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硫酸长春地辛

更新时间:2025-08-25 00:58:09

硫酸长春地辛结构式
硫酸长春地辛结构式
品牌特惠专场
常用名 硫酸长春地辛 英文名 Vindesine sulfate
CAS号 59917-39-4 分子量 852.00
密度 1.41 g/cm3 沸点 N/A
分子式 C43H57N5O11S 熔点 >250ºC
MSDS N/A 闪点 N/A

 硫酸长春地辛用途


硫酸长春地辛是一种有效的微管蛋白抑制剂,Ki为0.110µM。硫酸长春地辛在体外具有抗增殖作用。硫酸长春地辛在体内具有抗肿瘤作用[1]。

 硫酸长春地辛名称

中文名 硫酸长春地辛
英文名 vindesine sulfate
英文别名 更多

 硫酸长春地辛生物活性

描述 硫酸长春地辛是一种有效的微管蛋白抑制剂,Ki为0.110µM。硫酸长春地辛在体外具有抗增殖作用。硫酸长春地辛在体内具有抗肿瘤作用[1]。
相关类别
体外研究 硫酸长春地辛抑制L细胞生长,在40 nM处显示约25%的抑制作用【1】。
参考文献

[1]. Jordan MA, et al. Comparison of the effects of vinblastine, vincristine, vindesine, and vinepidine on microtubule dynamics and cell proliferation in vitro. Cancer Res. 1985 Jun;45(6):2741-7.

 硫酸长春地辛物理化学性质

密度 1.41 g/cm3
熔点 >250ºC
分子式 C43H57N5O11S
分子量 852.00
精确质量 851.377502
PSA 247.80000
LogP 3.80150
InChIKey COFJBSXICYYSKG-UNNXMZBYSA-N
SMILES CCC1(O)CC2CN(CCc3c([nH]c4ccccc34)C(C(=O)OC)(c3cc4c(cc3OC)N(C)C3C(O)(C(N)=O)C(O)C5(CC)C=CCN6CCC43C65)C2)C1.O=S(=O)(O)O
外观性状 非晶形的固体
储存条件 2-8°C
水溶解性 deionized water: ≥50mg/mL

 硫酸长春地辛毒性和生态

 硫酸长春地辛安全信息

危害码 (欧洲) Xn: Harmful;
风险声明 (欧洲) R40
安全声明 (欧洲) 26-36
危险品运输编码 UN 1544
RTECS号 YY8090000
包装等级 II
危险类别 6.1(a)
海关编码 2942000000

 硫酸长春地辛海关

海关编码 2942000000

 硫酸长春地辛文献4

更多文献
Validated HILIC-MS/MS assay for determination of vindesine in human plasma: Application to a population pharmacokinetic study

J. Pharm. Biomed. Anal. 96 , 31-6, (2014)

Mean plasma concentration–time profiles of intravenous injection of 3mg Vindesine Sulfate for Injection to 100 unrelated Chinese Han subjects with hematological malignant disorders.

Young patients with non-germinal center B-cell-like diffuse large B-cell lymphoma benefit from intensified chemotherapy with ACVBP plus rituximab compared with CHOP plus rituximab: analysis of data from the Groupe d'Etudes des Lymphomes de l'Adulte/lymphoma study association phase III trial LNH 03-2B.

J. Clin. Oncol. 32(35) , 3996-4003, (2014)

To determine whether any tumor biomarkers could account for the survival advantage observed in the LNH 03-2B trial among patients with diffuse large B-cell lymphoma (DLBCL) and low-intermediate risk a...

Reovirus cell entry requires functional microtubules.

MBio 4 , (2013)

Mammalian reovirus binds to cell-surface glycans and junctional adhesion molecule A and enters cells by receptor-mediated endocytosis in a process dependent on β1 integrin. Within the endocytic compar...

 硫酸长春地辛靶点实验

查看更多实验

实验名称:qHTS assay to identify small molecule antagonists of the androgen receptor (AR) signa...
来源:824
靶标:AR protein [Homo sapiens]
External Id:MDAN535
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:qHTS assay to identify small molecule antagonists of the androgen receptor (AR) sign...
来源:824
靶标:N/A
External Id:MDAV150
实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
实验名称:qHTS assay for small molecules that induce genotoxicity in human embryonic kidney cel...
来源:824
靶标:RecName: Full=ATPase family AAA domain-containing protein 5; AltName: Full=Chromosome fragility-associated gene 1 protein
External Id:ELG271
实验名称:qHTS assay to identify small molecule antagonists of the thyroid receptor (TR) signal...
来源:824
靶标:thyroid hormone receptor beta isoform 2 [Rattus norvegicus]
External Id:TRN186
实验名称:qHTS assay to identify small molecule antagonists of the thyroid receptor (TR) signal...
来源:824
靶标:N/A
External Id:TRV455
实验名称:qHTS for Inhibitors of binding or entry into cells for Marburg Virus
来源:NCGC
靶标:gene 4 small orf - Marburg virus
External Id:VSVM-OFFLINE
实验名称:qHTS for Inhibitors of binding or entry into cells for Lassa Virus
来源:NCGC
靶标:N/A
External Id:VSVL-OFFLINE
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 硫酸长春地辛英文别名

2H-3,7-Methanoazacycloundecino[5,4-b]indole-9-carboxylic acid, 9-[(2β,3β,4β,5α,12β,19α)-3-(aminocarbonyl)-6,7-didehydro-3,4-dihydroxy-16-methoxy-1-methylaspidospermidin-15-yl]-5-et hyl-1,4,5,6,7,8,9,10-octahydro-5-hydroxy-, methyl ester, (5S,7S,9S)-, sulfate (1:1) (salt)
methyl (5S,7S,9S)-9-[(2β,3β,4β,5α,12β,19α)-3-carbamoyl-3,4-dihydroxy-16-methoxy-1-methyl-6,7-didehydroaspidospermidin-15-yl]-5-ethyl-5-hydroxy-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indole-9-carboxylate sulfate (1:1)
Vindesine Sulfate Salt
2H-3,7-methanoazacycloundecino[5,4-b]indole-9-carboxylic acid, 9-[(2β,3β,4β,5α,12β,19α)-3-(aminocarbonyl)-6,7-didehydro-3,4-dihydroxy-16-methoxy-1-methylaspidospermidin-15-yl]-5-ethyl-1,4,5,6,7,8,9,10-octahydro-5-hydroxy-, methyl ester, (5S,7S,9S)-, sulfate (1:1) (salt)
Vindesine sulphate
Methyl (13S,15S,17S)-13-[(2β,3β,4β,5α,12β,19α)-3-carbamoyl-3,4-dihydroxy-16-methoxy-1-methyl-6,7-didehydroaspidospermidin-15-yl]-17-ethyl-17-hydroxy-1,11-diazatetracyclo[13.3.1.0.0]nonadeca-4(12),5,7,9-tetraene-13-carboxylate sulfate (1:1)
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