CAS 103476-89-7
:L-Leucinamida, N-acetil-L-leucil-N-[(1S)-4-[(aminoiminometil)amino]-1-formilbutil]-, sulfato (2:1)
Descrição:
L-Leucinamida, N-acetil-L-leucil-N-[(1S)-4-[(aminoiminometil)amino]-1-formilbutil]-, sulfato (2:1) é um composto orgânico complexo caracterizado por seus componentes estruturais, que incluem um derivado de aminoácido (L-leucina) e um grupo sulfato. Este composto apresenta uma disposição única de grupos funcionais, incluindo funcionalidades amida e acilo, que contribuem para sua atividade biológica e propriedades de solubilidade. A presença do grupo sulfato melhora seu caráter iônico, potencialmente influenciando sua interação com sistemas biológicos e solubilidade em ambientes aquosos. Como um derivado da L-leucina, pode exibir propriedades relacionadas à síntese de proteínas e ao metabolismo. A estereoquímica do composto, particularmente a configuração (1S), indica arranjos espaciais específicos que podem afetar suas interações biológicas. No geral, essa substância provavelmente será de interesse na pesquisa bioquímica, particularmente em estudos relacionados à síntese de peptídeos, design de fármacos e aplicações terapêuticas, embora atividades biológicas específicas e propriedades farmacológicas exijam investigação adicional.
Fórmula:C20H38N6O4H2O4S
InChI:InChI=1S/C20H38N6O4.H2O4S/c1-12(2)9-16(24-14(5)28)19(30)26-17(10-13(3)4)18(29)25-15(11-27)7-6-8-23-20(21)22;1-5(2,3)4/h11-13,15-17H,6-10H2,1-5H3,(H,24,28)(H,25,29)(H,26,30)(H4,21,22,23);(H2,1,2,3,4)/t15-,16-,17-;/m0./s1
Chave InChI:InChIKey=IBDASEYBOOUHFZ-FRKSIBALSA-N
SMILES:[C@@H](NC([C@H](CC(C)C)NC(C)=O)=O)(C(N[C@@H](CCCNC(=N)N)C=O)=O)CC(C)C.S(=O)(=O)(O)O
Sinónimos:- (2S)-2-(acetylamino)-N-[(2S)-2-({4-[(diaminomethylidene)amino]-1-formylbutyl}amino)-4-methylpentanoyl]-4-methylpentanamide (non-preferred name)
- 2-(2-Acetamido-4-methylvaleramido)-N-(1-formyl-4-guanidinobutyl)-4-methylvaleramide
- <span class="text-smallcaps">L</smallcap>-Leucinamide, N-acetyl-<smallcap>L</span>-leucyl-N-[(1S)-4-[(aminoiminomethyl)amino]-1-formylbutyl]-, sulfate (2:1)
- <span class="text-smallcaps">L</smallcap>-Leucinamide, N-acetyl-<smallcap>L</span>-leucyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-, (S)-, sulfate (2:1)
- Acetyl-L-leucyl-L-leucylargininal
- L-Leucinamide, N-acetyl-L-leucyl-N-(4-((aminoiminomethyl)amino)-1-formylbutyl)-
- Leupeptin Ac-LL
- Leupeptin Hemisulfate From Microbial*Source
- Leupeptin hemisulfate
- N-Acetyl-L-leucyl-L-leucyl-L-argininal
- N-acetyl-L-leucyl-N-{(2S)-5-[(diaminomethylidene)amino]-1-oxopentan-2-yl}-L-leucinamide
- Nk-381
- Valeramide, 2-(2-acetamido-4-methylvaleramido)-N-(1-formyl-4-guanidinobutyl)-4-methyl-
- L-Leucinamide, N-acetyl-L-leucyl-N-[(1S)-4-[(aminoiminomethyl)amino]-1-formylbutyl]-, sulfate (2:1)
- Ver mais sinónimos
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10 produtos.
Leupeptin
CAS:A reversible compeptitive protease inhibitor, which was shown to inhibit cathepsins B, H, L, and S, calpain and trypsin. Ac-LLR-CHO inhibits the trypsin-like activity of the proteasome endopeptidase complex. CAS Number (hemisulfate): 103476-89-7.Fórmula:C20H38N6O4·H2SO4Pureza:97.8380%Cor e Forma:WhitePeso molecular:951.2Leupeptin hemisulphate
CAS:Leupeptin hemisulphateFórmula:C20H38N6O4·H2SO4Pureza:>90%Cor e Forma: white to off white powderPeso molecular:951.18552g/molLeupeptin Hemisulfate
CAS:<p>Leupeptin hemisulfate is a protease inhibitor with cell membrane-permeable, reversible, competitive, and oral activities.</p>Fórmula:C20H38N6O4H2SO4Pureza:90% - ≥98%Cor e Forma:White SolidPeso molecular:475.59Leupeptin hemisulfate
CAS:Fórmula:C20H38N6O4·5H2SO4Pureza:≥ 95%Cor e Forma:White to off-white powderPeso molecular:475.59Leupeptin hemisulfate anhydrous
CAS:<p>Leupeptin is a protease inhibitor that inhibits the activity of proteases in cells. It has been shown to inhibit transcriptional regulation and apoptosis pathway, as well as possessing anti-inflammatory properties. Leupeptin has been shown to have inhibitory properties against a variety of proteases, including group P2 metalloproteases, cathepsin D, and proteinase 3. This drug has also been shown to prevent neuronal death in experimental models by inhibiting cell lysis. Leupeptin binds to the active site of the enzyme by forming hydrogen bonds with conserved amino acid residues and steric interactions with nearby amino acid residues. The redox potentials of leupeptin are not known, but it is assumed that they are low enough for its antioxidant properties to be effective.</p>Fórmula:C20H38N6O4H2SOPureza:Min. 90 Area-%Peso molecular:475.6 g/molLeupeptin hemisulfate anhydrous (vial)
CAS:<p>Leupeptin is an ion channel blocker that belongs to the group of protease inhibitors. It blocks the passage of ions across cell membranes by binding to the active site of a variety of enzymes in the membrane. Leupeptin is used as a research tool for studying protein interactions, and can be used for antibody production. Leupeptin is also useful in cell biology studies, because it inhibits the activation of many proteins involved in signal transduction and cell division.</p>Fórmula:C20H38N6O4Pureza:Min. 95%Peso molecular:426.55 g/molLeupeptin hemisulfate
CAS:<p>Leupeptin is a protein inhibitor that binds to the ubiquitin ligases and inhibits their activity. It has been shown to inhibit the transcriptional regulation of gene expression, which is important in cancer, chronic oral administration, and experimental models. Leupeptin also blocks the binding of proteins to DNA in cell culture and animal models. This leads to decreased production of fatty acids, which are needed for cellular growth and function. Leupeptin also has an anti-depressant effect by blocking the transcriptional regulation of gene expression for serotonin receptors.</p>Fórmula:C20H38N6O4•(H2SO4)0Pureza:Min. 90.0 Area-%Cor e Forma:White PowderPeso molecular:475.59 g/mol






