19 Results for "

GHS

" in MedChemExpress (MCE) Product Catalog:
Products (19)

19 Results for "GHS" in MCE Product Catalog:

3
3 Cited Publications
Referencia número: HY-U00433
No. CAS: 925238-89-7
Target:  

GHSR

Áreas de investigación:  

Neurological Disease Endocrinology

JMV 2959 is a growth hormone secretagogue receptor type 1a (GHS-R1a) antagonist with an IC50 of 32 nM.
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3
3 Cited Publications
Referencia número: HY-U00433A
No. CAS: 2448414-54-6
Target:  

GHSR

Áreas de investigación:  

Neurological Disease Endocrinology

JMV 2959 hydrochloride is a growth hormone secretagogue receptor type 1a (GHS-R1a) antagonist with an IC50 of 32±3 nM in LLC-PK1 cells.
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2
2 Cited Publications
Referencia número: HY-19884B
No. CAS: 2863659-22-5
Synonyms: RM-131 TFA; BIM-28131 TFA
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

Relamorelin (RM-131) TFA, a pentapeptide ghrelin analog, is a selective ghrelin/growth hormone secretagogue receptor (GHSR) agonist with a Ki of 0.42 nM for GHS-1a receptor. Relamorelin TFA is centrally penetrant. Relamorelin TFA increases growth hormone levels and accelerates gastric emptying. Relamorelin TFA has the potential for cachexia, gastroparesis, and gastric/intestinal dysmobility disorders research .
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1
1 Cited Publications
Referencia número: HY-P5645
No. CAS: 1683582-94-6
Synonyms: Human liver expressed antimicrobial peptide-2
LEAP-2 (Human liver expressed antimicrobial peptide-2) is a GHS-R1a antagonist, with an IC50 of 6.0 nM. LEAP-2 suppresses the orexigenic effect of ghrelin. LEAP-2 attenuates ghrelin-induced growth hormone (GH) release and reduces basal food intake. LEAP-2 exhibits antimicrobial activity against microbial model organisms. LEAP-2 can be used for the study of obesity and infection .
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Referencia número: HY-W002199
No. CAS: 647-42-7
Synonyms: 6:2 FTOH; 1H,1H,2H,2H-Perfluoro-1-octanol; 2-(Perfluorohexyl)ethanol
Áreas de investigación:  

Infection Neurological Disease

6:2 Fluorotelomer alcohol (6:2 FTOH) is an orally active, blood-brain barrier-permeable modulator of cyclin D1 and ETS1. 6:2 Fluorotelomer alcohol downregulates cyclin D1 expression, upregulates ETS1 via the TNF-α/ERK 1/2 pathway, impairs mitochondrial membrane potential and respiratory function, increases reactive oxygen species levels, disrupts calcium homeostasis and activates endoplasmic reticulum stress markers, and induces cell proliferation inhibition and endothelial-mesenchymal transition. Furthermore, 6:2 Fluorotelomer alcohol induces morphological abnormalities in zebrafish embryos and liver developmental damage, while disrupting the brain immune microenvironment in mice, causing systemic toxicity and delayed pup maturation in CD-1 mice. 6:2 Fluorotelomer alcohol also induces cortical neuron apoptosis, glial cell activation, synaptic abnormalities, colonic barrier damage, intestinal dysbiosis and autism spectrum disorder-like symptoms in mice. 6:2 Fluorotelomer alcohol shows no mutagenic, clastogenic, primary skin/eye irritation or skin sensitizing effects, exhibits no selective reproductive toxicity in CD-1 mice, and is classified as GHS Category 4 for acute oral toxicity. 6:2 Fluorotelomer alcohol can be used in studies of neurodevelopmental disorders and autism spectrum disorders .
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Referencia número: HY-113906A
No. CAS: 1092476-84-0
Pureza:  99.40%
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

(αR,8aS)-GSK1614343 is the isomer of GSK1614343 (HY-113906). GSK1614343 is the potent antagonist of growth hormone secretagogues type 1a (GHS1a) receptors .
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Referencia número: HY-P1139
No. CAS: 485803-62-1
Synonyms: PCFWKTCK
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

Cortistatin-8 (CST-8; PCFWKTCK), a neuropeptide, is a GHS-R1a antagonist by counteracting the response of ghrelin on gastric acid secretion. Cortistatin-8 can modulate GH release from somatotroph cells. Cortistatin-8 is a synthetic CST-analogue devoid of any binding affinity to SST-R but capable to bind the GHS-R1a. Cortistatin-8 can exert antagonistic effects on ghrelin actions either in vitro or in vivo in animals .
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Referencia número: HY-50760
No. CAS: 145455-35-2
Target:  

GHSR

Áreas de investigación:  

Endocrinology

L-692585 is a potent and nonpeptidyl growth hormone secretagogue receptor (GHS-R1a) agonist, with a Ki of 0.8 nM. L-692585 acts directly on somatotropes causing GH release .
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Referencia número: HY-19884
No. CAS: 661472-41-9
Synonyms: RM-131; BIM-28131
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

Relamorelin (RM-131), a pentapeptide ghrelin analog, is a selective ghrelin/growth hormone secretagogue receptor (GHSR) agonist with a Ki of 0.42 nM for GHS-1a receptor. Relamorelin is centrally penetrant. Relamorelin increases growth hormone levels and accelerates gastric emptying. Relamorelin has the potential for cachexia, gastroparesis, and gastric/intestinal dysmobility disorders research .
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Referencia número: HY-10957
No. CAS: 145455-23-8
Pureza:  99.90%
Synonyms: MK-0751
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

L-692429 (MK-0751) is a benzolactam derivative and a nonpeptidyl growth hormone secretagogue (GHS) agonist. L-692429 binds to G protein-coupled receptor with a Ki of 63 nM .
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Referencia número: HY-137061
No. CAS: 1143020-91-0
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

AZ-GHS-22 is a potent, non-CNS penetrant GHS-R1a inverse agonist (IC50=0.77 nM) .
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Referencia número: HY-19884A
No. CAS: 1809080-14-5
Synonyms: RM-131 acetate; BIM-28131 acetate
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

Relamorelin (RM-131) acetate, a pentapeptide ghrelin analog, is a selective ghrelin/growth hormone secretagogue receptor (GHSR) agonist with a Ki of 0.42 nM for GHS-1a receptor. Relamorelin acetate is centrally penetrant. Relamorelin acetate increases growth hormone levels and accelerates gastric emptying. Relamorelin acetate has the potential for cachexia, gastroparesis, and gastric/intestinal dysmobility disorders research .
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Referencia número: HY-116959
No. CAS: 259667-25-9
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

SM-130686 is an oxindole derivative and an active GH secretagogue (GHS). SM-130686 stimulates GH release with a Half-maximum stimulation of 6.3 nM. SM-130686 has an orally active .
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Referencia número: HY-15242
No. CAS: 193273-66-4
Synonyms: CP 424391
Target:  

GHSR

Áreas de investigación:  

Endocrinology

Capromorelin (CP 424391) is a pyrazolinone-piperidine dipeptide. Capromorelin is an orally active and potent growth hormone secretagogue (GHS) (hGHS-R1a Ki=7 nM, rat pituicyte EC50=3 nM) .
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Referencia número: HY-113906
No. CAS: 1092076-04-4
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

GSK1614343 is the potent antagonist of growth hormone secretagogues type 1a (GHS1a) receptors. GSK1614343 inhibits the calcium response induced by ghrelin with a pIC50 value of 7.90. GSK1614343 represents a useful tool to investigate the physiological relevance of the ghrelin system in rat models .
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Referencia número: HY-119125
No. CAS: 295337-71-2
Target:  

GHSR

Áreas de investigación:  

Cancer

BMS-317180 is an orally active and potent growth hormone secretagogue receptor (GHS-R) agonist (EC50=7.9 nM). BMS-317180 stimulates endogenous growth hormone (GH) release. BMS-317180 is promising for research of age-related frailty, osteoporosis, and cancer cachexia .
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Referencia número: HY-129287
No. CAS: 925239-09-4
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

JMV 3008 is a GHS-R1a antagonist with an IC50 of 5.6 nM. JMV 3008 can be used in the research of diseases such as diabetes and obesity .
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Referencia número: HY-10957A
No. CAS: 169188-19-6
Synonyms: MK-0751 hydrochloride
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

L-692429 (MK-0751) hydrochloride is a benzolactam derivative and a nonpeptidyl growth hormone secretagogue (GHS) agonist. L-692429 hydrochloride binds to G protein-coupled receptor with a Ki of 63 nM .
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Referencia número: HY-176995
No. CAS: 1143021-16-2
Target:  

GHSR

Áreas de investigación:  

Metabolic Disease

AZ-GHS-38 (compound 38) is an orally active CNS-penetrant inverse agonist of growth hormone secretagogue receptor (GHS-R1a) with an IC50 of 6.7 nM. AZ-GHS-38 results in acute reduction of food intake in wild-type mice. AZ-GHS-38 can be used for anti-obesity research .
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