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Cat. No. | Product Name | Target | Signaling Pathways |
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T23647 |
Zindoxifene
D 16726 |
Estrogen/progestogen Receptor | Endocrinology/Hormones |
Zindoxifene (D 16726) 是一种抗雌激素化合物,具有抗肿瘤活性,可用于研究乳腺癌和前列腺癌。 | |||
T7465 |
4-Methylbenzylidene camphor
Enzacamene,4-甲基苄亚基樟脑,3-(4-甲基苯亚甲基)樟脑,4-MBC |
AChE | Neuroscience |
4-Methylbenzylidene camphor 是有机的樟脑衍生物,应用于化妆品行业,具有保护皮肤抵抗紫外线(特别是紫外线B 辐射)的能力。 | |||
T12654 |
(Rac)-Acolbifene
(Rac)-EM-652,EM-343,阿考比芬 |
Estrogen Receptor/ERR | Endocrinology/Hormones |
(Rac)-Acolbifene (EM-343) 是 Acolbifene 的外消旋形式。Acolbifene 是一种 estrogen receptor 拮抗剂。(Rac)-Acolbifene 显示出抗雌激素和雌激素活性。 (Rac)-Acolbifene 包含哌啶环,显示出良好的药理作用,RBA=380。 | |||
T8981 |
WAY-169916
WAY 169916,WAY169916 |
NF-κB | NF-κB |
WAY-169916 是雌激素受体 (ER) 的通路选择性抑制剂。它通过抑制 NF-kB 转录活性而发挥作用,但没有常规的雌激素活性。 | |||
T9796 |
22393-62-0_peak 2
|
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22393-62-0_peak 2 exhibits some aspects of the antiestrogenic activity and other actions that may be connected to the estrogenic properties. A mixture of the (Z)- and (E)-isomers (Broparestrol, INN) is used in dermatology. | |||
T33876L |
Panomifene HCl
EGIS5650 HCl,GYKI 13504 HCl,Panomifene HCl(77599-17-8 Free base),EGIS 5650 HCl |
HER | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Panomifene HCl 是一种选择性抗雌激素化合物,具有抗肿瘤活性,可用于治疗乳腺癌。 | |||
T13684 |
Equilin
7-Dehydroestrone |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Equilin (7-Dehydroestrone) 是神经营养性雌激素类固醇,具有血管扩张活性,通过 NF-κB 信号传导增加单核细胞-内皮粘附。Equilin 通过阻断Ca(2+)进入平滑肌来同样放松肠系膜动脉的阻力。 | |||
T1514 |
Norethindrone
Norethisterone,炔诺酮 |
Estrogen/progestogen Receptor; Progesterone Receptor | Endocrinology/Hormones; Others |
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。 | |||
T8984 |
FLTX1
|
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
FLTX1 is a fluorescent derivative of Tamoxifen, designed to efficiently target and label intracellular Tamoxifen-binding sites (estrogen receptors) both under permeabilized and non-permeabilized conditions. Additionally, FLTX1 demonstrates strong antiestrogenic activity in breast cancer cells, resembling the potent antiestrogenic properties of Tamoxifen. Notably, FLTX1 does not exhibit any estrogenic agonistic effect on the uterus. | |||
T2569 |
Chlorotrianisene
tris(p-methoxyphenyl)chloroethylene,氯丁烯二烯,CTA,tri-p-anisylchloroethylene,氯烯雌醚,TACE |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; COX | Endocrinology/Hormones; Immunology/Inflammation; Neuroscience |
Chlorotrianisene (tri-p-anisylchloroethylene) 是长效、可口服、亲脂性高的合成三苯乙烯 (TPE) 衍生物和选择性雌激素受体调节剂,有雌激素活性,也有抗雌激素活性。它还有效抑制COX-1并抑制全血中的血小板聚集。 | |||
T20938 |
o,p'-DDT
2,4'-DDT,ortho,para'-DDT |
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O,P'-DDT, a chlorinated organic pesticide, has estrogenic activity. | |||
T38272 |
Thiacloprid
|
AChR; Parasite | Microbiology/Virology; Neuroscience |
Thiacloprid 属于氯烟碱类杀虫剂,主要用于防治蔬菜和果园中的蚜虫。它会破坏 DNA 的稳定性,通过疏水或氢相互作用,结合到小沟槽中,改变 DNA 的结构和稳定性。 | |||
T23737 |
Anordiol
H 241,H241,AF-45,AF 45,AF45 |
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Anordiol is an antiestrogen with estrogenic activity. It also is known to inhibit fertility. | |||
T20764 |
Dienestrol diacetate
NSC 81279,NSC81279,Cycladiene,Retalon-oral,Oestrasid C,NSC-81279 |
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Dienestrol diacetate, a derivative of the synthetic non-steroid phenolic compound, DIENESTROL, exhibits estrogenic activities. | |||
T70980 | PBRM | ||
PBRM is the first selective, potent, non-estrogenic, irreversible inhibitor of 17β-HSD1. | |||
T38379 |
4-tert-Octylphenol diethoxylate
|
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4-tert-Octylphenol diethoxylate is a degradation product of the multi-purpose surfactant, Triton X. A known environmental contaminant, 4-tert-octylphenol diethoxylate is reported to be an endocrine disruptor in animal and human research studies, producing weak estrogenic effects. | |||
T69696 | TAS-108 citrate | ||
TAS-108, also known as SR16234, is a synthetic, antiestrogenic steroidal compound with potential antitumor activity. TAS-108 binds to and inhibits estrogenic receptor alpha (ERa), mainly expressed in the mammary gland and uterus and upregulated in estrogen-dependent tumors. Blockage of ERa by TAS-108 prevents the binding and effects of estrogen and may lead to an inhibition of estrogen-dependent cancer cell proliferation. TAS-108 also is a partial agonist of the estrogenic receptor beta (ERb), e... | |||
T39259 |
Arzoxifene
LY353381,Arzoxifene,SERMIII |
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Arzoxifene (LY353381) is an orally active selective estrogen receptor modulator (SERM) exhibiting a fixed ring structure analogous to raloxifene. This compound demonstrates potent antiestrogenic effects on breast cancer and endometrium while displaying minimal side effects. Additionally, Arzoxifene elicits favorable estrogenic effects on bone health and lipid profile. | |||
T10273 |
AhR modulator-1
|
Others | Others |
AhR modulator-1 is a selective and orally active aryl hydrocarbon receptor (AhR) modulator. It inhibits metastasis, in part, by inhibiting prostatic VEGF production prior to tumor formation. It also possesses anti-estrogenic properties in rat uterus. | |||
T37647 |
5α-dihydro Levonorgestrel
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5α-dihydro Levonorgestrel is a metabolite of the synthetic progestin levonorgestrel . It lacks in vitro and in vivo estrogenic activity, but induces copulatory behavior in male rats when administered at a dose of 1 mg per animal per day. | |||
T82366 |
Fulvestrant 3-β-D-Glucuronide
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Fulvestrant 3-β-D-Glucuronide,Fulvestrant的代谢产物,为葡萄糖醛酸结合物,属于纯抗雌激素类固醇。该化合物可应用于乳腺癌研究领域。 | |||
T62572 |
Enclomiphene hydrochloride
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Enclomiphene ((E)-Clomiphene) hydrochloride 是一种口服具有活力的、有效的非甾体雌激素受体 (estrogen receptor) 拮抗剂,具有抗雌激素作用。Enclomiphene hydrochloride 能够用于研究卵巢功能障碍、睾酮缺乏、男性性腺功能减退症和 type 2 型糖尿病。 | |||
T35783 |
Zearalenone-13C18
Zearalenone-13C18 |
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Zearalenone-13C18is intended for use as an internal standard for the quantification of zearalenone by GC- or LC-MS. Zearalenone is a mycotoxin that has been found inFusariumand has estrogenic activities.1It binds to human estrogen receptor α (ERα) and ERβ (IC50s = 9 and 5.8 nM, respectively).2Zearalenone induces precocious development of mammary tissues in young female pigs and prepucial enlargement in young male pigs.3Zearalenone (1.5-5 mg/kg of diet) induces hyperestrogenism in pigs. It also i... | |||
T36913 |
17-Epiestriol
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17-Epiestriol is a metabolite of estrone .1It is formed from estroneviaa 16α-hydroxy estrone intermediate by reduction of the C-17 ketone. 17-Epiestriol binds to estrogen receptor α (ERα) and ERβ with relative binding affinities of 29 and 80 compared with 17β-estradiol .2 1.Brinton, L.A., Trabert, B., Anderson, G.L., et al.Serum estrogens and estrogen metabolites and endometrial cancer risk among postmenopausal womenCancer Epidemiol. Biomarkers Prev.25(7)1081-1089(2016) 2.Kuiper, G.G.J.M., Lemme... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T1009 |
Estrone
Oestrone,雌酮,Fluoroethyl,Aquacrine |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Estrone (Aquacrine) 是内源性雌激素的主要代表,由多种组织产生,尤其是脂肪组织。它是脂肪细胞中雄烯二酮芳构化过程的结果。 | |||
T12581 |
Puerarin-4'-O-β-D-glucopyranoside
Puerarin4'-O-glucoside,葛根素-4'-Β-D-葡萄糖苷 |
Others | Others |
Puerarin-4'-O-β-D-glucopyranoside (Puerarin4'-O-glucoside) 是一种从葛根 (PLR) 中提取的异黄酮。它具有雌激素活性和抗 MCF-7 人乳腺癌细胞增殖作用。 | |||
T9454 |
4-Hydroxyestrone
|
Estrogen Receptor/ERR; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
4-Hydroxyestrone 是一种内源性雌激素代谢物,可强烈保护神经元细胞免受氧化损伤。 | |||
T1424 |
Ethynyl estradiol
乙炔基雌二醇,17α-Ethynylestradiol,Ethinyl Estradiol,炔雌醇 |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Ethynyl estradio 是一种高效的生物活性雌激素。 | |||
T7957 |
2-Isopropyl Thioxanthone
|
Others | Others |
2-Isopropyl Thioxanthone 具有潜在的抗雌激素和抗雄激素特性。 | |||
T0345 |
Estropipate
雌酮硫酸酯哌嗪,Piperazine estrone sulfate,Pipestrone,Estrone sulfate piperazine salt |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Estropipate (Piperazine estrone sulfate) 是一种由硫酸雌酮和哌嗪组成的天然雌激素物质。 | |||
T6S0325 |
Glycitein
黄豆黄素,Glycetein |
Apoptosis; Others | Apoptosis; Others |
Glycitein (Glycetein) 是一种大豆异黄酮,可研究抗氧化和细胞凋亡。 | |||
TN1146 |
8-Prenylnaringenin
8-Prenylnaringenin,8-异戊烯基柚皮素 |
Apoptosis; ROS | Apoptosis; Immunology/Inflammation |
8-prenylnaringenin 是一种从啤酒花穗中分离到的异戊烯类黄酮,具有细胞毒性。它能通过激活小鼠 Akt 磷酸化途径,使其从静止诱导的停用性肌肉萎缩中恢复。它能通过诱导内源性和外源性通路介导的凋亡,对 HCT-116 结肠癌细胞产生抗增殖活性。 | |||
T3665 |
Tectoridin
射干苷,Shekanin |
Estrogen Receptor/ERR; Reductase | Endocrinology/Hormones; Metabolism |
Tectoridin (Shekanin) 是分离自 Maackia amurensis 中的异黄酮,是一种植物雌激素,能够激活雌激素和甲状腺激素受体。它通过 ER 依赖性基因组途径和 GPR30 依赖性非基因组途径发挥雌激素作用。 | |||
T5S0993 |
Kurarinone
苦参酮,苦参黄素 |
BCL; Others; IκB/IKK; TNF; NF-κB; JAK; STAT | Angiogenesis; Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling; NF-κB; Others; Stem Cells |
Kurarinone 是从灌木苦参中提取的黄酮类化合物,具有抗肿瘤、雌激素和抗炎活性,对免疫反应也有很强的抑制作用。 | |||
T5625 |
Zearalenone
玉米,Mycotoxin F2,玉米烯酮,RAL,F2 toxin,Toxin F2 |
Others | Others |
Zearalenone (F2 toxin) 是真菌毒素,主要由食物和饲料中的 Fusarium 产生。它会引起幼龄母猪乳房发育早熟或其它雌激素效应。它在猪、牛、羊体内具有雌激素活性,急性毒性低。 | |||
T64353 |
4-tert-Octylphenol
|
Endogenous Metabolite | Metabolism |
4-tert-Octylphenol 是一种干扰内分泌的化学物质及雌激素药物,能诱导子代小鼠脑神经元祖细胞的凋亡,并通过减少溴脱氧尿苷(BrdU)、有丝分裂标志物Ki67以及磷酸组蛋白H3(p-Histone-H3)的表达,导致神经元祖细胞的增殖减少。这种物质不仅会干扰小鼠的大脑发育,还会影响其行为。 | |||
T36914 |
2-Hydroxyanthraquinone
|
Others | Others |
2-Hydroxyanthraquinone 是一种天然产物,显示出抗肿瘤和免疫抑制活性。 | |||
T13577 | β-Zearalenol | Others | Others |
β-Zearalenol, a non-steroidal estrogenic mycotoxin synthesized by Fusarium species, potentially influences transcription and affects gene expression on the translational level. | |||
TN4875 | Quercetin 3,3'-dimethyl ether | Others | Others |
Quercetin 3,3'-dimethyl ether may have moderate estrogenic activity. | |||
TN1679 |
Genistein 7,4'-di-O-β-D-glucoside
染料木素-7,4'-二-O-Β-D-葡萄糖苷,Genistein 7,4'-di-O-beta-D-glucopyranoside,鲁冰花 |
Others; Estrogen/progestogen Receptor | Endocrinology/Hormones; Others |
Genistein 7,4'-di-O-beta-D-glucopyranoside shows significant estrogenic proliferative effect in MCF-7 cell in sub-cytotoxic concentration range. | |||
T13391 |
Zearalanone
|
Others | Others |
Zearalenone is a nonsteroidal estrogenic mycotoxin produced by Fusarium species, which colonizes several grains. | |||
TN1573 | Desmethylxanthohumol | Others | Others |
Desmethylxanthohumol shows estrogenic activity. | |||
TN2045 |
Pelargonidin-3-O-glucoside chloride
|
Others; Estrogen/progestogen Receptor | Endocrinology/Hormones; Others |
Pelargonidin-3-O-glucopyranoside is the glucoside of Pelargonidin, an potential antidiabetic agent. Pelargonidin-3-O-glucopyranoside has antioxidant, anti-inflammatory, anti-estrogenic, and angiotensin-converting enzyme inhibitory activities. | |||
TN2224 |
Soyasapogenol A
大豆甾醇A,大豆甾醇 A |
TNF | Apoptosis |
Soyasapogenol A shows estrogenic and hepatoprotective activities, it directly prevents apoptosis of hepatocytes, and secondly, inhibits the elevation of plasma TNF-α±, which consequently resulted in the prevention of liver damage in the concanavalin A-induced hepatitis model. | |||
TN4383 |
Kazinol U
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IL Receptor; IκB/IKK; NOS; NF-κB | Immunology/Inflammation; NF-κB |
Kazinol U may have therapeutic value in delaying pancreatic β-cell destruction in type 1 diabetes by blocking the NF-κB pathway in pancreatic β-cells reduces cell damage. Kazinol U shows estrogenic activity with ligand-activity of estrogen receptor, transcriptional activity of estrogen -responsive element-reporter genes, it may have beneficial effects in the treatment of menopausal symptoms. | |||
TN3397 | Alpinumisoflavone | ERK; LDL; NF-κB; MEK; MAPK; Antifection | MAPK; Metabolism; Microbiology/Virology; NF-κB |
Alpinumisoflavone has atheroprotective effects, may result from their ability to upregulate mechanisms promoting HDL-cholesterol and bile acid formation, it is endowed with estrogenic properties accounting, at least in part, for E. lysistemon effects. Alp | |||
TN5456 |
Isoerysenegalensein E
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Isoerysenegalensein E shows anti-estrogenic activity comparable to that of 4-hydroxytamoxifen, a typical estrogen receptor antagonist. It shows significant cytotoxicity against HL-60 cells, it induces apoptosis in HL-60 cells through activation of the cas | |||
T83301 |
5,7-Dimethoxy-2,3-phenanthrenediol
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5,7-Dimethoxy-2,3-phenanthrenediol 表现出雌激素活性,能够促进MCF-7细胞的增殖,并增强ERβ在MCF-7细胞系中的表达。 | |||
TN3380 |
Alloisoimperatorin
|
AChR | Neuroscience |
Alloisoimperatorin is a candidate of AChE inhibitors, it displays potent antioxidant effects against the DPPH radical and against renal epithelial cell injury by using AAPH to generate peroxyl radicals in vitro. Alloisoimperatorin has estrogenic activity | |||
TN3539 | Broussonin A | ERK; IL Receptor; IκB/IKK; NOS; NF-κB; Akt | Cytoskeletal Signaling; Immunology/Inflammation; MAPK; NF-κB; PI3K/Akt/mTOR signaling |
Broussonins A and B, new phytoalexins from diseased paper mulberry. Broussonin A shows estrogenic activity with ligand-binding activity of estrogen receptor, transcriptional activity of estrogen-responsive element-luciferase reporter genes. Broussonin A c |