NP-MRD: Showing NP-Card for (1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0194540)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 12:12:48 UTC

Updated at

2022-09-04 12:12:48 UTC

NP-MRD ID

NP0194540

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

Description

(1S,4S,5R,8R,10S,13S,14R,17S,18R,19S,20R)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]Tetracos-15-en-10-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate is found in Eucalyptus tereticornis. Based on a literature review very few articles have been published on (1S,4S,5R,8R,10S,13S,14R,17S,18R,19S,20R)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]Tetracos-15-en-10-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042214122D          

 44 50  0  0  1  0            999 V2000
    3.1500   -1.2737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5377   -0.7592    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7220   -1.2239    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6932   -2.0484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0223   -0.7868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0510    0.0377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7794    0.4251    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2497    1.1534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1044    1.1199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4536    0.3247    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9046    1.0155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9772   -0.4180    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4630   -1.1186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2975   -1.1122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7033   -0.3890    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5283   -0.3877    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1168   -1.1028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9418   -1.1016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7668   -1.1004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1783   -0.3853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0033   -0.3841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4168   -1.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2418   -1.0968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0054   -1.8130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4189   -2.5269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0075   -3.2420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4210   -3.9559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0096   -4.6709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1846   -4.6721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7731   -5.3872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7710   -3.9583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1825   -3.2432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7647    0.3285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5396    0.6118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6203    1.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9397    0.3273    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5262    1.0412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7012    1.0400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2897    0.3249    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3753    1.1455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2247   -0.9111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5162   -0.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7327   -0.6580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4791   -0.0121    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 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
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 26 32  1  0  0  0  0
 20 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 16 36  1  0  0  0  0
 36 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 15 39  1  0  0  0  0
 10 39  1  0  0  0  0
 39 40  1  1  0  0  0
 12 41  1  1  0  0  0
 41 42  1  0  0  0  0
  7 42  1  1  0  0  0
 42 43  2  0  0  0  0
 44 12  1  6  0  0  0
  2 44  1  0  0  0  0
  7 44  1  0  0  0  0
M  END

     RDKit          3D

 96102  0  0  0  0  0  0  0  0999 V2000
   -5.3283   -0.3885   -2.4038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9415   -0.0698   -1.0633 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.3538   -0.7115   -1.1336 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.3661    0.2625   -1.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7593   -1.2613    0.2111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2836   -0.4316    1.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8086   -0.2879    1.4008 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2804    0.9584    1.9625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0025    1.5049    1.4541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1721    0.6363    0.5804 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9835    1.4285   -0.7041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8387   -0.6882    0.3298 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0353   -1.6162   -0.4870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7546   -1.4899   -0.5701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0333   -0.4311    0.1320 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4071   -0.7557    0.4632 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5687   -1.7334    1.5704 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9823   -1.4248   -0.7719 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4256   -1.3029   -0.9830 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1468   -0.0980   -0.5390 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5535   -0.3350   -0.3551 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5292    0.2905   -1.1146 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1267    1.0972   -1.9942 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9630    0.0261   -0.9056 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9110    0.5909   -1.5978 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3306    0.3640   -1.4305 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8405   -0.5009   -0.4907 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2129   -0.6970   -0.3607 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0942   -0.0232   -1.1772 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4778   -0.1810   -1.0908 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5982    0.8379   -2.1138 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2288    1.0239   -2.2327 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5873    0.5468    0.6940 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9975    2.0367    0.7321 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2051   -0.0755    1.8937 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1265    0.5446    0.6108 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4362    1.3199    1.7411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9502    1.6520    1.2444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7603    0.3765    1.1418 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8825   -0.1491    2.5304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8555   -1.3820    1.6032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1334   -1.4213    2.1469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6423   -2.1550    3.0064 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2695   -0.6929    0.0455 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7909   -1.2720   -2.8891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2518   -0.5425   -2.3922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5490    0.4669   -3.0763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2128    1.0213   -0.9501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3445   -1.5837   -1.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1045    1.3227   -1.4816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3575    0.0054   -1.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5005    0.1416   -2.7957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4659   -2.3218    0.3449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8835   -1.2695    0.2362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6683   -0.9084    2.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7746    0.5688    1.2913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1270    1.7142    1.9305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1599    0.8079    3.0805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2742    2.5034    0.9727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3424    1.8866    2.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5553    2.4180   -0.4139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5480    0.9178   -1.5321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9921    1.8030   -1.0801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5492   -2.4057   -1.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1739   -2.1790   -1.1787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8399    0.3227   -0.7181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5198   -2.3368    1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6137   -1.3461    2.5812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2193   -2.5315    1.4221 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7379   -2.5270   -0.7777 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4733   -1.0478   -1.7082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6387   -1.4304   -2.0869 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9339   -2.1882   -0.5207 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0726    0.6549   -1.3722 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2334   -0.6764   -0.1340 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5731    1.2981   -2.3703 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2011   -1.0576    0.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6157   -1.3880    0.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.0532    0.3898   -0.4954 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.2852    1.3814   -2.7707 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9150    1.7223   -2.9985 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0003    2.1535    0.2800 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2362    2.6740    0.2733 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0841    2.3530    1.8078 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1503    0.4677    2.1252 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5951   -0.0130    2.8217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5638   -1.1302    1.7004 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8546    1.1407   -0.3156 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5296    0.6830    2.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0501    2.2464    1.8725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4389    2.4325    1.8632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7262    2.0635    0.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8780    0.0933    3.0225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7793   -1.2213    2.6604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2123    0.3350    3.2856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5249   -1.8066   -0.0306 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  6
 10 12  1  0
 12 41  1  1
 41 42  1  0
 42 43  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 29 31  1  0
 31 32  2  0
 20 33  1  0
 33 34  1  0
 33 35  1  0
 33 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  1
 12 44  1  0
 44  2  1  0
  2  1  1  0
  2  3  1  0
  7 42  1  1
 39 15  1  0
 44  7  1  0
 39 10  1  0
 36 16  1  0
 32 26  1  0
  4 50  1  0
  4 51  1  0
  4 52  1  0
  3 49  1  6
  5 53  1  0
  5 54  1  0
  6 55  1  0
  6 56  1  0
  8 57  1  0
  8 58  1  0
  9 59  1  0
  9 60  1  0
 11 61  1  0
 11 62  1  0
 11 63  1  0
 13 64  1  0
 14 65  1  0
 15 66  1  6
 17 67  1  0
 17 68  1  0
 17 69  1  0
 18 70  1  0
 18 71  1  0
 19 72  1  0
 19 73  1  0
 20 74  1  6
 24 75  1  0
 25 76  1  0
 27 77  1  0
 28 78  1  0
 30 79  1  0
 31 80  1  0
 32 81  1  0
 34 82  1  0
 34 83  1  0
 34 84  1  0
 35 85  1  0
 35 86  1  0
 35 87  1  0
 36 88  1  6
 37 89  1  0
 37 90  1  0
 38 91  1  0
 38 92  1  0
 40 93  1  0
 40 94  1  0
 40 95  1  0
 44 96  1  6
  2 48  1  1
  1 45  1  0
  1 46  1  0
  1 47  1  0
M  END


  Mrv1652309042214122D          

 44 50  0  0  1  0            999 V2000
    3.1500   -1.2737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5377   -0.7592    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7220   -1.2239    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6932   -2.0484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0223   -0.7868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0510    0.0377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7794    0.4251    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2497    1.1534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1044    1.1199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4536    0.3247    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9046    1.0155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9772   -0.4180    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4630   -1.1186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2975   -1.1122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7033   -0.3890    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5283   -0.3877    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1168   -1.1028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9418   -1.1016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7668   -1.1004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1783   -0.3853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0033   -0.3841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4168   -1.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2418   -1.0968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0054   -1.8130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4189   -2.5269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0075   -3.2420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4210   -3.9559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0096   -4.6709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1846   -4.6721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7731   -5.3872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7710   -3.9583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1825   -3.2432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7647    0.3285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5396    0.6118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6203    1.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9397    0.3273    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5262    1.0412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7012    1.0400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2897    0.3249    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3753    1.1455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2247   -0.9111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5162   -0.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7327   -0.6580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4791   -0.0121    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 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
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 26 32  1  0  0  0  0
 20 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 16 36  1  0  0  0  0
 36 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 15 39  1  0  0  0  0
 10 39  1  0  0  0  0
 39 40  1  1  0  0  0
 12 41  1  1  0  0  0
 41 42  1  0  0  0  0
  7 42  1  1  0  0  0
 42 43  2  0  0  0  0
 44 12  1  6  0  0  0
  2 44  1  0  0  0  0
  7 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0194540

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@@]23CC[C@]4(C)[C@](OC2=O)(C=C[C@@H]2[C@@]5(C)CC[C@H](OC(=O)\C=C\C6=CC=C(O)C=C6)C(C)(C)[C@@H]5CC[C@@]42C)[C@@H]3[C@H]1C

> <INCHI_IDENTIFIER>
InChI=1S/C39H52O5/c1-24-14-20-38-23-22-37(7)36(6)19-15-28-34(3,4)30(43-31(41)13-10-26-8-11-27(40)12-9-26)17-18-35(28,5)29(36)16-21-39(37,44-33(38)42)32(38)25(24)2/h8-13,16,21,24-25,28-30,32,40H,14-15,17-20,22-23H2,1-7H3/b13-10+/t24-,25+,28+,29-,30+,32-,35+,36-,37+,38+,39+/m1/s1

> <INCHI_KEY>
RIHYZKAATDJNMK-LDPPHYEASA-N

> <FORMULA>
C39H52O5

> <MOLECULAR_WEIGHT>
600.84

> <EXACT_MASS>
600.381474774

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
96

> <JCHEM_AVERAGE_POLARIZABILITY>
70.40019124920957

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4S,5R,8R,10S,13S,14R,17S,18R,19S,20R)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracos-15-en-10-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
9.094821180333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.398614366554039

> <JCHEM_PKA_STRONGEST_BASIC>
-5.954731874958935

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
173.31810000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,5R,8R,10S,13S,14R,17S,18R,19S,20R)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracos-15-en-10-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       5.880  -2.378   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.737  -1.417   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.214  -2.285   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.161  -3.824   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.908  -1.469   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.962   0.070   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.322   0.793   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.199   2.153   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.795   2.091   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.447   0.606   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.289   1.896   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.557  -0.780   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.464  -2.088   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.022  -2.076   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.779  -0.726   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.319  -0.724   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.551  -2.059   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.091  -2.056   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.631  -2.054   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.399  -0.719   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      14.939  -0.717   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      15.711  -2.050   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      17.251  -2.047   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      14.943  -3.384   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      15.715  -4.717   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.947  -6.052   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.719  -7.384   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      14.951  -8.719   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.411  -8.721   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      12.643 -10.056   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      12.639  -7.389   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.407  -6.054   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.628   0.613   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      14.074   1.142   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.358   2.129   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      11.088   0.611   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.316   1.944   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.776   1.941   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.008   0.606   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.167   2.138   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       4.153  -1.701   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       2.830  -0.746   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       1.368  -1.228   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       4.628  -0.023   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   44                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   42   44                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   39                                             
CONECT   11   10                                                            
CONECT   12   10   13   41   44                                             
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   39                                                  
CONECT   16   15   17   18   36                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   33                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   32                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   26                                                       
CONECT   33   20   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   33   16   37                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   15   10   40                                             
CONECT   40   39                                                            
CONECT   41   12   42                                                       
CONECT   42   41    7   43                                                  
CONECT   43   42                                                            
CONECT   44   12    2    7                                                  
MASTER        0    0    0    0    0    0    0    0   44    0  100    0
END

View in JSmol

Synonyms

Value	Source
(1S,4S,5R,8R,10S,13S,14R,17S,18R,19S,20R)-4,5,9,9,13,19,20-Heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0,.0,.0,.0,]tetracos-15-en-10-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₃₉H₅₂O₅

Average Mass

600.8400 Da

Monoisotopic Mass

600.38147 Da

IUPAC Name

(1S,4S,5R,8R,10S,13S,14R,17S,18R,19S,20R)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracos-15-en-10-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

(1S,4S,5R,8R,10S,13S,14R,17S,18R,19S,20R)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0^{1,18}.0^{4,17}.0^{5,14}.0^{8,13}]tetracos-15-en-10-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@@]23CC[C@]4(C)[C@](OC2=O)(C=C[C@@H]2[C@@]5(C)CC[C@H](OC(=O)\C=C\C6=CC=C(O)C=C6)C(C)(C)[C@@H]5CC[C@@]42C)[C@@H]3[C@H]1C

InChI Identifier

InChI=1S/C39H52O5/c1-24-14-20-38-23-22-37(7)36(6)19-15-28-34(3,4)30(43-31(41)13-10-26-8-11-27(40)12-9-26)17-18-35(28,5)29(36)16-21-39(37,44-33(38)42)32(38)25(24)2/h8-13,16,21,24-25,28-30,32,40H,14-15,17-20,22-23H2,1-7H3/b13-10+/t24-,25+,28+,29-,30+,32-,35+,36-,37+,38+,39+/m1/s1

InChI Key

RIHYZKAATDJNMK-LDPPHYEASA-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
Eucalyptus tereticornis	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
Coumaric acid ester
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Caprolactone
Styrene
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Oxepane
Phenol
Fatty acyl
Benzenoid
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Gamma butyrolactone
Tetrahydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	9.09	ChemAxon
pKa (Strongest Acidic)	9.4	ChemAxon
pKa (Strongest Basic)	-6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	173.32 m³·mol⁻¹	ChemAxon
Polarizability	70.4 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

163189189

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0194540)

MOL for NP0194540 ((1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D MOL for NP0194540 ((1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D SDF for NP0194540 ((1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D-SDF for NP0194540 ((1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

PDB for NP0194540 ((1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D PDB for NP0194540 ((1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

SMILES for NP0194540 ((1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

INCHI for NP0194540 ((1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

Structure for NP0194540 ((1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D Structure for NP0194540 ((1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20r)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)