NP-MRD: Showing NP-Card for (1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione (NP0180376)

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Record Information

Version

2.0

Created at

2022-09-03 18:43:30 UTC

Updated at

2022-09-03 18:43:30 UTC

NP-MRD ID

NP0180376

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione

Description

Pamamycin 649A 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. (1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione is found in Streptomyces alboniger. Based on a literature review very few articles have been published on Pamamycin 649A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032220432D          

 46 49  0  0  1  0            999 V2000
    7.3668    3.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9968    2.6252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4503    1.9360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0803    1.1987    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7313    0.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1388   -0.0254    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3378   -0.2229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2781   -1.0458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0422   -1.3568    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.5742   -0.7262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5150   -2.2905    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0991   -2.8731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8866   -3.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7976   -2.6980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0574   -3.4811    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9790   -2.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1836   -2.5809    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8135   -3.3183    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9900   -3.3665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6199   -4.1039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2671   -4.0074    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0912   -4.0456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3096   -4.8411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6205   -5.2947    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5824   -6.1188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8496   -6.4978    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8115   -7.3219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0787   -7.7010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0405   -8.5251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1549   -6.0527    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4222   -6.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1931   -5.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9762   -4.7794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5326   -2.0741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9085   -2.6138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1251   -1.3568    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3609   -1.0458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4206   -0.2229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2216   -0.0254    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6570   -0.7262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7489    0.9082    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1648    1.4909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3773    2.2880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4663    1.3158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2065    2.0988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2849    1.4177    0.0000 O   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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  6 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 21 18  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 26 30  1  1  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 24 33  1  0  0  0  0
 21 33  1  0  0  0  0
 17 34  1  0  0  0  0
 34 35  1  6  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  6  0  0  0
 36 40  1  6  0  0  0
 39 41  1  0  0  0  0
 41 42  1  1  0  0  0
 42 43  1  0  0  0  0
 41 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
  4 46  1  0  0  0  0
M  END

     RDKit          3D

113116  0  0  0  0  0  0  0  0999 V2000
    8.6298   -0.1960   -1.4912 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0611    0.9124   -2.3520 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5839    0.7313   -2.4797 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8379    0.7600   -1.1663 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0381    2.0681   -0.4766 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7951    2.9341   -0.4979 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7988    3.9799    0.6136 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3011    4.2248    0.8764 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6986    3.0933    0.1686 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6975    2.1733   -0.1638 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6181    2.3171    0.8894 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1612    1.8426    2.1907 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3408    0.9359    1.9561 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1506    1.1868    0.0215 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4157    1.3935   -1.2337 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5405    0.0662    0.3342 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5815   -0.4488    0.9284 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9070   -0.0014    0.3033 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9695    1.4451   -0.0399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1605    2.4331    1.0286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1149   -0.5520    0.9419 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5960   -0.0230    2.2267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9715   -0.7426    2.2829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3178   -0.7220    0.7853 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.5300    0.1558    0.6424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9652    0.2580   -0.7790 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.3231   -1.0715   -1.3465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4541   -1.7186   -0.5720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8280   -3.0624   -1.1412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0642    1.2140   -0.9383 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3011    1.3975   -2.3424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5757    2.4830   -0.3723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2265   -0.2424    0.1056 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4649   -1.9643    0.7566 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1300   -2.7774    1.8091 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9412   -2.4241    0.5957 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7745   -2.4890    1.8206 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1559   -2.7705    1.2052 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9131   -2.4245   -0.2505 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7314   -1.6751   -0.2695 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1131   -1.7263   -0.7807 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9616   -2.7672   -1.5264 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2837   -3.9472   -0.6455 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8605   -0.6302   -1.7187 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1061   -0.8459   -2.7081 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4621    0.6046   -1.4816 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0903   -1.1595   -1.6933 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5426    0.0369   -0.4180 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7016   -0.3874   -1.7035 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5474    0.7996   -3.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3986    1.8744   -1.9628 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2116    1.4952   -3.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4268   -0.2522   -3.0022 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1885   -0.0520   -0.4868 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3341    1.8942    0.5732 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8282    2.6534   -0.9767 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7273    3.3933   -1.4949 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2998    3.5968    1.4999 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3036    4.8667    0.2074 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1002    4.3649    1.9333 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0911    5.1718    0.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2947    3.4198   -0.8464 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8147    3.0463    1.1005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3799    1.3406    2.8185 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4948    2.7032    2.7953 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3627    0.2459    2.8557 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2247    0.2769    1.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3176    1.4615    1.9551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6855   -0.2570    2.0195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8794   -0.5080   -0.7201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1788    1.6777   -0.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9088    1.5329   -0.6953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5155    3.3300    0.7313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8343    2.1984    2.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1752    2.8691    1.0483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1568   -1.6573    0.9870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0197   -0.4104    3.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8645    1.0266    2.2981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8097   -1.7879    2.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6857   -0.1858    2.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5584   -1.7393    0.4399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2453    1.1557    1.0619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3353   -0.2338    1.2910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1310    0.6753   -1.3954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4670   -1.7540   -1.3393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6684   -0.9999   -2.4045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3120   -1.0195   -0.6366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1613   -1.9039    0.4890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7940   -2.9825   -1.7140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0240   -3.5180   -1.7593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0278   -3.8142   -0.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4586    0.9559   -2.9409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2844    0.9700   -2.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2785    2.4782   -2.5792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7845    2.5305    0.7232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0618    3.3266   -0.8872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4839    2.5615   -0.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9864   -2.1783   -0.2142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8454   -3.5400    1.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3998   -3.4808    2.3270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5689   -2.2240    2.6502 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8999   -3.4551    0.1570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5232   -3.2868    2.5482 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8328   -1.4952    2.2694 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9421   -2.1818    1.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2821   -3.8690    1.2642 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7178   -3.3348   -0.8589 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7341   -1.3822    0.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9000   -2.3140   -1.8955 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4080   -3.1530   -2.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5048   -3.6219    0.4062 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1990   -4.4740   -0.9766 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4755   -4.7046   -0.6371 H   0  0  0  0  0  0  0  0  0  0  0  0
 29 28  1  0
 28 27  1  0
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  4 46  1  0
 46 44  1  0
 44 45  2  0
 44 41  1  0
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 40 39  1  0
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 17 69  1  1
 11 63  1  1
 12 64  1  0
 12 65  1  0
 13 66  1  0
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 13 68  1  0
  9 62  1  6
  8 60  1  0
  8 61  1  0
  7 58  1  0
  7 59  1  0
  6 57  1  6
  5 55  1  0
  5 56  1  0
  4 54  1  1
  3 52  1  0
  3 53  1  0
  2 50  1  0
  2 51  1  0
  1 47  1  0
  1 48  1  0
  1 49  1  0
 41108  1  1
 42109  1  0
 42110  1  0
 43111  1  0
 43112  1  0
 43113  1  0
 39107  1  6
 38105  1  0
 38106  1  0
 37103  1  0
 37104  1  0
 36102  1  6
 34 98  1  6
 35 99  1  0
 35100  1  0
 35101  1  0
 31 92  1  0
 31 93  1  0
 31 94  1  0
 32 95  1  0
 32 96  1  0
 32 97  1  0
M  END


  Mrv1652309032220432D          

 46 49  0  0  1  0            999 V2000
    7.3668    3.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9968    2.6252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4503    1.9360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0803    1.1987    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7313    0.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1388   -0.0254    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3378   -0.2229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2781   -1.0458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0422   -1.3568    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.5742   -0.7262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5150   -2.2905    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0991   -2.8731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8866   -3.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7976   -2.6980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0574   -3.4811    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9790   -2.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1836   -2.5809    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8135   -3.3183    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9900   -3.3665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6199   -4.1039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2671   -4.0074    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0912   -4.0456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3096   -4.8411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6205   -5.2947    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5824   -6.1188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8496   -6.4978    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8115   -7.3219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0787   -7.7010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0405   -8.5251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1549   -6.0527    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4222   -6.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1931   -5.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9762   -4.7794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5326   -2.0741    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9085   -2.6138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1251   -1.3568    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3609   -1.0458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4206   -0.2229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2216   -0.0254    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6570   -0.7262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7489    0.9082    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1648    1.4909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3773    2.2880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4663    1.3158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2065    2.0988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2849    1.4177    0.0000 O   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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  6 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 21 18  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 26 30  1  1  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 24 33  1  0  0  0  0
 21 33  1  0  0  0  0
 17 34  1  0  0  0  0
 34 35  1  6  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  6  0  0  0
 36 40  1  6  0  0  0
 39 41  1  0  0  0  0
 41 42  1  1  0  0  0
 42 43  1  0  0  0  0
 41 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
  4 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0180376

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC[C@H](C[C@@H]1CC[C@@H](O1)[C@@H](CC)[C@@H]1OC(=O)[C@@H](CC)[C@H]2CC[C@@H](C[C@H](CCC)OC(=O)[C@H](CC)[C@H]3CC[C@H](O3)[C@H]1C)O2)N(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C38H67NO7/c1-9-14-25(39(7)8)22-27-16-18-33(42-27)29(11-3)36-24(6)32-20-21-35(45-32)31(13-5)37(40)44-26(15-10-2)23-28-17-19-34(43-28)30(12-4)38(41)46-36/h24-36H,9-23H2,1-8H3/t24-,25-,26+,27+,28+,29-,30+,31-,32+,33-,34-,35-,36-/m1/s1

> <INCHI_KEY>
JYJGXVRPMXVGID-FSQJWVLESA-N

> <FORMULA>
C38H67NO7

> <MOLECULAR_WEIGHT>
649.954

> <EXACT_MASS>
649.491753501

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
113

> <JCHEM_AVERAGE_POLARIZABILITY>
76.39087540804051

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,5R,6R,7S,10R,11R,14S,16S)-5-[(1R)-1-[(2R,5S)-5-[(2R)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1^{7,10}]icosane-3,12-dione

> <JCHEM_LOGP>
7.6207568843333355

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
10.0009104038788

> <JCHEM_POLAR_SURFACE_AREA>
83.53000000000002

> <JCHEM_REFRACTIVITY>
180.90419999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,5R,6R,7S,10R,11R,14S,16S)-5-[(1R)-1-[(2R,5S)-5-[(2R)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1^{7,10}]icosane-3,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      13.751   6.277   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.061   4.900   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.907   3.614   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.217   2.238   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.432   1.292   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.192  -0.047   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.697  -0.416   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.586  -1.952   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      15.012  -2.533   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      16.005  -1.356   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      14.028  -4.276   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.118  -5.363   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.722  -6.851   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.689  -5.036   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      13.174  -6.498   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      11.161  -5.227   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.676  -4.818   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.985  -6.194   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.448  -6.284   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.757  -7.661   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.832  -7.481   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.370  -7.552   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.778  -9.037   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.492  -9.883   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.420 -11.422   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.053 -12.129   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.981 -13.668   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.614 -14.375   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.542 -15.914   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       7.756 -11.298   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0       6.388 -12.006   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.827  -9.760   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       9.289  -8.922   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       8.461  -3.872   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.296  -4.879   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.700  -2.533   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.274  -1.952   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.385  -0.416   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.880  -0.047   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       8.693  -1.356   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       8.865   1.695   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       7.774   2.783   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       8.171   4.271   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      10.204   2.456   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       9.719   3.918   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      11.732   2.646   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   46                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9    6                                                       
CONECT   11    9   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   34                                                  
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22   33                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   33                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   30                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   26   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   24   21                                                       
CONECT   34   17   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   40                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39   36                                                       
CONECT   41   39   42   44                                                  
CONECT   42   41   43                                                       
CONECT   43   42                                                            
CONECT   44   41   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44    4                                                       
MASTER        0    0    0    0    0    0    0    0   46    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₆₇NO₇

Average Mass

649.9540 Da

Monoisotopic Mass

649.49175 Da

IUPAC Name

(1R,2S,5R,6R,7S,10R,11R,14S,16S)-5-[(1R)-1-[(2R,5S)-5-[(2R)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1^{7,10}]icosane-3,12-dione

Traditional Name

(1R,2S,5R,6R,7S,10R,11R,14S,16S)-5-[(1R)-1-[(2R,5S)-5-[(2R)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1^{7,10}]icosane-3,12-dione

CAS Registry Number

Not Available

SMILES

CCC[C@H](C[C@@H]1CC[C@@H](O1)[C@@H](CC)[C@@H]1OC(=O)[C@@H](CC)[C@H]2CC[C@@H](C[C@H](CCC)OC(=O)[C@H](CC)[C@H]3CC[C@H](O3)[C@H]1C)O2)N(C)C

InChI Identifier

InChI=1S/C38H67NO7/c1-9-14-25(39(7)8)22-27-16-18-33(42-27)29(11-3)36-24(6)32-20-21-35(45-32)31(13-5)37(40)44-26(15-10-2)23-28-17-19-34(43-28)30(12-4)38(41)46-36/h24-36H,9-23H2,1-8H3/t24-,25-,26+,27+,28+,29-,30+,31-,32+,33-,34-,35-,36-/m1/s1

InChI Key

JYJGXVRPMXVGID-FSQJWVLESA-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
Streptomyces alboniger	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
Dicarboxylic acid or derivatives
Tetrahydrofuran
Amino acid or derivatives
Carboxylic acid ester
Lactone
Tertiary amine
Tertiary aliphatic amine
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Organic oxide
Organic nitrogen compound
Organopnictogen compound
Amine
Organic oxygen compound
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	7.62	ChemAxon
pKa (Strongest Basic)	10	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	83.53 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	180.9 m³·mol⁻¹	ChemAxon
Polarizability	76.39 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

Not Available

Chemspider ID

78438647

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15694392

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione (NP0180376)

MOL for NP0180376 ((1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione)

3D MOL for NP0180376 ((1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione)

3D SDF for NP0180376 ((1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione)

3D-SDF for NP0180376 ((1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione)

PDB for NP0180376 ((1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione)

3D PDB for NP0180376 ((1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione)

SMILES for NP0180376 ((1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione)

INCHI for NP0180376 ((1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione)

Structure for NP0180376 ((1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione)

3D Structure for NP0180376 ((1r,2s,5r,6r,7s,10r,11r,14s,16s)-5-[(1r)-1-[(2r,5s)-5-[(2r)-2-(dimethylamino)pentyl]oxolan-2-yl]propyl]-2,11-diethyl-6-methyl-14-propyl-4,13,19,20-tetraoxatricyclo[14.2.1.1⁷,¹⁰]icosane-3,12-dione)