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Cat. No. | Product Name | ||
---|---|---|---|
L2800 | 5-羟色胺分子库 | 268 compounds | |
268 种生物活性小分子化合物,用于高通量、高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0322 |
Fipexide
|
Dopamine Receptor; AChR | GPCR/G Protein; Neuroscience |
Fipexide 是对氯苯乙酸衍生物,是哌嗪化学类的精神活性药物,作为促智药物,有用于老年痴呆的研究潜力。它可降低了纹状体腺苷酸环化酶的活性,通过多巴胺能神经传递对认知表现出积极的作用。 | |||
T6728 |
VUF 10166
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
VUF 10166 是一种新型的、有效的、竞争性的 5-HT3A 受体拮抗剂,Ki 为 0.04 nM,其对 5-HT3AB 受体的亲和力显着降低。 | |||
T21995 |
XAP044
|
GluR | Neuroscience |
XAP044 是高效的选择性mGlu7拮抗剂。代谢型谷氨酸受体亚型 7 是哺乳动物 CNS 中神经传递的重要突触前调节剂。它在啮齿动物行为测试中表现出较好的大脑暴露、广谱抗应激、抗抑郁以及抗焦虑作用。 | |||
T9461 |
AZ194
|
Sodium Channel | Membrane transporter/Ion channel |
CRMP2-Ubc9-NaV1.7 inhibitor 194 是一流的CRMP2-Ubc9相互作用抑制剂及NaV1.7抑制剂 (IC50=1.2 μM),口服有活性,具有抗伤害作用。AZ194 阻断 CRMP2 的 SUMOylation 以选择性地减少表面表达 NaV1.7 的量。 | |||
T11349 |
GABAA receptor agent 1
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
GABAA receptor agent 1 是GABAA 受体的高亲和力配体,有抗惊厥活性。 | |||
T7823 |
IDRA-21
7-氯-3-甲基-3,4-二氢-2H-1,2,4-苯并噻二嗪 1,1-二氧化物 |
GluR | Neuroscience |
IDRA-21 是一种阳性 AMPA 受体调节剂。 | |||
T8333 |
Aurintricarboxylic acid
ATA,NSC-4056,NSC4056,金精三羧酸,NSC 4056 |
Apoptosis; P2X Receptor; Influenza Virus; Topoisomerase | Apoptosis; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Aurintricarboxylic acid (NSC-4056) 是高效的αβ-亚甲基-ATP 敏感选择性P2X1Rs 和P2X3Rs 变构拮抗剂。 它是核糖核酸酶和拓扑异构酶 II 的有效抑制剂,可阻止核酸与酶结合。 | |||
T9409 |
Mesdopetam hemitartrate
IRL790 hemitartrate,1-Propanamine, N-[2-[3-fluoro-5-(methylsulfonyl)phenoxy]ethyl]-, (2R,3R)-2,3-dihydroxybutanedioate (2:1) |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Mesdopetam hemitartrate (IRL790 hemitartrate) 是一种多巴胺D3受体拮抗剂 (Ki=90 nM;IC50=9.8 μM),具有稳定精神运动的作用,可用于帕金森病的运动和精神并发症的研究。 | |||
T69552 |
Suzetrigine
VX-548 |
Sodium Channel | Membrane transporter/Ion channel |
Suzetrigine(VX-548) 是一种具有口服活性和特异性的 NaV1.8 抑制剂。 Suzetrigine 具有镇痛活性,可用于研究急性疼痛和神经通。 | |||
T7549 |
Talnetant
SB 223412 |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Talnetant (SB 223412) 是一种选择性、竞争性、脑渗透性 NK3 受体拮抗剂,Ki 为1.4 nM。它比对hNK-2受体的抑制性高100倍,具有调节中脑边缘和中脑皮质多巴胺能神经传递的能力。 | |||
T34399 |
Rovatirelin
KPS-0373,S0373,S-0373,S 0373 |
AChE | Neuroscience |
Rovatirelin (S-0373) 是一种新合成的促甲状腺激素释放激素(TRH)类似物,通过乙酰胆碱和多巴胺神经传递改善胞嘧啶阿拉伯糖苷诱导的脊髓小脑变性大鼠模型的运动功能障碍。 | |||
T20828 |
Citalopram
Cipram,Lu 10-171,Lu-10-171 Lu10-171 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Citalopram (Lu 10-171) 是一种具有口服活性的、选择性的血清素再摄取抑制剂 (SSRI),是一种选择性5-羟色胺再摄取抑制剂,是一种 S(+)-对映体 (Escitalopram) 和 R(-)-对映体的外消旋混合物。Citalopram 具有抗抑郁活性,可增强血清素能神经传递,可用于研究老年痴呆。 | |||
T16263 |
N6-Cyclopentyladenosine
UK-80882,CPA |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
N6-Cyclopentyladenosine (CPA) 是一个选择性的腺苷A1 受体 (Adenosine A1 receptor)的激动剂,可用于模拟腺苷A1受体的作用,对人A1、A2A 和 A3 受体的Ki 分别为 2.3 nM、790 nM 和 43 nM。N6-Cyclopentyladenosine (CPA) 可用于调节细胞信号传导、神经递质释放和其他生物学过程。 | |||
T1279 |
Vilazodone
维拉佐酮,SB659746A,EMD 68843 |
5-HT Receptor; Serotonin Transporter | GPCR/G Protein; Neuroscience |
Vilazodone (SB659746A) 是一种可口服的选择性 5 -羟色胺再摄取抑制剂 (SSRI) 和部分5-HT1A 受体激动剂。它有抗抑郁作用,可用于抑郁症和情绪性疾病的研究。 | |||
T2546 |
Pimozide
R6238,匹莫奇特,匹莫齐特 |
Potassium Channel; Dopamine Receptor; Adrenergic Receptor; STAT | GPCR/G Protein; JAK/STAT signaling; Membrane transporter/Ion channel; Neuroscience; Stem Cells |
Pimozide (R6238) 是多巴胺受体拮抗剂,对多巴胺 D1、D2 和 D3 受体的 Ki 值分别为 588、1.4 和 2.5 nM。它也是STAT3和STAT5的抑制剂,对 α1 肾上腺素受体也有较高亲和性,Ki 值为 39 nM。 | |||
T26778L |
Besipirdine hydrochloride
HP 749 hydrochloride,Besipirdine hydrochloride(119257-34-0 Free base) |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Besipirdine hydrochloride 是一种非受体依赖性拟胆碱化合物,具有α-肾上腺素能活性和心血管活性。Besipirdine hydrochloride 抑制电压依赖性钠钾通道,抑制生物胺的摄取。Besipirdine hydrochloride 可减少大鼠的时间表诱导的烦渴,增强中枢神经系统中的胆碱能和肾上腺素能神经传递。 | |||
T26778 |
Besipirdine
HP 749 free base,P-867493,P867493,HP 749,HP749,P 867493 |
Sodium Channel; Adrenergic Receptor | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Besipirdine (HP 749 free base)是一种非受体依赖性拟胆碱化合物,具有α-肾上腺素能活性和心血管活性。Besipirdine 抑制电压依赖性钠钾通道,抑制生物胺的摄取。Besipirdine 可减少大鼠的时间表诱导的烦渴,增强中枢神经系统中的胆碱能和肾上腺素能神经传递。 | |||
T27331 |
Flerobuterol HCl
CRL-40996,CRL40996,CRL 40996,Flerobuterol hydrochloride |
Others | Others |
Flerobuterol is a β adrenergic receptor agonist potentially for the treatment of major depressive disorder. Flerobuterol enhances serotonergic neurotransmission. Flerobuterol acutely increases 5-HT synthesis, in part, through an elevation of brain Trp ava | |||
T25558 |
JNJ-55511118
JNJ 55511118 |
Others | Others |
JNJ-55511118 is a selective negative modulator of AMPA receptors containing TARP-γ8 (Ki: 26 nM). It had excellent pharmacokinetic properties. JNJ-55511118 exhibited a dose-dependent inhibition of neurotransmission within the hippocampus and a strong antic | |||
T26200 |
Somatostatin RC 102
Somatostatin RC102,Somatostatin-RC-102,Somatostatin RC-102 |
Others | Others |
Somatostatin RC 102 is a peptide hormone. It regulates the endocrine system and affects neurotransmission and cell proliferation via interaction with G protein-coupled somatostatin receptors and inhibition of the release of numerous secondary hormones. | |||
T78584 |
Prostaglandin D3
PGD3 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Prostaglandin D3 (PGD3) 是具有抑制人类血小板聚集和调节自主神经传递功能的前列腺素类化合物。 | |||
T79692 |
BChE-IN-19
|
Others | Others |
BChE-IN-19 (Compound 7b) 是一种具有对 BChE 抑制活性(IC50=0.04 μM)的茚酮对位取代衍生物,可改善神经系统胆碱能调控,适用于抗阿尔茨海默病研究。 | |||
TP1732 |
Galanin (1-30), human
|
||
Galanin (1-30), human is a 30-amino acid neuropeptide, and acts as an agonist of GalR1 and GalR2 receptors, with Kis of both 1 nM. Endogenous peptide with multiple endocrine, metabolic and behavioral effects. Has been shown to have an action on intestinal | |||
T75944 |
Spadin TFA
|
||
Spadin TFA 是一种从血液中释放的前肽衍生的天然肽,是一种有效的 TREK-1 通道阻滞剂,其 IC50值为 10 nM。Spadin TFA 增强小鼠中缝背核 5-HT 神经传递,诱导海马 CREB 激活和神经发生。Spadin TFA 可用于抗抑郁研究。 | |||
T78126 |
Dothiepin
Dosulepin,Dothep |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Dothiepin(Dosulepin; Dothep)是一种具备镇静/抗焦虑作用的抗抑郁药物。该化合物主要通过抑制去甲肾上腺素的再摄取,而非血清素,以增强去肾上腺素能神经传递。同时,Dothiepin作为组胺H1受体的拮抗剂,具备显著的镇痛活性,适用于治疗心因性面部疼痛、特发性纤维肌痛综合征或类风湿关节炎,并且不具有心脏毒性。 | |||
T75916 |
Dynorphin A TFA
|
||
Dynorphin A TFA, 作为一种内源性阿片肽,主要在中枢神经系统(CNS)中发挥抑制性神经传导的作用。该化合物不仅是kappa阿片受体(KOR)的高效激动剂,还能激活其他阿片受体,包括mu(MOR)和delta(DOR)。Dynorphin A TFA具有诱导神经元死亡的能力,因此在神经系统疾病的研究中具有应用价值。 | |||
T78827 |
CVN417
|
Others | Others |
CVN417,一种含 α6 亚基的口服nAChR拮抗剂,通过脉冲依赖的方式调控多巴胺能神经传递,并对nAChR亚基介导的Ca(2+)流出显示出抑制效应,其IC50s为0.086 μM (α6),2.56 μM (α3),以及0.657 μM (α4)。在啮齿类动物模型之研究中,CVN417减缓静息震颤,并展现对帕金森病等运动功能障碍改善的可能性。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1023 |
Miltirone
|
P450; GABA Receptor | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Miltirone 是存在于丹参中的一种天然产物,可作为中枢苯二氮受体部分激动剂,IC50值为 0.3 μM。 | |||
T16533 |
Picrotin
|
Chloride channel | Membrane transporter/Ion channel |
Picrotin 是甘氨酸受体的抑制剂。 Picrotin 阻断 α2 GlyR、α1 GlyR 和 α3 GlyR,可用于神经传递研究。 | |||
T20089 |
ATP
Atipi,ATP disodium salt hydrate,Triphosphoric acid adenosine ester,Ara-ATP,Triphosphaden,Adenosine triphosphate;Ara-ATP,Adenosine triphosphate |
Endogenous Metabolite | Metabolism |
ATP (Adenosine triphosphate) 可为细胞提供能量,参与整体能量平衡,维持细胞内稳态。ATP 可以通过与特异性嘌呤能受体的相互作用充当细胞外信号分子,以介导神经传递、炎症、细胞凋亡和骨重塑等多种过程。 | |||
T1638 |
N-Acetylneuraminic acid
唾液酸,Acide aceneuramique,N-乙酰神经氨酸,NeuAc,Lactaminic acid |
Others; Influenza Virus; Endogenous Metabolite | Metabolism; Microbiology/Virology; Others |
N-Acetylneuraminic acid (Acide aceneuramique) 是一种九碳唾液酸单糖,通常存在于细胞膜上的糖蛋白和哺乳动物细胞中的神经节苷脂等糖脂中。它可用于神经传递、白细胞外渗、病毒或细菌感染以及碳水化合物-蛋白质识别。 | |||
T0266 |
Quinidine hydrochloride monohydrate
奎宁树,奎尼丁盐酸盐一水合物,奎尼丁盐酸盐,Quinidine hydrochloride |
Potassium Channel; Sodium Channel; Parasite | Membrane transporter/Ion channel; Microbiology/Virology |
Quinidine hydrochloride monohydrate 是一种抗心律失常剂,也是 K+通道 (K+channel) 的有效阻断剂,其IC50值为 19.9 μM。它是一种有效且选择性的细胞色素 P450db (cytochrome P450db) 抑制剂,也可用作疟疾的研究。 | |||
T6S0721 |
Orientin
荭草苷,Lutexin,Luteolin-8-glucoside |
Others | Others |
Orientin (Luteolin-8-glucoside) 是天然存在的生物活性类黄酮,是一种有前景的神经保护剂,具有多种生物特性,如抗炎、抗肿瘤、抗氧化、保护心脏等。它有用于神经性疼痛研究潜力。 | |||
T72733 |
Geissoschizoline
(+)-Geissoschizoline |
Others | Others |
Geissoschizoline ((+)-Geissoschizoline) 是一种有效的人AChE/BChE 抑制剂,其IC50s 分别为 20.40 µM 和 10.21 µM。Geissoschizoline 可用于预防神经变性和恢复神经传递方面的研究。Geissoschizoline 还具有抗炎作用。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-02929 |
ENTPD2 Protein, Human, Recombinant (aa 29-460, His)
ectonucleoside triphosphate diphosphohydrolase 2,NTPDase-2,R... |
Human | Baculovirus Insect Cells |
NTPDase 2, also known as ENTPD2, belongs to the ecto-nucleoside triphosphate diphosphohydrolase family (E-NTPDase). Members of E-NTPDase family are nucleotidases able to hydrolyze 5′-nucleoside tri- and/or diphosphates; the main role of these enzymes is the termination of purinergic signaling. NTPDases are ubiquitous and were previously shown in other parasites including the trypanosomatides of genus Leishmania and in T. brucei. NTPase activity would act as a timer and is crucial to T. gondii in... | |||
TMPH-00304 |
SV2A Protein, Bovine, Recombinant (His & Myc)
Synaptic vesicle glycoprotein 2A,p87,SV2A |
Bovine | HEK293 Cells |
Plays a role in the control of regulated secretion in neural and endocrine cells, enhancing selectively low-frequency neurotransmission. Positively regulates vesicle fusion by maintaining the readily releasable pool of secretory vesicles. SV2A Protein, Bovine, Recombinant (His & Myc) is expressed in HEK293 mammalian cells with N-10xHis and C-Myc tag. The predicted molecular weight is 22.8 kDa and the accession number is Q29397. | |||
TMPH-02165 |
STXBP1 Protein, Human, Recombinant (His)
MUNC18-1,Syntaxin-binding protein 1,N-Sec1,STXBP1,p67,Protei... |
Human | HEK293 Cells |
Participates in the regulation of synaptic vesicle docking and fusion through interaction with GTP-binding proteins. Essential for neurotransmission and binds syntaxin, a component of the synaptic vesicle fusion machinery probably in a 1:1 ratio. Can interact with syntaxins 1, 2, and 3 but not syntaxin 4. May play a role in determining the specificity of intracellular fusion reactions. | |||
TMPH-03283 |
CD39 Protein, Rat, Recombinant (His)
ATP diphosphohydrolase,Entpd1,Nucleoside triphosphate diphos... |
Rat | Baculovirus Insect Cells |
In the nervous system, could hydrolyze ATP and other nucleotides to regulate purinergic neurotransmission. Could also be implicated in the prevention of platelet aggregation by hydrolyzing platelet-activating ADP to AMP. Hydrolyzes ATP and ADP equally well. | |||
TMPH-03284 |
CD39 Protein, Rat, Recombinant (E. coli, His)
Entpd1,ATP-DPH,Ecto-ATP diphosphohydrolase 1,CD39,Ecto-ATPas... |
Rat | E. coli |
In the nervous system, could hydrolyze ATP and other nucleotides to regulate purinergic neurotransmission. Could also be implicated in the prevention of platelet aggregation by hydrolyzing platelet-activating ADP to AMP. Hydrolyzes ATP and ADP equally well. | |||
TMPH-02166 |
STXBP1 Protein, Human, Recombinant
p67,Protein unc-18 homolog A,Protein unc-18 homolog 1,STXBP1... |
Human | E. coli |
Participates in the regulation of synaptic vesicle docking and fusion through interaction with GTP-binding proteins. Essential for neurotransmission and binds syntaxin, a component of the synaptic vesicle fusion machinery probably in a 1:1 ratio. Can interact with syntaxins 1, 2, and 3 but not syntaxin 4. May play a role in determining the specificity of intracellular fusion reactions. | |||
TMPY-03991 |
DBI Protein, Human, Recombinant (His)
diazepam binding inhibitor (GABA receptor modulator, acyl-Co... |
Human | E. coli |
The diazepam binding inhibitor (DBI), alternatively known as the acyl-CoA binding protein (ACBP), is involved in multiple biological actions. The polypeptide binds to the peripheral, or mitochondrial, benzodiazepine receptor and facilitates transport of cholesterol to the inner membrane to stimulate steroid synthesis. Through this action, DBI indirectly modulates gamma-aminobutyric acid (GABA)-mediated inhibitory neurotransmission. DBI can be postulated as a candidate gene for psychiatric phenot... | |||
TMPY-01820 |
Munc18-1/STXBP1 Protein, Human, Recombinant (His & GST)
MUNC18-1,RBSEC1,P67,syntaxin binding protein 1,UNC18,NSEC1 |
Human | Baculovirus Insect Cells |
Syntaxin-binding protein 1, also known as N-Sec1, Protein unc-18 homolog 1, MUNC18-1 and STXBP1, is a peripheral membrane protein that belongs to the STXBP / unc-18 / SEC1 family. STXBP1 is an evolutionally conserved neuronal Sec1/Munc-18 (SM) protein that is essential in synaptic vesicle release in several species. It may participate in the regulation of synaptic vesicle docking and fusion, possibly through interaction with GTP-binding proteins. STXBP1 is essential for neurotransmission and bin... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIH-0159 |
Citalopram-d6
|
||
Citalopram-d6 是 Citalopram 的氘代化合物。Citalopram 的 CAS 号为 59729-33-8。Citalopram (Lu 10-171) 是一种具有口服活性的、选择性的血清素再摄取抑制剂 (SSRI),是一种选择性5-羟色胺再摄取抑制剂,是一种 S(+)-对映体 (Escitalopram) 和 R(-)-对映体的外消旋混合物。Citalopram 具有抗抑郁活性,可增强血清素能神经传递,可用于研究老年痴呆。 | |||
TMID-0120 |
Valproic Acid-d15
|
||
Valproic Acid-d15 是 Valproic Acid 的氘代化合物。Valproic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 | |||
TMIJ-0163 |
Valproic Acid-d4
|
||
Valproic Acid-d4 是 Valproic Acid 的氘代化合物。Valproic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 | |||
TMIJ-0431 |
2-(Propyl-3,3,3-d3)pentanoic-5,5,5-d3 Acid
|
||
2-(Propyl-3,3,3-d3)pentanoic-5,5,5-d3 Acid 是 2-pentanoic Acid 的氘代化合物。2-pentanoic Acid 的 CAS 号为 99-66-1。Valproic acid是一种 HDAC 抑制剂,可抑制HDAC1的活性,同时可诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、双相情感障碍和偏头痛等。 |