Proamanullin
WikiDoc Resources for Proamanullin |
Articles |
---|
Most recent articles on Proamanullin Most cited articles on Proamanullin |
Media |
Powerpoint slides on Proamanullin |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Proamanullin at Clinical Trials.gov Clinical Trials on Proamanullin at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Proamanullin
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Proamanullin Discussion groups on Proamanullin Patient Handouts on Proamanullin Directions to Hospitals Treating Proamanullin Risk calculators and risk factors for Proamanullin
|
Healthcare Provider Resources |
Causes & Risk Factors for Proamanullin |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
Template:Chembox E numberTemplate:Chembox AppearanceFile:Proamanullin structure.png | |
File:Proamanullin 3d chemical structure.png | |
Names | |
---|---|
Other names
2-L-Proline-3-isoleucine-alpha-amanitin
| |
Identifiers | |
3D model (JSmol)
|
|
ECHA InfoCard | Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). |
PubChem CID
|
|
| |
Properties | |
C39H54N10O11S | |
Molar mass | 870.97 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Promanullin is a cyclic nonribosomal peptide. It is an amatoxin, all of which are found in several members of the Amanita genus of mushrooms.
Toxicology
Like other amatoxins, proamanullin is an inhibitor of RNA polymerase II. Promanullin has a specific attraction to the enzyme RNA polymerase II. Upon ingestion, it binds to the RNA polymerase II enzyme, effectively causing cytolysis of hepatocytes (liver cells).[1]
References
See also
External links
- Pages with script errors
- Pages with citations using unsupported parameters
- Pages with broken file links
- Articles without InChI source
- Chemical pages without ChemSpiderID
- Articles without EBI source
- Articles without KEGG source
- Articles without UNII source
- ECHA InfoCard ID from Wikidata
- Articles containing unverified chemical infoboxes
- Chembox image size set
- Peptides
- Mycotoxins
- Hepatology
- Enzyme inhibitors