Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T15684 |
L-689560
|
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
L-689560 是 N-甲基-D-天冬氨酸受体(NMDA)的有效拮抗剂,抑制 NMDA 甘氨酸结合位点。它用于研究 NMDA 受体在正常神经系统过程以及疾病中的作用,也广泛用作结合研究中的放射性标记配体,也。 | |||
T32237 |
Isoxaben
EL 107,NA 8318,Isoxaben; EL 107; NA 8318 |
Cell wall | Immunology/Inflammation |
Isoxaben (EL 107) 是一种细胞壁生物合成的特异性抑制剂,常作为除草剂使用,可抑制放射性标记的葡萄糖掺入酸不溶性细胞壁部分。 | |||
T15629 |
JTE-013
|
Apoptosis; S1P Receptor; LPL Receptor | Apoptosis; GPCR/G Protein |
JTE-013 是一种选择性S1P2拮抗剂。它抑制放射性标记的 S1P 与人和大鼠 S1P2的特异性结合,IC50分别为 17 nM 和 22 nM。 | |||
T60336 |
CCR4 antagonist 3-1
|
CCR | Immunology/Inflammation; Microbiology/Virology |
CCR4 antagonist 3-1 是一种具有较低活性的趋化因子受体 4 (CCR4) 拮抗剂,对 [125I]TARC (胸腺和活化调节趋化因子) 具有抑制作用,IC50 值为 1.7 μM。CCR4 antagonist 3-1 对放射标记的[125I]TARC和巨噬细胞来源的趋化因子(MDC) 与 CEM 细胞表面的CCR4 受体的结合有抑制作用, 并对 TARC 介导的 CEM 细胞的体外迁移有抑制作用,IC50 值为 6.4 μM。 | |||
T24014 |
Dotanoc
DOTA-Nal3-octreotide,DOTA-NOC |
||
Dotanoc is a ligand to make gallium Ga 68-DOTANOC, which is a gallium Ga 68-radiolabeled analog of somatostatin. | |||
T31787 |
Fet F-18
Fet F18,18F-Fluoroethyltyrosine,18F-FET |
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Fet F-18 is an amino acid analog radiolabeled with fluorine F-18, a positron-emitting isotope, can be used as a tracer in positron emission tomography (PET). | |||
T18926 |
Biotin-probe 1
|
Others | Others |
Biotin-probe 1 is a non-radiolabeled probe and can be applied to in situ hybridization. | |||
T70599 | Asem F-18 | ||
Asem F-18 is a radiolabeled antagonist for imaging the α7-nicotinic acetylcholine receptor with PET . | |||
T68873 | Cornigerine | ||
Cornigerine is a natural product analog of colchicine produced by Colchicum cornigerum that inhibited tubulin polymerization both with and without microtubule-associated proteins, inhibited the binding of radiolabeled colchicine to tubulin, and stimulated tubulin-dependent GTP hydrolysis. | |||
T80238 |
NODAGA-LM3 TFA
|
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NODAGA-LM3 TFA 是一种可用68Ga标记的SSTR2拮抗剂,适用于PET成像,专门针对SSTR阳性副神经节瘤进行成像诊断。 | |||
T35448 |
10-Thiastearic Acid
|
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Heteroatom-substituted fatty acids have been observed to modulate the extension and desaturating of fatty acids, and to influence their distribution within phospholipids pools. 10-Thiastearic acid inhibits desaturation of radiolabeled stearate to oleate in rat hepatocytes and hepatoma cells by more than 80% at a concentration of 25 μM. This activity is associated with a hypolipidemic effect, making this 10-thiastearic acid a useful tool for evaluating new anti-obesity therapeutics. | |||
T80157 |
DOTA-JR11
|
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DOTA-JR11为SSTR2生长抑素受体拮抗剂,能经68Ga标记,应用于神经内分泌肿瘤(NETs)配对成像研究。 | |||
T37275 |
2,3-dinor-11β-Prostaglandin F2α
2,3-dinor-11β-Prostaglandin F2α |
||
2,3-dinor-11β-Prostaglandin F2α (2,3-dinor-11β-PGF2α) was recovered from the urine of both normal monkeys and humans when infused with radiolabeled PGD2, where it represented approximately 1% and 4% of the infused radiolabeled dose, respectively. 2,3-dinor-11β-PGF2α has also been recovered from the urine of mastocytosis patients, where it is excreted in large amounts. In human asthmatic patients, 2,3-dinor-11β-PGF2α represents about 40% (as determined by GC/MS) of the immunoreactive 11β-PGF2α wh... | |||
T76253 |
WL12
|
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WL12是一种专门针对程序性死亡配体1 (PD-L1)的结合肽,可通过多种放射性核素标记,生成放射性示踪剂,用于评估肿瘤中PD-L1的表达情况。 | |||
T39545 | MK-6884 | ||
MK-6884, a positive allosteric modulator (PAM) of M4 muscarinic receptors, exhibits a high affinity (Ki = 0.19 nM). It is a valuable compound for the investigation of neurodegenerative diseases. Additionally, MK-6884 can be efficiently radiolabeled with carbon-11, enabling its use as a PET imaging agent. | |||
T69712 |
Icapamespib HCl
|
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Icapamespib, also known as PU-HZ 151, is a heat shock protein 90 (HSP90) inhibitor. PU-HZ151 showed EC50 of 5 nM in the FP assay as compared to 11 nM for PU-H71 and a logD of 2.37 as compared to 1.21 for PU-H71. PU-HZ151 and radiolabeled PU-HZ151 showed selectivity for epichaperomes over the individual chaperome members. Icapamespib demonstrated the ability to productively engage the target in cells, mice, and humans. | |||
T68714 | Iobenguane I 131 | ||
Iobenguane I 131 is a guanidine analog with specific affinity for tissues of the sympathetic nervous system and related tumors. The radiolabeled forms are used as antineoplastic agents and radioactive imaging agents. MIBG serves as a neuron-blocking agent which has a strong affinity for, and retention in, the adrenal medulla and also inhibits ADP-ribosyltransferase. | |||
T61087 |
THK-5105
|
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THK-5105为芳基喹啉衍生物,具备与tau原纤维高度结合的亲和力。它对tau蛋白聚集体及含tau的阿尔茨海默病(AD)脑匀浆显示出显著的结合能力。18F-THK-5105展现出作为tau成像PET探针的潜能。 | |||
T70865 |
BMY-42393
|
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BMY-42393 is orally active and selective platelet aggregation inhibitor. BMY-42393 is also a prostacyclin partial agonist that inhibited ADP, collagen and thrombin-induced platelet aggregation (IC50 range 0.3 - 2.0 microM). BMY-42393 stimulated platelet adenylate cyclase activity (EC50 = 25 nM). Platelets treated with BMY 42393 showed an elevation of cAMP levels and activation of cAMP-dependent protein kinase. BMY 42393 also inhibited thrombin-induced elevation of intracellular free calcium. B... | |||
T75252 | Gemcitabine triphosphate | ||
Gemcitabine triphosphate (dFdCTP) 是 Gemcitabine 在细胞内的两种核苷代谢产物的一种。另一种是活性二磷酸 (dFdDTP)。Gemcitabine triphosphate 能够作为放射性标记探针成像研究的标准物,用于识别对 Gemcitabine 的肿瘤,并评估 Gemcitabine 被细胞摄取和保留性质。 | |||
T83813 |
8-Azidoadenosine-5'-O-diphosphate sodium
8-azido-ADP,Click Tag™ 8-Azidoadenosine-5'-O-diphosphate |
||
8-Azidoadenosine-5'-O-diphosphate(8-azido-ADP)是ATP前体和嘌呤受体配体ADP的可点击形式。8-azido-ADP的放射性标记形式已被用作各种蛋白质的光亲和标签,包括从牛脑中分离的谷氨酸脱氢酶(GDH)同工酶,以及从兔网织红细胞中分离的真核翻译起始因子2(eIF2)和鸟苷核苷酸交换因子(GEF)。 |