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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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