![]() Quinalizarin structure
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Common Name | Quinalizarin | ||
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CAS Number | 81-61-8 | Molecular Weight | 272.210 | |
Density | 1.8±0.1 g/cm3 | Boiling Point | 517.1±45.0 °C at 760 mmHg | |
Molecular Formula | C14H8O6 | Melting Point | 99 °C | |
MSDS | Chinese USA | Flash Point | 280.6±25.2 °C | |
Symbol |
![]() ![]() GHS07, GHS09 |
Signal Word | Warning |
Use of QuinalizarinQuinalizarin is a potent, selective and cell-permeable protein kinase CK2 inhibitor with an Ki of ~50 nM and an IC50 of 110 nM. Quinalizarin can induce apoptosis of certain cancer cells[1]. |
Name | quinalizarin |
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Synonym | More Synonyms |
Description | Quinalizarin is a potent, selective and cell-permeable protein kinase CK2 inhibitor with an Ki of ~50 nM and an IC50 of 110 nM. Quinalizarin can induce apoptosis of certain cancer cells[1]. |
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Related Catalog | |
Target |
CK2:~50 nM (Ki) CK2:110 nM (IC50) |
References |
Density | 1.8±0.1 g/cm3 |
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Boiling Point | 517.1±45.0 °C at 760 mmHg |
Melting Point | 99 °C |
Molecular Formula | C14H8O6 |
Molecular Weight | 272.210 |
Flash Point | 280.6±25.2 °C |
Exact Mass | 272.032074 |
PSA | 115.06000 |
LogP | 5.18 |
Vapour Pressure | 0.0±1.4 mmHg at 25°C |
Index of Refraction | 1.815 |
Storage condition | room temp |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
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~% Quinalizarin CAS#:81-61-8 |
Literature: DE60855 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 3, p. 198 Journal fuer Praktische Chemie (Leipzig), , vol. <2>43, p. 239 Chemische Berichte, , vol. 23, p. 3739 Justus Liebigs Annalen der Chemie, , vol. 349, p. 205 |
~% Quinalizarin CAS#:81-61-8 |
Literature: Justus Liebigs Annalen der Chemie, , vol. 240, p. 301 |
~% Quinalizarin CAS#:81-61-8 |
Literature: Journal of Organic Chemistry, , vol. 6, p. 732,747 Journal of Organic Chemistry, , vol. 7, p. 63,66 |
~% Quinalizarin CAS#:81-61-8 |
Literature: DE63693 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 3, p. 201 Journal fuer Praktische Chemie (Leipzig), , vol. <2>43, p. 249 |
~% Quinalizarin CAS#:81-61-8 |
Literature: DE161026 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 8, p. 256 |
Precursor 8 | |
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DownStream 4 | |
Protein kinase CK2 potentiates translation efficiency by phosphorylating eIF3j at Ser127.
Biochim. Biophys. Acta 1853 , 1693-701, (2015) In eukaryotic protein synthesis the translation initiation factor 3 (eIF3) is a key player in the recruitment and assembly of the translation initiation machinery. Mammalian eIF3 consists of 13 subuni... |
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A complex signaling network involving protein kinase CK2 is required for hepatitis C virus core protein-mediated modulation of the iron-regulatory hepcidin gene expression.
Cell. Mol. Life Sci. 71(21) , 4243-58, (2014) Hepatitis C virus (HCV) infection is associated with hepatic iron overload and elevated serum iron that correlate to poor antiviral responses. Hepcidin (HAMP), a 25-aa cysteine-rich liver-specific pep... |
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Quinalizarin enhances radiosensitivity of nasopharyngeal carcinoma cells partially by suppressing SHP-1 expression.
Int. J. Oncol. 48 , 1073-84, (2016) The purpose of this study was to investigate the influence of quinalizarin on the radiosensitivity of nasopharyngeal carcinoma (NPC) cells and the relevant underlying mechanisms. Human NPC cell lines ... |
1,2,5,8-tetrahydroxy-9,10-anthracenedione |
Alizarinbordeaux |
9,10-Anthracenedione, 1,2,5,8-tetrahydroxy- |
MFCD00001205 |
9,10-Anthracenedione,1,2,5,8-tetrahydroxy |
Alizarine Bordeaux B |
1,2,5,8-Tetrahydroxy-9,10-anthraquinone |
Mordant Violet 26 |
Khinalizarin |
Alizarine Bordeaux |
C.I. Mordant Violet 26 |
Alizarin bordeaux B |
1,2,5,8-tetrahydroxyanthracene-9,10-dione |
Quinalizarin |
1,2,5,8-tetrahydroxyanthraquinone |
EINECS 201-366-6 |