NP-MRD: Showing NP-Card for 4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide (NP0235197)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 17:41:27 UTC

Updated at

2022-09-06 17:41:28 UTC

NP-MRD ID

NP0235197

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide

Description

4-Bromo-N-{[(5R,6S,7S)-6-{[(4,5-dibromo-1H-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-2,3-dihydro-1H-imidazol-4-yl)-2,3,4,5,6,7-hexahydro-1H-1,3-benzodiazol-5-yl]methyl}-1-methyl-1H-pyrrole-2-carboxamide belongs to the class of organic compounds known as 2-heteroaryl carboxamides. 2-Heteroaryl carboxamides are compounds containing a heteroaromatic ring that carries a carboxamide group. 4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide is found in Astrosclera willeyana. Based on a literature review very few articles have been published on 4-bromo-N-{[(5R,6S,7S)-6-{[(4,5-dibromo-1H-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-2,3-dihydro-1H-imidazol-4-yl)-2,3,4,5,6,7-hexahydro-1H-1,3-benzodiazol-5-yl]methyl}-1-methyl-1H-pyrrole-2-carboxamide.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062219412D          

 38 42  0  0  1  0            999 V2000
    4.9511   -1.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1664   -1.8495    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9115   -2.6341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0865   -2.6341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6016   -3.3015    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.8316   -1.8495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -0.1271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4534    1.5229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3556    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6881    3.6579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9431    4.4425    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7681    4.4425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2530    5.1099    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0230    3.6579    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7845    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    1.9354    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5460    3.6579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8010    4.4425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3160    5.1099    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.6260    4.4425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1109    5.1099    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.8809    3.6579    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 26  1  0  0  0  0
 20 27  1  0  0  0  0
 12 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 32 38  1  0  0  0  0
M  END

     RDKit          3D

 63 67  0  0  0  0  0  0  0  0999 V2000
    1.6416   -3.8581   -4.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7128   -3.6622   -3.6647 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5785   -3.0775   -2.5223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5650   -2.7824   -1.8867 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3065   -2.1739   -0.7203 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0469   -2.0798   -0.6117 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5641   -2.6368   -1.7215 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7209   -1.4777    0.5328 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4705   -2.4591    1.3518 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7892   -2.8221    1.2169 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0994   -3.7526    2.1598 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9863   -3.9667    2.8738 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8988   -4.7864    3.8560 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6700   -5.3636    4.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0129   -3.1861    2.3821 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7890   -0.6386    1.4056 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5566    0.4455    2.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1303    1.4631    1.2355 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5177    2.4665    0.4794 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3135    2.6912    0.3670 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4107    3.3879   -0.2926 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9569    4.4128   -1.0727 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0822    5.0282   -1.6174 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1042    6.5216   -2.7915 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.1996    4.3760   -1.1662 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0186    4.7731   -1.5772 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.7328    3.3785   -0.3574 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4550   -0.2540    0.6892 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4638    0.3354    1.6442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7551    0.4243    1.0124 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0453    1.1271   -0.1605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2279    1.7778   -0.8360 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4290    1.1244   -0.6793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4931    0.4731   -0.1003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6320    0.6875   -0.8542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3964    0.0354   -0.5391 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -6.2264    1.4842   -1.9015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9007    1.7273   -1.7665 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1217    2.5362   -2.6907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1601   -1.6450    0.3377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5030   -3.0142   -2.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5871   -2.7301   -1.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4445   -0.7196    0.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4961   -2.4549    0.4968 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0517   -4.2098    2.2874 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0516   -3.1934    2.7931 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4631   -1.3134    2.2938 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8502    1.0209    2.7550 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3432    0.0311    2.7545 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2449    1.4771    1.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9412    4.7345   -1.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3820    2.7199    0.1244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3386    0.2749   -0.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2172    1.3152    2.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5346   -0.3874    2.5088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5695   -0.1035    1.4965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4897   -0.1270    0.8055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9007    1.8292   -2.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3506    1.9386   -3.2082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6515    3.3548   -2.0947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7940    3.0474   -3.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1607   -2.1663    1.2898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1714   -1.3790    0.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
 39 38  1  0
 38 37  1  0
 37 35  2  0
 35 36  1  0
 35 34  1  0
 34 33  2  0
 33 31  1  0
 31 32  2  0
 31 30  1  0
 30 29  1  0
 29 28  1  0
 28 40  1  0
 40  5  1  0
  5  6  2  0
  6  7  1  0
  7  3  1  0
  3  2  2  0
  3  4  1  0
  6  8  1  0
  8 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 25 26  1  0
 25 27  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 15  1  0
 33 38  1  0
 16 28  1  0
 27 21  1  0
 15  9  1  0
  4  5  1  0
 39 59  1  0
 39 60  1  0
 39 61  1  0
 37 58  1  0
 34 57  1  0
 30 56  1  0
 29 54  1  0
 29 55  1  0
 28 53  1  6
 40 62  1  0
 40 63  1  0
  7 42  1  0
  2  1  1  0
  4 41  1  0
  8 43  1  6
 16 47  1  1
 17 48  1  0
 17 49  1  0
 18 50  1  0
 22 51  1  0
 27 52  1  0
 10 44  1  0
 11 45  1  0
 13 14  1  0
 15 46  1  0
M  END


  Mrv1652309062219412D          

 38 42  0  0  1  0            999 V2000
    4.9511   -1.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1664   -1.8495    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9115   -2.6341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0865   -2.6341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6016   -3.3015    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.8316   -1.8495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -0.1271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.1104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4534    1.5229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3556    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6881    3.6579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9431    4.4425    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7681    4.4425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2530    5.1099    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0230    3.6579    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7845    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    1.9354    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5460    3.6579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8010    4.4425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3160    5.1099    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.6260    4.4425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1109    5.1099    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.8809    3.6579    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 26  1  0  0  0  0
 20 27  1  0  0  0  0
 12 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 32 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0235197

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C=C(Br)C=C1C(=O)NC[C@@H]1CC2=C(NC(=N)N2)[C@@H]([C@H]1CNC(=O)C1=CC(Br)=C(Br)N1)C1=CNC(=N)N1

> <INCHI_IDENTIFIER>
InChI=1S/C23H25Br3N10O2/c1-36-8-10(24)3-16(36)21(38)29-5-9-2-13-18(35-23(28)33-13)17(15-7-31-22(27)34-15)11(9)6-30-20(37)14-4-12(25)19(26)32-14/h3-4,7-9,11,17,32H,2,5-6H2,1H3,(H,29,38)(H,30,37)(H3,27,31,34)(H3,28,33,35)/t9-,11-,17-/m0/s1

> <INCHI_KEY>
NOQZFODGPSPCJC-NSTVUXKKSA-N

> <FORMULA>
C23H25Br3N10O2

> <MOLECULAR_WEIGHT>
713.233

> <EXACT_MASS>
709.971209

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
62.02038244163025

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-bromo-N-{[(5R,6S,7S)-6-{[(4,5-dibromo-1H-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-2,3-dihydro-1H-imidazol-4-yl)-2,3,4,5,6,7-hexahydro-1H-1,3-benzodiazol-5-yl]methyl}-1-methyl-1H-pyrrole-2-carboxamide

> <JCHEM_LOGP>
0.5483232166666678

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
12.002484151998

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.3954826445688715

> <JCHEM_PKA_STRONGEST_BASIC>
25.460262681918355

> <JCHEM_POLAR_SURFACE_AREA>
174.73999999999998

> <JCHEM_REFRACTIVITY>
176.79179999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-bromo-N-{[(5R,6S,7S)-6-{[(4,5-dibromo-1H-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       9.242  -2.976   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       7.777  -3.452   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       7.301  -4.917   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.761  -4.917   0.000  0.00  0.00           C+0
HETATM    5 Br   UNK     0       4.856  -6.163   0.000  0.00  0.00          Br+0
HETATM    6  C   UNK     0       5.286  -3.452   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.531  -2.547   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.531  -1.007   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.865  -0.237   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0       5.198  -0.237   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       5.198   1.303   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.864   2.073   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.530   1.303   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.197   2.073   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      -0.268   1.597   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      -1.173   2.843   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0      -2.713   2.843   0.000  0.00  0.00           N+0
HETATM   18  N   UNK     0      -0.268   4.089   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       1.197   3.613   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.530   4.383   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.530   5.923   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.285   6.828   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       1.760   8.293   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       3.300   8.293   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       4.206   9.539   0.000  0.00  0.00           N+0
HETATM   26  N   UNK     0       3.776   6.828   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       3.864   3.613   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.198   4.383   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       6.531   3.613   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       7.865   4.383   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       9.199   3.613   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       7.865   5.923   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.619   6.828   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.095   8.293   0.000  0.00  0.00           C+0
HETATM   35 Br   UNK     0       6.190   9.539   0.000  0.00  0.00          Br+0
HETATM   36  C   UNK     0       8.635   8.293   0.000  0.00  0.00           C+0
HETATM   37 Br   UNK     0       9.540   9.539   0.000  0.00  0.00          Br+0
HETATM   38  N   UNK     0       9.111   6.828   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   27                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   14   20                                                  
CONECT   20   19   21   27                                                  
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   21                                                       
CONECT   27   20   12   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   38                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   32                                                       
MASTER        0    0    0    0    0    0    0    0   38    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₅Br₃N₁₀O₂

Average Mass

713.2330 Da

Monoisotopic Mass

709.97121 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CN1C=C(Br)C=C1C(=O)NC[C@@H]1CC2=C(NC(=N)N2)[C@@H]([C@H]1CNC(=O)C1=CC(Br)=C(Br)N1)C1=CNC(=N)N1

InChI Identifier

InChI=1S/C23H25Br3N10O2/c1-36-8-10(24)3-16(36)21(38)29-5-9-2-13-18(35-23(28)33-13)17(15-7-31-22(27)34-15)11(9)6-30-20(37)14-4-12(25)19(26)32-14/h3-4,7-9,11,17,32H,2,5-6H2,1H3,(H,29,38)(H,30,37)(H3,27,31,34)(H3,28,33,35)/t9-,11-,17-/m0/s1

InChI Key

NOQZFODGPSPCJC-NSTVUXKKSA-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
Astrosclera willeyana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-heteroaryl carboxamides. 2-Heteroaryl carboxamides are compounds containing a heteroaromatic ring that carries a carboxamide group.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Carboxylic acid derivatives

Direct Parent

2-heteroaryl carboxamides

Alternative Parents

Substituents

2-heteroaryl carboxamide
Pyrrole-2-carboxylic acid or derivatives
Pyrrole-2-carboxamide
Aryl bromide
Aryl halide
N-methylpyrrole
Substituted pyrrole
Azole
Imidazole
Heteroaromatic compound
Pyrrole
Secondary carboxylic acid amide
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organobromide
Organohalogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen 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

163190486

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide (NP0235197)

MOL for NP0235197 (4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide)

3D MOL for NP0235197 (4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide)

3D SDF for NP0235197 (4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide)

3D-SDF for NP0235197 (4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide)

PDB for NP0235197 (4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide)

3D PDB for NP0235197 (4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide)

SMILES for NP0235197 (4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide)

INCHI for NP0235197 (4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide)

Structure for NP0235197 (4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide)

3D Structure for NP0235197 (4-bromo-n-{[(5r,6s,7s)-6-{[(4,5-dibromo-1h-pyrrol-2-yl)formamido]methyl}-2-imino-7-(2-imino-1,3-dihydroimidazol-4-yl)-1,3,4,5,6,7-hexahydro-1,3-benzodiazol-5-yl]methyl}-1-methylpyrrole-2-carboxamide)