NP-MRD: Showing NP-Card for [(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate (NP0199876)

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Record Information

Version

2.0

Created at

2022-09-04 18:36:15 UTC

Updated at

2022-09-04 18:36:15 UTC

NP-MRD ID

NP0199876

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate

Description

Mudanpioside H belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. [(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate is found in Paeonia suffruticosa. [(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate was first documented in 2006 (PMID: 17121173). Based on a literature review very few articles have been published on Mudanpioside H (PMID: 19586602).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042220362D          

 44 50  0  0  1  0            999 V2000
    2.1764    1.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2775    0.8305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0869    0.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9055   -0.3328    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7297   -0.3700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0042   -1.1697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2273   -0.8550    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4587    0.0289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3844   -0.6341    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6895   -1.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7273   -1.9030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4599   -2.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1547   -1.8377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4976   -3.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2302   -3.4859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2680   -4.3101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5731   -4.7548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6109   -5.5790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8405   -4.3754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8028   -3.5513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9457   -0.2077    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9856   -0.1389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5565    0.3344    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0589    0.9925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2402    0.8906    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0809    0.1306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.8629   -2.2511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1791   -1.6949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5002   -2.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3189   -2.5568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.6352   -2.0006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4954   -1.1388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3972    0.6868    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2159    0.5849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0761    1.4468    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5737    2.1048    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2574    1.5486    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0637    2.3086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  2  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
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 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 14 20  1  0  0  0  0
  9 21  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
  2 23  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  1  0  0  0
 25 24  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 32 38  1  0  0  0  0
 27 39  1  0  0  0  0
 39 40  1  1  0  0  0
 39 41  1  0  0  0  0
 41 42  1  6  0  0  0
 41 43  1  0  0  0  0
 25 43  1  0  0  0  0
 43 44  1  1  0  0  0
M  END

     RDKit          3D

 76 82  0  0  0  0  0  0  0  0999 V2000
   -0.0858   -0.0727   -3.7727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3790   -0.7164   -3.4338 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3786   -0.2146   -4.4908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7025   -0.7991   -4.1826 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7390   -0.3446   -4.9487 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6267   -2.4953   -3.2870 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3371   -2.1004   -3.5974 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0620   -1.6325   -2.1024 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -3.9638   -0.6520   -2.6814 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0726    0.4600   -2.1154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9452   -0.5516   -2.0964 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.9404   -0.6252   -0.5671 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0690   -0.0071   -0.1301 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2248   -0.9521    0.1045 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3776   -0.2689    0.5570 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5338   -0.9853    0.8219 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4962   -2.2289    0.6427 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.8090    1.0405    1.4929 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9438    1.6630    1.9312 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0905    0.9563    2.1946 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2383    1.5934    2.6389 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0498   -0.4130    1.9978 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8936   -1.0530    1.5504 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4670    1.9093    0.3395 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2022    1.0298   -3.8227 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.6358    1.2931    6.3688 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7063    0.2181    2.0108 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5664    1.2540    2.1343 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6304    0.3307    1.4142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7749    2.2188    1.2210 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1
  2  3  1  0
  3  4  1  0
  4  5  1  6
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  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  1
 10 11  1  0
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 12 13  2  0
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 23  9  1  0
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 38 70  1  0
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 41 73  1  6
 42 74  1  0
 43 75  1  1
 44 76  1  0
M  END


  Mrv1652309042220362D          

 44 50  0  0  1  0            999 V2000
    2.1764    1.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2775    0.8305    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0869    0.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9055   -0.3328    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7297   -0.3700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0042   -1.1697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4587    0.0289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3844   -0.6341    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6895   -1.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7273   -1.9030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4599   -2.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4976   -3.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2302   -3.4859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2680   -4.3101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6109   -5.5790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8405   -4.3754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8028   -3.5513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9457   -0.2077    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9856   -0.1389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5565    0.3344    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0589    0.9925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2402    0.8906    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0809    0.1306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8996    0.0288    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2207   -0.7312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0394   -0.8331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3605   -1.5930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8629   -2.2511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1791   -1.6949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5002   -2.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3189   -2.5568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8165   -1.8987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6352   -2.0006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4954   -1.1388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6767   -1.0369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3972    0.6868    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2159    0.5849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0761    1.4468    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5737    2.1048    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2574    1.5486    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0637    2.3086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  2  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 14 20  1  0  0  0  0
  9 21  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
  2 23  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  1  0  0  0
 25 24  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 32 38  1  0  0  0  0
 27 39  1  0  0  0  0
 39 40  1  1  0  0  0
 39 41  1  0  0  0  0
 41 42  1  6  0  0  0
 41 43  1  0  0  0  0
 25 43  1  0  0  0  0
 43 44  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0199876

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]12C[C@@]3(O)O[C@@H](O1)[C@]1(COC(=O)C4=CC=C(O)C=C4)[C@H]3C[C@]21O[C@@H]1O[C@H](COC(=O)C2=CC=C(O)C=C2)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C30H32O14/c1-27-12-29(38)19-10-30(27,28(19,26(43-27)44-29)13-40-24(37)15-4-8-17(32)9-5-15)42-25-22(35)21(34)20(33)18(41-25)11-39-23(36)14-2-6-16(31)7-3-14/h2-9,18-22,25-26,31-35,38H,10-13H2,1H3/t18-,19-,20-,21+,22-,25+,26-,27+,28+,29-,30+/m1/s1

> <INCHI_KEY>
ICDRIPCQQSUIDZ-HRCYFWENSA-N

> <FORMULA>
C30H32O14

> <MOLECULAR_WEIGHT>
616.572

> <EXACT_MASS>
616.17920571

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
56.42624615729568

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1R,2S,3R,5R,6R,8S)-6-hydroxy-8-methyl-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0^{2,5}.0^{3,8}]decan-2-yl]methyl 4-hydroxybenzoate

> <JCHEM_LOGP>
1.5016192300000009

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.7989908270786

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.197319921124897

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6490929336009525

> <JCHEM_POLAR_SURFACE_AREA>
210.89999999999998

> <JCHEM_REFRACTIVITY>
143.08750000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,2S,3R,5R,6R,8S)-6-hydroxy-8-methyl-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0^{2,5}.0^{3,8}]decan-2-yl]methyl 4-hydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       4.063   3.079   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.251   1.550   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.762   0.987   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.424  -0.621   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.962  -0.691   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       5.608  -2.184   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.158  -1.596   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.590   0.054   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.584  -1.184   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.287  -2.014   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.358  -3.552   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.725  -4.261   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.022  -3.430   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.796  -5.799   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.163  -6.507   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.234  -8.045   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.937  -8.876   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.007 -10.414   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.569  -8.168   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.499  -6.629   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.632  -0.388   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.840  -0.259   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.905   0.624   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.977   1.853   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.448   1.662   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -0.151   0.244   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.679   0.054   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.279  -1.365   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -3.807  -1.555   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -4.406  -2.974   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -3.477  -4.202   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -5.934  -3.164   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -6.534  -4.582   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -8.062  -4.773   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -8.991  -3.544   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0     -10.519  -3.734   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -8.391  -2.126   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -6.863  -1.936   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -2.608   1.282   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -4.136   1.092   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -2.009   2.701   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -2.937   3.929   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      -0.480   2.891   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       0.119   4.309   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8   23                                             
CONECT    3    2    4                                                       
CONECT    4    3    5    6   21                                             
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7    2                                                       
CONECT    9    7   10   21   23                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   14                                                       
CONECT   21    9    4   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22    2    9   24                                             
CONECT   24   23   25                                                       
CONECT   25   24   26   43                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   39                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   38                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   32                                                       
CONECT   39   27   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   25   44                                                  
CONECT   44   43                                                            
MASTER        0    0    0    0    0    0    0    0   44    0  100    0
END

View in JSmol

Synonyms

Value	Source
Mudanpioside-H	MeSH

Chemical Formula

C₃₀H₃₂O₁₄

Average Mass

616.5720 Da

Monoisotopic Mass

616.17921 Da

IUPAC Name

[(1R,2S,3R,5R,6R,8S)-6-hydroxy-8-methyl-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0^{2,5}.0^{3,8}]decan-2-yl]methyl 4-hydroxybenzoate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@]12C[C@@]3(O)O[C@@H](O1)[C@]1(COC(=O)C4=CC=C(O)C=C4)[C@H]3C[C@]21O[C@@H]1O[C@H](COC(=O)C2=CC=C(O)C=C2)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C30H32O14/c1-27-12-29(38)19-10-30(27,28(19,26(43-27)44-29)13-40-24(37)15-4-8-17(32)9-5-15)42-25-22(35)21(34)20(33)18(41-25)11-39-23(36)14-2-6-16(31)7-3-14/h2-9,18-22,25-26,31-35,38H,10-13H2,1H3/t18-,19-,20-,21+,22-,25+,26-,27+,28+,29-,30+/m1/s1

InChI Key

ICDRIPCQQSUIDZ-HRCYFWENSA-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
Paeonia suffruticosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Terpene glycosides

Alternative Parents

Substituents

Terpene glycoside
Hexose monosaccharide
P-hydroxybenzoic acid alkyl ester
P-hydroxybenzoic acid ester
Glycosyl compound
O-glycosyl compound
Aromatic monoterpenoid
Benzoate ester
Pinane monoterpenoid
Nopinane monoterpenoid
Monoterpenoid
Benzoic acid or derivatives
Furofuran
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Oxepane
Monocyclic benzene moiety
Meta-dioxane
Monosaccharide
Benzenoid
Oxane
Dicarboxylic acid or derivatives
Cyclic alcohol
Tetrahydrofuran
Hemiacetal
Carboxylic acid ester
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Carboxylic acid derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Alcohol
Hydrocarbon derivative
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	1.5	ChemAxon
pKa (Strongest Acidic)	8.2	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	210.9 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	143.09 m³·mol⁻¹	ChemAxon
Polarizability	56.43 Å³	ChemAxon
Number of Rings	7	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

28645382

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71457654

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ding HY, Lin HC, Chang TS: Tyrosinase inhibitors isolated from the roots of Paeonia suffruticosa. J Cosmet Sci. 2009 May-Jun;60(3):347-52. [PubMed:19586602 ]
An RB, Kim HC, Lee SH, Jeong GS, Sohn DH, Park H, Kwon DY, Lee JH, Kim YC: A new monoterpene glycoside and antibacterial monoterpene glycosides from Paeonia suffruticosa. Arch Pharm Res. 2006 Oct;29(10):815-20. doi: 10.1007/BF02973899. [PubMed:17121173 ]
LOTUS database [Link]

Showing NP-Card for [(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate (NP0199876)

MOL for NP0199876 ([(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate)

3D MOL for NP0199876 ([(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate)

3D SDF for NP0199876 ([(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate)

3D-SDF for NP0199876 ([(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate)

PDB for NP0199876 ([(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate)

3D PDB for NP0199876 ([(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate)

SMILES for NP0199876 ([(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate)

INCHI for NP0199876 ([(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate)

Structure for NP0199876 ([(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate)

3D Structure for NP0199876 ([(1r,2s,3r,5r,6r,8s)-6-hydroxy-8-methyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl 4-hydroxybenzoate)