NP-MRD: Showing NP-Card for 5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol (NP0192574)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 09:49:21 UTC

Updated at

2022-09-04 09:49:21 UTC

NP-MRD ID

NP0192574

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol

Description

5-Methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]Nonacosa-8(13),9,11,14(28),15(19),17,20(27),21,23,25-decaene-9,18-diol belongs to the class of organic compounds known as indolocarbazoles. These are polycyclic aromatic compounds containing an indole fused to a carbazole. 5-Methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]Nonacosa-8(13),9,11,14(28),15(19),17,20(27),21,23,25-decaene-9,18-diol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161523172D          

 36 43  0  0  0  0            999 V2000
    1.8747   -1.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6175   -1.1509    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6781   -0.3281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4346    0.0843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5340    1.0056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7829    1.0943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0392    1.0803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2158    1.0290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9976    0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2509   -0.1660    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1814   -0.9881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8845    1.9774    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0837    2.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3426    1.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2858    1.1036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3418    2.3873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2851    3.2104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4560    3.5728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1405    3.1121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9683    3.3508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4184    4.0586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1611    4.8424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8270    5.3294    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4960    4.8466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2798    5.1039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2434    4.0611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7056    3.3238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5328    3.0983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2085    3.5716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9563    3.2230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0283    2.4012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3526    1.9279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6048    2.2764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7857    1.9085    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2639    2.6119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4191    2.6519    0.0000 C   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  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 13 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  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
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
  5 34  1  0  0  0  0
 34 35  1  0  0  0  0
 27 35  2  0  0  0  0
 35 36  1  0  0  0  0
 12 36  1  0  0  0  0
 20 36  2  0  0  0  0
M  END

     RDKit          3D

 62 69  0  0  0  0  0  0  0  0999 V2000
    3.9498    0.3157   -1.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0328   -0.2815   -2.0439 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6791   -0.2714   -1.6315 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8271   -1.3504   -2.2230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5983   -1.0903   -1.9618 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1085    0.1378   -1.9536 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3229    1.2205   -1.5145 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9060    2.4450   -2.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0795    1.0699   -2.0120 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2011    1.1699   -3.3838 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0783    2.0563   -3.8982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3969    1.2546   -0.0666 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2065    2.3860    0.6991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2245    3.6675    0.4086 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5456    4.0561   -0.8691 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3323    4.5549    1.4723 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0334    4.1977    2.7602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3900    2.9217    3.0397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5069    2.0112    1.9839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599    0.6830    2.0225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2113   -0.2082    3.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4848   -1.5655    2.7524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3927   -2.0175    1.4556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5248   -3.2425    0.8432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8475   -4.5018    1.3041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8788   -5.5442    0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6074   -5.3661   -0.9492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2861   -4.1018   -1.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2491   -3.0434   -0.4773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9624   -1.7881   -0.7136 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0433   -1.1211    0.4639 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7840    0.2131    0.7328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8368   -2.2070    3.9830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1501   -3.3723    4.2328 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7722   -1.2030    5.0127 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3644    0.0492    4.4533 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3347   -0.4176   -0.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4187    1.1583   -0.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8498    0.7740   -1.6194 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3426   -0.8875   -2.7792 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6830   -0.3334   -0.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1240   -2.3151   -1.7109 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0765   -1.5589   -3.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1676   -1.6660   -2.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6821    2.0517   -3.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6030    3.0251   -1.6124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2540    2.9334   -2.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7289    1.8130   -1.5559 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9506    3.1263   -3.6674 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2692    1.9079   -5.0022 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1042    1.8353   -3.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8549    4.9928   -1.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6656    5.5527    1.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1142    4.8931    3.6116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6402    2.5715    4.0145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0691   -4.7022    2.3316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1387   -6.5259    0.7707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6320   -6.1912   -1.6770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0661   -3.9038   -2.4203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9962   -1.3888    6.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1610    0.7926    4.6729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3988    0.3287    4.8942 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
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7  9  1  0
  9 10  1  0
 10 11  1  0
  7 12  1  0
 12 32  1  0
 32 20  2  0
 20 21  1  0
 21 22  2  0
 22 33  1  0
 33 34  2  0
 33 35  1  0
 35 36  1  0
 22 23  1  0
 23 31  2  0
 31 30  1  0
 30 29  1  0
 29 28  2  0
 28 27  1  0
 27 26  2  0
 26 25  1  0
 25 24  2  0
 20 19  1  0
 19 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  2  0
  9  3  1  0
 13 12  1  0
 30  5  1  0
 24 29  1  0
 18 19  1  0
 31 32  1  0
 36 21  1  0
 24 23  1  0
  1 37  1  0
  1 38  1  0
  1 39  1  0
  2 40  1  0
  3 41  1  1
  4 42  1  0
  4 43  1  0
  5 44  1  6
  8 45  1  0
  8 46  1  0
  8 47  1  0
  9 48  1  1
 11 49  1  0
 11 50  1  0
 11 51  1  0
 35 60  1  0
 36 61  1  0
 36 62  1  0
 28 59  1  0
 27 58  1  0
 26 57  1  0
 25 56  1  0
 15 52  1  0
 16 53  1  0
 17 54  1  0
 18 55  1  0
M  END


  Mrv1533004161523172D          

 36 43  0  0  0  0            999 V2000
    1.8747   -1.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6175   -1.1509    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6781   -0.3281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4346    0.0843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5340    1.0056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7829    1.0943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0392    1.0803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2158    1.0290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9976    0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2509   -0.1660    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1814   -0.9881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8845    1.9774    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0837    2.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3426    1.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2858    1.1036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3418    2.3873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2851    3.2104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4560    3.5728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1405    3.1121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9683    3.3508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4184    4.0586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1611    4.8424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8270    5.3294    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4960    4.8466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2798    5.1039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2434    4.0611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7056    3.3238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5328    3.0983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2085    3.5716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9563    3.2230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0283    2.4012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3526    1.9279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6048    2.2764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7857    1.9085    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2639    2.6119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4191    2.6519    0.0000 C   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  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 13 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  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
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
  5 34  1  0  0  0  0
 34 35  1  0  0  0  0
 27 35  2  0  0  0  0
 35 36  1  0  0  0  0
 12 36  1  0  0  0  0
 20 36  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0192574

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CNC1CC2OC(C)(C1OC)N1C3=C(C4=C(C(=O)NC4)C4=C3N2C2=CC=CC=C42)C2=C1C(O)=CC=C2

> <INCHI_IDENTIFIER>
InChI=1S/C28H26N4O4/c1-28-26(35-3)16(29-2)11-19(36-28)31-17-9-5-4-7-13(17)21-22-15(12-30-27(22)34)20-14-8-6-10-18(33)23(14)32(28)25(20)24(21)31/h4-10,16,19,26,29,33H,11-12H2,1-3H3,(H,30,34)

> <INCHI_KEY>
YVTHZQUVPBXOSO-UHFFFAOYSA-N

> <FORMULA>
C28H26N4O4

> <MOLECULAR_WEIGHT>
482.54

> <EXACT_MASS>
482.195405333

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
52.06498708689067

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
25-hydroxy-3-methoxy-2-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8,10,12,14(28),15(19),20(27),21(26),22,24-nonaen-16-one

> <ALOGPS_LOGP>
3.06

> <JCHEM_LOGP>
2.8692732867039386

> <ALOGPS_LOGS>
-3.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.698211810053696

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.05868746867588

> <JCHEM_PKA_STRONGEST_BASIC>
9.721039740992866

> <JCHEM_POLAR_SURFACE_AREA>
89.68

> <JCHEM_REFRACTIVITY>
134.35299999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.45e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
25-hydroxy-3-methoxy-2-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8,10,12,14(28),15(19),20(27),21(26),22,24-nonaen-16-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       3.500  -2.818   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       4.886  -2.148   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       4.999  -0.612   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.411   0.157   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.597   1.877   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.195   2.043   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.807   2.016   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.269   1.921   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.729   0.345   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.335  -0.310   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.205  -1.844   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       3.518   3.691   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       2.023   4.273   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.639   3.596   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.534   2.060   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.638   4.456   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.532   5.993   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.851   6.669   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.129   5.809   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.674   6.255   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.514   7.576   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.034   9.039   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       5.277   9.948   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       6.526   9.047   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       7.989   9.527   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.054   7.581   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.917   6.204   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.461   5.783   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.723   6.667   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.118   6.016   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.253   4.482   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.991   3.599   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.596   4.249   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0       7.067   3.562   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0       6.093   4.876   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.516   4.950   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   34                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9   12                                             
CONECT    8    7                                                            
CONECT    9    7    3   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    7   13   36                                                  
CONECT   13   12   14   19                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   13   20                                                  
CONECT   20   19   21   36                                                  
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   27                                                  
CONECT   27   26   28   35                                                  
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   28   34                                                  
CONECT   34   33    5   35                                                  
CONECT   35   34   27   36                                                  
CONECT   36   35   12   20                                                  
MASTER        0    0    0    0    0    0    0    0   36    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₂₆N₄O₄

Average Mass

482.5400 Da

Monoisotopic Mass

482.19541 Da

IUPAC Name

25-hydroxy-3-methoxy-2-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8,10,12,14(28),15(19),20(27),21(26),22,24-nonaen-16-one

Traditional Name

CAS Registry Number

Not Available

SMILES

CNC1CC2OC(C)(C1OC)N1C3=C(C4=C(C(=O)NC4)C4=C3N2C2=CC=CC=C42)C2=C1C(O)=CC=C2

InChI Identifier

InChI=1S/C28H26N4O4/c1-28-26(35-3)16(29-2)11-19(36-28)31-17-9-5-4-7-13(17)21-22-15(12-30-27(22)34)20-14-8-6-10-18(33)23(14)32(28)25(20)24(21)31/h4-10,16,19,26,29,33H,11-12H2,1-3H3,(H,30,34)

InChI Key

YVTHZQUVPBXOSO-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indolocarbazoles. These are polycyclic aromatic compounds containing an indole fused to a carbazole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Indolocarbazoles

Alternative Parents

Substituents

Indolocarbazole
Pyrrolo[2,3-a]carbazole
Pyrroloindole
Hydroxyindole
Indole
Isoindole
Isoindole or derivatives
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Oxane
Benzenoid
Heteroaromatic compound
Pyrrole
Cyclic carboximidic acid
Dialkyl ether
Azacycle
Oxacycle
Ether
Secondary aliphatic amine
Secondary amine
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organooxygen compound
Organonitrogen compound
Amine
Hydrocarbon derivative
Organic oxygen compound
Organic nitrogen 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	3.06	ALOGPS
logP	2.87	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	9.06	ChemAxon
pKa (Strongest Basic)	9.72	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	89.68 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	134.35 m³·mol⁻¹	ChemAxon
Polarizability	52.06 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

73699095

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol (NP0192574)

MOL for NP0192574 (5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol)

3D MOL for NP0192574 (5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol)

3D SDF for NP0192574 (5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol)

3D-SDF for NP0192574 (5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol)

PDB for NP0192574 (5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol)

3D PDB for NP0192574 (5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol)

SMILES for NP0192574 (5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol)

INCHI for NP0192574 (5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol)

Structure for NP0192574 (5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol)

3D Structure for NP0192574 (5-methoxy-6-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.1²,⁶.0⁷,²⁸.0⁸,¹³.0¹⁵,¹⁹.0²⁰,²⁷.0²¹,²⁶]nonacosa-8(13),9,11,14(28),15(19),17,20(27),21(26),22,24-decaene-9,18-diol)