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41270-96-6

中文名稱(chēng) 4-IODO-6-PHENYLPYRIMIDINE
英文名稱(chēng) 4-IODO-6-PHENYLPYRIMIDINE
CAS 41270-96-6
分子式 C10H7IN2
分子量 282.08
MOL 文件 41270-96-6.mol
更新日期 2024/12/15 19:35:20
41270-96-6 結(jié)構(gòu)式 41270-96-6 結(jié)構(gòu)式

基本信息

中文別名
化合物4-IPP
4-碘-6-苯基嘧啶
英文別名
4-IPP
MIF Antagonist III, 4-IPP
4-IODO-6-PHENYLPYRIMIDINE
Pyrimidine, 4-iodo-6-phenyl-
4-IPP (4-Iodo-6-phenylpyrimidine)
MIF Antagonist III, 4-IPP - CAS 41270-96-6 - Calbiochem

物理化學(xué)性質(zhì)

沸點(diǎn)380.2±30.0 °C(Predicted)
密度1.728±0.06 g/cm3(Predicted)
儲(chǔ)存條件-20°C
溶解度在DMSO中的溶解度為10mg/mL(透明溶液,加熱)
酸度系數(shù)(pKa)-0.54±0.17(Predicted)
形態(tài)粉末
顏色白色至米色
InChIKeyZTCJXHNJVLUUMR-UHFFFAOYSA-N

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS07
警示詞危險(xiǎn)
危險(xiǎn)性描述H302-H315-H318-H335
防范說(shuō)明P261-P280-P305+P351+P338
危險(xiǎn)品標(biāo)志Xn
危險(xiǎn)類(lèi)別碼22-37/38-41
安全說(shuō)明26-39
WGK Germany3
4-IODO-6-PHENYLPYRIMIDINE價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱(chēng)CAS號(hào)包裝價(jià)格
2025/02/08HY-1100634-IPP41270-96-61 mg400元
2025/02/08HY-1100634-IODO-6-PHENYLPYRIMIDINE
4-IPP
41270-96-65mg1150元
2025/02/08HY-1100634-IODO-6-PHENYLPYRIMIDINE
4-IPP
41270-96-610mM * 1mLin DMSO1241元

常見(jiàn)問(wèn)題列表

生物活性
4-IPP (4-Iodo-6-phenylpyrimidine)是 macrophage migration inhibitory factor (MIF) 的不可逆抑制劑,是MIF的特異性自殺底物。4-IPP可以抑制NF-κB配體(RANKL)誘導(dǎo)的破骨細(xì)胞的受體激活劑,并在體外增強(qiáng)成骨細(xì)胞介導(dǎo)的礦化和骨結(jié)節(jié)的形成。
靶點(diǎn)
TargetValue
MIF
()
體外研究

4-IPP is a specific suicide substrate for MIF that binds covalently and irreversibly to MIF to inhibit its biologic activity.
4-IPP inhibits RANKL-induced p65 phosphorylation and nuclear translocation by preventing the interaction of MIF with thioredoxin-interacting protein-p65 complexes.
4-IPP can inhibit receptor activator of NF-κB ligand (RANKL)-induced osteoclastogenesis and potentiate osteoblast-mediated mineralization and bone nodule formation.
4-IPP (0.5-200μM;24-72 hours) inhibits osteoclastogenesis in a dose-dependent manner.
4-IPP(5-20μM; 5 days) inhibits RANKL-induced osteoclast differentiation and bone resorption .

Cell Cytotoxicity Assay

Cell Line: BMMs
Concentration: 0.5 μM, 1 μM, 2.5 μM, 5 μM, 10 μM, 25 μM, 50 μM, 100 μM, 200 μM
Incubation Time: 24 hours, 72 hours
Result: Inhibited osteoclastogenesis in a dose-dependent manner.

Western Blot Analysis

Cell Line: BMMs
Concentration: 5 μM,10 μM, 20 μM
Incubation Time: 1 day, 3 days, 5 days
Result: Inhibited RANKL-induced osteoclast differentiation and bone resorption.
體內(nèi)研究

4-IPP (1 mg/kg, 5 mg/kg; every 2 days; for 8 weeks) ameliorates the bone loss associated with estrogen deficiency by reducing osteoclastic activities and enhancing osteoblastic bone formation.

Animal Model: 8-weeks-old C57BL/6J male mice
Dosage: 1 mg/kg, 5 mg/kg
Administration: Intraperitoneal injection; every 2 days; for 8 weeks
Result: Alleviated OVX-induced osteoporosis.
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