H-Leu-Leu-Ome.Hcl (S)-2-((S)-2-氨基-4-甲基戊酰胺基)-4-甲基戊酸甲酯盐酸盐
CAS 6491-83-4 MFCD06491834
化学结构图
SMILES: COC(=O)C(CC(C)C)NC(=O)C(N)CC(C)C.Cl
化学属性
| Mol. Weight | 295 |
|---|---|
| Mol. Formula | C13H27ClN2O3 |
别名和识别编码
| Chemical Name Translation | (S)-2-((S)-2-氨基-4-甲基戊酰胺基)-4-甲基戊酸甲酯盐酸盐 |
|---|---|
| LabNetwork Molecule ID | LN01315594 |
| PubChem Substance ID | 15598024 |
| InChI | InChI=1S/C13H26N2O3.ClH/c1-8(2)6-10(14)12(16)15-11(7-9(3)4)13(17)18-5;/h8-11H,6-7,14H2,1-5H3,(H,15,16);1H/t10-,11-;/m0./s1 |
| MDL Number | |
| CAS Number | 6491-83-4 |
| Chemical Name | H-Leu-Leu-Ome.Hcl |
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相关文献及参考
- [2]. Thiele DL, et, al. Mechanism of L-leucyl-L-leucine methyl ester-mediated killing of cytotoxic lymphocytes: dependence on a lysosomal thiol protease, dipeptidyl peptidase I, that is enriched in these cells. Proc Natl Acad Sci U S A. 1990 Jan;87(1):83-7.
- [3]. Kalogeropulou AF, et, al. Endogenous Rab29 does not impact basal or stimulated LRRK2 pathway activity. Biochem J. 2020 Nov 27;477(22):4397-4423.
- [1]. Thiele DL, et, al. The immunosuppressive activity of L-leucyl-L-leucine methyl ester: selective ablation of cytotoxic lymphocytes and monocytes. J Immunol. 1986 Feb 1;136(3):1038-48.
- [1]. Thiele DL, et, al. The immunosuppressive activity of L-leucyl-L-leucine methyl ester: selective ablation of cytotoxic lymphocytes and monocytes. J Immunol. 1986 Feb 1;136(3):1038-48.
- [2]. Thiele DL, et, al. Mechanism of L-leucyl-L-leucine methyl ester-mediated killing of cytotoxic lymphocytes: dependence on a lysosomal thiol protease, dipeptidyl peptidas
