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  1. Apoptosis Anti-infection Autophagy Neuronal Signaling Membrane Transporter/Ion Channel
  2. Apoptosis Parasite Autophagy Caspase Calcium Channel
  3. Cinchonine

Cinchonine  (Synonyms: 辛可寧; (8R,9S)-Cinchonine; LA40221)

目錄號(hào): HY-Y0152 純度: 99.56%
COA 產(chǎn)品使用指南

Cinchonine 是金雞納樹皮中的天然化合物,對(duì)于瘧疾、腫瘤、炎癥、血小板凝結(jié)和肥胖都具有抑制作用。金雞納堿通過激活 Caspase-3 蛋白抑制細(xì)胞增殖和自噬 (autophagy),誘導(dǎo)細(xì)胞凋亡 (apoptosis)。Cinchonine 可激活內(nèi)質(zhì)網(wǎng)應(yīng)激誘導(dǎo)的人肝癌細(xì)胞凋亡。

MCE 的所有產(chǎn)品僅用作科學(xué)研究或藥證申報(bào),我們不為任何個(gè)人用途提供產(chǎn)品和服務(wù)

Cinchonine Chemical Structure

Cinchonine Chemical Structure

CAS No. : 118-10-5

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10 mM * 1 mL in DMSO ¥220
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5 g ¥420
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Other Forms of Cinchonine:

MCE 顧客使用本產(chǎn)品發(fā)表的 2 篇科研文獻(xiàn)

  • 生物活性

  • 純度 & 產(chǎn)品資料

  • 參考文獻(xiàn)

生物活性

Cinchonine is a natural compound present in Cinchona bark with antimalarial, antitumor, anti-inflammatory, anti platelet-aggregation and anti-obesity properties. Cinchonine inhibits cells proliferation and autophagy and induces apoptosis through activation of Caspase-3. Cinchonine activates endoplasmic reticulum stress-induced apoptosis in human liver cancer cells[1].

細(xì)胞效力
(Cellular Effect)
Cell Line Type Value Description References
HeLa EC50
697 μg/mL
Compound: I
Cytotoxicity against human HeLa cells by MTT assay
Cytotoxicity against human HeLa cells by MTT assay
[PMID: 22846917]
WI-38 IC50
> 20 μg/mL
Compound: 1c
Cytotoxicity against human WI38 cells by MTT assay
Cytotoxicity against human WI38 cells by MTT assay
[PMID: 23816880]
WI-38 IC50
> 68.03 μM
Compound: CN
Cytotoxicity against human WI38 cells by MTT assay
Cytotoxicity against human WI38 cells by MTT assay
[PMID: 26063305]
體外研究
(In Vitro)

Cinchonine 可以抑制 HepG2 和 SMCC7721 (180 μM, 24 h) 以及 HeLa 和 A549 (180 μM, 48-96 h) 細(xì)胞的增殖,誘導(dǎo)細(xì)胞凋亡[2][3]
Cinchonine (50-100 μM, 24 h) 在 A549 和 H1975 肺癌細(xì)胞中抑制腫瘤生長(zhǎng),IC[50] 值分別為 76.67 和 87.44 μM[4]
Cinchonine (0-20 μM, 24 h) 通過對(duì)成熟溶酶體水解酶的抑制作用阻斷自噬通路[4]。
Cinchonine (20 μM) 誘導(dǎo)破骨細(xì)胞分化和成骨作用[6]。
Cinchonine 通過抑制 Ca2+ 通量 (IC50: 300 μM) 和Kinase C (IC50: 20 μM) 來抑制血小板聚集[7]
Cinchonine 可以抑制 T. evansi 增殖 (0-100 μM, 72 h),24小時(shí)內(nèi)的 IC50為 16.96 μM[8]。

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[2][3][4]

Cell Line: HeLa, A549, HepG2, SMCC7721, H1975
Concentration: 180 μM (HeLa, A549, HepG2, SMCC7721), 200 μM (A549 and H1975)
Incubation Time: 24 h-96 h (HeLa and A549), 48 h (HepG2 and SMCC7721), 24 h (A549 and H1975)
Result: Inhibited cell proliferation in cells HeLa, A549, HepG2 and SMCC7721.
Cinchonine inhibited phosphorylation of AKT and TAK1.
Cinchonine activated Casapase-3, promoted GRP78 and phosphorylation of PERK and sIF2-α.
Cinchonine reduced mature cathepsin levels and increased immature cathespin levels.
體內(nèi)研究
(In Vivo)

Cinchonine (0.265-0.530 mg/kg,瘤內(nèi)注射,LLC細(xì)胞,14 天) 可以誘導(dǎo)細(xì)胞凋亡,抑制 BALB/c 裸鼠體內(nèi)的腫瘤生長(zhǎng),具有低毒性[2]。
Cinchonine (4 mg/kg/day,19 天,腹腔注射,LLC 細(xì)胞) 對(duì) BLAB/c 裸鼠的肺癌細(xì)胞具有低毒性的抗轉(zhuǎn)移活性[4]。
Cinchonine (50mg/kg,i.p.) 在 C57BL/6B 小鼠體內(nèi)具有抗肥胖活性[5]。

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: BALB/c nude mice [4]
Dosage: 4 mg/kg/day
Administration: Intraperitoneal injection, for 19 days
Result: Inhibited metastatic activity
Animal Model: BALB/c nude mice [2]
Dosage: 0.265 and 0.530 mg/kg
Administration: Intratumorally injection, for 14 days
Result: Inhibited tumor growth with more TUNEL positive cells (DNA fragmentation indicator).
Animal Model: High-fat-diet (HFD) induced obesity in C57BL/6B mice[5]
Dosage: 50 mg/kg
Administration: Intraperitoneal injection
Result: Reduced body weight gain (?38%), visceral fat-pad weights (?26%).
分子量

294.39

Formula

C19H22N2O

CAS 號(hào)
性狀

固體

顏色

White to off-white

中文名稱

辛可寧

結(jié)構(gòu)分類
初始來源
運(yùn)輸條件

Room temperature in continental US; may vary elsewhere.

儲(chǔ)存方式

4°C, protect from light, stored under nitrogen

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen)

溶解性數(shù)據(jù)
細(xì)胞實(shí)驗(yàn): 

DMSO 中的溶解度 : 4.76 mg/mL (16.17 mM; 超聲助溶; 吸濕的 DMSO 對(duì)產(chǎn)品的溶解度有顯著影響,請(qǐng)使用新開封的 DMSO)

配制儲(chǔ)備液
濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg
1 mM 3.3969 mL 16.9843 mL 33.9685 mL
5 mM 0.6794 mL 3.3969 mL 6.7937 mL
查看完整儲(chǔ)備液配制表

* 請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲(chǔ)備液;一旦配成溶液,請(qǐng)分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效。
儲(chǔ)備液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen)。-80°C儲(chǔ)存時(shí),請(qǐng)?jiān)?個(gè)月內(nèi)使用,-20°C儲(chǔ)存時(shí),請(qǐng)?jiān)?個(gè)月內(nèi)使用。

  • 摩爾計(jì)算器

  • 稀釋計(jì)算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

質(zhì)量
=
濃度
×
體積
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

濃度 (start)

C1

×
體積 (start)

V1

=
濃度 (final)

C2

×
體積 (final)

V2

動(dòng)物溶解方案計(jì)算器
請(qǐng)輸入動(dòng)物實(shí)驗(yàn)的基本信息:

給藥劑量

mg/kg

動(dòng)物的平均體重

g

每只動(dòng)物的給藥體積

μL

動(dòng)物數(shù)量

由于實(shí)驗(yàn)過程有損耗,建議您多配一只動(dòng)物的量
計(jì)算結(jié)果
工作液所需濃度 : mg/mL
純度 & 產(chǎn)品資料

純度: 99.56%

參考文獻(xiàn)

完整儲(chǔ)備液配制表

* 請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲(chǔ)備液;一旦配成溶液,請(qǐng)分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效
儲(chǔ)備液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen)。-80°C儲(chǔ)存時(shí),請(qǐng)?jiān)?個(gè)月內(nèi)使用,-20°C儲(chǔ)存時(shí),請(qǐng)?jiān)?個(gè)月內(nèi)使用。

可選溶劑 濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 3.3969 mL 16.9843 mL 33.9685 mL 84.9214 mL
5 mM 0.6794 mL 3.3969 mL 6.7937 mL 16.9843 mL
10 mM 0.3397 mL 1.6984 mL 3.3969 mL 8.4921 mL
15 mM 0.2265 mL 1.1323 mL 2.2646 mL 5.6614 mL
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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產(chǎn)品名稱:
Cinchonine
目錄號(hào):
HY-Y0152
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