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Merck
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Documentos

16702

Sigma-Aldrich

(R)-Pantetheine

≥95.0% (HPLC)

Sinónimos:

(2R)-2,4-Dihydroxy-N-[3-[(2-mercaptoethyl)amino]-3-oxopropyl]-3,3-dimethylbutanamide, (R)-2,4-Dihydroxy-N-[2-[(2-mercaptoethyl)carbamoyl]ethyl]-3,3-dimethylbutyramide, (D)-(+)-Pantetheine, N-(Pantothenyl)-β-aminoethanethiol, LBF, Lactobacillus bulgaricus factor

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About This Item

Fórmula empírica (notación de Hill):
C11H22N2O4S
Número de CAS:
496-65-1
Peso molecular:
278.37
Beilstein/REAXYS Number:
1714196
MDL number:
MFCD00056757
UNSPSC Code:
12352205
PubChem Substance ID:
329751343
NACRES:
NA.79

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

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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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C T Wittwer et al.
The Journal of biological chemistry, 258(16), 9733-9738 (1983-08-25)
A microsomal glycoprotein that catalyzes the hydrolysis of pantetheine to pantothenate and cysteamine was solubilized and purified to homogeneity as determined by sodium dodecyl sulfate electrophoresis. The enzyme from pig kidney cortex was solubilized on exposure to butanol and purified
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