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SMB00012

Sigma-Aldrich

Asterric acid

≥95% (LC/MS-ELSD)

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About This Item

Empirical Formula (Hill Notation):
C17H16O8
CAS Number:
Molecular Weight:
348.30
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.25

Assay

≥95% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

InChI

1S/C17H16O8/c1-8-4-11(19)14(16(20)21)12(5-8)25-15-10(17(22)24-3)6-9(18)7-13(15)23-2/h4-7,18-19H,1-3H3,(H,20,21)

InChI key

XOKVHFNTYHPEHN-UHFFFAOYSA-N

General description

Natural product derived from fungal source.

Pictograms

Environment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Yan Li et al.
Journal of natural products, 71(9), 1643-1646 (2008-08-30)
Five new asterric acid derivatives, ethyl asterrate (3), n-butyl asterrate (4), and geomycins A-C (6-8), have been isolated from cultures of an isolate of the Antarctic ascomycete fungus Geomyces sp. The structures of these metabolites were elucidated by NMR spectroscopy.
Shao-Hua Wu et al.
Journal of basic microbiology, 48(2), 140-142 (2008-04-03)
A new spiroketal, named aspergiketal (1) was isolated from the culture broth of Aspergillus terreus, an endophytic fungus in the stems of the plant Opuntia ficusindica Mill., together with two known compounds, physcion (2) and asterric acid (3). Their structures
Tomasz Boruta et al.
Applied microbiology and biotechnology, 100(7), 3009-3022 (2015-11-26)
Cultivation of Aspergillus terreus ATCC 20542 in a stirred tank bioreactor was performed to induce the biosynthesis of secondary metabolites and provide the bioprocess-related insights into the metabolic capabilities of the investigated strain. The activation of biosynthetic routes was attempted
Porntep Chomcheon et al.
Journal of natural products, 69(9), 1351-1353 (2006-09-23)
Two new natural products, 2-hydroxymethyl-3-methylcyclopent-2-enone (1) (synthetically known) and cis-2-hydroxymethyl-3-methylcyclopentanone (2), and a known compound, asterric acid (3), were isolated from the endophytic fungus mitosporic Dothideomycete sp. LRUB20, which was isolated from the stem of the Thai medicinal plant Leea
Asterric acid, a new endothelin binding inhibitor.
H Ohashi et al.
The Journal of antibiotics, 45(10), 1684-1685 (1992-10-01)

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