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131875-08-6

中文名稱 來沙骨化醇
英文名稱 Lexacalcitol
CAS 131875-08-6
分子式 C29H48O4
分子量 460.69
MOL 文件 131875-08-6.mol
更新日期 2026/02/24 11:11:13
131875-08-6 結(jié)構(gòu)式 131875-08-6 結(jié)構(gòu)式

基本信息

中文別名
來沙骨化醇
英文別名
KH 106
KH 1060
Lexacalcitol
Lenosacalcitol
Lexacalcideferol
(1S*,3R*,5Z),7aalpha))-(5Z,7E,20R)-20-((4-Ethyl-4-hydroxyhexyl)oxy)-9,10-secopregna-5,7,10(19)-triene-1alpha,3beta-diol
1,3-Cyclohexanediol, 5-[(2E)-2-[(1S,3aS,7aS)-1-[(1R)-1-[(4-ethyl-4-hydroxyhexyl)oxy]ethyl]octahydro-7a-methyl-4H-inden-4-ylidene]ethylidene]-4-methylene-, (1R,3S,5Z)-
(1R,3S,5Z)-5-[(2E)-2-[(1S,3aS,7aS)-1-[(1R)-1-(4-ethyl-4-hydroxyhexoxy)ethyl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexane-1,3-diol
所屬類別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

沸點(diǎn)600.3±55.0 °C(Predicted)
密度1.07±0.1 g/cm3(Predicted)
儲(chǔ)存條件-20°C, protect from light, stored under nitrogen,unstable in solution, ready to use.
溶解度DMSO
酸度系數(shù)(pKa)14.43±0.40(Predicted)
形態(tài)粉末
顏色White to off-white
來沙骨化醇價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2025/12/22HY-32340來沙骨化醇
Lexacalcitol
131875-08-61mg2560元
2024/08/19HY-32340來沙骨化醇
Lexacalcitol
131875-08-65mg6400元
2023/10/26HY-32340來沙骨化醇
Lexacalcitol
131875-08-610mg12500元

常見問題列表

生物活性
Lexacalcitol (KH1060) 是一種維生素 D 類似物,是細(xì)胞生長和免疫反應(yīng)的有效調(diào)節(jié)劑。Lexacalcitol 可用于移植排斥反應(yīng)、銀屑病、癌癥和自身免疫性疾病的研究。
體外研究

Lexacalcitol inhibits cell proliferation by 50% at 10 -12 M (14,000 times more active than la,25(OH) 2 D 3 ) in human histiocytic lymphoma cell line U 937.
Lexacalcitol inhibits interleukin-1-induced mouse thymocyte proliferation by 50% at 3×10 -16 M , allogeneic stimulation of mouse spleen lymphocytes at 5×10 -15 M.

體內(nèi)研究

Lexacalcitol (0.5 mg/kg/2 days; i.p.) in combination with cyclosporin A (CyA) can prevent autoimmune destruction of syngeneic islet grafts in spontaneously diabetic NOD recipients.

Animal Model: Male and female spontaneously diabetic NOD mice
Dosage: 0.5 mg/kg/2 days
Administration: Intraperitoneal injection
Result: Single treatment with KH1060 or CyA did not result in statistically significant suppression of early graft failure, while the combination of KH1060 and CyA can prevent early graft failure and delay graft rejection of xenogeneic islets in spontaneously diabetic NOD mice.
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