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16702

Sigma-Aldrich

(R)-Pantetheine

≥95.0% (HPLC)

Sinônimo(s):

(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 (Notação de Hill):
C11H22N2O4S
Número CAS:
496-65-1
Peso molecular:
278.37
Beilstein:
1714196
Número MDL:
MFCD00056757
Código UNSPSC:
12352205
ID de substância PubChem:
329751343
NACRES:
NA.79

Nível de qualidade

100

Ensaio

≥95.0% (HPLC)

forma

solid

atividade óptica

[α]/D 17±2°, c = 1 in H2O

cor

white

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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

chave InChI

ZNXZGRMVNNHPCA-VIFPVBQESA-N

Aplicação


  • 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).

Ações bioquímicas/fisiológicas

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

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