H-cHxOn-OH
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H-cHxOn-OH

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Category
Cyclic Amino Acids
Catalog number
BAT-005271
CAS number
285996-77-2
Molecular Formula
C7H11NO3
Molecular Weight
157.17
H-cHxOn-OH
IUPAC Name
1-amino-4-oxocyclohexane-1-carboxylic acid
Synonyms
1-Amino-1-carboxy-4-cyclohexanone; 1-amino-4-oxocyclohexane-1-carboxylic acid; Cyclohexanecarboxylic acid,1-amino-4-oxo-
Purity
97%
Density
1.296±0.060 g/cm3
Boiling Point
342.5±42.0 °C
InChI
InChI=1S/C7H11NO3/c8-7(6(10)11)3-1-5(9)2-4-7/h1-4,8H2,(H,10,11)
InChI Key
CESXXYZXSIXCFU-UHFFFAOYSA-N
Canonical SMILES
C1CC(CCC1=O)(C(=O)O)N
1. Vitamin D status and severity of COVID-19
Nete Munk Nielsen, et al. Sci Rep. 2022 Nov 17;12(1):19823. doi: 10.1038/s41598-022-21513-9.
We explored the association between COVID-19 severity and vitamin D status using information from Danish nation-wide health registers, the COVID-19 surveillance database and stored blood samples from the national biobank. 25-hydroxyvitamin D (25(OH)D) was measured using tandem mass spectroscopy. The association between 25(OH)D levels and COVID-19 severity, classified hierarchical as non-hospitalized, hospitalized but not admitted to an intensive care unit (ICU), admitted to ICU, and death, was evaluated by proportional odds ratios (POR) assuming proportionality between the four degrees of severity. Among 447 adults tested SARS-CoV-2 positive in the spring of 2020, low levels of 25(OH)D were associated with a higher risk of severe COVID-19. Thus, odds of experiencing more severe COVID-19 among individuals with insufficient (25 to < 50 nmol/L) and sufficient (≥ 50 nmol/L) 25(OH)D levels were approximately 50% of that among individuals with deficient levels (< 25 nmol/L) (POR = 0.49 (95% CI 0.25-0.94), POR = 0.51 (95% CI 0.27-0.96), respectively). Dividing sufficient vitamin D levels into 50 to < 75 nmol/L and ≥ 75 nmol/L revealed no additional beneficial effect of higher 25(OH)D levels. In this observational study, low levels of 25(OH)D were associated with a higher risk of severe COVID-19. A possible therapeutic role of vitamin D should be evaluated in well-designed interventional studies.
2. Epidemiology of Brain Tumors
Jill S Barnholtz-Sloan, Quinn T Ostrom, David Cote Neurol Clin. 2018 Aug;36(3):395-419. doi: 10.1016/j.ncl.2018.04.001. Epub 2018 Jun 15.
Incidence, prevalence, and survival for brain tumors varies by histologic type, age at diagnosis, sex, and race/ethnicity. Significant progress has been made in identifying potential risk factors for brain tumors, although more research is warranted. The strongest risk factors that have been identified thus far include allergies/atopic disease, ionizing radiation, and heritable genetic factors. Further analysis of large, multicenter, epidemiologic studies, as well as well annotated omic datasets (including genomic, epigenomic, transcriptomic, proteomic, or metabolomics data) can potentially lead to further understanding of the relationship between gene and environment in the process of brain tumor development.
3. COVID-19 and Cardiovascular Disease: From Bench to Bedside
Mina K Chung, et al. Circ Res. 2021 Apr 16;128(8):1214-1236. doi: 10.1161/CIRCRESAHA.121.317997. Epub 2021 Apr 15.
A pandemic of historic impact, coronavirus disease 2019 (COVID-19) has potential consequences on the cardiovascular health of millions of people who survive infection worldwide. Severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2), the etiologic agent of COVID-19, can infect the heart, vascular tissues, and circulating cells through ACE2 (angiotensin-converting enzyme 2), the host cell receptor for the viral spike protein. Acute cardiac injury is a common extrapulmonary manifestation of COVID-19 with potential chronic consequences. This update provides a review of the clinical manifestations of cardiovascular involvement, potential direct SARS-CoV-2 and indirect immune response mechanisms impacting the cardiovascular system, and implications for the management of patients after recovery from acute COVID-19 infection.
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