NP-MRD: Showing NP-Card for 6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate (NP0272186)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 18:43:35 UTC

Updated at

2022-09-08 18:43:35 UTC

NP-MRD ID

NP0272186

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate

Description

6-(5,13-Dihydroxy-1,6,6,11,15-pentamethyl-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-7-en-14-yl)-2-methyl-5-oxohept-3-en-2-yl acetate belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. 6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate is found in Neopicrorhiza scrophulariiflora and Picrorhiza kurrooa. 6-(5,13-Dihydroxy-1,6,6,11,15-pentamethyl-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-7-en-14-yl)-2-methyl-5-oxohept-3-en-2-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171515292D          

 49 53  0  0  0  0            999 V2000
   -2.6962    0.0341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0071   -0.7301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5008   -1.3814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7301   -2.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5060   -2.4542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0473   -2.6369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3959   -2.1305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1983   -2.9315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838   -2.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3035   -3.0516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5086   -3.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0404   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7601   -1.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2920   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1041   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6359   -0.6740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4480   -0.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7283   -1.5952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5404   -1.7404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8207   -2.5163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6328   -2.6615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0723   -1.1097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8844   -1.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7920   -0.3337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3238    0.2970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9798   -0.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6995    0.5874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3844   -2.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1965   -2.2259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8526   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4643   -3.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7358   -3.5281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0520   -1.6450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4798   -1.0143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3323   -0.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1444   -0.7239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6762   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0361   -0.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8244   -0.8429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3307   -0.1916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1353   -1.6071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9525   -1.7199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2634   -2.4841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0276   -2.1732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4992   -2.7950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5743   -3.2483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3915   -3.3612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7024   -4.1253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8979   -2.7098    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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 12 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 13 33  1  0  0  0  0
  9 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
  3 37  1  0  0  0  0
  7 37  1  0  0  0  0
 37 38  1  0  0  0  0
  2 39  1  0  0  0  0
 39 40  2  0  0  0  0
 41 39  1  4  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 43 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
M  END

     RDKit          3D

109113  0  0  0  0  0  0  0  0999 V2000
   10.2076    1.6679   -2.6634 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3536    0.6699   -1.9869 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7777   -0.2068   -2.6847 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1389    0.6283   -0.6321 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3492   -0.2808    0.0714 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3554    0.1239    1.5306 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8731   -1.6991    0.0025 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9348   -0.2041   -0.3956 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4569    0.8077   -1.0771 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1346    0.9884   -1.5702 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9401    2.0848   -2.2379 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9551    0.1114   -1.4262 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2696   -1.2533   -1.8430 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1997    0.4555   -0.2482 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6720    0.0201    1.1068 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0392   -1.3227    1.1799 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4889    0.2785    2.0612 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4981    0.9723    1.1772 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9654    2.4109    1.1088 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0795    0.8977    1.6492 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1484   -0.1345    2.7151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5051    0.0861    3.2863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4903    0.2344    2.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1771    0.1726    0.9682 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3736    0.7180    0.2348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6437   -0.0215    0.5923 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7514   -1.2226   -0.0961 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8368   -1.1596   -0.9524 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3875   -1.4702   -2.2295 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3190   -1.3161   -3.2256 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4551    0.1382   -3.6030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1793    0.5460   -4.0428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6216   -2.0003   -2.9751 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.5912   -1.4466   -3.7963 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0653   -1.9369   -1.5437 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.0907   -2.8418   -1.3406 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9056   -2.1785   -0.5908 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.3915   -1.7840    0.6766 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8323   -0.2766    2.0446 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7464   -1.6554    2.2770 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8600    0.4345    2.9572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9723   -0.3188    4.2999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2292    1.8552    3.2061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9599    1.0022    0.5955 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4848    2.4490    0.4669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5674    0.6085   -0.7979 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8772    0.8186   -1.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7365    0.2134   -0.1271 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4184   -1.2310    0.0101 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1068    2.6543   -2.1569 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.2654    1.3574   -2.5618 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8983    1.7545   -3.7117 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3697   -0.0715    2.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5832    1.1801    1.6906 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0991   -0.4696    2.1169 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9194   -2.1023   -1.0209 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8372   -1.7134    0.5392 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1708   -2.3218    0.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2887   -1.0296   -0.1635 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1979    1.6073   -1.2773 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2874    0.4844   -2.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3223   -2.0114   -1.0339 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5999   -1.6011   -2.6748 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2786   -1.2655   -2.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2870    1.6028   -0.1945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5219    0.6065    1.4994 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8984   -1.7050    2.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1561   -0.6345    2.5431 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7828    0.9874    2.8688 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3043    2.9628    1.8524 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9726    2.5743    1.5487 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8016    2.9181    0.1652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0518    1.8428    2.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5676    0.1050    3.5492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0968   -1.1700    2.3957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6801    0.1235    4.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0080   -0.8941    0.7018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2591    0.7210   -0.8589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5331    1.7656    0.5569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4986    0.6274    0.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3790   -0.1765   -0.9172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8730   -1.8153   -4.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1149    0.2629   -4.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7706    0.7891   -2.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2103    1.4249   -4.4915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4776   -3.0957   -3.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3712   -1.1070   -3.3276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3919   -0.8778   -1.3477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7402   -3.5914   -0.7861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5581   -3.2089   -0.6068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7376   -2.6113    1.0961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8511    0.0829    2.3881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1781   -2.1063    1.6115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4283   -1.2740    4.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0567   -0.5245    4.4342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5597    0.3054    5.1125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3423    2.5116    3.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7560    1.9507    4.1952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9521    2.1786    2.4191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0201    2.5935   -0.4897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5634    3.0753    0.3644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9842    2.8014    1.3629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9558   -0.4112   -1.0975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1253    1.2627   -1.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0367    1.8875   -1.3870 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0084    0.3073   -2.1595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8023   -1.7419    0.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7136   -1.7739   -0.9379 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3108   -1.4363    0.0504 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  6
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 30 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 26 39  1  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41 43  1  0
 24 44  1  0
 44 45  1  6
 44 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  1
 12 10  1  0
 10 11  2  0
 10  9  1  0
  9  8  2  0
  8  5  1  0
  5  6  1  0
  5  7  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 48 14  1  0
 48 18  1  0
 44 20  1  0
 41 23  1  0
 37 28  1  0
 13 62  1  0
 13 63  1  0
 13 64  1  0
 12 61  1  6
 14 65  1  1
 15 66  1  1
 16 67  1  0
 17 68  1  0
 17 69  1  0
 19 70  1  0
 19 71  1  0
 19 72  1  0
 20 73  1  1
 21 74  1  0
 21 75  1  0
 22 76  1  0
 24 77  1  6
 25 78  1  0
 25 79  1  0
 26 80  1  6
 28 81  1  6
 30 82  1  6
 31 83  1  0
 31 84  1  0
 32 85  1  0
 33 86  1  6
 34 87  1  0
 35 88  1  1
 36 89  1  0
 37 90  1  1
 38 91  1  0
 39 92  1  1
 40 93  1  0
 42 94  1  0
 42 95  1  0
 42 96  1  0
 43 97  1  0
 43 98  1  0
 43 99  1  0
 45100  1  0
 45101  1  0
 45102  1  0
 46103  1  0
 46104  1  0
 47105  1  0
 47106  1  0
 49107  1  0
 49108  1  0
 49109  1  0
  9 60  1  0
  8 59  1  0
  6 53  1  0
  6 54  1  0
  6 55  1  0
  7 56  1  0
  7 57  1  0
  7 58  1  0
  1 50  1  0
  1 51  1  0
  1 52  1  0
M  END


  Mrv1533004171515292D          

 49 53  0  0  0  0            999 V2000
   -2.6962    0.0341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0071   -0.7301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5008   -1.3814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7301   -2.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5060   -2.4542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0473   -2.6369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3959   -2.1305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1983   -2.9315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5838   -2.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3035   -3.0516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5086   -3.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0404   -2.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7601   -1.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2920   -1.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1041   -1.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6359   -0.6740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4480   -0.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7283   -1.5952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5404   -1.7404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8207   -2.5163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6328   -2.6615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0723   -1.1097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8844   -1.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7920   -0.3337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3238    0.2970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9798   -0.1885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6995    0.5874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3844   -2.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1965   -2.2259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8526   -2.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4643   -3.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7358   -3.5281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0520   -1.6450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4798   -1.0143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3323   -0.8691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1444   -0.7239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6762   -1.3546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0361   -0.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8244   -0.8429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3307   -0.1916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1353   -1.6071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9525   -1.7199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2634   -2.4841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0276   -2.1732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4992   -2.7950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5743   -3.2483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3915   -3.3612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7024   -4.1253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8979   -2.7098    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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 12 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 13 33  1  0  0  0  0
  9 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
  3 37  1  0  0  0  0
  7 37  1  0  0  0  0
 37 38  1  0  0  0  0
  2 39  1  0  0  0  0
 39 40  2  0  0  0  0
 41 39  1  4  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 43 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0272186

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C1C(O)CC2(C)C3CC=C4C(CC(OC5OC(CO)C(O)C(O)C5O)C(O)C4(C)C)C3(C)CCC12C)C(=O)C=CC(C)(C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C38H60O11/c1-19(23(41)12-13-34(3,4)49-20(2)40)28-24(42)17-38(9)27-11-10-21-22(36(27,7)14-15-37(28,38)8)16-25(32(46)35(21,5)6)47-33-31(45)30(44)29(43)26(18-39)48-33/h10,12-13,19,22,24-33,39,42-46H,11,14-18H2,1-9H3

> <INCHI_KEY>
AVRXZXZBXIWFEZ-UHFFFAOYSA-N

> <FORMULA>
C38H60O11

> <MOLECULAR_WEIGHT>
692.887

> <EXACT_MASS>
692.413562752

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
109

> <JCHEM_AVERAGE_POLARIZABILITY>
77.36693257399425

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-(5,13-dihydroxy-1,6,6,11,15-pentamethyl-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-14-yl)-2-methyl-5-oxohept-3-en-2-yl acetate

> <ALOGPS_LOGP>
2.86

> <JCHEM_LOGP>
2.2018969089999976

> <ALOGPS_LOGS>
-4.27

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.088599826828691

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.19572730606943

> <JCHEM_PKA_STRONGEST_BASIC>
-2.847443625892348

> <JCHEM_POLAR_SURFACE_AREA>
183.20999999999998

> <JCHEM_REFRACTIVITY>
181.92280000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.73e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(5,13-dihydroxy-1,6,6,11,15-pentamethyl-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-14-yl)-2-methyl-5-oxohept-3-en-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -5.033   0.064   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.613  -1.363   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.668  -2.579   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.096  -4.058   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -6.545  -4.581   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -3.822  -4.922   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.606  -3.977   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.237  -5.472   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.090  -4.248   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.567  -5.696   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.949  -5.967   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.942  -4.790   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.419  -3.342   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.412  -2.164   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.928  -2.436   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.920  -1.258   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.436  -1.529   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.960  -2.978   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.475  -3.249   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.999  -4.697   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.515  -4.968   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.468  -2.071   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.984  -2.342   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.945  -0.623   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.938   0.554   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.429  -0.352   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.906   1.096   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.451  -3.884   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.967  -4.155   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.458  -5.061   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.600  -6.094   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.240  -6.586   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -0.097  -3.071   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.896  -1.893   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -0.620  -1.622   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.136  -1.351   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -3.129  -2.529   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -3.801  -1.143   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -7.139  -1.573   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -8.084  -0.358   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -7.719  -3.000   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -9.245  -3.211   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -9.825  -4.637   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -11.252  -4.057   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -8.399  -5.217   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0     -10.405  -6.063   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0     -11.931  -6.274   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0     -12.511  -7.701   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0     -12.876  -5.058   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   39                                                  
CONECT    3    2    4   37                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9   37                                             
CONECT    8    7                                                            
CONECT    9    7   10   33                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   30                                                  
CONECT   13   12   14   33                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   28                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   26                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   17   27                                                  
CONECT   27   26                                                            
CONECT   28   15   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   12   31   32                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   13    9   34   35                                             
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36    3    7   38                                             
CONECT   38   37                                                            
CONECT   39    2   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   45   46                                             
CONECT   44   43                                                            
CONECT   45   43                                                            
CONECT   46   43   47                                                       
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  106    0
END

View in JSmol

Synonyms

Value	Source
6-(5,13-Dihydroxy-1,6,6,11,15-pentamethyl-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0,.0,]heptadec-7-en-14-yl)-2-methyl-5-oxohept-3-en-2-yl acetic acid	Generator
6-(5,13-Dihydroxy-1,6,6,11,15-pentamethyl-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-14-yl)-2-methyl-5-oxohept-3-en-2-yl acetic acid	Generator

Chemical Formula

C₃₈H₆₀O₁₁

Average Mass

692.8870 Da

Monoisotopic Mass

692.41356 Da

IUPAC Name

6-(5,13-dihydroxy-1,6,6,11,15-pentamethyl-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-14-yl)-2-methyl-5-oxohept-3-en-2-yl acetate

Traditional Name

6-(5,13-dihydroxy-1,6,6,11,15-pentamethyl-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-14-yl)-2-methyl-5-oxohept-3-en-2-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C1C(O)CC2(C)C3CC=C4C(CC(OC5OC(CO)C(O)C(O)C5O)C(O)C4(C)C)C3(C)CCC12C)C(=O)C=CC(C)(C)OC(C)=O

InChI Identifier

InChI=1S/C38H60O11/c1-19(23(41)12-13-34(3,4)49-20(2)40)28-24(42)17-38(9)27-11-10-21-22(36(27,7)14-15-37(28,38)8)16-25(32(46)35(21,5)6)47-33-31(45)30(44)29(43)26(18-39)48-33/h10,12-13,19,22,24-33,39,42-46H,11,14-18H2,1-9H3

InChI Key

AVRXZXZBXIWFEZ-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
Neopicrorhiza scrophulariiflora	LOTUS Database	35616633
Picrorhiza kurrooa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

Indoles

Alternative Parents

Substituents

Indole
Aryl alkyl ketone
Aryl ketone
Piperidine
Benzenoid
Pyrrole
Heteroaromatic compound
Ketone
Tertiary amine
Tertiary aliphatic amine
Azacycle
Amine
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen 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	2.86	ALOGPS
logP	2.2	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	183.21 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	181.92 m³·mol⁻¹	ChemAxon
Polarizability	77.37 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

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 6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate (NP0272186)

MOL for NP0272186 (6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate)

3D MOL for NP0272186 (6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate)

3D SDF for NP0272186 (6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate)

3D-SDF for NP0272186 (6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate)

PDB for NP0272186 (6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate)

3D PDB for NP0272186 (6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate)

SMILES for NP0272186 (6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate)

INCHI for NP0272186 (6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate)

Structure for NP0272186 (6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate)

3D Structure for NP0272186 (6-(2,7-dihydroxy-3a,6,6,9b,11a-pentamethyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthren-1-yl)-2-methyl-5-oxohept-3-en-2-yl acetate)