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20380-11-4

中文名稱 5,25R-膽甾烯-3BETA,26-二醇
英文名稱 27-Hydroxycholesterol
CAS 20380-11-4
分子式 C27H46O2
分子量 402.65
MOL 文件 20380-11-4.mol
更新日期 2024/12/30 09:00:55
20380-11-4 結(jié)構(gòu)式 20380-11-4 結(jié)構(gòu)式

基本信息

中文別名
27-羥基膽固醇
5,25R-膽甾烯-3BETA,26-二醇
英文別名
27-OHC
25(R)-27-hydroxy Cholesterol
cholest-(25R)-5-ene-3,27-diol
5,25R-Cholesten-3beta,26-diol
(25R)-Cholest-5-en-3β,26β-diol
(25R)-Cholest-5-ene-3β,26-diol
(3β,25R)-Cholest-5-ene-3,26-diol
(25R)-cholest-5-ene-3beta,26-diol
Cholest-5-ene-3,26-diol, (3β,25R)-
26-Hydroxycholesterol (not deuterated)
所屬類(lèi)別
醫(yī)藥中間體:原料藥中間體

物理化學(xué)性質(zhì)

熔點(diǎn)172-174 °C(Solv: hexane (110-54-3); ethyl acetate (141-78-6))
沸點(diǎn)517.1±23.0 °C(Predicted)
密度1.03
儲(chǔ)存條件-20°
溶解度可溶于 DMSO(高達(dá) 10 mg/ml)或乙醇(高達(dá) 10 mg/ml)。
酸度系數(shù)(pKa)15.03±0.70(Predicted)
形態(tài)白色固體。
顏色白色
穩(wěn)定性可在-20°下的DMSO或乙醇溶液保存長(zhǎng)達(dá)2個(gè)月。

常見(jiàn)問(wèn)題列表

簡(jiǎn)介

27-羥基膽固醇是一種內(nèi)源性的氧化膽固醇,有著多重生物學(xué)功能,包括選擇性雌激素受體調(diào)節(jié)物(SERM)活性,肝X受體(LXR)激動(dòng)劑等,由細(xì)胞色素P450氧化酶CYP27A1催化膽固醇生成。

生物活性
27-Hydroxycholesterol是選擇性的雌激素受體 (estrogen receptor) 調(diào)節(jié)劑和肝X 受體 (liver X receptor) 激動(dòng)劑。
靶點(diǎn)

Human Endogenous Metabolite

體外研究

27-Hydroxycholesterol is an endogenous selective estrogen receptor modulator that displays significant partial agonist activity in a variety of cellular models of estrogen receptor action. It positively regulates both gene transcription and cell proliferation in cellular models of breast cancer. 27-Hydroxycholesterol, through estrogen receptor activation, triggers deleterious effect in prostate cancer cell lines. 27-Hydroxycholesterol significantly increases cell proliferation of LNCaP and PC3 cells and this effect can be attenuated by estrogen receptor inhibitors. 27-Hydroxycholesterol is an oxysterol produced from cholesterol by the monooxygenase CYP27A1, which regulates intracellular cholesterol homeostasis. 27-Hydroxycholesterol also acts as an endogenous selective estrogen receptor modulator capable of increasing breast cancer growth and metastasis. 27-Hydroxycholesterol levels can be modulated by statins or direct inhibition of CYP27A1, thereby attenuating its pro-tumorigenic activities. 27-hydroxylation of cholesterol is an important pathway for LXR activation in response to cholesterol overload.

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