16702

(R)-Pantethein

≥95.0% (HPLC)

• Synonym(e): (2R)-2,4-Dihydroxy-N-[3-[(2-mercaptoethyl)-amino]-3-oxopropyl]-3,3-dimethylbutanamid, (R)-2,4-Dihydroxy-N-[2-[(2-mercaptoethyl)-carbamoyl]-ethyl]-3,3-dimethylbutyramid, (D)-(+)-Pantethein, N-(Pantothenyl)-β-aminoethanthiol, LBF, Lactobacillus bulgaricus factor
• Empirische Formel (Hill-System): C₁₁H₂₂N₂O₄S
• CAS-Nummer: 496-65-1
• Molekulargewicht: 278.37
• UNSPSC Code: 12352205
• NACRES: NA.79
• PubChem Substance ID: 329751343
• MDL number: MFCD00056757
• Beilstein/REAXYS Number: 1714196

Eigenschaften

• Quality Segment: 100
• assay: ≥95.0% (HPLC)
• form: solid
• optical activity: [α]/D 17±2°, c = 1 in H₂O
• color: white
• storage temp.: −20°C
• SMILES string: OCC(C)(C)[C@@H](O)C(NCCC(NCCS)=O)=O
• InChI: 1S/C11H22N2O4S/c1-11(2,7-14)9(16)10(17)13-4-3-8(15)12-5-6-18/h9,14,16,18H,3-7H2,1-2H3,(H,12,15)(H,13,17)/t9-/m0/s1
• InChI key: ZNXZGRMVNNHPCA-VIFPVBQESA-N

Beschreibung

Application

• Structures of carboxylic acid reductase reveal domain dynamics underlying catalysis: This study investigates the structural and dynamic aspects of carboxylic acid reductase enzymes, which are relevant for the conversion processes involving (R)-pantetheine and related compounds (Gahloth et al., 2017).

Biochem/physiol Actions

Metabolite in carbapenem biosynthesis, pantothenate and CoA biosynthesis and biosynthesis of secondary metabolites.

Sicherheitshinweise

• Lagerklasse: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable