NP-MRD: Showing NP-Card for (+)-6,7-Dehydroepivincadine (NP0066836)

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Record Information

Version

2.0

Created at

2022-04-28 11:04:21 UTC

Updated at

2022-04-28 11:04:21 UTC

NP-MRD ID

NP0066836

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-6,7-Dehydroepivincadine

Description

(7S)-7-Ethyl-3,7-methano-1,2,3,4,7,8,9,10-octahydroazacycloundecino[5,4-b]indole-9alpha-carboxylic acid methyl ester belongs to the class of organic compounds known as quebrachamine alkaloids. These are alkaloids with a structure based on the quebrachamine skeleton, a tetracyclic compound that is derived by fission of the 7,21 bond of the aspidospermidine skeleton. Some quebrachamine alkaloids lack the C-16 methoxycarbonyl group. (+)-6,7-Dehydroepivincadine is found in Catharanthus roseus . Based on a literature review very few articles have been published on (7S)-7-Ethyl-3,7-methano-1,2,3,4,7,8,9,10-octahydroazacycloundecino[5,4-b]indole-9alpha-carboxylic acid methyl ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282213042D          

 25 28  0  0  1  0            999 V2000
    7.4586    0.9239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0965    1.6651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2734    1.7222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8126    1.0379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1747    0.2966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9977    0.2396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5816   -0.2769    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8529    0.1100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9957    0.9225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5606    1.6463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7413    1.9062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9113    1.6448    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8517    0.8821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6479    0.1447    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3391   -0.3838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1979   -0.4187    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4569   -1.2020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9079   -1.8179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2647   -1.3695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5236   -2.1528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    0.3354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4860    1.1220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0441    1.7563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2992   -0.6030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7724   -1.2788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 12 23  1  0  0  0  0
 14 24  1  6  0  0  0
 24 25  1  0  0  0  0
M  END

     RDKit          3D

 51 54  0  0  0  0  0  0  0  0999 V2000
   -3.9450    0.5659   -1.5043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6270    0.3550   -0.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2526   -0.3124    0.1349 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4667   -1.7209   -0.3845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6034   -2.7283    0.4711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0086   -2.7764    1.8221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2131   -1.5429    2.0025 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0008   -1.7559    1.3170 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1561   -0.8852    1.6919 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8592   -0.3949    0.4654 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1921    0.5555   -0.2766 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0060    0.8505   -1.3326 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1227    0.1192   -1.2496 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2253    0.0606   -2.0621 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2699   -0.7967   -1.7508 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1758   -1.5751   -0.6250 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0637   -1.5392    0.2260 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0672   -0.6774   -0.1304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1428    1.1085    0.0596 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1117    2.5935   -0.2333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9164    3.0212   -1.0683 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7623    3.4478    0.3881 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7993    4.8365    0.1216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2653    0.4395   -0.6490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0537   -0.4670    1.6014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7035    1.6088   -1.7846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0277    0.3597   -1.6583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3461   -0.1687   -2.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6567    1.3389    0.4512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4189   -0.2596    0.4201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5087   -1.9096   -1.4509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2014   -3.5795    0.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4164   -3.6706    2.0281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8291   -2.6924    2.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3229   -2.8169    1.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0796   -1.7822    0.2113 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9470   -1.4490    2.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8955   -0.0564    2.3949 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7814    1.5405   -2.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3240    0.6624   -2.9535 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1353   -0.8247   -2.4129 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9963   -2.2465   -0.3831 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9998   -2.1544    1.1072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2251    1.0724    1.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7323    5.2255    0.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8450    4.9450   -0.9888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0838    5.3395    0.5576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7607    1.2320   -1.2922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8580   -0.2536   -1.4493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8721    0.4949    2.1539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0859   -0.7373    2.0092 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3 25  1  0
 25  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 11 19  1  0
 19 24  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
  4  3  1  0
 18 10  1  0
 24  3  1  0
 18 13  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
 25 50  1  0
 25 51  1  0
  6 33  1  0
  6 34  1  0
  5 32  1  0
  4 31  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 12 39  1  0
 14 40  1  0
 15 41  1  0
 16 42  1  0
 17 43  1  0
 19 44  1  1
 24 48  1  0
 24 49  1  0
 23 45  1  0
 23 46  1  0
 23 47  1  0
M  END


  Mrv1652304282213042D          

 25 28  0  0  1  0            999 V2000
    7.4586    0.9239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0965    1.6651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2734    1.7222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8126    1.0379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1747    0.2966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9977    0.2396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5816   -0.2769    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8529    0.1100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9957    0.9225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5606    1.6463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7413    1.9062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9113    1.6448    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8517    0.8821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6479    0.1447    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3391   -0.3838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1979   -0.4187    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4569   -1.2020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9079   -1.8179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2647   -1.3695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5236   -2.1528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    0.3354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4860    1.1220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0441    1.7563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2992   -0.6030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7724   -1.2788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 12 23  1  0  0  0  0
 14 24  1  6  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0066836

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@]12CN(CC=C1)CCC1=C(NC3=CC=CC=C13)[C@H](C2)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C21H26N2O2/c1-3-21-10-6-11-23(14-21)12-9-16-15-7-4-5-8-18(15)22-19(16)17(13-21)20(24)25-2/h4-8,10,17,22H,3,9,11-14H2,1-2H3/t17-,21+/m0/s1

> <INCHI_KEY>
DWRWMNKQJGGHFK-LAUBAEHRSA-N

> <FORMULA>
C21H26N2O2

> <MOLECULAR_WEIGHT>
338.451

> <EXACT_MASS>
338.199428085

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
38.19677185920579

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (13S,15S)-15-ethyl-1,11-diazatetracyclo[13.3.1.0^{4,12}.0^{5,10}]nonadeca-4(12),5,7,9,16-pentaene-13-carboxylate

> <ALOGPS_LOGP>
3.91

> <JCHEM_LOGP>
3.472295237

> <ALOGPS_LOGS>
-4.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.484641532192917

> <JCHEM_PKA_STRONGEST_BASIC>
7.944163457577181

> <JCHEM_POLAR_SURFACE_AREA>
45.33

> <JCHEM_REFRACTIVITY>
101.14299999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.88e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (13S,15S)-15-ethyl-1,11-diazatetracyclo[13.3.1.0^{4,12}.0^{5,10}]nonadeca-4(12),5,7,9,16-pentaene-13-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      13.923   1.725   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.247   3.108   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.710   3.215   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.850   1.937   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.526   0.554   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.062   0.447   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      10.419  -0.517   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       9.059   0.205   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.325   1.722   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.513   3.073   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.984   3.558   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       5.435   3.070   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       5.323   1.647   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.943   0.270   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.233  -0.716   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.836  -0.782   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.319  -2.244   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.295  -3.393   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       9.827  -2.556   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      10.311  -4.019   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.350   0.626   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.774   2.094   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.816   3.278   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.292  -1.126   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.175  -2.387   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8    4   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   23                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   21   24                                             
CONECT   15   14   16                                                       
CONECT   16   15    8   17                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   14   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   12                                                       
CONECT   24   14   25                                                       
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Value	Source
(7S)-7-Ethyl-3,7-methano-1,2,3,4,7,8,9,10-octahydroazacycloundecino[5,4-b]indole-9a-carboxylate methyl ester	Generator
(7S)-7-Ethyl-3,7-methano-1,2,3,4,7,8,9,10-octahydroazacycloundecino[5,4-b]indole-9a-carboxylic acid methyl ester	Generator
(7S)-7-Ethyl-3,7-methano-1,2,3,4,7,8,9,10-octahydroazacycloundecino[5,4-b]indole-9alpha-carboxylate methyl ester	Generator
(7S)-7-Ethyl-3,7-methano-1,2,3,4,7,8,9,10-octahydroazacycloundecino[5,4-b]indole-9α-carboxylate methyl ester	Generator
(7S)-7-Ethyl-3,7-methano-1,2,3,4,7,8,9,10-octahydroazacycloundecino[5,4-b]indole-9α-carboxylic acid methyl ester	Generator

Chemical Formula

C₂₁H₂₆N₂O₂

Average Mass

338.4510 Da

Monoisotopic Mass

338.19943 Da

IUPAC Name

methyl (13S,15S)-15-ethyl-1,11-diazatetracyclo[13.3.1.0^{4,12}.0^{5,10}]nonadeca-4(12),5,7,9,16-pentaene-13-carboxylate

Traditional Name

methyl (13S,15S)-15-ethyl-1,11-diazatetracyclo[13.3.1.0^{4,12}.0^{5,10}]nonadeca-4(12),5,7,9,16-pentaene-13-carboxylate

CAS Registry Number

Not Available

SMILES

CC[C@@]12CN(CC=C1)CCC1=C(NC3=CC=CC=C13)[C@H](C2)C(=O)OC

InChI Identifier

InChI=1S/C21H26N2O2/c1-3-21-10-6-11-23(14-21)12-9-16-15-7-4-5-8-18(15)22-19(16)17(13-21)20(24)25-2/h4-8,10,17,22H,3,9,11-14H2,1-2H3/t17-,21+/m0/s1

InChI Key

DWRWMNKQJGGHFK-LAUBAEHRSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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 roseus	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quebrachamine alkaloids. These are alkaloids with a structure based on the quebrachamine skeleton, a tetracyclic compound that is derived by fission of the 7,21 bond of the aspidospermidine skeleton. Some quebrachamine alkaloids lack the C-16 methoxycarbonyl group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Quebrachamine alkaloids

Sub Class

Not Available

Direct Parent

Quebrachamine alkaloids

Alternative Parents

Substituents

Quebrachamine skeleton
3-alkylindole
Indole
Indole or derivatives
Aralkylamine
Benzenoid
Heteroaromatic compound
Pyrrole
Methyl ester
Amino acid or derivatives
Carboxylic acid ester
Tertiary amine
Tertiary aliphatic amine
Monocarboxylic acid or derivatives
Azacycle
Carboxylic acid derivative
Organoheterocyclic compound
Organic oxide
Amine
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Hydrocarbon derivative
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	3.91	ALOGPS
logP	3.47	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	15.48	ChemAxon
pKa (Strongest Basic)	7.94	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	45.33 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	101.14 m³·mol⁻¹	ChemAxon
Polarizability	38.2 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

101202570

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-6,7-Dehydroepivincadine (NP0066836)

MOL for NP0066836 ((+)-6,7-Dehydroepivincadine)

3D MOL for NP0066836 ((+)-6,7-Dehydroepivincadine)

3D SDF for NP0066836 ((+)-6,7-Dehydroepivincadine)

3D-SDF for NP0066836 ((+)-6,7-Dehydroepivincadine)

PDB for NP0066836 ((+)-6,7-Dehydroepivincadine)

3D PDB for NP0066836 ((+)-6,7-Dehydroepivincadine)

SMILES for NP0066836 ((+)-6,7-Dehydroepivincadine)

INCHI for NP0066836 ((+)-6,7-Dehydroepivincadine)

Structure for NP0066836 ((+)-6,7-Dehydroepivincadine)

3D Structure for NP0066836 ((+)-6,7-Dehydroepivincadine)