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SB 271046 hydrochloride (SB 271046A) 是高效、选择性和具有口服活性的5-HT6受体拮抗剂，对大鼠、猪和人的pKi 分别为 9.02、8.55 和 8.81。它增加额叶皮层中的细胞外天冬氨酸和谷氨酸并表现出抗惊厥活性，EC50为 0.16 μM。它对 5-HT6 受体、结合位点和离子通道的选择性超过 200 倍。

Minamestane 是一种新型不可逆芳香化酶抑制剂。Minamestane 引起人胎盘芳香化酶的时间依赖性抑制，半衰期为4分钟，K 为59nM。Minamestane 具有抗肿瘤活性。

(Rac)-Telmesteine (3,4-Thiazolidinedicarboxylic Acid 3-Ethyl Ester) 是蛋白酶抑制剂，可用作含蛋白酶的洗涤剂和清洗剂中的酶稳定剂。

Mestranol (Devocin) 是一种雌激素受体激动剂，是一种非活性的前药，在转化为炔雌醇时具有生物活性。动物实验中，它可以与黄体酮联合使用，它可用于更年期激素或月经紊乱的研究。

Exemestane (EXE) 是一种选择性的、具有口服活性的、不可逆的甾体芳香酶抑制剂，能够作用于人胎盘芳香酶 (IC50:30 nM) 和大鼠卵巢芳香酶 (IC50:40 nM)，可用于研究激素依赖性乳腺癌。

Promestriene (3-propyl ethyl) 是局部有效的雌激素，是合成的雌二醇二乙醚。它对阴道萎缩有作用，但吸收量小。

Prudomestin (3,5,7-Trihydroxy-4',8-dimethoxyflavone) 是一种分离自 Prunus domestica 心材中，具有很强的黄嘌呤氧化酶(XO)抑制活性(IC50≈6 µM)。

Telmesteine is a mucolitic drug.

Domesticine, (-)- is an antagonist of alpha-1D-adrenoceptor.

Telomestatin is an inhibitor of the telomerase, it induces the formation of basket-type G-quadruplex (G4) structures from hybrid-type G-quadruplexes in the telomeric region.

Almestrone (developmental code names Ba 38372, Ciba 38372), also known as 7α-methylestrone, is a synthetic, steroidal estrogen which was synthesized in 1967 but was never marketed. It is used as a precursor in the synthesis of several highly active steroi

Dimestrol can induce DNA damage.

Lynestrenol mixture with mestranol is a bioactive chemical.

17β-hydroxy Exemestane is the primary active metabolite of exemestane . It is formed by metabolism of exemestane by the cytochrome P450 (CYP) isoforms CYP1A and CYP4A11. 17β-hydroxy Exemestane is an aromatase inhibitor (IC50 = 69 nM using human placental microsomes) and an androgen receptor (AR) agonist (IC50 = 39.6 nM) that is selective for AR over estrogen receptor α (ERα; IC50 = 21.2 μM). It stimulates growth of AR- and ERα-positive MCF-7 (EC50 = 2.7 μM) and T47D breast cancer cells (EC50s = 0.43 and 1,500 nM for AR- and ER-mediated growth, respectively) and inhibits proliferation of testosterone-treated aromatase-overexpressing MCF-7aro cells in a concentration-dependent manner. 17β-hydroxy Exemestane (20 mg/kg) inhibits increases in serum cholesterol and LDL levels and prevents decreases in bone mineral density in the lumbar vertebrae and femur, as well as femoral bending strength and compressive strength of the fifth lumbar vertebrae, in ovariectomized rats.

Emestrin is a mycotoxin originally isolated from E. striata that has antimicrobial, immunomodulatory, and cytotoxic activities.1,2,3,4,5 It is active against the fungi C. albicans and C. neoformans, as well as the bacteria E. coli, S. aureus, and methicillin-resistant S. aureus (MRSA; IC50s = 3.94, 0.6, 2.21, 4.55, and 2.21 μg/ml, respectively).2 Emestrin is a chemokine (C-C motif) receptor 2 (CCR2) antagonist (IC50 = 5.4 μM in a radioligand binding assay using isolated human monocytes).3 Emestrin (0.1 μg/ml) induces apoptosis in HL-60 cells.4 It induces heart, thymus, and liver tissue necrosis in mice when administered at doses ranging from 18 to 30 mg/kg.5 |1. Seya, H., Nakajima, S., Kawai, K.-i., et al. Structure and absolute configuration of emestrin, a new macrocyclic epidithiodioxopiperazine from Emericella striata. J. Chem. Soc. Chem. Commun. 10, 657-658 (1985).|2. Herath, H.M.T.B., Jacob, M., Wilson, A.D., et al. New secondary metabolites from bioactive extracts of the fungus Armillaria tabescens. Nat. Prod. Res. 27(17), 1562-1568 (2013).|3. Herath, K.B., Jayasuriya, H., Ondeyka, J.G., et al. Isolation and structures of novel fungal metabolites as chemokine receptor (CCR2) antagonists. J. Antibiot. (Tokyo) 58(11), 686-694 (2005).|4. Ueno, Y., Umemori, K., Niimi, E.-c., et al. Induction of apoptosis by T-2 toxin and other natural toxins in HL-60 human promyelotic leukemia cells. Nat. Toxins 3(3), 129-137 (1995).|5. Terao, K., Ito, E., Kawai, K.-i., et al. Experimental acute poisoning in mice induced by emestrin, a new mycotoxin isolated from Emericella species. Mycopathologia 112(2), 71-79 (1990).

Plomestane is a selective inhibitor of aromatization in human breast tissue and may provide a mechanism for controlling estrogen responsive processes.

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

Hedysarimcoumestan B为从Hedysarum multijugum根部提取的天然化合物。

Safimestomig 为IgG4κ型针对CD47/CD274的双特异性抗体，其同型对照为 HumanIgG4(S228P) kappa, Isotype Control。

Futermestotug 是一种靶向人细胞毒性 T 淋巴细胞相关蛋白 4 (CTLA4) 的人源化免疫球蛋白 G1-κ 单克隆抗体，有望用于多种恶性肿瘤的研究。

Exemestane-D3是Exemestane (T1587)的氘代化合物。Exemestane的CAS号为107868-30-4。Exemestane是一种选择性的、具有口服活性的、不可逆的甾体芳香酶抑制剂，能够作用于人胎盘芳香酶 (IC50:30 nM)和大鼠卵巢芳香酶 (IC50:40 nM)，可用于研究激素依赖性乳腺癌。

Exemestane-13C-D3是Exemestane (T1587)的 13C 和氘代化合物。Exemestane的CAS号为107868-30-4。Exemestane是一种选择性的、具有口服活性的、不可逆的甾体芳香酶抑制剂，能够作用于人胎盘芳香酶 (IC50:30 nM)和大鼠卵巢芳香酶 (IC50:40 nM)，可用于研究激素依赖性乳腺癌。

Mestranol (Standard) 是 Mestranol 的标准品，适用于定量分析、质量控制及生化实验等相关研究。Mestranol (Devocin) 是一种雌激素受体激动剂，是一种非活性的前药，在转化为炔雌醇时具有生物活性。动物实验中，它可以与黄体酮联合使用，它可用于更年期激素或月经紊乱的研究。

Coumestrol (Standard) 是 Coumestrol 的标准品。适用于定量分析、质量控制及生化实验等相关研究。Coumestrol 是一种大豆产品中存在的植物雌激素。它抑制ES2细胞增殖的IC50值为50 μM。它可用于癌症，神经障碍和自身免疫疾病的研究。