481-73-2
481-73-2
Chemical Structure
Citreorosein
Synonym(s): ω-Hydroxyemodin; NSC 624612
- CAS No.: 481-73-2
- Formula:C15H10O6
- Molecular Weight:286.24
IUPAC Name: 1,3,8-trihydroxy-6-(hydroxymethyl)anthracene-9,10-dione
InChIKey: YQHZABGPIPECSQ-UHFFFAOYSA-N
SMILES: O=C1C2=C(C=C(CO)C=C2O)C(C3=CC(O)=CC(O)=C13)=O
Biological Activity: Citreorosein is a natural product that can be isolated from Xanthoria parietina[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Citreorosein | 95.0% | Citreorosein is a natural product that can be isolated from Xanthoria parietina. | ||||||||||||||||||||
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Emodic acid | 98.00% | Emodic acid (NSC624610) is an anthraquinone compound isolated from A. microcarpus, which can inhibit the proliferation of cancer cells by inhibiting the activity of NF-κB. Emodic acid can also inhibit the phosphorylation of p38, ERK and JNK, the secretion of tumor-promoting cytokines IL-1β and IL-6, and the expression of VEGF and MMP, thereby inhibiting the invasion and migration potential of cancer cells. | ||||||||||||||||||||
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Emodin (Standard) | 98.84% | Emodin (Standard) is the analytical standard of Emodin. This product is intended for research and analytical applications. Emodin (Frangula emodin), an anthraquinone derivative, is an anti-SARS-CoV compound. Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 (ACE2) interaction. Emodin inhibits casein kinase-2 (CK2). Anti-inflammatory and anticancer effects. Emodin is a potent selective 11β-HSD1 inhibitor with the IC50 of 186 and 86 nM for human and mouse 11β-HSD1, respectively. Emodin ameliorates metabolic disorder in diet-induced obese mice. | ||||||||||||||||||||
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Aloe emodin | 98.32% | Aloe emodin (Rhabarberone) is a natural hydroxyanthraquinone with antitumor activities. aloe-emodin can bind with mTORC2 and inhibit its kinase activity. Aloe emodin exerts antiproliferation effects and induces cellular apoptosis. Aloe emodin also exhibits antiviral activity that against influenza A virus. | ||||||||||||||||||||
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Carviolin | Carviolin is a compound isolated from the mycelia of the ascomycete Neobulgaria pura. Carviolin inhibits the formation of appressoria in germinating conidia of Magnaporthe grisea on inductive (hydrophobic) surface. Carviolin exhibits moderate cytotoxic, but no antifungal, antibacterial, or phytotoxic activities. | |||||||||||||||||||||
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2-Hydroxyemodin | 2-Hydroxyemodin is an active metabolite of emodin in the hepatic microsomes. Emodin is an anthraquinone present in fungal metabolites and constituent of rhubarb. 2-Hydroxyemodin proves to be mutagenic to Salmonella typhimurium TA1537 in the absence of activation system. | |||||||||||||||||||||
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Paeciloquinone C | Paeciloquinone C can inhibit the EGFR protein tyrosine kinase. Paeciloquinone C inhibits the V-abl protein tyrosine Kinase with an IC50 of 0.56 μM. | |||||||||||||||||||||
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Flavokermesic acid | 98.18% | Flavokermesic acid is an anthraquinone dye that can be detected in extracts of insects from the family Diaspididae, and it is a minor pigment component thereof. Flavokermesic acid can be used to investigate the biosynthetic pathways of insect-derived anthraquinone pigments. | ||||||||||||||||||||
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Rheoemodin | Rheoemodin is an anthraquinone and antibacterial agent. Rheoemodin can be isolated from Cordyceps morakotii BCC 56811. Rheoemodin exhibits antibacterial activity against Acinetobacter baumannii (MIC: 12.5 μg/mL). Rheoemodin also exhibits weak to moderate antimycobacterial and antifungal activity. Rheoemodin also exhibits anticancer activity against breast cancer and small cell lung cancer. | |||||||||||||||||||||
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ω-Hydroxydigitoemodin | ω-Hydroxydigitoemodin is an anthraquinone derivative with anti-acetylcholinesterase activity, found in the marine fungus Trichoderma harzianum XS-20090075. | |||||||||||||||||||||
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Questinol | Questinol is a palmitic acid that can be isolated from Talaromyces stipitatus. Questinol has signi?cant anti-obesity activity in zebra?sh larvae. | |||||||||||||||||||||
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