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9
Cat. No. | Product Name | Target | Signaling Pathways |
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T13664 |
DSP-4 hydrochloride
Neurotoxin DSP 4 (hydrochloride) |
Others | Others |
DSP-4 hydrochloride (Neurotoxin DSP 4 (hydrochloride)) 是一种高选择性的神经毒素,主要是来自蓝斑 (LC) 的神经元,容易通过血脑屏障。它对成年和发育中大鼠去甲肾上腺素能神经元具有神经毒性作用,可用于中枢和外周去甲肾上腺素能神经元的暂时选择性降解。 | |||
T12214 | Neurotoxin Inhibitor | Others | Others |
Neurotoxin Inhibitor is an inhibitor of neurotoxin. | |||
T4081 |
MPTP hydrochloride
MPTP-hydrochloride |
Apoptosis; Dopamine Receptor | Apoptosis; GPCR/G Protein; Neuroscience |
MPTP hydrochloride 是 MPP+ 的前体,是一种多巴胺神经毒素,具有血脑屏障渗透性。MPTP hydrochloride 对多巴胺能神经元有毒,可以导致帕金森症,被广泛应用于帕金森动物模型的构建。 | |||
T27794 |
λ-Cyhalothrin
lambda-Cyhalothrin,Karate,λ-氯氟氰菊酯,Icon |
Sodium Channel; Parasite | Membrane transporter/Ion channel; Microbiology/Virology |
λ-Cyhalothrin (Icon) 是广谱的 II 型合成除虫菊酯杀虫剂,含有 α-氰基,用于防治多种害虫。它是一种钠通道神经毒素,靶向中枢神经系统中神经元膜。 | |||
T9354 |
2,4-Difluorobenzaldehyde
2,4-Difluoro-benzaldehyde,2,4-二氟苯甲醛 |
Others | Others |
2,4-Difluorobenzaldehyde 靶点-A 型肉毒杆菌神经毒素(肉毒杆菌)。 | |||
T28655 |
Sabeluzole
R 58735,R58735,R-58735 |
Microtubule Associated | Cytoskeletal Signaling |
Sabeluzole (R-58735) 具有抗癫痫和增强认知的作用,抑制神经毒素诱导的tau表达和细胞死亡。Sabeluzole 对氯氮卓诱导的习惯障碍有保护作用,可用于研究阿尔茨海默症。 | |||
TP1223L |
Apamin acetate
Apamine acetate,Apamin acetate(24345-16-2 Free base) |
Potassium Channel | Membrane transporter/Ion channel |
Apamin acetate (Apamine acetate) 是一种具有选择性的 Ca2+ 激活的 K+ (SK) 通道的阻断剂,是在蜂毒素中发现的一种 18 个氨基酸的肽类神经毒素。Apamin acetate 可增强皮质神经元撕裂损伤后的神经突生长和再生。Apamin acetate 具有抗炎和抗纤维化的作用。 | |||
T9169 |
MPP+ iodide
|
Mitochondrial Metabolism; Autophagy | Autophagy; Metabolism |
MPP+ iodide 是一种 5-羟色胺转运体的高亲和力底物,也是一种神经毒素 MPTP 的有毒代谢物,通过选择性破坏黑质多巴胺能神经元,在动物模型中引起帕金森病症状。它被多巴胺转运体吸收进入多巴胺能神经元,通过影响呼吸链复合体 I 对线粒体发挥神经毒性作用。 | |||
T26937 | C562-1101 | ||
C562-1101 is a novel potent botulinum neurotoxin serotype E (BoNT/E) inhibitor. | |||
T13819 |
Pi-Methylimidazoleacetic acid hydrochloride
|
Others | Others |
Pi-Methylimidazoleacetic acid hydrochloride is a potential neurotoxin. | |||
T14763 |
BoNT-IN-1
|
Others | Others |
BoNT-IN-1 is a potent Botulinum neurotoxin A light chain (BoNTA LC) inhibitor(IC50 : 0.9 uM). | |||
T33346 |
Methylaminoalanine-nickel(II)
L-Bmma-nickel(II),L-Medap-nickel(II) |
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Methylaminoalanine-nickel(II) can be regarded as a naturally occurring neurotoxin. | |||
T32850 |
Lolitrem A
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Lolitrem A is a neurotoxin from staggers-producing ryegrass pastures. | |||
T34794 |
Tecoram
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Tecoram is a dithiocarbamate and a possible neurotoxin. | |||
T25890 |
NSC-84096
CID 256758,CID-256758,CID256758 |
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NSC-84096 is an endopeptidase activity inhibitor of botulinum neurotoxin type A light chain (rBoNT/A-LC). | |||
T33644 |
Nephilatoxin 7
NPTX 7,NPTX7,NPTX-7 |
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Nephilatoxin 7 is a neurotoxin of the Joro spider (Nephila clavata). | |||
T69377 |
BoNT-IN-33
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BoNT-IN-33 is a potent inhibitor of Botulinum neurotoxin/A light chain (BoNT/A LC). | |||
T21464 |
Methiocarb
Mercaptodimethur,Mesurol |
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Methiocarb, a carbamate pesticide, is used as an insecticide, acaricide, bird repellent, and molluscicide. Methiocarb stimulates cholinergic by inhibiting reversibly acetylcholinesterase activity, making methiocarb a potent neurotoxin. | |||
TP2064 |
ω-Conotoxin MVIIC
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Peptide neurotoxin; wide spectrum blocker of N, P and Q type calcium channels. | |||
T26961 |
CBIP
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CBIP is a small-molecule inhibitors of botulinum neurotoxin serotype A light chain (BoNT/A LC). CBIP possesses low micromolar activity against BoNT/A. | |||
T31582 |
DSP 4
DSP4,UNII-PQ1P7JP5C1,DSP-4,az-Dsp 4 |
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DSP 4 is a selective neurotoxin selective for noradrenergic neurons in the locus coeruleus noradrenergic system and capable of crossing the blood–brain barrier and cyclizes to a reactive aziridinium derivative that is accumulated into the noradrenergic ne | |||
TP2062 |
ω-Conotoxin GVIA
|
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Peptide neurotoxin; selectively and reversibly blocks N-type calcium channels (IC50 = 0.15 nM). Reduces (RS)-3,5-DHPG -induced long term depression in vivo. | |||
TP1223 |
Apamin
Apamine |
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Apamin (Apamine) is an 18 amino acid peptide neurotoxin found in apitoxin (bee venom), is known as a specifically selective blocker of Ca2+-activated K+ (SK) channels and exhibits anti-inflammatory and anti-fibrotic activity. Apamin is a bee venom compone | |||
T80064 |
Dendrotoxin-I
DTX-I |
Potassium Channel | Membrane transporter/Ion channel |
Dendrotoxin-I是一种高效的K+通道阻滞剂,特异性针对KV1.1和KV1.2电压门控钾通道亚基。该化合物为从Dendroaspis蛇毒中提取的神经毒素。 | |||
T83223 |
AaHI
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AaHI,源自北非蝎子Androctonus australis hector的毒液,这种化合物是一种神经毒素,常用作开发能够中和毒素的活性物质的工具。 | |||
T80160 |
ω-Hexatoxin-Hv1a
ω-ACTX-Hv1,ω-Atracotoxin-HV1 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
ω-Hexatoxin-Hv1a,一种从毒液蜘蛛 (Hadronyche versuta) 分离得到的神经毒素,能够阻断电压门控钙通道 (calcium channels)。 | |||
TP2077 |
α-Bungarotoxin
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Neurotoxin that blocks neuromuscular transmission via irreversible inhibition of nicotinic ACh receptors (nAChRs). Prevents opening of nicotinic receptor-associated ion channels and is selective for α7 receptors over α3β4 receptors (IC50 values are 1.6 nM | |||
T80078 |
Calciseptin
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Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Calciseptine 是从黑曼巴Dendroaspis p. polylepis分离得到的天然神经毒素。含有60个氨基酸和四个二硫键,特异性阻断L型钙通道(calcium channel)[1]。 | |||
TP1576 |
SNAP-25 187-203
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This amino acids187 to 203 fragment is derived from the C-terminal helix of synaptosomal-associated protein of 25 kDa (SNAP-25). This peptide is able to rescue exocytosis from botulinum neurotoxin E (BoNT/E)-treated cells, albeit at higher concentrations | |||
T20396 |
Levadopa Related Compound A
6-Hydroxydopa, L-,L-Hydroxydopa |
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Levadopa Related Compound A is the 6-hydroxy derivative of the amino acid L-DOPA with neurotoxic properties. Exogenously administered 6-Hydroxy-L-DOPA is biotransformed by an amino acid decarboxylase to the highly potent and catecholamine-selective neurot | |||
T80454 |
BmK-M1
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Sodium Channel | Membrane transporter/Ion channel |
BmK-M1,一种含64个氨基酸通过四个二硫桥交联形成的蝎子毒素,作用于抑制Na+通道,属于心脏毒素和神经毒素类。 | |||
TP2016 |
Huwentoxin-IV
Huwentoxin IV |
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Selective NaV1.7 channel blocker. Preferentially inhibits neuronal NaV1.7, 1.2 and 1.3 (IC50 values are 26, 150 and 338 nM respectively), compared to muscle subtypes NaV1.4 and 1.5 (IC50 = >10 μM). Inhibits the channel by binding at the neurotoxin recepto | |||
T80704 |
α-Pompilidotoxin
α-PMTX |
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α-Pompilidotoxin (α-PMTX) 是从 Anoplius samariensis 的毒液中分离的一种神经毒素。它能剂量依赖性地增强兴奋性突触后电流(EPSCs),并且这种增强作用是可逆的。α-Pompilidotoxin 在神经科学研究中被作为实验工具广泛应用。 | |||
T75746 |
Apamin TFA
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Apamin TFA (Apamine TFA) 是在蜂毒素中发现的一种 18 个氨基酸的肽类神经毒素,是一种 Ca2+激活的 K+(SK) 通道的特异性和选择性的阻断剂,具有抗炎和抗纤维化的作用。 | |||
T80427 |
Jingzhaotoxin-II
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Sodium Channel | Membrane transporter/Ion channel |
Jingzhaotoxin-II是由32个氨基酸组成的神经毒素,包括两个酸性残基和两个碱性残基。该毒素能够抑制电压门控钠通道(VGSC),并在心肌细胞上明显减缓TTX抗性(TTX-R) VGSC的快速失活,其IC50值为0.26μM。 | |||
T80530 |
Spinoxin
SPX,α-KTx6.13,Potassium channel toxin alpha-KTx 6.13 |
Potassium Channel | Membrane transporter/Ion channel |
Spinoxin是一种从Heterometrus spinifer蝎子毒液中提取的神经毒素,由34个氨基酸残基组成,通过4个二硫桥交联。它能有效抑制Kv1.3钾通道(IC50= 63 nM),是研发诊断及治疗自身免疫性疾病和癌症策略时的潜在分子靶点。 | |||
T69578 | D-Ibotenic Acid | ||
D-Ibotenic Acid is a chemical compound and psychoactive drug which occurs naturally in Amanita muscaria and related species of mushrooms typically found in the temperate and boreal regions of the northern hemisphere. It is a conformationally-restricted analogue of the neurotransmitter glutamate, and due to its structural similarity to this neurotransmitter, acts as a non-selective glutamate receptor agonist. Because of this, ibotenic acid can be a powerful neurotoxin, and is employed as a brain-... | |||
T83136 |
alpha-Cobratoxin
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alpha-Cobratoxin 是从泰国眼镜蛇的毒液中提取的神经毒素,具有调节神经系统、抗病毒和镇痛的活性。此外,alpha-Cobratoxin 对急性及慢性多发性硬化症表现出免疫抑制作用,目前正在被进一步研究其在肾上腺脊髓神经病方面的潜在应用。 | |||
T80426 |
Jingzhaotoxin-IX
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Sodium Channel | Membrane transporter/Ion channel |
Jingzhaotoxin-IX是由35个氨基酸残基组成的C端酰胺化神经毒素。该化合物既抑制电压门控钠通道(包括河豚毒素抗性和河豚毒素敏感亚型)又抑制Kv2.1通道,但对延迟整流钾通道Kv1.1、1.2和1.3无效。 | |||
T81519 |
Pentapeptide-3
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Pentapeptide-3为源自韦氏腹蛇毒素waglerin-1的五肽神经毒素,作为尼古丁乙酰胆碱受体(nAChRs)的竞争性拮抗剂,能够在突触后膜发挥阻滞神经的效果。该化合物具有抗衰老功能,可与其他化妆品肽配合使用。 | |||
T75856 |
Huwentoxin-IV TFA
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Huwentoxin-IV TFA是一种具有高效性和选择性的钠通道阻滞剂,能够抑制Nav1.7、Nav1.2、Nav1.3和Nav1.4神经元,其IC50分别为26、150、338和400nM。通过优先结合于神经毒素受体位点4,Huwentoxin-IV TFA特异性地阻断周围神经的Nav1.7亚型。该化合物适用于炎症性及神经性疼痛动物模型的研究。 | |||
T80166 |
α-Conotoxin BuIA
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α-Conotoxin BuIA 是一种麻痹性肽类神经毒素,同时也是竞争性nAChR拮抗剂。它对nAChR亚型表现出不同的IC50值:0.258 nM(α6/α3β2)、1.54 nM(α6/α3β4)、5.72 nM(α3β2)。该化合物可用于鉴别包含β2与β4亚单位的nAChR亚型。此外,α-Conotoxin BuIA 对αxβ2nAChR的区分能力按照α6>α3>α2>α4的顺序减弱。 | |||
T80165 |
α-Conotoxin GID
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α-Conotoxin GID为一种麻痹性肽类神经毒素,能选择性地拮抗nAChR,具有不同亚型的IC50值:5 nM(α7)、3 nM(α3β2)和150 nM(α4β2)。该化合物是含有丰富二硫键的小分子肽,拥有缓解慢性疼痛的潜在效用。α-Conotoxin GID含C端羧酸酯结构,替换为羧酰胺会使其对α4β2nAChR的作用降低。该化合物可从锥螺科海洋生物中提取。 | |||
T83894 |
4A7C-301-Nurr1 Agonist
4A7C-301-Nuclear Receptor-Related 1 |
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4A7C-301-Nurr1激动剂是一种核受体相关1(Nurr1)的激动剂。它通过与Nurr1配体结合域(LBD;IC50 = 48.22 nM)结合,增加了在使用SK-N-BE(2)C人神经母细胞瘤细胞进行的报告基因测定中Nurr1-LBD和全长Nurr1的转录活性(EC50s = 6.53 和 50-70 µM,分别)。每天5 mg/kg的4A7C-301-Nurr1激动剂能减少在经MPTP神经毒素或α-突触核蛋白过表达诱导的帕金森病鼠模型中纹状体和黑质compacta部分多巴胺能细胞的死亡,并减少运动和嗅觉缺陷,而不诱发类似运动障碍的行为。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T22911 |
β-N-methylamino-L-alanine hydrochloride
L-BMAA hydrochloride |
Others | Others |
β-N-methylamino-L-alanine hydrochloride (L-BMAA hydrochloride) 是由蓝细菌产生的一种神经毒素,既有导致肌萎缩性侧索硬化症 (ALS) 以及其他可能的神经退行性疾病可能性。 | |||
T8264 |
3-Methyl-2-oxovaleric acid
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Endogenous Metabolite | Metabolism |
3-Methyl-2-oxovaleric acid 是神经毒素,代谢毒素和酸性原,它是支链氨基酸不完整分解产生的异常代谢物。 | |||
T5232 |
3-Methyl-2-oxobutanoic acid
3-甲基-2-氧丁酸,2-Oxoisovaleric acid,alpha-Ketoisovaleric acid |
Others; Endogenous Metabolite | Metabolism; Others |
3-Methyl-2-oxobutanoic acid (2-Oxoisovaleric acid) 是大肠杆菌中泛酸的前体。它是由支链氨基酸的不完全分解产生的一种异常代谢物。 | |||
T5071 |
4-Methyl-2-oxopentanoic acid
4-甲基-2-氧代戊酸,4-Methyl-2-oxovaleric acid |
Others; Endogenous Metabolite | Metabolism; Others |
4-Methyl-2-oxopentanoic acid (4-Methyl-2-oxovaleric acid) 是一种非正常代谢物,是一种神经毒素和代谢毒素。 | |||
T19130 |
Porphobilinogen
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Others | Others |
Porphobilinogen act as a phytotoxin, a metabotoxin, and a neurotoxin. | |||
T34885 |
Tinyatoxin
TNX,TTN,TTX |
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Tinyatoxin is a neurotoxin that works through vanillin receptors on sensory nerves. | |||
T13820 | Pi-Methylimidazoleacetic acid | Others | Others |
Pi-Methylimidazoleacetic acid is a potential neurotoxin. | |||
T75539 | Nereistoxin | ||
Nereistoxin (Nereistoxine) 是一种神经毒素,从海洋环节动物 Lumbriconereis heteropoda 中分离出来,可以通过阻断烟碱乙酰胆碱受体发挥作用。 | |||
T36068 |
Brevetoxin B
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Brevetoxin B is a polyketide neurotoxin produced by Karenia species and other dinoflagellates. It binds to site 5 on the alpha subunit of voltage-gated sodium channels (IC50 = 15 nM) on neurons at the neuromuscular junction, causing the channel to open irreversibly at potentials more negative than normal, discharging action potentials repetitively. Brevetoxin B is ichthyotoxic at nanomolar concentrations and is responsible for an illness described as neurotoxic shellfish poisoning. |