1、 HYPERLINK https:/www.MedChemE/Targets/GNRH Receptor.html GnRH HYPERLINK https:/www.MedChemE/Targets/GNRH Receptor.html HYPERLINK https:/www.MedChemE/Targets/GNRH Receptor.html ReceptorGonadotropin releasing hormone receptor; GNRHRThe GnRH receptor (Gonadotropin-releasing hormone receptor, GNRHR) is

2、 a member of the rhodopsin-like G protein-coupledreceptor (GPCR) family and consists of seven transmembrane helical domains connected via extra- and intra-cellular segments.GnRH receptor is located on the plasma membrane of gonadotrophs, pituitary cells that synthesize the gonadotrophins LH andFSH.M

3、ammalian type I and II GnRH receptors show differential ligand preference for GnRH-I and GnRH-II, respectively. All GnRH receptors activate the G family of G proteins, which activate phospholipase C-catalyzed production of second messengers thatq/11activate protein kinase C (PKC). GnRH receptor acti

4、vated by GnRH analogues stimulates the synthesis and release of LH and FSH.GnRH receptors can be used for the research of breast and prostate cancer, regulation of fertility, endometriosis and a range ofother medical and veterinary uses.www.MedChemE 1 HYPERLINK https:/www.MedChemE/Targets/GNRH Recep

5、tor.html GnRH HYPERLINK https:/www.MedChemE/Targets/GNRH Receptor.html HYPERLINK https:/www.MedChemE/Targets/GNRH Receptor.html Receptor HYPERLINK https:/www.MedChemE/Targets/GNRH Receptor.html HYPERLINK https:/www.MedChemE/Targets/GNRH Receptor.html Agonists HYPERLINK https:/www.MedChemE/Targets/GN

6、RH Receptor.html HYPERLINK https:/www.MedChemE/Targets/GNRH Receptor.html & HYPERLINK https:/www.MedChemE/Targets/GNRH Receptor.html HYPERLINK https:/www.MedChemE/Targets/GNRH Receptor.html Antagonists HYPERLINK https:/www.MedChemE/Elagolix.html (R)-Elagolix(NBI-56418) Cat. No.: HY-14789 HYPERLINK h

7、ttps:/www.MedChemE/Abarelix.html Abarelix(R3827; PPI 149) Cat. No.: HY-13534Elagolix is a highly potent, selective,orally-active, short-duration, non-peptideantagonist of the gonadotropin-releasing hormonereceptor (GnRHR) (KD = 54 pM).Abarelix (R3827; PPI 149) is a potentgonadotrophin-releasing horm

8、one (GnRH)used for prostate cancer treatment.antagonist,Purity: 95.74%Clinical Data: Phase 3Size: 10 mM 1 mL, 5 mg, 10 mg, 50 mg, 100 mgPurity: 99.62%Clinical Data: LaunchedSize: 10 mM 1 mL, 5 mg, 10 mg, 25 mg, 50 mg HYPERLINK https:/www.MedChemE/abarelix-acetate.html Abarelix HYPERLINK https:/www.M

9、edChemE/abarelix-acetate.html HYPERLINK https:/www.MedChemE/abarelix-acetate.html Acetate(PPI 149 Acetate; R 3827 Acetate) Cat. No.: HY-13534A HYPERLINK https:/www.MedChemE/Alarelin-Acetate.html Alarelin HYPERLINK https:/www.MedChemE/Alarelin-Acetate.html HYPERLINK https:/www.MedChemE/Alarelin-Aceta

10、te.html Acetate(Alarelin) Cat. No.: HY-17405Abarelix Acetate (PPI 149 Acetate; R 3827 Acetate)is a potent gonadotrophin-releasing hormone (GnRH)antagonist, used for prostate cancer research.Alarelin acetate is a synthetic GnRH agonist.Purity: 99.61%Clinical Data: LaunchedSize: 10 mM 1 mL, 5 mg, 10 m

11、g, 25 mg, 50 mgPurity: 99.43%Clinical Data: LaunchedSize: 10 mM 1 mL, 10 mg, 100 mg HYPERLINK https:/www.MedChemE/bay-1214784.html BAY HYPERLINK https:/www.MedChemE/bay-1214784.html HYPERLINK https:/www.MedChemE/bay-1214784.html 1214784 HYPERLINK https:/www.MedChemE/bay-1214784.html HYPERLINK https:

12、/www.MedChemE/bay-784.html BAY-784Cat. No.: HY-144863 Cat. No.: HY-133080BAY 1214784 is a potent, selective, and orallyactive antagonist of the humangonadotropin-releasing hormone receptor(hGnRH-R). BAY 1214784 is a spiroindolinederivative compound.BAY-784 is a gonadotropin releasing hormonereceptor

13、 (GnRH-R) antagonist probe with IC s of5021 and 24 nM for human and rat GnRH-R,respectively.Purity: 98%Clinical Data: No Development ReportedSize: 1 mg, 5 mgPurity: 98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg HYPERLINK https:/www.MedChemE/Cetrorelix-Acetate.html Cetrorelix HYPERLINK ht

14、tps:/www.MedChemE/Cetrorelix-Acetate.html HYPERLINK https:/www.MedChemE/Cetrorelix-Acetate.html Acetate HYPERLINK https:/www.MedChemE/Cetrorelix-Acetate.html HYPERLINK https:/www.MedChemE/cetrorelix-diacetate.html Cetrorelix HYPERLINK https:/www.MedChemE/cetrorelix-diacetate.html HYPERLINK https:/ww

15、w.MedChemE/cetrorelix-diacetate.html diacetate(SB-75 acetate) Cat. No.: HY-P0009A (SB-75 diacetate) Cat. No.: HY-P0009BCetrorelix Acetate (SB-75 acetate) is a potentgonadotropin-releasing hormone (GnRH) receptorantagonist with an IC of 1.21 nM.50Cetrorelix diacetate (SB-075 diacetate) is apotent gon

16、adotropin-releasing hormone (GnRH)receptor antagonist with an IC of 1.21 nM.50Purity: 99.69%Clinical Data: LaunchedSize: 10 mM 1 mL, 1 mg, 5 mg, 10 mg, 25 mg, 50 mgPurity: 98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg HYPERLINK https:/www.MedChemE/Degarelix.html Degarelix HYPERLINK https

17、:/www.MedChemE/Degarelix.html HYPERLINK https:/www.MedChemE/degarelix-d7.html Degarelix-d7Cat. No.: HY-16168A Cat. No.: HY-16168ASDegarelix is a competitive and reversiblegonadotropin-releasing hormone receptor (GnRHR)antagonist.Degarelix-d7 is deuterium labeled Degarelix.Degarelix is a competitive

18、and reversiblegonadotropin-releasing hormone receptor (GnRHR)antagonist.Purity: 99.92%Clinical Data: LaunchedSize: 2 mg, 5 mg, 10 mg, 50 mg, 100 mgPurity: 98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg2 Tel: 609-228-6898 Fax: 609-228-5909 Email: salesMedChemE HYPERLINK https:/www.MedChemE

19、/Elagolix_sodium.html Elagolix HYPERLINK https:/www.MedChemE/Elagolix_sodium.html HYPERLINK https:/www.MedChemE/Elagolix_sodium.html sodium(NBI-56418 sodium) Cat. No.: HY-14369 HYPERLINK https:/www.MedChemE/elagolix-13c-d3-sodium.html Elagolix-13C,d3 HYPERLINK https:/www.MedChemE/elagolix-13c-d3-sod

20、ium.html HYPERLINK https:/www.MedChemE/elagolix-13c-d3-sodium.html sodium(NBI-56418-13C,d3 sodium) Cat. No.: HY-14369SElagolix sodium is a human GnRH receptor(GnRHR) antagonist with an IC50 and Ki of 0.25and 3.7 nM, respectively.Elagolix-13C,d3 (sodium) is the 13C- and deuteriumlabeled. Elagolix sod

21、ium is a human GnRH receptor(GnRHR) antagonist with an IC50 and Ki of 0.25 and3.7 nM, respectively.Purity: 99.66%Clinical Data: LaunchedSize: 10 mM 1 mL, 5 mg, 10 mg, 50 mg, 100 mgPurity: 98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg HYPERLINK https:/www.MedChemE/gnrh-antagonist-2.html G

22、nRH HYPERLINK https:/www.MedChemE/gnrh-antagonist-2.html HYPERLINK https:/www.MedChemE/gnrh-antagonist-2.html antagonist HYPERLINK https:/www.MedChemE/gnrh-antagonist-2.html HYPERLINK https:/www.MedChemE/gnrh-antagonist-2.html 2Cat. No.: HY-134864 HYPERLINK https:/www.MedChemE/Goserelin.html Goserel

23、in(ICI 118630) Cat. No.: HY-13673GnRH antagonist 2 (formula I) is a GnRH receptorantagonist that can be used for endometriosisresearch.Goserelin (ICI 118630), a decapeptide analogue ofgonadotropin-releasing hormone (GnRH/LHRH),functions as a GnRH agonist. Goserelin can beused for the research of bre

24、ast cancer, epithelialovarian cancer and prostate cancer.Purity: 98.16%Clinical Data: No Development ReportedSize: 10 mM 1 mL, 5 mg, 10 mg, 25 mg, 50 mgPurity: 98%Clinical Data: LaunchedSize: 1 mg, 5 mg HYPERLINK https:/www.MedChemE/Goserelin-acetate.html Goserelin HYPERLINK https:/www.MedChemE/Gose

25、relin-acetate.html HYPERLINK https:/www.MedChemE/Goserelin-acetate.html acetate(ICI-118630 acetate) Cat. No.: HY-13673A HYPERLINK https:/www.MedChemE/kisspeptin-54-human.html Kisspeptin-54(human)(Metastin(human) Cat. No.: HY-P1022Goserelin acetate (ICI-118630 acetate), adecapeptide analogue of gonad

26、otropin-releasinghormone (GnRH/LHRH), functions as a GnRH agonist.Goserelin acetate can be used for the research ofbreast cancer, epithelial ovarian cancer andprostate cancer.Kisspeptin-54(human) (Metastin(human) is anendogenous ligand for kisspeptin receptor (KISS1,GPR54). Kisspeptin-54(human) bind

27、s to rat andhuman GPR54 receptors with K values of 1.81inM and 1.45 nM, respectively.Purity: 99.89%Clinical Data: LaunchedSize: 10 mM 1 mL, 5 mg, 10 mg, 50 mgPurity: 98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg HYPERLINK https:/www.MedChemE/kisspeptin-54-human-tfa.html Kisspeptin-54(hum

28、an) HYPERLINK https:/www.MedChemE/kisspeptin-54-human-tfa.html HYPERLINK https:/www.MedChemE/kisspeptin-54-human-tfa.html TFA HYPERLINK https:/www.MedChemE/kisspeptin-54-human-tfa.html HYPERLINK https:/www.MedChemE/Lecirelin.html Lecirelin(Metastin(human) TFA) Cat. No.: HY-P1022ACat. No.: HY-P0051Ki

29、sspeptin-54(human) TFA (Metastin(human) TFA) isan endogenous ligand for kisspeptin receptor(KISS1, GPR54). Kisspeptin-54(human) TFA binds torat and human GPR54 receptors with K valuesiof 1.81 nM and 1.45 nM, respectively.Lecirelin, a synthetic gonadotropin-releasinghormone (GnRH) analogue, acts as a

30、 GnRH agonist.Lecirelin is widely used for the research ofbovine ovarian follicular cysts.Purity: 98%Clinical Data: No Development ReportedSize: 1 mg, 5 mgPurity: 99.83%Clinical Data: No Development ReportedSize: 1 mg, 5 mg, 10 mg, 25 mg HYPERLINK https:/www.MedChemE/linzagolix.html Linzagolix HYPER

31、LINK https:/www.MedChemE/linzagolix.html HYPERLINK https:/www.MedChemE/_2R_-N-5-3-_2,5-Difluorophenyl_-2-_1,3-dihydro-2H-benzimidazol-2-ylidene_-1,3-dioxopropyl-2-fluorophenylsulfonyl-2-hydroxypropanimidamide.html opigolix(KLH-2109; OBE-2109) Cat. No.: HY-109093Cat. No.: HY-U00289Linzagolix (KLH-2109; OBE-2109) is a potent,non-peptid