NP-MRD: Showing NP-Card for (+)-Vincinine (NP0067339)

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Record Information

Version

2.0

Created at

2022-04-28 12:03:10 UTC

Updated at

2022-04-28 12:03:10 UTC

NP-MRD ID

NP0067339

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Vincinine

Description

Methyl (15R,17S,19S)-15-acetyl-17-hydroxy-4-methoxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]Nonadeca-2(7),3,5,8(18)-tetraene-17-carboxylate belongs to the class of organic compounds known as eburnan-type alkaloids. These are alkaloids with a structure based on the eburnan skeleton, that arises from rearrangement of the aspidospermidine ring system, involving migration of C-21 from C-7 to C-2, fission of the 2,16-bond, and attachment of C-16 to N-1. (+)-Vincinine is found in Vinca minor . Based on a literature review very few articles have been published on methyl (15R,17S,19S)-15-acetyl-17-hydroxy-4-methoxy-1,11-diazapentacyclo[9.6.2.0²,⁷.0⁸,¹⁸.0¹⁵,¹⁹]Nonadeca-2(7),3,5,8(18)-tetraene-17-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282214032D          

 29 33  0  0  1  0            999 V2000
    7.0341    0.4293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4868    1.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1158    1.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2921    1.9031    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8395    1.2133    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2105    0.4764    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7578   -0.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9342   -0.1661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5632    0.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0158    1.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6448    1.9973    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0975    2.6871    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9211    2.6399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4240    3.1635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4998    3.9850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6746    2.8185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0011    3.2949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1158    3.5119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7281    1.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7673    0.7881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0733    0.3421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3400    0.7202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3008    1.5443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9948    1.9902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5675    1.9223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8734    1.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7448    2.5928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3738    3.3297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5684    2.5456    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
  1  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
  9 10  2  0  0  0  0
  5 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  4 13  1  0  0  0  0
 12 14  1  1  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  6  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 19 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
  4 27  1  1  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 55 59  0  0  0  0  0  0  0  0999 V2000
    0.3002    4.5313   -0.0430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0867    3.1593    0.0754 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2085    2.4776    1.2471 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8001    3.0359    2.1902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2003    1.0303    1.3708 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2188    0.5839    2.6532 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6782    1.0109    1.2800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2956    0.0258    0.3264 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6611    0.4964   -0.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7022    0.6778    1.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0171    0.7642   -1.1509 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3957   -1.3572    0.9169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0812   -2.2404   -0.0917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2524   -2.2864   -1.3580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9441   -1.0151   -1.8781 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1060   -1.0992   -3.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3292   -1.5529   -2.7196 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7663   -0.8960   -1.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1026   -0.2049   -0.6742 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5106    0.2637    0.3821 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8069   -0.1095    0.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8882    0.1010    1.1581 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1456   -0.3934    0.8846 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2270   -0.1586    1.7548 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4811   -0.6867    1.4235 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3081   -1.1270   -0.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2524   -1.3601   -1.1282 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0183   -0.8646   -0.8427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5032   -0.0282   -0.9784 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9493    4.8244    0.8056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6472    5.1095   -0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8091    4.6928   -1.0158 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3964    1.3685    3.2487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1000    0.7520    2.2951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1374    2.0206    1.0673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6085    0.1368    0.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3439    0.3428    2.0451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9176    1.7848    1.0735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0236   -1.2649    1.8390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3921   -1.7798    1.1599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0836   -1.7992   -0.3015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2550   -3.2427    0.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7697   -2.9291   -2.0923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3022   -2.8092   -1.0903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5356   -1.7048   -3.8498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9730   -0.0411   -3.4027 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0041   -1.2512   -3.5463 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3246   -2.6412   -2.6615 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7481    0.6770    2.0608 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4526   -1.8050    1.3788 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8645   -0.3400    0.4386 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2226   -0.3963    2.1894 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2962   -1.5131   -0.4830 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4047   -1.9477   -2.0451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6177    0.9779   -1.4822 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  1
  5  7  1  0
  7  8  1  0
  8 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 29  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 23 26  2  0
 26 27  1  0
 27 28  2  0
  8  9  1  6
  9 10  1  0
  9 11  2  0
 20  5  1  0
 28 21  1  0
 29  8  1  0
 29 15  1  0
 28 18  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 14 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 29 55  1  6
 22 49  1  0
 25 50  1  0
 25 51  1  0
 25 52  1  0
 26 53  1  0
 27 54  1  0
 10 36  1  0
 10 37  1  0
 10 38  1  0
M  END


  Mrv1652304282214032D          

 29 33  0  0  1  0            999 V2000
    7.0341    0.4293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4868    1.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1158    1.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2921    1.9031    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8395    1.2133    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2105    0.4764    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7578   -0.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9342   -0.1661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5632    0.5707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0158    1.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6448    1.9973    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0975    2.6871    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9211    2.6399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4240    3.1635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4998    3.9850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6746    2.8185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0011    3.2949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1158    3.5119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7281    1.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7673    0.7881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0733    0.3421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3400    0.7202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3008    1.5443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9948    1.9902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5675    1.9223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8734    1.4763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7448    2.5928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3738    3.3297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5684    2.5456    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
  1  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
  9 10  2  0  0  0  0
  5 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  4 13  1  0  0  0  0
 12 14  1  1  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  6  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 19 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
  4 27  1  1  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0067339

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@]1(O)C[C@@]2(CCCN3CCC4=C([C@H]23)N1C1=CC(OC)=CC=C41)C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H26N2O5/c1-13(25)21-8-4-9-23-10-7-16-15-6-5-14(28-2)11-17(15)24(18(16)19(21)23)22(27,12-21)20(26)29-3/h5-6,11,19,27H,4,7-10,12H2,1-3H3/t19-,21+,22+/m1/s1

> <INCHI_KEY>
JSPRBHQBWMFUOZ-HJNYFJLDSA-N

> <FORMULA>
C22H26N2O5

> <MOLECULAR_WEIGHT>
398.459

> <EXACT_MASS>
398.184171945

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
42.63715208392013

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (15R,17S,19S)-15-acetyl-17-hydroxy-4-methoxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraene-17-carboxylate

> <ALOGPS_LOGP>
1.71

> <JCHEM_LOGP>
2.3098284846666686

> <ALOGPS_LOGS>
-2.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.23663085497555

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.504536421309517

> <JCHEM_PKA_STRONGEST_BASIC>
5.994558546161332

> <JCHEM_POLAR_SURFACE_AREA>
81.0

> <JCHEM_REFRACTIVITY>
106.7046

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.80e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (15R,17S,19S)-15-acetyl-17-hydroxy-4-methoxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraene-17-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      13.130   0.801   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.975   2.089   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.283   3.464   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.745   3.552   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.900   2.265   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      11.593   0.889   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      10.748  -0.398   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.210  -0.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.518   1.065   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.363   2.353   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       8.670   3.728   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       9.515   5.016   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.053   4.928   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.258   5.905   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.400   7.439   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       6.859   5.261   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.602   6.151   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.550   6.555   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.959   3.009   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.032   1.471   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.737   0.639   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.368   1.344   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.295   2.883   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.590   3.715   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.926   3.588   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.630   2.756   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.590   4.840   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.898   6.215   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      14.128   4.752   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   13   27                                             
CONECT    5    4    6   10                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   20                                                  
CONECT   10    9    5   11                                                  
CONECT   11   10   12   19                                                  
CONECT   12   11   13   14   18                                             
CONECT   13   12    4                                                       
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16                                                            
CONECT   18   12                                                            
CONECT   19   11   20   24                                                  
CONECT   20   19    9   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23   19                                                       
CONECT   25   23   26                                                       
CONECT   26   25                                                            
CONECT   27    4   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Value	Source
Methyl (15R,17S,19S)-15-acetyl-17-hydroxy-4-methoxy-1,11-diazapentacyclo[9.6.2.0,.0,.0,]nonadeca-2(7),3,5,8(18)-tetraene-17-carboxylic acid	Generator

Chemical Formula

C₂₂H₂₆N₂O₅

Average Mass

398.4590 Da

Monoisotopic Mass

398.18417 Da

IUPAC Name

methyl (15R,17S,19S)-15-acetyl-17-hydroxy-4-methoxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraene-17-carboxylate

Traditional Name

methyl (15R,17S,19S)-15-acetyl-17-hydroxy-4-methoxy-1,11-diazapentacyclo[9.6.2.0^{2,7}.0^{8,18}.0^{15,19}]nonadeca-2,4,6,8(18)-tetraene-17-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@]1(O)C[C@@]2(CCCN3CCC4=C([C@H]23)N1C1=CC(OC)=CC=C41)C(C)=O

InChI Identifier

InChI=1S/C22H26N2O5/c1-13(25)21-8-4-9-23-10-7-16-15-6-5-14(28-2)11-17(15)24(18(16)19(21)23)22(27,12-21)20(26)29-3/h5-6,11,19,27H,4,7-10,12H2,1-3H3/t19-,21+,22+/m1/s1

InChI Key

JSPRBHQBWMFUOZ-HJNYFJLDSA-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
Vinca minor	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eburnan-type alkaloids. These are alkaloids with a structure based on the eburnan skeleton, that arises from rearrangement of the aspidospermidine ring system, involving migration of C-21 from C-7 to C-2, fission of the 2,16-bond, and attachment of C-16 to N-1.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Eburnan-type alkaloids

Sub Class

Not Available

Direct Parent

Eburnan-type alkaloids

Alternative Parents

Substituents

Eburna alkaloid
Indolo[3,2-1de][1,5]naphthyridine
Pyridoindole
Beta-carboline
Alpha-amino acid or derivatives
Naphthyridine
Diazanaphthalene
3-alkylindole
Indole or derivatives
Indole
Anisole
Aralkylamine
Alkyl aryl ether
Beta-aminoketone
Benzenoid
Piperidine
Pyrrole
Heteroaromatic compound
Methyl ester
Ketone
Amino acid or derivatives
Carboxylic acid ester
Tertiary amine
Tertiary aliphatic amine
Alkanolamine
Azacycle
Carboxylic acid derivative
Organoheterocyclic compound
Ether
Monocarboxylic acid or derivatives
Carbonyl group
Organic nitrogen compound
Hydrocarbon derivative
Organic oxygen compound
Amine
Organooxygen compound
Organopnictogen compound
Organonitrogen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.71	ALOGPS
logP	2.31	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	10.5	ChemAxon
pKa (Strongest Basic)	5.99	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	81 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	106.7 m³·mol⁻¹	ChemAxon
Polarizability	42.64 Å³	ChemAxon
Number of Rings	5	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

139595637

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Vincinine (NP0067339)

MOL for NP0067339 ((+)-Vincinine)

3D MOL for NP0067339 ((+)-Vincinine)

3D SDF for NP0067339 ((+)-Vincinine)

3D-SDF for NP0067339 ((+)-Vincinine)

PDB for NP0067339 ((+)-Vincinine)

3D PDB for NP0067339 ((+)-Vincinine)

SMILES for NP0067339 ((+)-Vincinine)

INCHI for NP0067339 ((+)-Vincinine)

Structure for NP0067339 ((+)-Vincinine)

3D Structure for NP0067339 ((+)-Vincinine)