NP-MRD: Showing NP-Card for 14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid (NP0172750)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 09:44:51 UTC

Updated at

2022-09-03 09:44:51 UTC

NP-MRD ID

NP0172750

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid

Description

14-{2-[(2-{[2-(N,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-N-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]Icosa-1(18),2,4,6(20),9,12,15(19),16-octaene-8-carboxylic acid belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus. 14-{2-[(2-{[2-(N,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-N-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]Icosa-1(18),2,4,6(20),9,12,15(19),16-octaene-8-carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251505582D          

 63 65  0  0  0  0            999 V2000
   10.7171  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -13.6125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -14.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775  -13.6125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -14.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -12.3750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788  -11.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -14.0250    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   32.1512  -13.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -14.8500    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   28.5788  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -9.9000    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  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 49 50  2  0  0  0  0
 44 50  1  0  0  0  0
 49 51  1  0  0  0  0
 51 52  2  0  0  0  0
 51 53  1  0  0  0  0
 46 54  1  0  0  0  0
 54 55  2  0  0  0  0
 55 56  1  0  0  0  0
 33 56  1  0  0  0  0
 56 57  2  0  0  0  0
 57 58  1  0  0  0  0
 58 59  2  0  0  0  0
 54 59  1  0  0  0  0
 59 60  1  0  0  0  0
 42 61  1  0  0  0  0
 61 62  2  0  0  0  0
 61 63  1  0  0  0  0
M  CHG  2  51   1  53  -1
M  END

     RDKit          3D

124126  0  0  0  0  0  0  0  0999 V2000
   11.4667    3.1517   -1.0689 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5798    2.3204   -1.6410 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3635    0.8551   -1.4221 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.5517    0.1305   -2.0495 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2596    0.5479    0.0358 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0387   -0.9495    0.2804 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7715   -1.3763   -0.4227 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4605   -2.8191   -0.1774 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3249   -3.1945    1.2717 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3018   -2.3417    1.9497 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9744   -2.4853    1.2764 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9487   -1.5925    2.0611 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7229   -1.6899    1.2957 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7445   -2.0203    0.0669 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4306   -1.4219    1.8507 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2726   -1.0886    3.2204 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3063   -1.5390    0.9128 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3764   -2.6492    1.4435 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3596   -2.8517    0.5238 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5604   -0.2771    0.8206 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7221    0.6797    1.5749 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5349   -0.1105   -0.2145 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7651    1.1273   -0.1782 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4269    2.2336   -0.9480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6276    0.8563   -0.5081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0654   -0.2776   -0.8543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6222    1.9212   -0.4400 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9954    1.4710   -0.7563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8924    0.8735   -2.1100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0756    0.8105   -2.9230 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2186    0.1123   -2.4810 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0674   -0.5615   -3.7452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3062    0.3483   -1.6642 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3968    0.9436   -2.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8950   -0.0431   -3.2521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8595    2.2000   -2.7339 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8447    3.1195   -2.1920 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.5938    3.6597   -3.5061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9311    2.5644   -1.3854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8337    2.0423   -2.1722 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2333    2.4486   -0.0242 N   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1326    2.9662    0.9715 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.7153    4.2472    0.7828 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7550    5.1574   -0.0116 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5697    4.6042    1.9826 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1009    1.9525    1.5666 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6854    0.4938    1.5871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8105   -0.0883    0.7314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1532   -1.2366    1.1089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3003   -1.9459    2.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6459   -3.0746    2.6145 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2108   -1.3962    3.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6189   -1.9996    4.3691 N   0  0  0  0  0  4  0  0  0  0  0  0
  -11.0618   -1.2794    5.2684 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5634   -3.3358    4.6327 O   0  0  0  0  0  1  0  0  0  0  0  0
  -10.8784   -0.1785    2.7771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7395   -1.5520    0.4436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8685   -0.5091    0.1071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9156   -0.7711   -0.8730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8658   -2.0365   -1.4043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7484   -3.0650   -1.0139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7628   -2.8210   -0.0349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5212   -3.8794    0.1912 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4991    2.8902   -1.5530 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5959    4.2386   -1.2825 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3826    3.0225    0.0363 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5671    2.5122   -2.7708 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5731    2.6422   -1.2643 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3986    0.5769   -1.9470 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3186   -0.9817   -2.0206 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.4529    0.2646   -1.4363 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.7377    0.4397   -3.0931 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.1663    0.8570    0.5465 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3722    1.0586    0.4376 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8466   -1.0486    1.3867 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9171   -1.5313   -0.0309 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9669   -0.7230   -0.1173 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9401   -1.3133   -1.5352 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5113   -3.0960   -0.6935 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.2962   -3.4647   -0.5903 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9617   -4.2719    1.2519 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3078   -3.2604    1.7922 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2380   -2.5345    3.0286 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5835   -1.2455    1.8576 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9593   -2.1850    0.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6199   -3.5390    1.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8976   -1.9991    3.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3396   -0.5645    2.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9060   -0.0573    3.3619 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5151   -1.8111    3.6505 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2044   -1.2452    3.7958 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6582   -1.8427   -0.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9386   -3.5185    1.6666 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8899   -2.2559    2.3946 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7078   -3.1905   -0.3587 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3814   -0.8522   -0.9181 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7551    1.4928    0.8960 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9606    3.1921   -0.5468 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5243    2.2440   -0.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3412    2.1266   -2.0436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3330    2.8470   -0.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5882    2.3961   -0.7343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2306    0.7527    0.0253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1343    0.2173   -4.6063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8207   -1.2698   -4.0304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0166   -0.8995   -3.8413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9417    1.1774   -1.0069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3947    2.7104   -3.6393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3698    4.0554   -1.8270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9152    4.3530   -3.9958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7388    2.6803   -4.0427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5544    4.0042   -3.1508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5544    1.7474    0.5027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3903    3.1324    1.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0826    4.4434    2.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0914    2.1094    1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1465    2.2971    2.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8776    0.2286   -0.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7252   -3.5696    3.4393 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6229    0.2345    3.4895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8005    0.4417    0.7654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1371   -2.3495   -2.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6255   -4.0326   -1.4622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3219   -4.1141    0.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 59  1  0
 59 60  1  0
 60 61  2  0
 61 62  1  0
 62 63  1  0
 62 57  2  0
 57 58  1  0
 57 49  1  0
 49 50  1  0
 50 51  1  0
 50 52  2  0
 52 56  1  0
 56 47  2  0
 47 46  1  0
 46 42  1  0
 42 41  1  0
 41 39  1  0
 39 40  2  0
 39 37  1  0
 37 38  1  0
 37 36  1  0
 36 34  1  0
 34 35  2  0
 42 43  1  0
 43 45  1  0
 43 44  2  0
 47 48  1  0
 52 53  1  0
 53 55  1  0
 53 54  2  0
 34 33  1  0
 58 59  2  0
 48 49  2  0
  1 64  1  0
  1 65  1  0
  1 66  1  0
  2 67  1  0
  2 68  1  0
  3 69  1  6
  4 70  1  0
  4 71  1  0
  4 72  1  0
  5 73  1  0
  5 74  1  0
  6 75  1  0
  6 76  1  0
  7 77  1  0
  7 78  1  0
  8 79  1  0
  8 80  1  0
  9 81  1  0
  9 82  1  0
 10 83  1  0
 10 84  1  0
 11 85  1  0
 11 86  1  0
 12 87  1  0
 12 88  1  0
 16 89  1  0
 16 90  1  0
 16 91  1  0
 17 92  1  6
 18 93  1  0
 18 94  1  0
 19 95  1  0
 22 96  1  0
 23 97  1  1
 24 98  1  0
 24 99  1  0
 24100  1  0
 27101  1  0
 28102  1  0
 28103  1  0
 32104  1  0
 32105  1  0
 32106  1  0
 33107  1  1
 60122  1  0
 61123  1  0
 63124  1  0
 58121  1  0
 51119  1  0
 56120  1  0
 46116  1  0
 46117  1  0
 42114  1  1
 41113  1  0
 37109  1  1
 38110  1  0
 38111  1  0
 38112  1  0
 36108  1  0
 45115  1  0
 48118  1  0
M  CHG  2  53   1  55  -1
M  END


  Mrv1533004251505582D          

 63 65  0  0  0  0            999 V2000
   10.7171  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -13.6125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -14.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775  -13.6125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -14.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -12.3750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788  -11.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -14.0250    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   32.1512  -13.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -14.8500    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   28.5788  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -9.9000    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  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 49 50  2  0  0  0  0
 44 50  1  0  0  0  0
 49 51  1  0  0  0  0
 51 52  2  0  0  0  0
 51 53  1  0  0  0  0
 46 54  1  0  0  0  0
 54 55  2  0  0  0  0
 55 56  1  0  0  0  0
 33 56  1  0  0  0  0
 56 57  2  0  0  0  0
 57 58  1  0  0  0  0
 58 59  2  0  0  0  0
 54 59  1  0  0  0  0
 59 60  1  0  0  0  0
 42 61  1  0  0  0  0
 61 62  2  0  0  0  0
 61 63  1  0  0  0  0
M  CHG  2  51   1  53  -1
M  END
> <DATABASE_ID>
NP0172750

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)CCCCCCCCC(=O)N(C)C(CO)C(=O)NC(C)C(=O)NCC(=O)N(C)C1C2=CC=C(O)C(=C2)C2=C(O)C(=CC(CC(NC(=O)C(C)NC1=O)C(O)=O)=C2)[N+]([O-])=O

> <INCHI_IDENTIFIER>
InChI=1S/C43H61N7O13/c1-7-24(2)14-12-10-8-9-11-13-15-35(53)48(5)33(23-51)41(58)45-25(3)39(56)44-22-36(54)49(6)37-28-16-17-34(52)29(21-28)30-18-27(20-32(38(30)55)50(62)63)19-31(43(60)61)47-40(57)26(4)46-42(37)59/h16-18,20-21,24-26,31,33,37,51-52,55H,7-15,19,22-23H2,1-6H3,(H,44,56)(H,45,58)(H,46,59)(H,47,57)(H,60,61)

> <INCHI_KEY>
ULSQXBDNXAHTQS-UHFFFAOYSA-N

> <FORMULA>
C43H61N7O13

> <MOLECULAR_WEIGHT>
883.997

> <EXACT_MASS>
883.432735052

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
124

> <JCHEM_AVERAGE_POLARIZABILITY>
91.9439774162882

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-(2-{2-[2-(N,10-dimethyldodecanamido)-3-hydroxypropanamido]propanamido}-N-methylacetamido)-3,18-dihydroxy-11-methyl-4-nitro-10,13-dioxo-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),15,17-hexaene-8-carboxylic acid

> <ALOGPS_LOGP>
3.33

> <JCHEM_LOGP>
2.4087157746666663

> <ALOGPS_LOGS>
-5.08

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.24013356165606

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.158497820742058

> <JCHEM_PKA_STRONGEST_BASIC>
-2.847449974310183

> <JCHEM_POLAR_SURFACE_AREA>
298.15

> <JCHEM_REFRACTIVITY>
227.69930000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.28e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-(2-{2-[2-(N,10-dimethyldodecanamido)-3-hydroxypropanamido]propanamido}-N-methylacetamido)-3,18-dihydroxy-11-methyl-4-nitro-10,13-dioxo-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),15,17-hexaene-8-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      20.005 -25.410   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      21.339 -26.180   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      22.673 -25.410   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      22.673 -23.870   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      24.006 -26.180   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      25.340 -25.410   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      26.674 -26.180   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      28.007 -25.410   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      29.341 -26.180   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      30.675 -25.410   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      32.008 -26.180   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      33.342 -25.410   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      34.676 -26.180   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      34.676 -27.720   0.000  0.00  0.00           O+0
HETATM   15  N   UNK     0      36.009 -25.410   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      36.009 -23.870   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      37.343 -26.180   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      37.343 -27.720   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      38.677 -28.490   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      38.677 -25.410   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      38.677 -23.870   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0      40.010 -26.180   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0      41.344 -25.410   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      41.344 -23.870   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      42.678 -26.180   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      42.678 -27.720   0.000  0.00  0.00           O+0
HETATM   27  N   UNK     0      44.011 -25.410   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0      45.345 -26.180   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      46.679 -25.410   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      46.679 -23.870   0.000  0.00  0.00           O+0
HETATM   31  N   UNK     0      48.012 -26.180   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0      48.012 -27.720   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      49.346 -25.410   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      49.346 -23.870   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      48.012 -23.100   0.000  0.00  0.00           O+0
HETATM   36  N   UNK     0      50.680 -23.100   0.000  0.00  0.00           N+0
HETATM   37  C   UNK     0      50.680 -21.560   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      49.346 -20.790   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      52.013 -20.790   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      52.013 -19.250   0.000  0.00  0.00           O+0
HETATM   41  N   UNK     0      53.347 -21.560   0.000  0.00  0.00           N+0
HETATM   42  C   UNK     0      54.681 -20.790   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      56.015 -21.560   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      56.015 -23.100   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      54.681 -23.870   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      54.681 -25.410   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      56.015 -26.180   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      56.015 -27.720   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      57.348 -25.410   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      57.348 -23.870   0.000  0.00  0.00           C+0
HETATM   51  N   UNK     0      58.682 -26.180   0.000  0.00  0.00           N+1
HETATM   52  O   UNK     0      60.016 -25.410   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0      58.682 -27.720   0.000  0.00  0.00           O-1
HETATM   54  C   UNK     0      53.347 -26.180   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      52.013 -25.410   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      50.680 -26.180   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      50.680 -27.720   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      52.013 -28.490   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      53.347 -27.720   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0      54.681 -28.490   0.000  0.00  0.00           O+0
HETATM   61  C   UNK     0      54.681 -19.250   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      56.015 -18.480   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0      53.347 -18.480   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                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   56                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43   61                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45   50                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47   54                                                  
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   50   51                                                  
CONECT   50   49   44                                                       
CONECT   51   49   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51                                                            
CONECT   54   46   55   59                                                  
CONECT   55   54   56                                                       
CONECT   56   55   33   57                                                  
CONECT   57   56   58                                                       
CONECT   58   57   59                                                       
CONECT   59   58   54   60                                                  
CONECT   60   59                                                            
CONECT   61   42   62   63                                                  
CONECT   62   61                                                            
CONECT   63   61                                                            
MASTER        0    0    0    0    0    0    0    0   63    0  130    0
END

View in JSmol

Synonyms

Value	Source
14-{2-[(2-{[2-(N,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-N-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1,]icosa-1(18),2,4,6(20),9,12,15(19),16-octaene-8-carboxylate	Generator
14-{2-[(2-{[2-(N,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-N-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(18),2,4,6(20),9,12,15(19),16-octaene-8-carboxylate	Generator

Chemical Formula

C₄₃H₆₁N₇O₁₃

Average Mass

883.9970 Da

Monoisotopic Mass

883.43274 Da

IUPAC Name

14-(2-{2-[2-(N,10-dimethyldodecanamido)-3-hydroxypropanamido]propanamido}-N-methylacetamido)-3,18-dihydroxy-11-methyl-4-nitro-10,13-dioxo-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),15,17-hexaene-8-carboxylic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

CCC(C)CCCCCCCCC(=O)N(C)C(CO)C(=O)NC(C)C(=O)NCC(=O)N(C)C1C2=CC=C(O)C(=C2)C2=C(O)C(=CC(CC(NC(=O)C(C)NC1=O)C(O)=O)=C2)[N+]([O-])=O

InChI Identifier

InChI=1S/C43H61N7O13/c1-7-24(2)14-12-10-8-9-11-13-15-35(53)48(5)33(23-51)41(58)45-25(3)39(56)44-22-36(54)49(6)37-28-16-17-34(52)29(21-28)30-18-27(20-32(38(30)55)50(62)63)19-31(43(60)61)47-40(57)26(4)46-42(37)59/h16-18,20-21,24-26,31,33,37,51-52,55H,7-15,19,22-23H2,1-6H3,(H,44,56)(H,45,58)(H,46,59)(H,47,57)(H,60,61)

InChI Key

ULSQXBDNXAHTQS-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 cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Cucurbitacin glycosides

Alternative Parents

Substituents

Cucurbitacin glycoside skeleton
Cycloartanol-skeleton
9b,19-cyclo-lanostane-skeleton
Cycloartane-skeleton
Triterpenoid
21-hydroxysteroid
12-hydroxysteroid
15-hydroxysteroid
Hydroxysteroid
Glycosyl compound
O-glycosyl compound
Ketal
Oxepane
Oxane
Monosaccharide
Meta-dioxolane
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Polyol
Organoheterocyclic compound
Oxacycle
Acetal
Primary alcohol
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	3.33	ALOGPS
logP	2.41	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	3.16	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	298.15 Å²	ChemAxon
Rotatable Bond Count	20	ChemAxon
Refractivity	227.7 m³·mol⁻¹	ChemAxon
Polarizability	91.94 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73161295

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid (NP0172750)

MOL for NP0172750 (14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid)

3D MOL for NP0172750 (14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid)

3D SDF for NP0172750 (14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid)

3D-SDF for NP0172750 (14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid)

PDB for NP0172750 (14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid)

3D PDB for NP0172750 (14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid)

SMILES for NP0172750 (14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid)

INCHI for NP0172750 (14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid)

Structure for NP0172750 (14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid)

3D Structure for NP0172750 (14-{2-[(2-{[2-(n,10-dimethyldodecanamido)-1,3-dihydroxypropylidene]amino}-1-hydroxypropylidene)amino]-n-methylacetamido}-3,10,13,18-tetrahydroxy-11-methyl-4-nitro-9,12-diazatricyclo[13.3.1.1²,⁶]icosa-1(19),2,4,6(20),9,12,15,17-octaene-8-carboxylic acid)