NP-MRD: Showing NP-Card for (16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate (NP0328675)

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Record Information

Version

2.0

Created at

2022-09-12 12:21:13 UTC

Updated at

2022-09-12 12:21:14 UTC

NP-MRD ID

NP0328675

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate

Description

Trewiasine belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides. (16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate is found in Thamnobryum sandei and Mallotus nudiflorus. Based on a literature review very few articles have been published on Trewiasine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122214212D          

 52 55  0  0  0  0            999 V2000
    0.4757    9.4568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3465    9.3887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6986    8.6426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5208    8.5745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8728    7.8284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4028    7.1504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5806    7.2186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2285    7.9647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5937    8.0328    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.0876    6.4691    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8053    6.8758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3339    5.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1510    5.7950    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3111    4.8570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0219    4.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7363    3.6719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4508    4.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4508    4.9094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1653    3.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1653    2.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8797    4.0844    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8797    4.9094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5942    3.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5942    2.8469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3087    4.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0232    3.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3087    4.9094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5026    3.4475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2777    3.1797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4799    2.6229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2055    3.0155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0105    2.8351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9650    2.0114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8305    2.9259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1826    3.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0047    3.7401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8296    3.7580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4748    3.0621    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1227    2.3160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5928    1.6380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3006    2.2479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5404    4.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3153    4.3062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4576    3.4936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6537    5.4065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4956    6.2162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0831    6.9307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4609    7.4725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8930    8.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6966    7.7829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8770    8.5880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2700    9.1467    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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 34 41  1  0  0  0  0
 36 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 42 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
  5 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END

     RDKit          3D

104107  0  0  0  0  0  0  0  0999 V2000
   -4.5599    0.3493   -3.4306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5598    1.2681   -3.0473 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2639    1.4215   -1.7021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8893    0.7248   -0.7106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6042    0.8686    0.6682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6291    1.7667    1.0585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9697    2.4918    0.0737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3031    2.3048   -1.2939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5143    3.2206   -2.5958 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -0.9086    3.4678    0.1620 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0573    4.7335   -0.6225 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3284    3.3691    0.9125 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6972    4.4179    1.4995 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1447    2.1380    1.0167 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7157    1.6911   -0.3134 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0974    1.9473   -0.4320 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7122    2.8362   -1.2503 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9706    3.5377   -1.9985 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1784    3.0738   -1.3632 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5920    4.4732   -1.0425 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9107    2.0768   -0.5757 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7459    1.1130   -1.2625 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8258    2.0347    0.8314 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1333    2.8805    1.4283 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5713    0.9682    1.5642 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0426   -0.4052    1.1801 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4100    1.2234    3.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3641    0.2743   -0.6713 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2071   -0.0179   -2.1449 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2220   -0.1698    0.1659 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4773   -0.7279    0.2608 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5644   -2.1220   -0.3137 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8397   -2.7533    0.2617 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4240   -2.9086    0.2467 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8375   -2.8180   -0.5546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9090   -3.3625    0.3618 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7353   -2.7681    1.6357 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6958   -4.2906    0.3877 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2982   -3.1188   -0.1719 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4872   -4.0510   -1.2033 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2315   -3.3266    0.9664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4761   -2.8870    0.9212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9656   -1.6930    0.3134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6657   -0.4451    0.6088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5619    0.6892    0.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4752   -0.0743    1.4424 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9214    0.2739    2.6990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3717   -0.5075    3.7152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5127    0.5152   -2.8824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8107    0.5328   -4.5159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2366   -0.6982   -3.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6373    0.0013   -1.0803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3724    1.9155    2.1635 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8773    5.5012    0.2063 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4763    1.3233    1.3570 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.6420    0.8460   -0.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2005    0.1695   -1.4733 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1118    1.5079   -2.2375 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6545    0.9711    1.3417 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7594   -0.9804    0.5767 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0833   -0.2883    0.6242 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8409   -0.9535    2.1398 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0537    0.2882    3.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3712    1.5189    3.5119 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7188    2.0654    3.2215 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3030   -0.5638   -2.4150 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.0123    1.6447    0.1887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9000   -1.0122    1.5963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7433   -0.2134    4.7138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5827   -1.5888    3.5960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2462   -0.4399    3.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
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 52104  1  0
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 31 81  1  1
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 34 86  1  1
 35 87  1  0
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 37 89  1  0
 40 90  1  0
  1 53  1  0
  1 54  1  0
  1 55  1  0
  4 56  1  0
M  END


  Mrv1652309122214212D          

 52 55  0  0  0  0            999 V2000
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   -0.3465    9.3887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2285    7.9647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5937    8.0328    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.0876    6.4691    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8053    6.8758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3339    5.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1510    5.7950    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3111    4.8570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0219    4.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7363    3.6719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4508    4.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4508    4.9094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1653    3.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1653    2.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8797    4.0844    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8797    4.9094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5942    3.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5942    2.8469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3087    4.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0232    3.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3087    4.9094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5026    3.4475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2777    3.1797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4799    2.6229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2055    3.0155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0105    2.8351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9650    2.0114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8305    2.9259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1826    3.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0047    3.7401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8296    3.7580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4748    3.0621    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1227    2.3160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5928    1.6380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3006    2.2479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5404    4.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3153    4.3062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4576    3.4936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6537    5.4065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4956    6.2162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0831    6.9307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4609    7.4725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8930    8.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6966    7.7829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8770    8.5880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2700    9.1467    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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 34 41  1  0  0  0  0
 36 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 42 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
  5 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0328675

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1\C=C/C=C(C)\C(OC)C2=CC(N(C)C(=O)CC(OC(=O)C(C)N(C)C(=O)C(C)C)C3(C)OC3C(C)C3CC1(O)N=C(O)O3)=C(Cl)C(OC)=C2

> <INCHI_IDENTIFIER>
InChI=1S/C37H52ClN3O11/c1-19(2)33(43)40(7)22(5)34(44)51-28-17-29(42)41(8)24-15-23(16-25(47-9)30(24)38)31(49-11)20(3)13-12-14-27(48-10)37(46)18-26(50-35(45)39-37)21(4)32-36(28,6)52-32/h12-16,19,21-22,26-28,31-32,46H,17-18H2,1-11H3,(H,39,45)/b14-12-,20-13-

> <INCHI_KEY>
GNTFDQQBHGBGMN-AYSDVWJHSA-N

> <FORMULA>
C37H52ClN3O11

> <MOLECULAR_WEIGHT>
750.28

> <EXACT_MASS>
749.3290372

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
77.7854541884399

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(16Z,18Z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1^{10,14}.0^{3,5}]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(N,2-dimethylpropanamido)propanoate

> <JCHEM_LOGP>
4.624548391666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.719515652223848

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.665670584300675

> <JCHEM_PKA_STRONGEST_BASIC>
-1.298889117438216

> <JCHEM_POLAR_SURFACE_AREA>
169.18999999999997

> <JCHEM_REFRACTIVITY>
192.25809999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(16Z,18Z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1^{10,14}.0^{3,5}]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(N,2-dimethylpropanamido)propanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       0.888  17.653   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.647  17.526   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.304  16.133   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.839  16.006   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.496  14.613   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.618  13.347   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.084  13.475   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.426  14.867   0.000  0.00  0.00           C+0
HETATM    9 Cl   UNK     0       1.108  14.995   0.000  0.00  0.00          Cl+0
HETATM   10  N   UNK     0       0.163  12.076   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       1.503  12.835   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.623  10.606   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.149  10.817   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.581   9.066   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.041   7.624   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.374   6.854   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.708   7.624   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.708   9.164   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.042   6.854   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.042   5.314   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       5.376   7.624   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       5.376   9.164   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.709   6.854   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.709   5.314   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.043   7.624   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.377   6.854   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.043   9.164   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.938   6.435   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.518   5.935   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.896   4.896   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -2.250   5.629   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.753   5.292   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -3.668   3.755   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -5.284   5.462   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -5.941   6.854   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -7.476   6.981   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -9.015   7.015   0.000  0.00  0.00           O+0
HETATM   38  N   UNK     0      -8.353   5.716   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0      -7.696   4.323   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -8.573   3.058   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      -6.161   4.196   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -8.475   8.567   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -9.922   8.038   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0     -10.188   6.521   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -8.687  10.092   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -8.392  11.604   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -7.622  12.937   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -6.460  13.949   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -7.267  15.261   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -5.034  14.528   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      -5.370  16.031   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      -4.237  17.074   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   50                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   28                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   15   29   30   31                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   28   32                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   41                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38   42                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   34                                                       
CONECT   42   36   43   45                                                  
CONECT   43   42   44                                                       
CONECT   44   43                                                            
CONECT   45   42   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48    5   51                                                  
CONECT   51   50   52                                                       
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₅₂ClN₃O₁₁

Average Mass

750.2800 Da

Monoisotopic Mass

749.32904 Da

IUPAC Name

(16Z,18Z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1^{10,14}.0^{3,5}]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(N,2-dimethylpropanamido)propanoate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1\C=C/C=C(C)\C(OC)C2=CC(N(C)C(=O)CC(OC(=O)C(C)N(C)C(=O)C(C)C)C3(C)OC3C(C)C3CC1(O)N=C(O)O3)=C(Cl)C(OC)=C2

InChI Identifier

InChI=1S/C37H52ClN3O11/c1-19(2)33(43)40(7)22(5)34(44)51-28-17-29(42)41(8)24-15-23(16-25(47-9)30(24)38)31(49-11)20(3)13-12-14-27(48-10)37(46)18-26(50-35(45)39-37)21(4)32-36(28,6)52-32/h12-16,19,21-22,26-28,31-32,46H,17-18H2,1-11H3,(H,39,45)/b14-12-,20-13-

InChI Key

GNTFDQQBHGBGMN-AYSDVWJHSA-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
Thamnobryum sandei	LOTUS Database	35616633
Trewia nudiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolactams

Sub Class

Not Available

Direct Parent

Macrolactams

Alternative Parents

Substituents

Macrolactam
Alpha-amino acid ester
Alanine or derivatives
Alpha-amino acid or derivatives
Anisole
Phenol ether
Alkyl aryl ether
1,3-oxazinane
Oxazinane
Aryl chloride
Benzenoid
Aryl halide
Tertiary carboxylic acid amide
Carbamic acid ester
Carboxylic acid ester
Carboxamide group
Lactam
Alkanolamine
Oxacycle
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organonitrogen compound
Organic nitrogen compound
Organic oxygen compound
Organochloride
Organohalogen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	4.62	ChemAxon
pKa (Strongest Acidic)	3.67	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	169.19 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	192.26 m³·mol⁻¹	ChemAxon
Polarizability	77.79 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

C00047356

Chemspider ID

4875931

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6296530

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate (NP0328675)

MOL for NP0328675 ((16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

3D MOL for NP0328675 ((16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

3D SDF for NP0328675 ((16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

3D-SDF for NP0328675 ((16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

PDB for NP0328675 ((16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

3D PDB for NP0328675 ((16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

SMILES for NP0328675 ((16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

INCHI for NP0328675 ((16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

Structure for NP0328675 ((16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)

3D Structure for NP0328675 ((16z,18z)-11-chloro-21,23-dihydroxy-12,15,20-trimethoxy-2,5,9,16-tetramethyl-8-oxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.1¹⁰,¹⁴.0³,⁵]hexacosa-10,12,14(26),16,18,22-hexaen-6-yl 2-(n,2-dimethylpropanamido)propanoate)