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Cat. No.: HY-125538

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Deoxybrevianamide E

Deoxybrevianamide E, an indole alkaloid, is a biosynthetic precursor for advanced metabolites isolated from the marine-derived Aspergillus sp..

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

CAS No.: 34610-68-9
Formula: C₂₁H₂₅N₃O₂
Molecular Weight:351.44

Storage:

Powder -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month

Deoxybrevianamide E Chemical Structure

CAS No.: 34610-68-9

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Use of MCE Products

Fluorescent Dye

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

Biological Activity
- Description
- IC₅₀ & Target
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Bioz

Biological Activity

Description

Deoxybrevianamide E, an indole alkaloid, is a biosynthetic precursor for advanced metabolites isolated from the marine-derived Aspergillus sp.^[1].

IC₅₀ & Target

Microbial Metabolite

All Endogenous Metabolite Isoforms :

Chemical Information

CAS No. 34610-68-9
Appearance Solid
Molecular Weight 351.44
Formula C₂₁H₂₅N₃O₂
Color White to off-white
SMILES

O=C(N[C@H](C1=O)CC2=C(NC3=C2C=CC=C3)C(C)(C=C)C)[C@]4(N1CCC4)[H]
Structure Classification
- Alkaloids
- Indole Alkaloids
Initial Source
- Endogenous metabolite
- Human Gut Microbiota Metabolites
- Marine natural products
- Marine microorganism
- Microorganisms
Penicillium brevicompactum
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Powder	-20°C	3 years
In solvent	-80°C	6 months
	-20°C	1 month

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (274 KB)
SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Portuguese - PT (251 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]. Hikaru Kato, et al. Study on the biosynthesis of the notoamides: Pinacol-type rearrangement of the isoprenyl unit in deoxybrevianamide E and 6-hydroxydeoxybrevianamide E. Tetrahedron Lett. 2011 Dec 21;52(51):6923-6926. [Content Brief]

Calculators

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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.

Keywords

100 mg

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