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16702

Sigma-Aldrich

(R)-Pantetheine

≥95.0% (HPLC)

Sinonimo/i:

(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

Formula empirica (notazione di Hill):
C11H22N2O4S
Numero CAS:
496-65-1
Peso molecolare:
278.37
Beilstein:
1714196
Numero MDL:
MFCD00056757
Codice UNSPSC:
12352205
ID PubChem:
329751343
NACRES:
NA.79

Livello qualitativo

100

Saggio

≥95.0% (HPLC)

Stato

solid

Attività ottica

[α]/D 17±2°, c = 1 in H2O

Colore

white

Temperatura di conservazione

−20°C

Stringa SMILE

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
ZNXZGRMVNNHPCA-VIFPVBQESA-N

Applicazioni


  • 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).

Azioni biochim/fisiol

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
BCCB7634
BCBZ9006
BCBM8211V
BCBM8211

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