16 Results for "

pituitary LH

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "pituitary LH" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-P2293
CAS No.: 39341-83-8
Target:  

GnRH Receptor

Research Areas:  

Metabolic Disease

Luteinizing hormone (human), a heterodimeric glycoprotein hormone produced by the pituitary gland (LH), plays key roles in human reproduction .
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Cat. No.: HY-P1174
CAS No.: 100111-07-7
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

GnRH Associated Peptide (GAP) (1-13), human is an amino acid peptide fragment derived from GnRH. GAP can increase the secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) in rat anterior pituitary cells. GAP also inhibit the secretion of prolactin .
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Cat. No.: HY-E70001
Target:  

Others

Research Areas:  

Endocrinology

Recombinant Human Luteinizing Hormone is a recombinant form of Luteinizing hormone (human) (HY-P2293). Luteinizing hormone (human), a heterodimeric glycoprotein hormone produced by the pituitary gland (LH), plays key roles in human reproduction .
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Cat. No.: HY-P1250
CAS No.: 311309-27-0
Synonyms: Neuropeptide VF(124-131)(human); Neuropeptide NPVF (human)
Research Areas:  

Neurological Disease

RFRP-3 (Neuropeptide VF(124-131))(human), a human GnIH peptide homolog, is a potent inhibitor of gonadotropin secretion by inhibiting Ca 2+ mobilization. RFRP-3(human) is a NPFF1 receptor agonist, it inhibits forskolin-induced production of cAMP with an IC50 of 0.7 nM .
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Cat. No.: HY-P3675
CAS No.: 51776-33-1
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

LH-RH (4-10) is a heptapeptide, one of major degradation products of luteinising-hormone releasing hormone (LHRH) via pituitary and hypothalamus. LH-RH (4-10) produced in macrophages and type II pneumocytes .
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Cat. No.: HY-P3674
CAS No.: 38482-71-2
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

LH-RH (7-10) is a tetrapeptide, one of major degradation products of luteinising-hormone releasing hormone (LHRH) via pituitary and hypothalamus. LH-RH (7-10) produced in macrophages, type I-like and type II pneumocytes .
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Cat. No.: HY-P1905
CAS No.: 47922-48-5
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

[Gln8]-C517 (LH-RH), chicken is an avian hypothalamic peptide, which stimulates release of gonadotropins from anterior pituitary, thus regulating reproductive functions.
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Cat. No.: HY-P3084
CAS No.: 107873-08-5
Synonyms: hF-GRP
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

Human follicular gonadotropin releasing peptide (hF-GRP) is a hormone peptide. Human follicular gonadotropin releasing peptide can stimulate pituitary luteinizing hormone (LH) and follicle-stimulating hormone (FSH) secretion in vitro .
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Cat. No.: HY-P2357
CAS No.: 87565-51-3
Target:  

GnRH Receptor

Research Areas:  

Metabolic Disease

MI-1544 is a powerful GnRH antagonist. MI-1544 induces inhibitory effects on the pituitary LH release and on gonads. MI-1544 can be used for the research of antifertility effect .
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Cat. No.: HY-120767
CAS No.: 1321816-57-2
Synonyms: KLH-2109 choline; OBE-2109 choline
Target:  

GnRH Receptor

Research Areas:  

Inflammation/Immunology Cancer

Linzagolix choline (KLH-2109 choline) is a non-peptide gonadotropin-releasing hormone (GnRH) antagonist with oral activity. Linzagolix choline inhibits the release of endogenous gonadotropins such as luteinizing hormone LH and follicle-stimulating hormone FSH by binding to the GnRH receptor within the pituitary gland. This inhibition results in a reduction in the production of sex hormones such as estrogen and progesterone, which in turn affects the course of sex hormone-dependent diseases. Linzagolix choline can be used in the study of sex hormone-dependent diseases such as endometriosis and uterine fibroids .
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Cat. No.: HY-P2110
CAS No.: 109458-76-6
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

RS-18286 is a potent luteinizing-hormone (LH)-releasing hormone (LHRH) antagonist. RS-18286 blocks the pituitary LHRH receptor and suppresses pituitary luteinizing-hormone (LH) secretion and reduce serum concentrations of gonadal steroids .
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Cat. No.: HY-125611
CAS No.: 2529-45-5
Purity:  99.60%
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

Fluorogestone acetate is a progesterone compound. Fluorogestone acetate inhibits ovulation and synchronizes the estrous cycle in cattle by inhibiting the release of luteinizing hormone (LH) from the pituitary gland .
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Cat. No.: HY-P4564
CAS No.: 1926163-38-3
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

(D-Ser(tBu)6,D-Leu7,Azagly10)-LHRH is an analogue of luteinizing hormone-releasing hormone (LHRH). LHRH plays a central role in the control of reproduction by stimulating the release of pituitary luteinizing hormone (LH) and follicle-stimulating hormone (FSH) .
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Cat. No.: HY-P4568
CAS No.: 1926163-39-4
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

(D-Ser4,D-Ser(tBu)6,Azagly10)-LHRH is an analogue of luteinizing hormone-releasing hormone (LHRH). LHRH plays a central role in the control of reproduction by stimulating the release of pituitary luteinizing hormone (LH) and follicle-stimulating hormone (FSH) .
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Cat. No.: HY-P4577
CAS No.: 1426173-74-1
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

(D-Tyr5,D-Ser(tBu)6,Azagly10)-LHRH is an analogue of luteinizing hormone-releasing hormone (LHRH). LHRH plays a central role in the control of reproduction by stimulating the release of pituitary luteinizing hormone (LH) and follicle-stimulating hormone (FSH) .
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Cat. No.: HY-P2446
CAS No.: 83539-08-6
Synonyms: APTAA-LHRH
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

ORG 30276 (APTAA-LHRH) is a potent GnRH antagonist that effectively reduces serum LH and FSH levels in male rats. ORG 30276 significantly decreases unoccupied pituitary GnRH receptors, leading to suppressed gonadotropin secretion. ORG 30276 treatment results in a considerable reduction in mRNA levels of gonadotropin beta-subunits in the pituitary gland. ORG 30276's effects on gonadotropin dynamics can be selectively reversed by the replacement of specific sex steroids, with androgens being particularly effective for the FSH beta-subunit mRNA levels.
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