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
Matsuda T et al. Photocurable biodegradable liquid copolymers: synthesis of acrylate-end-capped trimethylene carbonate-based prepolymers, photocuring, and hydrolysis. 2004 Mar-Apr Biomacromolecules pmid:15002987
Hirabayashi C Studies on MMA-TBB resin II. The effect of dual use of TBB and other initiators on polymerization of PMMA/MMA resin. 2003 Dent Mater J pmid:12790296
Hirabayashi C and Imai Y Studies on MMA-tBB resin. I. Comparison of TBB and other initiators in the polymerization of PMMA/MMA resin. 2002 Dent Mater J pmid:12608421
Shimamura M et al. Comparison of antiandrogenic activities of vinclozolin and D,L-camphorquinone in androgen receptor gene transcription assay in vitro and mouse in utero exposure assay in vivo. 2002 Toxicology pmid:11985887
Thulasiram HV et al. Effect of ring size in R-(+)-pulegone-mediated hepatotoxicity: studies on the metabolism of R-(+)-4-methyl-2-(1-methylethylidene)-cyclopentanone and DL-camphorone in rats. 2001 Drug Metab. Dispos. pmid:11353750
Tanaka J et al. Polymer properties on resins composed of UDMA and methacrylates with the carboxyl group. 2001 Dent Mater J pmid:11806155
Hofmann N et al. Comparison between a plasma arc light source and conventional halogen curing units regarding flexural strength, modulus, and hardness of photoactivated resin composites. 2000 Clin Oral Investig pmid:11000318
Tilbrook DA et al. Photocurable epoxy-polyol matrices for use in dental composites I. 2000 Biomaterials pmid:10905456
Bryant SJ et al. Cytocompatibility of UV and visible light photoinitiating systems on cultured NIH/3T3 fibroblasts in vitro. 2000 J Biomater Sci Polym Ed pmid:10896041
Stansbury JW Curing dental resins and composites by photopolymerization. 2000 J Esthet Dent pmid:14743525