NP-MRD: Showing NP-Card for methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate (NP0316160)

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Record Information

Version

2.0

Created at

2022-09-11 15:10:01 UTC

Updated at

2022-09-11 15:10:01 UTC

NP-MRD ID

NP0316160

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate

Description

Methyl (1'R,3S,5'S,6R,11'R,12'R)-6-methoxy-3'-methyl-6-(propan-2-yl)-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]Pentadecan]-8'(14')-ene-12'-carboxylate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate is found in Daphniphyllum macropodum. Based on a literature review very few articles have been published on methyl (1'R,3S,5'S,6R,11'R,12'R)-6-methoxy-3'-methyl-6-(propan-2-yl)-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]Pentadecan]-8'(14')-ene-12'-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112217102D          

 30 34  0  0  1  0            999 V2000
    5.0510    2.3167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9028    1.5051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1258    1.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4971    1.7618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9777    0.4161    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2340    0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3438   -0.7587    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2792   -0.4068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8084   -0.9666    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9866   -0.8941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7130   -1.7493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7581   -2.1251    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4250   -2.6107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2205   -2.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5456   -1.6338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1554   -0.9069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5471   -0.1809    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4691   -0.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3575   -1.4874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7220   -1.3009    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0613   -1.7950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3031   -1.4700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2054   -0.6507    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8335    0.0857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2853    0.7760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4156   -0.8891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1857   -0.3243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2272   -1.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8661   -0.1566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6243   -0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
  7 16  1  0  0  0  0
 17 16  1  1  0  0  0
  5 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 19  1  0  0  0  0
 12 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 23 26  1  6  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 23 29  1  0  0  0  0
 29 30  1  0  0  0  0
 20 30  1  0  0  0  0
M  END

     RDKit          3D

 69 73  0  0  0  0  0  0  0  0999 V2000
   -3.2201    3.7560   -0.4941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7116    2.5408    0.0572 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8412    2.3089    1.4185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4043    3.1795    2.1250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3203    1.0637    1.9844 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8189    0.8959    1.6717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7156   -0.3636    0.8760 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5094   -1.5446    1.7975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7282   -2.7177    1.0682 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8231   -3.5402    1.4505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1940   -2.8729   -0.2139 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1529   -1.6492   -0.9913 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6883   -1.4971   -2.2070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0497   -0.9939   -2.1192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6492   -0.7914   -0.7968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0605   -0.4912    0.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9935   -0.1319    1.4094 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2756    0.0918    0.6939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1231   -0.8870   -0.4790 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3734   -0.4200   -0.1517 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6033    0.8213   -0.9125 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7909    1.6496   -0.5612 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0487    0.8353   -0.1855 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2898    1.0067    1.1479 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2222    0.2739    1.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1558    1.3125   -1.0494 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4875    0.6542   -0.9098 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7460    1.3176   -2.5240 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6711   -0.4850   -0.3667 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6772   -0.7183    0.6165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0915    3.6845   -1.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3125    3.7729   -0.2865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6937    4.6346   -0.0868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4392    1.0616    3.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2558    0.7577    2.6184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5165    1.8054    1.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4613   -1.4866    2.3374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2686   -1.4569    2.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6774   -4.5715    1.0726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8191   -3.1580    1.2138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7919   -3.6377    2.5754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9332   -3.4581   -0.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6774   -3.5916   -0.1222 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1849   -1.8582   -1.4360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7174   -2.5453   -2.6568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1375   -0.9360   -3.0260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1714   -0.0533   -2.7447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7585   -1.6981   -2.6551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1492   -0.9680    2.1371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4879    1.0919    0.3379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1426   -0.2742    1.3073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7484   -0.6171   -1.3284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3174   -1.9183   -0.1903 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6456    0.6289   -2.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2763    1.5416   -0.8457 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6212    2.3574    0.2750 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0312    2.2822   -1.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2755    0.3686    1.5005 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0056   -0.8487    1.7344 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2308    0.4672    2.9061 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3365    2.4072   -0.7948 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9515    0.6288   -1.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4455   -0.4117   -0.6371 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1951    1.2808   -0.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4870    2.3488   -2.7955 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6186    1.0435   -3.1659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7580   -1.8179    0.8120 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7703   -0.0875    1.4932 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  7  6  1  1
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  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
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 14 15  1  0
 15 16  2  0
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 12 20  1  0
 20 21  1  6
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 22 23  1  0
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 29 30  1  0
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 26 28  1  0
 17  5  1  0
 30 20  1  0
 16  7  1  0
 20  7  1  0
 19 15  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  5 34  1  1
  6 35  1  0
  6 36  1  0
  8 37  1  0
  8 38  1  0
 10 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  6
 13 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 17 49  1  1
 18 50  1  0
 18 51  1  0
 19 52  1  0
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 21 54  1  0
 21 55  1  0
 22 56  1  0
 22 57  1  0
 25 58  1  0
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 25 60  1  0
 30 68  1  0
 30 69  1  0
 26 61  1  0
 27 62  1  0
 27 63  1  0
 27 64  1  0
 28 65  1  0
 28 66  1  0
 28 67  1  0
M  END


  Mrv1652309112217102D          

 30 34  0  0  1  0            999 V2000
    5.0510    2.3167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9028    1.5051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1258    1.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4971    1.7618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9777    0.4161    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2340    0.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3438   -0.7587    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2792   -0.4068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8084   -0.9666    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9866   -0.8941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7130   -1.7493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7581   -2.1251    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4250   -2.6107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2205   -2.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5456   -1.6338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1554   -0.9069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5471   -0.1809    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4691   -0.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3575   -1.4874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7220   -1.3009    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0613   -1.7950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3031   -1.4700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2054   -0.6507    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8335    0.0857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2853    0.7760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4156   -0.8891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1857   -0.3243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2272   -1.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8661   -0.1566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6243   -0.4817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
  7 16  1  0  0  0  0
 17 16  1  1  0  0  0
  5 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 15 19  1  0  0  0  0
 12 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 23 26  1  6  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 23 29  1  0  0  0  0
 29 30  1  0  0  0  0
 20 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0316160

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H]1C[C@@]23CN(C)C[C@@H](CCC4=C2[C@@H]1CC4)[C@@]31CC[C@@](OC)(OC1)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C25H39NO4/c1-16(2)25(29-5)11-10-23(15-30-25)18-8-6-17-7-9-19-20(22(27)28-4)12-24(23,21(17)19)14-26(3)13-18/h16,18-20H,6-15H2,1-5H3/t18-,19-,20-,23+,24-,25-/m1/s1

> <INCHI_KEY>
NYUJYFZXEOGHOB-IWIGTOSWSA-N

> <FORMULA>
C25H39NO4

> <MOLECULAR_WEIGHT>
417.59

> <EXACT_MASS>
417.28790874

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
47.70856479439815

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1'R,3S,5'S,6R,11'R,12'R)-6-methoxy-3'-methyl-6-(propan-2-yl)-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1^{1,5}.0^{11,14}]pentadecan]-8'(14')-ene-12'-carboxylate

> <JCHEM_LOGP>
3.206386793666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
10.086378605467866

> <JCHEM_POLAR_SURFACE_AREA>
48.0

> <JCHEM_REFRACTIVITY>
117.32349999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1'R,3S,5'S,6R,11'R,12'R)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1^{1,5}.0^{11,14}]pentadecan]-8'(14')-ene-12'-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       9.428   4.324   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.152   2.810   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.702   2.292   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.528   3.289   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.425   0.777   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.037   0.110   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.242  -1.416   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.254  -0.759   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       3.376  -1.804   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       1.842  -1.669   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.198  -3.265   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.148  -3.967   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.393  -4.873   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.878  -4.465   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.485  -3.050   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.757  -1.693   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.488  -0.338   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.209  -1.251   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.001  -2.777   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.081  -2.428   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.848  -3.351   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.432  -2.744   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.250  -1.215   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.556   0.160   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.399   1.448   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.776  -1.660   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.347  -0.605   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.424  -3.159   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.483  -0.292   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.899  -0.899   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   16   20                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15    7   17                                                  
CONECT   17   16    5   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   15                                                       
CONECT   20   12    7   21   30                                             
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   26   29                                             
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   23   30                                                       
CONECT   30   29   20                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1'r,3S,5's,6R,11'r,12'r)-6-methoxy-3'-methyl-6-(propan-2-yl)-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1,.0,]pentadecan]-8'(14')-ene-12'-carboxylic acid	Generator

Chemical Formula

C₂₅H₃₉NO₄

Average Mass

417.5900 Da

Monoisotopic Mass

417.28791 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H]1C[C@@]23CN(C)C[C@@H](CCC4=C2[C@@H]1CC4)[C@@]31CC[C@@](OC)(OC1)C(C)C

InChI Identifier

InChI=1S/C25H39NO4/c1-16(2)25(29-5)11-10-23(15-30-25)18-8-6-17-7-9-19-20(22(27)28-4)12-24(23,21(17)19)14-26(3)13-18/h16,18-20H,6-15H2,1-5H3/t18-,19-,20-,23+,24-,25-/m1/s1

InChI Key

NYUJYFZXEOGHOB-IWIGTOSWSA-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
Daphniphyllum macropodum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Azaspirodecane
Ketal
Oxane
Piperidine
Methyl ester
Amino acid or derivatives
Carboxylic acid ester
Tertiary amine
Tertiary aliphatic amine
Acetal
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Azacycle
Organoheterocyclic compound
Organonitrogen compound
Amine
Organopnictogen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
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

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

12080809

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate (NP0316160)

MOL for NP0316160 (methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

3D MOL for NP0316160 (methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

3D SDF for NP0316160 (methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

3D-SDF for NP0316160 (methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

PDB for NP0316160 (methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

3D PDB for NP0316160 (methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

SMILES for NP0316160 (methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

INCHI for NP0316160 (methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

Structure for NP0316160 (methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)

3D Structure for NP0316160 (methyl (1'r,3s,5's,6r,11'r,12'r)-6-isopropyl-6-methoxy-3'-methyl-3'-azaspiro[oxane-3,15'-tetracyclo[6.5.1.1¹,⁵.0¹¹,¹⁴]pentadecan]-8'(14')-ene-12'-carboxylate)