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Cat. No.: HY-W095697

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N-Acetylhistidine

N-Acetylhistidine is a histidine derivative that is the acetylated enzyme intermediate in the N-acetyltransferase reaction.

For research use only. We do not sell to patients.

CAS No.: 2497-02-1
Formula: C₈H₁₁N₃O₃
Molecular Weight:197.19

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (269 KB)

N-Acetylhistidine Chemical Structure

CAS No.: 2497-02-1

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Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity

Description

N-Acetylhistidine is a histidine derivative that is the acetylated enzyme intermediate in the N-acetyltransferase reaction^[1]^[2].

All Endogenous Metabolite Isoforms :

Chemical Information

CAS No. 2497-02-1
Molecular Weight 197.19
Formula C₈H₁₁N₃O₃
SMILES

O=C(O)[C@H](CC1=CNC=N1)NC(C)=O
Initial Source
- Endogenous metabolite
- Human Gut Microbiota Metabolites
- Microorganisms
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (269 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Andersen S O, et al. Cuticle-catalyzed coupling between N-acetylhistidine and N-acetyldopamine[J]. Insect biochemistry and molecular biology, 1992, 22(5): 459-469.

[2]. Bame K J, et al. Acetyl-coenzyme A: alpha-glucosaminide N-acetyltransferase. Evidence for an active site histidine residue[J]. Journal of Biological Chemistry, 1986, 261(22): 10127-10132.

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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N-Acetylhistidine

All Endogenous Metabolite Isoforms

Biological Activity

Chemical Information

Purity & Documentation

References

Calculators

Help & FAQs

N-Acetylhistidine Related Classifications

HY-W095697 Related Classifications