Alkaloids

Alkaloids are nitrogen-containing small molecules which are mainly found in plants.1) To date, approximately 27 thousand alkaloids have been reported in which 21 thousand were of plant origin.
Since most of the alkaloids exhibit potent bioactivity, they are the main component of many herbal medicines. Some alkaloids are also used as pharmaceuticals. Alkaloids interact with proteins electrostatically due to the positive charge of the nitrogen atoms which facilitates binding to the negative charge of the proteins. Especially, pharmaceutical alkaloids tend to bind to the receptors in neural systems.

■Biosynthesis
Biosynthetic pathways to alkaloids vary greatly depending on the nitrogen source. Alkaloids are biosynthesized from various kinds of amino acids as depicted in Fig. 1. Further complex alkaloids are also biosynthesized by attaching another alkaloid to the original skeletons.

■Structure Classification
In the IUPAC Nomenclature Appendix, 67 alkaloid parent structures are shown.2) They can be classified into their basic skeletons based on their biosynthetic origins as shown in Fig. 1. In this section, alkaloids are categorized into nine: eight as shown above and purine alkaloids as the ninth. Polyamines which are occasionally considered as alkaloid-related substances, will be explained in the section “Polyamines”.

■Solubility
In general, alkaloids dissolve in acidic water. Their salts dissolve in neutral water. They are usually insoluble in neutral water as free forms, but soluble in polar organic solvents such as chloroform, methanol or DMSO.

■Analysis
HPLC:In the reversed phase mode using an ODS column, peak tailing is suppressed by addition of acetic acid or trifluoroacetic acid to the mobile phase. Effective analysis would be achieved by a mixed mode column, TCI-Dual, with ion-exchange and reversed phase modes simultaneously. Detection is generally conducted by a UV detector.
TLC:In a normal phase silica gel TLC analysis, a solvent system of chloroform-methanol-aqueous ammonia gives a relatively a good separation. NH2-type silica gel is also effective. Dragendorff’s reagent is a selective visualizing reagent for alkaloids. Tertiary amines and quaternary ammonium salts give orange spots.

■Storage Precautions
Alkaloids are relatively stable at room temperature, however, they tend to form carbonate salts due to their basicity by reaction with carbon dioxide in the air. In addition, they are usually colorized by reaction with oxygen. Therefore, opened bottles should be stored in the refrigerator or frozen with inert gas such as nitrogen or argon.

WARNING
Some of the alkaloids may cause serious physiological actions in very minute amounts. They may cause paralysis, convulsions, and death in the worst case. To avoid inhalation and contacting with skin, wear protective goggles, mask and eyeglasses when handling. Sufficient caution should be taken, when using these compounds, from the opening to the disposal of the reagents.

Tropane Alkaloids

Piperidine Alkaloids

Phenylethylamines

Isoquinoline Alkaloids

Quinoline Alkaloids

Pyridine Alkaloids

Indole Alkaloids

Imidazole Alkaloids

Purine Alkaloids

Others

Tropane Alkaloids

H0450 H0450 A0754 A0754 A0550 A0550
H0155 H0155 H0156 H0156 H0448 H0448
H0451 H0451 H0452 H0452 H0453 H0453
E0834 E0834 B3401 B3401 N0844 N0844
S0021 S0021 S0231 S0231 S0230 S0230
S0229 S0229 T0534 T0534
H0450 (-)-Hyoscyamine
A0754 Atropine
A0550 Atropine Sulfate Monohydrate
H0155 Homatropine Hydrobromide
H0156 Homatropine Hydrochloride
H0448 Homatropine Methyl Bromide
H0451 Hyoscyamine Hydrobromide
H0452 Hyoscyamine Hydrochloride
H0453 Hyoscyamine Sulfate Hydrate
E0834 N-(Ethoxycarbonyl)nortropinone
B3401 N-(tert-Butoxycarbonyl)nortropinone
N0844 Nortropinone Hydrochloride
S0021 Scopolamine Hydrobromide Trihydrate
S0231 Scopolamine Methyl Bromide
S0230 Scopolamine Methyl Nitrate
S0229 Scopolamine N-Oxide Hydrobromide
T0534 Tropine

Piperidine Alkaloids

L0096 L0096 P0460 P0460 S0067 S0067
L0096 Lobeline Hydrochloride
P0460 Piperine
S0067 Sparteine Sulfate

Phenylethylamines

P0398 P0398 M0844 M0844 D2104 D2104
M1891 M1891 E0387 E0387 A0305 A0305
A1234 A1234 A0172 A0172 A0909 A0909
N0389 N0389 P0397 P0397 E0381 E0381
D0651 D0651 I0261 I0261 I0260 I0260
A0173 A0173 A0175 A0175 A0906 A0906
P0395 P0395 P0396 P0396 S0232 S0232
S0233 S0233 A0302 A0302
P0398 (R)-Phenylephrine Hydrochloride
M0844 2-(2-Methoxyphenyl)ethylamine
D2104 2-(3,4-Dimethoxyphenyl)-N-methylethylamine
M1891 2-(3-Methoxyphenyl)ethylamine
E0387 2-Ethylamino-1-(4-methoxyphenyl)propane Hydrochloride
A0305 3-Hydroxytyramine Hydrochloride
A1234 Adrenalone Hydrochloride Hydrate
A0172 DL-Adrenaline
A0909 DL-Adrenaline Hydrochloride
N0389 DL-Norphenylephrine Hydrochloride
P0397 DL-Phenylephrine Hydrochloride
E0381 Etilefrine Hydrochloride
D0651 Hordenine Sulfate Dihydrate
I0261 Isoprenaline Sulfate
I0260 Isoproterenol Hydrochloride
A0173 L-Adrenaline
A0175 L-Adrenaline Bitartrate
A0906 L-Noradrenaline Bitartrate Monohydrate
P0395 L-Phenylephrine
P0396 L-Phenylephrine Bitartrate
S0232 Synephrine
S0233 Synephrine Tartrate
A0302 Tyramine

Isoquinoline Alkaloids

B0450 B0450 B0451 B0451 E0007 E0007
P0016 P0016 C0433 C0433
B0450 Berberine Chloride Hydrate
B0451 Berberine Sulfate Hydrate
E0007 Emetine Dihydrochloride Hydrate
P0016 Papaverine Hydrochloride
C0433 Tubocurarine Chloride

Quinoline Alkaloids

C1495 C1495 I0728 I0728 C0347 C0347
C0348 C0348 C0349 C0349 C0350 C0350
C0351 C0351 C0791 C0791 H0752 H0752
B1683 B1683 B1689 B1689 B1684 B1684
B1685 B1685 Q0006 Q0006 Q0010 Q0010
Q0028 Q0028 Q0030 Q0030
C1495 (S)-(+)-Camptothecin
I0728 beta-Isocupreidine
C0347 Cinchonidine
C0348 Cinchonidine Dihydrochloride
C0349 Cinchonidine Sulfate
C0350 Cinchonine
C0351 Cinchonine Hydrochloride Hydrate
C0791 Cinchonine Sulfate Dihydrate
H0752 Hydroquinidine Hydrochloride
B1683 N-Benzylcinchonidinium Chloride [Chiral Phase-Transfer Catalyst]
B1689 N-Benzylcinchoninium Chloride [Chiral Phase-Transfer Catalyst]
B1684 N-Benzylquinidinium Chloride [Chiral Phase-Transfer Catalyst]
B1685 N-Benzylquininium Chloride [Chiral Phase-Transfer Catalyst]
Q0006 Quinidine
Q0010 Quinidine Sulfate Dihydrate
Q0028 Quinine
Q0030 Quinine Hydrochloride Dihydrate

Pyridine Alkaloids

A0523 A0523 N0079 N0079 N0080 N0080
N0081 N0081 T1429 T1429
A0523 Arecoline Hydrobromide
N0079 Nicotine
N0080 Nicotine Bi-L-(+)-tartrate Dihydrate
N0081 Nicotine Sulfate (40-45% in Water as Nicotine base)
T1429 Trigonelline Hydrochloride

Indole Alkaloids

B0670 B0670 B0946 B0946 B0671 B0671
B0672 B0672 C0001 C0001 D2633 D2633
D1247 D1247 D0653 D0653 H0001 H0001
H0002 H0002 P0406 P0406 P0407 P0407
R0007 R0007 S0249 S0249 S0257 S0257
S0093 S0093 S0094 S0094 V0061 V0061
Y0002 Y0002
B0670 Brucine Dihydrate
B0946 Brucine Anhydrous
B0671 Brucine Hydrochloride
B0672 Brucine Sulfate Heptahydrate [for Nitrate Analysis]
C0001 Cacotheline Monohydrate
D2633 Dihydroergotamine Mesylate
D1247 Dihydroergotamine Tartrate
D0653 Gramine
H0001 Harmine
H0002 Harmine Hydrochloride
P0406 Physostigmine free base
P0407 Physostigmine Salicylate
R0007 Reserpine
S0249 Strychnine
S0257 Strychnine Hydrochloride Hydrate
S0093 Strychnine Nitrate
S0094 Strychnine Sulfate Pentahydrate
V0061 Vincamine
Y0002 Yohimbine Hydrochloride

Imidazole Alkaloids

H0146 H0146 H0147 H0147 P0434 P0434
P0399 P0399
H0146 Histamine Dihydrochloride
H0147 Histamine Diphosphate Hydrate
P0434 Pilocarpine Hydrochloride
P0399 Pilocarpine Nitrate

Purine Alkaloids

C1103 C1103 M1756 M1756 M2073 M2073
B3456 B3456 C0293 C0293 C2042 C2042
T0178 T0178 T0179 T0179
C1103 1-(3-Chloropropyl)theobromine
M1756 3-Methyl-7-propylxanthine
M2073 3-Methylxanthine
B3456 8-Bromotheophylline
C0293 8-Chlorotheophylline
C2042 Caffeine
T0178 Theobromine
T0179 Theophylline

Others

C0380 C0380 G0293 G0293 T0329 T0329
C0380 Colchicine (contains 5% Ethyl Acetate at maximum)
G0293 Galantamine Hydrobromide
T0329 Tomatine [for Cholesterol assay]

Literature

1) P. M. Dewick, in Medicinal Natural Products, 3rd ed., John Wiley & Sons Ltd, Chichester, 2009, p. 311.
2) P. M. Gills Jr., Pure Appl. Chem. 1999, 71, 587.


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