NP-MRD: Showing NP-Card for n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid (NP0219702)

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Record Information

Version

2.0

Created at

2022-09-05 20:47:33 UTC

Updated at

2022-09-05 20:47:33 UTC

NP-MRD ID

NP0219702

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid

Description

N-[2-({[(5R,8R)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]Nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom. n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid is found in Delphinium grandiflorum, Delphinium omeiense and Delphinium potaninii. Based on a literature review very few articles have been published on N-[2-({[(5R,8R)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]Nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309052222472D          

 50 56  0  0  1  0            999 V2000
    0.7927   -3.3124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5317   -2.4970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9484   -1.5670    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3871   -0.8573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7482   -0.0814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0699    0.3079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    1.0526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0654    1.7617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7595    1.7511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4687    2.4815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2936    2.4921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6969    3.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2752    3.9209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4503    3.9103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0470    3.1906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7779    3.1799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1996    3.8890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7963    4.6088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0245    3.8784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4462    4.5875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4278    3.1587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2527    3.1480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6560    2.4283    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6744    3.8571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9801    0.7437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7844    0.9753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3106    0.3360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6136    1.2152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4635    2.0871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1015   -0.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8839   -0.0973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6107    0.4679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4310   -0.2387    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7071   -1.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5654   -1.2281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0010   -1.9860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0889   -1.6713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2746   -1.4672    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4518   -2.3180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3570   -0.6352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0011    0.1063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7648    0.6934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5634    1.1153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3673   -1.7009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4068   -2.5742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3586   -1.3613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5176   -1.8655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3578   -1.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4484   -0.4576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7907   -1.5023    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
 16 15  1  4  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  5 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
 27 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 33 32  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  0  0  0  0
 31 40  1  0  0  0  0
 40 41  1  0  0  0  0
 33 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 38 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 46 49  1  0  0  0  0
  5 49  1  0  0  0  0
 30 49  1  0  0  0  0
 44 50  1  0  0  0  0
  3 50  1  0  0  0  0
 30 50  1  0  0  0  0
M  END


  Mrv1652309052222472D          

 50 56  0  0  1  0            999 V2000
    0.7927   -3.3124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5317   -2.4970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9484   -1.5670    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3871   -0.8573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7482   -0.0814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0699    0.3079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4871    1.0526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0654    1.7617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7595    1.7511    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4687    2.4815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2936    2.4921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6969    3.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2752    3.9209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4503    3.9103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0470    3.1906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7779    3.1799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1996    3.8890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7963    4.6088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0245    3.8784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4462    4.5875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4278    3.1587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2527    3.1480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6560    2.4283    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6744    3.8571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9801    0.7437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7844    0.9753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3106    0.3360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6136    1.2152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4635    2.0871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1015   -0.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8839   -0.0973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6107    0.4679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4310   -0.2387    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7071   -1.0844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5654   -1.2281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0010   -1.9860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0889   -1.6713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2746   -1.4672    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4518   -2.3180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3570   -0.6352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0011    0.1063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7648    0.6934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5634    1.1153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3673   -1.7009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4068   -2.5742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3586   -1.3613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5176   -1.8655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3578   -1.9429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4484   -0.4576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7907   -1.5023    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
 16 15  1  4  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  5 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
 27 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 33 32  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  0  0  0  0
 31 40  1  0  0  0  0
 40 41  1  0  0  0  0
 33 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 38 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 46 49  1  0  0  0  0
  5 49  1  0  0  0  0
 30 49  1  0  0  0  0
 44 50  1  0  0  0  0
  3 50  1  0  0  0  0
 30 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0219702

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCN1CC2(COC(=O)C3=CC=CC=C3N=C(O)C(C)CC(O)=N)CCC(OC)C34C5C[C@H]6C(OC)C5[C@](O)(CC6OC)C(O)(C(OC)C23)C14

> <INCHI_IDENTIFIER>
InChI=1S/C37H53N3O10/c1-7-40-17-34(18-50-32(43)20-10-8-9-11-23(20)39-31(42)19(2)14-26(38)41)13-12-25(47-4)36-22-15-21-24(46-3)16-35(44,27(22)28(21)48-5)37(45,33(36)40)30(49-6)29(34)36/h8-11,19,21-22,24-25,27-30,33,44-45H,7,12-18H2,1-6H3,(H2,38,41)(H,39,42)/t19?,21-,22?,24?,25?,27?,28?,29?,30?,33?,34?,35-,36?,37?/m1/s1

> <INCHI_KEY>
NXAZXMKMGPWXII-OWBGXFSJSA-N

> <FORMULA>
C37H53N3O10

> <MOLECULAR_WEIGHT>
699.842

> <EXACT_MASS>
699.373094919

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
75.49564933979448

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[2-({[(5R,8R)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1^{2,5}.0^{1,10}.0^{3,8}.0^{13,17}]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid

> <JCHEM_LOGP>
-3.9693054113032558

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
4.952704202899866

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.1830741456295533

> <JCHEM_PKA_STRONGEST_BASIC>
12.623869588239911

> <JCHEM_POLAR_SURFACE_AREA>
183.58999999999997

> <JCHEM_REFRACTIVITY>
193.98169999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-[2-({[(5R,8R)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1^{2,5}.0^{1,10}.0^{3,8}.0^{13,17}]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       1.480  -6.183   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.992  -4.661   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       1.770  -2.925   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       0.723  -1.600   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.397  -0.152   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.130   0.575   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.909   1.965   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.122   3.289   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.418   3.269   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.875   4.632   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.415   4.652   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.168   5.995   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.380   7.319   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.841   7.299   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.088   5.956   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       1.452   5.936   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       2.239   7.260   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.486   8.603   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.779   7.240   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.566   8.563   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.532   5.896   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.072   5.876   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       6.824   4.533   0.000  0.00  0.00           N+0
HETATM   24  O   UNK     0       6.859   7.200   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.830   1.388   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.331   1.821   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.313   0.627   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.879   2.268   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.599   3.896   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.923  -0.980   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.383  -0.182   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.740   0.873   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.271  -0.446   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.787  -2.024   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      10.389  -2.292   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      11.202  -3.707   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.633  -3.120   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.113  -2.739   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       6.443  -4.327   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       6.266  -1.186   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.469   0.198   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       8.894   1.294   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      10.385   2.082   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       4.419  -3.175   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       4.493  -4.805   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       2.536  -2.541   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       0.966  -3.482   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -0.668  -3.627   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       2.704  -0.854   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       3.343  -2.804   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   50                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   25   49                                             
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   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25    5   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   31   49   50                                             
CONECT   31   30   32   40                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   41                                                  
CONECT   34   33   35   37                                                  
CONECT   35   34   36                                                       
CONECT   36   35                                                            
CONECT   37   34   38                                                       
CONECT   38   37   39   40   44                                             
CONECT   39   38                                                            
CONECT   40   38   31   41                                                  
CONECT   41   40   33   42                                                  
CONECT   42   41   43                                                       
CONECT   43   42                                                            
CONECT   44   38   45   46   50                                             
CONECT   45   44                                                            
CONECT   46   44   47   49                                                  
CONECT   47   46   48                                                       
CONECT   48   47                                                            
CONECT   49   46    5   30                                                  
CONECT   50   44    3   30                                                  
MASTER        0    0    0    0    0    0    0    0   50    0  112    0
END

View in JSmol

Synonyms

Value	Source
N-[2-({[(5R,8R)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1,.0,.0,.0,]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidate	Generator

Chemical Formula

C₃₇H₅₃N₃O₁₀

Average Mass

699.8420 Da

Monoisotopic Mass

699.37309 Da

IUPAC Name

N-[2-({[(5R,8R)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1^{2,5}.0^{1,10}.0^{3,8}.0^{13,17}]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid

Traditional Name

N-[2-({[(5R,8R)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1^{2,5}.0^{1,10}.0^{3,8}.0^{13,17}]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid

CAS Registry Number

Not Available

SMILES

CCN1CC2(COC(=O)C3=CC=CC=C3N=C(O)C(C)CC(O)=N)CCC(OC)C34C5C[C@H]6C(OC)C5[C@](O)(CC6OC)C(O)(C(OC)C23)C14

InChI Identifier

InChI=1S/C37H53N3O10/c1-7-40-17-34(18-50-32(43)20-10-8-9-11-23(20)39-31(42)19(2)14-26(38)41)13-12-25(47-4)36-22-15-21-24(46-3)16-35(44,27(22)28(21)48-5)37(45,33(36)40)30(49-6)29(34)36/h8-11,19,21-22,24-25,27-30,33,44-45H,7,12-18H2,1-6H3,(H2,38,41)(H,39,42)/t19?,21-,22?,24?,25?,27?,28?,29?,30?,33?,34?,35-,36?,37?/m1/s1

InChI Key

NXAZXMKMGPWXII-OWBGXFSJSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Delphinium grandiflorum	LOTUS Database	35616633
Delphinium omeiense	LOTUS Database	35616633
Delphinium potaninii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aconitane-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the hexacyclic aconitane skeleton. These compounds have no oxygen functionality at the C7 atom.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Aconitane-type diterpenoid alkaloids

Alternative Parents

Substituents

Aconitane-type diterpenoid alkaloid
Quinolidine
Benzoate ester
Alkaloid or derivatives
Benzoic acid or derivatives
Benzoyl
Azepane
Benzenoid
Piperidine
Monocyclic benzene moiety
Tertiary alcohol
Cyclic alcohol
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid ester
Amino acid or derivatives
1,2-diol
1,2-aminoalcohol
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Carboximidic acid derivative
Carboximidic acid
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
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	-4	ChemAxon
pKa (Strongest Acidic)	-1.2	ChemAxon
pKa (Strongest Basic)	12.62	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	183.59 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	193.98 m³·mol⁻¹	ChemAxon
Polarizability	75.5 Å³	ChemAxon
Number of Rings	7	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

145994478

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-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid (NP0219702)

MOL for NP0219702 (n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid)

3D MOL for NP0219702 (n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid)

3D SDF for NP0219702 (n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid)

3D-SDF for NP0219702 (n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid)

PDB for NP0219702 (n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid)

3D PDB for NP0219702 (n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid)

SMILES for NP0219702 (n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid)

INCHI for NP0219702 (n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid)

Structure for NP0219702 (n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid)

3D Structure for NP0219702 (n-[2-({[(5r,8r)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.1²,⁵.0¹,¹⁰.0³,⁸.0¹³,¹⁷]nonadecan-13-yl]methoxy}carbonyl)phenyl]-2-methylbutanediimidic acid)