Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5015 |
Gonadorelin Acetate (33515-09-2 free base)
醋酸戈那瑞林,Luteinizing Hormone Releasing Hormone (LH-RH),Luteinizing Hormone Releasing Hormone (LH-RH), human,Gonadorelin Acetate |
Reductase | Endocrinology/Hormones; Metabolism |
Gonadorelin Acetate (33515-09-2 free base) (Luteinizing Hormone Releasing Hormone (LH-RH)) 是下丘脑神经肽,在控制生殖功能中起关键作用。 | |||
TP1112L |
LH-RH, salmon acetate(86073-88-3 free base)
Luteinizing Hormone Releasing Hormone (LH-RH), salmon acetate |
Others | Others |
LH-RH, salmon acetate(86073-88-3 free base) (Luteinizing Hormone Releasing Hormone (LH-RH), salmon acetate) 是一种在下丘脑中合成的垂体激素,在控制生殖功能中起着至关重要的作用。 | |||
TP1112 |
Luteinizing Hormone Releasing Hormone (LH-RH), salmon
LH-RH, salmon |
||
Luteinizing Hormone Releasing Hormone (LH-RH) is a pituitary Hormone synthesized in the hypothalamus and plays a crucial role in the control of reproductive function. | |||
T3538 |
Sufugolix
TAK-013 |
LHRH | Endocrinology/Hormones |
Sufugolix (TAK-013) 是一种高效的、有口服活性的黄体激素释放激素(LHRH) 受体拮抗剂(IC50:0.1 nM)。 | |||
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)。 | |||
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。 | |||
TP2107L |
Histrelin acetate
Histrelin acetate(76712-82-8 free base),醋酸组氨瑞林 |
GNRH Receptor | GPCR/G Protein |
Histrelin acetate 是促性腺激素释放激素 (GnRH) 的九肽类似物,具有增加的效力。当存在于血流中时,它作用于称为促性腺激素的垂体特定细胞。 Histrelin 刺激这些细胞释放促黄体激素和促卵泡激素。因此,它被认为是促性腺激素释放激素激动剂或 GnRH 激动剂。 | |||
T26040 |
Ramorelix
HOE 013,HOE013,HOE-013 |
||
Ramorelix is an antagonist of luteinizing hormone-releasing hormone (LHRH). | |||
T28954 |
Teverelix
|
||
Teverelix is a water-soluble antagonist of luteinizing hormone-releasing hormone (LHRH). | |||
T34055 |
Phtstllap
|
||
Phtstllap is a luteinizing hormone-releasing factor | |||
T68700 |
Avorelin acetate
|
||
Avorelin acetate is a luteinizing hormone releasing hormone (LH-RH) agonist. | |||
T25715 |
LHRH, Ala(6)-
L 1868,L-1868,L1868 |
||
LHRH, Ala(6)- is a synthetic luteinizing hormone-releasing hormone agonist agent. | |||
T26692 |
Avorelin
MF-6001,EP 23904,EP-23904,EP23904,MF6001 |
||
Avorelin, a luteinizing hormone releasing hormone (LH-RH) agonist, is used potentially for the treatment of prostate. | |||
T70819 | Argtide | ||
Argtide is an luteinizing hormone releasing hormone (LHRH) antagonist. | |||
T76351 | [D-Ala6]-LH-RH | ||
[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。 | |||
T76617 |
(D-Trp6)-LHRH free acid
|
||
(D-Trp6)-LHRH free acid 是促黄体生成素释放激素 (LHRH) 激动剂。 | |||
TP1648 |
[Gln8]-C517 (LH-RH), chicken
|
||
[Gln8] Luteinizing hormone releasing hormone ([Gln8] LH-RH), Avian hypothalamic peptide that stimulates release of gonadotropins from anterior pituitary, thus regulating reproductive functions. | |||
T76616 |
(D-Ser4,D-Ser(tBu)6,Azagly10)-LHRH
|
||
(D-Ser4,D-Ser(tBu)6,Azagly10)-LHRH 是一种黄体生成素释放激素 (LHRH) 的类似物,主要通过促进垂体分泌黄体生成素 (LH) 和促卵泡激素 (FSH) 来在生殖调控中发挥关键作用。 | |||
T83499 |
[D-Phe2,6, Pro3]-LH-RH
|
||
[D-Phe2,6, Pro3]-LH-RH是一种促黄体生成素释放激素(LHRH)的高效拮抗剂,具有特定氨基酸序列变异。 | |||
T76348 |
[D-Lys6]-LH-RH
|
||
[D-Lys6]-LH-RH 是一种黄体激素释放激素 (LHRH) 类似物,可作为GnRH 受体激动剂。 | |||
T76620 |
(D-Tyr5,D-Ser(tBu)6,Azagly10)-LHRH
|
||
(D-Ser4,D-Ser(tBu)6,Azagly10)-LHRH 是黄体生成素释放激素 (LHRH) 的类似物。LHRH 通过刺激垂体黄体生成素 (LH) 和促卵泡激素 (FSH) 的释放,在控制生殖中发挥核心作用。 | |||
T76615 |
(D-Ser(tBu)6,D-Leu7,Azagly10)-LHRH
|
||
(D-Ser(tBu)6,D-Leu7,Azagly10)-LHRH是一种LHRH(黄体生成素释放激素)的类似物,主要通过激活垂体分泌黄体生成素(LH)和促卵泡激素(FSH)来在生殖调控中发挥核心作用。 | |||
T80116 |
LHRH
|
GNRH Receptor | GPCR/G Protein |
LHRH是一种调节生殖功能的下丘脑神经肽,常用于癌症研究。 | |||
T82162 |
Human follicular gonadotropin releasing peptide
hF-GRP |
||
Human follicular gonadotropin releasing peptide (hF-GRP)是一种刺激垂体分泌促黄体激素(LH)及促卵泡激素(FSH)的激素类多肽,其作用可在体外实现。 | |||
T83498 |
[D-Phe2,D-Ala6]-LH-RH
Wy 18185 |
||
[D-Phe2,D-Ala6]-LH-RH 为有效LH-RH拮抗剂,展现了显著的抗LH/FSH-RH及抗排卵活性。 | |||
T75991 |
Ganirelix
|
||
Ganirelix为一种竞争性且选择性的促性腺激素释放激素(GnRH)拮抗剂,其主要作用机制为抑制内源性GnRH,从而抑制黄体生成素(LH)及促卵泡激素的释放。 | |||
T76324 |
GnRH Associated Peptide (1-24), human
|
||
GnRH Associated Peptide (GAP) (1-24), human 是人类的一个化合物,具体为促性腺激素释放激素相关肽(GAP)的第1至24个氨基酸片段(hGAP-1-24)。该化合物通过3个氨基酸加工位点与黄体生成素释放激素(LH-RH)序列连接。 | |||
TP1342 |
GnRH-I
|
||
GnRH-I is a small 10 amino acid long peptide (decapeptide) from the hypothalamus,It is also known as luteinizing hormone releasing hormone (LHRH), is a key molecule in the regulation of reproduction in vertebrates. GnRH, a decapeptide, is produced by neur | |||
T71149 | Triptorelin pamoate | ||
Triptorelin, a decapeptide (pGlu-His-Trp-Ser-Tyr-D-Trp-Leu-Arg-Pro-Gly-NH2), is a gonadotropin-releasing hormone agonist (GnRH agonist) used as the acetate or pamoate salts. By causing constant stimulation of the pituitary, it decreases pituitary secretion of gonadotropins luteinizing hormone (LH) and follicle stimulating hormone (FSH). Like other GnRH agonists, triptorelin may be used in the treatment of hormone-responsive cancers such as prostate cancer or breast cancer, precocious puberty, es... | |||
T76323 |
GnRH Associated Peptide (25-53), human
|
||
GnRH Associated Peptide (GAP) (25-53), human 是来源于人的促性腺激素释放激素相关肽(GAP)的一个特定片段,具体为第25至第53位氨基酸(hGAP-25-53)。本片段可用作免疫原,用以产生含有MC-1、MC-2和MC-3等抗体的抗血清。GAP通过其内含的三个氨基酸加工位点,能与黄体生成素释放激素(LH-RH)序列进行有效连接。 | |||
T76322 |
LH-RH II (chicken)
|
||
LH-RH II (chicken) 为家鸡下丘脑黄体生成素释放激素(LHRH)两种形式之一,亦为哺乳动物LHRH的结构变体。该化合物促进家鸡促性腺激素释放。 | |||
T76353 |
LH-RH (7-10)
|
||
LH-RH (7-10),一种由性腺激素释放激素 (LHRH) 在垂体和下丘脑降解过程中形成的主要四肽降解产物之一,存在于巨噬细胞、I 型样及II 型肺细胞中。 | |||
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) 作为一种CRF拮抗剂,能有效阻断IL-1a诱发的黄体生成素 (LH) 抑制作用。 | |||
T76558 |
Onvitrelin ucalontide
|
||
Onvitrelin ucalontide ([Phor18-LHRH (338613)]) 是一种 LHRH (黄体生成素释放激素) 的类似物,展现出抗肿瘤特性。这一化合物是一个具备序列 KFAKFAKKFAKFAKKFAKQHWSYGLRPG 的肽,能在小鼠模型上有效地抑制乳腺癌、卵巢癌和前列腺癌的异种移植物生长。 | |||
T70309 | Dicetrorelix pamoate | ||
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... | |||
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 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... | |||
T36912 |
17α,20β-Dihydroxy-4-pregnen-3-one
17α,20β-dihydroxy Progesterone,17α,20β-DHP,17α,20β-Dihydroxy-4-pregnen-3-one |
||
17α,20β-Dihydroxy-4-pregnen-3-one (17α,20β-DHP) is an endogenous, maturation-inducing steroid that stimulates oocyte maturation in females of several teleost species. For example, 1 μg/ml of 17α,20β-DHP applied to Persian sturgeon oocytes has been shown to effectively induce germinal vesicle breakdown, an essential step during oocyte maturation.1 Gonadotropin-releasing hormone and the gonadotropins, follicle-stimulating hormone and luteinizing hormone, have been shown to stimulate the production... | |||
T72990 |
BAY 1214784
|
||
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。 | |||
T68525 | Nafarelin acetate hydrate | ||
Nafarelin is a gonadotropin-releasing hormone agonist (GnRH agonist) which acts as an analog of GnRH. Nafarelin increases the release of FSH and LH by the anterior pituitary, which in turn leads to an increase of estrogen/progesterone. When administered, Nafarelin has the purpose of causing increase estrogen that will negatively feed back upon hypothalamus to decrease GnRH ( negative feedback loop ) Through negative feedback, Nafarelin causes a decrease in pituitary secretion of gonadotropins lu... | |||
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... |