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(410)
- AChR(53)
- AChE(101)
- Alzheimer(105)
- Amyloid β(119)
- BACE(4)
- CGRP (32)
- COX(293)
- DAPK(5)
- Dopamine Receptor(290)
- GABA Receptor(152)
- Gap Junction(16)
- GluR(116)
- Histamine(2)
- Histamine Receptor(232)
- 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(24)
- CaMK(33)
- Dopamine Transporter(19)
- Monoamine Oxidase(85)
- Serotonin Transporter(57)
- nAChR(97)
- iGluR(154)
- Neurokinin Receptor(73)
- MCHR1 (GPR24)(16)
- mAChR(179)
- GPR139(4)
- Cholecystokinin Receptor(25)
- Behavioral Neuroscience(345)
- DREADD(1)
- Huntington(14)
- Neuroendocrinology(58)
- Neuroprotection(115)
- Ophthalmology(157)
- Pain Research(221)
- Parkinson(71)
- Prion(7)
- Seizure Disorders(94)
- Cholinesterases(13)
- Neurodegenerative Disorders(3)
- Cat.No. 产品名称 Information
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GC61382
Xanthoangelol
黄色当归醇
Xanthoangelol, a chalcone found in the roots of Angelica keiskei, is a nonselective monoamine oxidase (MAO) inhibitor and a potent dopamine β-hydroxylase (DBH) inhibitor. It has anti-inflammatory, antibiotic and pro-apoptotic activities. - GC61378 VU0238441 VU0238441 is a pan muscarinic acetylcholine receptor (mAChR) positive allosteric modulator (PAM) with EC50 of 2.1 μM, 2.2 μM, 2.8 μM, 3.2 μM and >10 μM for M5, M3, M2, M1 and M4, respectively.
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GC61377
VU0119498
1-(4-溴苄基)吲哚-2,3-二酮
An M1, M3, and M5 muscarinic receptor positive allosteric modulator -
GC61371
Veratric acid
藜芦酸
Veratricacid(3,4-Dimethoxybenzoicacid)是从蔬菜和水果中得到的多酚物质,可口服,具有抗氧化、保护心血管和抗炎活性。当细胞受到UVB辐射时,Veratricacid能够减少上调的COX-2表达,降低PGE2和IL-6水平。 - GC61367 VAF347 VAF347是一种细胞可渗透且高度亲和力的芳烃受体(AhR)激动剂,可诱导AhR信号传导。VAF347抑制颗粒单核细胞(GM期)前体中CD14+CD11b+单核细胞的发育。VAF347具有抗炎作用。
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GC61337
Tolmetin
托麦汀;托美丁
Tolmetin (Tolectin) is a nonsteroidal anti-inflammatory drug of the heterocyclic acetic acid derivative class and also exhibits analgesic and antipyretic activity. -
GC61317
Tebanicline dihydrochloride
Ebanicline dihydrochloride; ABT-594 dihydrochloride
Tebaniclinedihydrochloride(Ebaniclinedihydrochloride)是nAChR的调节物,具有有效的口服止痛活性。抑制cytisine与神经元nAChR的结合的Ki值为37pM。 - GC61286 SP-8356 SP-8356, an anti-inflammatory synthetic verbenone derivative, is a CD147 inhibitor with respect to its regulation of breast cancer cell behavior and cancer progression.
- GC61281 SKF-83566 A dopamine D1 receptor antagonist
- GC61268 SB 243213 A 5-HT2C receptor inverse agonist
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GC61256
Rupatadine D4 fumarate
UR-12592 D4 fumarate
RupatadineD4fumarate(UR-12592D4fumarate)是Rupatadinefumarate的氘代标记物。RupatadineFumarate(UR-12592Fumarate)富马酸盐是PAF/H1受体双抑制剂,Ki值分别为0.55μM和0.1μM。 -
GC61255
Rubrofusarin triglucoside
红镰霉素三葡萄糖苷
Rubrofusarintriglucoside是一种从决明子种子中分离得到的糖苷化合物,可抑制人单胺氧化酶A(hMAO-A),IC50为85.5μM。 -
GC61238
Rehmapicrogenin
地黄苦苷元
Rehmapicrogenin可从Rehmanniaglutinosa的根部分离得到,通过抑制iNOS、COX-2和IL-6表现出有效的抗炎作用。
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GC61235
Regaloside B
王百合苷 B
RegalosideB是一种从Liliumlongiflorum中分离出来的苯丙烷。RegalosideB可以抑制iNOS和COX-2的表达,具有抗炎活性。 -
GC61234
Rebamipide D4
瑞巴派特 D4; OPC12759-d4; Proamipide-d4
An internal standard for the quantification of rebamipide -
GC61206
Profenofos
丙溴磷
Profenofos是一种乙酰胆碱酯酶抑制有机磷农药,广泛应用于农田作物、蔬菜和水果作物。 -
GC61193
Piroxicam D3
吡罗昔康 D3; CP-16171 D3
An internal standard for the quantification of piroxicam -
GC61186
Picrotoxinin
木防己苦毒宁
Picrotoxinin, a potent convulsant, is a chloride channel blocker. Picrotoxinin is a noncompetitive GABAA receptor antagonist, which negatively modulates the action of GABA on GABAAA receptors. -
GC61180
Phenidone
菲尼酮
Phenidone (1-phenyl-3-pyrazolidinone), a dual inhibitor of cyclooxygenase (COX) and lipoxygenase (LOX), is an organic compound that is primarily used as a photographic developer. -
GC61167
Paliperidone palmitate
棕榈酸帕利哌酮,9-Hydroxyrisperidone palmitate
Paliperidone Palmitate (9-hydroxyrisperidone palmitate) is a palmitate ester of paliperidone, which is a dopamine antagonist and 5-HT2A antagonist of the atypical antipsychotic class. -
GC61162
Osthenol
7-羟基-8-(3-甲基-2-丁烯)-二氢苯并吡喃,Ostenol
Osthenol(Ostenol)是从独活干根中分离得到的一种前酰化香豆素,是一种可逆的,选择性的竞争性人单胺氧化酶-A(hMAO-A)抑制剂(Ki=0.26µM)。Osthenol对重组hMAO-A具有潜在的选择性抑制作用,IC50为0.74µM,对hMAO-A和hMAO-B表现出较高的选择性指数。 -
GC61108
Naftidrofuryl oxalate
草酸萘呋胺; Nafronyl oxalate salt
Naftidrofuryloxalate(Nafronyloxalatesalt)是在外周血和脑血管病症如血管扩张药的管理中使用的药物,增加细胞氧化能力,且是一种5-HT2受体拮抗剂。 -
GC61067
Mirtazapine D3
米氮平 D3; Org3770 D3; 6-Azamianserin D3
An Analytical Reference Material -
GC61038
Mefenamic acid D4
甲芬那酸 D4
An internal standard for the quantification of mefenamic acid -
GC61017
Lycoramine hydrobromide
石蒜胺;氢溴酸二氢加兰他敏
Lycoraminehydrobromide是一种从Lycorisradiate中分离出的加兰他敏的二氢衍生物。Lycoraminehydrobromide是一种有效的乙酰胆碱酯酶(AChE)抑制剂。 -
GC60966
Ketorolac D5
酮咯酸D5
An internal standard for the quantification of ketorolac - GC60965 Keto Ziprasidone KetoZiprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。
- GC60957 Jatrorrhizine hydroxide Jatrorrhizine (Neprotin, Yatrorizine), one of the active constituents of Coptis chinensis Franch, has multiple bioactivities, such as hypoglycemic, antimicrobial, and antioxidant activities. It is an inhibitor of AChE with IC50 of 872 nM and demonstrates >115-fold selectivity for AChE over BuChE.
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GC60939
Iproniazid
异丙烟肼
Iproniazid (Marsilid, Iprazid) is a non-selective, irreversible monoamine oxidase (MAO) inhibitor (MAOI) that is used as an antidepressive agent. -
GC60938
Iprindole
伊普吲哚
Iprindole具有抗抑郁的生物活性,是一种弱的去甲肾上腺素和5-HT摄取的抑制剂。 -
GC60935
Indomethacin sodium hydrate
吲哚美辛钠盐三水合物; Indometacin sodium hydrate
A non-selective COX inhibitor -
GC60926
Ibuprofen impurity 1
布洛芬杂质
Ibuprofenimpurity1是Ibuprofen的杂质。Ibuprofen是COX-1和COX-2的抑制剂,IC50值分别为13μM和370μM,具有抗炎的活性。 -
GC60924
Hydroxyzine D8
安泰乐D8
An internal standard for the quantification of hydroxyzine -
GC60917
Hydroxyamine hydrochloride
羟胺盐酸盐
Hydroxylammonium chloride (Hydroxylamine hydrochloride) is the hydrochloric acid salt of hydroxylamine, which is a biological intermediate in the nitrification and in the anammox. -
GC60915
Hydroxy ziprasidone
齐拉西酮羟基化杂质
Hydroxyziprasidone是Ziprasidone的杂质。Ziprasidone,一种抗精神药物,是5-HT和多巴胺(dopaminereceptor)受体拮抗剂。 -
GC60913
Huperzine C
石杉碱丙
HuperzineC是从Huperziaserrate中分离的一种生物碱。HuperzineC是一种乙酰胆碱酯酶(AChE)抑制剂,其IC50值为0.6μM。HuperzineC可用于阿尔茨海默症的研究。 -
GC60890
Guvacine
去甲槟榔次碱
An inhibitor of GABA uptake - GC60886 GSK356278 A selective PDE4 inhbitor
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GC60875
GKT136901
NOX Inhibitor IV
A dual inhibitor of NOX1 and NOX4 - GC60866 Gap 26 TFA Gap 26, a connexin mimetic peptide that composeds of residue no. 63-75 of the extracellular loop 1 of connexin 43 (Cx43), is a gap junction inhibitor. Gap 26 blocks photoliberating inositol-1,4,5-trisphosphate triggers ATP release.
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GC60862
GABAA receptor agent 1
2-(4-氯苯基)-6-硝基-1H-苯并[D]咪唑
GABAA receptor agent 1 is a high affinity ligand for Gamma-aminobutyric acid A (GABAA) receptor that exerts potent anticonvulsant activity. -
GC60846
Flesinoxan
氟辛克生
Flesinoxan是一种降压剂,是一种有效的,高亲和力的选择性的5-羟色胺1A(5-HT1A)受体激动剂,EC50值为24nM。Flesinoxan还具有有效的抗焦虑/抗抑郁作用。 -
GC60791
Doxepin D3 Hydrochloride
盐酸多塞平 D3
DoxepinD3Hydrochloride是DoxepinHydrochloride的氘代物。Doxepinhydrochloride是一种口服活性的三环抗抑郁药。Doxepinhydrochloride是一种有效的选择性组胺受体H1拮抗剂。Doxepinhydrochloride也是一种有效的CYP450抑制剂,并显着抑制CYP4502C19和CYP4501A2。 -
GC60774
Dihydro Donepezil
盐酸多奈哌齐二氢杂质,Dihydro E2020
DihydroDonepezil(DihydroE2020)是Donepezil的代谢产物。Donepezil是一种有效的特异性AChE抑制剂,对bAChE和hAChE的IC50分别为8.12nM和11.6nM。 -
GC60758
Deschloroclozapine
氯氮平杂质
Deschloroclozapine, a metabolite of Clozapine, is a highly potent muscarinic DREADDs (muscarinic Designer Receptors Exclusively Activated by Designer Drugs) agonist, and binds to DREADD receptor subtypes hM3Dq and hM4Di with Ki of 6.3 and 4.2 nM, respectively. -
GC60740
Dapoxetine-D7 hydrochloride
LY-210448-d7 hydrochloride
Dapoxetine-D7(LY-210448-D7)hydrochloride是Dapoxetinehydrochloride的氘代物。Dapoxetinehydrochloride是一种短效的选择性5-羟色胺再摄取抑制剂(SSRI)。 - GC60723 COR659 COR659是GABAB的阳性变构调节剂(PAM)。COR659可缓解大鼠对酒精和巧克力的药物成瘾。
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GC60709
Cinnarizine D8
桂利嗪 D8
An internal standard for the quantification of cinnarizine -
GC60691
Cetirizine Impurity C
西替利嗪杂质C
CetirizineImpurityC是Cetirizine的一种杂质。Cetirizine是羟嗪的羧化代谢物,是第二代抗组胺剂。Cetirizine是一种特异的、具有口服活性的H1受体(histamineH1-receptor)的长效拮抗剂。 -
GC60662
Brexpiprazole S-oxide
依匹哌唑硫氧化杂质,DM-3411
BrexpiprazoleS-oxide(DM-3411)是Brexpiprazole的主要代谢产物,并通过细胞色素P4503A4(CYP3A4)代谢。Brexpiprazole是一种非典型抗精神病药,是人5-HT1A和多巴胺受体的部分激动剂,Ki分别为0.12nM和0.3nM。Brexpiprazole也是5-HT2A受体的拮抗剂,Ki为0.47nM。