63
10
Cat. No. | Product Name | Target | Signaling Pathways |
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T68260 | Calmidazolium (cation) | ||
Calmidazolium (cation) is a powerful inhibitor of or red blood cell Ca -ATPase & Ca transport into inside-out red blood cell vesicles; an antagonist of calmodulin. | |||
T32984 | LX-201 cation | ||
LX-201 cation is a bioactive chemical. | |||
T34817 |
Tetrabutylphosphonium cation
Tetra-n-butylphosphonium,J279H,Tetrabutylphosphonium ion,Tetrabutylphosphonium,Phosphonium, tetrabutyl- |
||
Tetrabutylphosphonium cation is a light orange solid and is the salt of the liphilic tetrabutylammonium cation and linear tribromide anion. | |||
T25628 |
Lapyrium
Lapyrium cation |
||
Lapyrium is a cationic surfactant that is used in personal care products as a biocide and antistatic. It is also used by the chloride salt, lapyrium chloride, in waste-water treatment and corrosion inhibition formulations. | |||
T25640 |
Laurolinium
Laurolinium ion,Laurolinium cation |
||
Laurolinium is an antimicrobial. | |||
T25636 |
Laudexium
Laudexium ion,Laudexium cation |
||
Laudexium is a neuromuscular blocking drug or skeletal muscle relaxant in the category of non-depolarizing neuromuscular-blocking drugs. It is used adjunctively in surgical anesthesia to facilitate endotracheal intubation and to provide skeletal muscle re | |||
T32592 |
Lauralkonium
Lauralkonium ion,Lauralkonium cation |
||
Lauralkonium is a bioactive chemical. | |||
T26666 |
ASM-024
|
AChR | Neuroscience |
ASM-024是一种有效的烟碱受体激动剂,是一种小分子合成哌嗪化合物,可促进β2-肾上腺素受体不同的靶点和信号通路介导平滑肌松弛,是治疗哮喘和慢性阻塞性支气管炎的潜在化合物,具有抗炎活性。 | |||
T21623 |
AS1269574
AS 1269574 |
GPR; TRP/TRPV Channel | Endocrinology/Hormones; GPCR/G Protein; Membrane transporter/Ion channel |
AS1269574 是口服有效的GPR119激动剂,在表达人 GPR119 的 HEK293 细胞中EC50为 2.5 μM。它激活 TRPA1 阳离子通道,刺激胰高血糖素样肽-1分泌。它仅在高糖条件下特异性诱导胰腺 β 细胞分泌葡萄糖依赖性胰岛素。它在 2 型糖尿病的研究中具有价值。 | |||
T9776 |
TRPM4 inhibitor 8
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
TRPM4 inhibitor 8 是瞬态受体电位 melastatin 4 (TRPM4) 的抑制剂,它有助于活力、迁移、细胞周期转变和粘附。 | |||
T68783 | Stercuronium | ||
Stercuronium is an aminosteroid neuromuscular blocking agent which was never marketed. It acts as a competitive antagonist of the nicotinic acetylcholine receptor, and is also reported to be an acetylcholinesterase inhibitor. | |||
T68735 | Ciclotropium (free base) | ||
Ciclotropium (free base) is quaternary ammonium compound with anticholinergic and parasympatholytic activity. Oral Cyclotropium bromide inhibited fasting and meal-stimulated colonic motility significantly without causing adverse side effects. After cyclotropium bromide, there was a significant correlation between antral contraction amplitude and gastric emptying. | |||
T68502 |
Dibrospidium Free Base
|
||
Dibrospidium Free Base is a dispirotripiperazine derivative and alkylating agent with potential antineoplastic and anti-inflammatory activities. The duration of DNA synthesis inhibition in tumor cells was found to correlate with spirobromine antitumor activity. Spirobromin is superior to prospidin by the power of the anti-inflammatory effect. Spyrobromin can diminish the latent period of the development of tumours in the experimental rats at intraperitoneal administration. At intragastric admini... | |||
T70310 | INCB-39110 | ||
INCB-39110 is a JAK1 inhibitor. | |||
T9245 |
TRPM4-IN-1
CBA,4-chloro-2-(2-(2-chlorophenoxy)acetamido)benzoic acid |
TRP/TRPV Channel | Membrane transporter/Ion channel |
TRPM4-IN-1 (4-chloro-2-(2-(2-chlorophenoxy)acetamido)benzoic acid) 是一种有效的阳离子通道TRPM4选择性抑制剂,IC50为 1.5 μM。TRPM4-IN-1 在心脏病和前列腺癌中具有研究价值。 | |||
T1050 |
Prazosin hydrochloride
Prazosin hydrochloride,哌唑嗪盐酸盐,Prazosin HCl,cp-12299-1,Peripress,Vasoflex,盐酸哌唑嗪,Minipress |
Potassium Channel; MRP; Adrenergic Receptor; ABC; Autophagy | Autophagy; GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
Prazosin hydrochloride (Vasoflex) 是一种选择性肾上腺素能 α-1 拮抗剂,可降低外周阻力并放松血管平滑肌。 它可用于研究高血压和酒精使用障碍。 它是一种合成哌嗪衍生物,具有降压抗肾上腺素能特性。它抑制有机阳离子转运蛋白 OCT-1 和 OCT-3,IC50分别为 1.8 和 13 μM 。 | |||
TQ0157 |
EIPA
L593754,MH 12-43 |
Sodium Channel; TRP/TRPV Channel | Membrane transporter/Ion channel |
EIPA (L593754) 是一种有效的TRPP3 channel 抑制剂,IC50为 10.5 μM。EIPA 对Na+/H+交换 (NHE) 和巨噬细胞也有抑制作用。 | |||
T80024 |
Cationic Bovine Serum Albumin
cBSA, chemically modified cationic bovine serum albumin |
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Cationic Bovine Serum Albumin(带正电荷的牛血清白蛋白)是由583个氨基酸组成的蛋白质,具有三个同源的全α结构域。该蛋白质与Tanshinone IIA联用,在缺血性脑卒中中展现出显著的神经保护作用。 | |||
T81449 |
PKC-ε translocation inhibitor peptide
|
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
PKC-ε translocation inhibitor peptide,作为一种特定的PKC-ε易位抑制剂,能够特异性地调控FcγR介导的调理珠内化速率,而对FcαR运输不产生影响。 | |||
T74550 |
Cemdisiran, terminal sugar modification-
|
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Cemdisiran(终端糖基修饰)是一种靶向C5 mRNA的siRNA,通过N-乙酰半乳糖胺缀合增强RNAi活性,能够抑制肝脏中补体成分C5的生成。 | |||
T7538 |
Tetraethylammonium chloride
|
Potassium Channel | Membrane transporter/Ion channel |
Tetraethylammonium chloride 是非选择性钾通道阻滞剂。它是有机阳离子转运蛋白的良好底物,并具有抗肿瘤特性。 | |||
T28020 |
Mesendogen
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
Mesendogen 是瞬时受体电位阳离子通道、亚家族 M、成员 6 (TRPM6) 和 7 (TRPM7) 的抑制剂,通过抑制 TRPM6/TRPM7 镁通道活性起作用。 | |||
T10247 |
Adenosine 5'-diphosphoribose sodium
Adenosine 5'-diphosphoribose sodium,ADP ribose sodium |
Endogenous Metabolite; TRP/TRPV Channel; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Adenosine 5'-diphosphoribose sodium (ADP ribose sodium) 是一种烟酰胺腺嘌呤核苷酸 (NAD+) 的代谢产物,广泛存在于生物体内。Adenosine 5'-diphosphoribose sodium (ADP ribose sodium) 是一种高效的细胞内 Ca2+ 渗透性阳离子 TRPM2 通道激活剂,还可以诱导自噬 (autophagy)。 | |||
T22537 |
9-Phenanthrol
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
9-Phenanthrol 是瞬时受体电位 melastatin 4 (TRPM) 通道的抑制剂,这是一种 Ca2+ 激活的非选择性阳离子通道。 | |||
T22353 |
Lanthanum(III) chloride heptahydrate
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Lanthanum(III) chloride heptahydrate 是一种无机化合物,用于生化研究,阻断二价阳离子通道,尤其是钙通道的活性。 | |||
T16763 |
RN-1747
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
RN-1747是瞬时受体电位阳离子通道 V 型亚家族成员4(TRPV4 )的选择性激动剂,对 hTRPV4、mTRPV4 和 rTRPV4 的 EC50分别为0.77 μM、4.0 μM 和4.1 μM。RN-1747也是 TRPM8的拮抗剂,IC50值为4.0 μM。 | |||
T16686 |
Pyr10
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
Pyr10 是吡唑衍生物,是TRPC3通道的选择性抑制剂。Pyr10抑制卡巴可刺激的TRPC3转染的 HEK293 细胞中的 Ca2+流入。它具有区分受体操纵的TRPC3和天然基质相互作用分子 1 (STIM1)/Orai1 通道的能力。 | |||
T1098 |
Denatonium benzoate
苯甲地那铵,THS-839 |
Others | Others |
Denatonium benzoate (THS-839) 是一种已知的最苦的化合物,可作为厌恶剂(苦味剂),加入到工业酒精、防冻液、咬指甲癖预防、呼吸器面罩配合测试、动物驱虫剂、液体皂和洗发水中,防止不适当的摄取。 | |||
TP1910L1 |
CALP1 acetate
CALP1 acetate(145224-99-3 free base) |
CaMK | Neuroscience |
CALP1 acetate 是一种钙调蛋白 (CaM) 激动剂(Kd 为 88 µM),可与 CaM EF-hand/Ca2+ 结合位点结合。 CALP1 通过抑制钙通道的开放来阻断钙流入和细胞凋亡(IC50 为 44.78 µM)。 CALP1 阻断谷氨酸受体通道并阻断储存操作的非选择性阳离子通道。 CALP1 激活依赖于 CaM 的磷酸二酯酶活性。 | |||
T70540 |
Pinokalant
LOE-908 |
SARS-CoV; TRP/TRPV Channel | Membrane transporter/Ion channel; Microbiology/Virology |
Pinokalant (LOE-908) 是一种新型非选性阳离子通道抑制剂。Pinokalant 在体内实验中可显著减少皮质梗死体积,可改善缺血半影区的代谢和电生理状态,可减少大鼠大脑中动脉闭塞后急性期磁共振图像上的病变大小。Pinokalant是一种潜在的SARS-CoV-2蛋白酶抑制剂,可用于研究脑卒中。 | |||
TP2158 |
TRV-120027 TFA
TRV-120027 TFA (1234510-46-3 free base) |
RAAS; Arrestin | Endocrinology/Hormones; GPCR/G Protein |
TRV-120027 TFA 是一种血管紧张素 II 介导的血管收缩抑制剂,可增加心肌细胞的收缩力。它是一种偏向 β-arrestin-1 的 AT1R 激动剂,可与 ß-arrestins 结合,同时阻断 G 蛋白信号传导。 它通过阳离子通道亚家族 C3 (TRPC3) 偶联诱导急性儿茶酚胺分泌,并促进在质膜上形成由 AT1R-β-arrestin-1-TRPC3-PLCγ 组成的大分子复合物。 | |||
T38516 |
IDT307
|
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IDT307, an analog of the organic cation MPP+, serves as a specific fluorescent substrate for DAT, identified as APP+. | |||
T22929 |
LOE 908 hydrochloride
|
Others | Others |
Broad spectrum cation channel blocker | |||
T40757 |
1-Stearoyl-2-arachidonoyl-sn-glycerol
|
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1-Stearoyl-2-arachidonoyl-sn-glycerol, a diacylglycerol (DAG) encompassing polyunsaturated fatty acids, possesses the ability to activate PKC. Moreover, this compound has the potential to enhance nonselective cation channel (NSCC) activity. | |||
T68693 |
AZ12099548
|
||
AZ12099548 is a transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonist. | |||
T0979L |
Dequalinium acetate
Dequadin acetate,Decalinium acetate |
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Dequalinium is a quaternary ammonium cation and bolaamphiphile commonly available as the dichloride salt. The bromide, iodide, acetate, and undecenoate salts are known as well. | |||
T37086 |
PDDHV
|
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PDDHV is a resiniferatoxin-type phorboid vanilloid with capsaicin-like selectivity for the cloned rat transient receptor potential cation channel subfamily V member 1 (TRPV1), formerly known as vanilloid receptor 1. It induces Ca2+-uptake by rat dorsal root ganglion neurons with an EC50 value of 70 nM. | |||
T22370 |
Mitoquinol mesylate
|
Others | Others |
Mitoquinol, a ubiquinone derivative, specifically accumulates in mitochondria due to the covalent attachment of the cation triphenylphosphonium. Mitoquinol is an antioxidant, protecting mitochondria from oxidative damage and preventing lipid peroxidation- | |||
T37658 |
MitoP
|
||
MitoP is a phenol product produced by the reaction of H2O2 with the ratiometric mass spectrometry probe MitoB . MitoB contains a triphenylphosphonium cation component that drives its accumulation in mitochondria where its arylboronic moiety selectively reacts with H2O2 to produce MitoP. Quantifying the MitoP/MitoB ratio by LC-MS/MS reflects the mitochondrial matrix H2O2 concentration. | |||
T76374 |
SPAI-1
|
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SPAI-1,特异性单价阳离子ATP酶抑制剂,源自猪十二指肠。能体外抑制Na+,K+-ATP酶和H+,K+-ATP酶,同时刺激Mg2+-ATP酶。 | |||
T81986 | Kayexalate | ||
Kayexalate,一种阳离子交换树脂,用作口服血浆钾离子抑制剂,适用于高钾血症的研究。 | |||
T35965 |
MitoTEMPOL
|
||
MitoTEMPOL is a mitochondria-targeting superoxide dismutase mimetic that reduces mitochondrial O2- to H2O2. Like the related compound MitoTEMPO , MitoTEMPOL combines an antioxidant moiety (here, TEMPOL, also known as 4-hydroxy-TEMPO) with the lipophilic cation triphenylphosphonium, which allows it to pass through lipid bilayers and accumulate in mitochondria. MitoTEMPOL has been used to elucidate the role of mitochondria-derived superoxide in mitochondrial, cellular, and whole animal signaling. | |||
T78513 |
Sodium zirconium cyclosilicate
|
Others | Others |
Sodium zirconium cyclosilicate 是一种新型口服、不吸收的无机微孔硅酸盐锆化合物,高选择性地作为阳离子交换剂,专门用于去除体内过量的K+。该化合物适用于慢性肾脏疾病(CKD)的研究。 | |||
T62272 |
TRPC6-IN-3
|
||
TRPC6-IN-3 (compound 17) 是一种口服具有活力的瞬时受体电位 C6 离子通道 (TRPC6) 抑制剂。TRPC6-IN-3 能够调节细胞内钙浓度,也能够调节包括钙离子和钠离子在内的阳离子通量来调节膜电位。TRPC6-IN-3 可以用于研究呼吸系统。 | |||
T28047 |
Mitoquinone-cyclodextrin
MitoQ10,Mitoubiquinone mesylate,MitoQ-10,MitoQ,Mito Q10,Mitoquinone mesylate-cyclodextrin |
||
Mitoquinone-cyclodextrin is a 1:1 molar ratio complex of Mitoquinone mesylate with cyclodextrin. Mitoquinone mesylate is a mitochondria-targeted antioxidant designed to accumulate within mitochondria in vivo in order to protect against oxidative damage. M | |||
T37550 |
Bacitracin Complex
|
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Bacitracin complex is a bacitracin antibiotic complex composed of cyclic dipeptides that has been found inBacillus.1It is metal-dependent and is complexed to a divalent metal cation, such as Cu2+, Ni2+, Co2+, Zn2+, or Mn2+, for its activity.1,2Bacitracin complex is a mixture of bacitracin polypeptides in complex with copper. 1.Piacham, T., Isarankura-Na-Ayudhya, C., Nantasenamat, C., et al.Metalloantibiotic Mn(II)-bacitracin complex mimicking manganese superoxide dismutaseBiochem. Biophys. Res. ... | |||
T35964 |
MitoTEMPO hydrate
|
||
MitoTEMPO is a mitochondria-targeted superoxide dismutase mimetic that possesses superoxide and alkyl radical scavenging properties.[1] This compound combines the antioxidant piperidine nitroxide TEMPO with the lipophilic cation triphenylphosphonium, which allows it to pass through lipid bilayers and accumulate in mitochondria. Mitochondrial targeting of superoxide scavenging via mitoTEMPO has been examined for potential therapeutic benefit to a variety of mitochondrial dysfunctions arising from... | |||
T35963 |
MitoPerOx
|
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MitoPerOx is a ratiometric fluorescent probe that can be used to assess changes in lipid peroxidation within mitochondria. It is composed of a BODIPY fluorophore conjugated via a dienyl link to a triphenylphosphonium cation component that drives its accumulation in mitochondria. MitoPerOx displays an excitation maximum of 495 nm and exhibits a shift in emission maxima from 590 to 520 nm upon mitochondrial lipid peroxidation, enabling determination of ratiometric measurements of lipid peroxidatio... | |||
T37697L |
D-GsMTx4 TFA
|
TRP/TRPV Channel; Piezo Channel | Membrane transporter/Ion channel |
D-GsMTx4 TFA 是一种具有选择性的蜘蛛毒液肽,是一种TRPC1 / 6和Piezo2抑制剂,可抑制属于 Piezo 和 TRP 通道家族的阳离子可渗透的机械敏感性通道 (MSCs),阻断阳离子选择性的拉伸激活通道 (SAC),减弱溶血磷脂酰胆碱 (LPC) 诱导的星形胶质细胞毒性和小胶质细胞反应性。D-GsMTx4 TFA 在小鼠缺血/再灌注模型中预防心肌梗死,可用于鉴定兴奋性 MSC 在正常生理学和病理学中的作用。 | |||
T36745 |
cDPCP
|
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cDPCP is a platinum-containing DNA-crosslinking agent.1Unlike cisplatin or oxaliplatin , cDPCP forms monofunctional DNA adducts. It is transported into cells by organic cation transporter 1 (OCT1) and OCT2, inhibiting proliferation of MDCK cells expressing the human transporters with IC50values of 8.1 and 1.5 μM, respectively. cDPCP inhibits RNA polymerase II-mediated transcription in a reporter assay using HeLa cells. It increases survival in murine S180 sarcoma and P388 leukemia models when ad... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T10662L |
Calcimycin
Antibiotic A-23187,离子载体(钙镁盐混合物),A-23187 |
Apoptosis; Antibacterial; Antibiotic; Autophagy; Antifungal | Apoptosis; Autophagy; Microbiology/Virology |
Calcimycin (A-23187) 是抗生素和二价阳离子离子载体。它抑制革兰氏阳性细菌和一些真菌生长,也抑制 ATP 酶的活性并解耦哺乳动物细胞的氧化磷酸化。它通过增加细胞内钙浓度诱导 Ca2+依赖性细胞死亡。 | |||
T1045 |
Trimipramine maleate
Surmontil maleate,马来酸三甲丙咪嗪,三甲丙咪嗪马来酸盐 |
Dopamine Receptor; 5-HT Receptor; Antibacterial; Adrenergic Receptor; Norepinephrine; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Trimipramine maleate (Surmontil maleate) 是一种 5-HT 受体拮抗剂,对 5-HT1C、5-HT2和 5-HT1A 受体的 pKi 值分别为 6.39、8.10和 4.66。 | |||
T4S0779 |
D-tetrahydropalmatine
|
Others; Dopamine Receptor | GPCR/G Protein; Neuroscience; Others |
D-Tetrahydropalmatine 是一种主要存在于延胡索类植物中的异喹啉生物碱。它是有机阳离子转运蛋白 1 抑制剂。它是多巴胺受体拮抗剂,对 D1 受体具有优先亲和力。 | |||
T1153 |
Trimethoprim
NIH 204,BW 56-72,甲氧苄啶,NSC-106568 |
DHFR; DNA/RNA Synthesis; Antifolate; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Trimethoprim (NSC-106568) 是抑菌抗生素,也是具有口服活性的二氢叶酸还原酶抑制剂。它对多种革兰氏阳性和革兰氏阴性需氧细菌具有活性,可用于尿路感染,肺孢子菌肺炎和志贺氏菌病的研究。 | |||
T2994 |
(E)-Cardamonin
Alpinetin chalcone,Cardamomin,小豆蔻明,Cardamonin,(E)-Cardamoni,豆蔻明 |
Apoptosis; TRP/TRPV Channel | Apoptosis; Membrane transporter/Ion channel |
(E)-Cardamonin (Alpinetin chalcone) 是一种新型hTRPA1阳离子通道拮抗剂,IC50值为454 nM。 | |||
TN2798 |
20-Deoxocarnosol
|
ROS; Antifection | Immunology/Inflammation; Microbiology/Virology |
20-Deoxocarnosol has antioxidant activity of measuring the decay of the radical cation diphenyl-picrylhydrazyl (DPPH).It also exhibits non-specific antiprotozoal activity due to high cytotoxicity. | |||
T10662 |
Calcimycin hemicalcium salt
Antibiotic A-23187 hemicalcium salt,A-23187 hemicalcium salt |
Others | Others |
Calcimycin (A-23187) hemicalcium salt is an antibiotic and a unique divalent cation ionophore (like calcium and magnesium). It induces Ca2+-dependent cell death by increasing intracellular calcium concentration. | |||
TN1361 |
(+)-Afzelechin
阿夫儿茶精,(+)-阿夫儿茶精 |
Others | Others |
(+)-Afzelechin has a neuroprotective effect on the glutamate-induced neurotoxicity in HT22 cells, it has ABTS cation radical scavenging effects with IC50 values of 23.7 microM | |||
TN1909 |
Malvidin-3-glucoside chloride
氯化锦葵色素-3-Β-葡糖苷,Malvidin-3-O-glucoside chloride,Oenin chloride |
Others | Others |
Malvidin-3-glucoside chloride (Oenin chloride) 是一种主要的葡萄酒花青素,能够调节大脑突触可塑性和外周炎症,促进应激反应的发生。 | |||
T36439 |
Gramicidin A
|
Antibacterial; HIF; Parasite | Angiogenesis; Chromatin/Epigenetic; Microbiology/Virology |
Gramicidin A 是一种从从 B. brevis 分离出来的多肽类抗生素。Gramicidin A 是一种高度疏水的通道形成离子载体,在人工膜中形成一价阳离子可渗透的通道。Gramicidin A 诱导缺氧诱导因子 1α (HIF-1α) 的降解,并能降低人肾细胞癌小鼠异种移植模型的生长。Gramicidin A 具有抗菌、抗疟活性以及溶血活性。 |