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
• Beilstein: 1714196
• MDL-Nummer: MFCD00056757
• UNSPSC-Code: 12352205
• PubChem Substanz-ID: 329751343
• NACRES: NA.79

Eigenschaften

• Assay: ≥95.0% (HPLC)
• Form: solid
• Optische Aktivität: [α]/D 17±2°, c = 1 in H₂O
• Farbe: white
• Lagertemp.: −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
• InChIKey: ZNXZGRMVNNHPCA-VIFPVBQESA-N

Beschreibung

Anwendung

• 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. Wirkung

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

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable