
Hello Bio/Dephostatin/HB0236/1mg
市场价:
¥2749.50
美元价:
2115.00
产品分类:
酸碱缓冲液
联系Q Q:
3392242852
电话号码:
4000-520-616
电子邮箱:
info@ebiomall.com
商品介绍
Product overview
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NameDephostatin
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Short descriptionCompetitive PTPase inhibitor
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Biological descriptionCompetitive tyrosine phosphatase (PTPase) inhibitor (IC50 = 7.7 µM). Enhances the release of amylase and intracellular calcium. Displays antibacterial and growth inhibition properties.
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Biological actionInhibitor
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Purity>90%
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Properties
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Chemical name2,5-Dihydroxy-N-methyl-N-nitrosoaniline
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Molecular Weight168.15
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Chemical structure
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Molecular FormulaC7H8N2O3
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CAS Number151606-30-3
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PubChem identifier5353574
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SMILESC1(=CC=C(C=C1N(N=O)C)O[H])O[H]
Storing and Using Your Product
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Solubility overviewsoluble in chloroform or DMSO (22mg/ml)
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ImportantThis product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.
References for Dephostatin
Dephostatin, a novel protein tyrosine phosphatase inhibitor produced by Streptomyces. I. Taxonomy, isolation, and characterization.
Imoto M et al (1993) J Antibiot (Tokyo) 46(9) : 1342-6.PubMedID: 8226312Effect of dephostatin on intracellular free calcium concentration and amylase secretion in isolated rat pancreatic acinar cells.
Lajas AI et al (2000) Mol Cell Biochem 205(1-2) : 163-9.PubMedID: 10821434Dephostatin, a novel protein tyrosine phosphatase inhibitor produced by Streptomyces. II. Structure determination.
Kakeya H et al (1993) J Antibiot (Tokyo) 46(11) : 1716-9.PubMedID: 8270494
品牌介绍
Hello Bio是由一群经验丰富的科学家和化学家们创立的充满活力的生物企业,总部位于英国布里斯托尔,在美国普林斯顿设有分公司,主旨在于提供质优价廉的生命科学研究工具,主要产品线为小分子化合物,如激动剂、拮抗剂、抑制剂等,部分产品价格甚至低至其他供应商的50%。热销产品线:酶抑制剂和激动剂ROCK inhibitor Y-27632, PKA inhibitor KT 5720 , adenylyl cyclase activator Forskolin, and novel GRK2/3 inhibitor Cmpd101等。 离子通道调节剂NMDA antagonist D-AP5, sodium channel blocker tetrodotoxin citrate, TRP antagonist capsazepine, and GABAA antagonist SR 95531 等。信号通路工具各种信号通路抑制剂、激动剂表观遗传学研究工具potent HDAC inhibitor Trichostatin A, DNA methyltransferase inhibitor 5-aza-2'-deoxycytidine,BET bromodomain inhibitor (+)-JQ1 and potent,selective GLP / G9a HMTase inhibitor BIX 01294 等受体配体novel selective GRK2/3 inhibitor, NMDA antagonist D-AP5, Group I mGlu agonist (S)-3,5-DHPG, and GABAA antagonist SR 95531.等干细胞调节剂ROCK inhibitor Y-27632, SB 431542 DAPT.
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