15052
Boc-Ala-ONp
≥96.0% (HPLC)
Synonym(s):
Boc-L-alanine 4-nitrophenyl ester
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About This Item
Empirical Formula (Hill Notation):
C14H18N2O6
CAS Number:
Molecular Weight:
310.30
UNSPSC Code:
12352202
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-621-5
Beilstein/REAXYS Number:
1892073
MDL number:
InChI key
SUHFNHHZORGDFI-VIFPVBQESA-N
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
SMILES string
C[C@H](NC(=O)OC(C)(C)C)C(=O)Oc1ccc(cc1)[N+]([O-])=O
assay
≥96.0% (HPLC)
reaction suitability
reaction type: Boc solid-phase peptide synthesis
application(s)
peptide synthesis
storage temp.
2-8°C
Quality Level
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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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