Endocrinology and Hormones
Endocrinology and Hormones(内分泌和激素)
Endocrinology and Hormones
The endocrine system is an information signaling system that coordinates most bodily functions. It senses environmental changes and secretes corresponding hormones to coordinate metabolism, maintain homeostasis, and regulate growth and development.read more
Endocrinology and Hormones 相关产品(940)
- GC10245Bazedoxifene HClCAS: 198480-56-7
Bazedoxifene HCl (TSE-424 hydrochloride) 是一种具有口服活性、可渗透 BBB 的非甾体选择性雌激素受体调节剂 (SERM),对 ERα 的 IC50 分别为 23 nM 和 99 nM;和ERβ,分别。盐酸巴多昔芬可用于骨质疏松症的研究。 Bazedoxifene HCl 作为 IL-6/GP130 蛋白质-蛋白质相互作用的抑制剂。 Bazedoxifene HCl 可用于胰腺癌的研究。
- GC10257Losartan Potassium (DuP 753)CAS: 124750-99-8纯度: >99.50%
Losartan Potassium (DuP 753)是一种血管紧张素II受体拮抗剂(IC 50 =20nM)。
- GC11813ExemestaneCAS: 107868-30-4纯度: >99.50%
A third generation, irreversible steroidal aromatase inhibitor
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC10076 | Leuprolide Acetate | 74381-53-6 | - | |
A synthetic GnRH receptor agonist | ||||
| GC10245 | Bazedoxifene HCl | 198480-56-7 | - | |
Bazedoxifene HCl (TSE-424 hydrochloride) 是一种具有口服活性、可渗透 BBB 的非甾体选择性雌激素受体调节剂 (SERM),对 ERα 的 IC50 分别为 23 nM 和 99 nM;和ERβ,分别。盐酸巴多昔芬可用于骨质疏松症的研究。 Bazedoxifene HCl 作为 IL-6/GP130 蛋白质-蛋白质相互作用的抑制剂。 Bazedoxifene HCl 可用于胰腺癌的研究。 | ||||
| GC10256 | Anastrozole | 120511-73-1 | >99.50% | |
An aromatase/CYP19A1 inhibitor | ||||
| GC10257 | Losartan Potassium (DuP 753) | 124750-99-8 | >99.50% | |
Losartan Potassium (DuP 753)是一种血管紧张素II受体拮抗剂(IC 50 =20nM)。 | ||||
| GC10702 | Trimebutine | 39133-31-8 | - | |
An opioid receptor agonist | ||||
| GC10726 | Letrozole | 112809-51-5 | >99.50% / >98.00% | |
Letrozole(来曲唑; CGS 20267)是一种口服活性非甾体类选择性芳香酶抑制剂,IC 50 为11.5nM。 | ||||
| GC10760 | XL335 | 629664-81-9 | >99.50% | |
A potent and selective FXR agonist | ||||
| GC10852 | Bazedoxifene acetate | 198481-33-3 | >99.50% | |
A selective estrogen receptor modulator | ||||
| GC10893 | Dutasteride | 164656-23-9 | >99.50% | |
An inhibitor of steroid 5α-reductase | ||||
| GC10975 | GW4064 | 278779-30-9 | >99.50% | |
GW4064作为合成的FXR激动剂,用于治疗胆汁淤积性肝病、代谢综合征和酒精性肝病。 | ||||
| GC11016 | Meptazinol HCl | 59263-76-2 | >99.00% | |
μ1 阿片受体的部分激动剂 | ||||
| GC11282 | β-Estradiol | 50-28-2 | >99.50% | |
The major premenopausal estrogen | ||||
| GC11436 | Ethisterone | 434-03-7 | - | |
A synthetic progestin | ||||
| GC11544 | Toremifene | 89778-26-7 | - | |
托瑞米芬(Z-托瑞米芬)是一种用于预防骨质疏松症的第二代选择性雌激素受体调节剂(SERM)。 | ||||
| GC11677 | Ulipristal acetate | 126784-99-4 | >99.50% | |
A selective progesterone receptor modulator | ||||
| GC11688 | Megestrol Acetate | 595-33-5 | >99.50% | |
A synthetic progestogen | ||||
| GC11781 | Medroxyprogesterone | 520-85-4 | >99.00% | |
A progesterone receptor agonist | ||||
| GC11813 | Exemestane | 107868-30-4 | >99.50% | |
A third generation, irreversible steroidal aromatase inhibitor | ||||
| GC11822 | Erteberel (LY500307) | 533884-09-2 | >98.00% | |
A potent and selective agonist of ERβ | ||||
| GC11826 | JTC-801 | 244218-51-7 | >99.50% | |
A selective nociceptin receptor antagonist | ||||
| GC11829 | ADL5859 HCl | 850173-95-4 | >99.50% | |
A δ-opioid receptor agonist | ||||
| GC12000 | Ethynodiol diacetate | 297-76-7 | >99.00% | |
A synthetic progestogen | ||||
| GC12041 | SNC 162 | 178803-51-5 | - | |
SNC 162 是一种 δ-阿片受体激动剂,IC50 为 0.94 nM。 | ||||
| GC12148 | Ethinyl Estradiol | 57-63-6 | >99.50% | |
A 17β-estradiol analog | ||||
