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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T40491 | Luteinizing hormone (human) | ||
Luteinizing hormone (LH), a heterodimeric glycoprotein hormone synthesized by the pituitary gland, serves vital functions in human reproductive processes. | |||
T5015 | Gonadorelin Acetate (33515-09-2 free base) | Luteinizing Hormone Releasing Hormone (LH-RH),Luteinizing Hormone Releasing Hormone (LH-RH), human,Gonadorelin Acetate | Reductase |
Gonadorelin Acetate (33515-09-2 free base) (Luteinizing Hormone Releasing Hormone (LH-RH)) is hypothalamic neuropeptide which plays a key role in the control of reproductive functions. | |||
T10476 | BAY-899 | Others | |
BAY-899 is an orally active and selective antagonist of the luteinizing hormone receptor (LH-R), exhibiting IC50 values of 185 nM and 46 nM for human LH (hLH) and rat LH (rLH) respectively. In vivo studies have demonstra... | |||
T82162 | Human follicular gonadotropin releasing peptide | hF-GRP | |
Human Follicular Gonadotropin Releasing Peptide (hF-GRP) is a hormonal peptide that, in vitro, can induce the secretion of pituitary luteinizing hormone (LH) and follicle-stimulating hormone (FSH) [1] [2]. | |||
T76324 | GnRH Associated Peptide (1-24), human | ||
Gonadotropin-Releasing Hormone-Associated Peptide (GAP) (1-24), human, also known as hGAP-1-24, is the 1-24 fragment of the human GAP, which is connected to the luteinizing hormone-releasing hormone (LH-RH) through a 3 a... | |||
T76602 | (D-Phe12,Nle21,38,α-Me-Leu37)-CRF (12-41) (human, rat) | ||
(D-Phe12,Nle21,38,α-Me-Leu37)-CRF (12-41) (human, rat) is a corticotropin-releasing factor (CRF) antagonist known to counteract the inhibitory effects of IL-1a on Luteinizing hormone (LH) production [1]. | |||
T63572 | Org 43553 | ||
Org 43553 is an orally active low molecular weight (LMW) luteinizing hormone receptor (LH-R) agonist capable of agonizing human LH (EC50: 3.7 nM) and FSH receptors (EC50: 110 nM).Org 43553 can be used for endocrine studi... | |||
T62881 | (R)-BAY-899 | ||
(R)-BAY-899 is an R-isomer of BAY-899. BAY-899 is a selective, orally active luteinizing hormone receptor (LH-R) antagonist that acts on hLH (human LH) (IC50: 185 nM) and rLH (rat LH) (IC50: 46 nM). | |||
T76323 | GnRH Associated Peptide (25-53), human | ||
Gonadotropin-Releasing Hormone-Associated Peptide (GAP) (25-53), Human, also known as hGAP-25-53, is a fragment of the human gonadotropin-releasing hormone-associated peptide that serves as an immunogen for producing ant... | |||
T68701 | Abarelix acetate | ||
Abarelix acetate is a synthetic third generation gonadotropin-releasing hormone receptor (GnRHR) antagonist. It increases histamine release from rat peritoneal mast cells in vitro and from a human skin model ex vivo. In ... | |||
T10469 | BAY-298 | Others | |
BAY-298 is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC 50 s of 96 nM, 23 nM and 78 nM for hLH (human LH) and rLH (rat LH) and cLH (cynomolgus monkey LH), respectively. BAY-298 is... | |||
T72990 | BAY 1214784 | ||
BAY 1214784, a potent, selective, and orally active spiroindoline derivative compound, serves as an antagonist of the human gonadotropin-releasing hormone receptor (hGnRH-R). It notably reduces plasma luteinizing hormone... | |||
T35794 | Kisspeptin-54 (human) (trifluoroacetate salt) | ||
Kisspeptin-54 is a peptide ligand of the orphan G protein-coupled receptor GPR54 (Kis = 1.81 and 1.45 nM for rat and human receptors, respectively).1 It is a 54 amino acid peptide encoded by the metastasis suppressor gen... |