NP-MRD: Showing NP-Card for 2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid (NP0275166)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 22:49:09 UTC

Updated at

2022-09-08 22:49:09 UTC

NP-MRD ID

NP0275166

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid

Description

Desotamide belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. 2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid was first documented in 2014 (PMID: 25072108). Based on a literature review a significant number of articles have been published on desotamide (PMID: 25747118) (PMID: 34073984) (PMID: 32727132) (PMID: 32002605) (PMID: 29431987) (PMID: 29129945).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092200492D          

 50 52  0  0  1  0            999 V2000
   -2.5986    1.8298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7916    1.6583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5367    0.8737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0887    0.2606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7297    0.7022    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4748   -0.0825    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0268   -0.6956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8338   -0.5240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7719   -1.4802    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3239   -2.0933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1309   -1.9218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6829   -2.5348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3858   -1.1371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0351   -1.6517    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2900   -2.4363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2620   -3.0494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0970   -2.6079    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3520   -3.3925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7999   -4.0056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0549   -4.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0071   -3.8340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6490   -1.9948    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4560   -2.1663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7110   -2.9509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0081   -1.5532    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8150   -1.7247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0700   -2.5093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5850   -3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0700   -3.8442    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546   -3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5691   -4.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2835   -3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2835   -2.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5691   -2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546   -2.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7531   -0.7686    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3051   -0.1555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1121   -0.3270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0502    0.6291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2432    0.8007    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9883    1.5853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5403    2.1984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1813    1.7568    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9264    2.5414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4784    3.1545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2235    3.9392    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2854    2.9830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6293    1.1437    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1777    1.3152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4326    2.0999    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  1  0  0  0
  5  3  1  6  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  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  4  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  4  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  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
 27 35  1  0  0  0  0
 30 35  1  0  0  0  0
 25 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  4  0  0  0
 37 39  1  0  0  0  0
 40 39  1  4  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  6  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 45 47  1  0  0  0  0
 43 48  1  0  0  0  0
 48 49  2  0  0  0  0
  5 49  1  0  0  0  0
 49 50  1  4  0  0  0
M  END

     RDKit          3D

102104  0  0  0  0  0  0  0  0999 V2000
   -2.0278   -6.3365   -2.2370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9259   -5.5959   -1.5075 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4123   -5.8023   -0.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9472   -7.0755   -0.0440 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2920   -4.7243    0.6201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7841   -3.4142    0.0171 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7773   -2.4626    1.1059 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4490   -1.3628    1.1653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2455   -0.6402    2.3431 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3576   -0.8969    0.0880 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8191   -1.1202    0.3558 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0918   -2.4536    1.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5401   -0.0866    1.1352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1668    0.0658    2.5663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9930    0.2456   -0.6065 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5216    1.3655   -0.5562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4329    2.0452   -1.8076 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0083    2.1754    0.5766 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2790    3.6321    0.4495 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6862    4.1022    0.4463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3382    3.7166    1.7658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5408    3.7429   -0.7158 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7608    1.8241    1.0985 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4287    1.7602    0.7978 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3674    1.3151    1.7262 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9477    2.1405   -0.5369 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9789    3.2441   -0.3276 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4559    3.6436   -1.7038 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5032    4.7262   -1.6695 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2752    4.2553   -2.4765 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3198    1.1344   -1.3811 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9468    0.2626   -1.8876 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4811   -0.4685   -3.0534 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2687   -0.2646   -1.4839 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0733    0.5888   -0.5608 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3950   -0.0684   -0.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6057    0.2038   -0.8465 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5696   -0.5744   -0.3388 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.0154   -1.3659    0.6115 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6189   -2.3233    1.4093 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8192   -2.9923    2.3172 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4721   -2.6909    2.3982 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8844   -1.7243    1.5864 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6674   -1.0578    0.6843 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2398   -1.6458   -1.1242 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3880   -2.3928   -0.5971 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7965   -3.7427   -0.4201 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0172   -2.0987   -0.1251 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0974   -2.4614   -1.1246 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0257   -2.9822   -1.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6233   -3.1760   -2.4379 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4970   -7.7755    0.4135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0152   -4.9232    1.4628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2601   -4.7065    0.9607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8600   -3.6711   -0.2713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4633   -0.9623    3.2552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1561   -1.7279   -0.7165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3645   -1.2035   -0.6348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1656   -3.2475    0.2754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1039   -2.4056    1.5186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3743   -2.6674    1.8346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6318   -0.4092    1.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6106    0.8988    0.5903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8711   -0.9062    3.0151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1005    0.3450    3.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4704    0.8903    2.7782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1467    1.9643   -2.5133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7570    1.8641    1.4215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8204    4.0022   -0.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7425    4.2431    1.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6416    5.2367    0.4529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8533    4.5936    2.2212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0617    2.9132    1.6495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5381    3.4062    2.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5243    4.2839   -0.5427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1049    4.1307   -1.6453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8315    2.6918   -0.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0857    0.5235    2.3044 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0895    2.7031   -1.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4284    4.1092    0.0973 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7640    2.9934    0.3741 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8337    2.7805   -2.2443 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5444    5.1764   -2.6883 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1777    5.5431   -0.9940 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4777    4.2816   -1.3688 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6266    3.4707   -2.8935 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7267    4.8300   -3.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6527    4.8703   -1.7964 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8622   -0.0514   -3.9078 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9472   -0.2751   -2.4398 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5841    0.7382    0.4026 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3609    1.5257   -1.0668 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7679    0.9322   -1.6215 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5812   -0.5905   -0.6093 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6915   -2.5336    1.3145 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2745   -3.7500    2.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8512   -3.2200    3.1134 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8507   -1.4961    1.6663 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5023   -4.3530   -1.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9038   -2.6715    0.8421 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8807   -1.0441    0.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0861   -3.5387   -3.2094 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 11  1  0
 11 12  1  0
 11 10  1  0
 10 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 18 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 26 31  1  0
 31 32  2  0
 32 33  1  0
 32 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  2  0
 37 38  1  0
 38 39  1  0
 39 40  2  0
 40 41  1  0
 41 42  2  0
 42 43  1  0
 43 44  2  0
 34 45  1  0
 45 46  2  0
 46 47  1  0
 46 48  1  0
 48 49  1  0
 49 50  2  0
 50 51  1  0
 50  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 44 36  1  0
 44 39  1  0
 14 64  1  0
 14 65  1  0
 14 66  1  0
 13 62  1  0
 13 63  1  0
 11 58  1  6
 12 59  1  0
 12 60  1  0
 12 61  1  0
 10 57  1  6
 17 67  1  0
 18 68  1  1
 19 69  1  0
 19 70  1  0
 20 71  1  0
 21 72  1  0
 21 73  1  0
 21 74  1  0
 22 75  1  0
 22 76  1  0
 22 77  1  0
 25 78  1  0
 26 79  1  6
 27 80  1  0
 27 81  1  0
 28 82  1  0
 29 83  1  0
 29 84  1  0
 29 85  1  0
 30 86  1  0
 30 87  1  0
 30 88  1  0
 33 89  1  0
 34 90  1  6
 35 91  1  0
 35 92  1  0
 37 93  1  0
 38 94  1  0
 40 95  1  0
 41 96  1  0
 42 97  1  0
 43 98  1  0
 47 99  1  0
 48100  1  0
 48101  1  0
 51102  1  0
  6 55  1  6
  5 53  1  0
  5 54  1  0
  4 52  1  0
  2  1  1  0
  9 56  1  0
M  END


  Mrv1652309092200492D          

 50 52  0  0  1  0            999 V2000
   -2.5986    1.8298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7916    1.6583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5367    0.8737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0887    0.2606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7297    0.7022    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4748   -0.0825    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0268   -0.6956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8338   -0.5240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7719   -1.4802    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3239   -2.0933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1309   -1.9218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6829   -2.5348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3858   -1.1371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0351   -1.6517    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2900   -2.4363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2620   -3.0494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0970   -2.6079    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3520   -3.3925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7999   -4.0056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0549   -4.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0071   -3.8340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6490   -1.9948    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4560   -2.1663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7110   -2.9509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0081   -1.5532    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8150   -1.7247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0700   -2.5093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5850   -3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0700   -3.8442    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546   -3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5691   -4.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2835   -3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2835   -2.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5691   -2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8546   -2.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7531   -0.7686    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3051   -0.1555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1121   -0.3270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0502    0.6291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2432    0.8007    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9883    1.5853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5403    2.1984    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1813    1.7568    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9264    2.5414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4784    3.1545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2235    3.9392    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2854    2.9830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6293    1.1437    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1777    1.3152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4326    2.0999    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  1  0  0  0
  5  3  1  6  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  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  4  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  4  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  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
 27 35  1  0  0  0  0
 30 35  1  0  0  0  0
 25 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  4  0  0  0
 37 39  1  0  0  0  0
 40 39  1  4  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  6  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 45 47  1  0  0  0  0
 43 48  1  0  0  0  0
 48 49  2  0  0  0  0
  5 49  1  0  0  0  0
 49 50  1  4  0  0  0
M  END
> <DATABASE_ID>
NP0275166

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C35H52N8O7/c1-7-20(6)30-35(50)42-27(15-28(36)44)31(46)38-17-29(45)39-26(14-21-16-37-23-11-9-8-10-22(21)23)33(48)40-24(12-18(2)3)32(47)41-25(13-19(4)5)34(49)43-30/h8-11,16,18-20,24-27,30,37H,7,12-15,17H2,1-6H3,(H2,36,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)(H,42,50)(H,43,49)/t20-,24+,25-,26+,27+,30+/m0/s1

> <INCHI_KEY>
LJGXNPVJAKBNOK-ZXCSEHFOSA-N

> <FORMULA>
C35H52N8O7

> <MOLECULAR_WEIGHT>
696.85

> <EXACT_MASS>
696.395896046

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
102

> <JCHEM_AVERAGE_POLARIZABILITY>
74.36405454378547

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(2R,8R,11R,14S,17R)-17-[(2S)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-[(1H-indol-3-yl)methyl]-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid

> <JCHEM_LOGP>
3.44478737207506

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.125716980754947

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.0716110624123978

> <JCHEM_PKA_STRONGEST_BASIC>
12.74983135937788

> <JCHEM_POLAR_SURFACE_AREA>
255.40999999999994

> <JCHEM_REFRACTIVITY>
197.86420000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-[(2R,8R,11R,14S,17R)-17-[(2S)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1H-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.851   3.416   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.344   3.095   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.868   1.631   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.899   0.486   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.362   1.311   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -0.886  -0.154   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      -1.917  -1.298   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.423  -0.978   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.441  -2.763   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.471  -3.907   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.978  -3.587   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.008  -4.732   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.454  -2.123   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       0.066  -3.083   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       0.541  -4.548   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.489  -5.692   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.048  -4.868   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.524  -6.333   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.493  -7.477   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.969  -8.942   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.013  -7.157   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       3.078  -3.724   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       4.585  -4.044   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.060  -5.508   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.615  -2.899   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.121  -3.219   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.597  -4.684   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.692  -5.930   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       7.597  -7.176   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       9.062  -6.700   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.396  -7.470   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      11.729  -6.700   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.729  -5.160   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.396  -4.390   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.062  -5.160   0.000  0.00  0.00           C+0
HETATM   36  N   UNK     0       5.139  -1.435   0.000  0.00  0.00           N+0
HETATM   37  C   UNK     0       6.170  -0.290   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       7.676  -0.610   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       5.694   1.174   0.000  0.00  0.00           C+0
HETATM   40  N   UNK     0       4.187   1.495   0.000  0.00  0.00           N+0
HETATM   41  C   UNK     0       3.711   2.959   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       4.742   4.104   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       2.205   3.279   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.729   4.744   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.760   5.888   0.000  0.00  0.00           C+0
HETATM   46  N   UNK     0       2.284   7.353   0.000  0.00  0.00           N+0
HETATM   47  O   UNK     0       4.266   5.568   0.000  0.00  0.00           O+0
HETATM   48  N   UNK     0       1.175   2.135   0.000  0.00  0.00           N+0
HETATM   49  C   UNK     0      -0.332   2.455   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      -0.808   3.920   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   49                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   36                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   35                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   27   30                                                  
CONECT   36   25   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44   48                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45                                                            
CONECT   48   43   49                                                       
CONECT   49   48    5   50                                                  
CONECT   50   49                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₅₂N₈O₇

Average Mass

696.8500 Da

Monoisotopic Mass

696.39590 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](CC(C)C)N=C(O)[C@@H](CC(C)C)N=C(O)[C@@H](CC2=CNC3=CC=CC=C23)N=C(O)CN=C(O)[C@@H](CC(O)=N)N=C1O

InChI Identifier

InChI=1S/C35H52N8O7/c1-7-20(6)30-35(50)42-27(15-28(36)44)31(46)38-17-29(45)39-26(14-21-16-37-23-11-9-8-10-22(21)23)33(48)40-24(12-18(2)3)32(47)41-25(13-19(4)5)34(49)43-30/h8-11,16,18-20,24-27,30,37H,7,12-15,17H2,1-6H3,(H2,36,44)(H,38,46)(H,39,45)(H,40,48)(H,41,47)(H,42,50)(H,43,49)/t20-,24+,25-,26+,27+,30+/m0/s1

InChI Key

LJGXNPVJAKBNOK-ZXCSEHFOSA-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

Not Available

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
Carboximidic acid derivative
Carboximidic acid
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
logP	3.44	ChemAxon
pKa (Strongest Acidic)	-1.1	ChemAxon
pKa (Strongest Basic)	12.75	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Rotatable Bond Count	10	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

133562661

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Song Y, Li Q, Liu X, Chen Y, Zhang Y, Sun A, Zhang W, Zhang J, Ju J: Cyclic Hexapeptides from the Deep South China Sea-Derived Streptomyces scopuliridis SCSIO ZJ46 Active Against Pathogenic Gram-Positive Bacteria. J Nat Prod. 2014 Aug 22;77(8):1937-41. doi: 10.1021/np500399v. [PubMed:25072108 ]
Li Q, Song Y, Qin X, Zhang X, Sun A, Ju J: Identification of the Biosynthetic Gene Cluster for the Anti-infective Desotamides and Production of a New Analogue in a Heterologous Host. J Nat Prod. 2015 Apr 24;78(4):944-8. doi: 10.1021/acs.jnatprod.5b00009. Epub 2015 Mar 6. [PubMed:25747118 ]
Xu R, Song Y, Li J, Ju J, Li Q: Chemical Synthesis and Structure-Activity Relationship Study Yield Desotamide a Analogues with Improved Antibacterial Activity. Mar Drugs. 2021 May 24;19(6). pii: md19060303. doi: 10.3390/md19060303. [PubMed:34073984 ]
Fazal A, Webb ME, Seipke RF: The Desotamide Family of Antibiotics. Antibiotics (Basel). 2020 Jul 27;9(8). pii: antibiotics9080452. doi: 10.3390/antibiotics9080452. [PubMed:32727132 ]
Ding W, Dong Y, Ju J, Li Q: The roles of genes associated with regulation, transportation, and macrocyclization in desotamide biosynthesis in Streptomyces scopuliridis SCSIO ZJ46. Appl Microbiol Biotechnol. 2020 Mar;104(6):2603-2610. doi: 10.1007/s00253-020-10414-4. Epub 2020 Jan 31. [PubMed:32002605 ]
Tsutsumi LS, Elmore JM, Dang UT, Wallace MJ, Marreddy R, Lee RB, Tan GT, Hurdle JG, Lee RE, Sun D: Solid-Phase Synthesis and Antibacterial Activity of Cyclohexapeptide Wollamide B Analogs. ACS Comb Sci. 2018 Mar 12;20(3):172-185. doi: 10.1021/acscombsci.7b00189. Epub 2018 Feb 20. [PubMed:29431987 ]
Tsutsumi LS, Tan GT, Sun D: Solid-phase synthesis of cyclic hexapeptides wollamides A, B and desotamide B. Tetrahedron Lett. 2017 Jul 5;58(27):2675-2680. doi: 10.1016/j.tetlet.2017.05.084. Epub 2017 May 25. [PubMed:29129945 ]
Chen YX, Liu C, Liu N, Wu Y, Zhao QJ, Hu HG, Li X, Zou Y: Total Synthesis and Antibacterial Study of Cyclohexapeptides Desotamide B, Wollamide B and Their Analogs. Chem Biodivers. 2018 Jan;15(1). doi: 10.1002/cbdv.201700414. Epub 2017 Dec 27. [PubMed:29125222 ]
Kamjam M, Sivalingam P, Deng Z, Hong K: Deep Sea Actinomycetes and Their Secondary Metabolites. Front Microbiol. 2017 May 1;8:760. doi: 10.3389/fmicb.2017.00760. eCollection 2017. [PubMed:28507537 ]
Li Q, Qin X, Liu J, Gui C, Wang B, Li J, Ju J: Deciphering the Biosynthetic Origin of L-allo-Isoleucine. J Am Chem Soc. 2016 Jan 13;138(1):408-15. doi: 10.1021/jacs.5b11380. Epub 2015 Dec 28. [PubMed:26669414 ]
LOTUS database [Link]

Showing NP-Card for 2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid (NP0275166)

MOL for NP0275166 (2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid)

3D MOL for NP0275166 (2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid)

3D SDF for NP0275166 (2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid)

3D-SDF for NP0275166 (2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid)

PDB for NP0275166 (2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid)

3D PDB for NP0275166 (2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid)

SMILES for NP0275166 (2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid)

INCHI for NP0275166 (2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid)

Structure for NP0275166 (2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid)

3D Structure for NP0275166 (2-[(2r,8r,11r,14s,17r)-17-[(2s)-butan-2-yl]-3,6,9,12,15,18-hexahydroxy-8-(1h-indol-3-ylmethyl)-11,14-bis(2-methylpropyl)-1,4,7,10,13,16-hexaazacyclooctadeca-1(18),3,6,9,12,15-hexaen-2-yl]ethanimidic acid)