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Search Results for " locomotor "

20

Compounds

Cat No. Product Name Synonyms Targets
T3278 Piribedil EU-4200,Trivastan,ET-495,Trivastal Dopamine Receptor , Histone Methyltransferase , Adrenergic Receptor
Piribedil (Trivastan) is a dopamine D2 agonist, used in the treatment of Parkinson's disease.
T21935L AMN082 free base AMN082 GluR
AMN082 free base is a metabotropic glutamate receptor 7 allosteric agonist.
T6140 SB-334867 free base SB334867A free base,SB-334867,SB 334867,SB334867 OX Receptor
SB-334867 free base (SB334867A free base) is a selective orexin-1 (OX1) receptor antagonist.
T21935 AMN082 AMN 082 dihydrochloride GluR
AMN082 (AMN 082 dihydrochloride) is a selective metabotropic glutamate mGlu7 receptor agonist reported to exhibit antidepressant activity.
T35033 Vamicamide FK 176,FK-176,FK176 AChE
Vamicamide (FK 176) is a novel anticholinergic compound. Vamicamide increases spontaneous locomotor activity in mice at 32 mg/kg (p.o.) or higher and inhibits cataleptic convulsions in mice at 100 mg/kg.
T35033L (S)-Vamicamide (S)-Vamicamide (Iso-132373-81-0) AChE
(S)-Vamicamide is a novel anticholinergic compound.Vamicamide increases spontaneous locomotor activity in mice at 32 mg/kg or higher (p.o.) and inhibits tonic convulsions in mice at 100 mg/kg.CAS 번호13483-86-1
TP1940L1 Ac-RYYRIK-NH2 acetate Opioid Receptor
Ac-RYYRIK-NH2 acetate is an agonist at nociceptin/orphanin FQ(noc/OFQ) receptors, affecting spontaneous locomotor activity. Ac-RYYRIK-NH2 acetate is a partial agonist on ORL1 transfected in CHO cells, antagonizes the sti...
TMS1461 Qingyangshengenin B Otophylloside B Beta Amyloid
Qingyangshengenin B (Otophylloside B) is a C-21 steroidal glycoside isolated from Qingyangshen. Qingyangshengenin B protects against Aβ toxicity, which decreases Aβ deposition by decreasing the expression of Aβ at the mR...
T21792 CGP 3466B maleate Omigapil (Maleate),Omigapil maleate Apoptosis
CGP 3466B maleate (Omigapil maleate) is an orally bioavailable GAPDH nitrosylation inhibitor. Omigapil maleate abrogates Aβ1-42-induced tau acetylation, memory impairment, and locomotor dysfunction in mice. Omigapil male...
T3685 SR9009 Stenabolic,REV-ERB Agonist II Autophagy
SR9009 (Stenabolic), a REV-ERB agonist, increases the constitutive repression of genes regulated by REV-ERBα/ERBβ (IC50: 670/800 nM). Through activation of REV-ERB, SR9009 can decrease circadian locomotor activity during...
T37190 L-Allylglycine Dehydrogenase , GABA Receptor
L-Allylglycine is an amino acid derivative that reduces glutamate decarboxylase (GAD) activity by 60% when administered at a dose of 39.8 μmol/g per hour ex vivo in mouse brain preparations. L-Allylglycine (1.2 mmol/kg, ...
T32440 L 363572 L363-572,L-363572,L-363-572,L363572,L 363-572
L 363572, a hexapeptide analog of MK 678, does not effect locomotor acitivity in rats.
T81659 NocII TFA
NocII TFA, an orphan neuropeptide, stimulates locomotor activity in mice [1].
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.
TN4722 Otophylloside F Others
Otophylloside F can suppress the seizure-like locomotor activity caused by pentylenetetrazole in zebrafish.
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 behavio...
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.
T28313 PD 117302 PD-117302,PD117302
PD 117302 is a nonpeptide opioid compound. It is a selective kappa-opioid agonist. PD 117302 causes naloxone-reversible locomotor impairment and diuresis. It is an Anti-Arrhythmia Agent, an Anticonvulsants, a Cardiovascu...
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 me...
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.
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TargetMol