Estrogen/progestogen Receptor
The estrogen/progestogen receptors are activated by the hormone estrogen/progesterone and regulate the gene transcription.
Products Related to Estrogen/progestogen Receptor(156)
- GC10245Bazedoxifene HClCAS: 198480-56-7Purity: >98%
Bazedoxifene HCl (TSE-424 hydrochloride) is an oral active, BBB-penetrant nonsteroidal selective estrogen receptor modulator (SERM), with IC50s of 23 nM and 99 nM for ERα and ERβ, respectively. Bazedoxifene HCl can be used for the research of osteoporosis. Bazedoxifene HCl acts as an inhibitor of IL-6/GP130 protein-protein interactions. Bazedoxifene HCl can be used for the research of pancreatic cancer.
- GC11677Ulipristal acetateCAS: 126784-99-4Purity: >99.50%
Novel selective progesterone receptor modulator (SPRM)
- GC11822Erteberel (LY500307)CAS: 533884-09-2Purity: >98.00%
Erteberel (LY500307) (LY500307) is a potent and selective estrogen receptor beta (ERβ) agonist with Ki and EC50 of 1.54 nM and 3.61 nM, respectively.
- GC12148Ethinyl EstradiolCAS: 57-63-6Purity: >99.50%
Ethinyl Estradiol (17α-Ethynylestradiol;Ethynylestradiol) is an orally bio-active estrogen used in almost all modern formulations of combined oral contraceptive pills.
- GC12974Medroxyprogesterone acetateCAS: 71-58-9Purity: >99.50%
Medroxyprogesterone acetate (MPA) is a synthetic progestin.
- GC13350Raloxifene HClCAS: 82640-04-8Purity: >99.50%
Raloxifene HCl (Keoxifene hydrochloride) is a second generationselective and orally active estrogen receptor modulator.
- GC13835Toremifene CitrateCAS: 89778-27-8Purity: >99.50%
Oral selective estrogen receptor modulator (SERM)
- GC14704LevonorgestrelCAS: 797-63-7Purity: >98.00%
Levonorgestrel is an effective oral progesterone inhibitor.
- GC18000Fulvestrant (ICI 182,780)CAS: 129453-61-8Purity: >98.00%
Fulvestrant is a selective estrogen receptor (ER) antagonist. It binds, blocks and degrades estrogen receptor, then inhibits estrogen receptor(ER)-mediated transcriptional activity with an IC 50 of 9.4 nM .
- GC10002CoumestrolCAS: 479-13-0Purity: >98.00%
Coumestrol is a natural, orally active coumestan phytoestrogen. Coumestrol competitively binds estrogen receptor ERα (IC 50 =11nM) and ERβ (IC 50 =2nM) to regulate estrogen-responsive genes.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC10245 | Bazedoxifene HCl | 198480-56-7 | >98% | |
Bazedoxifene HCl (TSE-424 hydrochloride) is an oral active, BBB-penetrant nonsteroidal selective estrogen receptor modulator (SERM), with IC50s of 23 nM and 99 nM for ERα and ERβ, respectively. Bazedoxifene HCl can be used for the research of osteoporosis. Bazedoxifene HCl acts as an inhibitor of IL-6/GP130 protein-protein interactions. Bazedoxifene HCl can be used for the research of pancreatic cancer. | ||||
| GC11282 | β-Estradiol | 50-28-2 | >99.50% | |
Sex hormone | ||||
| GC11436 | Ethisterone | 434-03-7 | >98% | |
Progestogen hormone | ||||
| GC11677 | Ulipristal acetate | 126784-99-4 | >99.50% | |
Novel selective progesterone receptor modulator (SPRM) | ||||
| GC11688 | Megestrol Acetate | 595-33-5 | >99.50% | |
Anti-estrogen agent | ||||
| GC11781 | Medroxyprogesterone | 520-85-4 | >99.00% | |
potent progesterone receptor agonist | ||||
| GC11822 | Erteberel (LY500307) | 533884-09-2 | >98.00% | |
Erteberel (LY500307) (LY500307) is a potent and selective estrogen receptor beta (ERβ) agonist with Ki and EC50 of 1.54 nM and 3.61 nM, respectively. | ||||
| GC12000 | Ethynodiol diacetate | 297-76-7 | >99.00% | |
Progestogen receptor agonist | ||||
| GC12148 | Ethinyl Estradiol | 57-63-6 | >99.50% | |
Ethinyl Estradiol (17α-Ethynylestradiol;Ethynylestradiol) is an orally bio-active estrogen used in almost all modern formulations of combined oral contraceptive pills. | ||||
| GC12182 | Estriol | 50-27-1 | >99.00% | |
Estriol is an agonist of estrogen receptors (ERα and ERβ) and G protein-coupled receptor 30 (GPR30) antagonist. | ||||
| GC12379 | Drospirenone | 67392-87-4 | >98.00% | |
Synthetic progestin | ||||
| GC12408 | Progesterone | 57-83-0 | >98.00% | |
Progesterone | ||||
| GC12974 | Medroxyprogesterone acetate | 71-58-9 | >99.50% | |
Medroxyprogesterone acetate (MPA) is a synthetic progestin. | ||||
| GC13297 | Altrenogest | 850-52-2 | >99.50% | |
Progestogen receptor agonist | ||||
| GC13350 | Raloxifene HCl | 82640-04-8 | >99.50% | |
Raloxifene HCl (Keoxifene hydrochloride) is a second generationselective and orally active estrogen receptor modulator. | ||||
| GC13835 | Toremifene Citrate | 89778-27-8 | >99.50% | |
Oral selective estrogen receptor modulator (SERM) | ||||
| GC14385 | Estrone | 53-16-7 | >98.00% | |
Estrone is one of the three major endogenous estrogens, the others being estradiol and estriol. | ||||
| GC14704 | Levonorgestrel | 797-63-7 | >98.00% | |
Levonorgestrel is an effective oral progesterone inhibitor. | ||||
| GC15324 | Hexestrol | 84-16-2 | >98.00% | |
Estrogen receptor agonist | ||||
| GC15366 | Clomiphene citrate | 50-41-9 | >98.00% | |
Selective estrogen receptor modulator | ||||
| GC15578 | Dienogest | 65928-58-7 | >98.00% | |
Orally active synthetic progesterone | ||||
| GC16292 | Equol | 94105-90-5 | >98.00% | |
non-steroidal estrogen | ||||
| GC18000 | Fulvestrant (ICI 182,780) | 129453-61-8 | >98.00% | |
Fulvestrant is a selective estrogen receptor (ER) antagonist. It binds, blocks and degrades estrogen receptor, then inhibits estrogen receptor(ER)-mediated transcriptional activity with an IC 50 of 9.4 nM . | ||||
| GC10002 | Coumestrol | 479-13-0 | >98.00% | |
Coumestrol is a natural, orally active coumestan phytoestrogen. Coumestrol competitively binds estrogen receptor ERα (IC 50 =11nM) and ERβ (IC 50 =2nM) to regulate estrogen-responsive genes. | ||||
