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Search Results for " locomotor activity "

28

抑制剂 & 化合物

2

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T3278	Piribedil EU-4200,Trivastan,ET-495,Trivastal	Dopamine Receptor; Histone Methyltransferase; Adrenergic Receptor	Chromatin/Epigenetic; GPCR/G Protein; Neuroscience
	Piribedil (Trivastan) 是多巴胺 D2受体激动剂，对 hα1A-肾上腺素受体也显示出拮抗作用。
T6140	SB-334867 free base SB334867A free base,SB-334867,SB 334867,SB334867	OX Receptor	GPCR/G Protein; Neuroscience
	SB-334867 free base (SB334867A free base) 是一种选择性 orexin-1(OX1) 受体拮抗剂，对 OX2有选择性，pKb 为7.4，对 5-HT2B、5-HT2C 的选择性是 100 倍，pKi 值分别为 5.4 和 5.3。它减少乙醇消耗，还抑制吗啡诱导的体内运动活动敏感性的获得。
T35033	Vamicamide FK 176,FK-176,FK176	AChE	Neuroscience
	Vamicamide (FK 176)是一种新型抗胆碱能化合物。Vamicamide 在 32 mg/kg （p.o.）或更高时增加小鼠的自发运动活动，并在 100 mg/kg 时抑制小鼠强直性惊厥。
T35033L	(S)-Vamicamide (S)-Vamicamide (Iso-132373-81-0)	AChE	Neuroscience
	(S)-Vamicamide 是一种新型抗抗胆碱能化合物。Vamicamide 在 32 mg/kg 或更高（p.o.）时增加小鼠的自发运动活动，并在 100 mg/kg 时抑制小鼠强直性惊厥。
TP1940L1	Ac-RYYRIK-NH2 acetate	Opioid Receptor	Endocrinology/Hormones; GPCR/G Protein; Neuroscience
	Ac-RYYRIK-NH2 acetate 是 nociceptin/orphanin FQ(noc/OFQ) 受体的激动剂，影响自发运动活动。它是转染在 CHO 细胞中的 ORL1 的部分激动剂，可拮抗大鼠脑膜和切片中 noc/OFQ 对 [35S]-GTPgammaS 与 G 蛋白结合的刺激。
T3685	SR9009 Stenabolic,REV-ERB Agonist II	Autophagy	Autophagy
	SR9009 (Stenabolic) 是一种REV-ERBα/β激动剂，可增加由 REV-ERBα/ERBβ 调节的基因的组成性抑制，IC50分别为 670 nM 和 800 nM。
T37190	L-Allylglycine	Dehydrogenase; GABA Receptor	Membrane transporter/Ion channel; Metabolism; Neuroscience
	L-Allylglycine 是 GABA 合成酶（谷氨酸脱羧酶）的有效抑制剂。
T75951	Neuropeptide S(Rat) TFA
	Neuropeptide S(Rat) TFA, a robust endogenous agonist for the neuropeptide S receptor (NSPR) with an EC50 of 3.2 nM, enhances locomotor activity and promotes wakefulness while concurrently diminishing anxiety-like behavior in mice.
TP1983	Neuropeptide S (human)
	Potent endogenous neuropeptide S receptor agonist (EC50 = 9.4 nM). Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice.
T81659	NocII TFA
	NocII TFA 是孤儿神经肽，能刺激小鼠运动。
TP1982	Neuropeptide S(Rat) Neuropeptide S (Rat)
	Potent endogenous neuropeptide S receptor (NSPR) agonist (EC50 = 3.2 nM). Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice.
TP1981	Neuropeptide S(Mouse) Neuropeptide S (Mouse)
	Potent endogenous neuropeptide S receptor (NPSR) agonist (EC50 = 3 nM). Induces mobilization of intracellular Ca2+. Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice.
TP1980	Neuromedin S(rat) Neuromedin S (rat)
	Potent, endogenous neuromedin U receptor agonist (EC50 values are 65 and 91 pM at NMU1 and NMU2 respectively). Induces phase shifts in the circadian rhythm of locomotor activity following i.c.v. administration. Potent endogenous anorexigenic peptide.
TP1940	Ac-RYYRIK-NH2
	High affinity ligand for the NOP site (Ki = 1.5 nM). Antagonizes nociceptin-stimulated GTP binding in rat brain and the chronotropic effect of nociceptin on rat cardiomyocytes. However, displays potent agonist properties in vivo, inhibiting locomotor acti
T82587	Delta (Phospho) Sleep Inducing Peptide DSIP-P
	Delta (Phospho) Sleep Inducing Peptide (DSIP-P) 是促进睡眠效应持久的多肽，能诱导大鼠昼夜运动行为的改变。
T29230	ZK-95962
	ZK-95962 is an agonist gamma-aminobutyric acid (GABA) receptor. ZK-95962 had selective effects on releasing exploratory locomotor activity suppressed by footshock (punished crossings). ZK-95962 had weak effects on the measures of anxiolytic activity. The
T60270	(R)-Preclamol
	(R)-Preclamol 是一种具有自身受体和突触后受体刺激特性的多巴胺 (DA) 激动剂。(R)-Preclamol 以低剂量抑制小鼠和大鼠的运动活动。
T75915	CTOP TFA
	CTOP TFA为高效、高选择性μ-阿片受体(μ-opioid receptor)拮抗剂。其能拮抗吗啡引发的急性镇痛效果及运动能力增强，同时升高伏隔核外多巴胺水平，并呈剂量依赖性增强运动能力。
T75950	Neuropeptide S(Mouse) TFA
	Neuropeptide S(Mouse) TFA, an endogenous agonist for the neuropeptide S receptor (NPSR) with an EC50 value of 3 nM, plays a significant role in physiological processes by inducing the mobilization of intracellular Ca2+. This compound elevates locomotor activity and wakefulness, and simultaneously decreases anxiety-like behavior in mice.
T29206	ZCZ011 ZCZ 011,ZCZ-011
	ZCZ011 is a positive allosteric modulator of the cannabinoid CB1 receptor. ZCZ011 is brain penetrant, increased the potency of orthosteric agonists in mouse behavioral assays indicative of cannabimimetic activity, including antinociception, hypothermia, c
T71327	Paraxanthine-d6
	Paraxanthine-d6 is intended for use as an internal standard for the quantification of paraxanthine by GC- or LC-MS. Paraxanthine is an active metabolite of caffeine. It is formed via N3-demethylation of caffeine by the cytochrome P450 (CYP) isoform CYP1A2. Paraxanthine is an adenosine A1 and A2 receptor antagonist. In vivo, paraxanthine increases striatal cGMP and extracellular striatal dopamine levels and locomotor activity, as well as inhibits motor depression induced by the adenosine A1 agoni...
T38172	RO 5263397 hydrochloride
	Potent trace amine 1 (TA1) receptor agonist (EC50 values are 0.12, 35 and 17-85 nM for mouse, rat and human receptors, respectively). Increases wakefulness and reduces REM and NREM sleep duration in wild type mice. Inhibits spontaneous locomotor activity in dopamine transport (DAT) knockout mice. Espinoza et al (2018) Biochemical and functional characterization of the trace amine-associated receptor 1 (TAAR1) agonist RO5263397. Front.Pharmacol. 9 645 PMID:29977204 \|Galley et al (2015) Discovery ...
TP1986	[Arg14,Lys15]Nociceptin
	Highly potent and selective NOP receptor agonist (EC50 = 1 nM). Displays > 875-fold selectivity over opioid receptors (IC50 values are 0.32, 280, > 10000 and 1500 for NOP, μ, δ and κ receptors respectively). Longer lasting and 30-fold more potent than noc
T35785	N-Oleoyl Leucine
	N-Oleoyl leucine is an N-acyl amide generated by PM20D1 that uncouples mitochondrial respiration independent of uncoupling protein 1 (UCP1) in vitro. N-Oleoyl leucine (25 mg/kg, i.p.) decreases body weight and food intake, preferentially decreasing fat mass in a diet-induced obesity mouse model. It improves glucose homeostasis in a fasting glucose tolerance test and increases VO2 while slightly decreasing overall locomotor activity.
T38221	N,N-Dipropyldopamine (hydrobromide)
	N,N-Dipropyldopamine is a dopamine receptor agonist.1,2,3 It decreases dihydrophenylalanine (DOPA) levels in the limbic forebrain and striatum of reserpinized rats (ED50s = 25 and 20 μmol/kg, respectively), as well as reduces homovanillic acid levels in rat striatum when administered at a dose of 80 μmol/kg.1 N,N-Dipropyldopamine (0.5-16 mg/kg) reduces spontaneous locomotor activity in mice, an effect that can be reversed by the antipsychotic spiroperidol.2,3
T71000	RO-5328673
	RO-5328673 is a dual NK2/NK3 antagonist. O5328673. [(3)H]RO5328673 bound to a single saturable site on hNK2, hNK3 and gpNK3 with high-affinity. RO5328673 acted as an insurmountable antagonist at both human and guinea-pig NK3 receptors in the [(3)H]IP accumulation assay. In binding kinetic analyses, [(3)H]RO5328673 had fast association and dissociation rates at hNK2 while it had a fast association rate and a remarkably slow dissociation rate at gp and hNK3. In electrophysiological recordings of g...
T83166	Adipokinetic hormone (Gryllus bimaculatus) Grybi-AKH
	Adipokinetic hormone Gryllus bimaculatus (Grybi-AKH) 是调节昆虫能量平衡的脂肪动力激素，主要功能是动员脂肪体内的脂质和碳水化合物。此外，Grybi-AKH也能增强双斑蟋蟀的运动活性，并在人体体重调节、体重减轻及糖原贮积障碍缓解的研究中具有应用潜力。
T37094	(S)-UFR2709 hydrochloride (S)-UFR2709 hydrochloride
	(S)-UFR2709 (hydrochloride) is a competitive nAChR antagonist and displays higher affinity for α4β2 nAChRs than for α7 nAChRs. (S)-UFR2709 (hydrochloride) decreases anxiety and reduces ethanol consumption and ethanol preference in alcohol-preferring rats. (S)-UFR2709 (hydrochloride) acts as an anxiolytic agent and can be used for the study of nicotine addiction[1][2]. Brain nicotinic acetylcholine receptors (nAChRs) is a heterogeneous family of pentameric acetylcholine-gated cation channels, whi...

化合物

Cat.No: T3278

Synonym: EU-4200,Trivastan,ET-495,Trivastal

Target: Dopamine Receptor, Histone Methyltransferase, Adrenergic Receptor

SB-334867 free base

Cat.No: T6140

Synonym: SB334867A free base,SB-334867,SB 334867,SB334867

Target: OX Receptor

Cat.No: T35033

Synonym: FK 176,FK-176,FK176

Target: AChE

Cat.No: T35033L

Synonym: (S)-Vamicamide (Iso-132373-81-0)

Target: AChE

Ac-RYYRIK-NH2 acetate

Cat.No: TP1940L1

Target: Opioid Receptor

Cat.No: T3685

Synonym: Stenabolic,REV-ERB Agonist II

Target: Autophagy

Cat.No: T37190

Target: Dehydrogenase, GABA Receptor

Neuropeptide S(Rat) TFA

Cat.No: T75951

Neuropeptide S (human)

Cat.No: TP1983

Cat.No: T81659

Neuropeptide S(Rat)

Cat.No: TP1982

Synonym: Neuropeptide S (Rat)

Neuropeptide S(Mouse)

Cat.No: TP1981

Synonym: Neuropeptide S (Mouse)

Neuromedin S(rat)

Cat.No: TP1980

Synonym: Neuromedin S (rat)

Cat.No: TP1940

Delta (Phospho) Sleep Inducing Peptide

Cat.No: T82587

Synonym: DSIP-P

Cat.No: T29230

Cat.No: T60270

Cat.No: T75915

Neuropeptide S(Mouse) TFA

Cat.No: T75950

Cat.No: T29206

Synonym: ZCZ 011,ZCZ-011

Paraxanthine-d6

Cat.No: T71327

RO 5263397 hydrochloride

Cat.No: T38172

[Arg14,Lys15]Nociceptin

Cat.No: TP1986

N-Oleoyl Leucine

Cat.No: T35785

N,N-Dipropyldopamine (hydrobromide)

Cat.No: T38221

Cat.No: T71000

Adipokinetic hormone (Gryllus bimaculatus)

Cat.No: T83166

Synonym: Grybi-AKH

(S)-UFR2709 hydrochloride

Cat.No: T37094

Synonym: (S)-UFR2709 hydrochloride

Cat. No.	Product Name	Target	Signaling Pathways
TMS1461	Qingyangshengenin B 青阳参甙元B,青阳参苷元B,Otophylloside B	Beta Amyloid	Neuroscience
	Qingyangshengenin B (Otophylloside B) 是一种分离自 Qingyangshen 的 C-21 甾体苷。它能够在 mRNA 水平上抑制 Aβ 的表达来减少 Aβ 的沉积，对 Aβ 的毒性有保护作用。它具有抗癫痫作用。
TN4722	Otophylloside F	Others	Others
	Otophylloside F can suppress the seizure-like locomotor activity caused by pentylenetetrazole in zebrafish.

天然产物

Qingyangshengenin B

Cat.No: TMS1461

Synonym: 青阳参甙元B,青阳参苷元B,Otophylloside B

Target: Beta Amyloid

Otophylloside F

Cat.No: TN4722

Target: Others

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