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Results for "

alkaloid

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    687
    TargetMol | Inhibitors_Agonists
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    TargetMol | Compound_Libraries
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Norharmane
β-Carboline, 2-Azacarbazole, 2,9-Diazafluorene
T4024244-63-3
Norharmane (β-Carboline) is a natural β-carboline first isolated from plants of the Zygophyllaceae family.
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Camptothecin
NSC-100880, CPT, Campathecin, (S)-(+)-Camptothecin
T11237689-03-4
Camptothecin (CPT) belongs to the alkaloid group of natural products and is a specific DNA topoisomerase I (Topo I) inhibitor (IC50=679 nM) with specificity. Camptothecin has antitumor activity and induces apoptosis.
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4-6 weeks
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TargetMol | Citations Cited
Harmane
Loturine, Harman, Aribine
T3158486-84-0
Harmane (Loturine) is a bio-active β-Carboline and monoamine oxidase inhibitor found in coffee and tobacco smoke.
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TargetMol | Citations Cited
Bicuculline
d-Bicuculline, (+)-Bicuculline
T2850485-49-4
Bicuculline ((+)-Bicuculline) is a light-sensitive competitive antagonist of GABAA receptors, originally identified in 1932 from plant alkaloid extracts, and isolated from Dicentra cucullaria, Adlumia fungosa, Fumariaceae, and various Corydalis species.
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TargetMol | Citations Cited
Guvacine ethyl ester
PT00442-2
TJS012318513-76-3
Guvacine ethyl ester (Arecoline) is an alkaloid found in betel nut that is used in the synthesis of GABA uptake inhibitors.
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Voacamine
Voacanginine
T2S02713371-85-5
Voacamine (Voacanginine) is an indole alkaloid. Voacamine exhibits potent cannabinoid CB1 receptor antagonistic activity. Voacamine also inhibits P-glycoprotein (P-gp) action in multidrug-resistant tumor cells.Voacanginine may have rhythmic effects.
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Thermopsine
Thermospine
T3S0970486-90-8
1. Thermopsine (Thermospine) exhibits antibacterial activity.
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Anisodamine Hydrobromide
6-Hydroxyhyoscyamine
T830455449-49-5
Anisodamine Hydrobromide (6-Hydroxyhyoscyamine) is an anticholinergic and α1-adrenergic receptor antagonist used in the treatment of acute circulatory shock.
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Laurolitsine
(+)-Norboldine
TN18555890-18-6
Laurolitsine ((+)-Norboldine), an alkaloid, is extracted from the leaves of Peumus boldus Molina.
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(+)-Magnoflorine
Thalictrin, Magnoflorine, Escholine, Escholin
T3S13192141-09-5
(+)-Magnoflorine (Thalictrin) has sedative and anxiolytic effects, probably mediated by Magnoflorine through a GABAergic mechanism of action. Magnoflorine and Sinomenine have protective effects, are mediated by some mechanism other than prevention of micelle formation or protection of the erythrocyte membrane against osmotic imbalance.
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TargetMol | Citations Cited
Cephaeline hydrochloride
T3S18523738-70-3
Cephaeline hydrochloride, a phenolic alkaloid found in Indian Ipecac, effectively inhibits the infection of viruses ZIKV and EBOV.
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Alkaloid SN-f
T128485
Alkaloid SN-f is a useful organic compound for research related to life sciences and the catalog number is T128485.
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Palmatine chloride
T271810605-02-4
Palmatine chloride an isoquinoline alkaloid, is an important medicinal herbal extract with diverse pharmacological and biological properties.
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TargetMol | Inhibitor Hot
Amakusamine
T730612923661-84-9In house
Amakusamine is an indole alkaloid from the sponge of Psammocinia sp. It inhibits RANKL-induced isolation of multinucleated osteoclasts and inhibits RANKL-induced multinucleated osteoclasts.
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6-8 weeks
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L-Clausenamide
(-)-Clausenamide
T32614201529-58-0In house
L-Clausenamide is an alkaloid extracted from the leaves of the yellow bark (Clausena lansium (Lour) skeels) and can be used to improve cognitive function. L-Clausenamide inhibits beta-amyloid (Aβ) toxicity and prevents the formation of neurofibrillary tangles by inhibiting tau phosphorylation. L-Clausenamide has neuroprotective activity and can be used to modulate stimuli triggered by Aβ25-35. L-Clausenamide can be used to study neurological disorders like Alzheimer's disease.
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6-8 weeks
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Bocconoline
T1250361322007-90-8In house
Bocconoline is an alkaloid found in Bocconia cordata WILLD with potential anticancer activity for the study of Parkinson's disease (PD).
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7-10 days
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Lamellarin D
Lamellarine D
T3254597614-65-8In house
Lamellarin D (Lamellarine D), a hexacyclic pyrrolizidine alkaloid isolated from marine invertebrates, is a mitochondria-targeted topoisomerase I inhibitor and a pro-apoptotic agent.
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6-8 weeks
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Girinimbine
Girinimbin
TN609723095-44-5In house
Girinimbine (Girinimbin) is a carbazole alkaloid isolated from the plants M. koenigii, M. koenigii, and Murraya koenigii. Girinimbine exhibits a wide range of biological effects, including apoptosis, antitrypanosomal, antiplatelet, antimicrobial, anti-inflammatory, antioxidant, and antitumor activities.
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Hymenidin
T27564107019-95-4In house
Hymenidin, an alkaloid isolated from the Okinawan sponge Hymeniacidon sp. is a 5-hydroxytryptaminergic receptor antagonist and voltage-gated potassium channel inhibitor with potential antiprotozoal effects.It selectively binds to FOXO1 DNA and reduces depolarization-induced elevation of cellular calcium.
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10-14 weeks
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1-Methoxycarbonyl-β-carboline
1-Methoxycarbonyl-beta-carboline
TN25493464-66-2In house
1-Methoxycarbonyl-β-carboline (1-Methoxycarbonyl-beta-carboline) is an alkaloid from Ailanthus altissima.
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Kukoamine B mesylate
T7026L1375179-86-4In house
Kukoamine B mesylate is a novel cationic alkaloid derived from dermatophytes with antioxidant activity, inhibits LPS internalization in Kupffer and RAW 264.7 cells, and can be used to study acute inflammation and diabetes.
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Evodiamine
Isoevodiamine, d-Evodiamine, (+)-Evodiamine
T2868518-17-2
Evodiamine (d-Evodiamine) is an alkaloid isolated from the fruit of daylily and has a variety of biological activities including anti-inflammatory, anti-obesity and anti-tumor.
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Vincamine
Angiopac, Oxybral, Devincan, Novicet, Equipur, Perval
T12861617-90-9
Vincamine (Perval) is a major alkaloid of Vinca minor L., Apocynaceae. It has been used therapeutically as a vasodilator and antihypertensive agent, particularly in cerebrovascular disorders.
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Arecoline hydrobromide
Arecoline HBr, Arecoline bromide
T2198300-08-3
Arecoline hydrobromide (Arecoline HBr) is a muscarinic acetylcholine receptor agonist.
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