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Review

13C-NMR Spectral Data of Alkaloids Isolated from Psychotria Species (Rubiaceae)

by
Almir Ribeiro de Carvalho Junior
1,
Ivo Jose Curcino Vieira
1,*,
Mario Geraldo de Carvalho
2,
Raimundo Braz-Filho
1,2,
Mary Anne S. Lima
3,
Rafaela Oliveira Ferreira
4,
Edmilson José Maria
1 and
Daniela Barros de Oliveira
5
1
Laboratório de Ciências Químicas, CCT, Universidade Estadual do Norte Fluminense Darcy Ribeiro, Campos dos Goytacazes, RJ 28013-602, Brazil
2
Departamento de Química, ICE, Universidade Federal Rural do Rio de Janeiro, Seropédica, RJ 23890-000, Brazil
3
Departamento de Química Orgânica e Inorgânica, Centro de Ciências, Universidade Federal do Ceará, Fortaleza, CE 60021-940, Brazil
4
Colegiado de Ciências Agrárias e Biotecnológicas, Universidade Federal do Tocantins, Gurupi, TO 77402-970, Brazil
5
Laboratório de Tecnologia de Alimentos, CCTA, Universidade Estadual do Norte Fluminense Darcy Ribeiro, Campos dos Goytacazes, RJ 28013-602, Brazil
*
Author to whom correspondence should be addressed.
Molecules 2017, 22(1), 103; https://doi.org/10.3390/molecules22010103
Submission received: 1 November 2016 / Revised: 9 December 2016 / Accepted: 28 December 2016 / Published: 11 January 2017
(This article belongs to the Special Issue Diversity of Alkaloids)
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Abstract

:
The genus Psychotria (Rubiaceae) comprises more than 2000 species, mainly found in tropical and subtropical forests. Several studies have been conducted concerning their chemical compositions, showing that this genus is a potential source of alkaloids. At least 70 indole alkaloids have been identified from this genus so far. This review aimed to compile 13C-NMR data of alkaloids isolated from the genus Psychotria as well as describe the main spectral features of different skeletons.

1. Introduction

In phytochemistry and related areas, structural elucidation techniques play a key role because precise knowledge of the chemistry of plants requires unequivocal structural characterization of its metabolites to obtain information related to the taxonomy of plant groups. Moreover, correct identification of biologically active compounds is important, both to understand their possible mechanisms of action and propose chemical modifications aimed at enhancing their activity.
The characterization of natural products requires, apart from patience and dedication, knowledge about spectroscopic techniques (interpretation of these data) and the biosynthesis of different types of metabolites. Comparison with literature data is another important auxiliary tool that aids the structural characterization of a given compound. In this context, finding a material that provides as much information as possible about the spectral data of metabolites isolated from a genus (such as Psychotria) may enable saving time.
The genus Psychotria (Rubiaceae) comprises more than 2000 species, which occur mostly in tropical and subtropical regions [1], with many of these species being employed in folk medicine to treat several diseases [2,3]. The biological potential of the chemical constituents of the species of this genus has possibly motivated several studies regarding the chemical composition of such species. Most of these have focused on investigating alkaloid fractions obtained by acid-base extraction, probably owing to the biological importance of this type of metabolite. Such efforts have led to the isolation and/or identification of various alkaloids, primarily indole-type. Some of them exhibit some biological properties such as analgesic [4,5], antioxidant [6], antiparasitic [7], and cytotoxic [8,9] activities. This review aimed to compile 13C-NMR spectral data of alkaloids isolated from Psychotria species as well as to discuss the main spectral features observed for the different types of skeletons.

2. Discussion

2.1. 13C-NMR Chemical Shifts of Monoterpene Indole Alkaloids Isolated from Psychotria Species

Monoterpene indole alkaloids (MIAs) comprise a wide group of secondary metabolites, found mainly in the Apocynaceae, Loganiaceae, and Rubiaceae families [10]. Their biosynthesis involves a reaction between tryptamine (derived from tryptophan) and the iridoid secologanin, catalyzed by strictosidine synthase [11]. This initial step leads to the formation of strictosidine (1, Table 1, Figure 1), the key precursor of other MIAs.
Strictosidine (1) was isolated from P. elata [12] and P. nuda (data not reported), and presents an ortho-substituted ring system (as do most of the MIAs isolated from this genus), characterized by the presence of four methine carbon signals at δC 118.8 (CH-9), 120.1 (CH-10), 122.7 (CH-11), and 112.0 (CH-12), and two quaternary carbon signals at δC 127.9 (C-8) and 137.9 (C-13). The signals of two quaternary carbons at δC 133.2 (C-2) and 107.7 (C-7), along with a methine carbon at δC 52.4 (CH-3) and two methylene carbons at δC 42.9 (CH2-5) and 21.0 (CH2-6) complete the tetrahydro-β-carboline system. The secologanin moiety is confirmed by the presence of signals resonating at δC 170.6 (C-22), δC 109.9 (C-16), and 156.1 (C-17), indicative of an α,β-unsaturated carboxyl group, a terminal vinyl at δC 135.7 (CH-19) and 119.5 (CH2-18), besides signals at δC 97.5 (CH-21), 45.6 (CH-20), 35.9 (CH2-14), and 32.5 (CH-15). The anomeric carbon signals of the glucose unit are observed at δC 100.3 (CH-1’), with four mono-oxygenated methines in the interval from δC 78.6 to 71.7 and one oxygenated methylene at δC 62.9 [13].
Strictosidine (1) may function as a precursor of other biosynthetic pathways, leading to different skeletons and consequently changes in spectral properties. Carbonylation at C-5 (δC = 176.5 ppm), as observed for 5α-carboxystrictosidine (4), for example, promotes a chemical shift displacement of CH2-6 (Δδ = 4.2 ppm, β effect) when compared with 1, as can be seen in Table 2. A similar pattern was observed for methylation of N-4 on correantoside (7) isolated from P. correa [14], where Δδ variations (β effect) of 5.4 and 3.5 ppm are observed for CH-3 and CH2-5, respectively. For 10-hydroxycorreantoside (8), it is possible to observe the electronic influence of a hydroxyl by the inductive effect at the ipso carbon (C-10) and an increase in the electron densities at the ortho(CH-9 and CH-11) and para (C-13) positions by the mesomeric effect. On the basis of this mesomeric effect, the signals corresponding to carbon atoms at the ortho, CH-9 (δC 118.8 (1) and 104.4 (8), ΔδC = −14.8 ppm) and CH-11 (δC 122.7 (1) and 114.2 (8), ΔδC = −8.5 ppm) and para positions, C-13 (δC 137.9 (1) and 131.4 (8), ΔδC = −6.5 ppm), are displaced upfield.
Other metabolic pathways of this class of alkaloid revealed cyclization reactions involving N-1(compounds 5 and 6) or N-4 (compounds 7–14) with C-22, or N-1 with C-18 and N-4 with C-22, as particularly observed for stachyoside (30) isolated from P. stachyoides [15] (Figure 2). Strictosamide (5), isolated from four different species, [16,17,18,19] is an example of lactam formation between N-4 and C-22. By examining Table 2, it is possible to notice, apart from the absence of a methoxyl group (carbomethoxy function) signal at δC 52.4, a slight difference in the chemical shift of C-22 (δC 167.1 ppm), when compared with compound 1 (δC 170.6 ppm), as well as a ΔδC variation of 6.9 ppm for C-17. In contrast, correantoside (7) exemplified the first possibility involving cyclization between N-1 and C-22. It is possible, in this case, to observe the variation in the chemical shifts of the orthoCH-12 (Δδ = 4.0 ppm) and para CH-10 (Δδ = 4.1 ppm) atoms, promoted by the inductive and mesomeric effects of the carboxyl group at C-22. These effects were also observed for compounds 8 (ΔδC = 4.8 (CH-12) ppm), 13 (ΔδC = 4.4 (CH-12) and 4.1 (CH-10) ppm), 14 (ΔδC = 4.4 (CH-12) and 4.5 (CH-10) ppm), 18 (ΔδC = 7.8 (CH-12) and 6.2 (CH-10) ppm), and 19 (ΔδC = 7.3 (CH-12) and 5.4 (CH-10) ppm), showing that the downfield displacements of the CH-12 and CH-10 signals may be used to suggest that N-1 is attached to C-22.
There are some examples of alkaloids isolated from this genus, whose biosynthesis involves hydrolysis of a glycoside moiety such as (E/Z)-vallesiachotamines, 23 and 24, isolated from P. bahiensis [17], and10-hydroxy-iso-deppeaninol (27) and N-oxide-10-hydroxyantirhine (29) isolated from P. prunifolia [20]. These types of skeletons may be suggested by analysis of the region of the 13C spectrum that is typical of sugars, revealing the absence of the typical signal of the anomeric carbon around δC 100.0, apart from additional signals of the oxy-carbons characteristic of this unit.
Kerber et al. reported the isolation of a new MIA from P. brachyceras leaves [21], named brachycerine (33), which showed a new alkaloid skeleton. Its biosynthesis involved the coupling of tryptamine to a 1-epi-loganin derivative. Psychollatine (34), a new MIA from P. umbellate [22], presented a terpenoid derivative from geniposide. Both alkaloids as well as compounds 21, 22, and 35 revealed an important characteristic in their 13C spectra: the absence of typical signals of a terminal vinyl group (~δC 119 ppm). In contrast, bahienosides A (38) and B (37), isolated from P. bahiensis [17], showed duplicate terminal vinyl group signals relative to two secologanin moieties. Figure 2 shows typical carbon assignments, which may indicate some different structural possibilities in comparison with those values observed for strictosidine (1).

2.2. 13C-NMR Chemical Shifts of Pyrrolidinoindoline Alkaloids Isolated from Psychotria Species

Some studies have also reported that the isolation of pyrrolidinoindoline alkaloids seems to be specific to the Psychotria species (Table 3). As shown in Figure 3, their chemical structures present the condensation of some N-methyltryptamine units with different connection patterns, mainly involving C-3a-C3’a, C-3’a-C-7, and N-C-3’a bonds or containing N-methyltryptamine units linked to a bisquinoline part. The compound (+)-chimonanthine (40) was isolated from several Psychotria species [40,41,42] and is an example of a dimer that presents a C-3a-C-3’a-type linkage between its two units. Its 13C-NMR spectrum exhibited 11 carbon-signal equivalents for both units. The signals at δC 52.4 (CH2-2) and 84.6 (C-8a) are typical of carbons bearing one and two nitrogen atoms, respectively. The signals at δC 33.2 and 63.6 were attributed to C-3 and C-3a, respectively, whereas the signal at δC 33.8 is consistent with a methyl carbon attached to a nitrogen atom. The ortho-substituted aromatic rings are characterized by signals at δC 124.9 (CH-4/CH-4’), 128.3 (C-4a/C-4a’), 122.3 (CH-5), 119.8 (CH-5’), 129.9 (CH-6/CH-6’), 110.5 (CH-7/CH-7’), and 150.5 (C-7a/C-7a’) [40] (Table 4).
Since some compounds with more than two units present a chimonanthine portion in their structures, the monitoring of C-3a and C-7 (main binding sites) and their neighborhood may be a good alternative, in order to determine the positions of the other monomeric units. Hodgkinsine (52) occurs frequently in the genus [41,42,43,44,45,46] and presents a third unit with a C-3’’a-C-7’ linkage. In this case, besides replacement of a methine aromatic carbon by a quaternary carbon (C-7’), observing the up field displacements of C-6’ and C-4’ (Δδ around 3.0 ppm) is possible probably because of the presence of a group that increases the electron densities of these positions (comparison with compound 40). Takayama et al. (2004), however, reported the isolation of psychopentamine (60) from P. rostrata2, which showed a new type of linkage between C-3’’’a and C-5’’ [2].
The chemical study of P. calocarpa leaves [43] led to the isolation of a new alkaloid named psychotriasine (45), which presents a tryptamine unit linked to a pyrroloindole unit by an N-C3’a linkage. This type of junction was also observed for psychohenin (46) and compound 48 isolated from P. henryi [47,48] and may be indicated by the presence of a quaternary carbon (C-3’a) that resonates at δC 79.4, 77.8, and 76.7 ppm, in the three compounds, respectively. In contrast, psychotrimine (53), isolated from P. rostrate [2] shows, besides the N-C-3’a bond, an N-C-7’ linkage indicated by the signal of a quaternary aromatic carbon C-7’ at δC 121.5 ppm.
Alkaloids with more complex structures, containing from four to seven units, such as quadrigemines A–C (55–57), psychotridine (61), oleoidine (64), and caledonine (65), have also been isolated from this genus; however, the structural elucidation of these compounds becomes more difficult as the number of units increases. Probably owing to this, some studies did not provide detailed attributions of their carbon signals. In such cases, mass spectrometry plays an important role in establishing the number of units present in their structures as well as the pattern of the junctions.

2.3. 13C-NMR Chemical Shifts of Benzoquinolizidine Alkaloids Isolated from Psychotria Species

Muhammad et al. reported the isolation of five benzoquinolizidine alkaloids from Psychotria klugii [7] (Table 5). Among them, klugine (66) and 7’-O-demethylisocephaeline (67) were reported for the first time, whereas cephaeline (68), isocephaeline (69), and 7-O-methylipecoside (70) were previously isolated from Cephaelis species [56,57].
Compound 68 (ipecac alkaloid) as along with compounds 66, 67, and 69 possesses an unusual skeleton with two tetrahydroisoquinoline ring systems [10] characterized by the presence of four quaternary carbon signs at δC 147.2, 147.5 (C-9 and C-10, oxygenated ortho-substituted carbons), 126.8 (C-7a), and 130.1 (C-11a), two methine carbons at δC 108.6 (CH-11) and 111.5 (C-8), and signals at δC 62.4 (CH-11b), 52.3 (CH2-6), and 29.2 (CH2-7). A similar system is observed for the lower unit, with the exception of the absence of a methoxyl group attaching C-6’ (a hydroxyl group in this position). The remarkable difference between compounds 68 and 69 (stereoisomers) is associated with the chemical shift of carbon C-1′ at δC 51.9 and 55.3 respectively, whereas compounds 66 and 67 differ from 68 and 69 in the number and positions of the methoxyl groups. Interestingly, compound 70 exhibits carbon assignments consistent with a tetrahydroisoquinoline ring attached to a secologanin moiety at C-1.The chemical structures of compounds 68–70 are shown in Figure 4, and their 13C-NMR data are listed in Table 6.

3. Conclusions

In this work, we attempted to compile 13C-NMR data of alkaloids isolated from the Psychotria genus and provide information that may be useful in order to distinguish different types of skeletons. For monoterpene indole alkaloids (MIAs), mainly found in tropical species, a good strategy for their structural elucidation is to compare their spectral data with those observed for strictosidine (1). The monitoring of differences in specific parts of the spectrum, such as the signals of C-22, CH-17, CH-12, CH2-5, and CH-1′, may suggest alternative structural possibilities. Note that all comparisons performed in this work are restricted where possible to compounds whose 13C-NMR experiments were run in the same solvent.
The main pyrrolidinoindoline alkaloids found in this genus are chimonanthine derivatives, with units linked mostly by C3a-C3’a or C-3a-C7a bonds. Some examples have shown different patterns of linkages between N (from tryptamine terminal units) and C-3a. For compounds with more than three units, such as quadrigemines A–C and psychotridine and its isomer, obtaining detailed assignments of these carbons is not possible owing to structural complexity.The occurrence of benzoquinolizidine alkaloids in Psychotria species is less common, comprising some compounds isolated from Psychotria klugii.

Acknowledgments

The authors are grateful to Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ) for grantsand a researchfellowship, to Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Coordenação de Aperfeiçoamento de Pessoal de Ensino Superior (CAPES) for researchfellowships.

Author Contributions

All authors have contributed with the collection and analysis of data as well as the confection of this manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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Molecules 22 00103 g001a 550Molecules 22 00103 g001b 550
Figure 1. Structures of monoterpene indole alkaloids from Psychotria species.
Figure 1. Structures of monoterpene indole alkaloids from Psychotria species.
Molecules 22 00103 g001aMolecules 22 00103 g001b
Molecules 22 00103 g002 550
Figure 2. Structural signaling based on specific signals compared with values for strictosidine (1): absence of a given signal in red and presence in green.
Figure 2. Structural signaling based on specific signals compared with values for strictosidine (1): absence of a given signal in red and presence in green.
Molecules 22 00103 g002
Molecules 22 00103 g003a 550Molecules 22 00103 g003b 550Molecules 22 00103 g003c 550
Figure 3. Structures of pyrrolidinoindoline alkaloids from Psychotria species.
Figure 3. Structures of pyrrolidinoindoline alkaloids from Psychotria species.
Molecules 22 00103 g003aMolecules 22 00103 g003bMolecules 22 00103 g003c
Molecules 22 00103 g004 550
Figure 4. Structures of Benzoquinolizidine Alkaloids from P. klugii.
Figure 4. Structures of Benzoquinolizidine Alkaloids from P. klugii.
Molecules 22 00103 g004
Table
Table 1. Monoterpene indole alkaloids from Psychotria species.
Table 1. Monoterpene indole alkaloids from Psychotria species.
CompoundsSpeciesReferences13C-NMR Data
Strictosidine (1)P. elata[12][13]
Strictosidinic acid (2)P. acuminata
P. barbiflora
P. myriantha		[1,23,24,25][25]
Palicoside (3)P. racemosa[12][26]
5α-Carboxystrictosidine (4)P. acuminata
P. bahiensis		[17,23][27]
Strictosamide (5)P. bahiensis
P. nuda
P. prunifolia
P. suterella		[16,17,18,19][18]
N,β-D-Glucopyranosilvincosamide (6)P. leiocarpa[28][28]
Correantoside (7)P. correae[14][14]
10-Hydroxycorreantoside (8)P. correae[14][14]
Correantine B (9)P. correae[14][14]
20-epi-Correantine B (10)P. correae[14][14]
Correantine A (11)P. correae[14][14]
Correantine C (12)P. correae[14][14]
N-Desmethyl-correantoside (13)P. stachyoides[29][29]
Nor-Methyl-23-oxo-correantoside (14)P. stachyoides[15][15]
14-Oxoprunifoleine (15)P. prunifolia[18,20][18]
17-Vinyl-19-oxa-2-azonia-12-azapentacyclo[14.3.1.02,14.05,13.06,11]icosa-2(14),3,5(13),6(11),7,9-hexaene (16)P. prunifolia[18][18]
Naucletine (17)P. suterella[19][30]
Correantosine E (18)P. stachyoides[31][31]
Correantosine F (19)P. stachyoides[31][31]
Lagamboside (20)P. acuminata[23][23]
N4-[1-((R)-2-Hydroxypropyl)]-psychollatine (21)P. umbellata[32][32]
N4-[1-((S)-2-Hydroxypropyl)]-psychollatine (22)P. umbellata[32][32]
(E/Z)-Vallesiachotamine (23 + 24)P. bahiensis
P. laciniata		[17,33][34]
Isodolichantoside (25)P. correae[14][14]
Angustine (26)P. bahiensis
P. laciniata		[17,33][35]
10-Hydroxy-iso-deppeaninol (27)P. prunifolia[20][20]
10-Hydroxy-antirhine (28)P. prunifolia[20][20]
N-Oxide-10-hydroxyantirhine (29)P. prunifolia[20][20]
Stachyoside (30)P. stachyoides[15][15]
Lyaloside (31)P. laciniata
P. suterella		[19,36][37]
Myrianthosine (32)P. myriantha[25][25]
Brachycerine (33)P. brachyceras[21][21]
Psychollatine (34)P. umbellata
P. umbellata		[5,22,38][22]
3,4-Dehydro-18,19-β-epoxy-psychollatine (35)P. umbellata[32][32]
Desoxycordifoline (36)P. acuminata[23][39]
Bahienoside B (37)P. acuminata
P. bahiensis		[17,23][17]
Bahienoside A (38)P. bahiensis[17][17]
Table
Table 2. 13C-NMR data of MIAs from Psychotria species.
Table 2. 13C-NMR data of MIAs from Psychotria species.
CarbonsCompounds/δC (ppm)
1 I2 III3 III4 I5 I6 I7 I8 I9 II10 II
C
2133.2132.3134.7133.2134.8136.1134.3133.8132.9133.0
7107.7106.0105.2109.0110.3111.5115.7115.3114.8114.8
8127.9126.1126.6128.0128.7129.5130.4131.3129.1129.1
13137.9135.8135.8138.4137.8137.7137.3131.4136.0136.0
22170.6170.0168.4170.9167.1166.3168.2167.8166.2166.2
16109.9113.4112.5109.9109.2109.1112.2112.0108.6109.6
CH
352.449.656.153.255.154.557.858.256.456.7
5---60.1------
9118.8117.8117.4118.8118.7119.3119.2104.4118.1118.0
10120.1118.7118.1120.1120.2121.3124.2155.1123.2123.2
11122.7121.2120.3122.6122.6122.9125.5114.2124.6124.6
12112.0111.5110.8112.1112.3114.8116.0116.8115.4115.2
1532.531.830.632.424.927.935.735.629.729.2
17156.1150.0151.8156.1149.2149.2155.7155.5158.0156.4
19135.7135.6135.6135.2134.4133.4135.1135.070.269.4
2045.644.344.045.744.744.145.445.451.853.9
2197.595.195.997.698.197.597.497.3--
CH2
542.940.045.260.144.841.646.446.745.545.5
621.019.215.925.222.122.318.818.817.617.7
1435.933.735.335.627.335.634.434.139.135.3
18119.5117.8117.8119.6120.6120.7119.2119.3--
CH3
MeN---39.8---41.441.2-41.5
Me--------18.319.3
Glucose
1′100.398.998.7100.5100.599.6100.5100.5--
2′78.669.873.074.774.374.974.774.7--
3′78.073.177.278.077.977.978.678.6--
4′74.677.270.071.971.371.6 a71.671.7--
5′71.776.576.678.678.278.378.078.0--
6′62.961.061.063.162.662.762.962.9--
1″-----87.6----
2″-----71.9----
3″-----75.1----
4″-----71.6 a----
5″-----81.2----
6″-----62.9----
CHO--------199.5199.2
CO2Me52.4--52.6------
CO2H---176.5------
CarbonsCompounds/δC (ppm)
11 II12 I13 I14 I15 I16 I17 II18 I19 I20 I
C
2136.2134.6136.0132.4134.4132.2127.4145.7134.4136.0
3----139.7139.5140.8-148.1-
7108.0117.4117.0116.2124.6132.9116.9138.0134.0111.3
8126.8130.6131.0130.1118.9119.7125.7123.9125.2129.7
13137.1137.7137.3137.7146.9144.6139.0140.0142.3136.0
14----191.6-----
15------141.1---
16111.2-112.7111.8--117.1113.5114.595.3
19------199.6---
20------138.8---
21-194.3--------
22167.5174.8168.6168.1--161.6167.9168.8171.8
CH
361.458.550.647.9---50.0-50.2
5----134.1132.5-137.0142.6-
6----120.6116.0-116.2114.5-
9118.5117.8119.2119.5123.6122.8119.3123.9122.3119.0
10119.8119.0124.4124.6123.4122.4119.9126.3125.5121.0
11121.5125.0125.5126.0137.2132.3120.9133.5131.3122.7
12109.2126.0116.4116.4113.7113.2112.0119.8119.3114.6
14------95.6---
1530.834.535.735.642.825.6-30.521.233.7
16-52.0--------
17155.267.5155.6156.587.986.7154.0157.2155.9149.3
1974.8149.7135.2134.9132.8134.9-133.6134.1140.8
2052.0-45.645.342.041.2-46.446.755.2
2175.5-97.597.6--155.497.997.9-
CH2
552.048.040.041.6--40.7--53.0
620.919.623.223.2--19.8--23.4
1436.735.936.734.8-24.8-36.739.835.1
16----42.825.6----
18-33.8119.3119.5118.9117.9-121.8121.3116.9
21----63.461.9---65.4
CH3
1818.6-----29.3---
MeN-43.041.9--------
Glucose
1′--100.7100.8---100.1100.187.6
2′--74.974.9---74.874.772.4
3′--78.778.2---78.077.979.4
4′--71.871.7---71.771.771.8
5′--78.278.7---78.078.681.2
6′--63.163.0---62.962.963.0
CHO---163.9------
CO2Me51.1--------51.2
CarbonsCompounds/δC (ppm)
21 I22 I23 III24 III25 I26 III27 I28 I29 I
C
2134.0133.4133.1133.6134.0126.8136.9130.5131.0
3-----136.9145.5--
7108.4108.4106.6107.4106.5114.8130.6106.0105.7
8138.6138.1126.2127.0128.1125.5123.1128.6128.3
10------152.6151.8152.0
13128.4128.0136.1136.8137.8138.5137.5133.1133.6
15-----139.0---
16112.2112.093.293.4112.0119.8---
19141.0142.1-------
20- -146.1143.9-127.8---
22169.7169.0166.9167.6169.8161.1---
CH
361.759.348.647.958.8--57.071.6
5------135.7--
6------114.6--
9118.6118.0117.4118.4118.7119.9106.6103.2103.3
10119.5120.0118.3119.2119.9119.9---
11121.9122.0120.7121.6122.3124.6120.4112.9113.2
12112.0112.0110.8111.8111.8112.0113.7112.8113.0
14-----93.8---
1533.035.327.430.530.5-36.431.130.6
17153.3153.0147.2148.5154.0149.7---
18132.6131.0-------
19--152.0146.3135.8130.2138.1138.7138.2
2049.048.4--45.5-51.050.852.3
2195.697.0--97.8147.7---
2565.166.3-------
CH2
549.049.649.850.747.940.4-52.469.0
621.419.721.322.217.919.2-18.120.6
1439.439.532.932.934.5-37.031.628.5
17------61.448.059.1
18----119.8119.8118.7118.5118.5
21------64.464.063.8
2462.461.6-------
CH3
18--14.313.8-----
2620.721.2-------
MeN-----40.6----
Glucose
1′100.1100.1--100.5----
2′74.674.8--74.7----
3′78.078.0--78.6----
4′78.271.6--71.6----
5′76.278.5--78.0----
6′62.762.5--62.9----
CHO--195.5191.5-- --
CO2Me51.651.749.750.851.9----
Carbons Compounds/δC (ppm)
30 I3132 III33 I34 I35 I36 I37 I38 I
C
2137.1140.3134.8130.7131.1128.8135.6135.0138.0
3-143.8---158.9142.9--
5------135.6--
7118.4121.0121.0108.3107.9118.8128.4107.3106.6
8129.2126.9121.5127.7127.6139.9121.7128.4128.0
13139.1134.6140.2112.3138.1126.1141.6137.8138.0
15
19----140.067.3---
16114.8109.9112.0111.8112.2110.2108.7112.1111.5
21169.0--------
22-166.6170.0169.1169.1168.9171.3169.7170.0
22b-- ----169.5169.4
CH
351.7-48.554.753.7--58.859.6
5-137.3137.0------
6-112.6118.0---114.2--
9119.7121.4126.6118.9119.0121.2121.4120.6118.7
10125.2119.0118.9120.2120.3121.1119.9119.7120.0
11126.8127.6127.5123.2123.6126.2128.4122.0122.5
12118.3111.8112.5112.3112.3113.6111.6112.0112.0
1532.930.1-35.537.531.734.531.531.6
17148.7151.6151.0153.5153.4153.1153.2154.0154.7
18---74.3138.562.5---
1953.3134.0134.549.0--133.8136.2136.1
2095.542.945.541.949.043.844.445.545.4
21-95.995.499.099.495.296.198.297.9
15b-- ----30.330.5
17b-- ----153.2153.5
19b-- ----135.7135.5
20b-- ----44.844.8
21b-- ----98.598.3
CH2
548.0--41.842.148.2-44.844.8
621.2--24.420.520.1-17.617.4
1443.732.145.643.540.534.734.036.936.7
15--30.0------
17---------
1872.4118.6118.9---117.6119.8119.8
3b-- ----52.051.9
14b-------28.027.4
18b-------120.1120.1
CH3
Me--10.4------
Glucose
1′100.398.7998.6100.6101.599.499.0100.4100.4
2′74.973.173.074.071.074.773.274.674.8 c
3′78.577.369.971.178.678.176.678.078.6 a
4′71.971.1077.378.374.672.170.471.671.7 d
5′78.577.876.877.777.678.876.678.478.2 b
6′63.061.261.062.161.863.361.862.962.9 e
1″-------100.3100.4
2″-------74.874.6 c
3″-------78.178.4 a
4″-------71.671.6 d
5″-------78.378.0 b
6″-------62.862.8 e
CO2Me-50.7-51.851.951.950.652.152.1
I CD3OD, II CDCl3 e III DMSO-d6, letters (a–e) indicate signals that may be interchanged.
Table
Table 3. Pyrrolidinoindoline alkaloids from Psychotria species.
Table 3. Pyrrolidinoindoline alkaloids from Psychotria species.
CompoundsSpeciesReferences13C-NMR Data
Meso-chimonanthine (39)P. forsteriana
P. muscosa		[41,49,50][50]
(+)-Chimonanthine (40)P. colorata
P. muscosa
P. rostrata
P. hoffmannseggiana		[40,41,42][40]
Iso-calycanthine (41)P. forsteriana[50][50]
Calycanthine (42)P. forsteriana[50][50]
(8-8a),(8’-8’a)-tetradehydroisocalycanthine 3a(R), 3’a(R) (43)P. colorata[42][42]
Nb-desmethyl-meso-chimonanthine (44)P. lyciiflora[49][49]
Psychotriasine (45)P. calocarpa[43][43]
Psychohenin (46)P. henryi[47][47]
Compound (47)P. henryi[48][48]
Compound (48)P. henryi[48][48]
Glomerulatine A (49)P. glumerulata[51][51]
Glomerulatine B (50)P. glumerulata[51][51]
Glomerulatine C (51)P. glumerulata[51][51]
Hodgkinsine (52)P. colorata
P. oleoides
P. lyciiflora
P. muscosa
P. beccarioides
P. rostrata		[41,42,43,44,45,46][42]
Psychotrimine (53)P. rostrata[2][2]
Psychotripine (54)P. pilifera[52][52]
Quadrigemine A (55)P. forsteriana[53][53]
Quadrigemine B (56)P. forsteriana
P. colorata
P. rostrata		[41,53][53]
Quadrigemine C (57)P. colorata
P. oleoides		[41,42,43,45,46,50,54][45]
Quadrigemine I (58)P. oleoides[49][49]
Psycholeine (59)P. oleoides[46,54][46]
Psychopentamine (60)P. rostrata[2][2]
Psychotridine (61)P. forsteriana
P. oleoides
P. colorata
P. beccarioides		[41,44,45,53][45]
Isopsychotridine C (62)P. forsteriana[53,55][55]
Isopsychotridine B (63)P. oleoides[49,50][45]
Oleoidine (64)P. oleoides[49][49]
Caledonine (65)P. oleoides[49][49]
Table
Table 4. 13C-NMR data of pyrrolidinoindoline alkaloids from Psychotria species.
Table 4. 13C-NMR data of pyrrolidinoindoline alkaloids from Psychotria species.
CarbonsCompounds/δC (ppm)
39 II40 II41 ns42 II43 II44 II45 I46 I47 II
C
3------112.7110.0112.3
3a64.763.637.836.848.962.8---
4a133.7128.3127.0125.9125.6132.2130.4130.5130.0
7a152.5150.5145.3146.2145.8151.7137.7138.0135.0
8a----165.0----
3′a64.763.637.836.848.963.979.477.875.3
4′a133.7128.3127.0125.9125.6130.0131.3131.3128.9
7′a152.5150.5145.3146.2145.8150.3152.5152.7152.4
8′a----165.0----
CH
2------125.0126.1123.4
4125.2124.9118.3117.1123.0123.9124.7119.5119.0
5119.2122.3122.2 b122.1118.5119.9119.3118.8 e119.1 f
6128.9129.9127.7127.3128.2128.2130.7123.0121.4
7109.5110.5112.9112.8123.9109.1120.1117.4112.8
8a83.984.671.771.82-79.3---
4′125.2124.9118.3117.1123.0124.4112.2124.9126.4
5′119.2119.8125.2125.2121.9117.9122.4119.8118.7
6′128.9129.9127.7127.3128.2128.4119.6130.9130.2
7′109.5110.5112.9112.8123.9108.2110.0110.4108.8
8′a83.984.671.771.82-82.487.087.386.6
CH2
253.152.446.947.348.544.9---
336.433.234.932.529.935.3---
2′53.152.446.947.448.551.852.052.353.6
3′36.433.234.932.529.938.139.940.037.7
2″--------69.1
CH3
Me-N1-nd33.846.943.431.1-36.333.940.6
MeN1′-nd33.846.943.431.135.1235.736.437.1
CarbonsCompounds/δC (ppm)
48 II49 III50 III51 III52 II53 II54 I + II55 II,*56 II,*
C
2129.6--------
3109.4----114.9---
3a-49.148.649.262.8-69.160.9 c60.1 c
4a128.0126.4126.1 a129.5131.7128.3133.8132.3 d133.2 e
7a137.4177.3147.1148.6150.8136.1152.2150.9 h150.6 h
8a-165.1164.7166.5--106.9--
3′a76.749.148.645.363.076.737.063.2 j63.9 i
4′a130.5126.4125.4 a122.3132.3132.0122.0132.4 d132.9 e
7′-----121.5130.9108.9 g-
8′a-165.1164.7------
3″-----112.5---
3″a----60.0-38.462.9 j63.3 i
8″-----25.7 b68.0--
9″-----52.0---
4″a----131.7129.8122.3132.6 d-
7″a----151.1136.1144.4--
3‴a-------60.8 c60.9 c
CH
2-----126.0---
4117.9123.7120.9123.0126.4119.4 a122.9-125.9 d
5119.2122.3122.2 b122.1118.5119.9119.3118.8 e119.1 f
6121.3128.9129.0 c128.8127.9122.4128.2127.9 f128.0 g
7112.1125.0125.2 d125.2109.0111.2107.7109.0 g108.9
8a----86.4--86.9 i85.9 i
4′124.5123.7124.0 d117.5121.9123.7123.7122.5125.1 d
5′119.0122.3122.6 b124.9116.8119.3 a122.0116.3 k118.3 f
6′129.6128.9128.8 c127.1126.0127.3121.1125.4127.8 g
7′108.9125.0124.4 d114.4-----
8′a86.5--76.581.786.169.786.1 i83.3 j
2″-----124.3---
4″----124.2119.3 a125.4--
5″----117.5119.3 a117.8118.7 e117.2 f
6″----127.4121.7127.6--
7″----108.1112.2112.5--
8″a----82.3-69.4-82.3 j
8‴a--------87.1 i
5‴-------116.2 k116.8 f
6‴-------126.4 f-
CH2
2-48.248.148.551.7-54.952.6 a52.3 a
3-30.330.331.737.6-36.338.8 b38.5 b
2′51.248.248.150.551.951.742.352.5 a52.2 a
3′40.630.330.334.036.739.133.138.7 b36.6 b
2″----51.9-45.952.2 a-
3″----38.0-33.738.5 b-
3‴-------36.6 b-
CH3
Me-N1-44.830.930.830.735.236.336.435.7 l35.8 k
MeN1′-36.130.9-36.635.036.4-35.5 l35.7 k
Me-N1″-----35.136.441.835.0l35.6 k
Me-N1‴---------35.2 k
CarbonsCompounds/δC (ppm)
57 II,*58 II,*59 II,*60 II61 II,*62 II,*63 II,*64 II,*65 II,*
C
3a60.660.059.6 b61.160.1 a60.9 c63.0 a60.4 c60.0 c
4a-132.0132.4 c132.9 b-132.7 d-132.8132.1 e
7a---152.8-150.6 f-150.7 e150.5 f
3′a62.663.037.5 f63.162.963.7 h63.3 a63.3 c63.0
4′a---132.8 b-132.0 d--132.4 e
7′-110.0 c-123.8----108.8
7′a---151.0-148.9 f-150.3 e148.9 f
5″---136.2-117.1---
3″a62.6-38.0 f64.262.963.2 h59.8 c60.9 c-
4″a---132.6-----
7″a---149.8----148.6
3‴a60.6-60.6 b62.360.6 a60.1 c59.8 c-60.5 c
4‴a--133.8 c138.6-----
7‴---120.4-----
7‴a---144.7-----
3″″---114.5-----
3″″a---128.360.8 a-60.7 c--
4″″a--- -----
CH
4-126.0-126.9-123.6-126.1 d125.3 d
4′-124.0-122.1-122.2-124.1125.2 d
5-117.0 b-118.8-119.1 e-116.3118.9
6-129.5-128.0-128.2-128.7128.1
7-109.0 c-110.5-109.0-109.3107.7
8a85.8 a88.0 d88.5 d87.386.0 b87.2 g81.8 b86.686.9
5′-118.5 b-116.2-118.4 e-119.4117.3
6′-127.5-126.5-126.1-126.2125.3
8′a82.383.0 d74.0 g82.482.6 c85.8 g86.8 b82.886.0
4″---121.4---125.7 d124.1
5″-119.0 b---117.1---
6″---126.1-125.4-128.4-
7″---108.5-----
8″a82.3-72.0 g83.482.3 c83.186.8 d83.0-
4‴---123.3---122.7123.6
5‴-119.5 b-118.8-----
6‴-128.5-125.1-----
7‴---120.4-----
8‴a86.7 a-87.5 d88.486.9 b82.185.5 d--
2″″---126.1-----
4″″---119.3---125.7123.2
5″″---111.2-----
6″″---122.3-----
7″″---119.7-----
8″″a----85.1 b-84.8 d--
CH2---------
2-53.047.17 a52.7 a-52.5 a-52 a52.1 a
3-38.0 a-37.8-38.8 b-38.7 b38.3 d
8 --------
9 --------
2′ --52.7 a-52.0 a-52.8 a52.4 a
3′ 39.0 a32.8 e35.8-38.5 b-38.7 b38.6 b
2″ --52.6a---52.9 a-
3″ -32.4 e37.2-----
2‴ -48.0 a52.5a-----
3‴ --39.2-----
3″″ --114.5-----
CH3 --------
Me-N1- 36.036.1 h34.8-35.6 i-35.735.4 g
Me-N1′- -42.6 i35.3-35.1 i--35.6 g
Me-N1″- -42.6 i35.8-----
Me-N1‴- -36.1 h35.7-----
Me-N1″″- --36.5-----
I CD3OD, II CDCl3 e III benzene-d6, ns not specified; letters indicate signals that may be interchanged, nd = not detected; * indicates cases for which there was no complete detailed attribution of carbon signals.
Table
Table 5. Benzoquinolizidine Alkaloids from P. klugii.
Table 5. Benzoquinolizidine Alkaloids from P. klugii.
CompoundReference13C-NMR Data
Klugine (66)[7][7]
7’-O-Demethylisocephaeline (67)[7][7]
Cephaeline (68)[7][56]
Isocephaeline (69)[7][56]
7-O-Methylipecoside (70)[7][57]
Table
Table 6. 13C-NMR Data of Benzoquinolizidine Alkaloids from P. klugii.
Table 6. 13C-NMR Data of Benzoquinolizidine Alkaloids from P. klugii.
CarbonsCompound/δC (ppm)
66 ns67 ns68 II69 II70 I
C
6----146.5 a
7----147.8 a
9146.5 a146.8147.2 a147.2 a-
10147.8 b148.0147.5 a147.4 a-
4a----126.9
7a127.8126.9126.8126.5-
8a----130.2
11a129.7127.9130.1129.9-
1′79.5----
4′----111.7
4’a127.7123.2127.6127.9-
6′146.4 a145.6143.9 b144.0-
7’
11’----169.2
8’a129.7126.0131.1131.0-
CH
1----50.6
2
342.541.341.761.5-
5----116.2
8116.2112.1111.5111.4111.1
11109.7109.0108.6108.2-
11b63.862.762.462.8-
1′-53.651.955.398.7
3′----153.1
4′28.527.629.029.3-
5′116.4115.2114.7114.827.5
8′110.0113.2108.4108.6136.3
9′----45.1
CH2
140.636.936.939.3-
3----36.1
462.261.661.352.629.1
653.351.952.352.6-
729.325.329.229.1-
1224.423.323.624.0-
1437.038.040.940.4-
3′41.039.540.141.4-
4′28.527.629.029.3-
6′----41.1
10′----120.1
CH311.510.111.211.3-
1311.510.111.211.3-
Me7-O---- 56.5
Me9-O--55.4 d55.8 e55.8 f-
Me10-O-56.8 c55.8 d56.0 e56.0 f-
Me7′-O-56.6 c-56.3 e56.0 f-
Glucose
1″----100.5
2″----74.8
3″----78.2 b
4″----71.5
5″----78.3 b
6″----62.7
CO2Me 51.7
I CD3OD, II CDCl3 e ns not specified; letters indicate signals that may be interchanged.

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Carvalho Junior, A.R.d.; Vieira, I.J.C.; Carvalho, M.G.d.; Braz-Filho, R.; S. Lima, M.A.; Ferreira, R.O.; José Maria, E.; Oliveira, D.B.d. 13C-NMR Spectral Data of Alkaloids Isolated from Psychotria Species (Rubiaceae). Molecules 2017, 22, 103. https://doi.org/10.3390/molecules22010103

AMA Style

Carvalho Junior ARd, Vieira IJC, Carvalho MGd, Braz-Filho R, S. Lima MA, Ferreira RO, José Maria E, Oliveira DBd. 13C-NMR Spectral Data of Alkaloids Isolated from Psychotria Species (Rubiaceae). Molecules. 2017; 22(1):103. https://doi.org/10.3390/molecules22010103

Chicago/Turabian Style

Carvalho Junior, Almir Ribeiro de, Ivo Jose Curcino Vieira, Mario Geraldo de Carvalho, Raimundo Braz-Filho, Mary Anne S. Lima, Rafaela Oliveira Ferreira, Edmilson José Maria, and Daniela Barros de Oliveira. 2017. "13C-NMR Spectral Data of Alkaloids Isolated from Psychotria Species (Rubiaceae)" Molecules 22, no. 1: 103. https://doi.org/10.3390/molecules22010103

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