9 Results for "

anorectic agent

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "anorectic agent" in MCE Product Catalog:

12
12 Cited Publications
Cat. No.: HY-Y0337
CAS No.: 52-90-4
Synonyms: Cysteine
L-Cysteine (Cysteine) is an orally active conditionally essential amino acid with hypoglycemic effects, which acts as a precursor for biologically active molecules such as hydrogen sulphide (H2S), glutathione and taurine. L-Cysteine promotes the proliferation and differentiation of neural stem cells via the CBS/H2S pathway. L-Cysteine suppresses ghrelin and reduces appetite in rodents and humans. L-Cysteine can be used as an anorectic agent .
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Cat. No.: HY-105955
CAS No.: 154132-95-3
Synonyms: ARL 14294
Research Areas:  

Metabolic Disease

FPL 14294 is a intranasally active anorectic agent and a cholecystokinin octapeptide (CCK) analog with enhanced metabolic stability. FPL 14294 induces satiety in many species and can be utilized in relevant research .
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Cat. No.: HY-164022
CAS No.: 47487-22-9
Synonyms: BS 7573a
Research Areas:  

Others

Acridorex (BS 7573a) is an anorectic agent .
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Cat. No.: HY-W700741
CAS No.: 13473-53-5
Target:  

Drug Metabolite

Research Areas:  

Neurological Disease

2-(2-Aminoethyl)-3-(4-chlorophenyl)-3-hydroxyisoindol-1-one hydrochloride is a metabolite of the anorectic agent Mazindol.
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Cat. No.: HY-12364C
CAS No.: 1234694-20-2
Synonyms: (+)-C75
(+)-trans-C75 ((+)-C75) is an enantiomer of C75 (HY-12364) (a fatty acid synthase inhibitor). (+)-trans-C75 is less potent than the racemic mixture or the (-) enantiomer in enhancing the cancer-killing ability of ionizing radiation. (+)-trans-C75 inhibits CPT1 and is an anorectic agent .
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Cat. No.: HY-W701814
CAS No.: 1276611-52-9
Mazindol metabolite-d4 hydrochloride is the deuterium labeled 2-(2-Aminoethyl)-3-(4-chlorophenyl)-3-hydroxyisoindol-1-one hydrochloride (HY-W700741). 2-(2-Aminoethyl)-3-(4-chlorophenyl)-3-hydroxyisoindol-1-one hydrochloride is a metabolite of the anorectic agent Mazindol.
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Cat. No.: HY-184316
CAS No.: 98644-22-5
Target:  

Serotonin Transporter

Research Areas:  

Metabolic Disease

CM 57373 is an orally active anorectic agent. CM 57373 releases serotonin and inhibits serotonin reuptake in rat brain synaptosomes. CM 57373 reduces food intake, decreases body weight and alleviates experimentally induced hyperphagia. CM 57373 can be used in obesity research .
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Cat. No.: HY-L121
424 compounds

5-HT receptors, also called Serotonin receptors, are a group of G protein-coupled receptors (GPCRs) and ligand-gated ion channels (LGICs) found in the central and peripheral nervous systems. These receptors are now classified into seven families, 5-HT1–7, comprising a total of 14 structurally and pharmacologically distinct mammalian 5-HT receptor subtypes. The 5-HT receptors influence various biological and neurological processes such as aggression, anxiety, appetite, cognition, learning, memory, mood, nausea, sleep, andthermoregulation. The serotonin receptors are the target of a variety of pharmaceutical drugs, including many antidepressants, antipsychotics, anorectics, antiemetics, gastroprokinetic agents, antimigraine agents, hallucinogens, and entactogens.

MCE 5-HT Receptor Compound Library consists of 424 5-HT receptor inhibitors and activators, which can be used for neuropsychiatric disorders drugs discovery.

Cat. No.: HY-182262
CAS No.: 31478-25-8
Target:  

Lipase

Research Areas:  

Metabolic Disease

Ro 20-0083 is an orally active pancreatic lipase inhibitor. Ro 20-0083 inhibits hPancreatic lipase activity, reduces lipid absorption and de novo fatty acid synthesis. Ro 20-0083 decreases food intake in Zucker rats. Ro 20-0083 can be used in obesity-related research .
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