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Key Documents

15052

Sigma-Aldrich

Boc-Ala-ONp

≥96.0% (HPLC)

同義詞:

Boc-L-丙氨酸-4-硝基苯酯

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About This Item

經驗公式(希爾表示法):
C14H18N2O6
CAS號碼:
分子量::
310.30
Beilstein:
1892073
EC號碼:
MDL號碼:
分類程式碼代碼:
12352202
PubChem物質ID:
NACRES:
NA.22

化驗

≥96.0% (HPLC)

反應適用性

reaction type: Boc solid-phase peptide synthesis

應用

peptide synthesis

儲存溫度

2-8°C

SMILES 字串

C[C@H](NC(=O)OC(C)(C)C)C(=O)Oc1ccc(cc1)[N+]([O-])=O

InChI

1S/C14H18N2O6/c1-9(15-13(18)22-14(2,3)4)12(17)21-11-7-5-10(6-8-11)16(19)20/h5-9H,1-4H3,(H,15,18)/t9-/m0/s1

InChI 密鑰

SUHFNHHZORGDFI-VIFPVBQESA-N

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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

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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分析證明 (COA)

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J L Sohl et al.
Biochemistry, 36(13), 3894-3902 (1997-04-01)
alpha-Lytic protease, a chymotrypsin-like serine protease, is synthesized with an N-terminal 166 amino acid pro region which is absolutely required for folding of the protease. The pro region is also the most potent inhibitor of the protease known with a
H M Korchak et al.
The Journal of biological chemistry, 259(12), 7439-7445 (1984-06-25)
Activated neutrophils aggregate, generate superoxide (O-2), and degranulate. The role of Ca as "second messenger" in neutrophil activation was examined using as agonist the chemotactic peptide fMet-Leu-Phe and its antagonist t-butoxycarbonyl-Phe-Leu-Phe-Leu-Phe to systematically vary the time of receptor occupancy. Release

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