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Cat. No. | Product Name | ||
---|---|---|---|
L7850 | 高溶解性3D结构多样性片段化合物库 | 1079 compounds | |
高溶解性3D 结构多样性片段库包含1079 个化合物。 | |||
L4520 | 抗菌活性库 | 904 compounds | |
904 种具有抗菌活性的化合物,是抗菌药物研发的有力工具; | |||
L3900 | DNA 损伤和修复分子库 | 910 compounds | |
910 个与 DNA 损伤和修复紧密相关的化合物集合,是高通量筛选,高内涵筛选的良好载体; | |||
L9410 | 共价抑制剂库 | 1920 compounds | |
1920 种小分子的独特集合,包含已发现的共价抑制剂以及包含某些共价反应基团常见弹头的分子,如氯乙酰基,2-氯丙酰基,丙烯酰基,1-丙-2-炔基,1-丁-2-炔基,酮羰基,二硫键等,可以用于共价抑制剂药物研发; | |||
L3980 | DNA损伤/修复库Plus | 667 compounds | |
667 种 DNA 损伤/修复靶向、结构新颖的化合物; | |||
L1720 | 核苷类化合物库 | 334 compounds | |
334 种核苷类化合物,包括核苷酸、核苷酸类似物及衍生物等,适用于抗病毒、抗肿瘤、抗真菌、抗抑郁等药物的研发; | |||
L2180 | 抗肿瘤库Plus | 1468 compounds | |
1468 种抗肿瘤相关、结构新颖的化合物; | |||
L2501 | 人内源代谢化合物库 Plus | 1283 compounds | |
1283种内源性生物活性化合物的独特集合,用于高通量、高内涵筛选。 | |||
L9240 | 农药化合物库 | 270 compounds | |
270种农药相关化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L7100 | 抗肥胖化合物库 | 2247 compounds | |
2247 个抗肥胖化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L9210 | 儿童药物库 | 972 compounds | |
972 种儿童药物的独特集合,可用于高通量筛选和高内涵筛选 | |||
L2190 | 抗肺癌化合物库 | 1702 compounds | |
1702 种与肺癌相关的化合物,可以用于抗肺癌药物研发和药理研究; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T23101 |
o-3M3FBS
|
Others | Others |
o-3M3FBS 是 m-3M3FBS 的阴性对照。它以独立于 PLC 的机制及拮抗方式抑制内向和外向电流。它以与 m-3M3FBS 竞争的方式增加 [Ca2+]i 增加。 | |||
T8581 |
Flecainide hydrochloride
|
Others | Others |
Flecainide hydrochloride 是一种用于预防和治疗异常快速心率的药物。这包括室性和室上性心动过速。 | |||
T4573 |
Cyclothiazide
|
GluR | Neuroscience |
Cyclothiazide 是AMPA 受体的正变构调节剂,可快速抑制 AMPA 受体脱敏,并缓慢增强 AMPA 电流。它可以阻断天然和异源表达的AMPA 受体脱敏。 | |||
T16348 |
NS5806
NS-5806 |
Potassium Channel | Membrane transporter/Ion channel |
NS5806 是钾电流的激活剂,可增加 KV4.3/KChIP2峰值电流幅度,EC50值为 5.3 μM。它会在包含 KChIP2 的通道复合体中降低 KV4.2 和 KV4.3 电流衰减。 | |||
T15286 |
Flindokalner
BMS-204352 |
Potassium Channel | Membrane transporter/Ion channel |
Flindokalner (BMS-204352) 是一种钾离子通道调节剂。它是大电导钙激活 K 通道正向调节剂。它是在 HEK293 细胞中表达的所有神经元 Kv7通道亚型的正调节剂。它在 Kv7.1 通道 (Ki=3.7 μM) 处显示负调节活性,并充当 GABAA 受体的负调节剂。它在体内显示出抗焦虑功效。 | |||
T23280 |
Ruthenium Red
钌红,Ammoniated ruthenium oxychloride |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Ruthenium Red (Ammoniated ruthenium oxychloride) 是一种 L 型钙电流 (ICa) 阻断剂,是一种聚阳离子染料,广泛用于电子显微镜 (EM) 下细胞、组织和营养细菌的观察。它能与磷脂和脂肪酸反应强烈,并与酸性粘多糖结合。 | |||
T16347 |
NS3623
|
Potassium Channel | Membrane transporter/Ion channel |
NS3623 是 hERG1 (KV11.1)钾通道激活剂,激活IKr 和Ito 电流,具有抗心律失常作用。NS3623也是 hERG1 通道抑制剂。 | |||
T2451 |
GlyH-101
GlyH 101 |
CFTR; Autophagy | Autophagy; Membrane transporter/Ion channel |
GlyH-101 是一种可渗透入细胞的 CFTR 阻断剂,Ki 为1.4 uM。 | |||
T7775 |
A2764 dihydrochloride
|
Potassium Channel | Membrane transporter/Ion channel |
A2764 dihydrochloride 是高选择性的TRESK (K2P18.1)抑制剂,对 TREK-1 和 TALK-1 有抑制作用。它相比基底 mTRESK 电流,对激活渠道更敏感 (IC50= 6.8 μM)。它可导致细胞去极化,增加细胞的兴奋性,在探索 TRESK 通道在偏头痛和痛觉中的作用中具有研究的价值。 | |||
T1434 |
Clarithromycin
A-56268,克拉霉素 |
P450; ribosome; MRP; Antibacterial; Antibiotic; Autophagy | Autophagy; Immunology/Inflammation; Metabolism; Microbiology/Virology |
Clarithromycin (A-56268) 具有广谱的抗菌活性。它抑制 CYP3A4催化的三唑仑 α-羟基化,IC50(Ki) 值为 56 (43) μM。它抑制 HERG 钾电流。它可削弱连接 hERG1 和 PI3K 的信号通路影响自噬流 。 | |||
T9009 |
ICA-105574
ICA,3-nitro-N-[4-phenoxyphenyl]-benzamide |
HER | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
ICA-105574 (ICA) 是 hERG 通道激活剂。它通过消除 hERG 通道的失活从而增强 hERG 通道活性。它可以把电流幅度急剧增加到原来的 10 倍以上,其EC50值为 0.5 +/- 0.1 μM,Hill 斜率 (n(H)) 为 3.3 +/- 0.2。 | |||
T3574 |
Sematilide hydrochloride
司美利特,CK-1752A,CK-1752,Sematilide HCl |
Potassium Channel | Membrane transporter/Ion channel |
Sematilide hydrochloride (CK-1752) 是一种选择性的 IKr 通道阻滞剂。Sematilide 以浓度依赖性抑制延迟整流钾通道 (K+current),IC50为 25 μM。Sematilide 是一种 III 类抗心律不齐剂。 | |||
T6541 |
Ibutilide Fumarate
Corvert Fumarate,U70226E,富马酸伊布利特 |
Calcium Channel; Sodium Channel | Membrane transporter/Ion channel; Metabolism |
Ibutilide Fumarate (U70226E) 是一种 III 类抗心律失常药物,可作用于急性心梗阻塞。 | |||
T15758 |
Linopirdine
利诺吡啶,DuP 996 |
Potassium Channel; TRP/TRPV Channel | Membrane transporter/Ion channel |
Linopirdine (DuP 996) 是一种口服有效的,选择性 M 型 K+电流 (IM;Kv7;KCNQ Channels) 抑制剂,IC50为 2.4 μM。Linopirdine 是TRPV1激活剂。Linopirdine 是一种公认的认知增强药物,可增加大鼠脑组织中乙酰胆碱的释放。 | |||
T15207 |
Eleclazine hydrochloride
GS 6615 hydrochloride |
Sodium Channel | Membrane transporter/Ion channel |
Eleclazine hydrochloride (GS 6615 hydrochloride) 是新型 Na+电流抑制剂,IC50是0.7 uM。 | |||
TP1858L |
Phe-Met-Arg-Phe, amide acetate
Phe-Met-Arg-Phe, amide acetate(64190-70-1 freebase) |
Potassium Channel | Membrane transporter/Ion channel |
Phe-Met-Arg-Phe, amide acetate(64190-70-1 freebase) 剂量依赖性 (ED50=23 nM) 激活肽能尾背神经元中的 K+ 电流。这种肽似乎在大脑的某些区域与神经肽 Y 一起定位。 | |||
T17262 |
XE 991 dihydrochloride
|
Others; Potassium Channel | Membrane transporter/Ion channel; Others |
XE 991 dihydrochloride 是有效的 Kv7 (KCNQ)通道阻滞剂,抑制 Kv7.1 (KCNQ1),Kv7.2 (KCNQ2),Kv7.2 + Kv7.3 (KCNQ3)通道以及 M-current,IC50分别为 0.75 µM、0.71 µM、0.6 μM、0.98 µM。 | |||
T10893 |
CS-722 Free base
|
Others | Others |
CS-722 Free base是一种合成的中枢作用肌肉松弛剂,它展现出肌肉松弛效果并抑制脊髓反射。可能通过限制钠和钙流动,从而在海马培养物中减少自发的抑制性和兴奋性突触后电流。 | |||
T13374 |
YM758
|
Others | Others |
YM758 是 If 电流通道的抑制剂。 | |||
T22745 |
DPO-1
|
Potassium Channel | Membrane transporter/Ion channel |
DPO-1 可以高效抑制电压门控钾离子通道Kv1.5,也可以阻断超快速延迟整流钾电流。它能够预防房性心律失常。 | |||
T26016 |
R 56865
R-56865,R56865 |
Sodium Channel | Membrane transporter/Ion channel |
R 56865 是一种弱电位操作通道抑制剂,抑制人分离心肌细胞的晚期钠电流。 | |||
T0193 |
Manidipine dihydrochloride
Manidipine 2HCl,盐酸马尼地平,CV-4093 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Manidipine dihydrochloride (Manidipine 2HCl) 是一种钙离子通道阻断剂,能抑制钙流,IC50=2.6 nM。 | |||
T30249 |
AZD 7009
AZD-7009,AZD7009 |
Sodium Channel | Membrane transporter/Ion channel |
AZD 7009是一种新型抗心律失常化合物,对CHO K1细胞中 hNav1.5的钠电流具有抑制作用,IC50为11 uM。AZD 7009 对离体兔心房和心室肌细胞的晚期钠电流具有抑制作用,对e -4031诱导的动作电位持续时间延长具有抑制作用,促使浦肯野纤维的早期后去极化(EADs)。 | |||
T78570 |
XE991
|
Potassium Channel | Membrane transporter/Ion channel |
XE991 是一种新型具有选择性的 Kv7 (KCNQ)通道阻滞剂。XE 991 抑制 Kv7.1 (KCNQ1)、Kv7.2 (KCNQ2)、Kv7.2 + Kv7.3 (KCNQ3)通道及M-current,可用于研究神经系统疾病。 | |||
T19765 |
MDK-4025
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
MDK-4025 是锥体神经元中高压激活 (HVA) Ca2+ 电流的抑制剂。 | |||
T1874 |
PPQ-102
PPQ102,CFTR Inhibitor,PPQ 102 |
CFTR; Autophagy | Autophagy; Membrane transporter/Ion channel |
PPQ-102 (CFTR Inhibitor) 是一种CFTR 抑制剂,可以完全抑制CFTR 氯化物电流,IC50为90 nM。 | |||
T21769L |
β-Pompilidotoxin Acetate
β-Pompilidotoxin Acetate(216064-36-7 Free base) |
Sodium Channel | Membrane transporter/Ion channel |
β-Pompilidotoxin Acetate 是一种黄蜂毒肽。 它可以减缓钠通道的失活并增加细胞中的稳态钠电流。 | |||
T2049 |
GS967
GS458967 |
Sodium Channel | Membrane transporter/Ion channel |
GS967 是一种有效的、选择性的心脏晚期钠电流(late I Na)抑制剂,心室肌细胞和心脏中的IC50分别为0.13和0.21 μM。 | |||
T31488 |
Dimethindene
Dimetindeno,Z 2001,Dimetindene,二甲茚定,Z-2001,Z2001 |
Potassium Channel; Endogenous Metabolite; AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Dimethindene (Dimetindeno) 是 H1受体的选择性拮抗剂,阻断 K+电流。Dimethindene 表现出抗组胺和抗胆碱作用。 | |||
T7505 |
Azimilide Dihydrochloride
NE-10064 Dihydrochloride,盐酸阿齐利特 |
Potassium Channel | Membrane transporter/Ion channel |
Azimilide Dihydrochloride (NE-10064 Dihydrochloride) 是 I(Ks) 和 I(Kr) 抑制剂,具有抗心律失常活性。 | |||
T27205 |
DPI 201-106
DPI-201-106 |
Sodium Channel | Membrane transporter/Ion channel |
DPI 201-106对电压门控钠通道的有心脏选择性调节活性,从而产生正性肌力作用。DPI 201-106 具有协同肌膜和细胞内作用机制。 | |||
T8839 |
ICCB280
|
Apoptosis; Others | Apoptosis; Others |
ICCB280 是一种 C/EBPα诱导剂,通过激活 C/EBPα 并影响其下游靶点,具有终末分化、增殖停滞和凋亡的抗白血病特性。 | |||
T73267 |
VU6036720
|
Potassium Channel | Membrane transporter/Ion channel |
VU6036720是一种有效且具有选择性的异构体Kir4.1/5.1抑制剂。VU6036720通过降低通道开路概率和单通道电流幅度来抑制Kir4.1/5.1活性。 | |||
T5585 |
AM-92016 hydrochloride
|
Potassium Channel | Membrane transporter/Ion channel |
AM-92016 hydrochloride 是一种整流钾电流的特异性阻断剂。它能够延迟整流钾通道,使膜复极化,限制神经冲动的持续时间。 | |||
T7578 |
REVERSE T3
碘塞罗宁,3,3',5'-triiodo-L-thyronine |
Thyroid hormone receptor(THR) | Endocrinology/Hormones |
Reverse T3 (3,3',5'-triiodo-L-thyronine) 是由甲状腺素原脱碘后产生的甲状腺激素。它可抑制由其它甲状腺激素类似物引起的新生大鼠心肌细胞中钠电流增加的作用。 | |||
T8617 |
GMQ hydrochloride
NSC 403387 hydrochloride |
Others | Others |
GMQ hydrochloride (NSC-403387 hydrochloride) 是一种有效的选择性酸感应离子通道 (ASIC) 调节剂。它在中性 pH 值下激活 ASIC3 通道并阻止酸引起的最大峰值电流。 | |||
T60536 |
Terodiline
|
Calcium Channel; HER; AChR | Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Metabolism; Neuroscience; Tyrosine Kinase/Adaptors |
Terodiline 是一种具有抗胆碱能和钙拮抗特性的仲胺,可阻断 hERG 电流(IC50:375 nM)。Terodiline 具有心脏毒性,可用于研究逼尿肌不稳定引起的疾病。 | |||
T60224 |
1H-Pyrrolo[2,1-c][1,2,4]benzothiadiazine, 2,3,3a,4-tetrahydro-, 5,5-dioxide, (3aR)-
|
GluR | Neuroscience |
1H-Pyrrolo[2,1-c][1,2,4]benzothiadiazine, 2,3,3a,4-tetrahydro-, 5,5-dioxide, (3aR)-是S 18986的低活性异构体。S 18986是一种AMPA 受体阳性调节剂,EC2(浓度为AMPA 诱导电流强度的两倍)为35μM。 | |||
TP1813L |
Dynorphin A 1-10 acetate(79994-24-4 free base)
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Dynorphin A 1-10 acetate(79994-24-4 free base) 是一种内源性 opioid 样物质神经肽,与 κ-opioid 样物质受体的细胞外环 2 结合。 Dynorphin A (1-10) 还阻断 NMDA 激活的电流,IC50 为 42.0 μM。 | |||
T0866 |
Propafenone
Rythmol,普罗帕酮,Propafenonum |
Potassium Channel; MRP; Sodium Channel | Immunology/Inflammation; Membrane transporter/Ion channel |
Propafenone (Propafenonum) 是钠通道阻滞剂,它对 β 受体具有高亲和力 (IC50=32 nM)。它能够阻断瞬时外向钾电流 (Ito) (IC50: 4.9 nM) 和持续延迟整流器K+电流 (Isus) (IC50: 8.6 nM) ,具有抗心律失常的作用。它能够诱导线粒体功能障碍及诱导细胞凋亡,从而抑制食管癌增殖。 | |||
T0207 |
Ranolazine dihydrochloride
盐酸雷诺嗪,雷诺嗪二盐酸盐,RS 43285,Ranolazine 2HCl |
Calcium Channel; Sodium Channel; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Ranolazine dihydrochloride (Ranolazine 2HCl) 是一种抗心绞痛和抗缺血剂,可通过抑制内向钠电流的后期作用来发挥功效,而不会影响心率或血压。它对 INa 和 IKr 的 IC50值分别为 6 μM 和 12 μM。它还是脂肪酸氧化的部分抑制剂。 | |||
T15555 |
IK1 inhibitor PA-6
|
Potassium Channel | Membrane transporter/Ion channel |
IK1 inhibitor PA-6 是一种喷他脒类似物,是选择性的 IK1(KIR2.x 离子通道携带向内整流电流) 抑制剂,对人和老鼠中 KIR2.x 电流的 IC50值为 12-15 nM。它可上调 KIR2.1 的蛋白表达,诱导细胞内 KIR2.1 的蛋白的积累。它在房颤和心律失常的研究中具有潜力。 | |||
T6476 |
Dofetilide
UK 68789,UK-68798,Tikosyn,多非利特 |
Potassium Channel | Membrane transporter/Ion channel |
Dofetilide (UK 68789) 是一种具有口服活性、有效的且特异性的IKr 阻滞剂,作为 III 类抗心律失常药物。Dofetilide 可用于心血管疾病研究。 | |||
TP1942L1 |
pep2-AVKI acetate(1315378-69-8 free base)
|
Others | Others |
pep2-AVKI acetate(1315378-69-8 free base) 选择性破坏 AMPA 受体亚基 GluA2(在 C 末端 PDZ 位点)与与 C 激酶 (PICK1) 相互作用的蛋白质结合的抑制剂肽。不影响 GluA2 与 GRIP 或 ABP 的结合,也不增加 AMPA 电流幅度或影响长期抑制 (LTD)。 | |||
T1046 |
Mexiletine hydrochloride
KOE-1173 (hydrochloride),Mexiletine HCl,KO1173,盐酸美西律 |
AhR; Sodium Channel | Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism |
Mexiletine hydrochloride (KOE-1173 hydrochloride) 是一种电压门控钠通道阻滞剂,是 IB 类抗心律失常药。 Mexiletine hydrochloride 通过抑制心肌细胞内钠电流,从而降低心脏动作电位(0相)上升速率,并且降低浦肯野纤维的自律性而发挥抗心律失常作用。 | |||
T16516 |
PG01
Phenylglycine-01 |
CFTR | Membrane transporter/Ion channel |
PG01是一种有效的CFTR Cl-通道增效剂,PG01对 ΔF508(Ka 为 0.3 μM)有效。PG01 对 E193K,G970R 和 G551D (CFTR 突变体)也 有效,Kd 值分别为 0.22 μM,0.45 μM 和 1.94 μM 。PG01在加入Forskolin 后可增加ΔF508-CFTR Cl-电流,纠正CFTR 突变体的门控缺陷。 | |||
TP1884L1 |
Neuropeptide SF(mouse,rat) acetate
Neuropeptide SF(mouse,rat) acetate(230960-31-3 free base) |
Neuropeptide Y Receptor | GPCR/G Protein; Neuroscience |
Neuropeptide SF(mouse,rat) acetate (Neuropeptide SF(mouse,rat) acetate (230960-31-3 free base)) 是一种有效的神经肽 FF 受体激动剂,对 NPFF1 和 NPFF2 的 Ki 分别为 48.4 nM 和 12.1 nM。它增加了异源表达的酸感应离子通道 3 (ASIC3) 的持续电流的幅度。 | |||
T2535 |
Ivabradine hydrochloride
盐酸伊伐布雷定,S 16257-2,Ivabradine HCl |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Ivabradine hydrochloride (S 16257-2) 是一种可口服的,超极化激活的环核苷酸门控离子通道通道阻滞剂。 | |||
T32191 |
Irdabisant
CEP-26401,CEP 26401,CEP26401 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Irdabisant (CEP-26401) 是选择性、口服活性和血脑屏障渗透性的组胺 H3 受体 (histamine H3 receptor, H3R) 拮抗剂/逆激动剂。Irdabisant 显示人 H3R 和大鼠 H3R 的 Ki 分别为 2.0 nM 和 7.2 nM。Irdabisant 抑制 hERG 电流的活性相对较低 (IC50= 13.8 μM)。在大鼠社会认知模型中,Irdabisant 具有认知增强和唤醒作用。Irdabisant 可用于研究精神分裂症或认知障碍。 | |||
T27117 |
DA-6886
DA6886,DA 6886 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
DA-6886 是一种 5-羟色胺受体 4(5-HT4)激动剂。DA-6886 以 5-HT4 受体拮抗剂敏感的方式诱导大鼠食道制剂松弛。在表达 hERG 通道的 CHO 细胞中对 DA-6886 进行的评估显示,它抑制 hERG 通道电流的 pIC50 值为 4.3,表明该化合物对 5-HT4 受体的选择性比 hERG 通道高 1000 倍。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T4550 |
Ajmaline
Cardiorythmine,Raugalline,阿义吗啉,阿义马林,Tachmalin,(+)-Ajmaline |
Sodium Channel | Membrane transporter/Ion channel |
Ajmaline (Cardiorythmine) 是一种钠通道阻断剂,属于1A 类抗心律失常剂。Ajmaline 阻断 HERG 电流,在 HEK 细胞的 IC50为 1 μM,爪蟾卵母细胞的IC50为 42.3 μM。Ajmaline 在室性心动过速方面具有研究价值。 | |||
T7056 |
Dronedarone
决奈达隆,SR 33589 |
P450; Potassium Channel; Calcium Channel; Sodium Channel; Adrenergic Receptor; AChR; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Dronedarone (SR 33589) 是一种胺碘酮类似物,对治疗心房颤动可能有效。它是CYP3A4的底物和中度抑制剂。它是多种离子电流的有效阻滞剂,通过非竞争性结合到肾上腺素能受体显示出抗肾上腺素能的效果。 | |||
T2732 |
(-)-Epicatechin gallate
表儿茶素没食子酸酯,(−)-Epicatechin 3-gallate,Epicatechin gallate,(-)-Epicatechin 3-gallate,(-)-Epicatechin 3-O-gallate,ECG |
Virus Protease; COX; Autophagy | Autophagy; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
(-)-Epicatechin gallate ((-)-Epicatechin 3-O-gallate) 抑制环加氧酶-1 的IC50值为 7.5 μM。 | |||
T2768 |
Saikosaponin A
柴胡皂苷A,柴胡皂苷 A |
NF-κB; Antibacterial; Liver X Receptor | Metabolism; Microbiology/Virology; NF-κB |
Saikosaponin A 是银柴胡中的主要活性成分,有抗炎活性,可上调 LXRα的表达。 | |||
T4A2458 |
Resibufogenin
酯蟾毒配基,Bufogenin,Recibufogenin,酯蟾毒配基,蟾力苏 |
Others | Others |
Resibufogenin (Bufogenin) 是华蟾素的成分之一,表现出抑制氧化应激及肿瘤再生的活性。 | |||
T8195 |
Lotusine
|
Others | Others |
Lotusine 是一种提取自Nelumbo nucifera Gaertn 的绿色种胚中的纯生物碱。它能够作用于心肌中动作电位及心脏浦肯野纤维缓慢内向电流。 | |||
TN1035 |
Irisolidone
尼泊尔鸢尾异黄酮,葛花苷元 |
IL Receptor; NF-κB; Chloride channel | Immunology/Inflammation; Membrane transporter/Ion channel; NF-κB |
Irisolidone 是葛根花中的一种异黄酮,具有较强的保肝活性。它是一种有效的体积调节阴离子通道 (VRAC) 电流抑制剂,有高效阻断作用,IC50 为 5-13 μM。 | |||
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。 | |||
TN1797 |
Isorhoifolin
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Isorhoifolin and vicenin II are main compounds of ethyl acetate fraction (EAcF) obtained from Erythrina velutina leaves, EAcF increases the cardiac contractile force by increasing the l-type calcium current and activating the adrenergic receptor pathway. | |||
TN3636 |
Chlorahololide C
|
Potassium Channel | Membrane transporter/Ion channel |
Chlorahololide C is a potent and selective potassium channel blocker, it exerts potent and selective inhibition on the delayed rectifier (I(K)) K(+) current with the IC(50) value of 3.6 +/- 10.1 mu M. | |||
T78489 |
Lotusine hydroxide
|
Others | Others |
Lotusine (hydroxide)为纯生物碱,源自Nelumbo nucifera Gaertn绿色种胚提取。该化合物能够影响心肌动作电位和心脏浦肯野纤维的缓慢内向电流。 | |||
TN4108 |
Ganoderic acid Z
|
Antifection | Microbiology/Virology |
The binding affinities of ganoderic acid DM and ganoderic acid Z (ÎGbind, -16.83 and-10.99 kcal mol-1) are comparable to that of current commercial drug oseltamivir (-23.62 kcal mol-1);Ganoderic acid DM is a potential source of anti-influenza ingredient, with novel binding pattern and advantage over oseltamivir, it has steric hindrance on the 150 cavity of N1 protein, and exerts activities across the H274Y and N294S mutations, is the attractive candidates of novel neuraminidase (NA) inhibitors.... | |||
TN3351 |
Aflatrem
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Aflatrem is a tremorgenic mycotoxin with acute neurotoxic effects, a single low dose of aflatrem is able to induce degeneration of neuronal processes in hippocampal neurotransmitter systems. Aflatrem potentiates the gamma-aminobutyric acid (GABA)-induced |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-02308 |
CACNA2D1 Protein, Human, Recombinant (His & SUMO)
MHS3,Voltage-dependent calcium channel subunit alpha-2/delta... |
Human | E. coli |
The alpha-2/delta subunit of voltage-dependent calcium channels regulates calcium current density and activation/inactivation kinetics of the calcium channel. Plays an important role in excitation-contraction coupling. | |||
TMPH-01663 |
GRM5 Protein, Human, Recombinant (His & Myc)
Metabotropic glutamate receptor 5,GRM5 |
Human | E. coli |
G-protein coupled receptor for glutamate. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors. Signaling activates a phosphatidylinositol-calcium second messenger system and generates a calcium-activated chloride current. Plays an important role in the regulation of synaptic plasticity and the modulation of the neural network activity. | |||
TMPH-01889 |
KCNK3 Protein, Human, Recombinant (His & Myc)
Potassium channel subfamily K member 3,TWIK-related acid-sen... |
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... | |||
TMPK-00976 |
AMHRII Protein, Human, Recombinant
MRII,AMHR2,AMH type II receptor,MIS type II receptor,AMHR,AM... |
Human | HEK293 Cells |
The aim of the current study was to explore whether anti-Müllerian hormone receptor II (AMHRII) genetic variants influence the hormonal profile and the ovarian response to standard gonadotropin stimulation of women undergoing medically assisted reproduction. Three hundred in vitro fertilization or intracytoplasmic sperm injection patients constituted the study population, while 300 women with at least one spontaneous pregnancy participated as controls. AMHRII Protein, Human, Recombinant is expre... | |||
TMPH-01306 |
EIF4A1 Protein, Human, Recombinant (His & Myc)
eIF4A-I,EIF4A1,eIF-4A-I,Eukaryotic initiation factor 4A-I,EI... |
Human | E. coli |
ATP-dependent RNA helicase which is a subunit of the eIF4F complex involved in cap recognition and is required for mRNA binding to ribosome. In the current model of translation initiation, eIF4A unwinds RNA secondary structures in the 5'-UTR of mRNAs which is necessary to allow efficient binding of the small ribosomal subunit, and subsequent scanning for the initiator codon. EIF4A1 Protein, Human, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The ... | |||
TMPK-01217 |
MFAP5 Protein, Mouse, Recombinant (hFc)
MP25,AAT9,MAGP2,MAGP-2,MFAP-5 |
Mouse | HEK293 Cells |
Human basal-like breast cancer (BLBC) is an aggressive malignancy with poor prognosis. Since most current treatments are ineffective, there is an urgent need to identify therapeutic targets for BLBC. Microfibrillar-associated protein 5 (MFAP5) plays an important role in the integration of elastic microfibers and the regulation of endothelial cell behaviors.MFAP5 was significantly overexpressed in BLBC tissues and associated with poor metastasis-free survival of patients with BLBC. MFAP5 Protein,... | |||
TMPK-00957 |
MFAP5 Protein, Human, Recombinant (hFc)
MAGP2,AAT9,MAGP-2,MP25,MFAP-5 |
Human | HEK293 Cells |
Human basal-like breast cancer (BLBC) is an aggressive malignancy with poor prognosis. Since most current treatments are ineffective, there is an urgent need to identify therapeutic targets for BLBC. Microfibrillar-associated protein 5 (MFAP5) plays an important role in the integration of elastic microfibers and the regulation of endothelial cell behaviors.MFAP5 was significantly overexpressed in BLBC tissues and associated with poor metastasis-free survival of patients with BLBC. MFAP5 Protein,... | |||
TMPK-00977 |
AMHRII Protein, Human, Recombinant (hFc)
MISR2,AMHR2,AMH type II receptor,AMHR,C14,MIS type II recept... |
Human | HEK293 Cells |
The aim of the current study was to explore whether anti-Müllerian hormone receptor II (AMHRII) genetic variants influence the hormonal profile and the ovarian response to standard gonadotropin stimulation of women undergoing medically assisted reproduction. Three hundred in vitro fertilization or intracytoplasmic sperm injection patients constituted the study population, while 300 women with at least one spontaneous pregnancy participated as controls. AMHRII Protein, Human, Recombinant (hFc) is... | |||
TMPH-00672 |
Metalloprotease stcE Protein, E. coli O157:H7, Recombinant (His)
stcE,Neutral zinc metalloprotease StcE,Metalloprotease StcE,... |
E. coli | E. coli |
Virulence factor that contributes to intimate adherence of enterohemorrhagic E.coli (EHEC) O157:H7 to host cells. Is able to cleave the secreted human mucin 7 (MUC7) and the glycoprotein 340 (DMBT1/GP340). Also cleaves human C1 inhibitor (SERPING1), a regulator of multiple inflammatory pathways, and binds and localizes it to bacterial and host cell surfaces, protecting them from complement-mediated lysis. Therefore, the current model proposes two roles for StcE during infection: it acts first as... | |||
TMPH-01671 |
Human metapneumovirus (strain CAN97-83) Fusion glycoprotein F0 (His & SUMO)
Fusion glycoprotein F0,F |
HMPV | E. coli |
Inactive precursor that is cleaved to give rise to the mature F1 and F2 fusion glycoproteins.; Class I viral fusion protein. Under the current model, the protein has at least 3 conformational states: pre-fusion native state, pre-hairpin intermediate state, and post-fusion hairpin state. During viral and plasma cell membrane fusion, the coiled coil regions assume a trimer-of-hairpins structure, positioning the fusion peptide in close proximity to the C-terminal region of the ectodomain. The forma... | |||
TMPY-00924 |
SMAC Protein, Human, Recombinant (His)
DFNA64,diablo, IAP-binding mitochondrial protein,SMAC |
Human | E. coli |
Apoptosis is an essential processes required for normal development and homeostasis of all metazoan organisms. Second Mitochondria-Derived Activator of Caspases (Smac) or Direct IAP Binding Protein with low isoelectric point, pI (Diablo) is a proapoptogenic mitochondrial protein that is released to the cytosol in response to diverse apoptotic stimuli, including commonly used chemotherapeutic drugs. The current knowlege about structure and function of Smac/Diablo during programmed cell death, bot... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37847 |
Zonisamide-13C2,15N
Zonisamide-13C2,15N |
||
Zonisamide-13C2,15N is intended for use as an internal standard for the quantification of zonisamide by GC- or LC-MS. Zonisamide is an antiepileptic agent.1 It selectively inhibits the repeated firing of sodium channels (IC50 = 2 μg/ml) in mouse embryo spinal cord neurons and inhibits spontaneous channel firing when used at concentrations greater than 10 μg/ml.2 In rat cerebral cortex neurons, zonisamide (1-1,000 μM) inhibits T-type calcium channels with a maximum reduction of 60% of the calcium... |