Fmoc-aspartic+acid-4-methyl+ester
Supplier:
AMBEED, INC
Description:
3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methoxybenzoic acid, Purity: 97%, CAS Number: 256935-69-0, Appearance: White to off-white powder or crystal, Storage: Sealed in dry, 2-8 C, Size: 5g
Supplier:
Matrix Scientific
Description:
N-BUTOXYCARBONYL TRIMETHYLPHOSPHONOGLYCINE MF=C10H20NO7P MW=297.25 CAS=89524-98-1 MDL=MFCD02178893
Supplier:
BeanTown Chemical
Description:
CAS: 89524-98-1; MDL No: MFCD02178893
Powder; Molecular Formula: C10H20NO7P; MW: 297.24
Melting Point: 67-71°
Supplier:
Bachem Americas
Description:
Sequence: Boc-Lys(Fmoc)-OH
Supplier:
Thermo Scientific Chemicals
Description:
N-Fmoc-L-citrulline, Purity: 98%, CAS Number: 133174-15-9, molecular formula: C21H23N3O5, color: White, Form: Powder, Synonyms: Fmoc-Cit-OH, 5g
Supplier:
Bachem Americas
Description:
Sequence: Fmoc-D-Tyr(tBu)-OH
Supplier:
AMBEED, INC
Description:
Fmoc-HomoArg(Pbf)-OH 97% (by HPLC)
Catalog Number:
(101852-260)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041557-1G , MDL Number: MFCD01311751
Catalog Number:
(10247-554)
Supplier:
Bioss
Description:
Caspases are cysteine proteases that cleave C-terminal aspartic acid residues on their substrate molecules. This gene is most highly related to members of the ICE subfamily of caspases that process inflammatory cytokines. In rodents, the homolog of this gene mediates apoptosis in response to endoplasmic reticulum stress. However, in humans this gene contains a polymorphism for the presence or absence of a premature stop codon. The majority of human individuals have the premature stop codon and produce a truncated non-functional protein. The read-through codon occurs primarily in individuals of African descent and carriers have endotoxin hypo-responsiveness and an increased susceptibility to severe sepsis. Several alternatively spliced transcript variants have been noted for this gene. [provided by RefSeq, Feb 2011].
Supplier:
AMBEED, INC
Description:
(R)-Methyl 2-amino-3-(4-chlorophenyl)propanoate hydrochloride, Purity: 97%, CAS number: 33965-47-8, Appearance: White to yellow powder or crystals, Storage: Inert atmosphere, 2-8C, Size: 5G
Catalog Number:
(10299-310)
Supplier:
Bioss
Description:
GOT1L1, Glutamate oxaloacetate transaminase 1-like protein 1, is a 421 amino acid member of the class-I pyridoxal-phosphate-dependent aminotransferase family. Similar to glutamate-oxaloacetate transaminase (GOT1), GOT1L1 is found primarily as a homodimer in the cytoplasmic space but also has mitochondrial and chloroplastic isozymes. GOT1L1 transaminates 2-oxoglutarate with L-aspartate to yield oxaloacetate and L-glutamate. This reaction requires a pyridoxal phosphate cofactor to occur. The GOT1L1 peptidase is predominately expressed in the liver and serum levels of this protein can be used as an indicator of liver disease. Also, elevated glutamate concentrations in the brain interstitial fluids can lead to pathological brain conditions. The glutamate-scavenging properties of these aminotranferase type enzymes likely prevent glutamate excitotoxicity and the long-lasting neurological deficits seen after stroke.
Supplier:
AMBEED, INC
Description:
(R)-5-((9H-Fluoren-9-yl)methoxy)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-5-oxopentanoic acid, Purity: 95%, CAS Number: 252049-17-5, Appearance: Solid, Storage: Sealed in dry, 2-8 C, Size: 250mg
Supplier:
AMBEED, INC
Description:
Fmoc-Val-Cit-OH, Purity: 95%, CAS number: 159858-21-6, Appearance: White to Yellow Solid, Storage: Keep in dark place, Sealed in dry, 2-8C, Size: 5G
Catalog Number:
(101851-520)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041372-50MG , MDL Number: MFCD09750523
Catalog Number:
(TCF0305-005G)
Supplier:
TCI America
Description:
Form: Crystal
Specific rotation [a]20/D: -18.5 deg (C=1, DMF)
Supplier:
Bachem Americas
Description:
SPPS employing the pure stereoisomer of Fmoc-Pamâ‚‚Cys-OH allows to obtain more homogeneous lipopeptides. The configuration of the bis-palmitoyloxypropyl moiety could influence the biological activity of the peptide conjugate.
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