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Merck
CN

16702

Sigma-Aldrich

(R)-Pantetheine

≥95.0% (HPLC)

Synonym(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

Empirical Formula (Hill Notation):
C11H22N2O4S
CAS Number:
496-65-1
Molecular Weight:
278.37
Beilstein:
1714196
MDL number:
MFCD00056757
UNSPSC Code:
12352205
PubChem Substance ID:
329751343
NACRES:
NA.79

Key Documents

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Quality Level

100

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

Related Categories

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCB7634
BCBZ9006
BCBM8211V
BCBM8211

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Johanna Busch et al.
PloS one, 14(5), e0214116-e0214116 (2019-05-03)
Acute gastrointestinal illness (AGI) is a global public health priority that often disproportionately effects Indigenous populations. While previous research examines the association between meteorological conditions and AGI, little is known about how socio-cultural factors may modify this relationship. This present
Assay of the enzymatic hydrolysis of pantetheine.
C Wittwer et al.
Analytical biochemistry, 122(2), 213-222 (1982-05-15)
H Kleinkauf et al.
Proceedings of the National Academy of Sciences of the United States of America, 68(9), 2069-2072 (1971-09-01)
To study the function of pantetheine in gramicidin S and tyrocidine biosynthesis, pepsin digests of the polymerizing enzymes, of which only the heavy ones contain pantetheine, were analyzed. The digests of gramicidin S enzymes charged with either [(14)C]proline or with
Jun Yang et al.
Applied optics, 57(10), 2490-2498 (2018-05-02)
On-site measurements and defect detection are of great importance for precision ground steel rollers due to their large dimension and weight. In addition to dimensional error, form accuracy, surface roughness, and surface/sub-surface cracks, there also exist optical defect requirements for
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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