NP-MRD: Showing NP-Card for 2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0188981)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2022-09-04 05:23:49 UTC

Updated at

2022-09-04 05:23:49 UTC

NP-MRD ID

NP0188981

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Description

174721-08-5 Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol is found in Panax ginseng. 174721-08-5 Is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161523222D          

 44 48  0  0  0  0            999 V2000
   -2.8505   -2.4190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0332   -2.3061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269   -2.9574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7096   -2.8446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3987   -2.0804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4185   -1.9676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7294   -1.2034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9249   -2.6189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6955   -3.4114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3784   -3.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0297   -3.3680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2274   -4.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7494   -2.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2812   -1.9614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0009   -1.1854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0934   -2.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3737   -2.8825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1858   -3.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9055   -2.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7176   -2.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5297   -2.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8100   -3.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6221   -3.4634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2782   -3.9489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9917   -4.3631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9942   -4.7234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4661   -3.8037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9343   -4.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1221   -4.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -3.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5309   -4.2774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2146   -5.2103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6827   -5.8410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9630   -6.6169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4312   -7.2476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7115   -8.0235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5236   -8.1688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6191   -7.1024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0873   -7.7331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3388   -6.3265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5267   -6.1813    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8706   -5.6958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5903   -4.9199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7223   -1.5419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  4  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  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
 11 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 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
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 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
 24 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 11 30  1  0  0  0  0
 17 30  1  0  0  0  0
 30 31  1  0  0  0  0
 28 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 35 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 33 42  1  0  0  0  0
 42 43  1  0  0  0  0
  2 44  1  0  0  0  0
M  END

     RDKit          3D

104108  0  0  0  0  0  0  0  0999 V2000
    8.3530    2.8566   -1.2622 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9569    1.4733   -0.8439 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9871    0.5973   -0.2243 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7157    1.0878   -1.0411 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6993    1.9854   -1.6662 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2149    1.3396   -2.8880 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9944    1.0066   -3.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7061    0.3440   -4.4728 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8454    1.2000   -2.2355 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7621    2.0839   -2.8068 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4480    1.5348   -2.3673 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6854    0.1128   -1.9023 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0794   -0.7793   -2.9660 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1601   -0.1233   -1.8938 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7190   -0.6031   -0.6093 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9793   -1.1849   -0.9038 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8806   -1.6527    0.0820 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3988   -1.4200   -0.0200 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3942   -1.9065    1.1712 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0801   -1.2666    2.4765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0082   -3.3849    1.3066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1441   -4.3144    1.0042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2605   -3.9447    1.9267 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2163   -4.9468    1.8767 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8105   -2.5723    1.6510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2254   -1.9032    2.9125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0716   -2.7851    0.8071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8466   -1.8276    0.7947 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2420   -0.4054    0.4739 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5598   -0.2441    0.2069 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2220    0.8059    0.8043 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1885    0.3843    1.7007 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6129    1.3218    2.5945 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8092    1.2090    3.8657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2066    2.1537    4.8119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4831    2.7374    2.0698 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4191    3.5183    2.7283 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7703    2.6883    0.5674 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1085    2.3671    0.3546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8217    1.7705   -0.1585 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8334    2.4949   -0.8278 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4692   -0.1166   -0.8361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0209   -0.0763   -0.5496 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3806    1.0894    0.3054 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2404    3.0167   -2.3489 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4190    3.0441   -1.0199 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7205    3.5703   -0.6825 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8568    0.4346   -0.8902 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3060    1.1028    0.7332 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5252   -0.3918   -0.0108 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4003    0.0986   -0.7509 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2516    2.9259   -1.9423 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9269    2.2478   -0.9628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9887    1.1234   -3.6640 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3420    0.8366   -5.2612 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6442    0.4694   -4.7237 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0542   -0.6882   -4.4069 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1828    1.7002   -1.3140 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9008    3.1508   -2.4643 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9097    2.1300   -3.8991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2134    1.5744   -3.2871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1065    2.1578   -1.6429 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1940   -1.8423   -2.8217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6674   -0.5435   -3.9045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9555   -0.4422   -3.2617 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4778   -0.8324   -2.6932 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9741    0.2510    0.0529 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0791   -2.0389   -0.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1926   -2.6321   -0.3937 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2604   -1.7275    1.1213 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0547   -2.1421   -0.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0061   -1.1506    2.6080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6711   -0.3827    2.7452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3571   -2.0280    3.2747 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3088   -3.6304    2.3622 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8295   -3.6793    0.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7934   -5.3317    1.3231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4135   -4.3905   -0.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8433   -3.9167    2.9616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3013   -5.4569    2.7027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0035   -0.8342    2.9613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3291   -2.0030    3.1096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7586   -2.4709    3.7720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3517   -3.8760    0.7573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9561   -2.3044    1.2723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9162   -2.5023   -0.2542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9001   -2.3808   -0.1996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8961    0.3471    1.2068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4680    1.3518    1.4198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6762    1.1050    2.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7129    1.3452    3.6564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9050    0.2079    4.3322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4385    2.3590    5.4047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4864    3.1096    2.2886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0939    4.4634    2.7930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5892    3.7223    0.1962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2319    1.4464    0.7302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4672    1.2211   -0.9090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9496    2.3514   -1.7997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8084    0.7548   -1.3629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6625   -1.0149   -1.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5587    1.6934    0.4947 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1457    1.7749   -0.1153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7723    0.8413    1.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  6
 12 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  1
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 25 28  1  0
 28 29  1  0
 29 42  1  0
 42 43  1  0
 43 44  1  1
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 33 36  1  0
 36 37  1  0
 36 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 14  9  1  0
 43 18  1  0
 40 31  1  0
 43 12  1  0
 28 19  1  0
  1 45  1  0
  1 46  1  0
  1 47  1  0
  3 48  1  0
  3 49  1  0
  3 50  1  0
  4 51  1  0
  5 52  1  0
  5 53  1  0
  6 54  1  0
  8 55  1  0
  8 56  1  0
  8 57  1  0
  9 58  1  1
 10 59  1  0
 10 60  1  0
 11 61  1  0
 11 62  1  0
 13 63  1  0
 13 64  1  0
 13 65  1  0
 14 66  1  6
 15 67  1  1
 16 68  1  0
 17 69  1  0
 17 70  1  0
 18 71  1  6
 20 72  1  0
 20 73  1  0
 20 74  1  0
 21 75  1  0
 21 76  1  0
 22 77  1  0
 22 78  1  0
 23 79  1  1
 24 80  1  0
 26 81  1  0
 26 82  1  0
 26 83  1  0
 27 84  1  0
 27 85  1  0
 27 86  1  0
 28 87  1  6
 29 88  1  1
 42100  1  0
 42101  1  0
 44102  1  0
 44103  1  0
 44104  1  0
 31 89  1  1
 33 90  1  1
 34 91  1  0
 34 92  1  0
 35 93  1  0
 36 94  1  6
 37 95  1  0
 38 96  1  6
 39 97  1  0
 40 98  1  6
 41 99  1  0
M  END


  Mrv1533004161523222D          

 44 48  0  0  0  0            999 V2000
   -2.8505   -2.4190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0332   -2.3061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269   -2.9574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7096   -2.8446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3987   -2.0804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4185   -1.9676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7294   -1.2034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9249   -2.6189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6955   -3.4114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3784   -3.8744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0297   -3.3680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2274   -4.1690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7494   -2.5921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2812   -1.9614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0009   -1.1854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0934   -2.1066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3737   -2.8825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1858   -3.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9055   -2.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7176   -2.3970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5297   -2.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8100   -3.3182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6221   -3.4634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2782   -3.9489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9917   -4.3631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9942   -4.7234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4661   -3.8037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9343   -4.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1221   -4.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8418   -3.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5309   -4.2774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2146   -5.2103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6827   -5.8410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9630   -6.6169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4312   -7.2476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7115   -8.0235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5236   -8.1688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6191   -7.1024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0873   -7.7331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3388   -6.3265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5267   -6.1813    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8706   -5.6958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5903   -4.9199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7223   -1.5419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  4  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  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
 11 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 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
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 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
 24 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 11 30  1  0  0  0  0
 17 30  1  0  0  0  0
 30 31  1  0  0  0  0
 28 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 35 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 33 42  1  0  0  0  0
 42 43  1  0  0  0  0
  2 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0188981

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC=C(C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(CC21C)OC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C36H60O8/c1-19(2)10-9-11-20(3)21-12-15-35(7)27(21)22(38)16-25-34(6)14-13-26(39)33(4,5)31(34)23(17-36(25,35)8)43-32-30(42)29(41)28(40)24(18-37)44-32/h10-11,21-32,37-42H,9,12-18H2,1-8H3

> <INCHI_KEY>
OZTXYFOXQFKYRP-UHFFFAOYSA-N

> <FORMULA>
C36H60O8

> <MOLECULAR_WEIGHT>
620.868

> <EXACT_MASS>
620.428818892

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
71.36510792190423

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[5,16-dihydroxy-2,6,6,10,11-pentamethyl-14-(6-methylhepta-2,5-dien-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
3.49

> <JCHEM_LOGP>
3.3619651059999986

> <ALOGPS_LOGS>
-4.39

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.188126658752765

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.209174729361132

> <JCHEM_PKA_STRONGEST_BASIC>
-0.44687248345506847

> <JCHEM_POLAR_SURFACE_AREA>
139.84

> <JCHEM_REFRACTIVITY>
170.40960000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.55e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{[5,16-dihydroxy-2,6,6,10,11-pentamethyl-14-(6-methylhepta-2,5-dien-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -5.321  -4.515   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.795  -4.305   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.850  -5.521   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.325  -5.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.744  -3.883   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.781  -3.673   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.362  -2.246   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.726  -4.889   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.298  -6.368   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.573  -7.232   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.789  -6.287   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.158  -7.782   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.266  -4.839   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.258  -3.661   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.735  -2.213   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.774  -3.932   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.297  -5.381   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.813  -5.652   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.290  -4.203   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.806  -4.474   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.322  -4.746   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.845  -6.194   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      12.361  -6.465   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       9.853  -7.371   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.184  -8.144   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.322  -8.817   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.337  -7.100   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.344  -8.277   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.828  -8.006   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.305  -6.558   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.724  -7.984   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.867  -9.726   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       6.874 -10.903   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       7.398 -12.352   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       6.405 -13.529   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.928 -14.977   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       8.444 -15.248   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       4.889 -13.258   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       3.896 -14.435   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       4.366 -11.809   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       2.850 -11.538   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       5.358 -10.632   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       4.835  -9.184   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -3.215  -2.878   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   44                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   30                                             
CONECT   12   11                                                            
CONECT   13   11    8   14                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   30                                                  
CONECT   18   17   19   20   27                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   24   18   28                                                  
CONECT   28   27   29   32                                                  
CONECT   29   28   30                                                       
CONECT   30   29   11   17   31                                             
CONECT   31   30                                                            
CONECT   32   28   33                                                       
CONECT   33   32   34   42                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   38                                                  
CONECT   36   35   37                                                       
CONECT   37   36                                                            
CONECT   38   35   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   33   43                                                  
CONECT   43   42                                                            
CONECT   44    2                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₆₀O₈

Average Mass

620.8680 Da

Monoisotopic Mass

620.42882 Da

IUPAC Name

2-{[5,16-dihydroxy-2,6,6,10,11-pentamethyl-14-(6-methylhepta-2,5-dien-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

2-{[5,16-dihydroxy-2,6,6,10,11-pentamethyl-14-(6-methylhepta-2,5-dien-2-yl)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-8-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CC(C)=CCC=C(C)C1CCC2(C)C1C(O)CC1C3(C)CCC(O)C(C)(C)C3C(CC21C)OC1OC(CO)C(O)C(O)C1O

InChI Identifier

InChI=1S/C36H60O8/c1-19(2)10-9-11-20(3)21-12-15-35(7)27(21)22(38)16-25-34(6)14-13-26(39)33(4,5)31(34)23(17-36(25,35)8)43-32-30(42)29(41)28(40)24(18-37)44-32/h10-11,21-32,37-42H,9,12-18H2,1-8H3

InChI Key

OZTXYFOXQFKYRP-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
Panax ginseng	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
3-hydroxysteroid
12-hydroxysteroid
Hydroxysteroid
Steroid
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Oxane
Monosaccharide
Cyclic alcohol
Secondary alcohol
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Primary alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.49	ALOGPS
logP	3.36	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-0.45	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	139.84 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	170.41 m³·mol⁻¹	ChemAxon
Polarizability	71.37 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

73812670

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0188981)

MOL for NP0188981 (2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0188981 (2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0188981 (2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0188981 (2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0188981 (2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0188981 (2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0188981 (2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0188981 (2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0188981 (2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0188981 (2-{[7,11-dihydroxy-3a,3b,6,6,9a-pentamethyl-1-(6-methylhepta-2,5-dien-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)