推荐产品
方案
98%
表单
solid
旋光性
[α]/D +22.8°, c = 1.2 in 1 M HCl
mp
93-95 °C (lit.)
官能团
amine
hydroxyl
phenyl
SMILES字符串
N[C@@H](CO)Cc1ccccc1
InChI
1S/C9H13NO/c10-9(7-11)6-8-4-2-1-3-5-8/h1-5,9,11H,6-7,10H2/t9-/m1/s1
InChI key
STVVMTBJNDTZBF-SECBINFHSA-N
警示用语:
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
Gretta C M'bitsi-Ibouily et al.
Scientific reports, 9(1), 4146-4146 (2019-03-13)
Sulpiride (SPR) is a selective antagonist of central dopamine receptors but has limited clinical use due to its poor pharmacokinetics. The aim of this study was to investigate how metal ligation to SPR may improve its solubility, intestinal permeability and
W W Mak et al.
Canadian journal of biochemistry, 58(12), 1421-1429 (1980-12-01)
The activities of a range of phenylalaninol-related compounds on capping of concanavalin A and induction of rounding of Chinese hamster ovary tsHl cells, as well as on the fluidity of phosphatidylcholine-cholesterol (1:1) liposomes, have been examined. These compounds include phenylalaninol
G P Zecchini et al.
Archiv der Pharmazie, 328(9), 673-676 (1995-09-01)
The synthesis and the biological activity towards human neutrophils of some N-formyl-Met-Leu-Phe-OMe analogues containing (S)-phenylalaninol (Pheol) or its derivatives in place of the native phenylalanine are reported. While the analogue containing Pheol (4) was found to be devoid of significant
H Hashizume et al.
Chemical & pharmaceutical bulletin, 40(11), 3113-3114 (1992-11-01)
The effects of phenylalaninol (D-isomer) on gastric acid secretion and gastric ulcer were studied in rats. The compound reduced the gastric acid secretion stimulated by intracisternal thyrotropin releasing hormone and intravenous 2-deoxy-D-glucose, but not that stimulated by subcutaneous carbachol or
B Weiss et al.
Research communications in chemical pathology and pharmacology, 62(1), 113-123 (1988-10-01)
An amino acid derivative, leucinethiol, was reported to be a strong inhibitor of aminopeptidase activity. In order to obtain selective inhibitors of various brain aminopeptidases, we tested the inhibition by amino acid analogs of brain aminopeptidase activity. In particular, we
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