Endocrinology and Hormones


Endocrinology is the study of hormones, their receptors and intracellular signaling pathways, as well as the related diseases. The endocrine system functions can be broadly classified into several categories, including reproduction and sexual differentiation, development and growth, maintenance of the internal environment, and regulation of metabolism/nutrient supply.
There are three types of hormones based on their chemical composition: Amines (e.g. dopamine, adrenalin and noradrenalin); Steroids (e.g. estrogen, testosterone and glucocorticoids); Peptides (e.g. the peptide hormones insulin, ghrelin and vasopressin). Peptide hormones produced by secretory nervous tissue are known as neuropeptides. For example, thyroid hormone plays important parts in development, homeostasis and metabolism, while cortisol is essential for growth, nutrient supply and immune function. Moreover, the regulation of blood glucose involves several pancreatic peptide insulin and its counter regulatory hormone, glucagon, as well as cortisol, growth hormone and epinephrine.
Dysregulations in endocrine system are implicated in diseases such as Acromegaly, Cushing Syndrome, Diabetes, Dwarfism, Graves Disease, Hermaphroditism, Delayed and Precocious Puberty and Thyroid Diseases.
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C4624 4’-hydroxy TamoxifenSummary: metabolite of tamoxifen, an estrogen receptor modulator -
C4747 OrmeloxifeneSummary: estrogen receptor modulator -
C4792 ML-335Summary: agonist for OPRM1-OPRD1 heterodimerization -
C5014 3,3',5'-Triiodo-L-thyronineSummary: TRΔα1 activator -
C5637 Lasofoxifene (tartrate)Summary: third-generation, non-steroidal selective estrogen receptor modulator (SERM) -
A1121 Melanocyte stimulating hormone release inhibiting factorSummary: MSH release-inhibiting factor -
C4895 BavachinSummary: estrogen receptors ERα and ERβ activator -
C5537 ZearalanoneSummary: estrogen receptor agonist -
B1049 Ulipristal acetateSummary: Novel selective progesterone receptor modulator (SPRM) -
B2110 Meptazinol HClSummary: Partial agonist at the μ1 opioid receptor

