品牌咨询
联系方式
公司地址
苏州工业园区生物纳米园A4#216
联系电话
4000-520-616 / 18915418616
传真号码
0512-67156496
电子邮箱
info@ebiomall.com
公司网址
https://www.ebiomall.com

ApexBio/Pepstatin A/10mM (in 1mL DMSO)/A2571

价格
¥5600.00
货号:A2571
浏览量:69
品牌:ApexBio
服务
全国联保
正品保证
正规发票
签订合同
商品描述
Related Products
  • o-Phenanthroline
  • E-64
  • Aprotinin
  • Phosphoramidon Disodium Salt
  • Bestatin
  • AEBSF.HCl
Molarity CalculatorDilution Calculator
Pepstatin AAspartic proteinases inhibitor

Catalog No.A2571
SizePriceStockQty
10mM (in 1mL DMSO)
$50.00
In stock
10mg
$45.00
In stock
50mg
$160.00
In stock
100mg
$280.00
In stock

Tel: +1-832-696-8203

Email: sales@apexbt.com

Worldwide Distributors

Sample solution is provided at 25 µL, 10mM.

Product Citations

1. Ying Long, Xuri Zhang, et al. "Initial events in the breakthrough of the epithelial barrier of the small intestine by Angiostrongylus cantonensis." Arch Biol Sci. 2016;68(2):375-383

Related Compound Libraries

  • DiscoveryProbe™ Bioactive Compound Library
  • DiscoveryProbe™ Protease Inhibitor Library

Quality Control

Quality Control & MSDS

View current batch:
    Purity = 98.58%
  • COA (Certificate Of Analysis)
  • HPLC
  • NMR (Nuclear Magnetic Resonance)
  • MSDS (Material Safety Data Sheet)
  • Datasheet

Chemical structure

Pepstatin A

Related Biological Data

CORM-3

Protocol

Kinase experiment [1]:

Binding assays

The inhibition of HIV protease, pepsin and cathepsin D activities was assayed using the solid-phase immunoassay at pH 5.6. After induction and harvesting, cells (50 g) were resuspended in 100 ml of 10 mM Tris-HCl buffer, pH 7.5, 1 mM EDTA, 1 mM DTT, 1 mM PMSF and 0.05% Triton X-100, sonicated and centrifuged at 10000g for 20 min, HIV-I protease activity in E. coli extracts was assayed by cleavage of a synthetic heptapeptide substrate and HPLC analysis of proctucts.

Cell experiment [2, 3]:

Cell lines

H9 cells, Bone marrow cells

Preparation method

The solubility of this compound in DMSO is >34.3mg/mL. General tips for obtaining a higher concentration: Please warm the tube at 37 ℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months.

Reacting condition

0.1 mM for 2, 4, or 11 days, 37 ℃

Applications

Pepstatin A inhibited the proteolytic processing of the HIV gag precursor in H9 cells. Pepstatin A inhibited the production of infectious HIV in H9 cell cultures. Pepstatin A (15–120 μM) dose-dependently suppressed the formation of TRAP-positive multinuclear cells. Pepstatin A dose-dependently suppressed the RANKL-induced osteoclastogenesis from stromal cell–deprived bone marrow cells in the co-culture system and bone marrow culture. Pepstatin A (15 μM) substantially inhibited the aspartic proteinase activity in bone marrow cells, while complete inhibition was seen at 90 μM.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1]. Sarubbi E, Seneci P F, Angelastro M R, et al. Peptide aldehydes as inhibitors of HIV protease. FEBS letters, 1993, 319(3): 253-256.

[2]. von der Helm K, Gürtler L, Eberle J, et al. Inhibition of HIV replication in cell culture by the specific aspartic protease inhibitor pepstatin A. FEBS letters, 1989, 247(2): 349-352.

[3] Yoshida H, Okamoto K, Iwamoto T, et al. Pepstatin A, an aspartic proteinase inhibitor, suppresses RANKL-induced osteoclast differentiation. Journal of biochemistry, 2006, 139(3): 583-590. >

Pepstatin A Dilution Calculator

Concentration (start)
x
Volume (start)
=
Concentration (final)
x
Volume (final)
C1
V1
C2
V2

calculate

Pepstatin A Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
g/mol

calculate

Chemical Properties

Cas No. 26305-03-3SDF Download SDF
Synonyms Pepstatin A,NSC272671,Isoval-Val-Val-Sta-Ala-Sta
Chemical Name 3-hydroxy-4-[2-[[3-hydroxy-6-methyl-4-[[3-methyl-2-[[3-methyl-2-(3-methylbutanoylamino)butanoyl]amino]butanoyl]amino]heptanoyl]amino]propanoylamino]-6-methylheptanoic acid
Canonical SMILES CC(C)CC(C(CC(=O)O)O)NC(=O)C(C)NC(=O)CC(C(CC(C)C)NC(=O)C(C(C)C)NC(=O)C(C(C)C)NC(=O)CC(C)C)O
Formula C34H63N5O9 M.Wt 685.9
Solubility ≥34.3mg/mL in DMSO Storage Store at -20°C
Physical AppearanceA solidShipping ConditionEvaluation sample solution : ship with blue ice.All other available size:ship with RT , or blue ice upon request
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.

Background

Pepstatin A is a well-known inhibitor of aspartic proteinases with IC50 values of 15 μM, 2 μM, < 5 nM and < 40 nM for human renin, HIV protease, pepsin and cathepsin D, respectively [1, 2].

Pepstatin A is a pentapeptide. It was originally isolated from the microbe. As a most potent renin inhibitor, pepstatinA inhibited porcine renin and human renin at weak acid pH value with IC50 values of 0.32 and 15 μM, respectively. The disadvantage is that, pepstatin Ais hydrophobic. To couple the charged hydrophilic residues to the C-terminal of pepstatinA can increase its solubility. Besides the renin, pepstatin A was also reported to have inhibitory effects on HIV protease and subsequently suppressed the virus replication. In cultured H9 cells, pepstatinA treatment blocked the proteolytic processing of the virus gag precursor and inhibited the production of infectious HIV. Moreover, pepstatin A was found to inhibit osteoclast differentiation due to its inhibitory efficacy of cathepsin D and E [1, 3 and 4].

References: 1. Eid M, Evin G, Castro B, et al.New renin inhibitors homologous with pepstatin.Biochem. J, 1981, 197: 465-471.2. Sarubbi E, Seneci P F, Angelastro M R, et al. Peptide aldehydes as inhibitors of HIV protease. FEBS letters, 1993, 319(3): 253-256.3. von der Helm K, Gürtler L, Eberle J, et al. Inhibition of HIV replication in cell culture by the specific aspartic protease inhibitor pepstatin A. FEBS letters, 1989, 247(2): 349-352.4. Yoshida H, Okamoto K, Iwamoto T, et al. Pepstatin A, an aspartic proteinase inhibitor, suppresses RANKL-induced osteoclast differentiation. Journal of biochemistry, 2006, 139(3): 583-590.>

ApexBio的3X FLAG Peptide FLAG标签系统利用与目标蛋白质1融合的短而亲水的8个氨基酸的肽段。FLAG肽与抗体M1结合。结合是钙依赖性方式2还是非依赖性3仍存在争议。该系统的缺点是单克隆抗体纯化基质不如其他基质稳定。通常,可以用特异性单克隆抗体检测小标签。为了改善对FLAG标签的检测,已经开发了3x FLAG系统。这种三级FLAG表位是亲水的,长22个氨基酸,可以检测到高达10 fmol的表达融合蛋白。激烈热球菌的带有FLAG标签的麦芽糖糊精结合蛋白已被结晶4,其晶体质量与未标记蛋白的晶体质量非常相似。 最后,可以通过用肠激酶处理去除FLAG标签,肠激酶对肽序列5的5个C末端氨基酸具有特异性。