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Spermine

Spermine is a naturally occurring polyamine, classified as an organic polycationic alkylamine with a linear tetramine structure consisting of four amino groups and the chemical formula C₁₀H₂₆N₄ (molecular weight 202.34 g/mol). It was named for its initial discovery in human semen.^[1] It is ubiquitous in all living organisms, where it plays essential roles in cellular processes, including the stabilization of nucleic acids and proteins through electrostatic interactions that help maintain helical structures, particularly in viruses and chromatin.^[1] Present at millimolar concentrations (1–2 mM) in the cell nucleus, spermine functions directly as an intracellular free radical scavenger, protecting DNA from oxidative damage by reactive oxygen species such as hydroxyl radicals, which it neutralizes by forming stable adducts like bis-oximes and dialdehydes.^[2] Biosynthetically, spermine is derived from the polyamine precursor spermidine through the action of the enzyme spermine synthase, which transfers an aminopropyl group from decarboxylated S-adenosyl-L-methionine (dcAdoMet).^[1] Its metabolism is regulated by enzymes such as spermine oxidase (SMOX), which oxidizes it to produce spermidine along with cytotoxic byproducts like hydrogen peroxide and reactive aldehydes, thereby influencing cellular redox balance and signaling.^[1] In the brain, spermine is actively transported into secretory vesicles of astrocytes by the vesicular polyamine transporter (VPAT, encoded by SLC18B1), operating via an electroneutral proton/spermine exchange mechanism (4:1 stoichiometry) that modulates its release during exocytosis to fine-tune neuronal activity.^[3] Spermine exerts diverse physiological effects by modulating ion channels (e.g., inwardly rectifying potassium channels like Kir, transient receptor potential channels like TRPC4, and NMDA receptors), enhancing gap junction communication, and regulating key cellular events such as proliferation, differentiation, autophagy, and apoptosis.^[1] It facilitates transcription, translation, and post-translational modifications, including the spermidine-mediated hypusination of eukaryotic initiation factor 5A (eIF5A), which is critical for protein synthesis and cell cycle progression.^[1] In both plant and human systems, spermine contributes to stress tolerance, developmental processes, and memory formation, with dietary sources like meat influencing its levels to support longevity and cognitive function.^[4] In human health, spermine levels are implicated in aging, where declining concentrations are associated with cognitive impairment, while supplementation can extend longevity by 15–40% in model organisms and mitigate age-related memory deficits through autophagy induction.^[4] Dysregulation is associated with diseases including cancer (e.g., promoting tumor growth in colorectal and neuroblastoma models), neurodegenerative disorders (e.g., Alzheimer's and Parkinson's via altered NMDA receptor function), and cardiovascular conditions, highlighting its dual role as both protective and pathological depending on context.^[1]^[3]

Chemical Properties

Molecular Structure and Nomenclature

Spermine is an organic polyamine compound with the molecular formula \ce{C10H26N4} and a molecular weight of 202.34 g/mol.^[5]^[6] Its systematic IUPAC name is N,N-bis(3-aminopropyl)butane-1,4-diamine, reflecting its structure as a butane-1,4-diamine core with two 3-aminopropyl substituents attached to the terminal nitrogen atoms.^[7]^[5] Structurally, spermine is a linear aliphatic tetraamine, characterized by four primary and secondary amine groups arranged along a flexible hydrocarbon chain. It can be represented as \ce{H2N-(CH2)3-NH-(CH2)4-NH-(CH2)3-NH2}, where the central butane segment connects two propylamine arms.^[5] This configuration positions the nitrogen atoms equivalently to those in a polyazaalkane derived from tetradecane, with nitrogens replacing carbons at positions 1, 5, 10, and 14, resulting in a total of 10 carbon atoms and a protonated polycationic form under physiological conditions.^[5] The symmetric placement of the aminopropyl groups imparts spermine with a high degree of flexibility and multiple protonation sites, contributing to its role as a polycation.^[5] Spermine belongs to the family of biogenic polyamines and shares structural similarities with shorter homologs. Putrescine, the simplest diamine precursor with the formula \ce{H2N-(CH2)4-NH2}, serves as the base for polyamine elongation.^[1] Spermidine, a triamine, is formed by attaching one aminopropyl group (\ce{-CH2-CH2-CH2-NH2}) to putrescine, yielding \ce{H2N-(CH2)3-NH-(CH2)4-NH2}.^[1] Spermine extends this motif by incorporating a second aminopropyl group onto spermidine, creating the tetraamine architecture that distinguishes it as the longest common endogenous polyamine in eukaryotic cells.^[1]^[8]

Physical and Chemical Characteristics

Spermine is a colorless to white, low-melting crystalline solid with a melting point of 28–30 °C and a boiling point of approximately 150 °C at reduced pressure (5 mmHg). Its density is 0.937 g/cm³, and it is highly soluble in water (>50 mg/mL at 20 °C) and other polar solvents, but insoluble in non-polar solvents such as diethyl ether. The compound is hygroscopic and absorbs carbon dioxide from the air, forming the corresponding carbonate. Due to its four primary and secondary amine groups, spermine exhibits strong basicity, with pKa values of 10.97, 10.27, 9.04, and 8.03 for successive protonations. This basic nature allows it to readily form salts with acids, such as the tetrahydrochloride salt commonly used in laboratory settings. Spermine also serves as a multidentate ligand in coordination chemistry, forming stable complexes with transition metals like copper(II) through its nitrogen donors. Additionally, it demonstrates free radical scavenging activity via oxidation of its amine groups, which helps mitigate oxidative stress in chemical systems. Spermine poses significant handling hazards, as it is corrosive to skin and eyes, potentially causing severe burns upon contact. It is classified as an irritant and requires protective equipment during use; inhalation or ingestion can lead to respiratory and gastrointestinal irritation. Safety data sheets recommend storage in a cool, dry place to prevent degradation or reaction with atmospheric CO₂.

Biosynthesis and Metabolism

Biosynthetic Pathways

In animals, spermine biosynthesis primarily follows a sequential pathway starting from the amino acid L-ornithine, which is decarboxylated to putrescine by the rate-limiting enzyme ornithine decarboxylase (ODC, encoded by the ODC1 gene in humans). Putrescine is then converted to spermidine by spermidine synthase (SRM), which transfers an aminopropyl group from decarboxylated S-adenosylmethionine (dcSAM), produced by S-adenosylmethionine decarboxylase (AdoMetDC). Finally, spermidine is transformed into spermine by spermine synthase (SMS), again utilizing dcSAM as the aminopropyl donor. This pathway is conserved across mammalian cells and is essential for maintaining intracellular polyamine homeostasis.^[1] Plants exhibit variations in the initial steps of polyamine biosynthesis, incorporating an additional route via arginine decarboxylase (ADC) alongside the ODC pathway. In the ADC route, predominant in many plant species such as Arabidopsis thaliana, arginine is decarboxylated to agmatine by ADC, followed by conversion to N-carbamoylputrescine and then putrescine via agmatinase (AGMAT) and N-carbamoylputrescine amidohydrolase. From putrescine, the pathway proceeds identically to the animal route through spermidine synthase and spermine synthase to yield spermine. The ODC pathway, while present in some plants like tomato, is absent in others such as Arabidopsis, making the ADC route critical for stress responses and development. In bacteria, the core pathway mirrors the eukaryotic aminopropyl transfer steps from putrescine to spermidine and spermine, often relying on ADC for putrescine production from arginine, though some species like Escherichia coli utilize ODC; hybrid variations exist, combining elements of both. Biosynthesis is tightly regulated, primarily through feedback inhibition of ODC by spermine and spermidine, which induce the expression of ornithine decarboxylase antizyme (OAZ1) via ribosomal frameshifting, leading to ODC degradation and reduced enzyme activity. This mechanism prevents polyamine overaccumulation, with spermine being particularly potent in stabilizing OAZ1 and enhancing its inhibitory effects. Gene expression of ODC1 and related enzymes is also modulated by cellular polyamine levels, ensuring balanced production. Recent findings have uncovered novel biosynthetic routes in certain organisms, including alternative decarboxylases in eukaryotes. In mammalian reproductive tissues, such as ovine conceptuses, an ADC/AGMAT pathway serves as a backup to the primary ODC route, converting arginine to agmatine and then putrescine to support embryonic development when ODC1 is deficient. In bacteria, a 2025 study identified an aspartate β-semialdehyde (ASA)-dependent pathway for spermine synthesis from spermidine via carboxyspermine intermediates, catalyzed by carboxyspermidine dehydrogenase (CASDH) and carboxyspermidine decarboxylase (CASDC), distinct from the classical dcSAM route; hybrid pathways blending ASA and dcSAM dependencies have also been observed in species like Clostridium leptum.^[9] These discoveries highlight evolutionary diversification in polyamine production across eukaryotes and prokaryotes.

Catabolic Processes

Spermine catabolism in biological systems is primarily mediated by spermine oxidase (SMOX), a flavin-dependent enzyme that catalyzes the oxidation of spermine to spermidine, 3-aminopropanal, and hydrogen peroxide (H₂O₂).^[10] This reaction generates reactive oxygen species (ROS), notably H₂O₂, which can induce cellular oxidative stress. SMOX preferentially acts on spermine and, to a lesser extent, N¹-acetylspermine, but shows minimal activity toward spermidine.^[11] The spermidine produced by SMOX undergoes further degradation via polyamine oxidase (PAO), an FAD-dependent enzyme that oxidizes N¹-acetylspermidine to putrescine, 3-acetamidopropanal, and H₂O₂, thereby completing the back-conversion pathway in polyamine homeostasis.^[12] PAO thus plays a crucial role in terminal catabolism by processing acetylated intermediates derived from spermidine.^[13] A key regulatory step in this catabolic process involves acetylation of spermine by spermidine/spermine N¹-acetyltransferase (SSAT), which forms N¹-acetylspermine that is oxidized by SMOX to N¹-acetylspermidine (and then by PAO to putrescine), helping to maintain intracellular polyamine levels.^[14]^[15] This acetylation facilitates polyamine export or degradation. SMOX expression and activity are tightly regulated, with significant upregulation occurring during inflammatory conditions in response to stimuli such as cytokines, leading to enhanced spermine breakdown and elevated ROS production that amplifies oxidative stress. In the gastrointestinal tract, SMOX activity is notably higher, particularly in gastric tissues, where it contributes to inflammation and cytotoxicity during infections like those caused by Helicobacter pylori.

Biological Functions

Roles in Cellular Processes

Spermine, a naturally occurring polyamine, is present at high concentrations in semen, where it reaches levels of 50–350 mg/dL, contributing to its name derivation from seminal fluid.^[16] It is also abundant in the brain, with intracellular concentrations in cortical neurons ranging from 0.5 to 1.5 mM, and in rapidly dividing cells, where polyamine levels, including spermine, increase to support growth and proliferation.^[17]^[18] Spermine plays a critical role in nucleic acid stabilization by binding electrostatically to the negatively charged phosphate backbone of DNA and RNA, thereby condensing chromatin structure and facilitating compact packaging.^[19] This interaction enhances the structural integrity of nucleic acids and protects DNA from degradation by nucleases, such as endonucleases, through strong binding that shields the polymer from enzymatic attack.^[20] In addition, spermine supports RNA-DNA hybrid stability, which is essential for processes like transcription.^[21] In ion channel modulation, spermine exerts inhibitory effects on NMDA receptors and inward rectifier potassium channels at physiological concentrations, reducing channel open probability through voltage-dependent block and charge screening mechanisms.^[22]^[23] Conversely, it potentiates the mitochondrial calcium uniporter by disrupting inhibitory interactions between MCU and MICU1-MICU2, thereby enhancing calcium uptake into mitochondria under normal intracellular levels.^[24] Spermine exhibits antioxidant activity by scavenging free radicals, such as superoxide, and inhibiting their generation, which reduces oxidative damage to lipids and proteins.^[25] This protective effect correlates with the number of amino groups in the polyamine structure, with spermine showing the strongest activity among common polyamines.^[26] Spermine is essential for cell proliferation, promoting DNA replication and RNA transcription by stabilizing nucleic acids and facilitating gene expression.^[27] Depletion of spermine arrests the cell cycle at the G1/S phase transition, inhibiting DNA synthesis and proliferation in epithelial cells.^[28] Spermine levels, derived from spermidine via enzymatic conversion, peak during the G1 to S phase to support these processes.^[29]

Physiological and Pathophysiological Significance

Spermine plays a crucial role in maintaining cellular homeostasis by stabilizing nucleic acids and facilitating protein synthesis, thereby supporting fundamental cellular functions essential for organismal health.^[1] In normal physiology, it contributes to growth processes in embryos and developing tissues, where elevated levels promote cell proliferation and differentiation during critical developmental stages. Spermine concentrations fluctuate dynamically with the cell cycle, increasing during the S phase to aid DNA replication and chromosome condensation, which underscores its importance in regulated tissue expansion and repair. Additionally, spermine briefly interacts with DNA through electrostatic binding, enhancing structural integrity during replication without dominating its broader physiological roles. In the context of aging and longevity, spermine supplementation has demonstrated potential to mimic caloric restriction effects by enhancing mitochondrial function and reducing oxidative damage in aged models, thereby extending lifespan in certain experimental organisms such as mice.^[30] This is linked to autophagy induction, a process shared with related polyamines like spermidine, where spermine helps clear damaged cellular components to promote metabolic resilience. Investigations, including a 2022 study, have shown that spermine administration in mouse models reduces body weight and adiposity by suppressing adipocyte differentiation.^[31] Moreover, polyamines including spermine contribute to gut microbiota regulation, influencing epithelial barrier integrity and microbial community balance, potentially mitigating age-related dysbiosis.^[32] Pathophysiological dysregulation of spermine is implicated in several diseases. In cancer, overproduction and accumulation of spermine drive tumor cell proliferation and migration by activating signaling pathways that support uncontrolled growth, as observed in colorectal and other malignancies.^[1] In neurodegeneration, such as Alzheimer's disease, altered spermine levels modulate NMDA receptor activity, contributing to excitotoxicity and synaptic dysfunction through excessive calcium influx and neuronal damage.^[3] During inflammation, upregulation of spermine oxidase (SMOX) leads to spermine oxidation, generating reactive oxygen species (ROS) that exacerbate tissue damage and chronic inflammatory states.^[1] Spermine deficiency, often modeled by spermine synthase disruptions, results in impaired growth, lysosomal dysfunction, and heightened oxidative stress, manifesting as developmental delays and increased vulnerability to cellular damage.^[1]

Derivatives and Applications

Synthetic Derivatives

Synthetic derivatives of spermine are engineered to alter its natural properties, such as improving cellular uptake or conferring resistance to enzymatic degradation, often serving as templates for therapeutic or diagnostic agents. These modifications typically involve alkylation or conjugation to enhance specificity and functionality while mimicking the polyamine transport systems in cells.^[33] A prominent example is N¹,N¹²-bis(ethyl)spermine (BESpm), developed in the 1980s as part of efforts to create antiproliferative agents that interfere with polyamine homeostasis. BESpm inhibits polyamine synthesis primarily by downregulating ornithine decarboxylase (ODC), the rate-limiting enzyme in the pathway, leading to depletion of natural polyamines like spermidine and spermine. This analog was synthesized through bis-ethylation of spermine, resulting in a structural mimic that is actively transported into cells but poorly metabolized.^[34]^[35]^[36] Other notable analogs include unsymmetrical polyamines, such as those conjugated to cytotoxic agents for targeted delivery to tumor cells exploiting polyamine uptake mechanisms. For instance, the epipodophyllotoxin-spermine conjugate F14512 targets topoisomerase II in cancer cells via polyamine transporters, enabling selective cytotoxicity.^[37] Additionally, macrocyclic polyamines derived from spermine scaffolds are utilized for metal chelation, forming stable complexes with transition metals or radiometals to support applications in diagnostics and radiotherapy. These cyclic structures provide a rigid cavity that enhances binding affinity and selectivity compared to linear polyamines.^[38]^[39]^[40] Design principles for these derivatives emphasize increasing lipophilicity to promote membrane penetration, often through alkyl substitutions like ethyl groups in BESpm, which improve partitioning into lipid bilayers without compromising uptake. Resistance to catabolism is another key focus, achieved by modifying amine groups to evade polyamine oxidases, thereby prolonging intracellular retention and activity. These strategies draw from natural polyamine biosynthesis as a scaffold but introduce non-natural elements to optimize pharmacological profiles.^[35]^[33] Common synthesis methods include alkylation of spermidine as a precursor to spermine analogs, where selective protection of amine groups allows stepwise introduction of substituents. Reductive amination is also widely employed, involving the reaction of polyamine precursors with aldehydes or ketones in the presence of reducing agents like sodium cyanoborohydride to form N-alkylated derivatives efficiently and with high regioselectivity. These approaches enable scalable production while minimizing side products from over-alkylation.^[41]^[33]^[42] In recent developments from 2024, functionalized macrocyclic polyamines have advanced for imaging and therapy, incorporating pendant groups for conjugation to fluorophores or radionuclides to enable targeted molecular imaging via MRI or PET. These derivatives also support therapeutic chelation in cancer treatment, where metal complexes deliver radiotherapy agents with reduced off-target effects, highlighting their potential in precision medicine.^[39]^[40]

Biomedical and Research Applications

Spermine and its analogs have been investigated for their potential in cancer therapy, primarily due to their ability to disrupt polyamine metabolism essential for tumor cell proliferation. The polyamine analog N¹,N¹¹-diethylnorspermine (DENSpm), a related compound, underwent Phase II clinical trials in the 1990s and 2000s, but showed limited activity in metastatic breast cancer patients despite depleting intracellular polyamine levels.^[43] More recent studies from 2023 have explored polyamine analogs such as DENSpm that suppress cancer cell proliferation by targeting polyamine transport and catabolism, showing promise in preclinical models of lung cancer.^[44] These analogs mimic natural polyamines to enter cells and interfere with biosynthetic pathways, reducing tumor burden without broadly affecting normal cells.^[45] In neurological applications, spermine exhibits potential neuroprotective effects through its modulation of N-methyl-D-aspartate (NMDA) receptors, which are implicated in excitotoxicity and neurodegeneration. Research indicates that low micromolar concentrations of spermine enhance NMDA receptor function under normal conditions but provide protection against anoxia and excessive NMDA activation in hippocampal models, preventing calcium overload and cell death.^[46] In Alzheimer's disease models, spermine's interaction with polyamine regulatory sites on NMDA receptors has been studied for its role in mitigating amyloid-beta-induced synaptic dysfunction, suggesting therapeutic potential in restoring cognitive processes.^[47] These effects highlight spermine's biphasic action, where context-dependent modulation could aid in managing neurodegenerative disorders. Diagnostic tools leveraging spermine have advanced with fluorescence-based detection methods using polyamine sensors, enabling sensitive quantification as clinical markers for diseases like cancer and neurodegeneration. In 2025, a poly-carboxylate receptor system was developed for fluorescence detection of spermine in real samples, offering high selectivity and low detection limits suitable for biofluid analysis.^[48] Smartphone-based sensor arrays incorporating fluorescent probes have also emerged, distinguishing spermine from other polyamines with clinical relevance for rapid point-of-care testing in tumor monitoring.^[49] These innovations improve upon traditional methods by providing non-invasive, real-time insights into polyamine dysregulation. Beyond oncology and neurology, spermine serves in gene delivery as complexes with DNA, facilitating transfection in therapeutic applications. Spermine condenses plasmid DNA into nanoparticles, enhancing cellular uptake and expression efficiency in non-viral vectors, as demonstrated in lung and cell culture models where it outperforms unmodified carriers.^[50] Additionally, spermine's antimicrobial properties support wound healing by potentiating antibiotic efficacy; it reduces minimum inhibitory concentrations of β-lactam antibiotics against bacterial strains, aiding infection control in cutaneous repair processes.^[51] Despite these applications, challenges persist, including toxicity from hydrogen peroxide (H₂O₂) production during spermine catabolism by oxidases, which generates reactive oxygen species leading to cellular damage and limits dosing in therapies.^[52] Ongoing clinical trials explore polyamine interventions, such as spermidine supplementation, for aging-related conditions like cardiovascular disease in the elderly, aiming to balance benefits against oxidative risks in age-associated decline.^[53]

History and Discovery

Initial Observations

In 1678, the Dutch microscopist Antonie van Leeuwenhoek first observed crystalline structures in human semen while examining samples under one of his early microscopes, describing them as small, elongated particles that appeared upon drying. These crystals, later identified as spermine phosphate, represented the initial empirical detection of spermine in a natural biological source, though van Leeuwenhoek did not characterize their chemical nature.^[54] During the 1870s, German chemist Philipp Schreiner successfully isolated spermine as a novel organic base from human seminal fluid in 1878, marking the first chemical extraction of the compound from its primary natural reservoir. Schreiner's work involved precipitating the base as a phosphate salt and noting its alkaline properties, which distinguished it from other nitrogenous substances in animal tissues. This isolation was part of emerging investigations into the composition of reproductive fluids, where spermine was recognized for its role in forming characteristic crystals observable in semen.^[55] Early characterizations of spermine highlighted its basic nature and a distinctive fishy odor, attributes typical of polyamines that contributed to the pungent smell of semen. In the late 19th century, researchers linked these properties to studies on fertility and semen quality, as the presence of spermine crystals was examined in relation to reproductive health in animal and human samples. This work positioned spermine within the broader context of polyamine research, which explored similar basic compounds in various animal fluids and tissues, laying groundwork for understanding their physiological distribution.^[56]

Structural Determination and Naming

The term "spermine" was coined in 1888 by German chemists Albert Ladenburg and John Jacob Abel, reflecting its initial isolation from human semen as a crystalline base.^[57] This naming followed earlier observations of the substance's basic properties, but its precise chemical identity remained elusive for decades.^[1] Efforts to determine spermine's structure began in earnest in the early 20th century through analytical techniques. In 1924, Otto Rosenheim and colleagues isolated spermine as its phosphate salt from semen and conducted elemental analysis, yielding a molecular formula of C₁₀H₂₆N₄ and confirming it as a tetraamine compound. Building on this, partial degradation studies in the 1910s and 1920s, including hydrolysis and oxidation, provided fragments consistent with a polyamine backbone, though ambiguities persisted regarding the exact carbon-nitrogen arrangement.^[57] The full structure was definitively elucidated in 1926 by Harold W. Dudley, Otto Rosenheim, and Walter W. Starling, who employed degradative methods alongside total synthesis to establish spermine as N¹-(3-aminopropyl)-N⁴-(3-aminobutyl)butane-1,4-diamine.^[58]^[59] Their synthetic route involved coupling appropriate amine precursors, yielding a product identical in properties to the natural isolate, thus resolving prior uncertainties without reliance on advanced spectroscopy at the time. Following this confirmation, post-1926 investigations further validated the structure indirectly. In 1958, isotopic labeling experiments using ¹⁴C-putrescine demonstrated its incorporation into spermine, aligning with the established carbon skeleton and supporting the structural framework in biosynthetic contexts.^[60]

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Spermine Significantly Increases the Transfection Efficiency of ... - NIH
Excessively high concentrations of spermine (above 120 μg/mL) can reduce transfection efficiency, possibly due to the over-condensation of nucleic acids into ...
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Polyamine Effects on Antibiotic Susceptibility in Bacteria - PMC - NIH
It was found that spermine and spermidine can decrease the MICs of β-lactam antibiotics in all strains as well as other types of antibiotics in a strain- ...
[48]
Toxicity of enzymatic oxidation products of spermine to human ...
Hydrogen peroxide was mainly responsible for the loss of cell viability. With about 20%, the aldehydes formed from spermine contribute also to cytotoxicity.Missing: H2O2 | Show results with:H2O2
[49]
POLYamine treatment in elderly patients with Coronary Artery ...
Oct 30, 2025 · This trial will investigate whether high-dose spermidine improves cardiac remodelling, exercise capacity, muscle mass, and systemic inflammation ...
[50]
The early history of polyamine research - PubMed
In 1678 Antonie van Leeuwenhoek identified crystalline substances in human semen. The structure of these crystals, named "spermine", was not elucidated by ...
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Ueber eine neue organische Basis in thierischen Organismen
Schreiner (1878) identified this new compound as an organic base, while Ladenburg and Abel (1888) named it as ''spermine''. Rosenheim (1924) synthesized the ...
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The polyamines: past, present and future | Essays in Biochemistry
Nov 4, 2009 · The polyamines, spermidine and spermine, were first discovered in 1678 by Antonie van Leeuwenhoek. In the early part of the 20th century ...
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The early history of polyamine research - ScienceDirect.com
In 1678 Antonie van Leeuwenhoek identified crystalline substances in human semen. The structure of these crystals, named “spermine”, was not elucidated by ...
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The Chemical Constitution of Spermine | Biochemical Journal
Get Permissions. Citation. Harold Ward Dudley, Otto Rosenheim, Walter William Starling; The Chemical Constitution of Spermine: Structure and Synthesis.
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The Chemical Constitution of Spermine: Structure and Synthesis
The Chemical Constitution of Spermine: Structure and Synthesis. Biochem J. 1926;20(5):1082-94. doi: 10.1042/bj0201082. Authors. H W Dudley , O Rosenheim, W W ...