NP-MRD: Showing NP-Card for methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate (NP0196902)

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Record Information

Version

2.0

Created at

2022-09-04 15:04:33 UTC

Updated at

2022-09-04 15:04:33 UTC

NP-MRD ID

NP0196902

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate

Description

Jaspofoliamoside D belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate is found in Jasminum polyanthum. Based on a literature review very few articles have been published on Jaspofoliamoside D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042217042D          

 39 41  0  0  1  0            999 V2000
    4.7345    0.1234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2202   -0.5217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0127   -1.3202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2175   -1.5397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6297   -0.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8344   -1.1804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6270   -1.9789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2467   -0.6015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4514   -0.8211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1364   -0.2422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0711    0.5563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5167    1.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8663    0.7759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0738    1.5744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8690    1.7940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4568    1.2150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2494    0.4166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2520    1.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4595    2.2331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8398    0.8557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6351    1.0753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2229    0.4964    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0154   -0.3021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6032   -0.8810    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3957   -1.6795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6005   -1.8991    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3930   -2.6976    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5978   -2.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0100   -2.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2148   -2.5578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3990   -2.4350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0073   -3.3563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5951   -3.9352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3984   -0.6614    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9862   -1.2403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6059    0.1371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4011    0.3567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0181    0.7160    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2256    1.5145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 26 25  1  6  0  0  0
  3 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
  4 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 24 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  0  0  0  0
 22 38  1  0  0  0  0
 38 39  1  1  0  0  0
M  END

     RDKit          3D

 77 79  0  0  0  0  0  0  0  0999 V2000
    4.3307    0.4996    1.9643 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5008   -0.6420    1.4726 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9652   -0.6069    0.2963 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1458    0.5477   -0.6067 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3721    0.0785   -1.9508 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3733   -1.2880   -2.2144 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9741   -2.2220   -1.3646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3442   -3.6080   -1.5634 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0176   -4.5506   -0.8153 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1320   -4.0110   -2.6600 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5000   -5.3601   -2.8659 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1470   -1.7147   -0.2349 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6654   -2.7158    0.7304 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4878   -2.1172    1.4501 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7068   -1.6099    2.5753 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7815   -2.1197    0.9072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4079   -3.1786    0.2496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7635   -3.5028    0.7920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8812   -2.6733    0.2559 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7959   -3.4859   -0.6697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4686   -1.3786   -0.3594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9852   -0.1859    0.4120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9539    1.0143   -0.4620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9511    2.2569   -0.0031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6534    3.3602   -0.7531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2838    2.6413    1.2356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8222    3.6003    1.8805 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1445    1.9976    1.6662 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9801    1.8038    0.8919 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0963    2.7594    1.4119 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3018    2.2306    1.1999 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9595    2.4449    0.0340 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9309    1.2666   -0.7120 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4790    3.6195   -0.7740 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5508    4.0768   -1.5524 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0752    4.6873    0.2300 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8813    5.9175   -0.3428 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1625    4.1411    0.9046 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6222    5.0122    1.8902 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7216    1.3965    2.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8510    0.2274    2.9035 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1584    0.7435    1.2391 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3887   -1.4880    2.1629 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9074    1.2529   -0.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7274   -1.6521   -3.1954 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7498   -5.8797   -1.9145 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4507   -5.3374   -3.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7535   -5.9093   -3.4733 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2249   -1.2736   -0.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1884   -3.5660    0.1599 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3631   -3.0693    1.4862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7850   -4.1112    0.3801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4784   -3.0582   -0.8542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9885   -4.5736    0.5346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7336   -3.4941    1.9172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5483   -2.4228    1.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8695   -3.2130   -0.5104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6722   -4.5720   -0.4916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5419   -3.1833   -1.7074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9658   -1.3260   -1.3716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3984   -1.2704   -0.5478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0537   -0.4262    0.6692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4485   -0.0520    1.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9323    0.8630   -1.5321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8771    3.7946   -1.4212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9601    4.1487   -0.0543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4564    2.9811   -1.3832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6093    0.7769    1.0850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1516    1.9192   -0.1902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0826    2.7992    2.5279 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0292    2.6402    0.2665 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6159    3.3932   -1.4106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1775    4.6460   -1.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8882    4.6937    1.0058 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3195    6.5999    0.2247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9501    4.0946    0.1238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2920    5.9225    1.6410 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10  8  1  0
  8  9  2  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  1  0
  4 33  1  0
 33 32  1  0
 32 31  1  0
 31 30  1  0
 30 29  1  0
 29 28  1  0
 28 26  1  0
 26 27  2  0
 26 24  1  0
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 24 23  2  0
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 22 21  1  0
 21 19  1  0
 19 20  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 14  1  0
 14 15  2  0
 14 13  1  0
 13 12  1  0
 12  3  1  0
  3  2  2  0
  2  1  1  0
 30 38  1  0
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 38 36  1  0
 36 37  1  0
 36 34  1  0
 34 35  1  0
 12  7  1  0
  3  4  1  0
 34 32  1  0
 11 46  1  0
 11 47  1  0
 11 48  1  0
  6 45  1  0
  4 44  1  1
 32 71  1  1
 30 70  1  1
 29 68  1  0
 29 69  1  0
 25 65  1  0
 25 66  1  0
 25 67  1  0
 23 64  1  0
 22 62  1  0
 22 63  1  0
 21 60  1  0
 21 61  1  0
 19 56  1  1
 20 57  1  0
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 20 59  1  0
 18 54  1  0
 18 55  1  0
 17 52  1  0
 17 53  1  0
 13 50  1  0
 13 51  1  0
 12 49  1  6
  2 43  1  0
  1 40  1  0
  1 41  1  0
  1 42  1  0
 38 76  1  6
 39 77  1  0
 36 74  1  1
 37 75  1  0
 34 72  1  6
 35 73  1  0
M  END


  Mrv1652309042217042D          

 39 41  0  0  1  0            999 V2000
    4.7345    0.1234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2202   -0.5217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0127   -1.3202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2175   -1.5397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6297   -0.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8344   -1.1804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6270   -1.9789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2467   -0.6015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4514   -0.8211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1364   -0.2422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0711    0.5563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5167    1.1352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8663    0.7759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0738    1.5744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8690    1.7940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4568    1.2150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2494    0.4166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2520    1.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4595    2.2331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8398    0.8557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6351    1.0753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2229    0.4964    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0154   -0.3021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6032   -0.8810    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3957   -1.6795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6005   -1.8991    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3930   -2.6976    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5978   -2.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0100   -2.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2148   -2.5578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3990   -2.4350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0073   -3.3563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5951   -3.9352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3984   -0.6614    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9862   -1.2403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6059    0.1371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4011    0.3567    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0181    0.7160    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2256    1.5145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 26 25  1  6  0  0  0
  3 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
  4 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 24 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  0  0  0  0
 22 38  1  0  0  0  0
 38 39  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0196902

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CO[C@H]2O[C@@H]3O[C@H](COC(=O)\C(C)=C\CCC(C)CCOC(=O)CC1\C2=C\C)[C@@H](O)[C@H](O)[C@H]3O

> <INCHI_IDENTIFIER>
InChI=1S/C27H38O12/c1-5-16-17-11-20(28)35-10-9-14(2)7-6-8-15(3)24(32)36-13-19-21(29)22(30)23(31)27(38-19)39-26(16)37-12-18(17)25(33)34-4/h5,8,12,14,17,19,21-23,26-27,29-31H,6-7,9-11,13H2,1-4H3/b15-8+,16-5-/t14?,17?,19-,21-,22+,23-,26+,27+/m1/s1

> <INCHI_KEY>
DDCMYHVJRJUSRK-FNUBTHORSA-N

> <FORMULA>
C27H38O12

> <MOLECULAR_WEIGHT>
554.589

> <EXACT_MASS>
554.236326664

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
56.94151374520709

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1S,3S,16E,21R,22S,23S,24R,26Z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1^{3,7}]hexacosa-5,16-diene-6-carboxylate

> <JCHEM_LOGP>
2.065401519666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.213217690084992

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.208174298305687

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6490950193256415

> <JCHEM_POLAR_SURFACE_AREA>
167.28

> <JCHEM_REFRACTIVITY>
135.3386

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,3S,16E,21R,22S,23S,24R,26Z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1^{3,7}]hexacosa-5,16-diene-6-carboxylate

> <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       8.838   0.230   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.878  -0.974   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.490  -2.464   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.006  -2.874   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.909  -1.794   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.424  -2.203   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.037  -3.694   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       2.327  -1.123   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.843  -1.533   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.255  -0.452   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.133   1.038   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.965   2.119   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.617   1.448   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.004   2.939   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.489   3.349   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.586   2.268   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.199   0.778   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.070   2.678   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.458   4.168   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       7.168   1.597   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.652   2.007   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.749   0.927   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.362  -0.564   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      10.459  -1.645   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.072  -3.135   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.588  -3.545   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.200  -5.035   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.716  -5.445   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.619  -4.365   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.134  -4.775   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       2.611  -4.545   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       3.747  -6.265   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.844  -7.346   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.944  -1.235   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      13.041  -2.315   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      12.331   0.256   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      13.815   0.666   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      11.234   1.337   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      11.621   2.827   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   26                                                  
CONECT    4    3    5   29                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   38                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   34                                                  
CONECT   25   24   26                                                       
CONECT   26   25    3   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28    4   30                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32                                                            
CONECT   34   24   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   22   39                                                  
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₈O₁₂

Average Mass

554.5890 Da

Monoisotopic Mass

554.23633 Da

IUPAC Name

methyl (1S,3S,16E,21R,22S,23S,24R,26Z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1^{3,7}]hexacosa-5,16-diene-6-carboxylate

Traditional Name

methyl (1S,3S,16E,21R,22S,23S,24R,26Z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1^{3,7}]hexacosa-5,16-diene-6-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CO[C@H]2O[C@@H]3O[C@H](COC(=O)\C(C)=C\CCC(C)CCOC(=O)CC1\C2=C\C)[C@@H](O)[C@H](O)[C@H]3O

InChI Identifier

InChI=1S/C27H38O12/c1-5-16-17-11-20(28)35-10-9-14(2)7-6-8-15(3)24(32)36-13-19-21(29)22(30)23(31)27(38-19)39-26(16)37-12-18(17)25(33)34-4/h5,8,12,14,17,19,21-23,26-27,29-31H,6-7,9-11,13H2,1-4H3/b15-8+,16-5-/t14?,17?,19-,21-,22+,23-,26+,27+/m1/s1

InChI Key

DDCMYHVJRJUSRK-FNUBTHORSA-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
Jasminum polyanthum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Tricarboxylic acid or derivatives
Oxane
Monosaccharide
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	2.07	ChemAxon
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	167.28 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	135.34 m³·mol⁻¹	ChemAxon
Polarizability	56.94 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	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

100917669

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,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate (NP0196902)

MOL for NP0196902 (methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate)

3D MOL for NP0196902 (methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate)

3D SDF for NP0196902 (methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate)

3D-SDF for NP0196902 (methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate)

PDB for NP0196902 (methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate)

3D PDB for NP0196902 (methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate)

SMILES for NP0196902 (methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate)

INCHI for NP0196902 (methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate)

Structure for NP0196902 (methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate)

3D Structure for NP0196902 (methyl (1s,3s,16e,21r,22s,23s,24r,26z)-26-ethylidene-22,23,24-trihydroxy-13,17-dimethyl-9,18-dioxo-2,4,10,19,25-pentaoxatricyclo[19.3.1.1³,⁷]hexacosa-5,16-diene-6-carboxylate)