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1568-80-5

中文名稱 3,3,3',3'-四甲基-1,1'-螺BI(茚滿)-6,6'-二醇
英文名稱 SPIROBIINDANE
CAS 1568-80-5
分子式 C21H24O2
分子量 308.42
MOL 文件 1568-80-5.mol
更新日期 2024/10/25 21:14:46
1568-80-5 結(jié)構式 1568-80-5 結(jié)構式

基本信息

中文別名
螺雙茚滿
螺二茚滿
3,3,3',3'-四甲基螺環(huán)二酚
3,3,3',3'-四甲基-1,1'-螺BI(茚滿)-6,6'-二醇
3,3,3',3'-四甲基-2,2',3,3'-四氫-1,1'-螺二[茚滿]-6,6'-二醇
英文別名
3,3,3'
SPIROBIINDANE
-tetrahydro-1,1'
-tetramethyl-2,2'
-spirobi[indene]-6,6'
HIV-1 integrase inhibitor 8
3,3,3',3'-Tetramethyl-1,1'-spirobi[indan]-6,6'-diol
tetrahydrotetramethyl-1,1'-spirobi-1H-indene-6,6'-diol
6,6'-Dihydroxy-3,3,3',3'-tetramethyl-1,1'-spirobiindan
6,6'-Dihydroxy-3,3,3',3'-tetramethyl-1,1'-spirobiindane
所屬類別
生物化工:激動劑抑制劑

物理化學性質(zhì)

熔點213-214 °C
沸點478.5±45.0 °C(Predicted)
密度1.21±0.1 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度DMSO : 125 mg/mL (405.30 mM; Need ultrasonic)
酸度系數(shù)(pKa)9.98±0.60(Predicted)
形態(tài)Solid
顏色White to off-white
CAS 數(shù)據(jù)庫1568-80-5
EPA化學物質(zhì)信息
危險性符號(GHS)GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS07,GHS09,GHS08
警示詞危險
毒性rat,LD50,oral,> 5gm/kg (5000mg/kg),BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY),International Journal of Toxicology. Vol. 19, Pg. 366, 2000.
3,3,3',3'-四甲基-1,1'-螺BI(茚滿)-6,6'-二醇價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/08/19HY-1074853,3,3',3'-四甲基-1,1'-螺BI(茚滿)-6,6'-二醇
HIV-1 integrase inhibitor 8
1568-80-550mg300元
2024/08/19HY-1074853,3,3',3'-四甲基-1,1'-螺BI(茚滿)-6,6'-二醇
HIV-1 integrase inhibitor 8
1568-80-5100mg500元

常見問題列表

生物活性
HIV-1 integrase inhibitor 8 是 HIV-1 整合酶 (HIV-1 integrase) 抑制劑,化合物 8。
體外研究

HIV-1 integrase inhibitor 8 is against 3′-processing (TC) and strand-transfer (ST) activities in the presence of Mn 2+ as the cationic cofactor by gel assay with IC 50 values of 275 μM and 200 μM, respectively. It inhibits the strand-transfer (ST) activity with an IC 50 value of 200 μM.The DNA relaxation activity of MCV topoisomerase is monitored by gel electrophoresis, while DNA cleavage and religation activities were monitored using a microtiter assay. HIV-1 integrase inhibitor 8 inhibits MCV topoisomerase and DNA religation with IC 50 values of 500 μM and 200 μM, respectively. This result demonstrates that compound 8 is inactive against topoisomerase in both assays. HIV-1 integrase inhibitor 8 induces cell cytotoxicity and yields a LD 50 (dose at which the signal is reduced 50% due to cell death) of 20 μM in HeLa cells.

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