Camphorquinone

Camphorquinone is a lipid of Prenol Lipids (PR) class. The involved functions are known as Polymerization. The related lipids are camphoroquinone.

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Introduction

To understand associated biological information of Camphorquinone, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with Camphorquinone?

There are no associated biomedical information in the current reference collection.

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Camphorquinone

PubChem Associated disorders and diseases

What pathways are associated with Camphorquinone

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with Camphorquinone?

There are no associated biomedical information in the current reference collection.

What functions are associated with Camphorquinone?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with Camphorquinone?

Related references are published most in these journals:

Lipid concept Cross reference Weighted score Related literatures
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What genes are associated with Camphorquinone?

There are no associated biomedical information in the current reference collection.

What common seen animal models are associated with Camphorquinone?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with Camphorquinone

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Authors Title Published Journal PubMed Link
Wang Z and Chiang MY System compliance dictates the effect of composite filler content on polymerization shrinkage stress. 2016 Dent Mater pmid:26916062
Ge X et al. Probing the dual function of a novel tertiary amine compound in dentin adhesive formulations. 2016 Dent Mater pmid:26764171
Zhang Y and Wang Y The effect of hydroxyapatite presence on the degree of conversion and polymerization rate in a model self-etching adhesive. 2012 Dent Mater pmid:22032933
Prakki A et al. Effect of propionaldehyde or 2,3-butanedione additives on the mechanical properties of Bis-GMA analog-based composites. 2009 Dent Mater pmid:18757084
Cadenaro M et al. Influence of different initiators on the degree of conversion of experimental adhesive blends in relation to their hydrophilicity and solvent content. 2010 Dent Mater pmid:20018363
Ely C et al. Polymerization kinetics and reactivity of alternative initiators systems for use in light-activated dental resins. 2012 Dent Mater pmid:23083514
Chen M et al. Effect of a non-thermal, atmospheric-pressure, plasma brush on conversion of model self-etch adhesive formulations compared to conventional photo-polymerization. 2012 Dent Mater pmid:23018084
Guo X et al. Effects of water content and initiator composition on photopolymerization of a model BisGMA/HEMA resin. 2008 Dent Mater pmid:18045679
Furche S et al. Quantification of elutable substances from methacrylate based sealers and their cytotoxicity effect on with human gingival fibroblasts. 2013 Dent Mater pmid:23570627
Prakki A et al. In vitro wear, surface roughness and hardness of propanal-containing and diacetyl-containing novel composites and copolymers based on bis-GMA analogs. 2008 Dent Mater pmid:17688931