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(S)-METHYL 2-((S)-2-AMINO-4-METHYLPENTANAMIDO)-4-METHYLPENTANOATE HYDROBROMIDE structure, CAS 16689-14-8

(S)-METHYL 2-((S)-2-AMINO-4-METHYLPENTANAMIDO)-4-METHYLPENTANOATE HYDROBROMIDE

CAS Number16689-14-8

Synonymsmethyl 2-[(2-amino-4-methylpentanoyl)amino]-4-methylpentanoate,hydrobromide; LLME,HBr Leu-Leu-Ome,HBr

Molecular FormulaC13H27BrN2O3

Molecular Weight339.27

Purity≥97 (TLC)%

Density

Boiling Point

Melting Point

Flash Point

Appearancepowder

EINECS0

MSDSChineseEnglish

Symboltransportation

Signal WordWarning

Cat. No.: 2A-0102015 Purity: ≥97 (TLC)%
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Quality Control of [ 16689-14-8 ] Purity: ≥97 (TLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number16689-14-8
Catalog No.2A-0102015
Chinese NameH-Leu-Leu-OMe·HCl
Synonymsmethyl 2-[(2-amino-4-methylpentanoyl)amino]-4-methylpentanoate,hydrobromide; LLME,HBr Leu-Leu-Ome,HBr
Molecular FormulaC13H27BrN2O3
Molecular Weight339.27
Purity≥97 (TLC)
Appearancepowder
Storage Condition-20°C, sealed, dry
ApplicationL-Leucyl-L-Leucine methyl ester (LLOMe) hydrobromide is a dipeptide condensation product of L-leucine methyl ester produced by human monocytes or polymorphonuclear leukocytes and can selectively elimi
EINECS0
HTC2924199090
UN(IATA)0
PubChem ID24896476
MDL NumberMFCD00216855
SMILESBr.COC(=O)C(CC(C)C)NC(=O)C(N)CC(C)C
InChI1S/C13H26N2O3.BrH/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
InChI KeyQIPBCIHWFATZOF-UHFFFAOYSA-N
NACRES CodeNA.26
UNSPSC12352209
Hazard Symbolstransportation
MSDSmsds/102015_1_16689_14_8.pdf
BioactivityL-Leucyl-L-Leucine methyl ester (LLOMe) hydrobromide, a dipeptide condensation product of L-leucine methyl ester generated by human monocytes or polymorphonuclear leukocytes, selectively eliminates lymphocytes with cytotoxic potential. L-Leucyl-L-Leucine methyl ester hydrobromide also can induce endolysosomal pathway stress[1][2][3]. Related Catalog Research Areas >> Inflammation/Immunology In Vitro L-Leucyl-L-Leucine methyl ester (1 mM; 0.5-2 h) enhances LRRK2-mediated Rab10 and Rab12 phosphorylation in MEFs and A549 cells[3]. L-Leucyl-L-Leucine methyl ester (10-250 μM; 15 min) is converted to a CCI3COOH-insoluble product by CD4- lymphocytes[2]. References [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 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. Chemical & Physical Properties Molecular Formula C13H27BrN2O3 Molecular Weight 339.26900 Exact Mass 338.12100 PSA 81.42000 LogP 3.11300 InChIKey QIPBCIHWFATZOF-ACMTZBLWSA-N SMILES Br.COC(=O)C(CC(C)C)NC(=O)C(N)CC(C)C
Use ofL-Leucyl-L-Leucine methyl ester (LLOMe) hydrobromide, a dipeptide condensation product of L-leucine methyl ester generated by human monocytes or polymorphonuclear leukocytes, selectively eliminates lymphocytes with cytotoxic potential. L-Leucyl-L-Leucine methyl ester hydrobromide also can induce endolysosomal pathway stress[1][2][3]. Properties Name Leu-Leu methyl ester hydrobromide Synonym More Synonyms Biological Activity Description L-Leucyl-L-Leucine methyl ester (LLOMe) hydrobromide, a dipeptide condensation product of L-leucine methyl ester generated by human monocytes or polymorphonuclear leukocytes, selectively eliminates lymphocytes with cytotoxic potential. L-Leucyl-L-Leucine methyl ester hydrobromide also can induce endolysosomal pathway stress[1][2][3]. Related Catalog Research Areas >> Inflammation/Immunology References [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 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. Chemical & Physical Properties Molecular Formula C13H27BrN2O3 Exact Mass 338.12100 PSA 81.42000 LogP 3.11300 InChIKey QIPBCIHWFATZOF-ACMTZBLWSA-N SMILES Br.COC(=O)C(CC(C)C)NC(=O)C(N)CC(C)C
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 30.0%
Transport InfoProduct name: Purity: 97.0%
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available
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