Boc-Cys(Mbzl)-OH
Bioactive Reagents
Leucine is one of nine essential amino acids in humans (provided by food), Leucine is important for protein synthesis and many metabolic functions. Leucine contributes to regulation of blood-sugar levels; growth and repair of muscle and bone tissue; growth hormone production; and wound healing. Leucine also prevents breakdown of muscle proteins after trauma or severe stress and may be beneficial for individuals with phenylketonuria. Leucine is available in many foods and deficiency is rare. (NCI04)
L-Leucine, also known as (S)-leucine or L-leucin, belongs to the class of organic compounds known as leucine and derivatives. Leucine and derivatives are compounds containing leucine or a derivative thereof resulting from reaction of leucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. L-Leucine exists as a solid, soluble (in water), and a moderately acidic compound (based on its pKa). L-Leucine has been found throughout most human tissues, and has also been detected in most biofluids, including breast milk, sweat, blood, and saliva. Within the cell, L-leucine is primarily located in the mitochondria and cytoplasm. L-Leucine exists in all eukaryotes, ranging from yeast to humans. L-Leucine and oxoglutaric acid can be converted into ketoleucine and L-glutamic acid through its interaction with the enzyme branched-chain-amino-acid aminotransferase, cytosolic. In humans, L-leucine is involved in the methacycline action pathway, the telithromycin action pathway, the josamycin action pathway, and the neomycin action pathway. L-Leucine is also involved in several metabolic disorders, some of which include the 3-methylglutaconic aciduria type IV pathway, the 3-methylglutaconic aciduria type I pathway, 2-methyl-3-hydroxybutryl CoA dehydrogenase deficiency, and the isovaleric acidemia pathway. L-Leucine is a potentially toxic compound.
L-leucine is the L-enantiomer of leucine. It has a role as a plant metabolite, an Escherichia coli metabolite, a Saccharomyces cerevisiae metabolite, a human metabolite, an algal metabolite and a mouse metabolite. It is a pyruvate family amino acid, a proteinogenic amino acid, a leucine and a L-alpha-amino acid. It is a conjugate base of a L-leucinium. It is a conjugate acid of a L-leucinate. It is an enantiomer of a D-leucine. It is a tautomer of a L-leucine zwitterion. 325.4 g/mol
L-Leucine, also known as (S)-leucine or L-leucin, belongs to the class of organic compounds known as leucine and derivatives. Leucine and derivatives are compounds containing leucine or a derivative thereof resulting from reaction of leucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. L-Leucine exists as a solid, soluble (in water), and a moderately acidic compound (based on its pKa). L-Leucine has been found throughout most human tissues, and has also been detected in most biofluids, including breast milk, sweat, blood, and saliva. Within the cell, L-leucine is primarily located in the mitochondria and cytoplasm. L-Leucine exists in all eukaryotes, ranging from yeast to humans. L-Leucine and oxoglutaric acid can be converted into ketoleucine and L-glutamic acid through its interaction with the enzyme branched-chain-amino-acid aminotransferase, cytosolic. In humans, L-leucine is involved in the methacycline action pathway, the telithromycin action pathway, the josamycin action pathway, and the neomycin action pathway. L-Leucine is also involved in several metabolic disorders, some of which include the 3-methylglutaconic aciduria type IV pathway, the 3-methylglutaconic aciduria type I pathway, 2-methyl-3-hydroxybutryl CoA dehydrogenase deficiency, and the isovaleric acidemia pathway. L-Leucine is a potentially toxic compound.
L-leucine is the L-enantiomer of leucine. It has a role as a plant metabolite, an Escherichia coli metabolite, a Saccharomyces cerevisiae metabolite, a human metabolite, an algal metabolite and a mouse metabolite. It is a pyruvate family amino acid, a proteinogenic amino acid, a leucine and a L-alpha-amino acid. It is a conjugate base of a L-leucinium. It is a conjugate acid of a L-leucinate. It is an enantiomer of a D-leucine. It is a tautomer of a L-leucine zwitterion. 325.4 g/mol
Formulation:
325.4 g/mol
Source:
Usage:
Boc-Cys(Mbzl)-OH
The product is for non-human research only. Not for therapeutic or veterinary use.
Catalog Number: BT-251306
CAS Number: 61925-77-7
Molecular Formula: C16H23NO4S
Molecular Weight: 325.4 g/mol
Purity: ≥ 98%
Inventory: In Stock
| Size | SKU | Price | |
|---|---|---|---|
| 1g | bt-251306-1g | $303.54 | |
| 5g | bt-251306-5g | $535.08 |
| CAS Number | 61925-77-7 |
|---|---|
| Product Name | Boc-Cys(Mbzl)-OH |
| Molecular Formula | C16H23NO4S |
| Molecular Weight | 325.4 g/mol |
| Boiling Point | Sublimes at 145-148 °C. Decomposes at 293-295 °C (rapid heating, sealed tube) |
| Colorform | White glistening hexagonal plates from aqueous alcohol White crystals |
| Density | 1.293 g/cu cm at 18 °C |
| Impurities | Heavy metals (as Pb): not more than 0.002%; Lead: not more than 10 mg/kg; Ash: not more than 0.1% |
| InChI | InChI=1S/C16H23NO4S/c1-11-5-7-12(8-6-11)9-22-10-13(14(18)19)17-15(20)21-16(2,3)4/h5-8,13H,9-10H2,1-4H3,(H,17,20)(H,18,19) |
| InChI Key | ROHFNLRQFUQHCH-YFKPBYRVSA-N |
| Isomeric SMILES | CC(C)C[C@@H](C(=O)[O-])[NH3+] |
| IUPAC Name | 3-[(4-methylphenyl)methylsulfanyl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid |
| Canonical SMILES | CC1=CC=C(C=C1)CSCC(C(=O)O)NC(=O)OC(C)(C)C |
| Description | Leucine is one of nine essential amino acids in humans (provided by food), Leucine is important for protein synthesis and many metabolic functions. Leucine contributes to regulation of blood-sugar levels; growth and repair of muscle and bone tissue; growth hormone production; and wound healing. Leucine also prevents breakdown of muscle proteins after trauma or severe stress and may be beneficial for individuals with phenylketonuria. Leucine is available in many foods and deficiency is rare. (NCI04) L-Leucine, also known as (S)-leucine or L-leucin, belongs to the class of organic compounds known as leucine and derivatives. Leucine and derivatives are compounds containing leucine or a derivative thereof resulting from reaction of leucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. L-Leucine exists as a solid, soluble (in water), and a moderately acidic compound (based on its pKa). L-Leucine has been found throughout most human tissues, and has also been detected in most biofluids, including breast milk, sweat, blood, and saliva. Within the cell, L-leucine is primarily located in the mitochondria and cytoplasm. L-Leucine exists in all eukaryotes, ranging from yeast to humans. L-Leucine and oxoglutaric acid can be converted into ketoleucine and L-glutamic acid through its interaction with the enzyme branched-chain-amino-acid aminotransferase, cytosolic. In humans, L-leucine is involved in the methacycline action pathway, the telithromycin action pathway, the josamycin action pathway, and the neomycin action pathway. L-Leucine is also involved in several metabolic disorders, some of which include the 3-methylglutaconic aciduria type IV pathway, the 3-methylglutaconic aciduria type I pathway, 2-methyl-3-hydroxybutryl CoA dehydrogenase deficiency, and the isovaleric acidemia pathway. L-Leucine is a potentially toxic compound. L-leucine is the L-enantiomer of leucine. It has a role as a plant metabolite, an Escherichia coli metabolite, a Saccharomyces cerevisiae metabolite, a human metabolite, an algal metabolite and a mouse metabolite. It is a pyruvate family amino acid, a proteinogenic amino acid, a leucine and a L-alpha-amino acid. It is a conjugate base of a L-leucinium. It is a conjugate acid of a L-leucinate. It is an enantiomer of a D-leucine. It is a tautomer of a L-leucine zwitterion. |
| Melting Point | 293 °C 293.0 °C 268-288°C |
| Other CAS Number | 21675-61-6 71000-80-1 61-90-5 |
| Physical Description | Solid Small white lustrous plates or crystalline powder; odourless |
| SMILES | CC1=CC=C(C=C1)CSCC(C(=O)O)NC(=O)OC(C)(C)C |
| Solubility | 21500 mg/L (at 25 °C) 0.14 M Solubility in 99% alcohol: 0.72; in acetic acid: 10.9. Insoluble in ether. Solubility in water (g/L): 22.7 (0 °C); 24.26 (25 °C); 28.87 (50 °C); 38.23 (75 °C); 56.38 (100 °C) In water, 2.15X10+4 mg/L at 25 °C 21.5 mg/mL Soluble in water, acetic acid, dilute HCl, and alkaline hydroxides and carbonates Slightly soluble (in ethanol) |
| Synonyms | L-leucine;leucine;61-90-5;(S)-2-Amino-4-methylpentanoicacid;(S)-Leucine;(2S)-2-amino-4-methylpentanoicacid;(S)-(+)-Leucine;(S)-2-Amino-4-methylvalericacid;L-(+)-Leucine;L-alpha-Aminoisocaproicacid;L-Norvaline,4-methyl-;LEUCINE,L-;Leucinum;Leucin;(2S)-alpha-leucine;L-leucin;2-amino-4-methylvalericacid;Leucin[German];L-(-)-2-Amino-4-methylpentanoicacid;Leucine(VAN);leu;Leucinum[INN-Latin];Leucina[INN-Spanish];L-a-Aminoisocaproicacid;Leucina[Latin,Spanish] |
| Vapor Pressure | 5.52X10-9 mm Hg at 25 °C (est) |
| PubChem Compound | Boc-Cys(Mbzl)-OH |
| Last Modified | Apr 24 2022 |