추천 제품
분석
98%
형태
powder
반응 적합성
reaction type: solution phase peptide synthesis
mp
192-195 °C (lit.)
응용 분야
peptide synthesis
SMILES string
NCCCCCCC(O)=O
InChI
1S/C7H15NO2/c8-6-4-2-1-3-5-7(9)10/h1-6,8H2,(H,9,10)
InChI key
XDOLZJYETYVRKV-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Is there any need for a TAFI(a) inhibitor as thrombolytic drug?
Ellen Vercauteren et al.
Thrombosis research, 130(4), 574-575 (2012-07-31)
V S De Serrano et al.
Biochemistry, 32(14), 3540-3548 (1993-04-13)
The involvement of specific aspartic acid (D) and glutamic acid (E) residues of the recombinant (r) kringle 2 (K2) domain of tissue-type plasminogen activator (tPA) in stabilizing its interaction with omega-amino acid ligands has been assessed by examination of these
Tomoyuki Sasaki et al.
Thrombosis research, 130(4), e222-e228 (2012-07-17)
Thrombin-activatable fibrinolysis inhibitor (TAFI) is a plasma zymogen that is activated by thrombin in plasma. In fibrinolytic processes, carboxy-terminal lysine (Lys) residues in partially degraded fibrin are important sites for plasminogen binding and activation, and an active form of TAFI
V S De Serrano et al.
Biochemistry, 31(47), 11698-11706 (1992-12-01)
The properties of the cationic locus within the recombinant (r) kringle 2 domain (residues 180-261) of tissue-type plasminogen activator ([K2tPA]) that are responsible for stabilization of its interaction with the carboxylate moiety of omega-amino acid ligands have been assessed by
Surface interactions of a homologous series of alpha,omega-amino acids on colloidal silver and gold.
A A Ooka et al.
Biospectroscopy, 5(1), 9-17 (1999-04-29)
Surface enhanced Raman spectroscopy (SERS) was used to characterize a homologous series of alpha,omega-amino acids on colloidal gold and silver. Raman and SER spectra of the alpha,omega-amino acids, NH2(CH2)nCOOH (n = 3-7), are presented and analyzed, revealing the probable conformations
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