Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1288 |
Fertirelin
|
Others | Others |
Fertirelin 是 GnRH 和 LH-RH 的类似物,可用于研究牛滤泡囊肿。 它是促性腺激素释放激素激动剂。 | |||
T1494 |
Alarelin Acetate
阿拉瑞林,Alarelin |
GNRH Receptor | GPCR/G Protein |
Alarelin Acetate 是一种合成的GnRH 激动剂。 | |||
T27837 |
Linzagolix
|
GNRH Receptor | GPCR/G Protein |
Linzagolix 是一种口服有活性的非多肽GnRH 拮抗剂。可用于研究子宫肌瘤、子宫腺肌症、子宫内膜异位症。 | |||
T11174 |
(R)-Elagolix
恶拉戈利,NBI-56418 |
GNRH Receptor | GPCR/G Protein |
(R)-Elagolix (NBI-56418) 是口服具有活性的、选择性高的非肽类促性腺激素释放激素受体短期有效拮抗剂 (KD = 54 pM)。 | |||
T5520 |
Cetrorelix Acetate
醋酸西曲瑞克,Cetrorelix |
GNRH Receptor | GPCR/G Protein |
Cetrorelix Acetate 是一种GnRH 受体的强效拮抗剂(IC50:1.21 nM)。 | |||
T5031 |
Elagolix sodium
NBI-56418 sodium,恶拉戈利钠 |
GNRH Receptor | GPCR/G Protein |
Elagolix sodium (NBI-56418 sodium) 是人GnRH 受体拮抗剂,其IC50=0.25 nM,Ki=3.7 nM。 | |||
T10217L |
Abarelix
R3827,阿巴瑞克,PPI 149 |
GNRH Receptor | GPCR/G Protein |
Abarelix (PPI 149) 是一种促性腺激素释放激素 (GnRH) 拮抗剂,用于前列腺癌研究。 | |||
T3630 |
Relugolix
RVT-601,瑞卢戈利,TAK-385 |
GNRH Receptor | GPCR/G Protein |
Relugolix (RVT-601) 是口服有活性的非肽性促性腺激素释放激素的拮抗剂。同 TAK-013 相比,它对人和猴子的受体具有高亲和力和强拮抗活性,它们的 IC50值分别为0.33 nM 和0.32 nM。它可用于研究性激素依赖性疾病,如子宫肌瘤、子宫内膜异位症、前列腺癌等。 | |||
T4102 |
Goserelin acetate
醋酸戈舍瑞林,Fertilan,ICI-118630 acetate,Zoladex |
Apoptosis; GNRH Receptor | Apoptosis; GPCR/G Protein |
Goserelin acetate (Fertilan) 是一种促性腺激素释放激素 (GnRH/LHRH) 十肽类似物,能作为GnRH 激动剂。它可研究乳腺癌、上皮性卵巢癌和前列腺癌。 | |||
T5520L |
Cetrorelix diacetate
NS-75A,醋酸西曲瑞克,SB-075 acetate,SB-075 diacetate,Cetrorelix acetate,NS-75A diacetate |
GNRH Receptor | GPCR/G Protein |
Cetrorelix diacetate (NS-75A) 是GnRH 受体的强效拮抗剂(IC50:1.21 nM)。 | |||
T10988L |
Degarelix acetate(214766-78-6 free base)
|
GNRH Receptor | GPCR/G Protein |
Degarelix acetate(214766-78-6 free base) 是促性腺激素释放激素受体 (GnRHR) 的竞争性可逆拮抗剂。 | |||
TP1307 |
Buserelin Acetate (57982-77-1 free base)
布舍瑞林,Buserelin Acetate |
GNRH Receptor | GPCR/G Protein |
Buserelin Acetate (57982-77-1 free base) (Buserelin Acetate) 是促性腺激素释放激素受体 (GnRHR) 的激动剂。 | |||
TP1342L |
GnRH-I acetate
GnRH-I acetate(33515-09-2 free base) |
Others | Others |
GnRH-I acetate 在血液中释放具有生物活性的促卵泡激素 (FSH) 和促黄体激素 (LH)。 | |||
T10988 |
Degarelix
|
GNRH Receptor | GPCR/G Protein |
Degarelix is a competitive and reversible gonadotropin-releasing hormone receptor (GnRHR) antagonist. | |||
T84706 |
DCOIT
Kathon 930 |
Others | Others |
DCOIT是一种典型的异噻唑啉酮,能激活促性腺激素释放激素受体(GnRHR)在大脑中引发卵泡刺激素和黄体生成素的合成。此外,DCOIT干扰了G蛋白偶联受体、MAPK和Ca2+信号传递途径。 | |||
T85273 |
Gonadorelin acetate
|
Others | Others |
Gonadorelin, a gonadotropin-releasing hormone receptor (GNRHR; Ki= 13 nM in CHO cells expressing the human receptor) agonist and tropic hormone, effectively stimulates the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) from rat anterior pituitary cultures at 0.1 μg doses. Additionally, it triggers LH release from bovine anterior pituitary cultures at a 1 μM concentration. In vivo, gonadorelin induces ovulation in rats pretreated with fluphenazine (ED50= 610.3 ng/kg). ... | |||
T68701 |
Abarelix acetate
|
Others | Others |
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 vivo, abarelix decreases plasma luteinizing hormone (LH) levels six hours post-treatment in castrated rats, with levels returning to baseline within 24 hours.3 Abarelix (2 mg/kg) also transiently decreases plasma testosterone levels in intact rats, with levels returning to baseli... | |||
T85183 |
Degarelix acetate
FE 200486 |
Others | Others |
Degarelix is a synthetic gonadotropin-releasing hormone receptor (GNRHR) antagonist (IC50= 3 nM in HEK293 cells expressing the human receptor), effective in inhibiting the growth of various prostate cell lines (WPMY-1, WPE1-NA22, BPH-1, and LNCaP) by activating caspase and inducing apoptosis after 72 hours of exposure to 10 μM. In vivo studies demonstrate that degarelix (2 mg/kg) significantly reduces plasma testosterone levels in rats to castrate levels for up to 49 days following administratio... | |||
T10475 |
BAY-784
|
Others | Others |
BAY-784 is a gonadotropin-releasing hormone receptor (GnRH-R) antagonist (IC50s: 21 and 24 nM for human and rat GnRH-R). |