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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。 | |||
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)。 | |||
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。 | |||
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)。 | |||
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。 | |||
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)。 | |||
TP2337 |
Ganirelix Acetate
|
GNRH Receptor | GPCR/G Protein |
Ganirelix Acetate 是一种促性腺激素释放激素 (GnRH) 受体拮抗剂。 | |||
T17301 |
Opigolix
ASP-1707 |
GNRH Receptor | GPCR/G Protein |
Opigolix (ASP-1707)是一种可口服促性腺激素释放激素 (GnRH) 受体拮抗剂,可用于研究子宫内膜异位症相关疼痛、风湿性关节炎和子宫肌瘤。 | |||
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。 | |||
TP1896L1 |
Kisspeptin 234 acetate(1145998-81-7 free base)
|
GPR; Kisspeptin | Endocrinology/Hormones; GPCR/G Protein |
Kisspeptin 234 acetate(1145998-81-7 free base) 是Kisspeptin 受体 (KISS1, GPR54) 拮抗剂; 是Kisspeptin-10 类似物。它抑制 Kisspeptin-10 对磷酸肌醇 (IP) (IC50 = 7 nM) 的刺激和促性腺激素释放激素 (GnRH) 的释放。 | |||
T23412 |
T 98475
|
Others | Others |
gonadotropin-releasing hormone (GnRH, LHRH) receptor antagonist,orally active | |||
T10988 |
Degarelix
|
GNRH Receptor | GPCR/G Protein |
Degarelix is a competitive and reversible gonadotropin-releasing hormone receptor (GnRHR) antagonist. | |||
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). | |||
T76351 |
[D-Ala6]-LH-RH
|
Others | Others |
[D-Ala6]-LH-RH,一种黄体激素释放激素(LHRH)模拟物,充当GnRH受体的激动剂。 | |||
T76350 |
[D-Glp1,D-Phe2,D-Trp3,6]-LH-RH
|
||
[D-Glp1,D-Phe2,D-Trp3,6]-LH-RH 是一种黄体激素释放激素 (LHRH) 类似物,可作为 GnRH 受体拮抗剂。 | |||
TP1936 |
RFRP-3(human)
RFRP 3 (human) |
||
Agonist of the NPFF1 receptor (IC50 = 0.7 nM for inhibition of forskolin-induced cAMP production). Homolog of gonadotropin-inhibitory hormone (GnIH); inhibits activity of gonadotropin-releasing hormone (GnRH) neurons. | |||
T28795 |
SKI2496
SKI 2496,SKI-2496 |
Others | Others |
SKI2496 is a potent and orally bioavailableantagonist of Gonadotropin-Releasing Hormone Receptor (hGnRHR IC50 = 0.46 nM; max. LH inh. inh. (%, h)= 84%, 12h; LH inh. (24h) = 76%.). SKI2496 exhibits more selective antagonistic activity toward the human GnRH | |||
T70309 |
Dicetrorelix pamoate
|
Others | Others |
Dicetrorelix pamoate is a synthetic decapeptide with gonadotropin-releasing hormone (GnRH) antagonistic activity. GnRH induces the production and release of luteinizing hormone (LH) and follicle stimulating hormone (FSH) from the gonadotrophic cells of the anterior pituitary. Due to a positive estradiol (E2) feedback at midcycle, GnRH liberation is enhanced resulting in an LH-surge. This LH-surge induces the ovulation of the dominant follicle, resumption of oocyte meiosis and subsequently lutein... | |||
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). ... | |||
T76436 |
[MePhe7]-Neurokinin B
|
||
[MePhe7]-Neurokinin B为NK-3受体(NK3R)激动剂,具有3 nM的IC50值。通过激活神经激肽3受体,[MePhe7]-Neurokinin B能够调节脉冲促性腺激素释放激素(GnRH)的分泌,成为调控该过程的潜在调节剂。 | |||
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... | |||
T72990 |
BAY 1214784
|
Others | Others |
BAY 1214784是一种针对人促性腺激素释放激素受体(hGnRH-R)的高效、选择性口服活性拮抗剂,属于螺二氢吲哚衍生物化合物。该化合物能显著降低血浆促黄体激素水平,最高可达49%,同时显示出较低的药代动力学变异性和良好的耐受性,表现出研究子宫肌瘤的潜力。 | |||
T70775 |
Zoptarelin doxorubicin
|
||
Zoptarelin doxorubicin, also known as AEZS-108, is an LHRH agonist. Zoptarelin doxorubicin is a peptide agonist of the gonadotropin releasing hormone-1 receptor (GnRH-1R) that is conjugated to the anthracycline antibiotic doxorubicin with potential antineoplastic activity. Zoptarelin doxorubicin binds to GnRH-1Rs, which may be highly expressed on endometrial and ovarian tumor cell membrane surfaces, and is internalized. Once inside the cell, the doxorubicin moiety of this agent intercalates in... | |||
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... | |||
T76047 |
TAK-683 TFA
|
||
TAK-683 TFA是一种高效的全KISS1R激动剂(IC50=170 pM),拥有较好的代谢稳定性,是九肽metastin的类似物,对KISS1R有激动效应,其对人和大鼠EC50值分别为0.96 nM和1.6 nM。TAK-683 TFA能够降低下丘脑GnRH水平,进而减少血浆FSH、LH、睾酮的浓度,显示出对激素依赖性前列腺癌研究的可能性。 | |||
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 gene KISS-1. Kisspeptin-54 induces calcium mobilization in CHO-K1 cells expressing rat and human receptors (EC50s = 1.39 and 5.47 nM, respectively). It also induces arachidonic acid release in CHO cells expressing rat and human GPR54 in a concentration-dependent manner. Kisspeptin-5... | |||
T81485 |
Phoenixin-14 TFA
PNX-14 TFA |
||
Phoenixin-14 (PNX-14) TFA 是具抗焦虑、心脏保护及神经保护效果的穿透大脑屏障神经肽。它通过上调GnRH受体mRNA调控垂体促性腺激素分泌,并促进胰岛素释放。此外,Phoenixin-14 TFA保护小鼠免受缺血/再灌注(IR)伤害,通过降低ROS、提高GSH减缓氧化应激。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-04307 |
GNRH2 Protein, Human, Recombinant (hFc)
LH-RHII,gonadotropin releasing hormone... |
Human | HEK293 Cells |
GNRH2 (Gonadotropin-Releasing Hormone 2) is a Protein Coding gene. This gene is a member of the gonadotropin-releasing hormone (GnRH) gene family. Proteins encoded by members of this gene family are proteolytically cleaved to form neuropeptides which, in part, regulate reproductive functions by stimulating the production and release of the gonadotropins follicle-stimulating hormone (FSH) and luteinizing hormone (LH). 3 alternatively spliced human isoforms have been reported. The second mammalian... | |||
TMPJ-00365 |
GAS6 Protein, Human, Recombinant (Avi & His), Biotinylated
AXLLG,Growth arrest-specific protein 6,AXL receptor... |
Human | HEK293 Cells |
Human Growth arrest-specific protein 6 (GAS6) is ligand for tyrosine-protein kinase receptors AXL, TYRO3 and MER whose signaling is implicated in cell growth and survival, cell adhesion and cell migration. GAS6/AXL signaling plays a role in various processes such as endothelial cell survival during acidification by preventing apoptosis, optimal cytokine signaling during human natural killer cell development, hepatic regeneration, gonadotropin-releasing hormone neuron survival and migration, plat... | |||
TMPJ-00366 |
GAS6 Protein, Human, Recombinant (hFc)
AXLLG,Gas6,GAS-6,AXLLGAXL stimulatory factor,growth arrest-s... |
Human | HEK293 Cells |
GAS6 (Growth arrest-specific protein 6) is also known as AXL receptor tyrosine kinase ligand, AXLLG, is a multimodular protein that is up-regulated by a wide variety of cell types in response to growth arrest. Gas6 binds and induces signaling through the receptor tyrosine kinases Axl, Dtk, and Mer whose signaling is implicated in cell growth and survival, cell adhesion and cell migration. GAS6/AXL signaling plays a role in various processes such as endothelial cell survival during acidification ... | |||
TMPY-04999 |
GAS6 Protein, Human, Recombinant (His)
|
Human | HEK293 cells |
GAS6 (Growth arrest-specific protein 6) is also known as AXL receptor tyrosine kinase ligand, AXLLG, is a multimodular protein that is up-regulated by a wide variety of cell types in response to growth arrest. Gas6 binds and induces signaling through the receptor tyrosine kinases Axl, Dtk, and Mer whose signaling is implicated in cell growth and survival, cell adhesion and cell migration. GAS6/AXL signaling plays a role in various processes such as endothelial cell survival during acidification ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIJ-0268 |
Relugolix-d6
|
||
Relugolix-d6 是 Relugolix 的氘代化合物。Relugolix 的 CAS 号为 737789-87-6。Relugolix 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。 |