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17927

Sigma-Aldrich

9-Oxo-10(9H)-acridineacetic acid

for HPLC derivatization, ≥99.0% (T)

Synonym(s):

(9,10-Dihydro-9-oxo-10-acridinyl)acetic acid, 10-(Carboxymethyl)-9(10H)acridone

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About This Item

Empirical Formula (Hill Notation):
C15H11NO3
CAS Number:
Molecular Weight:
253.25
Beilstein:
227508
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.32

grade

for HPLC derivatization

Quality Level

Assay

≥99.0% (T)

form

solid

mp

~289 °C (dec.)

SMILES string

OC(=O)CN1c2ccccc2C(=O)c3ccccc13

InChI

1S/C15H11NO3/c17-14(18)9-16-12-7-3-1-5-10(12)15(19)11-6-2-4-8-13(11)16/h1-8H,9H2,(H,17,18)

InChI key

UOMKBIIXHQIERR-UHFFFAOYSA-N

Application

9-Oxo-10(9H)-acridineacetic acid and its analogs are used to study their potential activity as interferon inducers.

Other Notes

Reagent for pre-column derivatization of amino acids for fluorescent determination in HPLC; Building block in pharmaceutics

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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The use of reamberin and cycloferon combination for increasing the antibacterial therapy efficacy in patients with chronic sepsis (CS) was studied. It was shown that the combination provided more rapid elimination of the CS exacerbation symptoms, normalization of the hematologic
Tolerance or hyperreactivity to interferon induction by sodium salt of 9-oxo-10-acridineacetic acid and analogs in mice and in the mouse macrophage cultures.
Szulc B, Inglot AD, Inglot O.
Arch. Immunol. Ther. Exp., 35, 389-395 (1987)
Competition of sodium salt of 9-oxo-10-acridineacetic acid with analogs during induction of interferon in the mouse bone marrow-derived macrophages.
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