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LDCA {[allProObj[0].p_purity_real_show]}

货号:A1680546

LDCA是一种双重作用的代谢调节剂,能够抑制乳酸脱氢酶 A (LDH-A) 活性并促进恶性细胞凋亡,广泛应用于癌症进展的研究中。

HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
LDCA 化学结构 CAS号:349106-80-5
LDCA 化学结构
CAS号:349106-80-5
LDCA 3D分子结构
CAS号:349106-80-5
LDCA 化学结构 CAS号:349106-80-5
LDCA 3D分子结构 CAS号:349106-80-5
规格 价格 会员价 库存 数量
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LDCA 纯度/质量文件 产品仅供科研

货号:A1680546 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 Dehydrogenase 其他靶点 纯度
Trilostane 99+%
AGI-6780 +++

IDH2 R140Q mutant, IC50: 23 nM

99%+
Gimeracil 98%
AGI-5198 ++

R132C-IDH1, IC50: 0.16 μM

R132H-IDH1, IC50: 70 nM

99%+
SW033291 ++++

15-PGDH, IC50: 1.5 nM

15-PGDH, Ki: 0.1 nM

99%+
Mycophenolic acid 99+%
Fomepizole 98%
Leflunomide 98%
3-Nitropropanoic acid 99%+
Isovaleramide 98%
Mycophenolate Mofetil +++

Inosine monophosphate dehydrogenase II, IC50: 27 nM

Inosine monophosphate dehydrogenase I, IC50: 39 nM

98%
MK-8245 ++++

SCD1 (rat), IC50: 3 nM

SCD1 (mouse), IC50: 1 nM

99%+
Vidofludimus ++

Human DHODH, IC50: 134 nM

99%+
Emodin 98%
Ivosidenib 98%
NCT-501 ++

ALDH1A1, IC50: 40 nM

98%
Gossypol 99%+
Devimistat 98%
Disulfiram 98%+
Enasidenib ++++

IDH2, IC50: 12 nM

98%
PluriSIn 1 99%+
ML390 +

DHODH, IC50: 0.56 μM

99%+
Teriflunomide 99%+
Daidzin +++

ALDH-Ⅰ, Ki: 20 nM

98+%
18β-Glycyrrhetinic acid 99%
RRx-001 95%
NCT-503 +

PHGDH, IC50: 2.5 μM

99%+
Vorasidenib 99%+
Ammonium Glycyrrhizinate(x:1) 98+%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

LDCA 生物活性

描述 LDCA acts as a dual-hit metabolic modulator, inhibiting LDH-A enzyme activity to promote apoptosis in cancer cells. It is used in cancer progression research[1].
体内研究

LDCA (2 mg/kg, intravenously, on the 6th day, once) combined with doxorubicin effectively impedes tumor growth kinetics, curbing oncogenic progression and enhancing survival in a murine melanoma model[1].

体外研究

LDCA, when used synergistically with doxorubicin in concentrations of 2-100 μM over 16-72 hours, enhances growth inhibition and triggers mitochondria-mediated apoptosis. This combination recruits the caspase cascade, limits cell migration, and prevents clonogenic expansion of melanoma cells[1].

LDCA 参考文献

[1]Saha, Suchandrima, et al. The dual-hit metabolic modulator LDCA synergistically potentiates doxorubicin to selectively combat cancer-associated hallmarks. RSC Advances, 7(84), 53322–53333. doi:10.1039/c7ra08625c.

[2]Keiser J, et al. Evaluation of the in vivo activity of tribendimidine against Schistosoma mansoni, Fasciola hepatica, Clonorchis sinensis, and Opisthorchis viverrini. Antimicrob Agents Chemother. 2007 Mar;51(3):1096-8.

LDCA 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.90mL

0.78mL

0.39mL

19.49mL

3.90mL

1.95mL

38.99mL

7.80mL

3.90mL

LDCA 技术信息

CAS号349106-80-5
分子式C8H5Cl3FNO
分子量 256.489
别名
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Inert atmosphere,2-8°C

溶解度

DMSO: 105 mg/mL(409.37 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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