174
3
1
13
9
Cat. No. | Product Name | ||
---|---|---|---|
L2610 | 神经递质受体化合物库 | 1513 compounds | |
1513 种与神经递质受体相关的化合物,用于高通量、高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T14319 |
Aripiprazole Lauroxil
|
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Aripiprazole lauroxil 是一种长效注射剂 (LAI) 的抗精神病药物,是阿立哌唑的 N-酰氧基甲基前药形式。它能够被体内酯酶裂解为 N-羟甲基阿立哌唑(月桂酸),再裂解为阿立哌唑,无毒性。 | |||
T8862 |
ML 254
|
GluR | Neuroscience |
是一种化学合成中的砌块 | |||
T21629 |
Loxapine
|
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Loxapine 是 D2DR 和 D4DR 抑制剂和5-羟色胺能受体拮抗剂,是一种抗精神病药物,主要用于治疗精神分裂症。 | |||
T9183 |
Ralmitaront
RO6889450 |
Others | Others |
Ralmitaront (RO6889450) 是口服具有活力的口服微量胺相关受体 1 (TAAR1) 的部分激动剂。它是一种神经抑制剂,可用于研究神经相关疾病,如精神分裂症 (SCZ)、分裂情感性障碍。 | |||
T21667 |
FAUC-365
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
FAUC-365 是一种高度选择性的多巴胺D3受体拮抗剂,能够作用于 D3 受体(Ki:0.5 nM)、D4.4 受体(Ki:340 nM)、D2short 受体(Ki:2600 nM)和 D2Long 受体(Ki:3600 nM)。它可用于研究帕金森病、精神分裂症等疾病。 | |||
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。 | |||
T5183 |
AUT1
|
Potassium Channel | Membrane transporter/Ion channel |
AUT1 是 Kv3 钾离子通道调节剂,对人重组 Kv3.1b 和 Kv3.2a 的pEC50值分别为 5.33 和 5.31,对其活性是对人重组 Kv3.3 通道的 10 倍,pEC50值为 4.5。 | |||
T13189 |
TP-10
|
PDE | Metabolism |
TP-10 是 PDE10A 对其他 PDE 的特异性抑制剂,IC50 为 0.8 nM。 | |||
T29137 |
VU0453595
VU 0453595,VU-0453595 |
AChR | Neuroscience |
VU0453595 是有效的、高选择性的、全身活性的M1正变构调节剂 (PAM, EC50=2140 nM),在精神分裂症方面有研究价值。 | |||
T9694 |
Emraclidine
CVL-231 |
AChR | Neuroscience |
Emraclidine (CVL-231) 是一种毒蕈碱 M4 受体阳性变构调节剂,可用于神经系统疾病研究。 | |||
T23348 |
SEN12333
SEN 12333 |
AChR | Neuroscience |
SEN12333 是强选择性和口服活性的 α7 nAChR 激动剂,可以用于 AD 和精神分裂症研究。它在功能性 Ca2+通量研究中起到完全激动剂的作用,对 GH4C1 细胞中表达的大鼠 α7 nAChRs 具有很高的亲和性。 | |||
T11095L |
DREADD agonist 21
|
5-HT Receptor; Adrenergic Receptor; AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
DREADD agonist 21 是一种人毒蕈碱乙酰胆碱 M3 受体激动剂,EC50为 1.7 nM。 | |||
T15260 |
Evenamide
NW-3509 |
Sodium Channel | Membrane transporter/Ion channel |
Evenamide (NW-3509) 是一种口服有效的电压门控钠通道 (sodium channel, VGSC) 阻滞剂,Ki 为 0.4 µM,在精神分裂症中有研究价值。Evenamide 在精神病,躁狂症,抑郁和攻击性的各种啮齿动物模型中具有显著功效。 | |||
T14830 |
Bromperidol
溴哌利多,R-11333 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Bromperidol (R-11333) 是一种苯丁酮衍生物,是一种强效长效精神安定药。它被用作治疗精神分裂症的抗精神病药。 | |||
T1539 |
Iloperidone
伊潘立酮,HP 873 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Iloperidone (HP 873) 是一种D2/5-HT2受体拮抗剂,是非典型抗精神病药,可治疗精神分裂症。 | |||
T7943 |
Fluphenazine decanoate
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Fluphenazine decanoate 是一种高度连续的多巴胺 D2受体阻滞剂,是一种长效吩噻嗪抗精神病药,用于精神分裂症的研究。 | |||
T11722 |
JNJ-37822681 dihydrochloride
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
JNJ-37822681 dihydrochloride 是特异性的、有中枢活性的,可快速解离的多巴胺 D2受体拮抗剂,与多巴胺 D2L 受体结合的亲和力适中 (Ki=158 nM)。JNJ-37822681 dihydrochloride 在精神分裂症和躁郁症领域有研究价值。 | |||
T0246 |
Betahistine dihydrochloride
PT-9,Betahistine 2HCl,盐酸倍他司汀 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Betahistine dihydrochloride (Betahistine 2HCl) 是可口服的组胺 H1 受体激动剂和 H3 受体的拮抗剂,可用作血管扩张剂,用于类风湿性关节炎的研究。 | |||
T4195 |
Betahistine
PT 9 base,倍他司汀,Vasomotal,Serc base |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Betahistine (Vasomotal) 是可口服的组胺 H1 受体激动剂和 H3 受体的拮抗剂,可用作血管扩张剂,用于类风湿性关节炎的研究。 | |||
T3086 |
Mesoridazine Besylate
Mesoridazine benzenesulfonate,Serentil,苯磺酸美索达嗪 |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Mesoridazine Besylate (Serentil) 是一种哌啶类精神安定药,属于称为吩噻嗪类的药物,用于治疗精神分裂症。它是硫利达嗪的代谢物。 | |||
T25487 |
Haloperidol decanoate
KD 16,KD-136,KD 136,Neoperidole,Haldol |
Others | Others |
Haloperidol decanoate (KD 16) 是一种典型的抗精神病药物,用作精神分裂症和情绪障碍的维持治疗,配制成用于肌肉注射的酯。 | |||
T24656 |
PQ-10
A844337,PQ 10,A-844337,A 844337 |
PDE | Metabolism |
PQ-10 (A-844337) 是磷酸二酯酶 10A 抑制剂,其IC50=4.6 nM,ED50=13 mg/kg。它能够诱导大脑葡萄糖代谢模式,这可能是潜在的转化生物标志物。它对精神分裂症等精神疾病具有研究潜力。 | |||
T9317 |
TAK-041
NBI-1065846 |
GPR | Endocrinology/Hormones; GPCR/G Protein |
TAK-041 (NBI-1065846) 是一种选择性 GPR139激动剂,EC50为 22 nM,有用于精神分裂症阴性症状的研究潜力。 | |||
T28368 |
PF-04859989 HCl
PF 04859989,PF04859989,PF-04859989HCl,PF-04859989 |
Others | Others |
PF-04859989 HCl 是不可逆的犬尿氨酸转氨酶 KAT II 抑制剂,可透过血脑屏障,抑制 hKATⅡ 和 rKATⅡ 的 IC50分别为 23 和 263 nM。它对 KATⅡ 的选择性高于人 KATⅠ、KATⅢ 和 KATⅣ (IC50分别为22、11和 >50 μM)。 | |||
T1180 |
Blonanserin
布南色林,AD-5423 |
Dopamine Receptor; Sigma receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Blonanserin (AD-5423) 是一种有效的5-HT2A 和多巴胺 D2 受体拮抗剂,Ki 为 0.812 和 0.142 nM,是一种非典型的抗精神病试剂。 | |||
T8389 |
Trifluoperazine
三氟拉嗪,trifluoroperazine |
CaMK; Dopamine Receptor; Influenza Virus; Adrenergic Receptor; P-gp; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Trifluoperazine (trifluoroperazine) 是一种多巴胺 D2 受体抑制剂,可治疗精神分裂症。它是NUPR1抑制剂,具有抗癌活性。它是α1-adrenergic 受体拮抗剂,是流感病毒形态发生的可逆抑制剂。 | |||
T7476 |
AS057278
3-Methylpyrazole-5-carboxylic acid,5-甲基-1H-吡唑-3-羧酸 |
Others | Others |
AS057278 (3-Methylpyrazole-5-carboxylic acid) 是一种 D-氨基酸氧化酶 (DAAO) 抑制剂。 | |||
TQ0084 |
lumateperone Tosylate
ITI-007,Lumateperone甲苯磺酸盐 |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
lumateperone Tosylate (ITI-007) 是5-HT 2A 受体拮抗剂,Ki 为 0.54 nM,突触前 D2受体的部分激动剂和突触后 D2受体的拮抗剂,Ki 为 32 nM。 | |||
T1412 |
Loxapine succinate
Daxolin,Loxapac,Cloxazepin,Loxapine succinate salt,丁二酸洛沙平,琥珀酸洛沙平 |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Loxapine succinate (Loxapac) 是D2/D4多巴胺受体,5-羟色胺受体抑制剂,用于精神分裂症。 | |||
T0455 |
Clozapine
氯氮平,HF 1854,LX 100-129 |
Dopamine Receptor; Adrenergic Receptor; AChR | GPCR/G Protein; Neuroscience |
Clozapine (HF 1854) 是一种三环二苯二氮卓类药物,属于非典型抗精神病药物。它结合几种类型的中枢神经系统受体,并显示出独特的药理学特征。 它是一种血清素拮抗剂,与 5-HT 2A/2C 受体亚型具有强结合力。它还对几种多巴胺能受体表现出很强的亲和力,但对多巴胺 D2 受体仅表现出较弱的拮抗作用,这种受体通常被认为可调节精神抑制活性。 | |||
T3619 |
VU0357017 hydrochloride
ML071 hydrochloride,CID-25010775,VU 0357017 hydrochloride,盐酸 VU 0357017 |
AChR | Neuroscience |
VU0357017 hydrochloride (ML071 hydrochloride) 是一种选择性和可透过血脑屏障的M1毒蕈碱乙酰胆碱受体变构激动剂,EC50值为 477 nM。它对 M1具有高度选择性,可用于阿尔茨海默症和精神分裂症的研究。 | |||
T21069 |
Lumateperone
ITI 722,ITI722,ITI-007,卢美哌隆,ITI007 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Lumateperone (ITI 722) 是一种 5HT2A 受体拮抗剂和多巴胺受体磷蛋白调节剂 (DPPM)。 | |||
T1884 |
CX516
Ampakine CX516,BDP 12,Ampalex,安帕来斯 |
GluR; iGluR | Membrane transporter/Ion channel; Neuroscience |
CX516 (Ampalex) 是AMPA 受体正向调节剂,可用于研究阿尔茨海默病,精神分裂等。 | |||
T5135 |
Flupentixol dihydrochloride
盐酸氟哌噻吨,Fupentixol Dihydrochloride,Flupenthixol dihydrochloride,(E/Z)-Flupentixol Dihydrochloride |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Flupentixol dihydrochloride 是噻克西酮类试剂,能够用于研究精神分裂症以及抗焦虑和抑郁障碍。 | |||
T10232 |
Acetophenazine dimaleate
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Acetophenazine dimaleate 是抗精神病试剂,能够有效治疗焦虑抑郁。 | |||
T1222 |
Trifluoperazine dihydrochloride
Trifluoperazine 2HCl,盐酸三氟拉嗪,SKF5019,Urinox |
CaMK; Dopamine Receptor; Influenza Virus; Adrenergic Receptor; P-gp; Autophagy | Autophagy; GPCR/G Protein; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Trifluoperazine dihydrochloride (SKF5019) 是一种抗精神病药物,靶向中枢多巴胺受体。它是流感病毒形态发生的可逆抑制剂,是NUPR1抑制剂,具有抗癌活性。它是钙调蛋白抑制剂,还可抑制 P-糖蛋白,可研究精神分裂症。 | |||
T9827 |
carfenazine
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
carfenazine 靶向多巴胺受体,用于精神分裂症研究。 | |||
T27865 |
LX-6171
LX6171 |
Others | Others |
LX-6171是一种脯氨酸转运体(SLC6A7)抑制剂,可用于治疗精神分裂症和阿尔茨海默病。 | |||
T39010 |
Xanomeline tartrate
LY 246708 tartrate,Xanomeline tartrate |
Others | Others |
Xanomeline (LY 246708), a potent agonist of muscarinic M1/M4 receptors, exhibits antipsychotic-like activity and enhances neuronal excitability. It is a valuable compound for studying schizophrenia. | |||
T30098 |
Aplindore Fumarate
Aplindore,DAB-452 Fumarate,DAB-452 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Aplindore Fumarate (DAB-452)是一种小分子多巴胺 D2 受体部分激动剂,Aplindore Fumarate 对多巴胺D2 和D3 受体表现出高亲和力,对多巴胺D4、5-羟色胺(5-HT2)和α1-肾上腺素受体表现出低亲和力。Aplindore Fumarate 可用于研究帕金森和精神分裂症。 | |||
T34616 |
Seridopidine
ACR-343,ACR 343,ACR343 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Seridopidine (ACR343) 是一种多巴胺能活性调节剂,可作为精神分裂症、帕金森病和抽动秽语综合征的口服疗法。 | |||
T23900 |
Clothiapine
S-805C,HF2159,HF 2159,HF-2159,LW 2159 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Clothiapine (HF 2159) 是一种非典型抗精神病剂,具有很强的抗 5-羟色胺能和血清素能活性活性,可用于研究精神分裂。 | |||
T32633 |
Lensiprazine
SLV314,SLV-314,SLV 314 |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Lensiprazine (SLV314)是一种有效的多巴胺 D(2)受体拮抗剂,可作为一种血清素再摄取抑制剂 ,可用于研究躁郁症和精神分裂症。 | |||
T23649 |
AF-710B
ANAVEX 3-71,AF 710B,AF710B |
Sigma receptor; AChR | GPCR/G Protein; Neuroscience |
AF-710B 是一种特异性变构 M1 毒蕈碱和 Sigma-1 受体激动剂,可用于研究阿尔茨海默病痴呆和神经分裂等神经系统疾病。 | |||
T24613 |
PF-00217830
PF-217830 |
Dopamine Receptor; Serotonin Transporter | GPCR/G Protein; Neuroscience |
PF-00217830 是一种血清素 1A 受体激动剂、多巴胺 D2 受体激动剂和血清素 2A 受体拮抗剂。PF-00217830 可用于研究精神分裂症。 | |||
TP1270L |
2:PN:US20040072744 SEQID:2 claimed protein acetate
2:PN:US20040072744 SEQID:2 claimed protein acetate(389572-87-6 free base) |
Others | Others |
2:PN:US20040072744 SEQID:2 claimed protein acetate 是一种合成肽,用于唐氏综合症和精神分裂症的研究。 | |||
T1567 |
Olanzapine
LY170053,奥氮平 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; AChR | GPCR/G Protein; Neuroscience |
Olanzapine (LY170053) 是一种非典型抗精神病药,目前用于治疗精神分裂症和双相情感障碍。 | |||
T31079 |
CP-810123
CP 810123,UNII-E6G4550EC4,CP810123 |
AChR | Neuroscience |
CP-810123 是一种新的α 7 nAChR 激动剂,可用于治疗与精神分裂症和阿尔茨海默病等精神或神经疾病相关的认知障碍。 | |||
T28809 |
SLV-310
SLV 310,SLV310 |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
SLV-310 是一种强效的多巴胺 D2 受体拮抗剂和 5-HT 再摄取受体抑制剂,可用于研究躁郁症和精神分裂症等神经系统疾病。 | |||
T84293 |
SSR 180
SSR180711 |
AChR | Neuroscience |
SSR 180 是一种高效性且亚型选择性的 α7 激动剂具有可用于研究阿尔茨海默病和精神分裂症。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0076 |
Paliperidone
9-羟基利培酮,帕潘立酮,9-hydroxyrisperidone |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Paliperidone (9-hydroxyrisperidone) 是 Risperidone 的主要活性代谢产物,是多巴胺 D2 拮抗剂和5-HT2A 拮抗剂。它用作非典型抗精神病药,用于精神分裂症的急性及维持治疗。它对α1和α2肾上腺素能受体和 H1组胺能受体也有拮抗作用。 | |||
T6975 |
Sarcosine
Sarcosinic acid,Methylaminoacetic acid,Sarcosin,肌氨酸,Methylglycine,N-Methylaminoacetic acid,N-methylglycine |
Others; GlyT; Endogenous Metabolite | Metabolism; Neuroscience; Others |
Sarcosine (Methylglycine) 是 I 型甘氨酸转运蛋白 (GlyT1) 的竞争性抑制剂和 N-甲基-D-天冬氨酸受体 (NMDAR) 共激动剂,通过增加甘氨酸的浓度增强 NMDA 受体的功能,可用于精神分裂症的研究。 | |||
T4877 |
L-Homocystine
|
Endogenous Metabolite | Metabolism |
L-Homocystine 是一种 L-homocysteine 的氧化物。其中 L-homocysteine 是抗血栓因子、血管舒张损害剂、促炎因子,也是研究心血管疾病发生机制的内质网应激反应的诱导剂。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-05054 |
Notch 4 Protein, Human, Recombinant (His)
INT3,notch 4 |
Human | Baculovirus Insect Cells |
NOTCH4 (Notch Receptor 4) is a Protein Coding gene. Notch4 belongs to a family of transmembrane receptors that play an important role in vascular development and maintenance. The NOTCH4 gene is located at 6p21.3 and is involved in the development and patterning of the central nervous systems. It regulates signaling pathways associated with neuronal maturation, a process involved in the development and patterning of the central nervous system. The NOTCH4 gene has also been identified as a possibl... | |||
TMPY-02377 |
14-3-3 eta/YWHAH Protein, Human, Recombinant (GST)
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activati... |
Human | E. coli |
YWHAH, the gene encoding the 14-3-3eta isoform, is highly expressed in retinal ganglion cells (RGC). YWHAH is a positional and functional candidate gene for both schizophrenia and bipolar disorder (BP). It is located on chromosome 22q12.3, a region that has been implicated by linkage studies in both BP and schizophrenia. | |||
TMPK-01200 |
Nogo Receptor/RTN4R Protein, Cynomolgus, Recombinant (His)
NGR,NOGOR,RTN4R,NgR1,Nogo receptor,Nogo-66 receptor |
Cynomolgus | HEK293 Cells |
NOGO Receptor 1 (RTN4R) regulates axonal growth, as well as axon regeneration after injury. The gene maps to the 22q11.2 schizophrenia susceptibility locus and is thus a strong functional and positional candidate gene.RTN4R may modulate the genetic risk or clinical expression of schizophrenia in a subset of patients and identify additional studies that will be necessary to clarify the role of RTN4R in psychiatric phenotypes. | |||
TMPY-01120 |
VPAC2 Protein, Human, Recombinant (mFc)
VPCAP2R,PACAP-R-3,VIP-R-2,vasoactive intestinal peptide rece... |
Human | HEK293 Cells |
VIP and PACAP receptor 2, or VIPR2 encodes the VPAC2 receptor, which binds both VIP and PACAP. VPAC2 is expressed throughout the central nervous system and the periphery. Mutations in the VIPR2 homolog in the mouse cause hypoactivity, as well as disruptions in circadian rhythm. Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia. | |||
TMPJ-01271 |
PIK3IP1 Protein, Human, Recombinant (His)
Kringle domain-containing protein HGFL,PIK3IP1,HGFL |
Human | HEK293 Cells |
Phosphoinositide-3-kinase-interacting protein 1(PIK3IP1) is an enzyme that in humans is encoded by the PIK3IP1 gene.It is a negative regulator of phosphatidylinositol-3-kinase (PI3K), suppresses the development of hepatocellular carcinoma. The gene encoding PIK3IP1 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibrom... | |||
TMPJ-01296 |
SULT4A1 Protein, Human, Recombinant
hBR-STL,SULTX3,Nervous System Sulfotransferase,SULT4A1,ST4A1... |
Human | E. coli |
Sulfotransferase 4A1 (ST4A1) is a member of the Sulfotransferase 1 family. ST4A1 is highly expressed in the cerebral cortex and frontal lobe, but no expression is detected in the pancreas. ST4A1 is a brain-specific sulfotransferase believed to be involved in the metabolism of neurotransmitters. ST4A1 acts on catecholamines and T4 in a manner that may not involve sulfonation. ST4A1 may have a role in the metabolism of drugs and neurotransmitters in the CNS. In addition, ST4A1 is related to schizo... | |||
TMPY-02511 |
PTP alpha/PTPRA Protein, Human, Recombinant (aa 174-793, His & GST)
LRP,PTP α/PTPRA Protein, Human, Recombinant (aa 174-793, His... |
Human | Baculovirus Insect Cells |
PTPRA is reported to be involved in cancer development and progression through activating the Src family kinase (SFK) signaling pathways. The higher PTPRA level was associated with worse prognosis of SCC patients and PTPRA could promote the cell cycle progression through stimulating the c-Src signaling pathways. The PTPRA gene, which encodes the protein RPTP-alpha, is critical to neurodevelopment. Previous linkage studies, genome-wide association studies, controlled expression analyses and anima... | |||
TMPJ-00383 |
SEMA3A Protein, Human, Recombinant (His & Flag)
Hsema-III,SemD,SEMA3A,Semaphorin III,SEMAD,Hsema-I,Sema III,... |
Human | HEK293 Cells |
emaphorin-3A is a secreted protein which belongs to the semaphorin family. Semaphorins are a family of secreted and cell-bound signaling molecules defined by the presence of a common 500 aa Sema domain.This protein can function as either a chemorepulsive agent, inhibiting axonal outgrowth, or as a chemoattractive agent, stimulating the growth of apical dendrites. In both cases, the protein is vital for normal neuronal pattern development. Increased expression of this protein is associated with s... | |||
TMPY-03852 |
Dopamine beta-Hydroxylase Protein, Human, Recombinant (His)
dopamine β-hydroxylase (dopamine β-monooxygenase),Dopamine β... |
Human | HEK293 Cells |
DBH is a 29 kDa copper-containing oxygenase. It can be detected in noradrenergic nerve terminals of the central and peripheral nervous systems, and is also expressed in chromaffin cells of the adrenal medulla. DBH contains our identical subunits, and its activity requires ascorbate as a cofactor. It functions in in the synthesis of small-molecule neurotransmitters that is membrane-bound, making norepinephrine the only transmitter synthesized inside vesicles. DBH has been shown to be associated ... | |||
TMPJ-00660 |
IMPase2 Protein, Human, Recombinant (His)
Inositol-1(or 4)-Monophosphatase 2,IMPA2,IMP 2,IMPase 2,Inos... |
Human | E. coli |
Inositol monophosphatase 2, also known as Inositol-1(or 4)-monophosphatase 2, Myo-inositol monophosphatase A2 and IMPA2, is an enzyme which belongs to the inositol monophosphatase family. IMPA2 catalyzes the dephosphoylration of inositol monophosphate with cofactor Magnesium and Inhibited by high Li+ and restricted Mg2+ concentrations. IMPA2 plays an important role in phosphatidylinositol signaling. IMPA2 can use the myo-inositol monophosphates, scylloinositol 1,4-diphosphate, glucose-1-phosphat... | |||
TMPY-03276 |
BLBP Protein, Human, Recombinant
fatty acid binding protein 7, brain,FABPB,MRG,B-FABP,BLBP,RP... |
Human | E. coli |
BLBP, also known as FABP7, is a brain fatty acid binding protein. Fatty acid binding proteins (FABPs) are a family of small, highly conserved, cytoplasmic proteins that bind long-chain fatty acids and other hydrophobic ligands. FABP7 binds DHA with the highest affinity among all of the FABPs. FABPs may play roles in fatty acid uptake, transport, and metabolism. BLBP is expressed, during development, in radial glia by the activation of notch receptors. It was shown that reelin induces FABP7 expre... | |||
TMPY-04408 |
CAMKII beta/CAMK2B Protein, Human, Recombinant (His & GST)
calcium/calmodulin-dependent protein kinase II beta,CAM2,CAM... |
Human | Baculovirus Insect Cells |
Calcium/calmodulin-dependent protein kinase II beta (CAMK2B) is a member of the serine/threonine protein kinase family and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. CaMKII is an important player in prostate cancer cells ability to escape apoptosis under androgen ablation and facilitate the progression of prostate cancer cells to an androgen independent state. As a multifunctional protein kinase, the loss of activity may play a critical role in initiating the changes leading to... | |||
TMPY-01695 |
CASPR2 Protein, Mouse, Recombinant (His)
5430425M22Rik,Caspr2,contactin associated protein-like 2,mKI... |
Mouse | HEK293 Cells |
CNTNAP2/CASPR2 is a member of the neurexin family which functions in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin N-terminal-like domains and a putative PDZ binding site. CNTNAP2/CASPR2 is localized at the juxtaparanodes of myelinated axons, and media... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T74145 |
Deutarserine
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Deutarserine 是内源性 D-丝氨酸 (CTP 692) 的氘代物,用于成人精神分裂症的研究。 | |||
TMIJ-0322 |
Olanzapine-d8
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Olanzapine-d8 是 Olanzapine 的氘代化合物。Olanzapine 的 CAS 号为 132539-06-1。Olanzapine 是一种非典型抗精神病药,目前用于治疗精神分裂症和双相情感障碍。 | |||
TMID-0025 |
Quetiapine-d8 Hemifumarate
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Quetiapine-d8 Hemifumarate 是 Quetiapine Hemifumarate 的氘代化合物。Quetiapine Hemifumarate 的 CAS 号为 111974-72-2。Quetiapine Fumarate 是5-HT受体激动剂和多巴胺受体拮抗剂,对人5-HT1A和人D2的pEC50值分别为 4.77 和 6.33,具有抗抑郁和抗焦虑作用。 | |||
TMIJ-0315 |
Quetiapine-d8 Fumarate
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Quetiapine-d8 Fumarate 是 Quetiapine Fumarate 的氘代化合物。Quetiapine Fumarate 的 CAS 号为 111974-72-2。Quetiapine Fumarate 是5-HT受体激动剂和多巴胺受体拮抗剂,对人5-HT1A和人D2的pEC50值分别为 4.77 和 6.33,具有抗抑郁和抗焦虑作用。 | |||
TMID-0053 |
Amisulpride-d5
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Amisulpride-d5 是 Amisulpride 的氘代化合物。Amisulpride 的 CAS 号为 71675-85-9。Amisulpride 是多巴胺D2/D3受体拮抗剂,对于人多巴胺D2和D3的Ki分别为 2.8 和 3.2 nM。 | |||
TMIH-0427 |
Perospirone hydrochloride-d8
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Perospirone hydrochloride-d8 是 Perospirone hydrochloride 的氘代化合物。Perospirone hydrochloride 的 CAS 号为 129273-38-7。Perospirone hydrochloride 是非典型的抗精神病剂,可用于精神分裂症的研究。它是可口服的5-HT2A受体和多巴胺D2受体的拮抗剂,也是5-HT1A受体的部分激动剂。 | |||
TMIJ-0269 |
Perospirone-d8 HCl
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Perospirone-d8 HCl 是 Perospirone HCl 的氘代化合物。Perospirone HCl 的 CAS 号为 129273-38-7。Perospirone hydrochloride 是非典型的抗精神病剂,可用于精神分裂症的研究。它是可口服的5-HT2A受体和多巴胺D2受体的拮抗剂,也是5-HT1A受体的部分激动剂。 | |||
TMIH-0314 |
Lurasidone-d8 HCl
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Lurasidone-d8 HCl 是 Lurasidone HCl 的氘代化合物。Lurasidone HCl 的 CAS 号为 367514-88-3。Lurasidone hydrochloride 是多巴胺 D2和5-HT7的拮抗剂,IC50值分别为 1.68 和 0.495 nM,用于治疗精神分裂症和双相情感障碍。它也是5-HT1A受体的部分激动剂,IC50值为 6.75 nM。 | |||
TMIH-0420 |
Paliperidone-d4
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Paliperidone-d4 是 Paliperidone 的氘代化合物。Paliperidone 的 CAS 号为 144598-75-4。Paliperidone 是 Risperidone 的主要活性代谢产物,是多巴胺 D2 拮抗剂和5-HT2A拮抗剂。它用作非典型抗精神病药,用于精神分裂症的急性及维持治疗。它对α1和α2肾上腺素能受体和H1组胺能受体也有拮抗作用。 |