ovulation

Saralasin acetate(34273-10-4 free base) 是一种非选择性血管紧张素 II 拮抗剂。

Nomegestrol acetate 是一种孕酮受体的完全激动剂，是一种高选择性孕激素。

Cyclofenil 是一种选择性雌激素受体调节剂和排卵诱导剂，具有抗登革热病毒活性。

Norethynodrel (Lynestrol) 是一种合成的孕激素，其作用和用途类似于孕酮。它已被用于治疗功能性子宫出血和子宫内膜异位症。它作为避孕药，通常与 MESTRANOL 联合使用。

Norethindrone (Norethisterone) 是孕激素，能够用于子宫内膜异位症、由激素水平异常引起的子宫出血和继发性闭经的研究。

Ulipristal acetate (CDB-2914) 是一种具有抗孕酮活性的选择性孕酮受体调节剂。它可抑制子宫平滑肌瘤病的生长。它通过抑制或延迟排卵和影响子宫内膜组织，可用作紧急避孕药。

Hydroxyprogesterone caproate (Delalutin) 是一种甾体，是一种人工合成的孕激素。

Pregnanediol (5Beta-Pregnane-3Alpha,20alpha-Diol) 是一种黄体酮的主要代谢物 (metabolite)，能够通过尿液排出。它提供了一种间接测定体内孕激素水平的方法。

Norgestomet is a steroidal progestin of the 19-norprogesterone group used in veterinary medicine to control estrus and ovulation in cattle. In addition to the progesterone receptor, norgestomet possesses a weak (micromolar) affinity for the glucocorticoid

Pregnant mare serum gonadotropin (PMSG) 是用于促进动物卵泡发育及排卵的促性腺激素。该激素可通过激活体内的血液激素、促性腺激素以及前脑垂体和下丘脑中的细胞质雌二醇受体，调节相关生理过程。在畜牧业中，Pregnant mare serum gonadotropin 用以增加繁殖效率；此外，它也被应用于研究发情周期的调节。

FSH receptor antagonist 1 (compound 10) 是一种高效的G(s)蛋白偶联人类促卵泡激素 (FSH) 受体拮抗剂，在表达人类FSH受体的细胞系中的IC50值为28 nM。该化合物在体外小鼠模型中显著抑制卵泡生长和排卵。

Clomifene is a selective estrogen receptor modulator (SERM), it has both estrogenic and anti-estrogenic activities. This agent causes the release of the pituitary gonadotropins follicle-stimulating hormone (FSH) and luteinizing hormone (LH), leading to ov

Coixol (MBOA) 是一种从薏苡仁中提取的多酚，有抗菌和抗肿瘤作用。

R 151885 delays ovulation in rats.

Retroprogesterone, a progestin, may be used for menstrual irregularities in adolescence, for the maintenance of threatened pregnancy, and possibly as an ovulation stimulant.

Clomesone 是一种合成的非甾体药物，可用作分子结构单元。它是一种常用于治疗女性不孕的药物，通过阻断大脑中雌激素的作用发挥作用，已被证明对患有多囊卵巢综合征和其他不孕问题的女性有效诱导排卵。

Clomifene hydrochloride 可以诱导排卵，能够用于不孕症。hydrochloride 是一种简单的、相对安全的、易于给药且耐受性良好的、口服具有活力的化合物。

Etamestrol is a synthetic, steroidal estrogen described as an ovulation inhibitor or hormonal contraceptive

Acyline is a novel GnRH antagonist found in animal studies to be a potent suppressor of circulating gonadotropin and testosterone (T) levels. Acyline inhibits basal and GnRH-stimulated serum testosterone concentrations in male dogs. Acyline prevented ovulation, but did not affect ovarian follicular development or gestational corpora lutea in the domestic cat. A single dose of the potent gonadotropin-releasing hormone antagonist acyline suppresses gonadotropins and testosterone for 2 weeks in healthy young men.

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 luteinization as indicated by rising progesterone levels. Cetrorelix competes with natural GnRH for binding to membrane receptors on pituitary cells and thus controls the release of LH and FSH in a dose-dependent manner. Cetrorelix binds to the gonadotropin releasing hormone receptor and acts as a potent inhibitor of gonadotropin secretion. It competes with natural GnRH for binding to membrane receptors on pituitary cells and thus controls the release of LH and FSH in a dose-dependent manner......

sGnRH-A，一种鲑鱼促性腺激素释放激素(GnRH)类似物，能够促进生长激素的分泌，并作为人工授精中的排卵诱导剂使用。

sGnRH-A醋酸盐是一种鲑鱼促性腺激素释放激素(GnRH)类似物。它能促进生长激素的分泌，并用作人工授精时的排卵诱导剂。

Lamprey LH-RH I 是一种促性腺激素释放激素，作用于提高血浆类固醇水平并刺激七鳃鳗排卵，而对其他动物模型无影响。

FSHreceptor-binding inhibitor fragment(bi-10) 是一种有效的 FSH 拮抗剂。FSHreceptor-binding inhibitor fragment(bi-10) 阻断 FSH 与 FSHR 的结合，并在受体水平上改变 FSH 的作用。FSHreceptor-binding inhibitor fragment(bi-10) 导致小鼠排卵抑制和卵泡闭锁。FSHreceptor-binding inhibitor fragment(bi-10) 通过下调卵巢中 FSHR 和 ERβ的过度表达来抑制卵巢癌发生。