46
5
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T15249 |
Estrogen receptor modulator 1
|
Estrogen Receptor/ERR | Endocrinology/Hormones |
Estrogen receptor modulator 1 是一种有效的、具有口服活性的、选择性雌激素受体(estrogen receptor)调节剂 (SERM),其 pIC50为 0.46。它能够诱导 Tamoxifen 耐药、激素非依赖性异种移植瘤的消退。 | |||
T40893 |
Estrogen receptor modulator 6
|
||
Estrogen receptor modulator 6 (compound 3a) is a highly specific and potent agonist of the estrogen receptor (ER) β with a remarkable affinity (K i = 0.44 nM). This compound exhibits an impressive 19-fold selectivity for ERβ over ERα, as evidenced by its affinity (K i = 8.4 nM). | |||
T79064 | Estrogen receptor modulator 7 | Estrogen Receptor/ERR | Endocrinology/Hormones |
Estrogen receptor modulator7 为一高效雌激素受体调节剂,主要用途涉及癌症研究领域。 | |||
T79109 |
Estrogen receptor modulator 8
|
Estrogen Receptor/ERR | Endocrinology/Hormones |
Estrogen receptor modulator8 (compound 4) 为一口服活性化合物,作用为抑制雌激素受体/ERR α(IC50=0.437 nM,MCF-7 细胞)。此化合物能有效抑制MCF-7细胞的增殖,其IC50值仅为0.1 nM。 | |||
T82439 |
Estrogen receptor modulator 10
|
Estrogen Receptor/ERR | Endocrinology/Hormones |
Estrogen receptor modulator10 (compound G-5b) 是一种具有高亲和力的ER拮抗剂,具有IC50值为6.7 nM,并且是一种有效的降解剂,DC50为0.4 nM。它能够通过蛋白酶体途径实现对ER的快速降解,并能诱导细胞凋亡,同时还能将细胞周期阻滞在G1/G0期,这使其成为癌症研究中的一个重要工具。 | |||
T7313 |
Enclomiphene citrate
恩氯米芬柠檬酸盐,Enclomifene citrate,(E)-Clomiphene citrate,trans-Clomiphene citrate |
Estrogen Receptor/ERR | Endocrinology/Hormones |
Enclomiphene citrate (trans-Clomiphene citrate) 是口服具有活力的 oestrogen receptor 拮抗剂,具有抗雌激素活性。 | |||
T2544 |
Bazedoxifene acetate
醋酸巴多昔芬,WAY-TES 424,TSE 424,WAY-140424 |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Bazedoxifene acetate (WAY-TES 424) 是一种非甾体的、有口服活性的、选择性的雌激素受体调节剂,能够作用于 ERα (IC50:26 nM) 和 ERβ (IC50:99 nM) ,可用于研究骨质疏松症。它也是一种IL-6/GP130蛋白相互作用抑制剂,可用于研究胰腺癌。 | |||
T6906 |
Tamoxifen
ICI 46474,他莫昔芬,Z-Tamoxifen,trans-Tamoxifen,ICI47699 |
Apoptosis; Estrogen Receptor/ERR; HSP; Estrogen/progestogen Receptor; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling; Endocrinology/Hormones; Metabolism |
Tamoxifen (ICI47699) 是一种雌激素受体调节剂 (SERM),具有选择性和口服有效性。Tamoxifen 对雌激素具有抑制活性 (如乳腺细胞) 和激活活性 (如骨、肝和子宫细胞)。 | |||
T0835 |
Tamoxifen Citrate
Tamoxifen Z-isomer citrate,ICI 46474,ICI 46474 Citrate,枸橼酸他莫昔芬,他莫昔芬柠檬酸盐 |
Apoptosis; Estrogen Receptor/ERR; HSP; Estrogen/progestogen Receptor; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling; Endocrinology/Hormones; Metabolism |
Tamoxifen Citrate 是一种口服有效的,选择性雌激素受体调节剂,可阻断乳腺细胞中的雌激素作用,并可激活如骨骼、肝脏和子宫细胞中的雌激素活性。它是 Hsp90激活剂,可增强 Hsp90 分子伴侣 ATPase 的活性,可激活自噬和诱导凋亡。 | |||
T6404 |
Bazedoxifene hydrochloride
Bazedoxifene HCl,盐酸巴多昔芬,TSE-424 |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Bazedoxifene hydrochloride (TSE-424) 是一种 IL-6/GP130蛋白相互作用抑制剂,可用于胰腺癌的研究。它也是一种有口服活性的,能透过血脑屏障的,非甾体、选择性的雌激素受体调节剂 (SERM),对 ERα 和 ERβ 作用的 IC50值分别为 26 nM 和 99 nM,可用于研究骨质疏松症。 | |||
T5348 |
SNG-1153
|
Estrogen/progestogen Receptor | Endocrinology/Hormones |
SNG-1153 是一种雌激素受体 ER-α36 调节剂。 | |||
T12482 |
Pipendoxifene hydrochloride
|
Estrogen Receptor/ERR | Endocrinology/Hormones |
Pipendoxifene hydrochloride 是雌激素受体的选择性调节剂。 | |||
T1193 |
Clomiphene citrate
NSC 35770,枸橼酸氯米芬,Clomifene citrate |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Clomiphene citrate (NSC 35770) 是一种雌激素受体调节剂。 | |||
T21897L |
MPP hydrochloride
MPP hydrochloride (289726-02-9 Free base) |
Estrogen Receptor/ERR | Endocrinology/Hormones |
MPP hydrochloride 是一种选择性雌激素受体(ERR)调节剂。 | |||
T27322 |
Fispemifene
HM-101,HM 101,HM101 |
Others | Others |
Fispemifene (HM-101) 是一种雌激素受体调节剂(SERM),可用于治疗泌尿生殖系统综合征和阴道萎缩。 | |||
T7839 |
Lasofoxifene Tartrate
CP-336156,酒石酸拉索昔芬 |
Estrogen Receptor/ERR | Endocrinology/Hormones |
Lasofoxifene Tartrate (CP-336156) 是一种非甾体类的雌激素受体选择性调节剂 (SERM)。 | |||
T68042 |
CHF-4227
Chf4227,Chf 4227 |
Estrogen Receptor/ERR | Endocrinology/Hormones |
CHF-4227 是一种新型高效且具有选择性的雌激素受体调节剂,可降低胆固醇合低密度脂蛋白胆固醇浓度。 | |||
T6743 |
(E/Z)-4-Hydroxytamoxifen
4-羟基他莫昔芬,(E/Z)-4-羟基他莫昔芬,Afimoxifene,4-Hydroxytamoxifen |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
(E/Z)-4-Hydroxytamoxifen (Afimoxifene) 是 tamoxifen 的活性代谢物和选择性雌激素受体(ER)调节剂,广泛用于乳腺癌的治疗和化学预防治疗。 | |||
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。 | |||
T4420 |
4-Hydroxytamoxifen
ICI 79280,(Z)-4-hydroxy Tamoxifen,4-羟基他莫昔芬,trans-4-Hydroxytamoxifen |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
4-Hydroxytamoxifen (ICI 79280) 是 Tamoxifen 的活性代谢产物,是一种雌激素受体调节剂 (SERM),具有选择性和口服有效性。4-Hydroxytamoxifen 具有抗肿瘤活性,可用于乳腺癌的研究。 | |||
T23113 | Ormeloxifene | Others | Others |
estrogen receptor modulator | |||
T10379 |
Arzoxifene hydrochloride
SERM 3,LY 353381 HCl |
Others | Others |
Arzoxifene hydrochloride is a selective estrogen receptor modulator that is a potent estrogen antagonist in mammary and uterine tissue. | |||
T14883 |
Idoxifene
CB7432 |
Others | Others |
Idoxifene is a tissue-specific selective estrogen receptor modulator. | |||
T29437 |
4-Hydroxytoremifene
4 Hydroxytoremifene,4-Hydroxy Toremifene,4-Hydroxy TOR,4OH-TOR |
||
4-Hydroxytoremifene is a selective estrogen receptor modulator toremifene active metabolite. | |||
T25700L |
Levormeloxifene fumarate
|
||
Levormeloxifene fumarate is an osteoporosis drug and selective estrogen receptor modulator (SERM). | |||
T23620 |
Acolbifene Hydrochloride
|
||
Acolbifene hydrochloride binds to estrogen receptors in the body. It is a type of selective estrogen receptor modulator | |||
T15800 |
LY117018
|
PI3K | PI3K/Akt/mTOR signaling |
LY117018 shows antiproliferative effects on breast cancer cell lines. LY117018 is a Raloxifene analog and is a selective estrogen receptor modulator. | |||
T12329 |
Ospemifene D4
FC-1271a D4 |
Estrogen/progestogen Receptor | Endocrinology/Hormones |
Ospemifene D4 is a deuterium labeled Ospemifene. Ospemifene is a selective and orally active modulator of estrogen receptor. | |||
T9001 |
Desketoraloxifene
|
Phospholipase | Metabolism |
Desketoraloxifene 是一种选择性雌激素受体调节剂,可抑制哺乳动物 PLD(PLD1 和 PLD2)。 | |||
T15186 |
(E)-4-Hydroxytamoxifen
|
Others | Others |
(E)-4-Hydroxytamoxifen is a less active isomer of (Z)-4-hydroxytamoxifen and also is an estrogen receptor modulator. | |||
T27946 |
LY-329146
LY 329146 |
||
LY-329146 is a selective estrogen receptor modulator (SERM). LY-329146 prevents doxorubicin resistance in tumor cells expressing multidrug resistance-associated protein (MRP) by inhibiting the binding of MRP substrates to the estrogen receptor. | |||
T25700 |
Levormeloxifene
|
||
Levormeloxifene is a selective modulator of the estrogen receptor. It inhibits the production of vaginal tropoelastin and transforming growth factor-beta 1. | |||
T68530 |
D 15414
|
||
D 15414 is a nonsteroidal weak estrogen of the 2-phenylindole group which was never marketed. It is the major metabolite of the selective estrogen receptor modulator zindoxifene. D-15414 has high affinity for the estrogen receptor and inhibits the growth of ER-positive MCF-7 breast cancer cells in vitro. | |||
T22512 |
4’-hydroxy Tamoxifen
|
Others | Others |
It is a metabolite of tamoxifen and an estrogen receptor modulator. | |||
T21375 |
Clomifene
Omifin,D,Chloramiphene,Clomiphene,Clomiphene free base,Citrate |
||
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 | |||
T13076 |
Tamoxifen-d5
ICI 47699-d5,(Z)-Tamoxifen-d5,trans-Tamoxifen-d5 |
HSP | Cytoskeletal Signaling; Metabolism |
Tamoxifen-d5 is a deuterium labeled Tamoxifen. Tamoxifen is a selective modulator of estrogen receptor (SERM). Tamoxifen is a potent activator of Hsp90 and enhances the Hsp90 molecular chaperone ATPase activity. | |||
T26037 |
RAD-140-Q
RAD 140,RAD-140Q,RAD-140 Q,RAD140,RAD-140 |
||
RAD-140-Q (RAD-140) is a selective androgen receptor modulator that inhibits the Growth of Androgen/Estrogen Receptor-Positive Breast Cancer Models with a Distinct Mechanism of Action. RAD-140-Q is neuroprotective in cultured neurons and kainate-lesioned | |||
T0139 |
Toremifene
GTx 006,Z-Toremifene,托瑞米芬 |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor | Endocrinology/Hormones |
Toremifene (GTx 006) 是第二代的选择性雌激素受体调节剂(IC50:1 μM)。它也可以有效抑制传染性 EBOV Zaire (IC50:0.07 μM) 和 Marburg (MARV) (IC50:2.6 μM)。 | |||
T71010 |
Norendoxifen
|
||
Norendoxifen, also known as 4-hydroxy-N, N-didesmethyltamoxifen, is a nonsteroidal aromatase inhibitor of the triphenylethylene group that was never marketed. It is an active metabolite of the selective estrogen receptor modulator tamoxifen. | |||
T39259 |
Arzoxifene
LY353381,Arzoxifene,SERMIII |
||
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. | |||
T79382 |
ER degrader 6
|
Estrogen Receptor/ERR | Endocrinology/Hormones |
ER degrader 6 (compound 35s) 是高效的雌激素受体 (ER)α降解剂,作用机制为通过抑制微管蛋白聚合破坏微管网络。该化合物能抑制肿瘤生长,并展现出较低的毒性特性。 | |||
T60674 | DK1 | ||
DK1 是有效的雌激素相关受体调节剂。DK1 影响 ERRα 受体的活性,具有降低血糖的能力。DK1 显示出研究糖尿病的潜力。 | |||
T71578 |
Endoxifen mesylate
|
||
Endoxifen, also known as N-desmethyl-4-hydroxytamoxifen, is a chemical that is under development for estrogen receptor-positive breast cancer. It is also being evaluated as an antipsychotic for treatment of mania and other psychotic disorders. Endoxifen is a nonsteroidal selective estrogen receptor modulator (SERM) of the triphenylethylene group. It is an active metabolite of tamoxifen and has been found to be effective in patients that have failed previous hormonal therapies (tamoxifen, aromat... | |||
T62119 |
Lasofoxifene
|
||
Lasofoxifene (CP-336156) 是一种选择性的、口服具有活力的雌激素受体调节剂 (SERM)。Lasofoxifene 对原生肿瘤的生长和转移具有抑制作用,也能够抗骨质疏松。Lasofoxifene 能够用于研究乳腺癌和绝经后骨质疏松症。 | |||
T20419 |
Raloxifene
Pharoxifene,雷洛昔芬,Raloxifenum,Keoxifene,LY-139481 |
Estrogen Receptor/ERR; Others | Endocrinology/Hormones; Others |
Raloxifene (LY-139481) 是一种苯并噻吩类化合物,是一种选择性雌激素受体 (estrogen receptor) 调节剂 (SERM),对骨、血脂有雌激素激动作用,对乳腺和子宫有雌激素拮抗作用。它用于乳腺癌和骨质疏松症研究。 | |||
TMIH-0414 |
Ospemifene-d4
|
||
Ospemifene-d4 是 Ospemifene 的氘代化合物。Ospemifene 的 CAS 号为 128607-22-7。Ospemifene 是非雌激素的选择性雌激素受体调节剂,能够作用于雌激素受体α (Kis:380 nM)和 Erβ (Kis:410 nM)。它可用于研究阴道萎缩乳腺癌。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TQ0274 |
27-Hydroxycholesterol
27-羟基胆固醇,5,25R-胆甾烯-3BETA,26-二醇,25(R)-27-hydroxy Cholesterol |
Estrogen/progestogen Receptor; Liver X Receptor | Endocrinology/Hormones; Metabolism |
27-Hydroxycholesterol (25(R)-27-hydroxy Cholesterol) 是一种有效的、选择性的雌激素受体调节剂和肝X 受体激动剂。 | |||
T1549 |
Raloxifene hydrochloride
LY156758 hydrochloride,盐酸雷洛昔芬,Raloxifene HCl,LY139481 hydrochloride,Keoxifene hydrochloride,LY156758 (Keoxifene) HCl |
Estrogen Receptor/ERR; Others; MAO; Estrogen/progestogen Receptor; Autophagy | Autophagy; Endocrinology/Hormones; Metabolism; Neuroscience; Others |
Raloxifene hydrochloride (LY156758 hydrochloride) 是一种选择性且可口服的雌激素受体调节剂,用于预防绝经后妇女的骨质疏松症。它对骨骼和胆固醇代谢具有雌激素激动作用,但对乳腺和子宫组织具有完全的雌激素拮抗作用。 | |||
T15248 |
Estetrol
Donesta |
Estrogen Receptor/ERR; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Estetrol(Donesta) 是可口服且具有选择性核雌激素受体 (estrogen receptor) 调节剂,是一种在怀孕期间由人类胎儿肝脏合成的天然雌激素。Estetrol 对子宫内膜或中枢神经系统有作用,但对乳房有拮抗作用。Estetrol 在低浓度时可能有助于降低血栓形成。Estetrol 可用于缓解更年期症状。 | |||
T3923 |
Calycosin
Cyclosin,3'-Hydroxyformononetin,异黄酮,毛异黄酮 |
Apoptosis; Tyrosinase | Apoptosis; Proteases/Proteasome |
Calycosin (Cyclosin) 是一抗氧化和抗炎症活性天然产物。 | |||
TMA0424 |
Martynoside
|
ROS | Immunology/Inflammation |
Martynoside is a natural selective estrogen receptor modulator, which has antioxidative, anti-muscle fatigue, anticancer and antimetastatic activities. Martynoside has the potential of antagonizing sports anaemia, the mechanism of this effect might be rel |