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A5730

Sigma-Aldrich

Abz-SDK(Dnp)P-OH 三氟乙酸盐

≥91% (HPLC), lyophilized powder

别名:

o-aminobenzoic acid-Ser-Asp-Lys(DNP)Pro-OH 三氟乙酸盐

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About This Item

经验公式（希尔记法）:
C31H38N8O13 · xC2HF3O2
CAS号:
1217465-57-0
分子量:
730.68 (free base basis)
MDL號碼:
MFCD09753055
分類程式碼代碼:
12352200
PubChem物質ID:
24891013
NACRES:
NA.77

品質等級

100

化驗

≥91% (HPLC)

形狀

lyophilized powder

溶解度

H2O: freely soluble

儲存溫度

2-8°C

SMILES 字串

OC(=O)C(F)(F)F.Nc1ccccc1C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCNc2ccc(cc2[N+]([O-])=O)[N+]([O-])=O)C(=O)N3CCC[C@H]3C(O)=O

InChI

1S/C31H38N8O13.C2HF3O2/c32-19-7-2-1-6-18(19)27(43)36-23(16-40)29(45)35-22(15-26(41)42)28(44)34-21(30(46)37-13-5-9-24(37)31(47)48)8-3-4-12-33-20-11-10-17(38(49)50)14-25(20)39(51)52;3-2(4,5)1(6)7/h1-2,6-7,10-11,14,21-24,33,40H,3-5,8-9,12-13,15-16,32H2,(H,34,44)(H,35,45)(H,36,43)(H,41,42)(H,47,48);(H,6,7)/t21-,22-,23-,24-;/m0./s1

InChI 密鑰

IFSUGURCQHMSJS-JPIABUGISA-N

相关类别

Amino Acid Sequence

Abz-Ser-Asp-Lys-DNP

應用

Abz-SDK(Dnp)P-OH trifluoroacetate is an Angiotensin Converting Enzyme (ACE) fluorescent peptide substrate that specifically binds to the N domain of ACE. Abz-SDK(Dnp)P-OH has been used to study tipifarnib-induced apoptosis in acute myeloid leukemia and multiple myeloma cells.

生化／生理作用

Abz-SDK(Dnp)P-OH is an Angiotensin Converting Enzyme (ACE) fluorescent peptide substrate specific for the N domain for real time fluorescent assay (ACE, Peptidyl Dipeptidase, Kininase II, E.C. 3.4.15.1).

特點和優勢

This compound is featured on the Angiotensin Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
037K4704V
037K4704

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Christopher D Cerruti et al.
Analytical and bioanalytical chemistry, 401(1), 75-87 (2011-03-08)
Mass spectrometry imaging of lipids using MALDI-TOF/TOF mass spectrometers is of growing interest for chemical mapping of organic compounds at the surface of tissue sections. Many efforts have been devoted to the best matrix choice and deposition technique. Nevertheless, the
Niranjan Yanamandra et al.
The Journal of pharmacology and experimental therapeutics, 337(3), 636-643 (2011-03-08)
A major contributing factor to the high mortality rate associated with acute myeloid leukemia and multiple myeloma is the development of resistance to chemotherapy. We have shown that the combination of tipifarnib, a nonpeptidomimetic farnesyltransferase inhibitor (FTI), with bortezomib, a
Jun Lu et al.
Bioorganic & medicinal chemistry, 18(21), 7628-7638 (2010-10-05)
An efficient synthesis has provided access to a novel α-tocopherol analogue (2), as well as its trifluoroacetate salt and acetate ester. An annulation reaction was used to establish the pyridinol core structure and a Stille coupling reaction was employed for

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