NP-MRD: Showing NP-Card for (-)-19-Epivoacangarine (NP0067893)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 12:43:49 UTC

Updated at

2022-04-28 12:43:49 UTC

NP-MRD ID

NP0067893

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-19-Epivoacangarine

Description

Ibogamine-18-carboxylic acid, 20-hydroxy-12-methoxy-, methyl ester, (20R)- belongs to the class of organic compounds known as ibogan-type alkaloids. These are indole alkaloids with a structure based on the ibogamine skeleton or a derivative thereof. Ibogamine is a pentacyclic heterocyclic compound consisting of an indole fused to an azepane-containing tricyclic moiety ring. Iboga alkaloids arise from the cyclization of a secodine-type precursor through the formation of a 16,21 bond. (-)-19-Epivoacangarine is found in Tabernaemontana divaricata, Peschiera affinis, Tabernaemontana calcarea, Tabernaemontana catharinensis, Tabernaemontana dichotoma Roxb.ex Wall , Tabernaemontana echinata Vell., Tabernaemontana lundii A.DC. and Tabernaemontana mocquerysii Aug.DC.. Based on a literature review very few articles have been published on Ibogamine-18-carboxylic acid, 20-hydroxy-12-methoxy-, methyl ester, (20R)-.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282214442D          

 28 32  0  0  1  0            999 V2000
    2.4050   -1.1015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9808   -0.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5227    0.2282    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818   -0.0950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2090   -0.9168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8843   -1.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6324   -1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7052   -0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0299    0.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3077   -1.5168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0557   -1.1689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0359   -0.2350    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4310   -1.1245    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7271   -1.8624    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4186   -2.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1734   -1.9332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4613   -1.4761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3956   -0.3913    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7214   -0.9065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668   -0.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1864   -0.6917    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0057   -0.7890    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3310   -1.5471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4996   -0.1282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7120    0.5237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2071    1.1836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1070    0.6226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4310    1.3813    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  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  4  9  2  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  1 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 12 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 22 24  1  1  0  0  0
 12 25  1  1  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 56 60  0  0  0  0  0  0  0  0999 V2000
   -0.6309    4.5896   -0.2293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4787    3.2848    0.2942 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1733    2.1908   -0.1683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9880    2.3265   -1.0987 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9563    0.8655    0.4319 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1906    0.8811    1.9380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9267   -0.4200    2.2543 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3470   -0.2088    1.7359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2690    0.1109    0.2520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2180   -0.8756   -0.4387 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2240   -0.6507   -1.9354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8540   -2.1857   -0.1998 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8586   -0.1483   -0.2411 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5317   -1.4973    0.1030 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6169   -2.1593   -0.7313 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3258   -1.3129   -1.5049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0503   -0.4066   -0.5836 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4737    0.5258    0.2427 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4846    1.1221    0.8979 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6549    0.6137    0.5260 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9414    0.8827    0.8980 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0029    0.1706    0.3240 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7621   -0.8043   -0.6175 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8156   -1.5263   -1.2015 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1278   -1.2141   -0.7865 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4647   -1.0772   -0.9941 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4340   -0.3617   -0.4141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2415   -1.5494    1.5159 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2500    5.2134    0.0115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5208    5.1084    0.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7373    4.5927   -1.3356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8524    1.7265    2.1926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2592    0.9575    2.5123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9198   -0.6609    3.3152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7317    0.6811    2.3119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0005   -1.0491    1.9653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6265    1.1204    0.0514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2575   -0.7349   -0.0846 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3512   -1.1203   -2.4398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3172    0.4339   -2.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1304   -1.1301   -2.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0137   -2.7776   -0.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8448    0.0558   -1.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0013   -2.8736   -0.1139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1432   -2.8341   -1.4682 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0949   -1.9945   -1.9643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1250   -0.7308   -2.3154 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3110    1.8937    1.6094 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2002    1.6323    1.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0247    0.3755    0.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2748   -0.1056   -0.9271 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2607   -1.4265    0.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8924   -1.7451   -1.3696 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2161   -1.8217   -1.7190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1650   -1.4373    1.6603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599   -2.5150    1.9681 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
  5  3  1  6
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
  9 13  1  0
 13 14  1  0
 14 28  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
 23 26  1  0
 26 27  2  0
 13  5  1  0
 27 17  1  0
 18  5  1  0
 27 20  1  0
 28  7  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  6 32  1  0
  6 33  1  0
  7 34  1  1
  8 35  1  0
  8 36  1  0
  9 37  1  1
 10 38  1  1
 11 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  0
 13 43  1  6
 28 55  1  0
 28 56  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 16 47  1  0
 19 48  1  0
 21 49  1  0
 22 50  1  0
 25 51  1  0
 25 52  1  0
 25 53  1  0
 26 54  1  0
M  END


  Mrv1652304282214442D          

 28 32  0  0  1  0            999 V2000
    2.4050   -1.1015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9808   -0.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5227    0.2282    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818   -0.0950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2090   -0.9168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8843   -1.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6324   -1.0429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7052   -0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0299    0.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3077   -1.5168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0557   -1.1689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0359   -0.2350    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4310   -1.1245    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7271   -1.8624    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4186   -2.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1734   -1.9332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4613   -1.4761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3956   -0.3913    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7214   -0.9065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3668   -0.0646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1864   -0.6917    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0057   -0.7890    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3310   -1.5471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4996   -0.1282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7120    0.5237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2071    1.1836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1070    0.6226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4310    1.3813    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  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  4  9  2  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  1 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 12 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 22 24  1  1  0  0  0
 12 25  1  1  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0067893

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@]12C[C@H]3C[C@H]([C@@H](C)O)[C@@H]1N(C3)CCC1=C2NC2=CC=C(OC)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C22H28N2O4/c1-12(25)16-8-13-10-22(21(26)28-3)19-15(6-7-24(11-13)20(16)22)17-9-14(27-2)4-5-18(17)23-19/h4-5,9,12-13,16,20,23,25H,6-8,10-11H2,1-3H3/t12-,13-,16-,20+,22-/m1/s1

> <INCHI_KEY>
OYMQKBZMKFJPMH-MDIKWQLESA-N

> <FORMULA>
C22H28N2O4

> <MOLECULAR_WEIGHT>
384.476

> <EXACT_MASS>
384.20490739

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.55220044175804

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,15R,17S,18S)-17-[(1R)-1-hydroxyethyl]-7-methoxy-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-carboxylate

> <ALOGPS_LOGP>
2.68

> <JCHEM_LOGP>
1.9380818983333348

> <ALOGPS_LOGS>
-3.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
16.66992357447108

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.202127040915691

> <JCHEM_PKA_STRONGEST_BASIC>
8.087011924133225

> <JCHEM_POLAR_SURFACE_AREA>
74.79

> <JCHEM_REFRACTIVITY>
106.04940000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.91e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,15R,17S,18S)-17-[(1R)-1-hydroxyethyl]-7-methoxy-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-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       4.489  -2.056   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.698  -0.735   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       4.709   0.426   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       6.126  -0.177   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.990  -1.711   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.251  -2.596   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.647  -1.947   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.783  -0.413   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.522   0.472   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.908  -2.831   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      11.304  -2.182   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.934  -0.439   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.805  -2.099   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       1.357  -3.476   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       2.648  -4.307   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.057  -3.609   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.728  -2.755   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.605  -0.730   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.213  -1.692   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.685  -0.121   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.348  -1.291   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.877  -1.473   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.485  -2.888   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.799  -0.239   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.329   0.978   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.253   2.209   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -0.200   1.162   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -0.804   2.578   0.000  0.00  0.00           C+0
CONECT    1    2    5   16                                                  
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    1    6                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8    4                                                       
CONECT   10    7   11                                                       
CONECT   11   10                                                            
CONECT   12    2   13   19   25                                             
CONECT   13   12   14   21                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15    1                                                       
CONECT   17   14   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18   12                                                       
CONECT   20   18   21                                                       
CONECT   21   20   13   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   12   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₈N₂O₄

Average Mass

384.4760 Da

Monoisotopic Mass

384.20491 Da

IUPAC Name

methyl (1S,15R,17S,18S)-17-[(1R)-1-hydroxyethyl]-7-methoxy-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-carboxylate

Traditional Name

methyl (1S,15R,17S,18S)-17-[(1R)-1-hydroxyethyl]-7-methoxy-3,13-diazapentacyclo[13.3.1.0^{2,10}.0^{4,9}.0^{13,18}]nonadeca-2(10),4,6,8-tetraene-1-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@]12C[C@H]3C[C@H]([C@@H](C)O)[C@@H]1N(C3)CCC1=C2NC2=CC=C(OC)C=C12

InChI Identifier

InChI=1S/C22H28N2O4/c1-12(25)16-8-13-10-22(21(26)28-3)19-15(6-7-24(11-13)20(16)22)17-9-14(27-2)4-5-18(17)23-19/h4-5,9,12-13,16,20,23,25H,6-8,10-11H2,1-3H3/t12-,13-,16-,20+,22-/m1/s1

InChI Key

OYMQKBZMKFJPMH-MDIKWQLESA-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
Ervatamia coronaria	LOTUS Database	35616633
Peschiera affinis	Plant	KNApSAcK
Tabernaemontana calcarea	Plant	KNApSAcK
Tabernaemontana catharinensis	LOTUS Database	35616633
Tabernaemontana dichotoma Roxb.ex Wall	Plant	KNApSAcK
Tabernaemontana echinata Vell.	Plant	KNApSAcK
Tabernaemontana lundii A.DC.	Plant	KNApSAcK
Tabernaemontana mocquerysii Aug.DC.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ibogan-type alkaloids. These are indole alkaloids with a structure based on the ibogamine skeleton or a derivative thereof. Ibogamine is a pentacyclic heterocyclic compound consisting of an indole fused to an azepane-containing tricyclic moiety ring. Iboga alkaloids arise from the cyclization of a secodine-type precursor through the formation of a 16,21 bond.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Ibogan-type alkaloids

Sub Class

Not Available

Direct Parent

Ibogan-type alkaloids

Alternative Parents

Substituents

Ibogan skeleton
Catharanthine skeleton
Pyrroloazepine
3-alkylindole
Indole
Indole or derivatives
Piperidinecarboxylic acid
Anisole
Phenol ether
Aralkylamine
Alkyl aryl ether
Azepine
Benzenoid
Piperidine
Pyrrole
Heteroaromatic compound
Methyl ester
1,3-aminoalcohol
Tertiary amine
Secondary alcohol
Amino acid or derivatives
Tertiary aliphatic amine
Carboxylic acid ester
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Ether
Alcohol
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Amine
Organonitrogen compound
Organooxygen compound
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	2.68	ALOGPS
logP	1.94	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	15.2	ChemAxon
pKa (Strongest Basic)	8.09	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.79 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	106.05 m³·mol⁻¹	ChemAxon
Polarizability	42.55 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

57523176

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

56842093

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (-)-19-Epivoacangarine (NP0067893)

MOL for NP0067893 ((-)-19-Epivoacangarine)

3D MOL for NP0067893 ((-)-19-Epivoacangarine)

3D SDF for NP0067893 ((-)-19-Epivoacangarine)

3D-SDF for NP0067893 ((-)-19-Epivoacangarine)

PDB for NP0067893 ((-)-19-Epivoacangarine)

3D PDB for NP0067893 ((-)-19-Epivoacangarine)

SMILES for NP0067893 ((-)-19-Epivoacangarine)

INCHI for NP0067893 ((-)-19-Epivoacangarine)

Structure for NP0067893 ((-)-19-Epivoacangarine)

3D Structure for NP0067893 ((-)-19-Epivoacangarine)