NP-MRD: Showing NP-Card for n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine (NP0268164)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 13:11:53 UTC

Updated at

2022-09-08 13:11:53 UTC

NP-MRD ID

NP0268164

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine

Description

N-(3-{1,8,14-trihydroxy-10-[(1H-indol-3-yl)methyl]-6-(4-methylpentyl)-4,11-dioxo-3H,4H,6H,7H,10H,11H,13H,14H,15H,15aH-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl}propyl)guanidine belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating. n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine is found in Elysia rufescens. N-(3-{1,8,14-trihydroxy-10-[(1H-indol-3-yl)methyl]-6-(4-methylpentyl)-4,11-dioxo-3H,4H,6H,7H,10H,11H,13H,14H,15H,15aH-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl}propyl)guanidine is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171517542D          

 44 47  0  0  0  0            999 V2000
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6753   -0.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4389   -0.0232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1232    0.2775    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5357    0.9920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2002    1.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6203    1.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1723    1.2188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9260    1.5544    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8398    2.3749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3918    2.9880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1368    3.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3299    3.9441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7778    3.3310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0328    2.5464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3427    0.8205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7012    0.0774    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3149    2.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1354    2.1307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5479    2.8452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4710    1.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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
  2  4  1  0  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  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  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
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 14 22  1  0  0  0  0
 17 22  1  0  0  0  0
 12 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
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 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
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 34 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
  7 44  1  0  0  0  0
M  END

     RDKit          3D

 89 92  0  0  0  0  0  0  0  0999 V2000
   -4.1472    7.3319    1.8735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4512    7.3089    0.8953 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0190    6.5361   -0.0276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5521    6.6390   -1.3293 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0143    5.5868    0.2594 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2808    4.1418    0.1282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9933    3.4397    0.5235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1886    1.9506    0.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5276    1.3903   -0.8684 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6550    1.5047   -1.9865 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2768    1.4824   -2.2049 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0980    0.3557   -2.7695 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8362    2.3614   -1.9826 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6234    3.7695   -2.5571 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7836    4.4757   -1.9097 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6546    5.8595   -1.9189 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6878    3.9550   -0.5229 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4266    2.5049   -0.6766 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7084    1.4666    0.2411 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2417    1.6393    1.4284 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4553    0.2193    0.0501 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0577   -0.2711    1.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0297   -1.3414    1.1716 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8853   -2.7110    1.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0283   -3.3181    1.0334 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9315   -2.4054    0.6222 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2161   -2.5205    0.1876 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8806   -1.3699   -0.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2965   -0.1238   -0.0932 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0012   -0.0389    0.3483 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3156   -1.1697    0.7059 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8328   -0.9000   -0.5231 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9566   -1.8551   -0.0150 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1648   -3.0725   -0.3725 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1951   -1.6702    0.8875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4908   -1.8992    0.1538 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2382   -3.0232    0.9044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4868   -4.3022    0.9478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2637   -5.3401    1.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5676   -5.6141    1.0160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2979   -6.6956    1.8299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2536   -6.1522   -0.3766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3444   -0.8452    0.1134 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0227   -0.0453   -0.6892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0630   -0.3147   -1.3508 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2286    7.4190   -1.9585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2606    5.9889   -1.7305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0943    5.9514    0.5620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5070    3.9575   -0.9596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1571    3.8319    0.6920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2445    3.7653   -0.1962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7531    3.7232    1.5715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4240    1.3900    1.0175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1184    1.7828    1.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4643    2.0080   -1.1726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2715    1.6120   -2.9050 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7630    2.0383   -2.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3541    4.1568   -2.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7554    3.7007   -3.6695 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7227    4.1249   -2.3626 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9359    6.1753   -2.8133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9287    4.4043    0.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6608    4.1826   -0.0403 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4073    0.4503   -0.5363 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2507   -0.6392    2.0500 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4668    0.6395    1.8616 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9925   -3.1722    1.7268 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2374   -4.3498    1.0693 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6745   -3.5099    0.1333 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9040   -1.4808   -0.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8648    0.7732   -0.3853 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5439    0.9560    0.4044 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0674   -1.0767   -1.5624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2578   -0.6435    1.2985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0397   -2.3202    1.7681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2035   -2.3903   -0.8042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3680   -2.6536    1.9469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2423   -3.0993    0.4804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4890   -4.2211    1.4686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1984   -4.6670   -0.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6650   -6.2874    1.8098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4794   -5.0285    2.7461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2135   -4.7198    0.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9831   -7.6723    1.4399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0084   -6.5888    2.9074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3857   -6.5355    1.7022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1215   -6.7347   -0.7006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0513   -5.3375   -1.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3739   -6.8236   -0.3512 H   0  0  0  0  0  0  0  0  0  0  0  0
 41 40  1  0
 40 42  1  0
 40 39  1  0
 39 38  1  0
 38 37  1  0
 37 36  1  0
 36 35  1  0
 35 33  1  0
 33 34  2  0
 33 32  1  0
 32 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 21 19  1  0
 19 20  2  0
 19 18  1  0
 18 17  1  0
 17 15  1  0
 15 16  1  0
 15 14  1  0
 14 13  1  0
 13 11  1  0
 11 12  2  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  9 44  1  0
 44 45  2  0
 44 43  1  0
 43 36  1  0
 31 23  1  0
 13 18  1  0
 31 26  1  0
 41 84  1  0
 41 85  1  0
 41 86  1  0
 40 83  1  0
 42 87  1  0
 42 88  1  0
 42 89  1  0
 39 81  1  0
 39 82  1  0
 38 79  1  0
 38 80  1  0
 37 77  1  0
 37 78  1  0
 36 76  1  6
 35 74  1  0
 35 75  1  0
 32 73  1  0
 21 64  1  6
 22 65  1  0
 22 66  1  0
 24 67  1  0
 25 68  1  0
 27 69  1  0
 28 70  1  0
 29 71  1  0
 30 72  1  0
 17 62  1  0
 17 63  1  0
 15 60  1  6
 16 61  1  0
 14 58  1  0
 14 59  1  0
 13 57  1  6
 10 56  1  0
  9 55  1  6
  8 53  1  0
  8 54  1  0
  7 51  1  0
  7 52  1  0
  6 49  1  0
  6 50  1  0
  5 48  1  0
  4 46  1  0
  4 47  1  0
  2  1  1  0
M  END


  Mrv1533004171517542D          

 44 47  0  0  0  0            999 V2000
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6753   -0.3355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4389   -0.0232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1232    0.2775    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5357    0.9920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2002    1.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6203    1.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1723    1.2188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9260    1.5544    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8398    2.3749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3918    2.9880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1368    3.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3299    3.9441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7778    3.3310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0328    2.5464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3427    0.8205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7012    0.0774    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3149    2.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1354    2.1307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5479    2.8452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4710    1.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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
  2  4  1  0  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  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  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
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 14 22  1  0  0  0  0
 17 22  1  0  0  0  0
 12 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
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 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
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 34 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
  7 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0268164

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCCC1CC(=O)NC(CC2=CNC3=CC=CC=C23)C(=O)N2CC(O)CC2C(=O)NC(CCCNC(N)=N)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C31H45N7O6/c1-18(2)7-5-8-21-15-27(40)36-25(13-19-16-35-23-10-4-3-9-22(19)23)29(42)38-17-20(39)14-26(38)28(41)37-24(30(43)44-21)11-6-12-34-31(32)33/h3-4,9-10,16,18,20-21,24-26,35,39H,5-8,11-15,17H2,1-2H3,(H,36,40)(H,37,41)(H4,32,33,34)

> <INCHI_KEY>
YWSRTGORAXAKFR-UHFFFAOYSA-N

> <FORMULA>
C31H45N7O6

> <MOLECULAR_WEIGHT>
611.744

> <EXACT_MASS>
611.343132197

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
65.41024197705282

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-(3-{14-hydroxy-10-[(1H-indol-3-yl)methyl]-6-(4-methylpentyl)-1,4,8,11-tetraoxo-tetradecahydropyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl}propyl)guanidine

> <ALOGPS_LOGP>
1.09

> <JCHEM_LOGP>
0.23151624816123925

> <ALOGPS_LOGS>
-4.20

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
11.476998546482834

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.941698093609888

> <JCHEM_PKA_STRONGEST_BASIC>
12.070943880513783

> <JCHEM_POLAR_SURFACE_AREA>
202.73

> <JCHEM_REFRACTIVITY>
172.878

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.85e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-{3-[14-hydroxy-10-(1H-indol-3-ylmethyl)-6-(4-methylpentyl)-1,4,8,11-tetraoxo-decahydropyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.261  -0.626   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.686  -0.043   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0       0.230   0.518   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       1.000   1.852   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.374   3.259   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.158   3.420   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.188   2.275   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      -3.595   2.902   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      -3.434   4.433   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.465   5.578   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.989   7.042   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.482   7.362   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.452   6.218   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.928   4.753   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.506   1.532   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.176   0.145   0.000  0.00  0.00           O+0
HETATM   25  N   UNK     0       4.001   2.310   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       4.321   3.816   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.853   3.977   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.623   5.311   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.479   2.570   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   33  N   UNK     0       6.668  -0.770   0.000  0.00  0.00           N+0
HETATM   34  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0      12.003  -2.310   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0      13.337  -3.080   0.000  0.00  0.00           C+0
HETATM   40  N   UNK     0      14.670  -2.310   0.000  0.00  0.00           N+0
HETATM   41  N   UNK     0      13.337  -4.620   0.000  0.00  0.00           N+0
HETATM   42  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   44                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   23                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   14   17                                                  
CONECT   23   12   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   25   31                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   42                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   34   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42    7                                                       
MASTER        0    0    0    0    0    0    0    0   44    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₄₅N₇O₆

Average Mass

611.7440 Da

Monoisotopic Mass

611.34313 Da

IUPAC Name

N-(3-{14-hydroxy-10-[(1H-indol-3-yl)methyl]-6-(4-methylpentyl)-1,4,8,11-tetraoxo-tetradecahydropyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl}propyl)guanidine

Traditional Name

N-{3-[14-hydroxy-10-(1H-indol-3-ylmethyl)-6-(4-methylpentyl)-1,4,8,11-tetraoxo-decahydropyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine

CAS Registry Number

Not Available

SMILES

CC(C)CCCC1CC(=O)NC(CC2=CNC3=CC=CC=C23)C(=O)N2CC(O)CC2C(=O)NC(CCCNC(N)=N)C(=O)O1

InChI Identifier

InChI=1S/C31H45N7O6/c1-18(2)7-5-8-21-15-27(40)36-25(13-19-16-35-23-10-4-3-9-22(19)23)29(42)38-17-20(39)14-26(38)28(41)37-24(30(43)44-21)11-6-12-34-31(32)33/h3-4,9-10,16,18,20-21,24-26,35,39H,5-8,11-15,17H2,1-2H3,(H,36,40)(H,37,41)(H4,32,33,34)

InChI Key

YWSRTGORAXAKFR-UHFFFAOYSA-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
Elysia rufescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Peptidomimetics

Sub Class

Depsipeptides

Direct Parent

Cyclic depsipeptides

Alternative Parents

Substituents

Cyclic depsipeptide
Macrolide lactam
Alpha-amino acid ester
Macrolactam
Alpha-amino acid or derivatives
3-alkylindole
Indole
Indole or derivatives
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Pyrrole
Pyrrolidine
Tertiary carboxylic acid amide
Carboxamide group
Carboxylic acid ester
Guanidine
Lactam
Lactone
Secondary alcohol
Secondary carboxylic acid amide
Azacycle
Oxacycle
Carboxylic acid derivative
Carboximidamide
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carbonyl group
Imine
Organic oxygen compound
Organopnictogen compound
Organic nitrogen compound
Organic oxide
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Alcohol
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	1.09	ALOGPS
logP	0.23	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	10.94	ChemAxon
pKa (Strongest Basic)	12.07	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	202.73 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	172.88 m³·mol⁻¹	ChemAxon
Polarizability	65.41 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine (NP0268164)

MOL for NP0268164 (n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine)

3D MOL for NP0268164 (n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine)

3D SDF for NP0268164 (n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine)

3D-SDF for NP0268164 (n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine)

PDB for NP0268164 (n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine)

3D PDB for NP0268164 (n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine)

SMILES for NP0268164 (n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine)

INCHI for NP0268164 (n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine)

Structure for NP0268164 (n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine)

3D Structure for NP0268164 (n-{3-[1,8,14-trihydroxy-10-(1h-indol-3-ylmethyl)-6-(4-methylpentyl)-4,11-dioxo-3h,6h,7h,10h,13h,14h,15h,15ah-pyrrolo[2,1-f]1-oxa-4,7,10-triazacyclotridecan-3-yl]propyl}guanidine)