NP-MRD: Showing NP-Card for 4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate (NP0266280)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 10:34:35 UTC

Updated at

2022-09-08 10:34:35 UTC

NP-MRD ID

NP0266280

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate

Description

(4-{[3-(Acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2H-spiro[naphthalene-1,3'-oxolane]-5-yl)methyl acetate belongs to the class of organic compounds known as diterpene glycosides. 4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate is found in Teucrium flavum. These are diterpenoids in which an isoprene unit is glycosylated (4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2H-spiro[naphthalene-1,3'-oxolane]-5-yl)methyl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251513022D          

 41 45  0  0  0  0            999 V2000
    2.2871    1.4612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0765    1.2215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6789    1.7852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4683    1.5454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0706    2.1092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8836    2.9127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0942    3.1525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9071    3.9560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1177    4.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9307    4.9993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5095    4.5197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3224    5.3232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2989    4.2799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9012    4.8437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4859    3.4764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2753    3.2367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8776    3.8004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6906    4.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6670    3.5606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6553    0.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4447    0.5021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0470    1.0659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8364    0.8261    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4388    1.3898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2517    2.1934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2281    1.1501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6317   -0.3014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0294   -0.8651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2400   -0.6253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0530    0.1782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2636    0.4179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3656   -0.4007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6185   -0.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0548   -0.1484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4534    0.5739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8897    1.1762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4626   -1.5609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0263   -2.1632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6277   -2.8855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8175   -2.7296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7155   -1.9109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  4 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 20 30  1  0  0  0  0
 30 31  1  0  0  0  0
  2 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
 31 35  1  0  0  0  0
 35 36  2  0  0  0  0
 33 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 37 41  1  0  0  0  0
M  END

     RDKit          3D

 79 83  0  0  0  0  0  0  0  0999 V2000
    0.3153    5.9624   -0.1157 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0505    4.4926   -0.0379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5260    3.7738    0.8522 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7470    3.9521   -0.9945 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1246    2.5740   -1.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1383    1.7970   -1.2226 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5331    0.8469   -0.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3454    0.5141    0.7774 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2879   -0.4415    0.4901 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5790   -0.2133    0.8143 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9845   -1.1109    1.8104 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2142   -0.8548    2.3352 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1510    0.2346    3.3981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2906   -0.2529    4.3816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3145   -0.5828    1.3701 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1056   -1.7334    1.1331 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9316    0.0618    0.0908 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1418    1.4433    0.1217 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5237   -0.2402   -0.3641 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4287   -1.3897   -1.1396 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0422   -1.3636   -2.4482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9275   -2.5696   -3.3114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7710   -0.2579   -2.9406 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5078   -0.1434    1.8951 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2866   -1.2740    1.3127 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4301   -2.2817    0.6268 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3521   -0.7065    0.4259 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1093   -1.8224   -0.2576 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2872   -2.0545    0.6420 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4098   -2.5742   -0.1550 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7423   -2.4409    0.1501 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4393   -3.0648   -0.8501 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5692   -3.5440   -1.7047 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3491   -3.2762   -1.3321 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6009   -0.7273    1.0506 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3918   -0.0497    1.2552 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3430    0.9299    2.0378 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8189    0.2061   -0.6463 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9025    1.2069   -0.9927 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4552    2.2814   -1.9255 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0453    2.0568   -2.4073 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2151    6.1831   -0.7318 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4731    6.4014    0.8750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5318    6.4688   -0.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6902    2.5223   -2.0629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7526    2.3113   -0.2624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7562    1.4193    1.2072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6744    0.7851    1.2848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5164   -1.7851    2.9045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1617    0.2580    3.8749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8562    1.1891    2.9667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6338   -0.8846    4.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0330    0.1246    1.8860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7926   -2.4150    1.7487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6028   -0.3400   -0.7178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0031    1.8535   -0.7583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2319    0.6095   -1.0119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4034   -3.3447   -2.6824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3163   -2.3777   -4.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9126   -3.0028   -3.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2568   -0.5623    2.6142 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0968    0.5792    2.4433 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8174   -1.8045    2.1509 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9056   -3.3123    0.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1552   -2.0199   -0.4120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4795   -2.4438    1.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4559   -1.5124   -1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5384   -2.7479   -0.3931 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0377   -2.6585    1.5201 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2013   -1.9510    0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5196   -3.1599   -0.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4595   -3.5561   -1.8551 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6845   -0.4119   -1.5817 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6982    0.6184   -1.5425 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3350    1.7091   -0.1077 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1193    2.3682   -2.8337 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5096    3.3082   -1.4546 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7218    2.9836   -2.9353 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9686    1.2340   -3.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 25  1  0
 25 24  1  0
 24  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  6 41  1  0
 41 40  1  0
 40 39  1  0
 39 38  1  0
 38 27  1  0
 27 28  1  0
 28 29  1  0
 29 35  1  0
 35 36  1  0
 36 37  2  0
 29 30  1  0
 30 34  2  0
 34 33  1  0
 33 32  1  0
 32 31  2  0
 27 25  1  0
 27 36  1  1
 31 30  1  0
 19 10  1  0
 38  7  1  0
 26 64  1  0
 26 65  1  0
 26 66  1  0
 25 63  1  1
 24 61  1  0
 24 62  1  0
  8 47  1  1
 10 48  1  1
 12 49  1  1
 13 50  1  0
 13 51  1  0
 14 52  1  0
 15 53  1  1
 16 54  1  0
 17 55  1  6
 18 56  1  0
 19 57  1  6
 22 58  1  0
 22 59  1  0
 22 60  1  0
  5 45  1  0
  5 46  1  0
  1 42  1  0
  1 43  1  0
  1 44  1  0
 41 78  1  0
 41 79  1  0
 40 76  1  0
 40 77  1  0
 39 74  1  0
 39 75  1  0
 38 73  1  6
 28 67  1  0
 28 68  1  0
 29 69  1  1
 34 72  1  0
 32 71  1  0
 31 70  1  0
M  END


  Mrv1533004251513022D          

 41 45  0  0  0  0            999 V2000
    2.2871    1.4612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0765    1.2215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6789    1.7852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4683    1.5454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0706    2.1092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8836    2.9127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0942    3.1525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9071    3.9560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1177    4.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9307    4.9993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5095    4.5197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3224    5.3232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2989    4.2799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9012    4.8437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4859    3.4764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2753    3.2367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8776    3.8004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6906    4.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6670    3.5606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6553    0.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4447    0.5021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0470    1.0659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8364    0.8261    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4388    1.3898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2517    2.1934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2281    1.1501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6317   -0.3014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0294   -0.8651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2400   -0.6253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0530    0.1782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2636    0.4179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3656   -0.4007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6185   -0.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0548   -0.1484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4534    0.5739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8897    1.1762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4626   -1.5609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0263   -2.1632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6277   -2.8855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8175   -2.7296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7155   -1.9109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  4 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 20 30  1  0  0  0  0
 30 31  1  0  0  0  0
  2 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
 31 35  1  0  0  0  0
 35 36  2  0  0  0  0
 33 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 37 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0266280

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(OC2OC(CO)C(O)C(O)C2OC(C)=O)C2=C(COC(C)=O)CCCC2C11CC(OC1=O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C29H38O12/c1-14-9-20(39-27-26(38-16(3)32)25(34)24(33)22(11-30)40-27)23-18(13-37-15(2)31)5-4-6-19(23)29(14)10-21(41-28(29)35)17-7-8-36-12-17/h7-8,12,14,19-22,24-27,30,33-34H,4-6,9-11,13H2,1-3H3

> <INCHI_KEY>
SKRDIJQANJDROJ-UHFFFAOYSA-N

> <FORMULA>
C29H38O12

> <MOLECULAR_WEIGHT>
578.611

> <EXACT_MASS>
578.236326664

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
57.9447028636335

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2H-spiro[naphthalene-1,3'-oxolane]-5-yl)methyl acetate

> <ALOGPS_LOGP>
1.64

> <JCHEM_LOGP>
0.7671011439999994

> <ALOGPS_LOGS>
-3.10

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.01753648309872

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.695653270362609

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8620627652730786

> <JCHEM_POLAR_SURFACE_AREA>
171.19

> <JCHEM_REFRACTIVITY>
138.36469999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.63e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2H-spiro[naphthalene-1,3'-oxolane]-5-ylmethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       4.269   2.728   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.743   2.280   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.867   3.332   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.341   2.885   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.465   3.937   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.116   5.437   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.642   5.885   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.293   7.384   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.820   7.832   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.471   9.332   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.418   8.437   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.069   9.937   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       9.891   7.989   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      11.016   9.042   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.240   6.489   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      11.714   6.042   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      12.838   7.094   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      12.489   8.594   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      14.312   6.647   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.690   1.385   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.163   0.937   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.288   1.990   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      12.761   1.542   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      13.886   2.594   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.537   4.094   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      15.359   2.147   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.513  -0.563   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.388  -1.615   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.915  -1.167   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.566   0.333   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.092   0.780   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.282  -0.748   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.888  -1.401   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.836  -0.277   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       4.580   1.071   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.527   2.196   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       4.597  -2.914   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.649  -4.038   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       4.905  -5.386   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       3.393  -5.095   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.202  -3.567   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   31                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   20                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    6   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20    4   21   30                                                  
CONECT   21   20   22   27                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   21   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   20   31                                                  
CONECT   31   30    2   32   35                                             
CONECT   32   31   33                                                       
CONECT   33   32   34   37                                                  
CONECT   34   33   35                                                       
CONECT   35   34   31   36                                                  
CONECT   36   35                                                            
CONECT   37   33   38   41                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   37                                                       
MASTER        0    0    0    0    0    0    0    0   41    0   90    0
END

View in JSmol

Synonyms

Value	Source
(4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2H-spiro[naphthalene-1,3'-oxolane]-5-yl)methyl acetic acid	Generator

Chemical Formula

C₂₉H₃₈O₁₂

Average Mass

578.6110 Da

Monoisotopic Mass

578.23633 Da

IUPAC Name

(4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2H-spiro[naphthalene-1,3'-oxolane]-5-yl)methyl acetate

Traditional Name

4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2H-spiro[naphthalene-1,3'-oxolane]-5-ylmethyl acetate

CAS Registry Number

Not Available

SMILES

CC1CC(OC2OC(CO)C(O)C(O)C2OC(C)=O)C2=C(COC(C)=O)CCCC2C11CC(OC1=O)C1=COC=C1

InChI Identifier

InChI=1S/C29H38O12/c1-14-9-20(39-27-26(38-16(3)32)25(34)24(33)22(11-30)40-27)23-18(13-37-15(2)31)5-4-6-19(23)29(14)10-21(41-28(29)35)17-7-8-36-12-17/h7-8,12,14,19-22,24-27,30,33-34H,4-6,9-11,13H2,1-3H3

InChI Key

SKRDIJQANJDROJ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Teucrium flavum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Diterpene glycosides

Alternative Parents

Substituents

Diterpene glycoside
Diterpene lactone
Diterpenoid
Clerodane diterpenoid
Glycosyl compound
O-glycosyl compound
Tricarboxylic acid or derivatives
Gamma butyrolactone
Monosaccharide
Oxane
Heteroaromatic compound
Furan
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Lactone
Organoheterocyclic compound
Acetal
Carboxylic acid derivative
Oxacycle
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organic oxide
Carbonyl group
Primary alcohol
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	1.64	ALOGPS
logP	0.77	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	12.7	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	171.19 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	138.36 m³·mol⁻¹	ChemAxon
Polarizability	57.94 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate (NP0266280)

MOL for NP0266280 (4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate)

3D MOL for NP0266280 (4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate)

3D SDF for NP0266280 (4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate)

3D-SDF for NP0266280 (4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate)

PDB for NP0266280 (4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate)

3D PDB for NP0266280 (4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate)

SMILES for NP0266280 (4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate)

INCHI for NP0266280 (4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate)

Structure for NP0266280 (4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate)

3D Structure for NP0266280 (4-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5'-(furan-3-yl)-2-methyl-2'-oxo-3,4,6,7,8,8a-hexahydro-2h-spiro[naphthalene-1,3'-oxolan]-5-ylmethyl acetate)