37
6
Cat. No. | Product Name | Target | Signaling Pathways |
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T9796 |
22393-62-0_peak 2
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22393-62-0_peak 2 exhibits some aspects of the antiestrogenic activity and other actions that may be connected to the estrogenic properties. A mixture of the (Z)- and (E)-isomers (Broparestrol, INN) is used in dermatology. | |||
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。 | |||
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。 | |||
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。 | |||
T3644 |
U93631
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
U93631 是一种具有新型化学结构的 GABAA 受体配体,IC50 为 100 nM,它在重组 GABAA 受体中诱导 GABA 诱导的全细胞 Cl 电流快速,这种效果随时间依赖性衰减。 | |||
T28491 |
R-1663
R1663 |
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R-1663 is a factor Xa inhibitor. R-1663 prolonged clotting times, inhibited thrombin generation (peak height and endogenous thrombin potential [ETP]) and anti-factor Xa activity in a concentration-dependent manner without increasing bleeding time. Pharmac | |||
T26862 | BMS-902483 | ||
BMS-902483 is a potent α7 partial agonist. BMS-902483 improved cognition in preclinical rodent models. BMS-902483 showed FLIR α7 EC50=9.3nM; α7 Electrophysiology, rat; Area EC50 = 140 nM; Peak, Area (Ymax %) = 40, 54. 5-HT3A IC50 = 480 nm. | |||
T83352 |
3-Methyl-8-(2'-deoxy-β-D-ribofuranosyl)isoxanthopterin
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3-Methyl-8-(2'-deoxy-β-D-ribofuranosyl)isoxanthopterin 是一种基于蝶啶的荧光鸟苷类似物,用作DNA吸收示踪剂。此化合物在DNA结合及动力学研究中有着广泛应用,其吸光度和发射光度的最大值分别为350 nm 和430 nm。 | |||
T32426 |
KT 1
KT-1,KT1 |
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KT 1 decreased aortic pressure, renal blood flow, left ventricular enddiastolic pressure and resistances of total peripheral, vertebral, coronary and renal vasculatures and increased aortic blood flow, vertebral blood flow, coronary blood flow, peak posit | |||
T19304 |
EC-17 disodium salt
|
Others | Others |
The peak excitation and emission wavelengths of EC-17 are 470/520 nm.EC-17 (disodium salt) is a folate receptor alpha (FRα) targeting contrast agent with fluorescent properties in the visible light spectrum. | |||
T36916 |
Estrone-3-Glucuronide (sodium salt hydrate)
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Estrone-3-Glucuronide is a metabolite of the primary premenopausal estrogen 17β-estradiol .1,2Urinary levels of estrone-3-Glucuronide peak approximately 36 hours prior to ovulation and have been used as a marker of fertility in women. 1.Blackwell, L.F., Brown, J.B., and Cooke, D.Definition of the potentially fertile period from urinary steroid excretion rates. Part II. A threshold value for pregnanediol glucuronide as a marker for the end of the potentially fertile period in the human menstrual ... | |||
T82726 |
Chromotrope 2R
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Chromotrope 2R 是一种用于蛋白质定量的显色分析探针,其特征在于能够将碱性蛋白染成红色,吸收光谱在pH调整下呈现从501.6nm向567nm的红移特性。 | |||
T70773 |
Noberastine citrate
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Noberastine citrate, a histamine H1 antagonist, has potent and specific peripheral antihistaminic activity. Noberastine, a furan derivative of nor-astemizole (an astemizole metabolite), has been shown to have a more rapid onset, and shorter duration of action than astemizole with peak antihistaminic activity at 4h following ingestion. Noberastine is rapidly absorbed and the peak plasma levels are obtained within 2 h of oral dosing. In preclinical studies Noberastine has been shown to lack centra... | |||
T71398 |
RO5126946
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RO5126946 is a Novel α7 nicotinic acetylcholine receptor-positive allosteric modulator. RO5126946 allosterically modulates α7nAChR activity. RO5126946 increased acetylcholine-evoked peak current and delayed current decay but did not affect the recovery of α7nAChRs from desensitization. In addition, RO5126946's effects were absent when nicotine-evoked currents were completely blocked by coapplication of the α7nAChR-selective antagonist methyl-lycaconitine. | |||
T37764 |
Cal Green™ 1 (potassium salt)
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Cal Green 1 is a cell-impermeant fluorescent calcium indicator that is characterized by high quantum yield and low phototoxicity. Its peak excitation and emission wavelengths (506 and 531 nm, respectively) are comparable to standard fluorescein dyes, making Cal Green 1 appropriate for fluorescent microscopy. Cal Green 1 is ~5-fold brighter than fluo-3 at saturating calcium levels. | |||
T41171 |
BODIPY FL VH032
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BODIPY FL VH032 is a high-affinity VHL fluorescent probe (Kd= 3.01 nM) with application in time-resolved fluorescence resonance energy-transfer (TR-FRET) assays for high-throughput identification and characterization of VHL ligands. BODIPY FL VH032 consists of a derivative of von Hippel-Lindau (VHL) ligand VH 032 and a fluorophore BODIPY FL(with excitation peak at 504 nm and emission peak at 520 nm), joined by a polyethylene glycol (PEG) 4 linker. The BODIPY FL VH032 VHL TR-FRET signal is stable... | |||
T71425 |
Noberastine maleate
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Noberastine maleate, a histamine H1 antagonist, has potent and specific peripheral antihistaminic activity. Noberastine, a furan derivative of nor-astemizole (an astemizole metabolite), has been shown to have a more rapid onset, and shorter duration of action than astemizole with peak antihistaminic activity at 4h following ingestion. Noberastine is rapidly absorbed and the peak plasma levels are obtained within 2 h of oral dosing. In preclinical studies Noberastine has been shown to lack centra... | |||
T39717 |
VGSC blocker-1
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VGSC blocker-1 is a powerful small molecule that serves as a blocker for the neonatal isoform of the VGSC subtype known as Nav1.5 (nNav1.5). It effectively blocks INa peak currents by 34.9% at a concentration of 1 μM, and demonstrates a 0.3% inhibition of cell invasion at the same concentration in the MDA-MB-231 human breast cancer cell line, without compromising cell viability. | |||
T62376 |
GNE-9278
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GNE-9278 是一种高度选择性的 NMDAR 正变构调节剂,能够作用于 GluN1 跨膜结构域 (TMD)。GNE-9278 可以作用于活化的 NMDAR,能够提高峰值电流和激动剂亲和力。 | |||
T82495 |
eGFP mRNA(N1-Me-Pseudo UTP)
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eGFP mRNA可以在哺乳动物细胞培养中直接表达出明亮的绿色荧光蛋白,该荧光蛋白源自水母Aequorea victoria,并在509 nm的激发光下发出绿色荧光。作为一种常用的报告蛋白,eGFP用于检测基因表达。 | |||
T39254 |
ICG-carboxylic acid
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ICG-carboxylic acid is a fluorescent probe in the near-infrared (NIR) range. It is derived from indocyanine green (ICG), a commonly used fluorescent dye in medical diagnostics. ICG exhibits a peak absorption at 800 nm, allowing it to efficiently absorb energy from near-infrared lasers and release heat within the dyed tissue. | |||
T35798 |
Massarigenin C
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Massarigenin C is a fungal metabolite that has been found inM. flavoroseaand has enzyme inhibitory activities.1,2Massarigenin C inhibits neuraminidasein vitro(IC50= 4.15 μM).2It is also an inhibitor of yeast α-glucosidase (IC50= 1.25 mM).1It reduces the postprandial peak in blood glucose levels in an oral sucrose tolerance test in normo- and hyperglycemic mice when administered at doses of 3.2, 10, and 31.6 mg/kg. | |||
T78385 |
BODIPY FL alkyne
BOD FL alkyne |
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BODIPY FL alkyne(BOD FL alkyne)为绿色荧光染料(Ex=503 nm;Em=512 nm),具备高亮度及优良的光稳定性,在荧光素(FAM)通道中发射光。该化合物能够通过铜催化的Click Chemistry与叠氮分子发生共轭反应。 | |||
T78454 |
Lucifer Yellow CH dipotassium salt
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Lucifer Yellow CH dipotassium为一高亮度荧光探针,含有游离肼基。它能在室温条件下与脂肪醛发生作用,并被广泛应用于作为生物示踪剂,监测神经元分支、再生、间隙连接以及细胞特定区域损伤后的反应。该探针 Ex-max 和 Em-max 分别为 430 nm和540 nm。 | |||
T82497 |
eGFP circRNA
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eGFP circRNA,能够编码由Aequorea victoria水母分离得到的绿色荧光蛋白。作为哺乳动物细胞培养中的常规直接检测报告蛋白,其在509 nm波长下发出鲜明的绿光。eGFP circRNA作为环状RNA转染的首选阳性对照,对于监测及提升转染效率具有重要意义。 | |||
T74335 | PSDalpha | ||
PSDalpha 是一种ERα降解剂,通过乙炔键结合光敏剂 (PS)、三苯胺苯并噻二唑 (TB) 和 17β-雌二醇。PSDalpha 对 MCF-7 细胞表现出优异的抗增殖性能。PSDalpha 在可见光区的 λmax 位于 465 nm。 | |||
T60463 | Bifemelane | ||
Bifemelane 是一种益智化合物, 通过刺激细胞内 Ca2+储存的释放产生第一个峰值,通过储存操作的 Ca2+通道的电容进入产生第二个峰值。Bifemelane 可作为星形胶质细胞基础研究的药理学工具。 | |||
TP1972 |
OD1
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Potent rat Nav1.7, human Nav1.4 and rat Nav1.6 channel activator (EC50 values are 7, 10 and 47 nM, respectively). Exhibits minimal activation at mammalian Nav1.2, Nav1.3 and Nav1.5 (EC50 values >3 μM). Inhibits fast inactivation on all channels. Increases | |||
TD0001 |
SYBR GREEN 1
SUPER Green I (效果同SYBR Green I)核酸染料(10,000× DMSO溶液)(电泳级),SYBR(R) GREEN I NUCLEIC ACID GEL STAIN *10,000× concentrate in DMSO,SYBRGREENⅠ核苷酸胶体染料 |
Others | Others |
SYBR GREEN 1 是一种不对称花青染料,用于检测核酸。它由一个 N-烷基化的苯并噻唑或苯并恶唑环系统组成,通过一甲基桥连接到吡啶鎓或喹啉鎓环系统。 SYBR Green I 与 dsDNA 的小沟结合,在 480 nm 波长处被激发。它具有 520 nm 的峰值荧光发射。 | |||
T83843 |
2'(3')-O-Anthraniloylguanosine-5'-O-triphosphate sodium
2'(3')-ANT-GTP |
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2'(3')-O-Anthraniloylguanosine-5'-O-triphosphate(2'-ANT-GTP)及3'-ANT-GTP是荧光GTP衍生物,能够自发进行异构化。2'(3')-ANT-GTP在水中的激发波长为330 nm时,发射最大波长为428 nm。它抑制哺乳动物腺苷酸环化酶1(AC1;在锰存在下Ki=10 nM)、B. anthracis AC毒素水肿因子(在锰和镁存在下Kis分别为4.1 和 13 µM)及B. pertussis AC毒素CyaA(在锰存在下Ki=29 µM)。 | |||
T83941 |
Mag-Fura-2 AM
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Mag-Fura-2 AM是一种可渗透细胞的荧光镁离子(Mg2+)指示剂,对Mg2+具有高度选择性,相较于其他二价离子(Zn2+、Cu2+和Ca2+)。其对Mg2+的选择性超过13,000倍(Mg2+Kd为1.9 nM,相对于Ca2+Kd的25 μM)。激发和发射峰值(λ)分别为369 nm和511 nm。Mag-Fura-2 AM可作为间接指示ATP消耗/产生的指标。 | |||
T83829 |
2'-Deoxy-1,N6-ethenoadenosine-5'-O-triphosphate sodium
ε-dATP |
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ε-dATP是一种具有荧光性的嘌呤核苷酸2’-脱氧腺苷-5’-O-三磷酸(dATP)衍生物。它能在50至150µM的浓度范围内诱导初级小鼠脾脏T细胞和B细胞在脂多糖(LPS)或刀豆蛋白A刺激下发生姊妹染色单体交换。ε-dATP已被用于研究乙烯氯诱导的突变过程中模糊碱基配对的情况。相关的ATP衍生物ε-ATP,在300 nm激发下显示415 nm的发射峰值。 | |||
T13460 |
(+)-Cevimeline hydrochloride hemihydrate
(+)-AF102B hydrochloride hemihydrate,(+)-SNI-2011 |
Others | Others |
(+)-Cevimeline hydrochloride hemihydrate ((+)-SNI-2011) 是一种有效的 mAChR 激动剂。 | |||
T13421 |
(-)-Cevimeline hydrochloride hemihydrate
(-)-SNI-2011,(-)-AF102B hydrochloride hemihydrate |
ALK | Angiogenesis; Tyrosine Kinase/Adaptors |
(-)-Cevimeline hydrochloride hemihydrate ((-)-SNI-2011) 是一种新型mAChR 激动剂,是一种治疗干燥综合征口干症的候选治疗药物。 | |||
T83820 |
TNP-GTP sodium
TNP-Guanosine 5'-triphosphate |
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TNP-GTP是一种荧光衍生物,源自蛋白质合成与糖异生的能量底物鸟苷三磷酸(GTP)。其在水中激发波长为410 nm时,发射最大波长为552 nm,而在40%和80%的N,N-二甲基甲酰胺中,其荧光强度增加,发射波长分别向544 nm和532 nm移动,这是因为N,N-二甲基甲酰胺的极性比水小。TNP-GTP是谷氨酸脱氢酶的抑制剂(Ki = 2.7 μM)。当与谷氨酸脱氢酶结合时,TNP-GTP的荧光强度增加,且发射波长从552 nm变为545 nm,此效果可以通过加入GTP来阻断。TNP-GTP还是嘌呤P2X2和P2X2/3受体的拮抗剂(IC50s分别为0.4和1.2 nM)。它还选择性抑制大鼠可溶性鸟苷酸环化酶(sGC; Ki = 11 nM)高于牛肝谷氨酸脱氢酶(GDH; Ki = 2.7 µM)以及钙调素依赖的B. pertussis腺苷酸环化酶(AC)毒素(Kis在存在锰或镁时分别为20和320 µM)。 | |||
T83802 |
TNP-ATP sodium
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TNP-ATP是ATP的衍生物,同时是嘌呤P2Y1、P2X3和P2X2/3受体的拮抗剂(IC50s分别为6、0.9和7 nM,在表达人类受体的HEK293细胞中)。该化合物相对于嘌呤P2X2、P2X4和P2X7受体显示出选择性(IC50s分别为2、15.2和>30 µM,在表达人类受体的HEK293细胞中)。TNP-ATP能降低表达P2X3和P2X2/3受体的1321N1细胞中乙酸诱导的钙流量(IC50s分别为100和62 nM)。它还可以减轻小鼠模型中由乙酸诱发的痛性绞曲(ED50 = 6.35 µmol/kg)。在403 nm激发下,其发射最大峰值为547 nm,当结合于胰岛素降解酶(IDE)时,其相对荧光强度增加四倍,并且发射峰移至538 nm。 | |||
T37880 |
OPC-167832
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OPC-167832 is a potent and orally active dprE1 Inhibitor with an IC50 of 0.258 μM. OPC-167832 has antituberculosis activity and can be used for the research of tuberculosis caused by Mycobacterium tuberculosis[1]. OPC-167832 exhibits very low MICs against laboratory strains of M. tuberculosis H37Rv (MIC: 0.0005 μg/ml) and Kurono (MIC: 0.0005 μg/ml) and strains with monoresistance to rifampin (RIF), isoniazid (INH), ethambutol (EMB), streptomycin (STR), and pyrazinamide (PZA) (MIC: 0.00024-0.001 ... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T33492 |
Methyl pyropheophorbide-a
MPPa (Methyl pyropheophorbide-a),NSC267052,Pyropheophorbidea,MPPa,NSC-267052,NSC 267052 |
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Pyropheophorbide-a methyl ester (MPPa) is a PDT photosensitizer, and is also a semisynthetic natural product derived from chlorophyll a. The absorption peak of MPPa in organic solvent and in cells was at 667 and 674 nm, respectively. 3-(4,5-Dimethylthiazo | |||
TN2347 |
Methylsticin
麻醉椒苦素,Methysticin |
Others | Others |
Methylsticin (Methysticin) 是一种卡瓦内酯,从卡瓦根中分离得到。它能够抑制破骨细胞形成的活性。 | |||
TN1918 |
Medicarpin
美迪紫檀素 |
Apoptosis; BCL; ROS; JNK | Apoptosis; Immunology/Inflammation; MAPK |
Medicarpin 是从紫花苜蓿中分离出的一种类黄酮。它通过调节 P-gp 介导的药物外流,诱导白血病 P388 细胞凋亡并克服多药耐药性。 | |||
TN6514 | 2-Carboxybenzaldehyde | ||
The major peak of 2-Carboxybenzaldehyde reductase activity in human liver co-purifies with hAFAR protein. Sulphydryl substances and some proteins play important roles in preserving the molecular and catalytic properties of 2-Carboxybenzaldehyde reductase. | |||
T80007 |
Stevisalioside A
|
Phosphatase | Metabolism |
Stevisalioside A (Compound 2),一种从甜叶菊根提取的化合物,展现出抗糖尿病的口服活性。该化合物有效抑制PTP1B,IC50为526.8 μM,并能降低Stevisalioside A引起的高血糖小鼠血糖水平,改善餐后血糖峰值及口服葡萄糖和胰岛素耐量测试结果。 | |||
T37609 |
(rel)-Asperparaline A
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Aspergillimide is a fungal metabolite originally isolated from A. japonicus.1 It reduces nicotinic acetylcholine receptor (nAChR) peak and slowly-desensitizing amplitudes induced by acetylcholine in silkworm (B. mori) larval neurons (IC50s = 20.2 and 39.6 nM, respectively) but has no effect on chicken α3β4-, α4β2-, and α7-containing nAChRs.2 Dietary administration of aspergillimide A (10 μg/g of diet) induces paralysis in silkworm fourth instar larvae.1 Aspergillimide A (10 and 20 mg/kg) reduces... |