Chemical structure
Cat.No.
Product Name
CAS no.
Target
Goserelin, a gonadotropin-releasing hormone (GnRH) analogue, functions as aGnRHagonist. Goserelin can be used for the research of breast cancer, epithelial ovarian cancer and prostate cancer.
YN320783 Leuprolide Acetate 74381-53-6
Leuprolide acetate is a synthetic nonapeptide that is a potent gonadotropin-releasing hormone receptor (GnRHR) agonist used for diverse clinical applications, including the treatment of prostate cancer, endometriosis, uterine fibroids,...
YN321130 Alarelin Acetate 79561-22-1
Alarelin Acetate is a synthetic LH-RH agonist that is found in higher amounts than that of LH-RH in rat hypophyseal stimulation of gonadotropin secretion in vivo and in vitro and in ovulation inductions.
YN321782 Cetrorelix diacetate 130143-01-0
Cetrorelix diacetate (SB-075 diacetate) is a potent gonadotropin-releasing hormone(GnRH)receptor antagonist with an IC50 of 1.21nM.
YN321781 Cetrorelix Acetate 145672-81-7
Cetrorelix Acetate (SB-75 acetate) is a potent gonadotropin-releasing hormone(GnRH)receptor antagonist with an IC50 of 1.21nM.
YN320785 Goserelin acetate 145781-92-6
Goserelin is a luteinizing hormone releasing hormone (LHRH) agonist, which is used to suppress production of the sex hormones.
Abarelix (R3827; PPI 149) is a potentgonadotrophin-releasing hormone (GnRH)antagonist, used for prostate cancer treatment.
YN321055 Degarelix 214766-78-6
Degarelix is a competitive and reversible gonadotropin-releasing hormone receptor (GnRHR) antagonist.
YN321838 Kisspeptin-54(human) 374683-24-6
Kisspeptin-54(human) (Metastin(human)) is an endogenous lig and forkisspeptin receptor (KISS1, GPR54). Kisspeptin-54(human) binds torat and human GPR54 receptorswith Ki values of 1.81nM and 1.45nM, respectively. Kisspept...
YN321063 Relugolix 737789-87-6
Relugolix is a selective antagonist of the gonadotropin-releasing hormone receptor (GnRHR) with an IC50 of 0.12 nM.
YN320860 Elagolix sodium 832720-36-2
Elagolix Soidum is a potent, selective, orally active, non-peptide antagonist of the gonadotropin-releasing hormone receptor (GnRHR) with Kd value of 54 pM. Concentration at 10 μM shows no significant activity on ion channels, en...
YN320913 (R)-Elagolix 834153-87-6
Elagolix is a highly potent, selective, orally-active, short-duration, non-peptide antagonist of the gonadotropin-releasing hormone receptor (GnRHR) (KD = 54 pM).
BAY-784 is a gonadotropin releasing hormone receptor (GnRH-R) antagonist probe with IC50s of 21 and 24nM for human and rat GnRH-R, respectively.
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