NP-MRD: Showing NP-Card for (+)-Smilaside C (NP0078752)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 23:49:20 UTC

Updated at

2022-04-28 23:49:20 UTC

NP-MRD ID

NP0078752

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Smilaside C

Description

SMILASIDE C belongs to the class of organic compounds known as coumaric acid esters. These are aromatic compounds containing an ester derivative of coumaric acid. (+)-Smilaside C is found in Smilax bracteata and Smilax china . Based on a literature review very few articles have been published on SMILASIDE C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292201492D          

 60 64  0  0  1  0            999 V2000
   -1.6242   -5.0437    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4492   -5.0437    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7041   -4.2590    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0367   -3.7741    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3693   -4.2590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6317   -3.0554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8068   -3.0467    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4018   -2.3280    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4232   -2.3193    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8432   -3.0294    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4382   -3.7482    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3868   -3.7568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8581   -4.4583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4531   -5.1771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6681   -3.0208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8282   -1.6006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8217   -1.6179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4417   -3.0554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2667   -3.0467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6717   -2.3280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4966   -2.3193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2517   -1.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6567   -0.8991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2367   -0.1890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6417    0.5298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2218    1.2399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3968    1.2312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9918    0.5125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4118   -0.1976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9769    1.9413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4888   -4.0041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1019   -4.5561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9303   -5.3631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8865   -4.3012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4996   -4.8532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2842   -4.5983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8973   -5.1503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6819   -4.8954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8534   -4.0884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2403   -3.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4557   -3.7913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4119   -2.7294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7988   -2.1774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6381   -3.8335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9341   -5.7111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1393   -5.7111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3188   -5.6249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1661   -6.2923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1694   -7.0460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9866   -6.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4715   -6.8735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2920   -6.7873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6276   -6.0336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4480   -5.9473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9330   -6.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5974   -7.3685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7769   -7.4547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0823   -8.0359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7468   -8.7896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7534   -6.5286    0.0000 O   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
  1  5  1  0  0  0  0
  4  6  1  6  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  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
  7 12  1  0  0  0  0
 11 13  1  1  0  0  0
 13 14  1  0  0  0  0
 10 15  1  6  0  0  0
  9 16  1  1  0  0  0
  8 17  1  6  0  0  0
  4 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 24 29  1  0  0  0  0
 27 30  1  0  0  0  0
  3 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 36 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 39 44  1  0  0  0  0
  2 45  1  1  0  0  0
  1 46  1  6  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
 53 54  1  0  0  0  0
 54 55  2  0  0  0  0
 55 56  1  0  0  0  0
 56 57  2  0  0  0  0
 52 57  1  0  0  0  0
 56 58  1  0  0  0  0
 58 59  1  0  0  0  0
 55 60  1  0  0  0  0
M  END

     RDKit          3D

104108  0  0  0  0  0  0  0  0999 V2000
   -7.3155   -2.0414   -5.4167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5008   -2.8935   -6.1550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3440   -3.5116   -5.6915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9245   -3.2992   -4.3743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8019   -3.8724   -3.8459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4172   -3.6166   -2.4793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0497   -2.8215   -1.6548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5295   -2.6692   -0.2846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5147   -3.3309    0.0240 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1031   -1.8473    0.6439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6815   -1.6436    1.9737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3160   -1.1465    2.0127 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0141    0.0590    1.4242 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7842    0.5070    1.9627 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2310    0.6598    0.8743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1456    1.5539   -0.1519 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6721    1.7674   -1.2335 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7547    1.1622   -1.2888 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3134    2.6836   -2.3375 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1110    2.8460   -3.3631 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8683    3.7104   -4.4976 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7829    3.7584   -5.5599 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6046    4.5435   -6.6655 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4929    5.3413   -6.7875 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3285    6.1326   -7.9220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4492    5.3281   -5.7501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2311    4.5101   -4.6338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0267    1.5970    2.7347 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5951    2.6679    2.1106 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8182    3.0243    2.6844 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4869    3.9397    1.9014 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5906    3.2608    1.1547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2956    4.1746    0.3386 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5982    4.6323    0.8941 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2790    5.8179    0.5311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2748    5.0169    1.4908 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3615    5.4199    0.5229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6745    3.8755    2.2431 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5830    4.1705    3.6091 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3257   -0.6122    2.8680 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6198   -0.2312    3.7685 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8273   -0.8997    3.9655 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9671   -1.9130    3.2263 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8719   -0.5327    4.9082 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9675   -1.2610    5.0155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0874   -1.0242    5.8991 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1864    0.0561    6.7483 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2841    0.2342    7.5855 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3069   -0.7112    7.5576 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4370   -0.5678    8.3889 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2445   -1.8038    6.7246 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2917   -2.7206    6.7384 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3055   -3.8749    5.9248 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1497   -1.9260    5.9289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6934   -1.0252    3.4302 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6615   -2.3017    3.9517 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0450   -4.7071   -4.6699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4454   -4.9352   -5.9932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5795   -4.3398   -6.4835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9873   -4.5650   -7.8138 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3958   -2.2394   -4.3475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9614   -0.9835   -5.5560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3222   -2.0553   -5.9111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5547   -2.6363   -3.7881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5075   -4.1525   -2.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9237   -2.3019   -1.9806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3942   -0.9196    2.4486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7226   -2.6403    2.4810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6399   -1.9070    1.5106 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3970   -0.3213    0.3766 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2332    0.9202    1.3235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6129    3.2367   -2.3215 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0480    2.2734   -3.3511 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6543    3.1269   -5.4659 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3234    4.5714   -7.4914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4532    6.7302   -8.0796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3186    5.9567   -5.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9703    4.5146   -3.8395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7943    2.4446    1.0585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9648    4.7353    2.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3152    2.7221    1.8333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1581    2.5044    0.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5052    3.7987   -0.5446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4513    4.0584   -0.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6352    5.7445   -0.3984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4531    5.9002    2.1528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7606    5.3662   -0.3948 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3365    3.5860    1.8960 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3271    4.0145    3.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0474   -1.4732    2.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7892    0.3277    5.5390 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0044   -2.1297    4.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4018    0.7923    6.7827 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3617    1.0782    8.2516 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1804   -1.2718    8.3571 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4053   -4.4699    6.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0362   -3.5598    4.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2286   -4.4457    5.9993 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1037   -2.7819    5.2767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1659   -0.2604    4.0268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1603   -2.3064    4.7996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1616   -5.1884   -4.3313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9042   -5.5709   -6.6701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8270   -4.1120   -8.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  2  0
 14 28  1  1
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 31 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 14 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  2  0
 42 44  1  0
 44 45  2  0
 45 46  1  0
 46 47  2  0
 47 48  1  0
 48 49  2  0
 49 50  1  0
 49 51  1  0
 51 52  1  0
 52 53  1  0
 51 54  2  0
 40 55  1  0
 55 56  1  0
  5 57  2  0
 57 58  1  0
 58 59  2  0
 59 60  1  0
 59  3  1  0
 55 12  1  0
 27 21  1  0
 38 29  1  0
 54 46  1  0
  1 61  1  0
  1 62  1  0
  1 63  1  0
  4 64  1  0
  6 65  1  0
  7 66  1  0
 11 67  1  0
 11 68  1  0
 12 69  1  6
 15 70  1  0
 15 71  1  0
 19 72  1  0
 20 73  1  0
 22 74  1  0
 23 75  1  0
 25 76  1  0
 26 77  1  0
 27 78  1  0
 29 79  1  6
 31 80  1  1
 32 81  1  0
 32 82  1  0
 33 83  1  0
 34 84  1  6
 35 85  1  0
 36 86  1  1
 37 87  1  0
 38 88  1  6
 39 89  1  0
 40 90  1  6
 44 91  1  0
 45 92  1  0
 47 93  1  0
 48 94  1  0
 50 95  1  0
 53 96  1  0
 53 97  1  0
 53 98  1  0
 54 99  1  0
 55100  1  1
 56101  1  0
 57102  1  0
 58103  1  0
 60104  1  0
M  END


  Mrv1652304292201492D          

 60 64  0  0  1  0            999 V2000
   -1.6242   -5.0437    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4492   -5.0437    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7041   -4.2590    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0367   -3.7741    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3693   -4.2590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6317   -3.0554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8068   -3.0467    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4018   -2.3280    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4232   -2.3193    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8432   -3.0294    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4382   -3.7482    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3868   -3.7568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8581   -4.4583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4531   -5.1771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6681   -3.0208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8282   -1.6006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8217   -1.6179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4417   -3.0554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2667   -3.0467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6717   -2.3280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4966   -2.3193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2517   -1.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6567   -0.8991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2367   -0.1890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6417    0.5298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2218    1.2399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3968    1.2312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9918    0.5125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4118   -0.1976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9769    1.9413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4888   -4.0041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1019   -4.5561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9303   -5.3631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8865   -4.3012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4996   -4.8532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2842   -4.5983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8973   -5.1503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6819   -4.8954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8534   -4.0884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2403   -3.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4557   -3.7913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4119   -2.7294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7988   -2.1774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6381   -3.8335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9341   -5.7111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1393   -5.7111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3188   -5.6249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1661   -6.2923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1694   -7.0460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9866   -6.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4715   -6.8735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2920   -6.7873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6276   -6.0336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4480   -5.9473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9330   -6.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5974   -7.3685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7769   -7.4547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0823   -8.0359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7468   -8.7896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7534   -6.5286    0.0000 O   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
  1  5  1  0  0  0  0
  4  6  1  6  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  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
  7 12  1  0  0  0  0
 11 13  1  1  0  0  0
 13 14  1  0  0  0  0
 10 15  1  6  0  0  0
  9 16  1  1  0  0  0
  8 17  1  6  0  0  0
  4 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 24 29  1  0  0  0  0
 27 30  1  0  0  0  0
  3 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 36 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 39 44  1  0  0  0  0
  2 45  1  1  0  0  0
  1 46  1  6  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 48 50  1  0  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
 53 54  1  0  0  0  0
 54 55  2  0  0  0  0
 55 56  1  0  0  0  0
 56 57  2  0  0  0  0
 52 57  1  0  0  0  0
 56 58  1  0  0  0  0
 58 59  1  0  0  0  0
 55 60  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0078752

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C\C(=O)OC[C@H]2O[C@@](COC(=O)\C=C\C3=CC=C(O)C=C3)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](OC(=O)\C=C\C3=CC=C(O)C(OC)=C3)[C@@H]2O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C41H44O19/c1-53-28-17-23(5-12-26(28)44)8-15-32(46)55-20-31-36(50)39(58-34(48)16-9-24-6-13-27(45)29(18-24)54-2)41(59-31,60-40-38(52)37(51)35(49)30(19-42)57-40)21-56-33(47)14-7-22-3-10-25(43)11-4-22/h3-18,30-31,35-40,42-45,49-52H,19-21H2,1-2H3/b14-7+,15-8+,16-9+/t30-,31-,35-,36-,37+,38-,39+,40-,41+/m1/s1

> <INCHI_KEY>
XPMSXAVTDBNKAT-SZPLYKBJSA-N

> <FORMULA>
C41H44O19

> <MOLECULAR_WEIGHT>
840.784

> <EXACT_MASS>
840.247679197

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
84.26076965786085

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2S,3S,4R,5R)-4-hydroxy-3-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-5-({[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-2-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
2.68

> <JCHEM_LOGP>
3.3467986939999994

> <ALOGPS_LOGS>
-4.09

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.72247304478362

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.173083958948455

> <JCHEM_PKA_STRONGEST_BASIC>
-2.98108491281414

> <JCHEM_POLAR_SURFACE_AREA>
286.89

> <JCHEM_REFRACTIVITY>
206.3463

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.84e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2S,3S,4R,5R)-4-hydroxy-3-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-5-({[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-2-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <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      -3.032  -9.415   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.572  -9.415   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.048  -7.950   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.802  -7.045   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.556  -7.950   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      -3.046  -5.703   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.506  -5.687   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.750  -4.346   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.790  -4.329   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.574  -5.655   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.818  -6.997   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.722  -7.013   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.602  -8.322   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.846  -9.664   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       3.114  -5.639   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       1.546  -2.988   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -1.534  -3.020   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -4.558  -5.703   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -6.098  -5.687   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -6.854  -4.346   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -8.394  -4.329   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -6.070  -3.020   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.826  -1.678   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -6.042  -0.353   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -6.798   0.989   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.014   2.314   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.474   2.298   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.718   0.957   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.502  -0.369   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -3.690   3.624   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -6.512  -7.474   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -7.657  -8.505   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -7.337 -10.011   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -9.121  -8.029   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -10.266  -9.059   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0     -11.731  -8.583   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -12.875  -9.614   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -14.340  -9.138   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -14.660  -7.632   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -13.515  -6.601   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0     -12.051  -7.077   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0     -13.836  -5.095   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0     -12.691  -4.064   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0     -16.124  -7.156   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      -5.477 -10.661   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      -2.127 -10.661   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -0.595 -10.500   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       0.310 -11.746   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -0.316 -13.152   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       1.842 -11.585   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       2.747 -12.831   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       4.278 -12.670   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       4.905 -11.263   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       6.436 -11.102   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       7.342 -12.348   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       6.715 -13.754   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0       5.184 -13.915   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0       7.620 -15.000   0.000  0.00  0.00           O+0
HETATM   59  C   UNK     0       6.994 -16.407   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0       8.873 -12.187   0.000  0.00  0.00           O+0
CONECT    1    2    5   46                                                  
CONECT    2    1    3   45                                                  
CONECT    3    2    4   31                                                  
CONECT    4    3    5    6   18                                             
CONECT    5    4    1                                                       
CONECT    6    4    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9   17                                                  
CONECT    9    8   10   16                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11    7                                                       
CONECT   13   11   14                                                       
CONECT   14   13                                                            
CONECT   15   10                                                            
CONECT   16    9                                                            
CONECT   17    8                                                            
CONECT   18    4   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28   24                                                       
CONECT   30   27                                                            
CONECT   31    3   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   41                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   44                                                  
CONECT   40   39   41   42                                                  
CONECT   41   40   36                                                       
CONECT   42   40   43                                                       
CONECT   43   42                                                            
CONECT   44   39                                                            
CONECT   45    2                                                            
CONECT   46    1   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53   57                                                  
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   56   60                                                  
CONECT   56   55   57   58                                                  
CONECT   57   56   52                                                       
CONECT   58   56   59                                                       
CONECT   59   58                                                            
CONECT   60   55                                                            
MASTER        0    0    0    0    0    0    0    0   60    0  128    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₄₄O₁₉

Average Mass

840.7840 Da

Monoisotopic Mass

840.24768 Da

IUPAC Name

[(2S,3S,4R,5R)-4-hydroxy-3-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-5-({[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-2-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC(\C=C\C(=O)OC[C@H]2O[C@@](COC(=O)\C=C\C3=CC=C(O)C=C3)(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](OC(=O)\C=C\C3=CC=C(O)C(OC)=C3)[C@@H]2O)=CC=C1O

InChI Identifier

InChI=1S/C41H44O19/c1-53-28-17-23(5-12-26(28)44)8-15-32(46)55-20-31-36(50)39(58-34(48)16-9-24-6-13-27(45)29(18-24)54-2)41(59-31,60-40-38(52)37(51)35(49)30(19-42)57-40)21-56-33(47)14-7-22-3-10-25(43)11-4-22/h3-18,30-31,35-40,42-45,49-52H,19-21H2,1-2H3/b14-7+,15-8+,16-9+/t30-,31-,35-,36-,37+,38-,39+,40-,41+/m1/s1

InChI Key

XPMSXAVTDBNKAT-SZPLYKBJSA-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
Smilax bracteata	LOTUS Database	35616633
Smilax china	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acid esters. These are aromatic compounds containing an ester derivative of coumaric acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acid esters

Alternative Parents

Substituents

Coumaric acid ester
Coumaric acid or derivatives
Cinnamic acid ester
C-glycosyl compound
Disaccharide
Glycosyl compound
O-glycosyl compound
Methoxyphenol
Tricarboxylic acid or derivatives
Anisole
Phenoxy compound
Phenol ether
Styrene
Methoxybenzene
1-hydroxy-2-unsubstituted benzenoid
Ketal
Fatty acid ester
Alkyl aryl ether
Phenol
Fatty acyl
Oxane
Benzenoid
Monocyclic benzene moiety
Enoate ester
Oxolane
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Carboxylic acid ester
Acetal
Oxacycle
Polyol
Ether
Organoheterocyclic compound
Carboxylic acid derivative
Organooxygen compound
Carbonyl group
Alcohol
Organic oxygen compound
Organic oxide
Primary alcohol
Hydrocarbon derivative
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	2.68	ALOGPS
logP	3.35	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	9.17	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	286.89 Å²	ChemAxon
Rotatable Bond Count	19	ChemAxon
Refractivity	206.35 m³·mol⁻¹	ChemAxon
Polarizability	84.26 Å³	ChemAxon
Number of Rings	5	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

C00043005

Chemspider ID

9095196

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10919948

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (+)-Smilaside C (NP0078752)

MOL for NP0078752 ((+)-Smilaside C)

3D MOL for NP0078752 ((+)-Smilaside C)

3D SDF for NP0078752 ((+)-Smilaside C)

3D-SDF for NP0078752 ((+)-Smilaside C)

PDB for NP0078752 ((+)-Smilaside C)

3D PDB for NP0078752 ((+)-Smilaside C)

SMILES for NP0078752 ((+)-Smilaside C)

INCHI for NP0078752 ((+)-Smilaside C)

Structure for NP0078752 ((+)-Smilaside C)

3D Structure for NP0078752 ((+)-Smilaside C)