NP-MRD: Showing NP-Card for n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid (NP0196605)

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Record Information

Version

2.0

Created at

2022-09-04 14:43:33 UTC

Updated at

2022-09-04 14:43:33 UTC

NP-MRD ID

NP0196605

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid

Description

N-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]Nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid belongs to the class of organic compounds known as lappaconitine-type diterpenoid alkaloids. These are c18-bisnorditerpenoid alkaloids with a structure based on the heptacyclic lappaconitine skeleton. Lappaconitine similar to aconitane, with the difference that the former lacks a carbon atom at the 18-position. N-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]Nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191520322D          

 42 48  0  0  0  0            999 V2000
   -0.3274   -2.3893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4962   -2.3415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8666   -1.6043    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4197   -0.8647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7821   -0.0895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0090    0.1985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1282    1.0120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5078    1.5376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2809    1.2496    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3706    2.3511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4026    2.6390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5397    3.4525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962    3.9781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8693    3.6901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0065    2.8766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7796    2.5887    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4155    3.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1887    2.8263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2784    3.9278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0155    0.7352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1498    0.5079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3937    1.2960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6456    0.4548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0354    0.0925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9630    0.9143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6386    1.3879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5387   -1.3033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7618   -2.0976    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
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
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 10 15  1  0  0  0  0
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  5 20  1  0  0  0  0
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  5 35  1  0  0  0  0
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 33 36  1  0  0  0  0
  3 36  1  0  0  0  0
 25 36  1  0  0  0  0
 31 37  1  0  0  0  0
 26 37  1  0  0  0  0
 37 38  1  0  0  0  0
 28 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 29 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END

     RDKit          3D

 88 94  0  0  0  0  0  0  0  0999 V2000
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   -0.2040   -0.1217    3.7930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0955   -0.0495    2.3725 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2006    0.0414    1.8547 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2035    0.1672    0.3819 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1854    1.1509   -0.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4798    0.8710    0.0012 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4380    0.7198    0.8754 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1129    0.9003    2.1093 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8206    0.3700    0.6345 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6726    0.1714    1.7266 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9665   -0.2179    1.5494 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4690   -0.4255    0.2895 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.0300    1.5894   -1.3520 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0921    2.3735   -1.8689 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9341    3.0501   -2.9926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7438    2.0808   -0.0017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3067    1.1800    1.1104 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0581    1.2978    2.2762 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5424   -1.0265    1.2597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0913   -1.4032   -0.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2996   -0.9842   -0.3737 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  1
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 31 75  1  0
 35 79  1  1
 36 80  1  0
 36 81  1  0
 37 82  1  6
 38 83  1  1
M  END


  Mrv1533004191520322D          

 42 48  0  0  0  0            999 V2000
   -0.3274   -2.3893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4962   -2.3415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8666   -1.6043    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4197   -0.8647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7821   -0.0895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0090    0.1985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1282    1.0120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5078    1.5376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2809    1.2496    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3706    2.3511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4026    2.6390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5397    3.4525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962    3.9781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8693    3.6901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0065    2.8766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7796    2.5887    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4155    3.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1887    2.8263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2784    3.9278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0155    0.7352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8202    0.9654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3453    0.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1498    0.5079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3937    1.2960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1346   -0.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9178   -0.1091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6456    0.4548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4646   -0.2533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7393   -1.0995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1200   -1.6852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3060   -1.4797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3073   -2.3047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3984   -1.7119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3902   -1.3704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4816   -0.4669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8221   -1.5122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3899   -0.6478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0354    0.0925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9630    0.9143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6386    1.3879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5387   -1.3033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7618   -2.0976    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
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  5 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
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 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  1  0  0  0  0
  5 35  1  0  0  0  0
 25 35  1  0  0  0  0
 33 36  1  0  0  0  0
  3 36  1  0  0  0  0
 25 36  1  0  0  0  0
 31 37  1  0  0  0  0
 26 37  1  0  0  0  0
 37 38  1  0  0  0  0
 28 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 29 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0196605

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1CC2(COC(=O)C3=CC=CC=C3NC(C)=O)CCC(OC)C34C5CC6C(OC)C5C(O)(CC6OC)C(CC23)C14

> <INCHI_IDENTIFIER>
InChI=1S/C33H46N2O7/c1-6-35-16-31(17-42-30(37)19-9-7-8-10-23(19)34-18(2)36)12-11-26(40-4)33-21-13-20-24(39-3)15-32(38,27(21)28(20)41-5)22(29(33)35)14-25(31)33/h7-10,20-22,24-29,38H,6,11-17H2,1-5H3,(H,34,36)

> <INCHI_KEY>
DJZIEWQFQQMVTG-UHFFFAOYSA-N

> <FORMULA>
C33H46N2O7

> <MOLECULAR_WEIGHT>
582.738

> <EXACT_MASS>
582.330501829

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
64.88041832562858

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methyl 2-acetamidobenzoate

> <ALOGPS_LOGP>
2.45

> <JCHEM_LOGP>
2.1129113083333326

> <ALOGPS_LOGS>
-4.41

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.137166419622979

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.536051226837749

> <JCHEM_PKA_STRONGEST_BASIC>
10.006978165215752

> <JCHEM_POLAR_SURFACE_AREA>
106.56000000000002

> <JCHEM_REFRACTIVITY>
157.72239999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.26e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methyl 2-acetamidobenzoate

> <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      -0.611  -4.460   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.926  -4.371   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       1.618  -2.995   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       0.783  -1.614   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.460  -0.167   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.017   0.370   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.239   1.889   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.948   2.870   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.391   2.333   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.692   4.389   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.751   4.926   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.008   6.445   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.180   7.426   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.623   6.888   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.879   5.370   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       3.322   4.832   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       4.509   5.813   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.952   5.276   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.253   7.332   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.896   1.372   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.398   1.802   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.378   0.607   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.880   0.948   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.335   2.419   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.985  -0.999   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.447  -0.204   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.805   0.849   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.334  -0.473   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.847  -2.052   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.691  -3.146   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.171  -2.762   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       6.174  -4.302   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.477  -3.195   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.595  -2.558   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.766  -0.872   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.401  -2.823   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.328  -1.209   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.533   0.173   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       7.398   1.707   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       8.659   2.591   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      10.339  -2.433   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      10.755  -3.915   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   36                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   20   35                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20    5   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26   35   36                                             
CONECT   26   25   27   37                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   38                                                  
CONECT   29   28   30   41                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33   37                                             
CONECT   32   31                                                            
CONECT   33   31   34   36                                                  
CONECT   34   33   35                                                       
CONECT   35   34    5   25                                                  
CONECT   36   33    3   25                                                  
CONECT   37   31   26   38                                                  
CONECT   38   37   28   39                                                  
CONECT   39   38   40                                                       
CONECT   40   39                                                            
CONECT   41   29   42                                                       
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   96    0
END

View in JSmol

Synonyms

Value	Source
N-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1,.0,.0,.0,]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidate	Generator
N-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidate	Generator

Chemical Formula

C₃₃H₄₆N₂O₇

Average Mass

582.7380 Da

Monoisotopic Mass

582.33050 Da

IUPAC Name

{11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methyl 2-acetamidobenzoate

Traditional Name

{11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methyl 2-acetamidobenzoate

CAS Registry Number

Not Available

SMILES

CCN1CC2(COC(=O)C3=CC=CC=C3NC(C)=O)CCC(OC)C34C5CC6C(OC)C5C(O)(CC6OC)C(CC23)C14

InChI Identifier

InChI=1S/C33H46N2O7/c1-6-35-16-31(17-42-30(37)19-9-7-8-10-23(19)34-18(2)36)12-11-26(40-4)33-21-13-20-24(39-3)15-32(38,27(21)28(20)41-5)22(29(33)35)14-25(31)33/h7-10,20-22,24-29,38H,6,11-17H2,1-5H3,(H,34,36)

InChI Key

DJZIEWQFQQMVTG-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 lappaconitine-type diterpenoid alkaloids. These are c18-bisnorditerpenoid alkaloids with a structure based on the heptacyclic lappaconitine skeleton. Lappaconitine similar to aconitane, with the difference that the former lacks a carbon atom at the 18-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Lappaconitine-type diterpenoid alkaloids

Alternative Parents

Substituents

Lappaconitine-type diterpenoid alkaloid
Quinolidine
Alkaloid or derivatives
Azepane
Piperidine
Cyclic alcohol
Tertiary alcohol
1,2-aminoalcohol
Secondary alcohol
Tertiary aliphatic amine
Tertiary amine
Dialkyl ether
Ether
Polyol
Azacycle
Organoheterocyclic compound
Organonitrogen compound
Alcohol
Organic nitrogen compound
Organopnictogen compound
Organooxygen compound
Hydrocarbon derivative
Amine
Organic oxygen 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	2.45	ALOGPS
logP	2.11	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	12.54	ChemAxon
pKa (Strongest Basic)	10.01	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	106.56 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	157.72 m³·mol⁻¹	ChemAxon
Polarizability	64.88 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid (NP0196605)

MOL for NP0196605 (n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid)

3D MOL for NP0196605 (n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid)

3D SDF for NP0196605 (n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid)

3D-SDF for NP0196605 (n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid)

PDB for NP0196605 (n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid)

3D PDB for NP0196605 (n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid)

SMILES for NP0196605 (n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid)

INCHI for NP0196605 (n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid)

Structure for NP0196605 (n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid)

3D Structure for NP0196605 (n-{2-[({11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl}methoxy)carbonyl]phenyl}ethanimidic acid)