cladrin

cladrin is a lipid of Polyketides (PK) class.

Cross Reference

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

Current reference collection contains 53 references associated with cladrin in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

Users can download the reference list at the bottom of this page and read the reference manually to find out biomedical information.


Here are additional resources we collected from PubChem and MeSH for cladrin

Possible diseases from mapped MeSH terms on references

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

MeSH term MeSH ID Detail
Body Weight D001835 333 associated lipids
Bone Diseases, Metabolic D001851 9 associated lipids
Total 2

PubChem Biomolecular Interactions and Pathways

NCBI Entrez Crosslinks

All references with cladrin

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Total 9
Authors Title Published Journal PubMed Link
Rashid M et al. Development and validation of UPLC-MS/MS assay for quantification of cladrin: Absolute bioavailability and dose proportionality study in rats. 2018 J Pharm Biomed Anal pmid:29454264
Gautam J et al. An isoflavone cladrin prevents high-fat diet-induced bone loss and inhibits the expression of adipogenic gene regulators in 3T3-L1 adipocyte. 2016 J. Pharm. Pharmacol. pmid:27265669
Singh S et al. Study of conformational stability, structural, electronic and charge transfer properties of cladrin using vibrational spectroscopy and DFT calculations. 2014 Spectrochim Acta A Mol Biomol Spectrosc pmid:24892542
Khan K et al. Positive skeletal effects of cladrin, a naturally occurring dimethoxydaidzein, in osteopenic rats that were maintained after treatment discontinuation. 2013 Osteoporos Int pmid:22932734
Gautam AK et al. Differential effects of formononetin and cladrin on osteoblast function, peak bone mass achievement and bioavailability in rats. 2011 J. Nutr. Biochem. pmid:20579866
Lee S et al. Isoflavone derivatives inhibit NF-κB-dependent transcriptional activity. 2010 Bioorg. Med. Chem. Lett. pmid:20829041
Crombie L and Whiting DA Review article number 135 biosynthesis in the rotenoid group of natural products: applications of isotope methodology. 1998 Phytochemistry pmid:11711058
Pandey R et al. Total extract and standardized fraction from the stem bark of Butea monosperma have osteoprotective action: evidence for the nonestrogenic osteogenic effect of the standardized fraction. Menopause pmid:20395887
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