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                同义名:
                    
                        
                            二氢丹参酮Ⅰ
                            
                             / 15,16-Dihydrotanshinone I; DHTS
                            
                        
                    
                
                
                
                    
                     
                
            
Dihydrotanshinone I是一种从丹参中提取的天然产物,对 PL(pro) 的 IC50 为 4.9 μM,对 3CLpro 的 IC50 为 14.4 μM,广泛用于心血管疾病和病毒研究。
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| 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+ | 
 
                                 
                                
                            

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| 描述 | Dihydrotanshinone I, a natural product isolated and purified from the roots of Salvia miltiorrhiza Bge., exhibits dose-dependent inhibition towards HLM-catalyzed propofol glucuronidation. | 
| Concentration | Treated Time | Description | References | |
| 4T1 cells | IC50: 6.97 μM | 24 hours | Inhibited cell proliferation, IC50 of 6.97 μM | Int J Mol Sci. 2022 Dec 2;23(23):15180 | 
| 8505C-PTX cells | 2.5 µM | 72 hours | Evaluate the effect of DHT on the viability of PTX-resistant cells, results showed DHT significantly reduced cell viability | Int J Mol Sci. 2021 Jul 28;22(15):8083 | 
| SW1736-PTX cells | 2.5 µM | 72 hours | Evaluate the effect of DHT on the viability of PTX-resistant cells, results showed DHT significantly reduced cell viability | Int J Mol Sci. 2021 Jul 28;22(15):8083 | 
| PMNs cells | 0.5–128 μM | 8 hours | Increased cell viability | Int J Mol Sci. 2022 Dec 2;23(23):15180 | 
| SKBR-3 cells | IC50: 17.87 μM | 24 hours | Inhibited cell proliferation, IC50 of 17.87 μM | Int J Mol Sci. 2022 Dec 2;23(23):15180 | 
| MCF-7 cells | IC50: 34.11 μM | 24 hours | Inhibited cell proliferation, IC50 of 34.11 μM | Int J Mol Sci. 2022 Dec 2;23(23):15180 | 
| MDA-MB-231 cells | IC50: 117.71 μM | 24 hours | Inhibited cell proliferation, IC50 of 117.71 μM | Int J Mol Sci. 2022 Dec 2;23(23):15180 | 
| HCT116 cells | 10 µM | 15 days | To assess the inhibitory effect of DHTS on tumor spheroid growth | Nucleic Acids Res. 2017 Sep 19;45(16):9514-9527 | 
| HeLa cells | 10 µM | To evaluate the interference of DHTS with HuR binding to target mRNAs | Nucleic Acids Res. 2017 Sep 19;45(16):9514-9527 | |
| NIH-3T3 fibroblasts | 37.5, 75, 150 nM | 12 hours | Blocking the downstream of CD44-RhoA-YAP signaling pathway, reducing YAP nuclear translocation, and inhibiting fibroblast migration, invasion, proliferation, and collagen deposition. | Theranostics. 2019 Jul 9;9(17):4993-5008 | 
| RAW264.7 macrophages | 10, 50, 100 nM | 24 hours | To evaluate the inhibitory effect of DHT on LPS-induced inflammatory response in macrophages, results showed DHT reduced the release of TNF-α and IL-1β and inhibited the activation of M1 macrophages | J Exp Clin Cancer Res. 2020 May 24;39(1):93 | 
| H9C2 cardiomyocytes | 10 nM | 24 hours | To evaluate the inhibitory effect of DHT on DOX-induced inflammatory response in cardiomyocytes, results showed DHT downregulated the expressions of p-NF-κB, TNF-α, and COX2 | J Exp Clin Cancer Res. 2020 May 24;39(1):93 | 
| Rat primary hepatic stellate cells (pHSCs) | 1, 5, 10 μmol/L | DHI dose-dependently inhibited the mRNA expression of various fibrogenic genes, including TGFβ1, α-SMA and COL1A1, in rat pHSCs. | Br J Pharmacol. 2017 May;174(10):1147-1160 | |
| LX-2 cells | 1, 5, 10 μmol/L | DHI dose-dependently inhibited the mRNA expression of various fibrogenic genes, including TGFβ1, α-SMA and COL1A1, in LX-2 cells. | Br J Pharmacol. 2017 May;174(10):1147-1160 | |
| HL-60 cells | 0.5~2.5 μg/mL | 24 hours | DHTS significantly inhibited HL-60 cell proliferation, induced apoptosis, activated caspase-3, -8, and -9, leading to PARP cleavage. | Int J Mol Sci. 2015 Aug 17;16(8):19387-400 | 
| Administration | Dosage | Frequency | Description | References | ||
| BALB/c nude mice | 4T1 spontaneous metastasis model | Intraperitoneal injection | 10 mg/kg or 20 mg/kg | Once daily for 25 days | Inhibited tumor growth and lung metastasis, lung fluorescence intensity decreased by 74.9% in DHT-H group | Int J Mol Sci. 2022 Dec 2;23(23):15180 | 
| Nude mice | HCT116 xenograft model | Intraperitoneal injection | 10 mg/kg | Every 48 hours for 31 days | To evaluate the inhibitory effect of DHTS on tumor growth | Nucleic Acids Res. 2017 Sep 19;45(16):9514-9527 | 
| C57BL/6 mice | Crystalline silica-induced silicosis model | Intragastric administration | 150, 75, 37.5 mg/kg | Once daily for 7 days | By blocking the CD44-RhoA-YAP signaling pathway, it alleviates crystalline silica-induced pulmonary fibrosis and improves pulmonary function. | Theranostics. 2019 Jul 9;9(17):4993-5008 | 
| C57BL/6 mice | Doxorubicin-induced cardiotoxicity model | Oral | 20 mg/kg | Once daily for 4 weeks | To evaluate the protective effect of DHT on doxorubicin-induced cardiotoxicity, results showed DHT improved cardiac function, reduced inflammatory cell infiltration, and inhibited the activation of M1 macrophages and NF-κB signaling pathway | J Exp Clin Cancer Res. 2020 May 24;39(1):93 | 
| Sprague-Dawley rats | Bile duct ligation (BDL)-induced hepatic fibrosis model | Intraperitoneal injection | 25 mg/kg/day | Once daily for 14 days | DHI treatment attenuated liver necrosis, bile duct proliferation and collagen accumulation, and reduced the expression of fibrogenesis-associated genes in BDL rats. | Br J Pharmacol. 2017 May;174(10):1147-1160 | 
| Nude mice | HL-60 xenograft model | Intraperitoneal injection | 12.5 and 25.0 mg/kg | Once daily for one week | 25 mg/kg DHTS significantly inhibited HL-60 tumor growth by about 68.0% with no effect on body weight. | Int J Mol Sci. 2015 Aug 17;16(8):19387-400 | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 3.59mL 0.72mL 0.36mL | 17.97mL 3.59mL 1.80mL | 35.93mL 7.19mL 3.59mL | |
| CAS号 | 87205-99-0 | 
| 分子式 | C18H14O3 | 
| 分子量 | 278.3 | 
| SMILES Code | O=C(C1=C2C=CC3=C1C=CC=C3C)C(C4=C2OC[C@@H]4C)=O | 
| MDL No. | MFCD28016070 | 
| 别名 | 二氢丹参酮Ⅰ ;15,16-Dihydrotanshinone I; DHTS | 
| 运输 | 蓝冰 | 
| InChI Key | HARGZZNYNSYSGJ-JTQLQIEISA-N | 
| Pubchem ID | 11425923 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, sealed in dry, 2-8°C | 
| 溶解方案 | DMSO: 2 mg/mL(7.19 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 | 
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