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Acridine (Synonyms: 2,3,5,6-Dibenzopyridine, 10-Azaanthracene, Dibenzopyridine, NSC 3408)

Katalog-Nr.GC49804 Copy One-Click Copy Product Info

An azaarene

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Acridine Chemische Struktur

Cas No.: 260-94-6

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5 g
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10 g
117,00 $
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25 g
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50 g
465,00 $
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Sample solution is provided at 25 µL, 10mM.



Description of Acridine

Acridine is an azaarene.1 It is a scaffold component of many pharmacologically active compounds, including topoisomerase inhibitors and DNA intercalators, as well as compounds with anticancer and antimalarial activities.2,3,4,5 Acridine is also the backbone of some fluorescent probes, such as acridine orange and ICAAc .6,7 It is genotoxic to bacteria when used at a concentration of 50 µg/ml.1

1.Skarek, M., Cupr, P., RÉblova, K., et al.Assessment of toxic and genotoxic effects of N-heterocyclic polyaromatic hydrocarbons with miniaturized in vitro screening bioassays1-4() 2.Nelson, E.M., Tewey, K.M., and Liu, L.F.Mechanism of antitumor drug action: Poisoning of mammalian DNA topoisomerase II on DNA by 4’-(9-acridinylamino)-methanesulfon-m-anisidideProc. Natl. Acad. Sci. USA81(5)1361-1365(1984) 3.Fukui, K., Tanaka, K., Fujitsuka, M., et al.Distance dpendence of electron transfer in acridine-intercalated DNAJ. Photochem. Photobiol. B Biol.5018-27(1999) 4.Heald, R.A., Modi, C., Cookson, J.C., et al.Antitumor polycyclic acridines. 8.1 Synthesis and telomerase-inhibitory activity of methylated pentacyclic acridinium saltsJ. Med. Chem.45(3)590-597(2002) 5.Kumar, R., Kaur, M., and Kumari, M.Acridine: A versatile heterocyclic nucleusActa Pol. Pharm.69(1)3-9(2012) 6.Han, J., and Burgess, K.Fluorescent indicators for intracellular pHChem. Revs.110(5)2709-2728(2010) 7.Nagy, M., Racz, D., Nagy, Z.L., et al.Amino-isocyanoacridines: Novel, tunable solvatochromic fluorophores as phystiological pH probesSci. Rep.98250(2019)

Chemical Properties of Acridine

Cas No. 260-94-6 SDF
Überlieferungen 2,3,5,6-Dibenzopyridine, 10-Azaanthracene, Dibenzopyridine, NSC 3408
Canonical SMILES C1(N=C2C=CC=CC2=C3)=C3C=CC=C1
Formula C13H9N M.Wt 179.2
Löslichkeit DMF: 2 mg/ml,DMSO: 10 mg/ml,Ethanol: 10 mg/ml,PBS (pH 7.2): insol Storage -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of Acridine

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 5.5804 mL 27.9018 mL 55.8036 mL
5 mM 1.1161 mL 5.5804 mL 11.1607 mL
10 mM 558 μL 2.7902 mL 5.5804 mL
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In vivo Formulation Calculator (Clear solution) of Acridine

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL saline, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.

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Review for Acridine

Average Rating: 5 ★★★★★ (Based on Reviews and 18 reference(s) in Google Scholar.)

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