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4-庚氧基苯酚

4-庚氧基苯酚结构式
4-庚氧基苯酚结构式
品牌特惠专场
常用名 4-庚氧基苯酚 英文名 4-(Heptyloxy)phenol
CAS号 13037-86-0 分子量 208.297
密度 1.0±0.1 g/cm3 沸点 325.3±15.0 °C at 760 mmHg
分子式 C13H20O2 熔点 60-63 °C(lit.)
MSDS 中文版 美版 闪点 144.8±5.3 °C
符号 GHS07
GHS07
信号词 Warning

Impact of induced fit on ligand binding to the androgen receptor: a multidimensional QSAR study to predict endocrine-disrupting effects of environmental chemicals.

J. Med. Chem. 48 , 5666-74, (2005)

We investigated the influence of induced fit of the androgen receptor binding pocket on free energies of ligand binding. On the basis of a novel alignment procedure using flexible docking, molecular dynamics simulations, and linear-interaction energy analysis...

The expression of Steroidogenic Factor-1 and its role in bovine steroidogenic ovarian cells during the estrus cycle and first trimester of pregnancy.

Anim. Reprod. Sci. , doi:10.1016/j.anireprosci.2013.01.008, (2013)

The orphan receptor Steroidogenic Factor-1 (SF-1, NR5A1), a member of the nuclear receptor superfamily, is present in fetal and adult steroidogenic tissues and also participates in the regulation of ovarian function. In this study, the expression levels of SF...

The orphan nuclear receptor SF-1 is involved in the effect of PCBs, DDT, and DDE on the secretion of steroid hormones and oxytocin from bovine luteal cells during the estrous cycle in vitro.

Theriogenology 81(7) , 877-86, (2014)

The orphan receptor steroidogenic factor-1 (SF-1) is involved in the regulation of ovarian steroidogenesis in cows. It is hypothesized that estrogen-like chlorinated compounds might affect SF-1, and thus impair the function of the ovary. Bovine luteal cells f...

Small molecule agonists of the orphan nuclear receptors steroidogenic factor-1 (SF-1, NR5A1) and liver receptor homologue-1 (LRH-1, NR5A2).

J. Med. Chem. 54 , 2266-81, (2011)

The crystal structure of LRH-1 ligand binding domain bound to our previously reported agonist 3-(E-oct-4-en-4-yl)-1-phenylamino-2-phenyl-cis-bicyclo[3.3.0]oct-2-ene 5 is described. Two new classes of agonists in which the bridgehead anilino group from our fir...