Neuroscience(神经科学)

Neuroscience
Neurons communicate with each other, effector organs and sensory organs through the neurotransmitter – receptor pathway at synapses. Neurotransmitters can be divided into 4 major groups: 1. Amino acids (glumate, aspartate, serine, glycine and GABA); 2. Monoamines (norepinephrine, epinephrine, dopamine, histamine, and serotonin); 3. Peptides (opioid peptides, substance P, somatostatin); and 4. Others (acetylcholine, NO, nucleosides). read more
Products for Neuroscience
- 5-HT Receptor(420)
- AChR(53)
- AChE(100)
- Alzheimer(107)
- Amyloid β(118)
- BACE(4)
- CGRP (33)
- COX(294)
- DAPK(7)
- Dopamine Receptor(290)
- GABA Receptor(155)
- Gap Junction(16)
- GluR(116)
- Histamine(2)
- Histamine Receptor(236)
- mPEGS-1(4)
- Muscarinic Receptor(41)
- Neuroscience Peptides(38)
- Nicotinic Receptor(62)
- P2 Receptor(2)
- P2X7 receptor(3)
- SSRIs(5)
- Substance P/NK1 Receptor(20)
- NMDA(2)
- Beta-secretase(25)
- CaMK(32)
- Dopamine Transporter(20)
- Monoamine Oxidase(91)
- Serotonin Transporter(57)
- nAChR(100)
- iGluR(155)
- Neurokinin Receptor(75)
- MCHR1 (GPR24)(16)
- mAChR(183)
- GPR139(4)
- Cholecystokinin Receptor(25)
- Behavioral Neuroscience(353)
- DREADD(1)
- Huntington(14)
- Neuroendocrinology(64)
- Neuroprotection(117)
- Ophthalmology(158)
- Pain Research(229)
- Parkinson(73)
- Prion(7)
- Seizure Disorders(94)
- Cholinesterases(13)
- Tau Protein(4)
- Neurodegenerative Disorders(5)
- Cholinesterase (ChE)(3)
- Amyloid-β(9)
- γ-secretase(1)
- Ischemia(3)
- Cat.No. 产品名称 Information
-
GC41339
Pioglitazone Ketone
吡格列酮
An active metabolite of pioglitazone -
GC36924
Pipamperone
酰胺哌啶酮,Floropipamide; McN-JR 3345; R 3345
Pipamperone (Floropipamide; McN-JR 3345; R 3345) 是 5-HT2A 受体 (pKi=8.2) 和 D4 受体 (pKi=8.0) 的高亲和力拮抗剂。Pipamperone (Floropipamide; McN-JR 3345; R 3345) 是 D2 受体 (pKi=6.7) 的低亲和力拮抗剂。 -
GC38938
Pipecuronium bromide
哌库溴铵
Pipecuronium bromide 是一种有效的长效非去极化甾体神经肌肉阻滞剂 (NMBA),是一种双季铵化合物。Pipecuronium bromide 是一种功能强大的竞争性 nAChR 拮抗剂,Kd 为 3.06 μM。 -
GC30827
Pipequaline (PK-8165)
哌夸林,PK-8165
A partial agonist of central benzodiazepine receptors -
GC31183
Piperidine-MO-1
Piperidine-MO-1是来自专利WO/2005/121087A1化合物实例2的多巴胺受体(dopaminereceptor)调节剂,在大鼠纹状体中增加DOPAC的ED50值为68μmol/kg。
-
GC31056
Piperidolate
二苯哌酯
Piperidolate是一种抗胆碱剂,作用于大鼠和狗,可抑制乙酰胆碱引起的肠抽筋。 -
GC30912
Piperidolate hydrochloride
盐酸哌立度酯
Piperidolate盐酸盐是一种抗胆碱剂,作用于大鼠和狗,可抑制乙酰胆碱引起的肠抽筋。 -
GC13469
Piracetam
吡拉西坦; UCB-6215
An Analytical Reference Standard -
GC49192
Piracetam-d6
UCB-6215-d6
An internal standard for the quantification of piracetam -
GC25756
Pirenperone
R-47456, R-50656
Pirenperone (R-47456, R-50656), a quinazoline derivative, is a selective antagonist of SR-2A (5-HT2 serotonin receptor) when employed in low doses. Pirenperone behaves like a typical neuroleptic when used in higher doses (greater than 0.1 mg/kg). -
GC13403
Pirenzepine dihydrochloride
盐酸哌仑西平,LS 519; Pirenzepin dihydrochloride; Gastrozepin dihydrochloride
A muscarinic M1 receptor antagonist -
GC36929
Piribedil
吡贝地尔; 双哌嘧啶
A dopamine receptor agonist -
GC30396
Piribedil D8 (ET-495 D8)
吡贝地尔D8,ET-495 D8
Piribedil D8 (ET-495 D8) (ET-495 D8) 是氘标记的 Piribedil,它是一种抗帕金森病药物。 -
GC11602
Piribedil dihydrochloride
盐酸吡贝地尔;盐酸双哌嘧啶;盐酸泰舒达
A dopamine receptor agonist -
GC49845
Piribedil N-oxide
吡贝地尔氮氧化物
A metabolite of piribedil -
GC60291
Pirimiphos-methyl
甲基嘧啶磷
Pirimiphos-methyl 是一种快速作用的有机磷杀虫剂和杀螨剂,可抑制目标生物体中的乙酰胆碱酯酶 (AChE)。Pirimiphos-methyl 经常在农业谷物的储存过程中用于预防和控制甲虫,鼻子甲虫,飞蛾和埃氏小球藻。 -
GC14323
Pirinixic Acid Aminothiazole
A dual inhibitor of mPGES-1 and 5-LO
-
GC41251
Pirlindole
坡尔吲哚
A selective and reversible MAO-A inhibitor -
GC48853
Pirlindole-d4 (hydrochloride)
An internal standard for the quantification of pirlindole
-
GC32478
Pirmenol hydrochloride (Cl-845)
盐酸吡美诺; Cl-845; (±)-Pirmenol hydrochlorid
A class I antiarrhythmic agent -
GC31897
Pirolate (CP-32387)
匹罗酯,CP-32387
Pirolate (CP-32387) 是一种组胺 H1 受体拮抗剂。 -
GC16790
Piroxicam
吡罗昔康; CP-16171
A COX inhibitor and NSAID -
GC61193
Piroxicam D3
吡罗昔康 D3; CP-16171 D3
An internal standard for the quantification of piroxicam -
GC18207
Pitofenone (hydrochloride)
吡托非农盐酸盐
An antispasmodic agent -
GC36931
Pitolisant
替洛利生,Tiprolisant
A histamine H3 receptor antagonist and inverse agonist -
GC11382
Pitolisant hydrochloride
1-[3-[3-(4-氯丙基)丙氧基]丙基]-哌啶盐酸盐,Ciproxidine;BF 2649;BF2649;BF-2649
A histamine H3 receptor antagonist and inverse agonist -
GC36932
Pitolisant oxalate
PITOLISANT草酸盐,Tiprolisant oxalate
A histamine H3 receptor antagonist and inverse agonist -
GC13053
Pizotifen
苯噻啶; Pizotyline; BC-105
A triptan -
GC13478
Pizotifen Malate
苯噻啶苹果酸盐,Pizotyline malate; BC-105 malate
A triptan -
GC47962
PKCε Inhibitor Scramble Peptide
H-Leu-Ser-Glu-Thr-Lys-Pro-Ala-Val-OH, H-LSETKPAV-OH
A negative control for PKCε inhibitor peptide -
GC92078
PKG Inhibitor (trifluoroacetate salt)
Arginyl-
PKG Inhibitor (trifluoroacetate salt)是一种特定的cGMP依赖性PKG抑制剂Ki=86μM。lysyl- arginyl- alanyl- arginyl- lysyl- glutamic acid; Protein Kinase G Inhibitor -
GC49265
PKI (14-22) amide (myristoylated) (trifluoroacetate salt)
Myr-Gly-Arg-Thr-Gly-Arg-Arg-Asn-Ala-Ile-NH2, Myr-GRTGRRNAI-NH2, Myristoylated PKI-(14-22)-amide, PKI-(Myr-14-22)-amide
A PKA inhibitor -
GC65954
Plazinemdor
Plazinemdor 是一种 N-甲基-D-天冬氨酸 (NMDA) 受体正变构调节剂,用于精神、神经、神经发育障碍以及神经系统疾病的研究。
-
GC48362
PMX-205 (trifluoroacetate salt)
A potent antagonist of C5aR
-
GC90490
PMX-53 (trifluoroacetate salt)
AcF-OPdChaWR, AcPhe-Orn-Pro-D-Cyclohexylalanine-Trp-Arg, 3D53
一种C5a受体拮抗剂
-
GC71040
PNB-001
PNB-001是一种口服活性CCK2选择性配体和拮抗剂。
-
GC17854
PNU 142633
PNU 142633 是一种高亲和力、选择性和口服活性的 5-HT1D 受体激动剂,对人 5-HT1D 受体和人 5-HT1B 受体的 Kis 分别为 6 nM 和 \u003e 18 000 nM。
-
GC15763
PNU 177864 hydrochloride
dopamine D3 receptor antagonist
-
GC12952
PNU 282987
PNU 282987是一种选择性α7烟碱乙酰胆碱受体(α7nAChR)激动剂,与抗炎途径相关,也是5-HT3受体的拮抗剂,PNU 282987对α7nAChR的EC50为154nM (Ki α7nAChR=27nM,大鼠脑匀浆),对5-HT3受体的IC50为4541nM (Ki 5-HT3R=1662nM, GR-65630)。
-
GC11902
PNU 96415E
PNU 96415E 是一种选择性 D4/5-HT2A 拮抗剂。
-
GC11643
PNU-120596
NSC 216666
PNU-120596是α7神经元烟碱乙酰胆碱受体(α7nAChR)的正变构调节剂,EC50值为216nM。 -
GC36942
PNU-282987 S enantiomer free base
PNU-282987 S enantiomer free base is the S-enantiomer of PNU-282987 free base, which is an α7 nicotinic acetylcholine receptor (α7 nAChR) agonist.
-
GN10578
Polygalacic acid
毛果一枝黄花皂苷元G
A triterpenoid saponin with antioxidant and neuroprotective activities -
GC74619
Posdinemab
JNJ-63733657
Posdinemab是一种针对微管相关蛋白tau(MAPT)的人源化IgG1κ抗体。 -
GC36952
Pozanicline
ABT-089
Pozanicline (ABT-089) 是一种新型的胆碱能药物,是 α4β2* nAChRs 部分激动剂,显示对 α6β2* 和 α4α5β2 nAChR 亚型的高选择性。Pozanicline 与 [3H] cytisine位点的结合亲和力 (Ki; rat) 为 16.7 nM。Pozanicline 逆转尼古丁戒断诱导的认知缺陷,可能是尼古丁成瘾的新治疗策略的有效组成部分。 -
GC38940
Pozanicline dihydrochloride
ABT-089 dihydrochloride
Pozanicline dihydrochloride (ABT-089 dihydrochloride) 是一种具有口服活性的烟碱型乙酰胆碱受体 (nAChR) 激动剂,与 [3H] 胱氨酸位点结合,Ki 为 16.7 nM。Pozanicline dihydrochloride 是一种 α4β2 选择性 nAChR 激动剂,与大鼠脑 α4β2 nAChR 结合,Ki 为 17 nM,而与 α7nAChR 的结合力很弱。 -
GC44673
PQ-10
6,7-二甲氧基-4-[(3R)-3-(2-喹喔啉基氧基)-1-吡咯烷基]喹唑啉
A selective PDE10 inhibitor -
GC63153
PQCA
PQCA 是一种高度选择性且有效的毒蕈碱 M1 受体阳性变构调节剂。PQCA 在恒河猴和人 M1 受体上的 EC50 值分别为 49 nM 和 135 nM,并对其他毒蕈碱受体无活性。PQCA 具有减少与阿尔茨海默氏病相关的认知缺陷的潜力。
-
GC36954
PQM130
PQM130是一种能透过大脑的、魏罗酮-多奈哌齐杂化化合物,是多靶点的候选药物,可用于Aβ1-42 低聚物引起的神经毒性,还具有抗炎活性。PQM130 是具有神经保护作用的、有潜力的抗 AD 药物。
-
GC33684
Pralidoxime chloride (2-PAM chloride)
氯解磷定,2-PAM chloride
An AChE reactivator