NP-MRD: Showing NP-Card for methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate (NP0283601)

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Record Information

Version

2.0

Created at

2022-09-09 10:56:08 UTC

Updated at

2022-09-09 10:56:08 UTC

NP-MRD ID

NP0283601

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate

Description

Methyl (1R,9R,10R,11S,12R,19R)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]Icosa-2,4,6-triene-10-carboxylate belongs to the class of organic compounds known as aspidospermatan-type alkaloids. These are tryptophan-derived alkaloids that are derived from the fusion of tryptamine and a terpene unit (generally either 9 or 10 carbons). Aspidospermine and aspidospermidine (along with tabersonine) are the archetypical members of the Aspidosperma alkaloids. methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate is found in Catharanthus lanceus and Catharanthus ovalis. Based on a literature review very few articles have been published on methyl (1R,9R,10R,11S,12R,19R)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]Icosa-2,4,6-triene-10-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092212562D          

 31 36  0  0  1  0            999 V2000
    0.9961    0.8338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9787   -0.1175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3103   -0.7254    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3815   -1.0010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3284   -1.8954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4013   -2.3427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1342   -1.9282    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9711   -2.0644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3111   -1.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7331   -0.6243    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5939   -0.4916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1874   -1.0647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9804   -0.8373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1800   -0.0368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5865    0.5363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7935    0.3089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0763    0.7220    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5321    1.4687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4217    0.2023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5031    0.3279    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3754    1.2533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2316    1.7346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2227    1.9528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1508    2.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5071   -0.0988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0270    0.1763    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9135    0.3664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3795   -0.5050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0662   -1.3110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2475   -0.6595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0509   -1.0948    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  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  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 17  1  6  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
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 20 25  1  0  0  0  0
  4 25  1  0  0  0  0
 20 26  1  0  0  0  0
  3 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 10 31  1  0  0  0  0
 31  7  1  1  0  0  0
  3 31  1  0  0  0  0
M  END

     RDKit          3D

 61 66  0  0  0  0  0  0  0  0999 V2000
    3.0176   -2.3844    0.4602 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0313   -0.2401   -0.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1612    1.1046   -0.3710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0252    1.7622   -0.8037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8166    1.1158   -0.9704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5327    1.6103   -1.4106 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4127    2.8993   -2.0539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5578    0.5997   -1.0903 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4012    0.9270    0.0072 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9270    2.3013   -0.0695 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3008    2.7544   -1.1656 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0158    3.1008    1.0447 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5125    4.4300    1.0333 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1648    0.6453    1.3110 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5452   -0.0773   -0.3116 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7104    0.3384    0.3651 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8413    0.6177   -0.3907 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0742    1.0544    0.2895 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8301    0.5040   -1.6440 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6845   -1.1556    0.2680 C   0  0  2  0  0  0  0  0  0  0  0  0
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    1.5174   -2.6775   -0.9234 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1706   -3.3688    0.5990 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7515   -0.7607    3.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7788   -2.5799    2.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2139   -3.4657   -0.8051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5505   -3.8427   -0.9801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2483   -1.8900   -2.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9953   -2.0155   -2.4508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8488   -1.9648   -0.0326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8997   -0.7967    0.2317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0945    1.6428   -0.2509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1274    2.8222   -1.0088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2188    3.7197   -1.3555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4013    3.1900   -2.5420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7232    2.8812   -2.9454 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0541    0.5157   -2.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8563    4.7420    0.0286 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6938   -0.1629   -1.3808 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2613   -0.5715    1.0521 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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 23 24  1  0
 31  3  1  0
 11 16  1  0
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  1 32  1  0
  1 33  1  0
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  6 40  1  0
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 31 61  1  1
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 26 57  1  6
 29 58  1  0
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 24 54  1  0
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 24 56  1  0
M  END


  Mrv1652309092212562D          

 31 36  0  0  1  0            999 V2000
    0.9961    0.8338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9787   -0.1175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3103   -0.7254    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3815   -1.0010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3284   -1.8954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4013   -2.3427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1342   -1.9282    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9711   -2.0644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7331   -0.6243    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5939   -0.4916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1874   -1.0647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9804   -0.8373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1800   -0.0368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7935    0.3089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3754    1.2533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2316    1.7346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2227    1.9528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1508    2.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5071   -0.0988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0270    0.1763    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9135    0.3664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3795   -0.5050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0662   -1.3110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2475   -0.6595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0509   -1.0948    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  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  1  0  0  0  0
 10  9  1  1  0  0  0
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  4 25  1  0  0  0  0
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 27 28  1  0  0  0  0
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 28 30  2  0  0  0  0
 10 31  1  0  0  0  0
 31  7  1  1  0  0  0
  3 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0283601

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@]12C3CCN4CC[C@@]5([C@H]14)[C@@H](N(C)C1=CC=CC=C51)[C@@](O3)([C@H]2OC(C)=O)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C24H30N2O5/c1-5-22-17-10-12-26-13-11-23(18(22)26)15-8-6-7-9-16(15)25(3)19(23)24(31-17,21(28)29-4)20(22)30-14(2)27/h6-9,17-20H,5,10-13H2,1-4H3/t17?,18-,19+,20-,22-,23+,24+/m0/s1

> <INCHI_KEY>
HHQSRWIDLJYBKB-CEGOXWABSA-N

> <FORMULA>
C24H30N2O5

> <MOLECULAR_WEIGHT>
426.513

> <EXACT_MASS>
426.215472074

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
45.582254375352534

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1R,9R,10R,11S,12R,19R)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1^{10,13}.0^{1,9}.0^{2,7}.0^{16,19}]icosa-2,4,6-triene-10-carboxylate

> <JCHEM_LOGP>
2.1044214159999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
10.011142362510109

> <JCHEM_POLAR_SURFACE_AREA>
68.31

> <JCHEM_REFRACTIVITY>
112.83409999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,9R,10R,11S,12R,19R)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1^{10,13}.0^{1,9}.0^{2,7}.0^{16,19}]icosa-2,4,6-triene-10-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       1.859   1.556   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.827  -0.219   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.579  -1.354   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.712  -1.869   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.613  -3.538   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.749  -4.373   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       2.117  -3.599   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       3.679  -3.854   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.314  -2.442   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.235  -1.165   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.842  -0.918   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.950  -1.987   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.430  -1.563   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.803  -0.069   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.695   1.001   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.214   0.577   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       3.876   1.348   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       4.727   2.741   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.654   0.378   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.939   0.612   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.701   2.339   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.299   3.238   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -0.416   3.645   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.281   5.253   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.947  -0.184   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -0.050   0.329   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.705   0.684   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -2.575  -0.943   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.990  -2.447   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -4.195  -1.231   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.962  -2.044   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   26   31                                             
CONECT    4    3    5   25                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   31                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   19   31                                             
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   10   20                                                  
CONECT   20   19   21   25   26                                             
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23                                                            
CONECT   25   20    4                                                       
CONECT   26   20    3   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   10    7    3                                                  
MASTER        0    0    0    0    0    0    0    0   31    0   72    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1R,9R,10R,11S,12R,19R)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1,.0,.0,.0,]icosa-2,4,6-triene-10-carboxylic acid	Generator

Chemical Formula

C₂₄H₃₀N₂O₅

Average Mass

426.5130 Da

Monoisotopic Mass

426.21547 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC[C@]12C3CCN4CC[C@@]5([C@H]14)[C@@H](N(C)C1=CC=CC=C51)[C@@](O3)([C@H]2OC(C)=O)C(=O)OC

InChI Identifier

InChI=1S/C24H30N2O5/c1-5-22-17-10-12-26-13-11-23(18(22)26)15-8-6-7-9-16(15)25(3)19(23)24(31-17,21(28)29-4)20(22)30-14(2)27/h6-9,17-20H,5,10-13H2,1-4H3/t17?,18-,19+,20-,22-,23+,24+/m0/s1

InChI Key

HHQSRWIDLJYBKB-CEGOXWABSA-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
Catharanthus lanceus	LOTUS Database	35616633
Catharanthus ovalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aspidospermatan-type alkaloids. These are tryptophan-derived alkaloids that are derived from the fusion of tryptamine and a terpene unit (generally either 9 or 10 carbons). Aspidospermine and aspidospermidine (along with tabersonine) are the archetypical members of the Aspidosperma alkaloids.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Aspidospermatan-type alkaloids

Sub Class

Not Available

Direct Parent

Aspidospermatan-type alkaloids

Alternative Parents

Substituents

Aspidosperma alkaloid
Plumeran-type alkaloid
Carbazole
Quinolidine
Indolizidine
Indole or derivatives
Dialkylarylamine
Tertiary aliphatic/aromatic amine
Aralkylamine
Oxepane
Benzenoid
N-alkylpyrrolidine
Piperidine
Monosaccharide
Dicarboxylic acid or derivatives
Methyl ester
Tetrahydrofuran
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid ester
Amino acid or derivatives
Oxacycle
Azacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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

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

163193332

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate (NP0283601)

MOL for NP0283601 (methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate)

3D MOL for NP0283601 (methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate)

3D SDF for NP0283601 (methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate)

3D-SDF for NP0283601 (methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate)

PDB for NP0283601 (methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate)

3D PDB for NP0283601 (methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate)

SMILES for NP0283601 (methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate)

INCHI for NP0283601 (methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate)

Structure for NP0283601 (methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate)

3D Structure for NP0283601 (methyl (1r,9r,10r,11s,12r,19r)-11-(acetyloxy)-12-ethyl-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.1¹⁰,¹³.0¹,⁹.0²,⁷.0¹⁶,¹⁹]icosa-2,4,6-triene-10-carboxylate)