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Boc-N-methyl-L-leucine

Boc-N-methyl-L-leucine Structure
CAS No.
53363-89-6
Chemical Name:
Boc-N-methyl-L-leucine
Synonyms
Tyr(Me);BOC-MELEU-OH;BOC-LEU(ME)-OH;BOC-L-MELEU-OH;BOC-ALA(TBU)-OH;BOC-N-ME-LEU-OH;BOC-N-ME-LEUCINE;Boc-N-Me-L-Leu-OH;BOC-BETA-TBU-ALA-OH;BOC-BETA-TBU-ALANINE
CBNumber:
CB3197622
Molecular Formula:
C12H23NO4
Molecular Weight:
245.32
MOL File:
53363-89-6.mol
MSDS File:
SDS
Modify Date:
2024/7/2 8:55:06

Boc-N-methyl-L-leucine Properties

Melting point 55-60 °C
Boiling point 338.2±21.0 °C(Predicted)
Density 1.053±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
pka 4.04±0.21(Predicted)
form Solid
color White to off-white
optical activity [α]20/D 36±2°, c = 1% in methylene chloride
BRN 2373250
InChI InChI=1S/C12H23NO4/c1-8(2)7-9(10(14)15)13(6)11(16)17-12(3,4)5/h8-9H,7H2,1-6H3,(H,14,15)/t9-/m0/s1
InChIKey YXJFAOXATCRIKU-VIFPVBQESA-N
SMILES C(O)(=O)[C@H](CC(C)C)N(C(OC(C)(C)C)=O)C
CAS DataBase Reference 53363-89-6(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
WGK Germany  3
HS Code  2924 19 00
HazardClass  IRRITANT

Boc-N-methyl-L-leucine price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 8.53083 Boc-N-Me-Leu-OH Novabiochem? 53363-89-6 5G ₹9270 2022-06-14 Buy
Sigma-Aldrich(India) 15446 Boc-N-Me-Leu-OH ≥99.0% (sum of enantiomers, TLC) 53363-89-6 5G ₹20870.6 2022-06-14 Buy
Product number Packaging Price Buy
8.53083 5G ₹9270 Buy
15446 5G ₹20870.6 Buy

Boc-N-methyl-L-leucine Chemical Properties,Uses,Production

Description

Boc-N-methyl-L-leucine is the BOC (tert-butyloxycarbonyl) protected N-methylated leucine. The N-methylated amino acid is quite useful in the peptide synthesis, giving a lot of improved properties to peptide. Studies have shown that peptide containing N-methylated amino acids obtain increased proteolytic stability, increased membrane permeability, and altered conformation. The effects of N-methylated amino acids are quite important in the development of therapeutic peptide compound as well as in the assay of biological activity of some modified peptides. BOC group can be easily removed by treatment with strong acids such as trifluoroacetic acid.

Biological Activity

Boc-N-methyl-L-leucine is a peptidyl nucleobase that has been shown to inhibit tumor cell growth and induce tumor regression in animal models. It is an amide of leucine and the antibiotic aminouracil, which is a guanine analogue. Boc-N-methyl-L-leucine has also shown to inhibit tumor growth by inhibiting mitochondrial membrane potential, which may lead to cell death in cancer cells. This compound has been shown to be effective against both solid tumors and leukemia cell lines. Boc-N-methyl-L-leucine also inhibits the proliferation of human prostate cancer cells by blocking the synthesis of nucleic acids and proteins.

References

https://en.wikipedia.org/wiki/Tert-Butyloxycarbonyl_protecting_group
http://pubs.acs.org/doi/abs/10.1021/cr030024z?src=recsys&journalCode=chreay

Boc-N-methyl-L-leucine Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 171)Suppliers
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A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
Capot Chemical Co.,Ltd. 571-85586718 +8613336195806 China 29798 60 Inquiry
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SIMAGCHEM CORP +86-13806087780 China 17367 58 Inquiry
Hubei Ipure Biology Co., Ltd +8613367258412 China 10326 58 Inquiry

Boc-N-methyl-L-leucine Spectrum

N-ALPHA-T-BUTYLOXYCARBONYL-N-ALPHA-METHYL-L-LEUCINE N-ALPHA-T-BUTOXYCARBONYL-N-ALPHA-METHYL-L-LEUCINE N-ALPHA-T-BUTOXYCARBONYL-BETA-T-BUTYL-L-ALANINE N-ALPHA-T-BUTOXYCARBONYL-GAMMA-METHYL-L-LEUCINE N-ALPHA-TERT-BUTYLOXYCARBONYL-N-ALPHA-METHYL-L-LEUCINE N-ALPHA-T-BOC-N-ALPHA-METHYL-L-LEUCINE BOC-BETA-TBU-ALANINE BOC-BETA-TBU-ALA-OH BOC-BETA-T-BUTYL-L-ALANINE BOC-ALA(TBU)-OH BOC-N-ME-LEUCINE BOC-N-ME-LEU-OH BOC-N-METHYL-L-LEUCINE BOC-N-METHYL-L-LEU-OH BOC-MELEU-OH BOC-NEOPENTYLGLYCINE BOC-(NEOPENTYL)GLY-OH BOC-N-ALPHA-METHYL-L-LEUCINE BOC-L-BETA-T-BUTYLALANINE BOC-LEU(ME)-OH BOC-L-NEOPENTYLGLYCINE BOC-L-MELEU-OH BOC-T-BUTYL-L-ALANINE N-ALPHA-TERT-BUTYLOXYCABONYL-N-ALPHA-METHYL-L-LEUCINE DANSYL-L-GLUTAMIC ACID BIS(CYCLOHEXYLAMMONIUM) NALPHA-tert-Butoxycarbonyl-N-methyl-L-leucine N-tert-Butyloxycarbonyl-N-methyl-L-leucine N-(tert-butoxycarbonyl)-N-methyl-L-leucine L-Leucine, N-[(1,1-diMethylethoxy)carbonyl]-N-Methyl- (S)-2-((tert-butoxycarbonyl)(Methyl)aMino)-4-Methylpentanoic acid Tyr(Me) Boc-N-Me-L-Leu-OH Boc-N-Me-Leu-OH Boc-N-Methyl Leucine Boc-N-methyl-L-leucine98+% N-α-t-butoxycarbonyl-β-t-butyl-L-alanine (Tert-Butoxy)Carbonyl N-Me-Leu-OH (2S)-2-{[(tert-butoxy)carbonyl](methyl)amino}-4-methylpentanoic acid (2S)-4-methyl-2-[methyl-[(2-methylpropan-2-yl)oxy-oxomethyl]amino]pentanoic acid Boc-N-L-methylleucine Boc-N-methyl-L-leucine USP/EP/BP 2-((TERT-BUTOXYCARBONYL)(METHYL)AMINO)-4-METHYLPENTANOIC ACID N-[(1,1-Dimethylethoxy)carbonyl]-N-methyl-L-leucine N-BOC-N-Methyl-L-leucine BOC-N-methyl tert leucine 53363-89-6 Peptide Synthesis N-Methyl Amino Acids Unnatural Amino Acid Derivatives Specialty Synthesis amino acids Amino Acid Derivatives N-Methyl Amino Acids