Details
Stereochemistry | ACHIRAL |
Molecular Formula | C20H19NO5 |
Molecular Weight | 353.3686 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1CCC2=C(C=C3OCOC3=C2)C(=O)CC4=C(C1)C5=C(OCO5)C=C4
InChI
InChIKey=GPTFURBXHJWNHR-UHFFFAOYSA-N
InChI=1S/C20H19NO5/c1-21-5-4-13-7-18-19(25-10-24-18)8-14(13)16(22)6-12-2-3-17-20(15(12)9-21)26-11-23-17/h2-3,7-8H,4-6,9-11H2,1H3
Protopine is the isoquinoline alkaloid found primarily in the plant families Berberidaceae, Ranunculaceae, Rutaceae, Fumariaceae. It has diverse biological activities, such as anti-thrombotic, anti-inflammatory, anti-parasitic activity, antimicrobial activity, as well as hepatoprotective effects in animal models. The biological activities of protopine are associated with its ability selectively inhibits K(ATP) channels by targeting on SUR1 subunit. In addition, was discovered that β2 -adrenoceptor (β2 -AR) is a target for antiasthma activities of protopine. On this target, binding of the drug occurs on the amino acid residual of Ser 169 through the formation of hydrogen bonds and receptor‐drug bumps.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23245239
Curator's Comment: Known to be CNS penetrant in rats. Human data not available.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL210 Sources: https://www.ncbi.nlm.nih.gov/pubmed/28124461 |
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Target ID: Q09428 Gene ID: 6833.0 Gene Symbol: ABCC8 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/15588728 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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PubMed
Title | Date | PubMed |
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Assay of nematocidal activity of isoquinoline alkaloids using third-stage larvae of Strongyloides ratti and S. venezuelensis. | 2002 Mar 1 |
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Direct determination of alkaloid contents in Fumaria species by GC-MS. | 2002 Nov-Dec |
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Inhibition of mouse liver respiration by Chelidonium majus isoquinoline alkaloids. | 2003 Dec 15 |
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Cytotoxic activity and quality control determinations on Chelidonium majus. | 2003 Feb |
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In vitro anti-influenza virus activity of isoquinoline alkaloids from thalictrum species. | 2003 Feb |
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Antifungal activity of the methanolic extract and alkaloids of Glaucium oxylobum. | 2003 Jul |
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Cytochrome P450 isoenzymes involved in rat liver microsomal metabolism of californine and protopine. | 2004 Feb 6 |
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How to treat tremor. | 2004 May |
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1H and 13C NMR signal assignment of benzylisoquinoline alkaloids from Fumaria officinalis L. (Papaveraceae). | 2004 Oct |
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Regulation of glutamate level in rat brain through activation of glutamate dehydrogenase by Corydalis ternata. | 2005 Aug 31 |
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[Studies on the alkaloids from the herb of Corydalis adunca]. | 2005 Feb |
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Effect of binary combination of some plant-derived molluscicides with MGK-264 or piperonyl butoxide on the reproduction of the snail Lymnaea acuminata. | 2005 Feb |
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Identification and quantification of isoquinoline alkaloids in the genus Sarcocapnos by GC-MS. | 2005 Sep-Oct |
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Intestinal spasmolytic effects of STW 5 (Iberogast) and its components. | 2006 |
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Proapoptotic activity of Ukrain is based on Chelidonium majus L. alkaloids and mediated via a mitochondrial death pathway. | 2006 Jan 17 |
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Effect of isoquinoline alkaloids of different structural types on antiplatelet aggregation in vitro. | 2006 Oct |
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Gene transcript and metabolite profiling of elicitor-induced opium poppy cell cultures reveals the coordinate regulation of primary and secondary metabolism. | 2007 Apr |
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Hepatoprotective potential of Fumaria indica Pugsley whole plant extracts, fractions and an isolated alkaloid protopine. | 2008 Jun |
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Protective effects of protopine on hydrogen peroxide-induced oxidative injury of PC12 cells via Ca(2+) antagonism and antioxidant mechanisms. | 2008 Sep 4 |
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Simultaneous determination of tetrahydropalmatine, protopine, and palmatine in rat plasma by LC-ESI-MS and its application to a pharmacokinetic study. | 2009 Feb 20 |
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[Alkaloids from Macleaya cordata]. | 2009 Jul |
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Analysis of alkaloids in Macleaya cordata (Willd.) R. Br. using high-performance liquid chromatography with diode array detection and electrospray ionization mass spectrometry. | 2009 Mar 13 |
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Simultaneous determination of seven main alkaloids of Chelidonium majus L. by ultra-performance LC with photodiode-array detection. | 2010 Apr |
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Antiplasmodial agents from the Bhutanese medicinal plant Corydalis calliantha. | 2010 Apr |
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Phytochemical and antimicrobial characterization of Macleaya cordata herb. | 2010 Dec |
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Optimization of microwave-assisted extraction of protopine and allocryptopine from stems of Macleaya cordata (Willd) R. Br. using response surface methodology. | 2010 Jul |
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A study on separation and extraction of four main alkaloids in Macleaya cordata (Willd) R. Br. with strip dispersion hybrid liquid membrane. | 2010 Jul |
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Screening of antinociceptive components in Corydalis yanhusuo W.T. Wang by comprehensive two-dimensional liquid chromatography/tandem mass spectrometry. | 2010 Mar |
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Validated liquid chromatography-tandem mass spectrometry method for quantitative determination of dauricine in human plasma and its application to pharmacokinetic study. | 2010 May 1 |
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Acetylcholinesterase and butyrylcholinesterase inhibitory compounds from Chelidonium majus (Papaveraceae). | 2010 Nov |
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Integration of deep transcriptome and proteome analyses reveals the components of alkaloid metabolism in opium poppy cell cultures. | 2010 Nov 18 |
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[Determination of protopine in Corydalis racemose by HPLC]. | 2010 Sep |
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Protopine and allocryptopine increase mRNA levels of cytochromes P450 1A in human hepatocytes and HepG2 cells independently of AhR. | 2011 Jun 10 |
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Antimalarial alkaloids from a Bhutanese traditional medicinal plant Corydalis dubia. | 2012 Aug 30 |
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A new protoberberine alkaloid from Meconopsis simplicifolia (D. Don) Walpers with potent antimalarial activity against a multidrug resistant Plasmodium falciparum strain. | 2013 Dec 12 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11498866
Protective action of protopine against experimental liver injury in mice: administration of two doses of protopine at 50 and 100 mg.kg-1 in an interval of 8 to 24 h before i.p. injection of CCl4, acetaminophen or thioacetamide.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9368908
The effects of protopine on human platelet aggregation and arachidonic acid (AA) metabolism via cyclooxygenase (COX) and lipoxygenase (LOP) enzymes were examined. Platelet aggregation induced by various platelet agonists (AA, ADP, collagen and PAF) was strongly inhibited by protopine in a concentration-related manner. The IC50 values (microM) of protopine (mean +/- SEM) against: AA; 12 +/- 2: ADP; 9 +/- 2: collagen; 16 +/- 2 and PAF; 11 +/- 1, were much less than those observed for aspirin.
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PROTOPINE
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SUBSTANCE RECORD