Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T13016 |
SR59230A
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
SR59230A 是可透过血脑屏障的、选择性的 β3-肾上腺素能受体拮抗剂,对 β3,β1 和 β2 受体的 IC50分别为 40、408 和 648 nM。 | |||
T8452 |
Dantrolene
|
Others | Others |
Dantrolene 是一种肌肉松弛剂,是人红细胞谷胱甘肽还原酶的非竞争性抑制剂,其Ki 和IC50值分别为 111.6 μM 和 52.3 μM。它是兰尼碱受体拮抗剂及Ca2+信号稳定剂。它可用于研究恶性高热、亨廷顿病、肌肉痉挛和其他神经阻滞剂恶性综合征。 | |||
T4176 |
rac-BHFF
(R,S)-BHFF |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
rac-BHFF ((R,S)-BHFF) 是具有口服活性的 GABAB 受体的异构增强剂,有抗焦虑活性。 | |||
T0235 |
Modaline sulfate
|
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Modaline sulfate 是一种 MAO 抑制剂,用于研究抑郁症。 | |||
T23778 |
BCTP
|
||
BCTP is a polymodal inhibitor of TRPV1. It has a reduced liability for hyperthermia. | |||
T68959 |
Fenobam hydrate
|
||
Fenobam hydrate is a noncompetitive antagonist and inverse agonist of metabotropic glutamate receptor 5 (mGluR5). It inhibits intracellular calcium mobilization induced by the glutamate analog quisqualate and inhibits basal activity of mGluR5. Fenobam reduces stress-induced hyperthermia, exhibits anxiolytic-like activity, and may induce analgesia. | |||
TP1958 |
PL-017
PL 017 |
||
Selective μ opioid receptor agonist (IC50 values are 5.5 and > 10000 nM for inhibition of 125I-FK 33,824 and 125I-DADLE binding to μ and δ sites respectively). Produces naloxone-reversible analgesia, catalepsy and hyperthermia following central administra | |||
T37732 |
AMG 21629
|
||
Potent and selective TRPV1 antagonist. Blocks Ca2+ uptake by CHO cells expressing TRPV1 receptors and acid-induced Ca2+ uptake, respectively). Exhibits >4000-fold selectivity for TRPV1 over other TRP channels. Blocks capsaicin-induced flinch response and causes hyperthermia in rats. Orally available and non-CNS penetrant. Tamayo et al (2008) Design and synthesis of peripherally restricted transient receptor potential vanilloid 1 (TRPV1) antagonists. J.Med.Chem. 51 2744 PMID:18386885 |Gavva et al... |