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About This Item
化学式:
C6H5CH2CH2CH(NH2)CO2H · HCl
CAS番号:
分子量:
215.68
MDL番号:
UNSPSCコード:
12352209
PubChem Substance ID:
NACRES:
NA.22
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品質水準
アッセイ
97%
光学活性
[α]20/D +38°, c = 1 in 3 M HCl
反応適合性
reaction type: solution phase peptide synthesis
mp
262-265 °C (dec.) (lit.)
アプリケーション
peptide synthesis
SMILES記法
Cl.N[C@@H](CCc1ccccc1)C(O)=O
InChI
1S/C10H13NO2.ClH/c11-9(10(12)13)7-6-8-4-2-1-3-5-8;/h1-5,9H,6-7,11H2,(H,12,13);1H/t9-;/m0./s1
InChI Key
CHBMONIBOQCTCF-FVGYRXGTSA-N
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
Eyeshields, Gloves, type N95 (US)
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
544051-1G:
544051-VAR:
544051-5G:
544051-BULK:
最新バージョンのいずれかを選択してください：
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A series of highly potent and selective inhibitors of DPP-4 was optimized for ADMET properties. The effort resulted in the discovery of inhibitor 1g, that exhibits excellent efficacy in an oral glucose tolerance test and an attractive pharmacokinetic profile.
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European journal of medicinal chemistry, 44(9), 3731-3738 (2009-06-03)
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Biotechnology progress, 25(6), 1637-1642 (2009-09-22)
L-Homophenylalanine (L-HPA) and N(6)-protected-2-oxo-6-amino-hexanoic acid (N(6)-protected-OAHA) can be used as building blocks for the manufacture of angiotensin-converting enzyme inhibitors. To synthesize L-HPA and N(6)-protected-OAHA simultaneously from 2-oxo-4-phenylbutanoic acid (OPBA) and N(6)-protected-L-lysine, several variants of Escherichia coli aspartate aminotransferase (AAT) were
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