513
83
3
26
17
Cat. No. | Product Name | ||
---|---|---|---|
L7300 | 钾通道分子库 | 152 compounds | |
152 种钾通道相关化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L7400 | 钠通道分子库 | 118 compounds | |
118 种钠通道相关化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L7110 | 抗高血压化合物库 | 678 compounds | |
678 种高血压相关的小分子,用于高通量和高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5987 |
Potassium oxonate
Oxonic Acid (potassium salt),氧嗪酸钾,Potassium otastat,Potassium azaorotate |
Others | Others |
Potassium oxonate (Potassium azaorotate) 是用作尿酸酶抑制剂,都5-FU 磷酸化为5-fluorouridine-5'-monophosphate 具有抑制作用。 | |||
T68022L |
Sulotroban potassium
BM 13177 potassium,Sulotroban potassium(72131-33-0 Free base) |
PPAR | DNA Damage/DNA Repair; Metabolism |
Sulotroban potassium 是一种小分子血栓素A2受体(TXA2R)拮抗剂,可用于研究心肌梗塞和血栓形成。 | |||
T3096 |
Canrenoate potassium
坎利酸钾,Potassium aldadiene,Canrenoic acid potassium salt,Potassium canrenoate,Soldactone |
Glucocorticoid Receptor | Endocrinology/Hormones |
Canrenoate potassium (Soldactone) 是一种有效的竞争性盐皮质激素受体 (mineralocorticoid receptor) 拮抗剂,是一种释放 canrenone 的前药。它作为一种利尿剂,用于高血压的研究。 | |||
T35381 |
Aluminum potassium sulfate
Potassium Aluminium Sulfate,APS |
Others | Others |
Aluminum potassium sulfate (Potassium Aluminium Sulfate) 可用于研究严重急性呼吸系统综合症,可用于预防和治疗癌症。 | |||
T2239 |
Raltegravir potassium
MK 0518 potassium salt,Raltegravir potassium salt,雷特格韦钾盐 |
HIV Protease; Integrase | Microbiology/Virology; Proteases/Proteasome |
Raltegravir potassium (MK 0518 potassium salt) 是一种整合酶抑制剂,用于研究 HIV 感染。 | |||
T8129 |
Potassium acetate
Diuretic salt,Potassium ethanoate,乙酸钾 |
Antifungal | Microbiology/Virology |
Potassium acetate (Diuretic salt) 是一种钾盐,能够用于补充电解质,恢复水电解质平衡,也能用于制备细菌碱性裂解的中和液,以及纯化 DNA 和蛋白质。 | |||
T0481 |
Azilsartan Medoxomil Potassium
TAK-491 Potassium |
||
Azilsartan Medoxomil Potassium (TAK-491 Potassium) 是一种具有口服活性的1型血管紧张素 II 受体拮抗剂(IC50: 0.62 nM)。 | |||
T19498 |
p-Cresyl sulfate potassium
p-Tolyl sulfate potassium salt,p-Cresol sulfate potassium,p-Methylphenyl potassium sulfate,对甲基硫酸钾,Potassium p-tolyl sulfate |
Endogenous Metabolite | Metabolism |
p-Cresyl sulfate potassium (p-Tolyl sulfate potassium salt) 是一种尿毒症毒素,能够与原型蛋白质结合。 | |||
T3267 |
Potassium guaiacolsulfonate hemihydrate
愈创木酚磺酸钾水合物,Potassium guaiacolsulfonate,Potassium 4-guaiacolsulfonate hemihydrate,愈创木酚磺酸钾 |
Antibacterial; Antibiotic | Microbiology/Virology |
Potassium guaiacolsulfonate hemihydrate (Potassium guaiacolsulfonate) 是一种芳香族磺酸,在医药中用作祛痰剂,可治疗急性呼吸道感染。它可松弛粘液,与其他药物合用,可治疗普通感冒、感染或过敏引起的咳嗽。 | |||
T22328 |
Ethyl potassium malonate
Potassium 3-ethoxy-3-oxopropanoate,Malonic Acid Monoethyl Ester Potassium Salt,丙二酸单乙酯钾盐 |
Others | Others |
Ethyl potassium malonate 是琥珀酸脱氢酶的竞争性抑制剂,可作为生产丙二酸(三甲基甲硅烷基)乙酯的前体,丙二酸乙酯用于通过酰化制备 β-酮酯,并作为制备丙二酸叔丁酯的中间体。 | |||
T5580 |
1-Naphthaleneacetic acid potassium salt
α-萘醋酸钾,α-Naphthaleneacetic acid,Potassium alpha-naphthylacetate,Potassium 1-Naphthaleneacetate,1-NAA Potassium Salt |
Phospholipase | Metabolism |
1-Naphthaleneacetic acid potassium salt (1-NAA Potassium Salt) 是一种合成的植物生长素,能够促进植物生长,也是一种PLA2抑制剂,IC50=13.16 μM。 | |||
T0215 |
Losartan potassium
DuP-753 potassium,洛沙坦钾,氯沙坦钾,MK 954,DuP 753 |
RAAS | Endocrinology/Hormones |
Losartan potassium (DuP-753 potassium) 是一种血管紧张素 II 受体 1 型(AT1)拮抗剂,能够与血管紧张素 II 与 AT1 的结合竞争,其 IC50=20 nM。 | |||
T36008 |
Nebentan potassium
YM598 |
Endothelin Receptor | GPCR/G Protein |
Nebentan potassium (YM598) 是一种具有口服活性和选择性的非肽类内皮素受体 (ETA receptor) 拮抗剂。Nebentan potassium 抑制肺动脉高压,可用于研究神经系统疾病和心血管疾病。 | |||
T4139 |
D-Luciferin potassium
D-Luciferin K Salt,D-Luciferin Potassium Salt,D-萤光素钾盐,D-荧光素钾盐 |
Others | Others |
D-Luciferin potassium (D-Luciferin K Salt) 是一种荧光素酶 (Luc) 的底物,能够催化生物发光昆虫产生典型的黄绿光 (560 nm)。D-Luciferin potassium 可以用于荧光素酶实验。 | |||
T22402 |
Potassium thioacetate
|
Others | Others |
Potassium thioacetate 它已被用于合成聚合物、杂环、纳米颗粒、过渡金属配体、生物活性化合物和大分子包合物。 | |||
T0357 |
Potassium iodide
|
Tyrosinase | Proteases/Proteasome |
Potassium iodide 用于治疗过度活跃的甲状腺,并保护甲状腺免受吞咽或吸入放射性碘的辐射影响。可在意外接触放射性碘后或服用含放射性碘的药物前后使用。 | |||
T0940 |
Acesulfame Potassium
|
Others | Others |
Acesulfame potassium 是一种人造甜味剂,长期使用会影响认知功能,可能改变小鼠的神经代谢功能。 | |||
T68006 |
Orilotimod potassium
APO805K1 |
Others | Others |
Orilotimod potassium (APO805K1)可用于研究斑块状银屑病。 | |||
T23175 |
Potassium phosphate monobasic
|
Others | Others |
Potassium phosphate monobasic 是生物测定时常用的缓冲液。它是中等浓度至高浓度的磷酸二氢钾水溶液,可用于制备磷酸盐缓冲液以及其他实验试剂。 | |||
T6415 |
Bismuth Subcitrate Potassium
|
SARS-CoV | Microbiology/Virology |
Bismuth Subcitrate Potassium 是一种对 12 种幽门螺杆菌有作用的抗生素,抑制组胺H2受体,可用于研究 SARS-CoV-2 感染脆弱患者的腹泻和消化性溃疡病。 | |||
T67732 |
Potassium trimethylsilanolate
Trimethylsiloxypotassium |
Others | Others |
Potassium trimethylsilanolate 是一种催化剂。Potassium trimethylsilanolate 通过(TMSOK)通过硼酸途径促进 Suzuki Miyaura 反应。 | |||
T6470 |
Diclofenac Potassium
双氯芬酸钾,CGP-45840B,Cataflam,Voltfast |
Apoptosis; Others; COX | Apoptosis; Immunology/Inflammation; Neuroscience; Others |
Diclofenac Potassium (CGP-45840B) 是一种非甾体抗炎药,用于减轻炎症并在某些情况下作为镇痛剂减轻疼痛。它通过活化 caspase 级联反应来诱导神经干细胞凋亡。它是一种COX 抑制剂,在 CHO 细胞中,对人 COX-1 和 COX-2 的IC50值分别为 4 和 1.3 nM。它对绵羊 COX-1 和 COX-2 的IC50值分别为 5.1 μM 和0.84 μM。 | |||
T1425 |
Pemirolast potassium
BMY 26517,TWT-8152,吡嘧司特钾 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Pemirolast potassium (TWT-8152) 是 H1组胺受体拮抗剂和肥大细胞稳定剂,是一种具有抗过敏特性的嘧啶酮衍生物。 | |||
T7827 |
Glycyrrhizinic acid, potassium salt
|
Others | Others |
Glycyrrhizinic acid, potassium salt 可减轻藜芦醇引起的室性心律失常。 | |||
T22215 |
1-Naphthyl phosphate potassium salt
|
Phosphatase | Metabolism |
1-Naphthyl phosphate potassium salt 是非特异性磷酸酶 (phosphatase) 抑制剂,能够降低剪接校正作用。 | |||
T77688 |
Dipotassium tetrachloroplatinate
Potassium tetrachloroplatinate |
Others | Others |
Dipotassium tetrachloroplatinate (Potassium tetrachloroplatinate) 在实体肿瘤系中表现出抗肿瘤活性,可用于有治疗肿瘤疾病。Dipotassium tetrachloroplatinate 还可充当放射增敏剂,可增强热疗杀伤作用。 | |||
T72272 |
Glibenclamide potassium
Glyburide potassium |
Others | Others |
Glibenclamide (Glyburide) potassium 是 Glibenclamide 的钾盐形式。Glibenclamid potassium 以无水和水合物形式存在,与纯 Glibenclamide 相比具有更高的溶解度。 | |||
T10674 |
Potassium Channel Activator 1
钾离子通道激活剂1,ZINC34634569 |
Potassium Channel | Membrane transporter/Ion channel |
Potassium Channel Activator 1 可用于治疗多巴胺能系统被破坏的疾病或病症的研究,例如情绪障碍 ADHD、精神分裂症和其他精神病状态。 | |||
T78614 |
Selnoflast potassium
RO-7486967 potassium |
NOD-like Receptor (NLR) | Immunology/Inflammation |
Selnoflast (potassium) (example 6) 作为NLRP3抑制剂。 | |||
T24551 |
NSC339614 potassium
NSC 339614 potassium,NSC-339614 potassium,NSC339614 potassium salt |
Others | Others |
NSC339614 potassium is a selective GluN1/GluN2C and GluN1/GluN2D receptors potentiator. | |||
T24630 |
Phenethicillin potassium
ALPHA-PHENOXYETHYLPENICILLINIC ACID POTASSIUM SALT,PHENETHICILLIN POTASSIUM SALT,Phenethicillin-potassium,Phenethicillinpotassium |
Others | Others |
Phenethicillin potassium is a potassium salt form of phenethicillin with antibacterial activity. | |||
T20365 |
Monopotassium glutamate
L-谷氨酸钾盐,Potassium glutamate,Potassium L-glutamate |
Others | Others |
Monopotassium glutamate (Potassium glutamate) 可在食品中用作增味剂。 | |||
T34116 |
Potassium caprate
Potassium decanoate |
Others | Others |
Potassium caprate is a biochemical. | |||
T38715 |
MSDC-0602K
MSDC-0602K,Azemiglitazone potassium |
PPAR | DNA Damage/DNA Repair; Metabolism |
MSDC-0602K (Azemiglitazone potassium) (Azemiglitazone potassium) is a PPARγ-sparing thiazolidinedione (Ps-TZD) compound that binds to PPARγ with an IC50 of 18.25 μM. It also modulates the mitochondrial pyruvate carrier (MPC). This compound, MSDC-0602K, has potential applications in researching fatty liver conditions, including dysfunctional lipid metabolism, inflammation, and insulin resistance. MSDC-0602K acts as an insulin sensitizer, improving insulinemia and fatty liver disease in mice both ... | |||
T39715 |
MeCY5-NHS ester potassium
Sulfo-Cyanine5 NHS ester potassium,MeCY5-NHS ester potassium |
||
MeCY5-NHS ester (potassium) is a reactive dye designed for labeling proteins and nucleic acids. | |||
T12524 |
Potassium clavulanate cellulose
Potassium clavulanate:cellulose (1:1) |
Others | Others |
Potassium clavulanate cellulose is a mixture of potassium clavulanate and cellulose, is an inhibitor of beta-lactamase. | |||
T22623 |
Carboxy-PTIO potassium
Carboxy-PTIO, potassium salt |
Others | Others |
reacts with nitric oxide to form carboxy-PTI derivatives which in turn inhibits nitric oxide synthase | |||
T24900 |
Troclosene potassium
Fluonon,NSC-251767,NSC 251767,Neochlor 59,Potassium dichloroisocyanurate,NSC251767 |
Others | Others |
Troclosene potassium acts as an anti-infective agent on denture cleansers, in hospitals, and in wastewater treatment. | |||
T19948 |
Grazoprevir potassium salt
MK 5172 potassium,Grazoprevir,Grazoprevir potassium,MK 5172,MK5172,MK-5172 |
Others | Others |
Grazoprevir is a drug approved for the treatment of hepatitis C. Grazoprevir is a second-generation hepatitis C virus protease inhibitor acting at the NS3/4a protease targets. | |||
T41058 |
Nelonemdaz potassium
Neu2000potassium,Salfaprodil |
Others | Others |
Nelonemdaz potassium (also known as Salfaprodil) is a potent NR2B-selective and uncompetitive antagonist of N-methyl-D-aspartate (NMDA). This compound exhibits remarkable neuroprotection against cell death induced by both NMDA and free radicals, in addition to its role as a free radical scavenger. | |||
T68270 |
Avutometinib potassium
|
Others | Others |
Avutometinib potassium is a MEK inhibitor (MEKi) that enhanced the inhibition of pseudovirus infection by GLPG-0187. It Blocks SARS-CoV-2 Delta and Omicron Pseudovirus Infection of Airway Epithelial Cells In Vitro, Which Could Attenuate Disease Severity | |||
T27724 |
KDT 501 potassium
KDT 501 potassium salt,KDT-501,KDT 501,Tetrahydroisohumulone |
Others | Others |
KDT 501, a PPAR agonist and G protein-coupled receptor (GPR) 120 agonist, is used potentially for the treatment of type 2 diabetes. | |||
T69273 |
Mexrenoate potassium
|
Others | Others |
Mexrenoate potassium is a steroidal aldosterone antagonist and antihypertensive. | |||
T71844 |
Methyl potassium malonate
|
Others | Others |
Methyl potassium malonate is a protein advanced glycosylation inhibitor. | |||
T70589 |
Saprisartan potassium
|
Others | Others |
Saprisartan potassium is an Angiotensin II Type 1 receptor antagonist and antihypertensive agent. | |||
T35382 |
Potassium phosphate dibasic
Dipotassium phosphate |
Others | Others |
Potassium phosphate dibasic (Dipotassium phosphate, K2HPO4)常被用作肥料、食品添加剂和缓冲剂。 | |||
T38510 |
ABT-072 potassium trihydrate
|
Others | Others |
ABT-072, also known as potassium trihydrate, is a highly effective non-nucleoside inhibitor of the HCV NS5B polymerase, administered orally. This compound exhibits potent activity against HCV GT1a (with an EC50 of 1 nM) and HCV GT1b (with an EC50 of 0.3 nM). | |||
T70743 |
IS-741 potassium
|
Others | Others |
IS-741 potassium is a phospholipase A2 inhibitor. | |||
T70203 |
Galloflavin Potassium
|
Others | Others |
Galloflavin Potassium is an inhibitor of lactate dehydrogenase. | |||
T33228 |
MCPA-potassium
|
Others | Others |
MCPA-potassium is a bioactive chemical. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4807 |
Potassium sorbate
Sorbic acid potassium salt,山梨酸钾,Potassium 2,4-hexadienoate |
Others; Endogenous Metabolite; Antibacterial; Antibiotic; Antifungal | Metabolism; Microbiology/Virology; Others |
Potassium sorbate (Sorbic acid potassium salt) 是一种高效安全无毒的食品防腐剂,可有效抑制大多数霉菌,酵母和某些细菌。 | |||
TN1698 |
Glucotropaeolin potassium
金莲葡糖硫苷钾盐,Glucotropaeolin,Benzylglucosinolate potassium,Glucotropaeolin Potassium Salt |
Others | Others |
Glucotropaeolin potassium (Benzylglucosinolate potassium) 存在于十字花科蔬菜中,并且 可适度减少动物的自发性DNA 损伤。 | |||
T1126 |
Penicillin V Potassium
青霉素V钾,Penicillin V potassium salt,Phenoxymethylpenicillin potassium salt |
Antibacterial; Antibiotic | Microbiology/Virology |
Penicillin V Potassium (Phenoxymethylpenicillin potassium salt) 是一种有口服活性的抗生素。它可抑制链球菌,艰难梭菌和金黄色葡萄球菌的生长,可研究中耳炎,鼻窦炎,咽炎和扁桃体炎。 | |||
T5602 |
Penicillin G potassium
青霉素钾,Benzylpenicillin potassium |
Anti-infection; Antibacterial; Antibiotic | Microbiology/Virology |
Penicillin G potassium (Benzylpenicillin potassium) 是青霉素家族的一种速效抗生素。 | |||
T20198 |
Potassium gluconate
Kalium-beta,Kalium Gluconate,Kaon elixir,Kaon,Potassium D-gluconate,HSDB 3165,K-Iao |
Endogenous Metabolite; Antifungal | Metabolism; Microbiology/Virology |
Potassium gluconate (Potassium D-gluconate) 是一种具有口服活性和螯合性质的氧化型羧酸,具有杀菌活性。 | |||
T4938 |
Potassium 1H-indol-3-yl sulfate
硫酸吲哚钾盐,Indoxyl sulfate potassium salt,Potassium 3-indoxyl sulfate |
AhR; Endogenous Metabolite | Immunology/Inflammation; Metabolism |
Potassium 1H-indol-3-yl sulfate (Potassium 3-indoxyl sulfate) 是人芳烃受体(AhR)的激动剂。芳烃受体(AhR)最近被发现是免疫炎症条件的病理生理调节剂,Potassium 1H-indol-3-yl sulfate 已被证明是AhR的配体。Potassium 1H-indol-3-yl sulfate 也是膳食蛋白质中色氨酸的代谢物。色氨酸被肠道细菌代谢为吲哚,吲哚被吸收到血液中,然后在肝脏中进一步代谢为硫酸吲哚,通常通过尿液排出体外。在肾功能受损的慢性肾病患者中,Potassium 1H-indol-3-yl sulfate 可作为尿毒症毒素在血清中积累,诱导氧化应激并加速疾病进展。250 μM Potassium 1H-indol-3-yl sulfate 可诱导NF-Κb活化,促进大鼠近端小管细胞TGF-β1和Smad3的表达,与促纤维化活性相关。 | |||
T5213 |
Acetyl phosphate(lithium potassium)
乙酰磷酸锂钾盐,Lithium potassium acetyl phosphate,Acetylphosphoric acid |
Others; Endogenous Metabolite | Metabolism; Others |
Acetyl phosphate lithium potassium (Lithium potassium acetyl phosphate) 是内源性代谢产物的一种。 | |||
TN7050 |
Potassium 7-hydroxy-1-naphthalenesulfona
藏红花酸,2-Naphthol-8-sulfonic Acid Potassium Salt |
Others | Others |
Potassium 7-hydroxy-1-naphthalenesulfona (2-Naphthol-8-sulfonic Acid Potassium Salt) 天然存在于茜草科栀子花的果实、鸢尾科番红花的花和玄参科玄参科的花叶中。 | |||
T4916 |
D-Glucaric acid potassium
D-Saccharic acid potassium salt,Glucosaccharic acid,D-葡萄糖二酸单钾盐,Glucaric Acid |
Others; Endogenous Metabolite | Metabolism; Others |
D-Glucaric acid potassium (D-Saccharic acid potassium salt) 是内源性代谢产物的一种。 | |||
T4948 |
Potassium 2-hydroxy-2-methylsuccinate
(±)-柠苹酸钾 一水合物,(±)-Potassium citramalate monohydrate,(±)-2-Hydroxy-2-methylsuccinic acid dipotassium salt |
Others; Endogenous Metabolite | Metabolism; Others |
Potassium 2-hydroxy-2-methylsuccinate ((±)-2-Hydroxy-2-methylsuccinic acid dipotassium salt) 是内源性代谢产物的一种。 | |||
T4898 |
Potassium 1-carboxyvinyl hydrogenphosphate
PEP-K,磷酸烯醇丙酮酸单钾盐,Phospho(enol)pyruvic acid monopotassium |
Others; Endogenous Metabolite | Metabolism; Others |
Potassium 1-carboxyvinyl hydrogenphosphate (PEP-K) 是内源性代谢产物的一种。 | |||
T3S0156 |
Atractyloside potassium salt
Atractyloside Dipotassium Salt,苍术苷钾盐,苍术苷二钾盐 |
Others | Others |
Atractyloside potassium salt (Atractyloside Dipotassium Salt) 是一种从苍术果实中分离出得到的二萜苷类化合物,具有毒性。它能抑制大鼠心脏线粒体膜的氯离子通道。它是高效、特异性的线粒体 ADP/ATP 转运 (ADP/ATP transport) 抑制剂。 | |||
T5069 |
D-Glucose 6-phosphate potassium salt
|
Others | Others |
在细胞中,当葡萄糖被己糖激酶或葡萄糖激酶磷酸化或在糖原分解过程中通过磷酸葡萄糖变位酶转化葡萄糖 1-磷酸时,会产生D-glucose 6-phosphate (G6P)。 G6P 位于糖酵解和戊糖磷酸途径的起点。当血糖水平高时,它也可以作为糖原储存。 | |||
T5075 |
Phytic acid potassium
植酸二钾盐,Inositol hexakisphosphate dipotassium salt,Phytic acid dipotassium salt,Fytic Acid dipotassium salt,Inositol polyphosphate dipotassium salt |
Others; BACE; Endogenous Metabolite | Metabolism; Neuroscience; Others |
Phytic acid dipotassium salt 是内源性代谢产物的一种,抑制 β-分泌酶 1 (BACE1) 。 | |||
T82304 |
Glucobrassicanapin potassium
4-Pentenylglucosinolate potassium |
Others | Others |
Glucobrassicanapin (4-Pentenylglucosinolate) potassium 是脂肪族硫代葡萄糖苷类化合物,主要存在于白菜等蔬菜作物中。 | |||
T4942 |
Galactose 1-phosphate Potassium salt
D-半乳糖 1-磷酸二钾盐五水合物,α-D-Galactose-1-phosphate Dipotassium Pentahydrate |
Others; Endogenous Metabolite | Metabolism; Others |
Galactose 1-phosphate Potassium salt (α-D-Galactose-1-phosphate Dipotassium Pentahydrate) 是一种半乳糖代谢中的中间体和核苷酸糖。 | |||
TN2212 |
Glucosinalbate potassium
白芥子钾盐,Sinalbin potassium salt |
Others | Others |
Sinalbin potassium salt is a natural product | |||
T19457 |
N-Hydroxypipecolic acid potassium
NHP potassium,1-Hydroxy-2-piperidinecarboxylic acid potassium |
Others | Others |
N-Hydroxypipecolic acid potassium is a metabolite of plant and a systemic acquired resistance (SAR) regulator. | |||
T73772 |
Estrone sulfate potassium
|
Endogenous Metabolite | Metabolism |
Estrone sulfate potassium 是一种雌激素酯和共轭物,是一种天然内源性类固醇。 | |||
T78471 |
α,α-Trehalose 6-phosphate potassium
Tre6P potassium |
Endogenous Metabolite | Metabolism |
α,α-Trehalose 6-phosphate (Tre6P) potassium 是一种α,α′-trehalose的6-磷酸衍生物及内源代谢物。在Tre6P磷酸酶 (T6PP) 的催化下,α,α-Trehalose 6-phosphate可被高效转化为α,α′-trehalose。 | |||
T65269 |
L-Aspartic acid potasium salt
Aspartic acid potasium salt,Potassium L-aspartate |
Others | Others |
L-aspartic acid potasium salt(VX-548) 是一种广泛存在于动植物体内的氨基酸。L-aspartic acid potasium salt驱动氮氧化物的产生,从而促进吞噬作用,有助于提高鱼类的成活率。L-aspartic acid potasium salt 可对抗生素产生刺激,刺激作用可能与参与天冬氨酸-4-半醛生物合成的前体有关。 | |||
T11589 |
Hydroxycitric acid tripotassium hydrate
柠檬酸钾一水合物,三水合钾柠檬酸,Potassium citrate monohydrate |
ATP Citrate Lyase; HIF/HIF Prolyl-Hydroxylase; HIF | Angiogenesis; Chromatin/Epigenetic; Metabolism |
Hydroxycitric acid tripotassium hydrate (Potassium citrate monohydrate) 是一种藤黄果的主要活性成分,也是一种柠檬酸的衍生物。它可竞争性抑制柠檬酸裂解酶 (ATP citrate lyase) ,并具有减肥作用。它有效抑制结石形成,并抑制HIF,具有抗氧化,抗炎和抗肿瘤活性。 | |||
T35415 |
α-D-Glucose-1,6-bisphosphate (potassium salt hydrate)
|
Others | Others |
α-D-Glucose-1,6-bisphosphate is abis-phosphorylated derivative of α-D-glucose that has roles in carbohydrate metabolism.1It is the product of the reaction of glucose-1- or 6-phosphate with glucose-1,6-bisphosphate synthase (PGM2LI) in the conversion of 1,3-bisphosphoglycerate to 3-phosphoglycerate.2It is also a cofactor for the bacterial enzyme phosphopentomutase.3,4α-D-Glucose-1,6-bisphosphate has been used in the study of carbohydrate metabolism. 1.Beitner, R.Regulation of carbohydrate metabol... | |||
TN7336 |
Glucobrassicin potassium
|
Others | Others |
Glucobrassicin (potassium) 是一种从野生胡萝卜 (Raphanus raphanistrumL.) 中分离的硫代葡萄糖苷 (GSL),适用于生物熏蒸和化感植物在杂草管理研究中的应用。 | |||
T82301 |
Gluconapin potassium
|
||
Gluconapin potassium为萝卜硫素前体,后者为一抗癌效能显著的异硫氰酸酯。 | |||
TN7337 |
Glucoraphenin potassium
|
Others | Others |
Glucoraphenin potassium 是一种具口服活性的硫代葡萄糖苷,能通过芥子酶水解产生萝卜硫素,发挥抗癌作用,并可诱导激活异生物质代谢酶(XMEs)。 | |||
T78466 |
Erythronic acid potassium
|
Endogenous Metabolite | Metabolism |
Erythronic acid potassium为糖类内源性代谢物,关键作用于高尿酸血症发病及改善过程,并与转醛缩酶缺乏症相关的线粒体功能障碍有关,常用于代谢性疾病研究。 | |||
T0690 |
Quinine
奎宁树 |
Potassium Channel; Platelet aggregation; Parasite | Membrane transporter/Ion channel; Microbiology/Virology; Others |
Quinine 是一种从金鸡纳树皮中提取的生物碱,用于预防和治疗疟疾。它也用于特发性肌肉痉挛,可抑制电压脉冲引起的 MT mSlo3 (KCa5.1) 通道 +100 mV 电流, 其IC50值为 169 μM,是一种钾离子通道抑制剂。 | |||
T1719 |
Bufalin
|
ATPase | Membrane transporter/Ion channel |
Bufalin 是蟾酥中的一种成分,是Na+/K+-ATPase 抑制剂,具有抗肿瘤活性,可与其基 α1、α2 和 α3 结合,Kd 值分别为 42.5、45 和 40 nM。 | |||
T8189 |
Dihydroberberine
|
Potassium Channel; HSP; HER | Angiogenesis; Cytoskeletal Signaling; JAK/STAT signaling; Membrane transporter/Ion channel; Metabolism; Tyrosine Kinase/Adaptors |
Dihydroberberine 可抑制人类 ether-a-go-go 相关基因 (hERG) 通道并显着降低 Hsp90 表达及其与 hERG 的相互作用,具有抗动脉粥样硬化、抗炎、降血脂和抗肿瘤活性。 | |||
T37709 |
2,2,2-Trichloroethanol
|
Potassium Channel; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism |
2,2,2-Trichloroethanol 是非经典的 K2P 通道 TREK-1和 TRAAK 的激动剂。 | |||
TN1092 |
O-Nornuciferine
|
Potassium Channel; HER | Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors |
O-Noruciferine 是分离自荷叶的卟啉型生物碱,是有效的 hERG 通道抑制剂。 | |||
T0801 |
Tannic acid
单宁酸,Gallotannic acid |
Potassium Channel; HER; CXCR | Angiogenesis; Autophagy; GPCR/G Protein; Immunology/Inflammation; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors |
Tannic acid (Gallotannic acid) 属于多酚类天然产物,是一种 hERG 通道阻塞剂,也是一种 CXCL12/CXCR4 抑制剂。Tannic acid 具有抗菌、抗氧化、抗炎和抗肿瘤等多种生物活性。 | |||
T3S1873 |
Talatisamine
塔拉乌头胺,塔拉萨敏 |
Potassium Channel | Membrane transporter/Ion channel |
Talatisamine 是一种乌头生物碱,对K+通道有特异性阻滞作用。它能减弱 beta- 淀粉样低聚物对培养的皮层神经元的毒性。 | |||
T3A2467 |
Allocryptopine
Thalictrimine,Fagarine I,别隐品碱 |
Potassium Channel | Membrane transporter/Ion channel |
Allocryptopine (Thalictrimine) 是一种延胡索乙素的衍生物,提取自Corydalis decumbens。Allocryptopine 具有抗心律失常作用,能有效阻断hERG 电流。 | |||
T1186 |
Ifenprodil Tartrate
|
Potassium Channel; NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Ifenprodil tartrate 是典型的非竞争性 NMDA 受体拮抗剂,抑制 GIRK (Kir3),通过基底 GIRK 活性减少内向电流,有用做脑血管舒张试剂的潜力。它对 NR1A/NR2B 受体亲和力是 NR1A/NR2A 受体的 400 倍。 | |||
T3054 |
Daurisoline
蝙蝠葛苏林碱,(R,R)-Daurisoline |
Others; Potassium Channel; Autophagy | Autophagy; Membrane transporter/Ion channel; Others |
Daurisoline ((R,R)-Daurisoline) 是一种 hERG 抑制剂,也是一种自噬阻滞剂。 | |||
TJP2872 |
Acevaltrate
Acevaltratum,乙酰缬草三酯,Acetoxyvaltrate |
ATPase; Others | Membrane transporter/Ion channel; Others |
Acevaltrate (Acevaltratum) 对人小细胞肺癌细胞系 GLC(4) 和人结肠直肠癌细胞系 COLO 320 具有高细胞毒性,IC50 值为 1-6 uM。它抑制大鼠肾和脑半球中 Na+/K+-ATP 酶活性,IC50分别为 22.8 和 42.3 μM。 | |||
T4333 |
Quinine dihydrochloride
盐酸奎宁,Quinine bimuriate |
Others | Others |
Quinine dihydrochloride (Quinine bimuriate) 是Cinchona(Rubiaceae) 各种物种的主要生物碱。它也是一种抗疟药和肌肉松弛剂(骨骼)。 | |||
T3S0081 |
Oxypeucedanin
(+-)-Oxypeucedanin,氧化前胡素,Oxypeucadanin |
Potassium Channel | Membrane transporter/Ion channel |
Oxypeucedanin ((+-)-Oxypeucedanin) 是呋喃香豆素衍生物,分离自Angelica dahurica。它是选择性开放通道阻滞剂,可抑制hKv1.5通道电流,IC50值为 76 nM。它延长心脏动作电位持续时间,是潜在的抗心律失常试剂。它通过抑制癌细胞迁移来诱导细胞凋亡。 | |||
T7938 |
Quinidine
奎尼丁,奎宁树 |
Parasite | Microbiology/Virology |
Quinidine 是一种抗心律失常剂,也是 K+通道的有效阻断剂,其 IC50值为 19.9 μM。它是一种选择性细胞色素 P450db 的有效抑制剂,也可研究疟疾。 | |||
TMS2171 |
(±)-Naringenin
(±)-柚皮素,Salipurpol,柚皮素,Naringenine,Naringenin |
Potassium Channel | Membrane transporter/Ion channel |
(±)-Naringenin (Naringenine) 是一种天然的类黄酮。它通过激活肌细胞中 BKCa 通道发挥对内皮剥脱血管的舒张作用。 | |||
T3876 |
Loureirin B
龙血素B,龙血素 B |
PAI-1; ERK; Potassium Channel; JNK | MAPK; Membrane transporter/Ion channel; Metabolism |
Loureirin B 是从剑叶龙血树中分离到的一种黄酮,是 PAI-1抑制剂,IC50值为 26.10 μM。它抑制 KATP,以及 ERK 和 JNK 的磷酸化,具有抗糖尿病的功效。 | |||
T8182 |
Guanfu base A
Guan-fu base A,关附甲素 |
P450; Potassium Channel; HER | Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Metabolism; Tyrosine Kinase/Adaptors |
Guanfu base A 是一种生物碱,分离自 Aconitum coreanum,是非竞争性 CYP2D6抑制剂,对人肝微粒体 (HLM) 的 Ki 为 1.20 μM,对人重组体 (rCYP2D6) 的 Ki 为 0.37 μM。它也是 CYP2D 的有效竞争抑制剂。它还能抑制 HERG 通道电流。Guan-fu base A 具有抗心律失常的作用。 | |||
T5S0890 |
Oleandrin
Neriostene,Folinerin,Foliandrin,欧夹竹桃苷 |
Apoptosis; ATPase; Potassium Channel; Sodium Channel | Apoptosis; Membrane transporter/Ion channel |
Oleandrin (Folinerin) 是夹竹桃属中的一种类固醇,可抑制Na+/K+-ATPase 活性,IC50为 620 nM。 | |||
T3667 |
Kalii Dehydrographolidi Succinas
Ddhads,穿琥宁,Dehydroandrographolide Succinate Potasium Salt |
Others | Others |
Kalii Dehydrographolidi Succinas (Dehydroandrographolide Succinate Potasium Salt) 从中药穿心莲中提取得到,具有免疫刺激、抗感染和抗炎作用,对病毒性肺炎和病毒性上呼吸道感染具有潜在的研究价值。 | |||
T3092 |
Nigericin sodium salt
尼日利亚菌素,尼日利亚菌素钠盐 |
Potassium Channel; NOD-like Receptor (NLR); Antibacterial; Antibiotic; NOD | Immunology/Inflammation; Membrane transporter/Ion channel; Microbiology/Virology; NF-κB |
Nigericin sodium salt 属于抗生素,是一种 NLRP3 激活剂,也是一种阳离子离子载体。Nigericin sodium 可以触发 NALP3 炎性体的激活,可抑制高尔基体功能并抑制革兰氏阳性菌的生长。 | |||
T2850 |
Bicuculline
荷包牡丹碱,(+)-Bicuculline,d-Bicuculline |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Bicuculline ((+)-Bicuculline) 是从东北延胡索中提取的一种生物碱,能阻断 Ca2+激活钾 (SK) 通道。它是一种竞争性的神经递质 GABAA 受体拮抗剂,IC50为 2 μM。 | |||
TN5073 |
Strophanthidin
毒毛旋花子甙元,Strophanthidine,葡萄球菌素 |
ATPase; Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Strophanthidin (Strophanthidine) 是黄花夹竹桃中的一种类固醇,可增加舒张期和收缩期胞内 Ca2+浓度。它在 0.1 和 1 nmol/L 增加Na+/K+-ATPase 活性,1到100 μ mol/L 抑制Na+/K+-ATPase 活性,10 和 100 nmol/L 对Na+/K+-ATPase 活性无影响。 | |||
T3S0870 |
Paederosidic acid methyl ester
鸡屎藤苷酸甲酯,紫草酸甲酯 |
ATPase; Potassium Channel; NO Synthase | Immunology/Inflammation; Membrane transporter/Ion channel |
Paederosidic acid methyl ester 是 ATP 敏感的 K+channel 通道激活剂,分离自 P. scandens。它通过激活脑中和脊髓水平中 ATP 敏感型 K+通道提高了痛觉阈值,表现出显著的中枢缓解疼痛活性。 | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01890 |
KCNA1 Protein, Human, Recombinant (His)
Voltage-gated potassium channel subunit Kv1.1,Volta... |
Human | E. coli |
KCNA1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 22.2 kDa and the accession number is Q09470. | |||
TMPH-03603 |
KcsA Protein, S. coelicolor, Recombinant (His)
pH-gated potassium channel KcsA,kcsA |
Streptomyces coelicolor | E. coli |
Acts as a pH-gated potassium ion channel; changing the cytosolic pH from 7 to 4 opens the channel. KcsA Protein, S. coelicolor, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 23.7 kDa and the accession number is P0A333. | |||
TMPH-01891 |
KCNE2 Protein, Human, Recombinant (His)
MinK-related peptide 1,Potassium voltage-gated chan... |
Human | E. coli |
KCNE2 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 17.3 kDa and the accession number is Q9Y6J6. | |||
TMPH-01889 |
KCNK3 Protein, Human, Recombinant (His & Myc)
Potassium channel subfamily K member 3,TWIK-related... |
Human | E. coli |
pH-dependent, voltage-insensitive, background potassium channel protein. Rectification direction results from potassium ion concentration on either side of the membrane. Acts as an outward rectifier when external potassium concentration is low. When external potassium concentration is high, current is inward. KCNK3 Protein, Human, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 50.5 kDa and the accession number is O... | |||
TMPH-01892 |
ATP4A Protein, Human, Recombinant (His & Myc)
ATP4A,Gastric H(+)/K(+) ATPase subunit alpha,Potassium |
Human | E. coli |
ATP4A Protein, Human, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 54.6 kDa and the accession number is P20648. | |||
TMPH-01028 |
KCNMA1 Protein, Human, Recombinant
K(VCA)alpha,Calcium-activated potassium channel sub... |
Human | E. coli |
KCNMA1 Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 17.2 kDa and the accession number is Q12791. | |||
TMPH-01893 |
ATP4B Protein, Human, Recombinant (GST)
Proton pump beta chain,Gastric H(+)/K(+) ATPase subunit beta... |
Human | E. coli |
ATP4B Protein, Human, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 53.6 kDa and the accession number is P51164. | |||
TMPH-01894 |
ATP4B Protein, Human, Recombinant
Proton pump beta chain,Potassium-transporting ATPas... |
Human | E. coli |
ATP4B Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 26.6 kDa and the accession number is P51164. | |||
TMPH-02309 |
KCNAB2 Protein, Human, Recombinant (His & SUMO)
Kv-beta-2,K(+) channel subunit beta-2,KCNAB2,Voltage-gated <... |
Human | E. coli |
KCNAB2 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 57.0 kDa and the accession number is Q13303. | |||
TMPH-01358 |
FXYD3 Protein, Human, Recombinant (His & SUMO)
Phospholemman-like,Chloride conductance inducer protein Mat-... |
Human | E. coli |
FXYD3 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 20.5 kDa and the accession number is Q14802. | |||
TMPH-01714 |
CHRM1 Protein, Human, Recombinant (His)
Muscarinic acetylcholine receptor M1,CHRM1 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 20.8 kDa and the accession number is P11229. | |||
TMPH-01717 |
CHRM5 Protein, Human, Recombinant (His)
CHRM5,Muscarinic acetylcholine receptor M5 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM5 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 31.5 kDa and the accession number is P08912. | |||
TMPY-03615 |
CSEN Protein, Human, Recombinant (His)
Kv channel interacting protein 3, calsenilin,DREAM,KCHIP3,CS... |
Human | E. coli |
KCNIP3 (Potassium Voltage-Gated Channel Interacting Protein 3, also known as CSEN) is a Protein Coding gene. CSEN is a member of the family of voltage-gated potassium (Kv) channel-interacting proteins, which belong to the recoverin branch of the EF-hand superfamily. Members of this family are integral subunit components of native Kv4 channel complexes that may regulate A-type currents, and hence neuronal excitability, in response to changes in intracellular calcium. CSEN also functions as a calc... | |||
TMPH-01716 |
CHRM3 Protein, Human, Recombinant (B2M & His)
Muscarinic acetylcholine receptor M3,CHRM3 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM3 Protein, Human, Recombinant (B2M & His) is expressed in E. coli expression system with N-6xHis-B2M tag. The predicted molecular weight is 40.7 kDa and the accession number is P20309. | |||
TMPH-03338 |
CHRM1 Protein, Rat, Recombinant (His)
Muscarinic acetylcholine receptor M1,CHRM1 |
Rat | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. CHRM1 Protein, Rat, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 21.1 kDa and the accession number is P08482. | |||
TMPJ-00652 |
PSD-95 Protein, Rat, Recombinant (His)
PSD95,SAP90,Disks large homolog 4,SAP-90,PSD-95,Postsynaptic... |
Rat | E. coli |
Disks large homolog 4(DLG4) is a cell membrane protein and it is a member of the membrane-associated guanylate kinase (MAGUK) family. The protein contains 1 guanylate kinase-like domain,3 PDZ (DHR) domains and 1 SH3 domain. With PSD-93 it is recruited into the same NMDA receptor and potassium channel clusters. These two MAGUK proteins may interact at postsynaptic sites to form a multimeric scaffold for the clustering of receptors, ion channels, and associated signaling proteins. DLG4 is the be... | |||
TMPH-01609 |
LGI1 Protein, Human, Recombinant (His & Myc)
Leucine-rich glioma-inactivated protein 1,Epitempin-1,LGI1 |
Human | E. coli |
Regulates voltage-gated potassium channels assembled from KCNA1, KCNA4 and KCNAB1. It slows down channel inactivation by precluding channel closure mediated by the KCNAB1 subunit. Ligand for ADAM22 that positively regulates synaptic transmission mediated by AMPA-type glutamate receptors. Plays a role in suppressing the production of MMP1/3 through the phosphatidylinositol 3-kinase/ERK pathway. May play a role in the control of neuroblastoma cell survival. | |||
TMPY-01854 |
DPP10 Protein, Human, Recombinant (His)
DPPY,DPRP3,DPRP-3,DPL2,dipeptidyl-peptidase 10 (non-function... |
Human | HEK293 Cells |
Inactive dipeptidyl peptidase 1, also known as Dipeptidyl peptidase IV-related protein 3, Dipeptidyl peptidase X, Dipeptidyl peptidase-like protein 2, DPRP-3, DPL2 and DPP1, is a single-pass type II membrane protein which belongs to thepeptidase S9B family.DPPIV subfamily. It may modulate cell surface expression and activity of the potassium channels KCND1 and KCND2. DPP1 / DPRP3 has no detectable protease activity, most likely due to the absence of the conserved serine residue normally p... | |||
TMPH-01715 |
CHRM2 Protein, Human, Recombinant (His)
CHRM2,Muscarinic acetylcholine receptor M2 |
Human | E. coli |
The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is adenylate cyclase inhibition. Signaling promotes phospholipase C activity, leading to the release of inositol trisphosphate (IP3); this then triggers calcium ion release into the cytosol. CHRM2 Protein, Human, Recombinant (His) is expressed in E. col... | |||
TMPH-03399 |
VAMP2 Protein, Rat, Recombinant (His)
Vesicle-associated membrane protein 2,Vamp2,Synaptobrevin-2 |
Rat | E. coli |
Involved in the targeting and/or fusion of transport vesicles to their target membrane. Major SNARE protein of synaptic vesicles which mediates fusion of synaptic vesicles to release neurotransmitters. Essential for fast vesicular exocytosis and activity-dependent neurotransmitter release as well as fast endocytosis that mediates rapid reuse of synaptic vesicles. Modulates the gating characteristics of the delayed rectifier voltage-dependent potassium channel KCNB1. VAMP2 Protein, Rat, Recombina... | |||
TMPJ-00988 |
SEPHS1 Protein, Human, Recombinant (His)
water dikinase 1,SELD,Selenophosphate synthase 1,SEPHS1,SPS1... |
Human | HEK293 Cells |
Selenophosphate synthetase 1 (SEPHS1) belongs to the selenophosphate synthase 1 family, Class II subfamily. It has four different isoforms by alternative splicing. Isoform 1 and isoform 2 are gradually expressed during the cell cycle until G2/M phase and then decreased, which Isoform 3 is gradually expressed during the cell cycle until S phase and then decreased. SEPHS1 can be activated by phosphate ions and by potassium ions. It can synthesize synthesizes selenophosphate from selenide and ATP.... | |||
TMPY-03491 |
Lysozyme 2 Protein, Human, Recombinant (His)
lysozyme like 2,LYZL2 |
Human | Baculovirus Insect Cells |
The lysozyme 2 gene is a member of a family of lysozyme-like genes. Lysozymes, especially C-type lysozymes, are well-recognized bacteriolytic factors widely distributed in the animal kingdom and play a mainly protective role in host defense. Lysozymes damage bacterial cell walls by catalyzing the hydrolysis of 1,4-beta-linkages between N-acetylmuramic acid and N-acetyl-D-glucosamine residues in a peptidoglycan and between N-acetyl-D-glucosamine residues in chitodextrins. Lysozyme is part of the ... | |||
TMPY-01695 |
CASPR2 Protein, Mouse, Recombinant (His)
5430425M22Rik,Caspr2,contactin associated protein-like 2,mKI... |
Mouse | HEK293 Cells |
CNTNAP2/CASPR2 is a member of the neurexin family which functions in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin N-terminal-like domains and a putative PDZ binding site. CNTNAP2/CASPR2 is localized at the juxtaparanodes of myelinated axons, and media... | |||
TMPY-04561 |
SGK3 Protein, Human, Recombinant (His & GST)
serum/glucocorticoid regulated kinase family, member 3,SGK2,... |
Human | Baculovirus Insect Cells |
Serine / threonine-protein kinase Sgk3, also known as Serum / glucocorticoid-regulated kinase 3, Serum / glucocorticoid-regulated kinase-like and SGK3, is a cytoplasmic vesicle protein that belongs to the protein kinase superfamily and AGC Ser/Thr protein kinase family. SGK3 contains one AGC-kinase C-terminal domain, one protein kinase domain and one PX (phox homology) domain. Two specific sites of SGK3, one in the kinase domain (Thr-32) and the other in the C-terminal regulatory region (Ser-486... | |||
TMPY-06599 |
ATP1B4 Protein, Human, Recombinant (His)
ATPase, Na+/K+ transporting, β 4 polypeptide,ATPase, Na+/K+ ... |
Human | E. coli |
ATP1B4 is a member of the X(+)/potassium ATPases subunit beta family. It is highly expressed in skeletal muscle and at a lower level in heart. ATP1B4 gene can be found in all vertebrate genomes sequenced to date. However, this gene has undergone a change in function in placental mammals compared to other species. Specifically, in fish, avian, and amphibian species, this gene encodes plasma membrane-bound beta-subunits of Na, K-ATPase. In placental mammals, the encoded protein interacts with the ... | |||
TMPH-02521 |
PYCARD Protein, Mouse, Recombinant (His & Myc)
Pycard,PYD and CARD domain-containing protein,Apoptosis-asso... |
Mouse | E. coli |
Functions as key mediator in apoptosis and inflammation. Promotes caspase-mediated apoptosis involving predominantly caspase-8 and also caspase-9 in a probable cell type-specific manner. Involved in activation of the mitochondrial apoptotic pathway, promotes caspase-8-dependent proteolytic maturation of BID independently of FADD in certain cell types and also mediates mitochondrial translocation of BAX and activates BAX-dependent apoptosis coupled to activation of caspase-9, -2 and -3. Involved ... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T70313 |
Indoxyl Sulfate-d5 potassium salt
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Indoxyl sulfate-d5 is intended for use as an internal standard for the quantification of indoxyl sulfate by GC- or LC-MS. Indoxyl sulfate is a uremic toxin and a metabolite of tryptophan. It is formed via sulfation of indole, an intermediate generated from tryptophan by intestinal bacteria, by the sulfotransferase (SULT) isoform 1A1 variant 2 (SULT1A1*2) in the liver. Indoxyl sulfate activates the aryl hydrocarbon receptor (AhR) in HepG2 40/6 hepatoma cells (EC50 = 12.1 nM in a reporter assay). ... | |||
TMID-0234 |
Penicillin G-d5 potassium salt
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Penicillin G-d5 potassium salt 是 Penicillin G potassium salt 的氘代化合物。Penicillin G potassium salt 的 CAS 号为 113-98-4。Benzylpenicillin potassium是青霉素家族的一种速效抗生素。 | |||
TMIH-0434 |
PHPB-d7
(R/S)-2-(1-hydroxy-n-pentyl)benzoic acid potassium salt-d7 |
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PHPB-d7 是 PHPB 的氘代化合物。 | |||
TMID-0125 |
Canrenone-d4
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Canrenone-d4 是 Canrenone 的氘代化合物。Canrenone 的 CAS 号为 976-71-6。Canrenone 是一种醛固酮 (aldosterone) 拮抗剂,广泛用作利尿剂。 | |||
TMID-0124 |
Canrenone-d6
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Canrenone-d6 是 Canrenone 的氘代化合物。Canrenone 的 CAS 号为 976-71-6。Canrenone 是一种醛固酮 (aldosterone) 拮抗剂,广泛用作利尿剂。 | |||
T73713 |
Flupirtine-d4 hydrochloride
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Flupirtine-d4 (D 9998-d4) hydrochloride,Flupirtine (D 9998) hydrochloride的氘代物,为神经元钾通道开放剂,具有拮抗NMDA受体的作用。 | |||
TMIH-0601 |
Vonoprazan-d3
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Vonoprazan-d3 是 Vonoprazan 的氘代化合物。Vonoprazan 的 CAS 号为 881681-00-1。Vonoprazan 是一种质子泵抑制剂,是口服活性钾竞争性酸阻断剂,有抗分泌作用。在 pH 为 6.5 时,它抑制猪胃微粒体中的 H+,K+-ATPase 酶活性,IC50值为 19 nM。它可用于研究胃酸相关疾病。 | |||
TMIH-0086 |
Amifampridine-d3 2HCl
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Amifampridine-d3 2HCl 是 Amifampridine 2HCl 的氘代化合物。Amifampridine 2HCl 的 CAS 号为 54-96-6。Amifampridine 可用于罕见肌肉疾病的研究。 | |||
TMIH-0602 |
Vonoprazan-d4
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Vonoprazan-d4 是 Vonoprazan 的氘代化合物。Vonoprazan 的 CAS 号为 881681-00-1。Vonoprazan 是一种质子泵抑制剂,是口服活性钾竞争性酸阻断剂,有抗分泌作用。在 pH 为 6.5 时,它抑制猪胃微粒体中的 H+,K+-ATPase 酶活性,IC50值为 19 nM。它可用于研究胃酸相关疾病。 | |||
TMIJ-0210 |
Bupivacaine-d9
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Bupivacaine-d9 是 Bupivacaine 的氘代化合物。Bupivacaine 的 CAS 号为 38396-39-3。Bupivacaine 是一种 NMDA 受体抑制剂。Bupivacaine 可以阻断钠、L-钙和钾通道。Bupivacaine 有效阻断 SCN5A 通道,IC50 为 69.5 μM。Bupivacaine 可用于慢性疼痛的研究。 | |||
T36059 |
Dichlorphenamide-13C6
Dichlorphenamide-13C6 |
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Dichlorphenamide-13C6is intended for use as an internal standard for the quantification of dichlorphenamide by GC- or LC-MS. Dichlorphenamide is a sulfonamide and an orally bioavailable carbonic anhydrase (CA) inhibitor (Kis = 1.20, 38, 50, and 50 nM for the human CA isoforms CAI, CAII, CAIX, and CAXII, respectively).1It lowers intraocular pressure in rabbits when 50 μl of a 10% solution is applied topically to the eye.2Dichlorphenamide rescues the potassium deficiency and prevents insulin-induc... | |||
TMID-0070 |
Amiodarone-d10 Hydrochloride
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Amiodarone-d10 Hydrochloride 是 Amiodarone Hydrochloride 的氘代化合物。Amiodarone Hydrochloride 的 CAS 号为 19774-82-4。Amiodarone hydrochloride是一种抗心绞痛和 III 类抗心律失常药物,通过抑制钾通道和电压门控钠通道来增加心室和心房肌肉作用的持续时间,可导致心率和血管阻力降低。它通过成纤维细胞中的ERK1/2和p38 MAPK信号传导诱导细胞增殖和肌成纤维细胞分化,可研究室上性和室性心律失常。 | |||
TMID-0069 |
Amiodarone-d4 HCl
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Amiodarone-d4 HCl 是 Amiodarone HCl 的氘代化合物。Amiodarone HCl 的 CAS 号为 19774-82-4。Amiodarone hydrochloride是一种抗心绞痛和 III 类抗心律失常药物,通过抑制钾通道和电压门控钠通道来增加心室和心房肌肉作用的持续时间,可导致心率和血管阻力降低。它通过成纤维细胞中的ERK1/2和p38 MAPK信号传导诱导细胞增殖和肌成纤维细胞分化,可研究室上性和室性心律失常。 | |||
T69600 |
Spermidine-d6
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Spermidine-d6 is intended for use as an internal standard for the quantification of spermidine by GC- or LC-MS. Spermidine is an endogenous polyamine. It is formed from putrescine by spermidine synthase. Spermidine (25 µM) inhibits the activity of the human inward-rectifying potassium channel Kir2.3 in a patch-clamp assay. It induces autophagy in HeLa cells when used at a concentration of 100 µM and increases the lifespan of D. melanogaster, yeast, and C. elegans. Spermidine (30 mM in the drinki... | |||
T71402 |
Nicorandil-d4
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Nicorandil-d4 is intended for use as an internal standard for the quantification of nicorandil by GC- or LC-MS. Nicorandil is an activator of sulfonylurea receptor 2B (SUR2B) linked to ATP-sensitive potassium channel Kir6.2 (EC50 = ~10 µM) and a nitric oxide (NO) donor. It is selective for SUR2B/Kir6.2 over the SUR2A/Kir6.2 channel (EC50 = >500 µM). Nicorandil activates soluble guanylate cyclase in a cell-free assay and relaxes partially depolarized isolated bovine coronary artery strips (EC50 =... | |||
T71981 |
Gliclazide-d4
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Gliclazide-d4 is intended for use as an internal standard for the quantification of gliclazide by GC- or LC-MS. Gliclazide is a sulfonylurea and an inhibitor of pancreatic β-cell ATP-sensitive potassium (KATP) channels. It is selective for pancreatic β-cell over cardiac and arterial smooth muscle cell KATP channels. Gliclazide (5 μM) increases insulin-induced glucose uptake and glucose transporter 4 (GLUT4) translocation to the plasma membrane in a differentiated 3T3L1 adipocyte model of insulin... | |||
T71303 |
Flufenamic Acid-d4
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Flufenamic acid-d4 is intended for use as an internal standard for the quantification of flufenamic acid by GC- or LC-MS. Flufenamic acid is a non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor (IC50s = 3 and 9.3 µM for human COX-1 and COX-2, respectively). Flufenamic acid inhibits TNF-α-induced increases in COX-2 levels and NF-κB activation in HT-29 colon cancer cells in a concentration-dependent manner. It inhibits calcium influx induced by fMLP or A23187 in human polymorphonuclear... |