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99009-20-8

中文名稱 NSC 366140 無結(jié)構(gòu)圖
英文名稱 NSC 366140
CAS 99009-20-8
分子式 C19H21N5O3
分子量 367.4
MOL 文件 99009-20-8.mol
更新日期 2023/03/20 15:41:25
99009-20-8 結(jié)構(gòu)式 99009-20-8 結(jié)構(gòu)式

基本信息

中文別名
NSC 366140 無結(jié)構(gòu)圖
英文別名
Pd 115934
NSC 366140
Pd 115,934
Brn 4211902
Pyrazoloacridine
N,N-Dimethyl-9-methoxy-5-nitropyrazolo(3,4,5-kl)acridine-2(6H)-propanamine
Pyrazolo(3,4,5-kl)acridine-2(6H)-propanamine, N,N-dimethyl-9-methoxy-5-nitro-
9-Methoxy-N,N-dimethyl-5-nitropyrazolo[3,4,5-kl]acridine-2(6H)-propane-1-amine
(3-(9-METHOXY-5-NITRO-6H-PYRAZOLO(3,4,5-KL)ACRIDIN-2-YL)-PROPYL)-DIMETHYL-AMINE
2,6-Dihydro-2-(3-dimethylaminopropyl)-9-methoxy-5-nitropyrazolo[3,4,5-kl]acridine

物理化學(xué)性質(zhì)

沸點(diǎn)584.3±50.0 °C(Predicted)
密度1.38±0.1 g/cm3(Predicted)
儲(chǔ)存條件-20°C儲(chǔ)存
酸度系數(shù)(pKa)9.35±0.28(Predicted)
形態(tài)Solid
顏色Light brown to orange
NSC 366140 無結(jié)構(gòu)圖價(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
2024/11/08HY-108969NSC 366140 無結(jié)構(gòu)圖
Pyrazoloacridine
99009-20-85mg900元
2024/11/08HY-108969NSC 366140 無結(jié)構(gòu)圖
Pyrazoloacridine
99009-20-810 mg1450元
2024/11/08HY-108969NSC 366140 無結(jié)構(gòu)圖
Pyrazoloacridine
99009-20-825 mg2700元

常見問題列表

生物活性
Pyrazoloacridine (NSC 366140) 具有抗癌活性,抑制拓?fù)洚悩?gòu)酶 1 和 2 的活性 (topoisomerases 1 and 2)。Pyrazoloacridine (NSC 366140) 對(duì) K562 髓系白血病細(xì)胞中的 IC50 值為 1.25 μM (24 h)。
體外研究

Pyrazoloacridine (NSC 366140, PD 115934) exhibits IC 50 values of 10.7 μM and 4.5 μM for oxic and hypoxic HCT-8 cells.
Pyrazoloacridine (NSC 366140, 2-4 μM) abolishes the catalytic activity of both topo I and topo II in vitro.
Pyrazoloacridine (NSC 366140) displays activity against cisplatin- and paclitaxel-resistant ovarian cancer.
Pyrazoloacridine (NSC 366140) has been shown to cause delayed DNA fragmentation in MCF-7 breast cancer cells.
Pyrazoloacridine (NSC 366140) induces apoptosis in P53-deficient Hep 3B human hepatoma cells.

Cell Cytotoxicity Assay

Cell Line: K562 Myeloid Leukemia Cells.
Concentration: 0-500 μM.
Incubation Time: 1 h or 24 h.
Result: When K562 cells were incubated with PA for 1 h and then plated in soft agar, an IC 50 of -50 μM was observed. In contrast, when cells were incubated for 24 h with PA, the IC 50 was 1.25 μM.
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