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680C91 {[allProObj[0].p_purity_real_show]}

货号:A393978

680C91是一种选择性色氨酸2,3-双加氧酶(TDO)抑制剂,能够调节色氨酸代谢,适用于肿瘤免疫和阿尔茨海默症研究。

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+
680C91 化学结构 CAS号:163239-22-3
680C91 化学结构
CAS号:163239-22-3
680C91 3D分子结构
CAS号:163239-22-3
680C91 化学结构 CAS号:163239-22-3
680C91 3D分子结构 CAS号:163239-22-3
规格 价格 会员价 库存 数量
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680C91 纯度/质量文件 产品仅供科研

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680C91 细胞实验

Cell Line
Concentration Treated Time Description References
Fibroid explants 50μM 48 hours To investigate the effect of 680C91 on mRNA expression in fibroid explants, results showed that 680C91 blocked tryptophan-induced expression of CYP1B1, TGF-β3, FN1, CDK2, E2F1, IL8, and SPARC mRNA. Fertil Steril. 2024 Apr;121(4):669-678.
HCT15 colon cancer cells 25 µM 3 days Reduction in cell number was caused by cell death or cell cycle arrest Genes Dev. 2019 Sep 1;33(17-18):1236-1251.
DLD1 colon cancer cells 25 µM 3 days Reduction in cell number was caused by cell death or cell cycle arrest Genes Dev. 2019 Sep 1;33(17-18):1236-1251.
SK-Mel-28 melanoma cells 40 μM 24 hours 680C91 significantly inhibited dexamethasone-induced migration and MMP2 activity in SK-Mel-28 cells. Pharmaceuticals (Basel). 2021 Mar 4;14(3):211.
SK-Mel-28 melanoma cells 40 μM 3 hours 680C91 partially but significantly inhibited dexamethasone-induced Akt phosphorylation. Pharmaceuticals (Basel). 2021 Mar 4;14(3):211.
SK-Mel-28 melanoma cells 40 μM 48 hours 680C91 significantly inhibited dexamethasone-induced proliferation of SK-Mel-28 cells by 41.2 ±7.1%, without affecting cell viability or FGF2-induced cell proliferation. Pharmaceuticals (Basel). 2021 Mar 4;14(3):211.
A172 cells 10 μM 24 hours 680C91 treatment resulted in decreased hpol κ expression. Chem Res Toxicol. 2016 Jan 19;29(1):101-8.
U-87-MG cells 10 μM 24 hours 680C91 treatment resulted in decreased hpol κ expression. Chem Res Toxicol. 2016 Jan 19;29(1):101-8.
T98G cells 10 μM or 100 μM 24 hours Inhibition of TDO activity led to reduced Kyn production and decreased hpol κ expression levels. Chem Res Toxicol. 2016 Jan 19;29(1):101-8.
ECFCs 40 µM 24 hours 680C91 significantly impaired ECFCs' tube formation ability Pharmaceuticals (Basel). 2024 Apr 27;17(5):558.
HUVECs 40 µM 48 hours 680C91 significantly inhibited HUVEC proliferation, with maximal effect at 40 µM inhibiting cell growth by 79.3 ± 28% Pharmaceuticals (Basel). 2024 Apr 27;17(5):558.
A375 cells 40 µM 24 hours 680C91 significantly abolished the dex-induced upregulation of stem cell markers Front Pharmacol. 2022 Jun 30;13:911019.
SK-Mel-28 cells 40 µM 24 hours 680C91 significantly abolished the dex-induced upregulation of stem cell markers Front Pharmacol. 2022 Jun 30;13:911019.
HepG2 cells 10, 20, 40, 80 µmol/L 72 hours To investigate the effect of 680C91 on TDO-mediated tryptophan degradation, results showed that 680C91 significantly inhibited tryptophan degradation and kynurenine accumulation J Clin Med. 2022 Aug 16;11(16):4794.

680C91 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
SCID/Beige mice Human fibroid xenograft model Intraperitoneal injection 10 mg/kg Daily for two months To evaluate the therapeutic effects of 680C91 on fibroid xenografts, results showed a 30% reduction in fibroid weight after two months of treatment with 680C91, along with decreased levels of kynurenine and reduced mRNA and protein expression of multiple genes (CYP1B1, TGF-β3, FN1, CDK2, E2F1, IL-8, and SPARC) in the xenografts. Fertil Steril. 2024 Apr;121(4):669-678.

680C91 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.20mL

0.84mL

0.42mL

20.99mL

4.20mL

2.10mL

41.97mL

8.39mL

4.20mL

680C91 技术信息

CAS号163239-22-3
分子式C15H11FN2
分子量 238.26
SMILES Code FC1=CC2=C(C=C1)C(/C=C/C3=CC=CN=C3)=CN2
MDL No. MFCD20926361
别名
运输蓝冰
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry, 2-8°C

溶解方案

DMSO: 120 mg/mL(503.65 mM),配合低频超声助溶,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

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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