NP-MRD: Showing NP-Card for methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate (NP0233082)

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Record Information

Version

2.0

Created at

2022-09-06 14:33:31 UTC

Updated at

2022-09-06 14:33:31 UTC

NP-MRD ID

NP0233082

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate

Description

15Alpha-Angeloyloxy-9beta-hydroxykaur-16-en-19-oic acid methyl 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. methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate is found in Helianthus occidentalis, Sphagneticola trilobata and Viguiera hypargyrea. Based on a literature review very few articles have been published on 15alpha-Angeloyloxy-9beta-hydroxykaur-16-en-19-oic acid methyl.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062216332D          

 31 34  0  0  1  0            999 V2000
    0.0435   -0.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8566   -0.1407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4794    0.4660    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3435    1.2798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5709    1.5690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0659    1.0445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4350    2.3827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0718    2.9073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3376    2.6720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9744    2.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2893    0.0832    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5946    0.8699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4039    1.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9582    0.4175    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7638    0.5954    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4487    1.3579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4599    1.0381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1914    0.6566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4246    1.8624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6931    2.2439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3206   -0.0133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0719   -0.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2663   -0.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7095   -0.3691    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4700   -1.1586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8883   -0.5708    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0004   -1.3882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6431   -1.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7976   -1.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2377   -0.9152    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8140   -0.4494    0.0000 C   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  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
  3 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  6  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  2 30  1  0  0  0  0
 30 31  1  6  0  0  0
 11 31  1  6  0  0  0
M  END

     RDKit          3D

 69 72  0  0  0  0  0  0  0  0999 V2000
    3.2744    0.7757    3.6021 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1457    0.4075    3.0786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7883    0.2431    1.6200 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4179    1.1849    0.8177 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3765    0.8150   -0.1144 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6373   -0.4140   -0.1870 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0490    1.7969   -0.9677 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7221    3.2398   -0.8611 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9579    1.4189   -1.8471 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3364   -0.0270   -2.0066 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2782    0.3079    1.5534 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2211    1.3319    0.5733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3998    0.8133   -0.8168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1196   -0.4869   -0.9198 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2809   -0.4744   -1.8692 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6534   -0.2412   -3.2627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1916    0.6810   -1.7045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1595    1.5562   -0.8439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2175    0.7711   -2.6655 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1504    1.8521   -2.5946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9939   -1.7763   -1.9287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7928   -2.7659   -0.8691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6105   -2.6294    0.0275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4171   -1.1446    0.3959 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7202   -0.7513    1.0223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2427   -1.0734    1.2997 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7659   -1.8876    0.7303 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5178   -1.7006    2.6529 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6677   -1.4303    3.5735 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8915    0.0466    3.7952 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1032    0.8308    2.9378 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3659    0.8440    4.6824 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1734    1.0332    3.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1890   -0.7622    1.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4677    3.6600   -1.8780 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7926    3.3438   -0.2631 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5572    3.8406   -0.4447 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4316    2.1924   -2.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0966   -0.0838   -2.8054 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4669   -0.6211   -2.3624 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7953   -0.4313   -1.0861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1176    1.8792    0.9659 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5766    2.1334    0.5320 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6375    0.7935   -1.2750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8986    1.6451   -1.3982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3927   -1.1867   -1.4483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3818    0.8244   -3.3614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4842   -0.4219   -3.9760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8256   -0.9315   -3.4436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5358    2.7481   -2.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6051    2.0599   -3.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8850    1.7065   -1.7741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1017   -1.5259   -1.9503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8660   -2.2835   -2.9341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7248   -3.8092   -1.3081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6933   -2.8634   -0.1889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7611   -3.2393    0.9158 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6555   -2.9403   -0.4433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7508    0.2102    1.5116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5378   -0.8965    0.3052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9219   -1.5225    1.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0879   -1.5813   -0.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5961   -2.8052    2.5786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4018   -1.3346    3.1599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.9290    3.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5153   -1.9384    4.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8813    0.3494    4.8397 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1801    1.8933    2.9857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1344    0.6807    3.2130 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 17  1  0
 17 18  2  0
 15 17  1  1
 15 16  1  0
 15 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  1
 24 14  1  0
 14 13  1  0
 13 12  1  0
 11 12  1  6
 11 31  1  0
 31 30  1  0
 30 29  1  0
 29 28  1  0
 28 26  1  0
 26 27  1  6
 30  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 14 15  1  0
 26 11  1  0
 26 24  1  0
  3 11  1  0
 20 50  1  0
 20 51  1  0
 20 52  1  0
 16 47  1  0
 16 48  1  0
 16 49  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 23 57  1  0
 23 58  1  0
 25 59  1  0
 25 60  1  0
 25 61  1  0
 14 46  1  6
 13 44  1  0
 13 45  1  0
 12 42  1  0
 12 43  1  0
 31 68  1  0
 31 69  1  0
 30 67  1  1
 29 65  1  0
 29 66  1  0
 28 63  1  0
 28 64  1  0
 27 62  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  6
  8 35  1  0
  8 36  1  0
  8 37  1  0
  9 38  1  0
 10 39  1  0
 10 40  1  0
 10 41  1  0
M  END


  Mrv1652309062216332D          

 31 34  0  0  1  0            999 V2000
    0.0435   -0.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8566   -0.1407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4794    0.4660    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3435    1.2798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5709    1.5690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0659    1.0445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4350    2.3827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0718    2.9073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3376    2.6720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9744    2.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2893    0.0832    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5946    0.8699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4039    1.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9582    0.4175    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7638    0.5954    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4487    1.3579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4599    1.0381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1914    0.6566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4246    1.8624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6931    2.2439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3206   -0.0133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0719   -0.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2663   -0.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7095   -0.3691    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4700   -1.1586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8883   -0.5708    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0004   -1.3882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6431   -1.4156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7976   -1.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2377   -0.9152    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8140   -0.4494    0.0000 C   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  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
  3 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  6  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  2 30  1  0  0  0  0
 30 31  1  6  0  0  0
 11 31  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0233082

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@]1(C)CCC[C@]2(C)[C@@H]1CC[C@@]13C[C@@H](CC[C@@]21O)C(=C)[C@@H]3OC(=O)C(\C)=C/C

> <INCHI_IDENTIFIER>
InChI=1S/C26H38O5/c1-7-16(2)21(27)31-20-17(3)18-9-14-26(29)24(5)12-8-11-23(4,22(28)30-6)19(24)10-13-25(20,26)15-18/h7,18-20,29H,3,8-15H2,1-2,4-6H3/b16-7-/t18-,19-,20+,23-,24-,25+,26-/m1/s1

> <INCHI_KEY>
YTLOZRSCDVGDQP-REAVOEKPSA-N

> <FORMULA>
C26H38O5

> <MOLECULAR_WEIGHT>
430.585

> <EXACT_MASS>
430.271924324

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
48.190281523383454

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,4S,5R,9R,10R,13R,15S)-10-hydroxy-5,9-dimethyl-15-{[(2Z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecane-5-carboxylate

> <JCHEM_LOGP>
5.088366142999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.939763607268635

> <JCHEM_PKA_STRONGEST_BASIC>
-3.262547398180698

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
118.69809999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,4S,5R,9R,10R,13R,15S)-10-hydroxy-5,9-dimethyl-15-{[(2Z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadecane-5-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       0.081  -0.001   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.599  -0.263   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.761   0.870   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       2.508   2.389   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.066   2.929   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.123   1.950   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.812   4.448   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.001   5.427   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.630   4.988   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.819   4.009   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.273   0.155   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.843   1.624   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.354   1.935   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.389   0.779   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.892   1.111   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.304   2.535   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.192   1.938   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      11.557   1.226   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      10.126   3.476   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.760   4.189   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.932  -0.025   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.468  -1.493   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.964  -1.825   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.924  -0.689   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.477  -2.163   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.392  -1.066   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.601  -2.591   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.934  -2.642   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.356  -2.939   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.310  -1.708   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.386  -0.839   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4   11                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9                                                            
CONECT   11    3   12   26   31                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   24                                                  
CONECT   15   14   16   17   21                                             
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   15   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   14   25   26                                             
CONECT   25   24                                                            
CONECT   26   24   11   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    2   31                                                  
CONECT   31   30   11                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Value	Source
15a-Angeloyloxy-9b-hydroxykaur-16-en-19-Oate methyl	Generator
15a-Angeloyloxy-9b-hydroxykaur-16-en-19-Oic acid methyl	Generator
15alpha-Angeloyloxy-9beta-hydroxykaur-16-en-19-Oate methyl	Generator
15Α-angeloyloxy-9β-hydroxykaur-16-en-19-Oate methyl	Generator
15Α-angeloyloxy-9β-hydroxykaur-16-en-19-Oic acid methyl	Generator

Chemical Formula

C₂₆H₃₈O₅

Average Mass

430.5850 Da

Monoisotopic Mass

430.27192 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]1(C)CCC[C@]2(C)[C@@H]1CC[C@@]13C[C@@H](CC[C@@]21O)C(=C)[C@@H]3OC(=O)C(\C)=C/C

InChI Identifier

InChI=1S/C26H38O5/c1-7-16(2)21(27)31-20-17(3)18-9-14-26(29)24(5)12-8-11-23(4,22(28)30-6)19(24)10-13-25(20,26)15-18/h7,18-20,29H,3,8-15H2,1-2,4-6H3/b16-7-/t18-,19-,20+,23-,24-,25+,26-/m1/s1

InChI Key

YTLOZRSCDVGDQP-REAVOEKPSA-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
Helianthus occidentalis	LOTUS Database	35616633
Sphagneticola trilobata	LOTUS Database	35616633
Viguiera hypargyrea	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
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Cyclic alcohol
Tertiary alcohol
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Carboxylic acid derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Hydrocarbon derivative
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

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

101596879

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate (NP0233082)

MOL for NP0233082 (methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate)

3D MOL for NP0233082 (methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate)

3D SDF for NP0233082 (methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate)

3D-SDF for NP0233082 (methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate)

PDB for NP0233082 (methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate)

3D PDB for NP0233082 (methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate)

SMILES for NP0233082 (methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate)

INCHI for NP0233082 (methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate)

Structure for NP0233082 (methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate)

3D Structure for NP0233082 (methyl (1s,4s,5r,9r,10r,13r,15s)-10-hydroxy-5,9-dimethyl-15-{[(2z)-2-methylbut-2-enoyl]oxy}-14-methylidenetetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecane-5-carboxylate)