FSHR agonist 1 structure
|
Common Name | FSHR agonist 1 | ||
---|---|---|---|---|
CAS Number | 1256776-89-2 | Molecular Weight | 467.62 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C26H33N3O3S | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of FSHR agonist 1FSHR agonist 1 is a high affinity and allosteric follicle stimulating hormone receptor (FSHR) agonist with a pEC50 of 7.72. FSHR agonist 1 formes extensive interactions with the TMD to directly activate FSHR[1]. |
Name | FSHR agonist 1 |
---|
Description | FSHR agonist 1 is a high affinity and allosteric follicle stimulating hormone receptor (FSHR) agonist with a pEC50 of 7.72. FSHR agonist 1 formes extensive interactions with the TMD to directly activate FSHR[1]. |
---|---|
Related Catalog | |
Target |
pEC50: 7.72 (FSHR)[1] |
In Vitro | FSHR agonist 1 (compound 21f) 与 FSHR TMD 口袋的结合诱导 TM6 和 TM7 向内运动,这直接导致 FSHR 激活[1]。 FSHR agonist 1 (compound 21f) 可以高效激活 FSHR、LHCGR 和 TSHR,而对 FSHR 的激活效力比 LHCGR(pEC50 为 6.26)和 TSHR(pEC50 为 6.48)高 10 倍以上[1]。 |
References |
Molecular Formula | C26H33N3O3S |
---|---|
Molecular Weight | 467.62 |