Estrogen/progestogen Receptor
Estrogen/progestogen Receptor(雌激素/孕激素受体)
The estrogen/progestogen receptors are activated by the hormone estrogen/progesterone and regulate the gene transcription.
Estrogen/progestogen Receptor 相关产品(157)
- GC489102-HydroxyanthraquinoneCAS: 605-32-3纯度: >98.00%
An anthraquinone with antibacterial and estrogenic activities
- GC48979Estradiol 17-(β-D-Glucuronide) (sodium salt hydrate)纯度: >95.00%
A substrate of multidrug resistance protein 2
- GC4916116α-hydroxy DehydroepiandrosteroneCAS: 1232-73-1纯度: >95.00%
A metabolite of dehydroepiandrosterone
- GC49189(E/Z)-4-hydroxy Tamoxifen-d5CAS: 2470232-57-4纯度: >99.00%
An internal standard for the quantification of (E/Z)-4-hydroxy tamoxifen
- GC493265β-DihydroprogesteroneCAS: 128-23-4纯度: >95.00%
A progesterone receptor agonist and metabolite of progesterone
- GC496092-bromo 17β-EstradiolCAS: 15833-07-5纯度: >98.00%
A synthetic steroid and inhibitor of estrogen 2-hydroxylase
- GC49757Bazedoxifene N-oxideCAS: 1174289-22-5纯度: >90.00%
An oxidative degradation product of bazedoxifene
- GC49878Fulvestrant 9-sulfoneCAS: 98008-06-1纯度: >98.00%
An estrogen receptor antagonist and a derivative of fulvestrant
- GC523654-tert-Octylphenol monoethoxylateCAS: 2315-67-5纯度: >98.00%
An alkylphenolethoxylate and a degradation product of non-ionic surfactants
- GC61267SAR439859CAS: 2114339-57-8纯度: >99.50%
Amcenestrant (SAR439859, compound 43d) is an orally available and nonsteroidal selective estrogen receptor degrader (SERD) with potential antineoplastic activity. SAR439859 is a potent estrogen receptor (ER) antagonist with EC50 of 0.2 nM for ERα degradation.
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC48910 | 2-Hydroxyanthraquinone | 605-32-3 | >98.00% | |
An anthraquinone with antibacterial and estrogenic activities | ||||
| GC48979 | Estradiol 17-(β-D-Glucuronide) (sodium salt hydrate) | - | >95.00% | |
A substrate of multidrug resistance protein 2 | ||||
| GC49025 | Desogestrel-13C2-d2 | - | >99.00% | |
An internal standard for the quantification of desogestrel | ||||
| GC49068 | 16-Epiestriol | 547-81-9 | >90.00% | |
A metabolite of estrone | ||||
| GC49161 | 16α-hydroxy Dehydroepiandrosterone | 1232-73-1 | >95.00% | |
A metabolite of dehydroepiandrosterone | ||||
| GC49172 | 2-hydroxy Estrone | 362-06-1 | >95.00% | |
An active metabolite of estrone | ||||
| GC49189 | (E/Z)-4-hydroxy Tamoxifen-d5 | 2470232-57-4 | >99.00% | |
An internal standard for the quantification of (E/Z)-4-hydroxy tamoxifen | ||||
| GC49254 | Estrone-3-Glucuronide (sodium salt hydrate) | - | >98.00% | |
A metabolite of 17β-estradiol | ||||
| GC49326 | 5β-Dihydroprogesterone | 128-23-4 | >95.00% | |
A progesterone receptor agonist and metabolite of progesterone | ||||
| GC49391 | 7α-Thiospironolactone | 38753-76-3 | >90.00% | |
An active metabolite of spironolactone | ||||
| GC49520 | (S)-Equol | 531-95-3 | >98.00% | |
(S)-Equol是一种由部分人群肠道微生物产生的异黄烷类化合物，主要来源于大豆中的大豆素在特定肠道菌群的作用下生成。(S)-Equol具有显著的雌激素样活性和抗氧化特性，能够与雌激素受体结合，对 ERβ的亲和力为Ki=0.73±0.2nM，对ERα的亲和力为Ki=6.41±1nM。 | ||||
| GC49562 | 4-methoxy Estrone | 58562-33-7 | >95.00% | |
An active metabolite of estrone | ||||
| GC49563 | Fenhexamid | 126833-17-8 | >98.00% | |
A fungicide | ||||
| GC49609 | 2-bromo 17β-Estradiol | 15833-07-5 | >98.00% | |
A synthetic steroid and inhibitor of estrogen 2-hydroxylase | ||||
| GC49757 | Bazedoxifene N-oxide | 1174289-22-5 | >90.00% | |
An oxidative degradation product of bazedoxifene | ||||
| GC49848 | 16-Ketoestradiol | 566-75-6 | >95.00% | |
An active metabolite of estrone | ||||
| GC49878 | Fulvestrant 9-sulfone | 98008-06-1 | >98.00% | |
An estrogen receptor antagonist and a derivative of fulvestrant | ||||
| GC50091 | AC 186 | 1421854-16-1 | - | |
A non-steroidal ERβ agonist | ||||
| GC52180 | WAY-169916 | 669764-18-5 | >98.00% | |
A pathway-selective estrogen receptor ligand | ||||
| GC52189 | Nomegestrol | 58691-88-6 | >95.00% | |
A derivative of 19-norprogesterone | ||||
| GC52365 | 4-tert-Octylphenol monoethoxylate | 2315-67-5 | >98.00% | |
An alkylphenolethoxylate and a degradation product of non-ionic surfactants | ||||
| GC52420 | Drospirenone-13C3 | - | >95.00% | |
An internal standard for the quantification of drospirenone | ||||
| GC61267 | SAR439859 | 2114339-57-8 | >99.50% | |
Amcenestrant (SAR439859, compound 43d) is an orally available and nonsteroidal selective estrogen receptor degrader (SERD) with potential antineoplastic activity. SAR439859 is a potent estrogen receptor (ER) antagonist with EC50 of 0.2 nM for ERα degradation. | ||||
| GC61971 | Liarozole | 115575-11-6 | >98.50% | |
A CYP26A1 inhibitor | ||||