NP-MRD: Showing NP-Card for (3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol (NP0246690)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 08:14:38 UTC

Updated at

2022-09-07 08:14:39 UTC

NP-MRD ID

NP0246690

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol

Description

(3R,6R,9R,12S,15R,18R)-12-[(2R)-butan-2-yl]-3-[(1H-indol-3-yl)methyl]-6,18-dimethyl-9,15-bis(propan-2-yl)-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. (3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol is found in Aspergillus unguis. Based on a literature review very few articles have been published on (3R,6R,9R,12S,15R,18R)-12-[(2R)-butan-2-yl]-3-[(1H-indol-3-yl)methyl]-6,18-dimethyl-9,15-bis(propan-2-yl)-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072210142D          

 52 54  0  0  1  0            999 V2000
   13.3480   -9.2421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7065   -8.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2423   -7.8171    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.6007   -7.0740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4195   -7.8781    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.7551   -8.6318    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.1420   -9.1838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2282  -10.0043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4275   -8.7713    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.2808   -9.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9105  -10.1162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5044   -9.8620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5371   -8.9205    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9851   -8.3074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2400   -7.5228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1781   -8.4789    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9232   -9.2636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6261   -7.8658    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8191   -8.0374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5642   -8.8220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2671   -7.4243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4601   -7.5958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9081   -6.9827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1630   -6.1981    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9700   -6.0266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5220   -6.6397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2249   -5.2419    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6729   -4.6288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9278   -3.8442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4429   -3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9278   -2.5093    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7125   -2.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4269   -2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1414   -2.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1414   -3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4269   -4.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7125   -3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0319   -5.0704    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5839   -5.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3290   -6.4681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3909   -5.5120    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.6459   -4.7274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9429   -6.1251    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.7499   -5.9535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0049   -5.1689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3020   -6.5666    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.5569   -5.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3639   -5.6105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4707   -4.9615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1089   -6.3951    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.6610   -7.0082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4640   -6.8192    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
  3  4  1  6  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  4  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  4  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  4  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  4  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 29 37  1  0  0  0  0
 32 37  1  0  0  0  0
 27 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  4  0  0  0
 39 41  1  0  0  0  0
 41 42  1  1  0  0  0
 41 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  4  0  0  0
 44 46  1  0  0  0  0
 46 47  1  6  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 46 50  1  0  0  0  0
 50 51  2  0  0  0  0
  5 51  1  0  0  0  0
 51 52  1  4  0  0  0
M  END

     RDKit          3D

108110  0  0  0  0  0  0  0  0999 V2000
   -5.6501   -3.2515    2.2924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6625   -2.1166    1.9448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2996   -2.1173    0.5034 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4079   -1.8651   -0.4471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0488   -1.2602    0.3089 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2067    0.0377    0.6628 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3459    1.1857    0.9589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4260    1.6291    2.2854 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4629    2.2658   -0.0979 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5813    2.0336   -1.0661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5153    3.1287   -2.1108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9123    2.3036   -0.3485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8342    3.5095    0.6236 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0421    4.4225    0.9417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5664    5.5612    1.6481 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5960    4.4282    0.6302 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2200    5.9215    0.4867 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8266    3.7927    1.6401 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4108    3.7886    1.8535 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9661    3.0627    2.9474 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3906    4.5051    1.0197 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4812    3.9658   -0.3613 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3548    2.6870   -0.4127 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9219    1.8962   -1.4855 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2288    0.6899   -1.8769 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6740    0.0906   -2.9886 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2420   -0.0508   -1.0673 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5051    0.7498   -0.9779 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5101    0.3891    0.0065 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1817    0.1119    1.3527 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3209   -0.0520    2.0208 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3712    0.1020    1.1770 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7506    0.0627    1.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6243    0.3070    0.3982 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1314    0.5839   -0.8832 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7733    0.6067   -1.0726 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8731    0.3720   -0.0633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7321   -0.6793    0.0560 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3960   -1.9030    0.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9043   -2.1832    1.5323 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4473   -3.0127   -0.7494 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9147   -4.3175   -0.1084 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4251   -3.1315   -1.6531 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3457   -3.3217   -2.0969 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1205   -3.1966   -3.4978 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9143   -3.6943   -1.3467 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6317   -4.5807   -0.1772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9628   -4.9060    0.5557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3216   -5.9788   -0.7556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6925   -2.5683   -1.2459 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3903   -1.6503   -0.9543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6989   -0.6862   -1.9846 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0231   -3.1583    3.3043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0391   -4.2137    2.1681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4674   -3.3038    1.5784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1626   -1.1777    2.2654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7481   -2.3238    2.5435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9694   -3.1489    0.2654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1054   -2.0985   -1.4931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2683   -2.5026   -0.1929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7610   -0.8111   -0.4107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3723   -1.7302    1.1340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2503    1.9583    2.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5054    2.4660   -0.5665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6447    1.0229   -1.4544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2797    4.0688   -1.5965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4977    3.1127   -2.6213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7297    2.8772   -2.8907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3482    1.3929    0.0697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7736    3.0746    0.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6524    2.7136   -1.0914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4854    5.5053    2.6743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4238    4.0093   -0.3792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1655    6.4655    0.2315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9178    6.2622    1.4719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5331    6.0660   -0.3426 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0270    3.6489    3.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4357    4.3835    1.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2712    5.6202    1.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5601    3.7492   -0.8602 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0837    4.7333   -0.9704 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3712    3.1402   -0.4474 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2661    2.1988    0.6028 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9924    0.6257   -3.5169 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5901   -0.9328   -1.8034 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3815    1.7744   -1.2218 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1058    0.4339   -2.0110 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1629    0.0455    1.7549 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4318   -0.2574    3.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0622   -0.1583    2.4105 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6986    0.2986    0.5138 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8239    0.7831   -1.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3669    0.8102   -2.0758 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6837   -2.5914    2.1013 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4049   -2.7694   -1.3660 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0056   -4.2881    0.1467 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6924   -5.1418   -0.8163 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3876   -4.4480    0.8355 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0427   -2.2106   -3.8017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4474   -4.4788   -2.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1087   -4.2476    0.5298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1476   -4.1280    1.2819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9087   -5.8825    1.0791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7694   -4.9540   -0.2014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5051   -6.7222    0.0666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0879   -6.1817   -1.5288 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6603   -6.0905   -1.1595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4081   -0.9561   -2.6381 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  7  9  1  0
  9 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  1  0
 32 33  2  0
 33 34  1  0
 34 35  2  0
 35 36  1  0
 36 37  2  0
 27 38  1  0
 38 39  2  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41 43  1  0
 43 44  2  0
 44 45  1  0
 44 46  1  0
 46 50  1  0
 50 51  2  0
 51 52  1  0
 46 47  1  0
 47 48  1  0
 47 49  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 51  5  1  0
 37 29  1  0
 37 32  1  0
  1 53  1  0
  1 54  1  0
  1 55  1  0
  2 56  1  0
  2 57  1  0
  3 58  1  6
  4 59  1  0
  4 60  1  0
  4 61  1  0
  5 62  1  1
  8 63  1  0
  9 64  1  6
 15 72  1  0
 16 73  1  6
 17 74  1  0
 17 75  1  0
 17 76  1  0
 20 77  1  0
 21 78  1  0
 21 79  1  0
 22 80  1  0
 22 81  1  0
 23 82  1  0
 23 83  1  0
 26 84  1  0
 27 85  1  6
 28 86  1  0
 28 87  1  0
 30 88  1  0
 31 89  1  0
 33 90  1  0
 34 91  1  0
 35 92  1  0
 36 93  1  0
 40 94  1  0
 41 95  1  6
 42 96  1  0
 42 97  1  0
 42 98  1  0
 45 99  1  0
 46100  1  6
 52108  1  0
 47101  1  0
 48102  1  0
 48103  1  0
 48104  1  0
 49105  1  0
 49106  1  0
 49107  1  0
 10 65  1  0
 11 66  1  0
 11 67  1  0
 11 68  1  0
 12 69  1  0
 12 70  1  0
 12 71  1  0
M  END


  Mrv1652309072210142D          

 52 54  0  0  1  0            999 V2000
   13.3480   -9.2421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7065   -8.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2423   -7.8171    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.6007   -7.0740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4195   -7.8781    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.7551   -8.6318    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.1420   -9.1838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2282  -10.0043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4275   -8.7713    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.2808   -9.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9105  -10.1162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5044   -9.8620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5371   -8.9205    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9851   -8.3074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2400   -7.5228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1781   -8.4789    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9232   -9.2636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6261   -7.8658    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.8191   -8.0374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5642   -8.8220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2671   -7.4243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4601   -7.5958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9081   -6.9827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1630   -6.1981    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9700   -6.0266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5220   -6.6397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2249   -5.2419    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6729   -4.6288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9278   -3.8442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4429   -3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9278   -2.5093    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.7125   -2.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4269   -2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1414   -2.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1414   -3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4269   -4.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7125   -3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0319   -5.0704    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5839   -5.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3290   -6.4681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3909   -5.5120    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.6459   -4.7274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9429   -6.1251    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.7499   -5.9535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0049   -5.1689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3020   -6.5666    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.5569   -5.7820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3639   -5.6105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4707   -4.9615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1089   -6.3951    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.6610   -7.0082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4640   -6.8192    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
  3  4  1  6  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  4  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  4  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  4  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  4  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 29 37  1  0  0  0  0
 32 37  1  0  0  0  0
 27 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  4  0  0  0
 39 41  1  0  0  0  0
 41 42  1  1  0  0  0
 41 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  4  0  0  0
 44 46  1  0  0  0  0
 46 47  1  6  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 46 50  1  0  0  0  0
 50 51  2  0  0  0  0
  5 51  1  0  0  0  0
 51 52  1  4  0  0  0
M  END
> <DATABASE_ID>
NP0246690

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H](C)[C@@H]1N=C(O)[C@H](N=C(O)[C@@H](C)N=C(O)CCCN=C(O)[C@@H](CC2=CNC3=CC=CC=C23)N=C(O)[C@@H](C)N=C(O)[C@H](N=C1O)C(C)C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C37H56N8O7/c1-9-21(6)31-37(52)44-29(19(2)3)35(50)41-23(8)32(47)42-27(17-24-18-39-26-14-11-10-13-25(24)26)34(49)38-16-12-15-28(46)40-22(7)33(48)43-30(20(4)5)36(51)45-31/h10-11,13-14,18-23,27,29-31,39H,9,12,15-17H2,1-8H3,(H,38,49)(H,40,46)(H,41,50)(H,42,47)(H,43,48)(H,44,52)(H,45,51)/t21-,22-,23-,27-,29-,30-,31+/m1/s1

> <INCHI_KEY>
DLGQVTFCVCCOEO-TZEXHMFTSA-N

> <FORMULA>
C37H56N8O7

> <MOLECULAR_WEIGHT>
724.904

> <EXACT_MASS>
724.427196175

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
77.45636563042605

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,6R,9R,12S,15R,18R)-12-[(2R)-butan-2-yl]-3-[(1H-indol-3-yl)methyl]-6,18-dimethyl-9,15-bis(propan-2-yl)-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol

> <JCHEM_LOGP>
4.155420918791462

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.1914901635667943

> <JCHEM_PKA_STRONGEST_ACIDIC>
-4.196610862668064

> <JCHEM_PKA_STRONGEST_BASIC>
12.212233274304042

> <JCHEM_POLAR_SURFACE_AREA>
243.91999999999993

> <JCHEM_REFRACTIVITY>
196.98750000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R,6R,9R,12S,15R,18R)-12-[(2R)-butan-2-yl]-3-(1H-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      24.916 -17.252   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      25.585 -15.865   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      24.719 -14.592   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      25.388 -13.205   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      23.183 -14.706   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      23.809 -16.113   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      22.665 -17.143   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      22.826 -18.675   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      21.331 -16.373   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      21.057 -17.889   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      22.233 -18.883   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      19.608 -18.409   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      19.669 -16.652   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      18.639 -15.507   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      19.115 -14.043   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      17.133 -15.827   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      16.657 -17.292   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0      16.102 -14.683   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      14.596 -15.003   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      14.120 -16.468   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      13.565 -13.859   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.059 -14.179   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.028 -13.034   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0      11.504 -11.570   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0      13.011 -11.250   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      14.041 -12.394   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      13.487  -9.785   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.456  -8.641   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.932  -7.176   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      12.027  -5.930   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0      12.932  -4.684   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0      14.397  -5.160   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      15.730  -4.390   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      17.064  -5.160   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      17.064  -6.700   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      15.730  -7.470   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.397  -6.700   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0      14.993  -9.465   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0      16.023 -10.609   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      15.547 -12.074   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      17.530 -10.289   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      18.006  -8.824   0.000  0.00  0.00           C+0
HETATM   43  N   UNK     0      18.560 -11.433   0.000  0.00  0.00           N+0
HETATM   44  C   UNK     0      20.067 -11.113   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      20.542  -9.649   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      21.097 -12.258   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      21.573 -10.793   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      23.079 -10.473   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      21.412  -9.262   0.000  0.00  0.00           C+0
HETATM   50  N   UNK     0      22.603 -11.938   0.000  0.00  0.00           N+0
HETATM   51  C   UNK     0      23.634 -13.082   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      25.133 -12.729   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   51                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   13                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    9   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   38                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   37                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   29   32                                                  
CONECT   38   27   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   50                                                  
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47                                                            
CONECT   50   46   51                                                       
CONECT   51   50    5   52                                                  
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  108    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₅₆N₈O₇

Average Mass

724.9040 Da

Monoisotopic Mass

724.42720 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC[C@@H](C)[C@@H]1N=C(O)[C@H](N=C(O)[C@@H](C)N=C(O)CCCN=C(O)[C@@H](CC2=CNC3=CC=CC=C23)N=C(O)[C@@H](C)N=C(O)[C@H](N=C1O)C(C)C)C(C)C

InChI Identifier

InChI=1S/C37H56N8O7/c1-9-21(6)31-37(52)44-29(19(2)3)35(50)41-23(8)32(47)42-27(17-24-18-39-26-14-11-10-13-25(24)26)34(49)38-16-12-15-28(46)40-22(7)33(48)43-30(20(4)5)36(51)45-31/h10-11,13-14,18-23,27,29-31,39H,9,12,15-17H2,1-8H3,(H,38,49)(H,40,46)(H,41,50)(H,42,47)(H,43,48)(H,44,52)(H,45,51)/t21-,22-,23-,27-,29-,30-,31+/m1/s1

InChI Key

DLGQVTFCVCCOEO-TZEXHMFTSA-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
Aspergillus unguis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Cyclic peptides

Alternative Parents

Substituents

Cyclic alpha peptide
3-alkylindole
Indole or derivatives
Indole
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Cyclic carboximidic acid
Pyrrole
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
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

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

163103854

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol (NP0246690)

MOL for NP0246690 ((3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol)

3D MOL for NP0246690 ((3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol)

3D SDF for NP0246690 ((3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol)

3D-SDF for NP0246690 ((3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol)

PDB for NP0246690 ((3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol)

3D PDB for NP0246690 ((3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol)

SMILES for NP0246690 ((3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol)

INCHI for NP0246690 ((3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol)

Structure for NP0246690 ((3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol)

3D Structure for NP0246690 ((3r,6r,9r,12s,15r,18r)-12-[(2r)-butan-2-yl]-3-(1h-indol-3-ylmethyl)-9,15-diisopropyl-6,18-dimethyl-1,4,7,10,13,16,19-heptaazacyclotricosa-1,4,7,10,13,16,19-heptaene-2,5,8,11,14,17,20-heptol)