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CAS: 138-14-7
分子式: C25H48N6O8.CH4O3S
分子量: 656.79
英文名称: 
propionohydroxamic acid, n-(5-(3-((5-aminopentyl)hydroxycarbamoyl)propionamido)
monomethanesulfonate (sa
deferoxamine b mesylate
deferoxamine mesilate
deferoxamine mesylate
deferoxamine methanesulfonate
desferal
desferal mesylate
desferal methanesulfonate
desferrioxamine b mesylate
desferrioxamine b methanesulfonate
desferrioxamine methanesulfonate
展开更多英文名
用途: Deferoxamine mesylate is the mesylate salt of Deferoxamine, which forms iron complexes and is used as a chelating agent.
推荐供应商
货号品牌产品名称规格包装、参考价格详情
D875507MACKLIN甲磺酸去铁胺≥92.5%128元/25mg;   358元/100mg;   966元/500mg;   展开
储存:-20℃
状态:白色到灰白色粉末
D873692MACKLIN甲磺酸去铁胺≥98%58元/5mg;   185元/25mg;   395元/100mg;   1110元/500mg;   1619元/1g;   6599元/5g;   展开
储存:-20℃
状态:白色到灰白色固体
454081J&KDeferoxamine mesylate salt97%465元/250MG;   1559元/1G;   5456元/5G;   展开

基本信息

分子式C26H52N6O11S
分子量656.79
熔点145-149
MDL编码MFCD00058605
Beilstein4122177
EINECS 编号205-314-3
存储条件Freezer -20℃

安全信息

防范说明P262
WGK2
RTECSUG5310000
C46177Alfa AesarDeferoxamine mesylate95%4104元/1g;   展开

基本信息

Ref#
46177

分子式
C25H48N6O8.CH4O3S

分子量
292.13

252750MilliporeDeferoxamine Mesylate-CAS 138-14-7-CalbiochemParenteral iron chelating agent. Commonly used in therapy as a chelator of ferric iron in disorders of iron overload.1877.44元/1 G;   展开

产品说明

一般描述

Parenteral iron chelating agent. Commonly used in therapy as a chelator of ferric iron in disorders of iron overload. Completely protects against dopamine-induced cell death. Has also been shown to interfere with hydroxyl radical formation, which mediates tissue damage in several disease states. Shows anti-proliferative effect on vascular smooth muscle cells in vitro and in vivo. Can also inhibit the oxidative chemistry of peroxynitrite by reaction of the hydroxamic acid moieties with trans-peroxynitrous acid.
Parenteral iron chelating agent. Commonly used in therapy as a chelator of ferric iron in disorders of iron overload. Completely protects against dopamine-induced cell death. Has also been shown to interfere with hydroxyl radical formation, which mediates tissue damage in several disease states. Shows antiproliferative effects on vascular smooth muscle cells in vitro and in vivo. Can also inhibit the oxidative chemistry of peroxynitrite by reaction of the hydroxamic moieties with trans-peroxynitrous acid.

包装

1 g in Plastic ampoule

警告

Toxicity: Harmful & Carcinogenic / Teratogenic (E)

其他说明

Bergeron, R.J., et al. 1996. J. Med. Chem. 39, 1575.
Ben-Shachar, D., et al. 1995. J. Neurochem. 64, 718.
Denicola, A., et al. 1995. Free Radic. Biol. Med. 19, 11.
Dzwigaj, S., and pererat, H., 1995. Free Radic. Res.14, 103.
Dang, S., et al. 1994. Res. Commun. Mol. Pathol. Pharmacol. 86, 43.
Porreca, E., et al. 1994. Arterioscler. Thromb. 14, 299.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

基本信息

经验(实验)分子式C25H48N6O8 · xCH4O3S
分子量560.68 (free base basis)
MDL编号MFCD00058605

产品性质

质量水平100
测定92.5-100% (TLC)
形式powder
manufacturer/tradenameCalbiochem®
储存条件OK to freeze
desiccated (hygroscopic)
颜色faint yellow
溶解性water: 50 mg/mL
运输ambient
储存温度2-8℃
InChI1S/C25H48N6O8.CH4O3S/c1-21(32)29(37)18-9-3-6-16-27-22(33)12-14-25(36)31(39)20-10-4-7-17-28-23(34)11-13-24(35)30(38)19-8-2-5-15-26;1-5(2,3)4/h37-39H,2-20,26H2,1H3,(H,27,33)(H,28,34);1H3,(H,2,3,4)
InChI keyIDDIJAWJANBQLJ-UHFFFAOYSA-N

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 2
闪点(F)Not applicable
闪点(C)Not applicable
D9533Sigma-AldrichDeferoxamine mesylate salt≥92.5% (TLC), powder1649.92元/1 g;   展开

产品说明

生化/生理作用

去铁胺被用作一个缺氧模拟物质去稳定低氧诱导因子1 (HIF-1)。 去铁胺通过抑制以HIF-1为靶点的脯氨酰羟化酶(PHDs)降解来稳定HIF-1。 去铁胺的抑制机制可能是通过Fe2+ 与酶活性所需的PHD活性位点的螯合作用而实现的。
一种铁螯合剂,常用于研究细胞增殖和凋亡。 体外体内 实验均显示其对血管平滑肌细胞具有抗增殖作用,并抑制G1期细胞的增殖。 据报道,它也诱导p53。 通过螯合铁诱导HL-60细胞凋亡。 经过1μM去铁胺处理48小时后,DNA明显断裂。 细胞经1μM去铁胺处理仅24小时后发生凋亡;48小时后观察到核坍塌。 一些研究表明,它具有抗氧化性能,并保护细胞免受H2O2诱导的损伤。

基本信息

经验(实验)分子式C25H48N6O8 · CH4O3S
分子量656.79
EC 号205-314-3
MDL编号MFCD00058605
PubChem化学物质编号24894304
NACRESNA.32

产品性质

质量水平200
测定≥92.5% (TLC)
形式powder
颜色 white to off-white
溶解性H2O: 50 mg/mL
储存温度−20℃
SMILES stringCS(O)(=O)=O.CC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCN
InChI1S/C25H48N6O8.CH4O3S/c1-21(32)29(37)18-9-3-6-16-27-22(33)12-14-25(36)31(39)20-10-4-7-17-28-23(34)11-13-24(35)30(38)19-8-2-5-15-26;1-5(2,3)4/h37-39H,2-20,26H2,1H3,(H,27,33)(H,28,34);1H3,(H,2,3,4)
InChI keyIDDIJAWJANBQLJ-UHFFFAOYSA-N

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 2
闪点(F)Not applicable
闪点(C)Not applicable
个人防护装备Eyeshields, Gloves, type N95 (US)
D0160000Deferoxamine mesylate saltEuropean Pharmacopoeia (EP) Reference Standard1572.27元/ ;   展开

产品说明

一般描述

本产品按照发行药典的发行和规定提供。支持本产品的所有信息,包括安全数据表和任何产品信息传单,都是在发行药典的授权下开发和发布的。 如需进一步信息和支持,请访问现行药典网站。

生化/生理作用

一种铁螯合剂,常用于研究细胞增殖和凋亡。 体外体内 实验均显示其对血管平滑肌细胞具有抗增殖作用,并抑制G1期细胞的增殖。 据报道,它也诱导p53。 通过螯合铁诱导HL-60细胞凋亡。 经过1μM去铁胺处理48小时后,DNA明显断裂。 细胞经1μM去铁胺处理仅24小时后发生凋亡;48小时后观察到核坍塌。 一些研究表明,它具有抗氧化性能,并保护细胞免受H2O2诱导的损伤。

包装

单位数量:30 mg。随时可能改变。产品按照发行药典的规定交付。有关当前单位数量,请访问EDQM对照品目录。

注意

请参见 由EDQM提供的SDS。。

其他说明

可能适用相应的销售限制。

基本信息

经验(实验)分子式C25H48N6O8 · CH4O3S
分子量656.79
MDL编号MFCD00058605
PubChem化学物质编号329798589
NACRESNA.24

产品性质

等级pharmaceutical primary standard
manufacturer/tradenameEDQM
application(s)pharmaceutical (small molecule)
格式neat
SMILES stringCS(O)(=O)=O.CC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCN
InChI1S/C25H48N6O8.CH4O3S/c1-21(32)29(37)18-9-3-6-16-27-22(33)12-14-25(36)31(39)20-10-4-7-17-28-23(34)11-13-24(35)30(38)19-8-2-5-15-26;1-5(2,3)4/h37-39H,2-20,26H2,1H3,(H,27,33)(H,28,34);1H3,(H,2,3,4)
InChI keyIDDIJAWJANBQLJ-UHFFFAOYSA-N

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 2
闪点(F)Not applicable
闪点(C)Not applicable
Y0001934Deferoxamine for system suitabilityEuropean Pharmacopoeia (EP) Reference Standard1548.8元/ ;   展开

产品说明

一般描述

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

生化/生理作用

一种铁螯合剂,常用于研究细胞增殖和凋亡。 体外体内 实验均显示其对血管平滑肌细胞具有抗增殖作用,并抑制G1期细胞的增殖。 据报道,它也诱导p53。 通过螯合铁诱导HL-60细胞凋亡。 经过1μM去铁胺处理48小时后,DNA明显断裂。 细胞经1μM去铁胺处理仅24小时后发生凋亡;48小时后观察到核坍塌。 一些研究表明,它具有抗氧化性能,并保护细胞免受H2O2诱导的损伤。

包装

Unit quantity: 15 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

其他说明

Sales restrictions may apply.

基本信息

经验(实验)分子式C25H48N6O8 · CH4O3S
分子量656.79
MDL编号MFCD00058605
NACRESNA.24

产品性质

等级pharmaceutical primary standard
manufacturer/tradenameEDQM
格式neat
储存温度2-8℃
SMILES stringCS(O)(=O)=O.CC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCN
InChI1S/C25H48N6O8.CH4O3S/c1-21(32)29(37)18-9-3-6-16-27-22(33)12-14-25(36)31(39)20-10-4-7-17-28-23(34)11-13-24(35)30(38)19-8-2-5-15-26;1-5(2,3)4/h37-39H,2-20,26H2,1H3,(H,27,33)(H,28,34);1H3,(H,2,3,4)
InChI keyIDDIJAWJANBQLJ-UHFFFAOYSA-N

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 2
闪点(F)Not applicable
闪点(C)Not applicable
PHR3411SupelcoDeferoxamine mesylatecertified reference material, pharmaceutical secondary standard2000.81元/500 mg;   展开

产品说明

一般描述

Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards

生化/生理作用

一种铁螯合剂,常用于研究细胞增殖和凋亡。 体外体内 实验均显示其对血管平滑肌细胞具有抗增殖作用,并抑制G1期细胞的增殖。 据报道,它也诱导p53。 通过螯合铁诱导HL-60细胞凋亡。 经过1μM去铁胺处理48小时后,DNA明显断裂。 细胞经1μM去铁胺处理仅24小时后发生凋亡;48小时后观察到核坍塌。 一些研究表明,它具有抗氧化性能,并保护细胞免受H2O2诱导的损伤。

分析说明

These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.

其他说明

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

附注

To see an example of a Certificate of Analysis for this material enter LRAA6959(changes by product) in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

基本信息

经验(实验)分子式C25H48N6O8 · CH4O3S
分子量656.79
MDL编号MFCD00058605

产品性质

质量水平300
等级certified reference material
pharmaceutical secondary standard
CofAcurrent certificate can be downloaded
包装pkg of 500 mg
application(s)pharmaceutical
SMILES stringCS(O)(=O)=O.CC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCN
InChI1S/C25H48N6O8.CH4O3S/c1-21(32)29(37)18-9-3-6-16-27-22(33)12-14-25(36)31(39)20-10-4-7-17-28-23(34)11-13-24(35)30(38)19-8-2-5-15-26;1-5(2,3)4/h37-39H,2-20,26H2,1H3,(H,27,33)(H,28,34);1H3,(H,2,3,4)
InChI keyIDDIJAWJANBQLJ-UHFFFAOYSA-N

安全信息

储存分类代码13 - Non Combustible Solids
WGKWGK 2
闪点(F)Not applicable
闪点(C)Not applicable
1166003USPDeferoxamine mesylateUnited States Pharmacopeia (USP) Reference Standard3231.47元/300 MG;   展开

产品说明

一般描述

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.
For further information and support please go to the website of the issuing Pharmacopoeia.

生化/生理作用

一种铁螯合剂,常用于研究细胞增殖和凋亡。 体外体内 实验均显示其对血管平滑肌细胞具有抗增殖作用,并抑制G1期细胞的增殖。 据报道,它也诱导p53。 通过螯合铁诱导HL-60细胞凋亡。 经过1μM去铁胺处理48小时后,DNA明显断裂。 细胞经1μM去铁胺处理仅24小时后发生凋亡;48小时后观察到核坍塌。 一些研究表明,它具有抗氧化性能,并保护细胞免受H2O2诱导的损伤。

分析说明

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

其他说明

USP issued SDS can be found here.
Sales restrictions may apply.

基本信息

经验(实验)分子式C25H48N6O8 · CH4O3S
分子量656.79
MDL编号MFCD00058605
PubChem化学物质编号329749526
NACRESNA.24

产品性质

等级pharmaceutical primary standard
manufacturer/tradenameUSP
application(s)pharmaceutical (small molecule)
格式neat
储存温度2-8℃
SMILES stringCS(O)(=O)=O.CC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCN
InChI1S/C25H48N6O8.CH4O3S/c1-21(32)29(37)18-9-3-6-16-27-22(33)12-14-25(36)31(39)20-10-4-7-17-28-23(34)11-13-24(35)30(38)19-8-2-5-15-26;1-5(2,3)4/h37-39H,2-20,26H2,1H3,(H,27,33)(H,28,34);1H3,(H,2,3,4)
InChI keyIDDIJAWJANBQLJ-UHFFFAOYSA-N

安全信息

储存分类代码13 - Non Combustible Solids
WGKWGK 2
闪点(F)Not applicable
闪点(C)Not applicable
BP987Desferrioxamine mesilateBritish Pharmacopoeia (BP) Reference Standard1916.08元/30 MG;   展开

产品说明

一般描述

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.

生化/生理作用

一种铁螯合剂,常用于研究细胞增殖和凋亡。 体外体内 实验均显示其对血管平滑肌细胞具有抗增殖作用,并抑制G1期细胞的增殖。 据报道,它也诱导p53。 通过螯合铁诱导HL-60细胞凋亡。 经过1μM去铁胺处理48小时后,DNA明显断裂。 细胞经1μM去铁胺处理仅24小时后发生凋亡;48小时后观察到核坍塌。 一些研究表明,它具有抗氧化性能,并保护细胞免受H2O2诱导的损伤。

包装

Unit quantity: 30 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity please visit British Pharmacopoeia

其他说明

Sales restrictions may apply.

基本信息

经验(实验)分子式C25H48N6O8 · CH4O3S
分子量656.79
MDL编号MFCD00058605

产品性质

等级pharmaceutical primary standard
manufacturer/tradenameBP
格式neat
储存温度2-8℃
SMILES stringCS(O)(=O)=O.CC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCN
InChI1S/C25H48N6O8.CH4O3S/c1-21(32)29(37)18-9-3-6-16-27-22(33)12-14-25(36)31(39)20-10-4-7-17-28-23(34)11-13-24(35)30(38)19-8-2-5-15-26;1-5(2,3)4/h37-39H,2-20,26H2,1H3,(H,27,33)(H,28,34);1H3,(H,2,3,4)
InChI keyIDDIJAWJANBQLJ-UHFFFAOYSA-N

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 2
闪点(F)Not applicable
闪点(C)Not applicable
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