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Merck

SMB00978

Sigma-Aldrich

L-Hercynine

≥95% (HPLC)

Synonim(y):

α-N,N,N-Trimethylhistidine, N-α-trimethyl histidine, Histidine-betaine

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About This Item

Wzór empiryczny (zapis Hilla):
C9H15N3O2
Numer CAS:
Masa cząsteczkowa:
197.23
NACRES:
NA.26

Poziom jakości

Próba

≥95% (HPLC)

Postać

solid

temp. przechowywania

2-8°C

ciąg SMILES

C[N+](C)(C)[C@H](C([O-])=O)CC1=CN=CN1

InChI

1S/C9H15N3O2/c1-12(2,3)8(9(13)14)4-7-5-10-6-11-7/h5-6,8H,4H2,1-3H3,(H-,10,11,13,14)/t8-/m0/s1

Klucz InChI

GPPYTCRVKHULJH-QMMMGPOBSA-N

Opis ogólny

Hercynine is the precursor and redox metabolite of ergothioneine, which regulates microbial physiology and enables the survival of microbes under stressful conditions encountered in their natural environments. Ergothioneine is primarily present as a thione physiological pH, which makes it resistant to autoxidation. Ergothioneine enables pathogenic microbes, such as Mycobacterium tuberculosis (Mtb) to withstand hostile environments within the host to establish infection.

Zastosowanie

Hercynine is a versatile molecule and it finds application in biochemical and metabolomics research.

Cechy i korzyści

  • Can be used in Metabolomics and Biochemical research
  • High-quality compound suitable for multiple research applications

Inne uwagi

For additional information on our range of Biochemicals, please complete this form.
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Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Salvatore Sotgia et al.
Antioxidants (Basel, Switzerland), 9(9) (2020-09-17)
The dependence of a stallion's spermatozoa on oxidative phosphorylation for energy requirements results in an unconventional relationship between reactive oxygen species (ROS) production and fertility. In such a scenario, antioxidant activity must be finely controlled and not affect the essential
Tomoyuki Kamide et al.
Journal of agricultural and food chemistry, 68(23), 6390-6394 (2020-05-22)
We previously constructed a heterologous production system for ergothioneine (ERG) in Escherichia coli using five ERG biosynthesis genes (egtABCDE) from Mycobacterium smegmatis. However, significant amounts of hercynine (HER), an intermediate of ERG, as ERG were accumulated, suggesting that the reaction

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