52452-60-5
52452-60-5
Chemical Structure
Terphenyllin
- CAS No.: 52452-60-5
- Formula:C20H18O5
- Molecular Weight:338.35
IUPAC Name: 3',6'-dimethoxy-[1,1':4',1''-terphenyl]-2',4,4''-triol
InChIKey: YNEMPXKRLPZFAX-UHFFFAOYSA-N
SMILES: OC1=CC=C(C=C1)C2=C(C(O)=C(C(OC)=C2)C3=CC=C(C=C3)O)OC
Biological Activity: Terphenyllin is a naturally abundant p-terphenyl metabolite isolated from the coral derived fungus Aspergillus candidus, has significant α-glucosidase inhibitory activity[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Terphenyllin | 97.16% | Terphenyllin is a naturally abundant p-terphenyl metabolite isolated from the coral derived fungus Aspergillus candidus, has significant α-glucosidase inhibitory activity. | ||||||||||||||||||||
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Terphenyllin (Standard) | ≥98% | Thiamiprine (Standard) is the analytical standard of Thiamiprine. This product is intended for research and analytical applications. Thiamiprine (BW 57-323) is a compound related to azathioprine. Its nucleoside forms are similar to the parent compound in terms of cytotoxicity in vitro (except for the arabinoside). In the rat adjuvant arthritis model in vivo, its riboside and 2'-deoxyriboside are less active than the parent compound. The arabinoside is inactive and nontoxic. It has similar potency to the other parent compounds tested, but has a different safety profile. | ||||||||||||||||||||
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References
Keywords
