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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2711 |
Chembridge-5861528
TCS 5861528 |
TRP/TRPV Channel | Membrane transporter/Ion channel |
Chembridge-5861528 (TCS 5861528) 是有效的 TRPA1离子通道阻断剂。 | |||
T1092 |
Zolmitriptan
佐米曲普坦,311C90,BW-311C90 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Zolmitriptan (311C90) 是一种5-HT1B/1D 受体部分激动剂,可用于偏头痛的研究,对 5-HT1B、5-HT1D、5-HT1F 受体的Ki 分别为 5.01、0.63 和 63.09 nM。 | |||
T2547 |
Droxidopa
屈昔多巴,屈西多巴,SM5688,DOPS,L-DOPS |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Droxidopa (L-DOPS) 是 Droxidopa (w/w80%) 和 Pharmaceutical starch (w/w20%) 的混合物,能透过血脑屏障,可作为神经递质去甲肾上腺素和肾上腺素的原药。 | |||
T9263 |
cim0216
N-(5-methyl-1,2-oxazol-3-yl)-2-phenyl-2-(1,2,3,4-tetrahydroquinolin-1-yl)acetamide |
TRP/TRPV Channel | Membrane transporter/Ion channel |
CIM0216 是选择性的TRPM3激动剂,对 TRPM3 的选择性高于 TRPM1、TRPM2 和 TRPM4-8。它以TRPM3依赖性的方式引起疼痛并唤起感觉神经末梢的神经肽释放,可用于神经源性炎症的相关研究。 | |||
T20423 |
Dibenzylamine
二苄胺,Dibenzyl-amine,N-Benzylbenzylamine,Bibenzylamine,N-benzyl-1-phenylmethanamine,Benzenemethanamine, N-(phenylmethyl)-,AI315327,AI3-15327,AI3 15327 |
Others | Others |
Dibenzylamine (N-Benzylbenzylamine) 是强效神经生成剂的一种成分。 | |||
T1833 |
NSI189
NSI-189,NSI 189 |
Others | Others |
NSI189 (NSI-189) 是一种促智和神经源性研究化学品,源自烟酰胺和吡嗪。 | |||
T21244 |
NSI-189 Phosphate
NSI189 Phosphate,NSI 189 Phosphate,NSI-189磷酸盐 |
Others | Others |
NSI-189 Phosphate 是一种新型神经源性分子,具有多效性,包括临床前研究中证明的抗抑郁、促认知、突触和神经营养活性。其抗抑郁活性不依赖于单胺。 | |||
T25615 |
Lanepitant
LY303870,LY-303870,LY 303870 |
Others | Others |
Lanepitant (LY303870) 是一种非肽类神经激肽-1(NK-1)拮抗剂,具有镇痛活性,可抑制神经源性硬脑膜炎症,可用于预防偏头痛。 | |||
T10012 |
P7C3-OMe
|
Others | Others |
P7C3-OMe 是促神经原性化合物,其 R-对映体活性远高于 S-对映体。可以用于研究神经精神疾病和神经退行性疾病。 | |||
T25616 |
Lanepitant 2HCl
LY303870 dihydrochloride,LY 303870 dihydrochloride,LY-303870 dihydrochloride,Lanepitant dihydrochloride |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Lanepitant 2HCl 是一种非肽类神经激肽-1 受体拮抗剂,具有镇痛和抗炎活性。Lanepitant 2HCl 抑制 P 物质与神经激肽-1 受体的结合,抑制神经源性炎症和疼痛传递,可用于研究偏头痛等疼痛性神经病变类疾病。 | |||
T1993 |
J-147
J147 |
Epigenetic Reader Domain; Dopamine Receptor; Monoamine Oxidase | Chromatin/Epigenetic; GPCR/G Protein; Neuroscience |
J-147 是一种高效的、具有口服活性的、可透过血脑屏障神经保护剂,可增强认知能力。它抑制单胺氧化酶 B 和多巴胺转运体,EC50分别为 1.88 μM 和 0.649 μM。它有研究阿尔茨海默氏症的潜力。 | |||
T39733 |
Hu7691 free base
|
Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
Hu7691 free base 是一种具有口服活性、高效性和选择性的 Akt 抑制剂,对多种神经母细胞瘤细胞系的抗增殖和神经发生作用。Hu7691 free base 抑制 Akt1、Akt2 和 Akt3 ,诱导神经母细胞瘤细胞分化。 | |||
T27059 |
CP-122288
|
||
CP-122288 is a potent and selective agonist for the 5-HT1B, 5-HT1D and 5-HT1F serotonin receptor subtypes. CP-122288 is potent as an inhibitor of plasma protein extravasation and neurogenic inflammation. | |||
T3290L |
Pikamilone Sodium
GABA-NG,Nicotinoyl-GABA sodium salt,GABA NG,GABANG,Pikamilone Na |
||
Pikamilone Sodium is a prodrug of GABA used for therapy of neurogenic bladder in spinal and benign prostatic hyperplasia. | |||
T7825 |
Distigmine Bromide
BC 51,Ubretid,BC51,Hexamarium,BC-51 |
||
Distigmine Bromide is an acetylcholinesterase inhibitor. It is used for the treatment of underactive neurogenic bladder and myasthenia gravis. | |||
T33652 |
Neurodazole
|
||
Neurodazole is a neurogenic inducer for converting pluripotent P19 cells into electrophysiologically active neurons. | |||
T27915 |
LY 302148
LY-302148,LY302148 |
||
LY 302148 , a 5-HT1F receptor agonist, inhibits neurogenic dural inflammation in guinea pigs. It has potential for migraine therapeutics. | |||
T78606 | P2X3-IN-1 | P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
P2X3-IN-1(示例7)为P2X3受体抑制剂,适用于神经源性疾病的研究。 | |||
T25617 |
Lanepitant HCl trihydrate
Lanepitant dihydrochloride trihydrate |
||
Lanepitant HCl trihydrate is an effective non-peptide neurokinin-1 receptor antagonist, suppresses neurogenic dural inflammation, and may have a role in migraine therapy. | |||
T70248 |
4991W93
|
||
4991W93 is a 5HT(1B/1D) receptor partial agonist, inhibiting electrically induced plasma extravasation, blocking neurogenic plasma protein extravasation, inhibiting release of calcitonin gene-related peptide. | |||
T28516 |
ReN-1869
NNC-05-1869,NNC 05-1869,NNC-051869,ReN 1869 |
||
ReN-1869 is a histamine H1 receptor antagonist. ReN 1869 is active against inflammation and neurogenic pain. ReN-1869 produces potent and selective antinociceptive effects on dorsal horn neurons after inflammation and neuropathy. | |||
T26781 |
BF-1
BF1 |
||
BF-1 is a 5-Hydroxytryptamine receptor 2B antagonist. BF-1 was tested as potential migraine prophylactic drug by blocking BW723C86 (5-((thiophen-2-yl)methoxy)-α-methyltryptamine) or meta-chlorophenylpiperazine (mCPP) induced neurogenic dural plasma protei | |||
T61309 |
(R)-Oxybutynin
|
||
(R)-Oxybutynin (Aroxybutynin) is an orally active muscarinic receptor antagonist, which exhibits antimuscarinic, antispasmodic, and anticholinergic activity. This compound, being the (R)-isomer of Oxybutynin, competitively antagonizes Carbachol-induced contractions. It is particularly useful in researching neurogenic bladder dysfunction-related incontinence [1] [2] [3]. | |||
T76429 |
Neurokinin Receptor (393-407), rat
|
||
Neurokinin Receptor(393-407), rat (SPR393–407) 是一段属于大鼠神经激肽1受体(NK1R)的特定肽。它与P物质(SP)结合后,通过内吞作用迅速被NK1R内化,并循环至质膜。此化合物主要应用于神经源性炎症研究领域。 | |||
T80172 |
Stromatoxin 1
|
Potassium Channel | Membrane transporter/Ion channel |
Stromatoxin 1是从狼蛛中分离出的肽类钾通道抑制剂,特异性地抑制K(V)2.1、K(V)2.2、K(V)4.2和K(V)2.1/9.3通道。其中,K(V)2.1和K(V)2.2通道亚基对大鼠肌源性和神经源性膀胱平滑肌(UBSM)的收缩起关键调控作用,然而K(V)4.2则不参与此作用。 | |||
T60369 |
Droxidopa hydrochloride
|
||
Droxidopa (L-DOPS) hydrochloride 是一种有效的、具有口服活性的去甲肾上腺素前体。Droxidopa hydrochloride 可增加站立血压,改善直立性低血压症状并提高站立能力。Droxidopa hydrochloride 具有研究神经源性直立性低血压(nOH)和替代性多动症 (注意缺陷多动障碍) 的潜力[3]。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN5757 |
p-Hydroxybenzaldehyde glucoside
4-formylphenyl b-d-glucopyranoside,Gastrodin Impurity |
||
p-Hydroxybenzaldehyde glucoside (4-formylphenyl b-d-glucopyranoside) 是抑制天麻素衍生物,具有镇痛活性,可以用于研究神经源性疼痛。 | |||
TN6872 |
Trypsin
|
Protease-activated Receptor | GPCR/G Protein |
Trypsin 是一种可从鱼类分离出的丝氨酸蛋白酶,可水解赖氨酸或精氨酸羧基侧蛋白质。Trypsin 具有抗炎活性,可通过 PDCoV 的 S 糖蛋白与 pAPN 的相互作用诱导 PDCoV 感染的细胞膜融合,可激活 PAR2 和 PAR4,促进细胞增殖和分化。Trypsin 可用于促进伤口愈合和研究神经源性炎症。 |