NP-MRD: Showing NP-Card for (1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate (NP0291106)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 22:04:35 UTC

Updated at

2022-09-09 22:04:36 UTC

NP-MRD ID

NP0291106

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate

Description

(1R,2R,4R,6S,8S,9S,10S,11S,13S)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]Hexadecan-11-yl acetate belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. (1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate is found in Isodon adenanthus, Isodon calcicola, Isodon nervosus, Isodon tenuifolius and Isodon wikstroemioides. Based on a literature review very few articles have been published on (1R,2R,4R,6S,8S,9S,10S,11S,13S)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]Hexadecan-11-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102200042D          

 35 38  0  0  1  0            999 V2000
   -1.5987   -0.3788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7854   -0.2403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1637   -0.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3012   -1.6618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6469   -0.4671    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1725    0.0666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4028    0.5335    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1586    1.1914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0038    1.0309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5595    1.6407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3092    2.4269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5032    2.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8648    3.0367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2474    0.1857    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0661   -0.0115    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8257    0.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6242    0.5960    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3771    1.3831    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9352    1.9907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6881    2.7778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7404    1.8111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4294    0.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6765   -0.3707    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4817   -0.5503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1184   -0.9782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8017   -1.7400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8136   -1.4224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3132   -0.7987    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7596   -1.4229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0191   -2.2061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9506   -1.2543    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4166   -1.8832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6941   -2.6601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5057   -2.8081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1601   -3.2889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  1  0  0  0
  7  6  1  1  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  9 14  1  0  0  0  0
 14  5  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
  5 31  1  0  0  0  0
 31 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
M  END

     RDKit          3D

 69 72  0  0  0  0  0  0  0  0999 V2000
   -1.5785    0.2226   -4.0720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7620   -0.1576   -2.8117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1065   -1.2363   -2.0716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5421   -2.2108   -2.5716 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3241   -0.8116   -0.6586 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8032   -0.5045   -0.8016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7484    0.5210   -1.9002 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2158    1.7692   -1.2889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3975    1.4873    0.0031 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8592    2.7265    0.3044 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2551    3.3825    1.4706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7231    4.7143    1.8636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1022    2.8060    2.2124 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4670    0.3846   -0.3804 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7131    0.1378    0.4979 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5616    0.6419    1.9108 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9387    0.8978   -0.0372 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5843    2.1548   -0.4505 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7132    2.6118   -1.7512 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3168    3.9826   -2.1710 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1945    1.7679   -2.5476 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0610    0.8195    0.9458 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4668   -0.5668    1.2647 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6450   -0.9141    0.5501 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4160   -1.6156    1.2019 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1486   -2.2144    2.5886 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0629   -2.7940    0.4230 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1870   -1.2990    0.4311 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1537   -2.3116    0.6511 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3204   -3.4273    1.0657 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2432   -1.9168    0.3273 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0511   -2.9722   -0.0846 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1492   -3.4105    0.6393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0140   -4.5220    0.2218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3729   -2.7893    1.7028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8474   -0.3242   -4.6532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1123    1.0290   -4.5240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2623   -1.4179   -1.2721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3339   -0.2505    0.0911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7168    0.6704   -2.3959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5235    2.3323   -1.9497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0617    2.4350   -1.0409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0820    1.1531    0.8014 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0993    4.6346    2.6031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5577    5.2346    2.4053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4825    5.3554    0.9979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0371    0.7416   -1.3705 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9530    1.7000    2.0206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4394    0.5194    2.3272 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3268    0.1027    2.5453 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3145    0.3379   -0.9470 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2334    4.1551   -2.0970 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9272    4.7190   -1.6379 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5811    4.0749   -3.2557 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9320    1.4588    1.8425 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9371    1.3159    0.4191 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8485   -0.5392    2.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3659   -0.9685   -0.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7801   -1.6298    3.3247 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1022   -2.2289    2.8786 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5204   -3.2494    2.6980 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6140   -3.7546    0.7577 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8315   -2.7014   -0.6591 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1498   -2.7738    0.5350 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4609   -1.4008   -0.6701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6596   -1.5497    1.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3467   -5.3308   -0.1821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7345   -4.2338   -0.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5484   -4.9700    1.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 13  2  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 33 35  2  0
 31 29  1  0
 29 30  2  0
 29 28  1  0
 28 25  1  0
 25 26  1  0
 25 27  1  0
 25 23  1  0
 23 24  1  0
 23 22  1  0
 22 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 17 15  1  0
 15 16  1  1
 15 14  1  0
  5  3  1  6
  3  4  2  0
  3  2  1  0
  2  1  2  3
 14  9  1  0
  2  7  1  0
 14  5  1  0
 15 28  1  0
 12 44  1  0
 12 45  1  0
 12 46  1  0
  9 43  1  1
  8 41  1  0
  8 42  1  0
  7 40  1  6
  6 38  1  0
  6 39  1  0
 31 66  1  1
 34 67  1  0
 34 68  1  0
 34 69  1  0
 28 65  1  6
 26 59  1  0
 26 60  1  0
 26 61  1  0
 27 62  1  0
 27 63  1  0
 27 64  1  0
 23 57  1  1
 24 58  1  0
 22 55  1  0
 22 56  1  0
 17 51  1  6
 20 52  1  0
 20 53  1  0
 20 54  1  0
 16 48  1  0
 16 49  1  0
 16 50  1  0
 14 47  1  6
  1 36  1  0
  1 37  1  0
M  END


  Mrv1652309102200042D          

 35 38  0  0  1  0            999 V2000
   -1.5987   -0.3788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7854   -0.2403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1637   -0.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3012   -1.6618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6469   -0.4671    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1725    0.0666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4028    0.5335    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1586    1.1914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0038    1.0309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5595    1.6407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3092    2.4269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5032    2.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8648    3.0367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2474    0.1857    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0661   -0.0115    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8257    0.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6242    0.5960    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3771    1.3831    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9352    1.9907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6881    2.7778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7404    1.8111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4294    0.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6765   -0.3707    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4817   -0.5503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1184   -0.9782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8017   -1.7400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8136   -1.4224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3132   -0.7987    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7596   -1.4229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0191   -2.2061    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9506   -1.2543    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4166   -1.8832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6941   -2.6601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5057   -2.8081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1601   -3.2889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  1  0  0  0
  7  6  1  1  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  9 14  1  0  0  0  0
 14  5  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
  5 31  1  0  0  0  0
 31 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0291106

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@@H]2C[C@@]3([C@@H](OC(C)=O)C(=O)[C@@H]4C(C)(C)[C@@H](O)C[C@H](OC(C)=O)[C@@]4(C)[C@H]13)C(=O)C2=C

> <INCHI_IDENTIFIER>
InChI=1S/C26H34O9/c1-11-15-8-16(33-12(2)27)20-25(7)18(34-13(3)28)9-17(30)24(5,6)21(25)19(31)23(35-14(4)29)26(20,10-15)22(11)32/h15-18,20-21,23,30H,1,8-10H2,2-7H3/t15-,16+,17+,18+,20+,21-,23+,25+,26+/m1/s1

> <INCHI_KEY>
WQVYSFSBBFDGRG-FYHXSELJSA-N

> <FORMULA>
C26H34O9

> <MOLECULAR_WEIGHT>
490.549

> <EXACT_MASS>
490.220282675

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
49.823935995195285

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,4R,6S,8S,9S,10S,11S,13S)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecan-11-yl acetate

> <JCHEM_LOGP>
1.3025754580000015

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.782730205891724

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.116948692442023

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9701089789976143

> <JCHEM_POLAR_SURFACE_AREA>
133.27000000000004

> <JCHEM_REFRACTIVITY>
120.4313

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,4R,6S,8S,9S,10S,11S,13S)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecan-11-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.984  -0.707   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.466  -0.449   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.306  -1.583   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.562  -3.102   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.208  -0.872   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.322   0.124   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.752   0.996   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.296   2.224   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.874   1.924   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.911   3.063   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.444   4.530   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.939   4.859   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.481   5.668   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       2.328   0.347   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.857  -0.022   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.408   1.452   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.899   1.113   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.437   2.582   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.479   3.716   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.018   5.185   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.982   3.381   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.402   0.777   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.863  -0.692   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.366  -1.027   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.821  -1.826   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.230  -3.248   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.119  -2.655   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.318  -1.491   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.285  -2.656   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.769  -4.118   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.774  -2.341   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       0.778  -3.515   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.296  -4.965   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.811  -5.242   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       0.299  -6.139   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   14   31                                             
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9    5   15                                                  
CONECT   15   14   16   17   28                                             
CONECT   16   15                                                            
CONECT   17   15   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   15   29                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29    5   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,4R,6S,8S,9S,10S,11S,13S)-2,8-Bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0,.0,]hexadecan-11-yl acetic acid	Generator

Chemical Formula

C₂₆H₃₄O₉

Average Mass

490.5490 Da

Monoisotopic Mass

490.22028 Da

IUPAC Name

(1R,2R,4R,6S,8S,9S,10S,11S,13S)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecan-11-yl acetate

Traditional Name

(1R,2R,4R,6S,8S,9S,10S,11S,13S)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecan-11-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@@H]2C[C@@]3([C@@H](OC(C)=O)C(=O)[C@@H]4C(C)(C)[C@@H](O)C[C@H](OC(C)=O)[C@@]4(C)[C@H]13)C(=O)C2=C

InChI Identifier

InChI=1S/C26H34O9/c1-11-15-8-16(33-12(2)27)20-25(7)18(34-13(3)28)9-17(30)24(5,6)21(25)19(31)23(35-14(4)29)26(20,10-15)22(11)32/h15-18,20-21,23,30H,1,8-10H2,2-7H3/t15-,16+,17+,18+,20+,21-,23+,25+,26+/m1/s1

InChI Key

WQVYSFSBBFDGRG-FYHXSELJSA-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
Isodon adenanthus	LOTUS Database	35616633
Isodon calcicola	LOTUS Database	35616633
Isodon nervosus	LOTUS Database	35616633
Isodon tenuifolius	LOTUS Database	35616633
Isodon wikstroemioides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Tricarboxylic acid or derivatives
Alpha-acyloxy ketone
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	1.3	ChemAxon
pKa (Strongest Acidic)	14.12	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	133.27 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	120.43 m³·mol⁻¹	ChemAxon
Polarizability	49.82 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

24715558

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15011073

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate (NP0291106)

MOL for NP0291106 ((1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate)

3D MOL for NP0291106 ((1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate)

3D SDF for NP0291106 ((1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate)

3D-SDF for NP0291106 ((1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate)

PDB for NP0291106 ((1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate)

3D PDB for NP0291106 ((1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate)

SMILES for NP0291106 ((1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate)

INCHI for NP0291106 ((1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate)

Structure for NP0291106 ((1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate)

3D Structure for NP0291106 ((1r,2r,4r,6s,8s,9s,10s,11s,13s)-2,8-bis(acetyloxy)-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxotetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-11-yl acetate)