NP-MRD: Showing NP-Card for 2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate (NP0200011)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 18:46:03 UTC

Updated at

2022-09-04 18:46:03 UTC

NP-MRD ID

NP0200011

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate

Description

2,18-Dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]Henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate belongs to the class of organic compounds known as indolecarboxylic acids. Indolecarboxylic acids are compounds containing a carboxylic acid group linked to an indole. 2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate is found in Kopsia pauciflora. 2,18-Dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]Henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191516242D          

 35 39  0  0  0  0            999 V2000
    0.0180    2.8206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7482    2.2453    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2119    1.2545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2429    1.0959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1958    0.6319    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2074    0.7352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9704    1.0489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4920    1.8098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2130    2.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6236    0.5450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5039    0.6203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2531    0.2071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5138   -0.2727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7508   -0.5864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0976   -0.0825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4956    0.8761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8590    1.6745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1835    2.1764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3210    1.7706    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6157    1.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0434    0.7116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0627   -0.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5360   -0.8422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2354   -1.3406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0147   -0.9866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1883   -0.1128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5529    0.2187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7365    0.7786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6973   -0.0580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1045    1.2916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7671    0.4564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7374    2.3423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1691    3.1463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7347    1.0202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0773    0.3115    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  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  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  5 26  1  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 23 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 19 34  1  0  0  0  0
 16 34  1  0  0  0  0
 34 35  2  0  0  0  0
M  END

     RDKit          3D

 65 69  0  0  0  0  0  0  0  0999 V2000
    1.7864    3.9913   -2.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6675    2.8191   -1.3624 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6177    1.9575   -1.5842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1713    2.2968   -2.4856 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4548    0.7774   -0.8245 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5317    0.1581   -0.1099 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0222   -0.8894    0.5672 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8027   -1.6626    1.3917 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1507   -1.4103    1.5700 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6817   -0.3647    0.8948 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0315   -0.0508    1.0232 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9122   -0.7678    1.8326 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8872    0.4243    0.0528 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5188    1.4538   -0.6023 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1628    1.1190   -1.8503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3960   -1.0818    0.2089 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0922   -1.5862    1.3839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6115   -3.0130    1.0893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7173   -2.8373   -0.3977 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9034   -3.1811   -1.1043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1686   -2.8602   -0.3357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3237   -1.4608    0.0944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4640   -0.4276   -0.5527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9733   -0.3328   -1.7356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4523   -0.2206   -1.8583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8108    0.0866   -0.5584 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6552    1.1167    0.1474 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7809    2.1752   -0.8109 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0002    1.7820    1.2862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6891    1.1684    2.3233 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6778    3.1613    1.2855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0472    3.7561    2.4061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0906    0.7365    0.3695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4850   -2.3026   -0.7416 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4906   -2.5021   -1.5242 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3989    3.7242   -3.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2663    4.8293   -1.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7766    4.2616   -2.5036 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3895   -2.5145    1.9347 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7426   -2.0391    2.2309 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6092   -0.7071    2.8943 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9163   -1.8307    1.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9307   -0.3829    1.7150 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3942    0.6065   -2.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4421    2.0985   -2.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9978    0.4374   -1.6932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353   -1.0850    1.8148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4024   -1.7629    2.2694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5352   -3.2383    1.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8653   -3.7843    1.3378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8985   -4.3135   -1.1751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0602   -2.8309   -2.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2148   -3.5906    0.4968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0120   -3.1596   -1.0248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2004   -1.4421    1.2017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4243   -1.1951   -0.0115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4190   -0.3061   -2.7527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1752   -1.2322   -2.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2008    0.4621   -2.6854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9543    3.0314   -0.3503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2158    4.8488    2.3719 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0467    3.5522    2.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4785    3.3701    3.3686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7946    1.6033    0.1216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3324    0.5604    1.4154 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6 13  2  0
 13 14  1  0
 14 15  1  0
 13 10  1  0
 10 11  1  0
 11 12  1  0
 10  9  2  0
  9  8  1  0
  8  7  2  0
  7 16  1  0
 16 17  1  1
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  6
 27 33  1  0
 27 29  1  0
 29 30  2  0
 29 31  1  0
 31 32  1  0
 19 34  1  0
 34 35  2  0
 26  5  1  6
  7  6  1  0
 26 16  1  0
 34 16  1  0
 33 23  1  0
  1 36  1  0
  1 37  1  0
  1 38  1  0
 15 44  1  0
 15 45  1  0
 15 46  1  0
 12 41  1  0
 12 42  1  0
 12 43  1  0
  9 40  1  0
  8 39  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 24 57  1  0
 25 58  1  0
 25 59  1  0
 28 60  1  0
 33 64  1  0
 33 65  1  0
 32 61  1  0
 32 62  1  0
 32 63  1  0
M  END


  Mrv1533004191516242D          

 35 39  0  0  0  0            999 V2000
    0.0180    2.8206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7482    2.2453    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2119    1.2545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2429    1.0959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1958    0.6319    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2074    0.7352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9704    1.0489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4920    1.8098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2130    2.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6236    0.5450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5039    0.6203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2531    0.2071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5138   -0.2727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7508   -0.5864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0976   -0.0825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4956    0.8761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8590    1.6745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1835    2.1764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3210    1.7706    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6157    1.3921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0434    0.7116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0627   -0.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5360   -0.8422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2354   -1.3406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0147   -0.9866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1883   -0.1128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5529    0.2187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7365    0.7786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6973   -0.0580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1045    1.2916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7671    0.4564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7374    2.3423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1691    3.1463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7347    1.0202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0773    0.3115    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  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  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  5 26  1  0  0  0  0
 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 23 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 19 34  1  0  0  0  0
 16 34  1  0  0  0  0
 34 35  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0200011

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)N1C2=C(OC)C(OC)=CC=C2C23CCN(CCCC4=CCC12C(O)(C4)C(=O)OC)C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H30N2O8/c1-32-17-8-7-16-18(19(17)33-2)27(22(30)35-4)25-10-9-15(14-24(25,31)21(29)34-3)6-5-12-26-13-11-23(16,25)20(26)28/h7-9,31H,5-6,10-14H2,1-4H3

> <INCHI_KEY>
SQMISQBTNOKVMW-UHFFFAOYSA-N

> <FORMULA>
C25H30N2O8

> <MOLECULAR_WEIGHT>
486.521

> <EXACT_MASS>
486.200215934

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
48.92890817692303

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3,5,7,16(20)-tetraene-2,18-dicarboxylate

> <ALOGPS_LOGP>
1.06

> <JCHEM_LOGP>
0.8730378216666668

> <ALOGPS_LOGS>
-3.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.522092372588494

> <JCHEM_PKA_STRONGEST_BASIC>
-1.4177340044930835

> <JCHEM_POLAR_SURFACE_AREA>
114.84

> <JCHEM_REFRACTIVITY>
123.79419999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.15e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3,5,7,16(20)-tetraene-2,18-dicarboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       0.034   5.265   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.397   4.191   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.262   2.342   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.453   2.046   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0       4.099   1.180   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       5.987   1.372   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.411   1.958   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.385   3.378   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.731   4.289   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.631   1.017   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.274   1.158   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.673   0.387   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.426  -0.509   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.001  -1.095   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.782  -0.154   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.658   1.635   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.337   3.126   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.076   4.063   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       2.466   3.305   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       1.149   2.598   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.081   1.328   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.117  -0.328   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.001  -1.572   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.306  -2.502   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.761  -1.842   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.085  -0.210   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.899   0.408   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.375   1.453   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.302  -0.108   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.928   2.411   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       5.165   0.852   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       3.243   4.372   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.049   5.873   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.238   1.904   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       2.011   0.582   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   26                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    6   16                                                  
CONECT   16   15   17   26   34                                             
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   34                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    5   16   27                                             
CONECT   27   26   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27   23                                                       
CONECT   30   27   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32                                                            
CONECT   34   19   16   35                                                  
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Value	Source
2,18-Dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1,.0,.0,]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylic acid	Generator
2,18-Dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylic acid	Generator

Chemical Formula

C₂₅H₃₀N₂O₈

Average Mass

486.5210 Da

Monoisotopic Mass

486.20022 Da

IUPAC Name

2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3,5,7,16(20)-tetraene-2,18-dicarboxylate

Traditional Name

2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3,5,7,16(20)-tetraene-2,18-dicarboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)N1C2=C(OC)C(OC)=CC=C2C23CCN(CCCC4=CCC12C(O)(C4)C(=O)OC)C3=O

InChI Identifier

InChI=1S/C25H30N2O8/c1-32-17-8-7-16-18(19(17)33-2)27(22(30)35-4)25-10-9-15(14-24(25,31)21(29)34-3)6-5-12-26-13-11-23(16,25)20(26)28/h7-9,31H,5-6,10-14H2,1-4H3

InChI Key

SQMISQBTNOKVMW-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

Species Name	Source	Reference
Kopsia pauciflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indolecarboxylic acids. Indolecarboxylic acids are compounds containing a carboxylic acid group linked to an indole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indolecarboxylic acids and derivatives

Direct Parent

Indolecarboxylic acids

Alternative Parents

Substituents

Indolecarboxylic acid
Anisole
Phenol ether
Alkyl aryl ether
Pyrrolidone
Benzenoid
N-alkylpyrrolidine
2-pyrrolidone
Pyrrolidine
Methyl ester
Tertiary alcohol
Tertiary carboxylic acid amide
Carbamic acid ester
Lactam
Carboxylic acid ester
Carboxamide group
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Azacycle
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic nitrogen compound
Organic oxygen compound
Carbonyl group
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	1.06	ALOGPS
logP	0.87	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	11.52	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	114.84 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	123.79 m³·mol⁻¹	ChemAxon
Polarizability	48.93 Å³	ChemAxon
Number of Rings	5	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

85182567

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate (NP0200011)

MOL for NP0200011 (2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate)

3D MOL for NP0200011 (2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate)

3D SDF for NP0200011 (2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate)

3D-SDF for NP0200011 (2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate)

PDB for NP0200011 (2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate)

3D PDB for NP0200011 (2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate)

SMILES for NP0200011 (2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate)

INCHI for NP0200011 (2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate)

Structure for NP0200011 (2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate)

3D Structure for NP0200011 (2,18-dimethyl 18-hydroxy-4,5-dimethoxy-21-oxo-2,12-diazapentacyclo[14.2.2.1⁹,¹².0¹,⁹.0³,⁸]henicosa-3(8),4,6,16(20)-tetraene-2,18-dicarboxylate)