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化驗
≥98.0% (sum of enantiomers, HPLC)
光學活性
[α]20/D −18±1°, c = 1% in DMF
反應適用性
reaction type: Fmoc solid-phase peptide synthesis
mp
141-144 °C (lit.)
應用
peptide synthesis
官能基
Fmoc
儲存溫度
2-8°C
SMILES 字串
CCCC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
InChI
1S/C21H23NO4/c1-2-3-12-19(20(23)24)22-21(25)26-13-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,18-19H,2-3,12-13H2,1H3,(H,22,25)(H,23,24)/t19-/m0/s1
InChI 密鑰
VCFCFPNRQDANPN-IBGZPJMESA-N
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儲存類別代碼
13 - Non 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)
Oncogene (2018-06-22)
The antiviral metabolites from bacterial stress response to bacteriophage infection can maintain homeostasis of host cells, while metabolism disorder is a remarkable characteristic of tumorigenesis. In the aspect of metabolic homeostasis, therefore, the antiviral homeostasis-maintaining metabolites of bacteria may possess
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