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Dihydrotanshinone I/二氢丹参酮I {[allProObj[0].p_purity_real_show]}

货号:A831392 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+
Dihydrotanshinone I/二氢丹参酮I 化学结构 CAS号:87205-99-0
Dihydrotanshinone I/二氢丹参酮I 化学结构
CAS号:87205-99-0
Dihydrotanshinone I/二氢丹参酮I 3D分子结构
CAS号:87205-99-0
Dihydrotanshinone I/二氢丹参酮I 化学结构 CAS号:87205-99-0
Dihydrotanshinone I/二氢丹参酮I 3D分子结构 CAS号:87205-99-0
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Dihydrotanshinone I/二氢丹参酮I 纯度/质量文件 产品仅供科研

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Dihydrotanshinone I/二氢丹参酮I 生物活性

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.

Dihydrotanshinone I/二氢丹参酮I 细胞实验

Cell Line
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

Dihydrotanshinone I/二氢丹参酮I 动物实验

Species
Animal Model
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

Dihydrotanshinone I/二氢丹参酮I 参考文献

[1]Cheung J, Beri V, Shiomi K, Rosenberry TL. Acetylcholinesterase complexes with the natural product inhibitors dihydrotanshinone I and territrem B: binding site assignment from inhibitor competition and validation through crystal structure determination. J Mol Neurosci. 2014 Jul;53(3):506-10.

[2]Cong M, Hu CM, et al. Cryptotanshinone and dihydrotanshinone I exhibit strong inhibition towards human liver microsome (HLM)-catalyzed propofol glucuronidation. Fitoterapia. 2013 Mar;85:109-13.

Dihydrotanshinone I/二氢丹参酮I 实验方案

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

Dihydrotanshinone I/二氢丹参酮I 技术信息

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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