777   -1.3634 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4785   -2.3112   -2.6624 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9416    0.7670   -1.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1625    0.2074   -3.5206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3044    1.3044    1.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  1
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7 27  1  0
 27 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 14 13  1  0
 13 12  1  0
 12  8  2  0
  8  9  1  0
  9 11  1  0
  9 10  2  0
 27  2  1  0
 25 16  1  0
  8  7  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  4 32  1  6
  5 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  1
 27 51  1  1
 14 39  1  1
 16 40  1  1
 18 41  1  1
 19 42  1  0
 19 43  1  0
 20 44  1  0
 21 45  1  6
 22 46  1  0
 23 47  1  1
 24 48  1  0
 25 49  1  6
 26 50  1  0
 12 38  1  0
 11 37  1  0
M  END


  Mrv1652304292200402D          

 27 29  0  0  1  0            999 V2000
    3.3523    1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.5854    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3523    4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    4.8229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7812    4.4104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7812    3.5854    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    3.1729    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    4.8229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    5.6479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    6.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3018    2.9991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5314    2.7488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.5396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  8  7  1  6  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
 13 14  1  1  0  0  0
 12 15  1  6  0  0  0
 11 16  1  1  0  0  0
 10 17  1  6  0  0  0
 17 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  4 21  1  1  0  0  0
 20 22  1  6  0  0  0
 19 23  1  1  0  0  0
 19 24  1  6  0  0  0
  3 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0077549

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]1(O)[C@@H](O)C[C@H]2[C@@H]1[C@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)OC=C2C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H24O11/c1-16(24)8(18)2-5-6(13(22)23)4-25-14(9(5)16)27-15-12(21)11(20)10(19)7(3-17)26-15/h4-5,7-12,14-15,17-21,24H,2-3H2,1H3,(H,22,23)/t5-,7-,8+,9-,10-,11+,12-,14+,15+,16+/m1/s1

> <INCHI_KEY>
WAXHVHOTAZULHY-UKJXUXBJSA-N

> <FORMULA>
C16H24O11

> <MOLECULAR_WEIGHT>
392.357

> <EXACT_MASS>
392.131861593

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
37.04843580117507

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4aS,6S,7R,7aS)-6,7-dihydroxy-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

> <ALOGPS_LOGP>
-1.96

> <JCHEM_LOGP>
-3.1145934676666664

> <ALOGPS_LOGS>
-0.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.185016477986288

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.187511158476738

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847601928367

> <JCHEM_POLAR_SURFACE_AREA>
186.36999999999998

> <JCHEM_REFRACTIVITY>
83.87259999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.82e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4aS,6S,7R,7aS)-6,7-dihydroxy-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-carboxylic acid

> <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  O   UNK     0       6.258   3.613   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.924   5.923   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.258   6.693   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.258   8.233   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.591   9.003   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.925   8.233   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.925   6.693   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.591   5.923   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.591   4.383   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      10.259   5.923   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      10.259   9.003   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.591  10.543   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.925  11.313   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.126   4.089   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.126   1.597   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.320   2.843   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.430   5.598   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.992   5.131   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.924  -0.237   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.590  -1.007   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       6.258  -1.007   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5   21                                                  
CONECT    5    4    6   19                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13   15                                                  
CONECT   13   12    8   14                                                  
CONECT   14   13                                                            
CONECT   15   12                                                            
CONECT   16   11                                                            
CONECT   17   10   18                                                       
CONECT   18   17                                                            
CONECT   19    5   20   23   24                                             
CONECT   20   19   21   22                                                  
CONECT   21   20    4                                                       
CONECT   22   20                                                            
CONECT   23   19                                                            
CONECT   24   19                                                            
CONECT   25    3   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Value	Source
(1S)-1a-(b-D-Glucopyranosyloxy)-6a,7-dihydroxy-7b-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylate	Generator
(1S)-1a-(b-D-Glucopyranosyloxy)-6a,7-dihydroxy-7b-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylic acid	Generator
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-6alpha,7-dihydroxy-7beta-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylate	Generator
(1S)-1Α-(β-D-glucopyranosyloxy)-6α,7-dihydroxy-7β-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylate	Generator
(1S)-1Α-(β-D-glucopyranosyloxy)-6α,7-dihydroxy-7β-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylic acid	Generator

Chemical Formula

C₁₆H₂₄O₁₁

Average Mass

392.3570 Da

Monoisotopic Mass

392.13186 Da

IUPAC Name

(1S,4aS,6S,7R,7aS)-6,7-dihydroxy-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

Traditional Name

(1S,4aS,6S,7R,7aS)-6,7-dihydroxy-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-carboxylic acid

CAS Registry Number

Not Available

SMILES

C[C@]1(O)[C@@H](O)C[C@H]2[C@@H]1[C@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)OC=C2C(O)=O

InChI Identifier

InChI=1S/C16H24O11/c1-16(24)8(18)2-5-6(13(22)23)4-25-14(9(5)16)27-15-12(21)11(20)10(19)7(3-17)26-15/h4-5,7-12,14-15,17-21,24H,2-3H2,1H3,(H,22,23)/t5-,7-,8+,9-,10-,11+,12-,14+,15+,16+/m1/s1

InChI Key

WAXHVHOTAZULHY-UKJXUXBJSA-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
Lippia graveolens	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
Hexose monosaccharide
Glycosyl compound
Iridoid-skeleton
O-glycosyl compound
Bicyclic monoterpenoid
Monoterpenoid
Monosaccharide
Oxane
Cyclic alcohol
Vinylogous ester
Tertiary alcohol
Secondary alcohol
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Oxacycle
Acetal
Carboxylic acid
Carboxylic acid derivative
Polyol
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Primary 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	-2	ALOGPS
logP	-3.1	ChemAxon
logS	-0.6	ALOGPS
pKa (Strongest Acidic)	4.19	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	186.37 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	83.87 m³·mol⁻¹	ChemAxon
Polarizability	37.05 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

103882849

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

72709988

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (-)-Caryoptosidic acid (NP0077549)

MOL for NP0077549 ((-)-Caryoptosidic acid)

3D MOL for NP0077549 ((-)-Caryoptosidic acid)

3D SDF for NP0077549 ((-)-Caryoptosidic acid)

3D-SDF for NP0077549 ((-)-Caryoptosidic acid)

PDB for NP0077549 ((-)-Caryoptosidic acid)

3D PDB for NP0077549 ((-)-Caryoptosidic acid)

SMILES for NP0077549 ((-)-Caryoptosidic acid)

INCHI for NP0077549 ((-)-Caryoptosidic acid)

Structure for NP0077549 ((-)-Caryoptosidic acid)

3D Structure for NP0077549 ((-)-Caryoptosidic acid)