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Article Synopsis
  • Five new pregnane C21-steroids were identified from the roots of Cynanchum bungei, including three previously unknown 5,6-epoxy steroids and two 8,14-seco-steroids.
  • Compound 3 is notable for being the first 5a,6a-epoxy steroid discovered in Cynanchum plants, with their structures confirmed through various spectroscopic methods and theoretical calculations.
  • All isolated compounds showed anti-inflammatory properties by inhibiting nitric oxide release in RAW264.7 cells, with compounds 3 and 4 demonstrating stronger activity than the commonly used anti-inflammatory drug indomethacin at a concentration of 50 μM.
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Integrated proteomics and metabolomics network analysis across different delivery modes in human pregnancy: a pilot study.

BMC Pregnancy Childbirth

December 2024

Ministry of Education-Shanghai Key Laboratory of Children's Environmental Health, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Background: Delivery mode has been linked to child health, e.g., allergic disease.

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Dai-Bai-Jie, the root of the plant Marsdenia tenacissima from the Asclepiadaceae family, is well-known for its therapeutic effects in clearing heat, detoxifying, reducing swelling, and relieving pain as one of the most commonly used Dai medicine. Due to numerous structurally similar C21 steroidal compounds in Dai-Bai-Jie, chemical composition profiling has been substantially challenged. In this study, an offline two-dimensional chromatographic method (LC × SFC separation system) was developed to address these issues.

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Three New Steroids from the Roots of Marsdenia tenacissima.

Chem Biodivers

December 2024

The MOE Key Laboratory of Standardization of Chinese Medicines and SATCM Key Laboratory of New Resources and Quality Evaluation of Chinese Medicines, Institute of Chinese Materia Medica (ICMM), Shanghai University of Traditional Chinese Medicine (SHUTCM), Shanghai, 201203, PR China.

Three undescribed pregnane steroids, 12β-O-4-hydroxybenzoyl tenacigenin D (1), 12β-O-4-hydroxybenzoyl tenacigenin A (2), and 11α-nicotinoyl-17β-marsdenin (3), along with two known analogues (4 and 5), were isolated from the roots of Marsdenia tenacissima. Their structures were elucidated using one- and two-dimensional NMR, high-resolution electron ionization-mass spectrometry, single-crystal X-ray diffraction data, and experimental and density-functional-theory-calculated electronic circular dichroism measurements. All isolated compounds were evaluated for their cytotoxic activities against human lung cancer cells (A549), ovarian carcinoma cells (SKOV-3), gastric cancer cells (MGC 803) and breast cancer cells (MCF-7).

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Prostate cancer (PCa) is the most commonly diagnosed cancer in male individuals, principally affecting men over 50 years old, and is the leading cause of cancer-related deaths. Actually, the measurement of prostate-specific antigen level in blood is affected by limited sensitivity and specificity and cannot discriminate PCa from benign prostatic hyperplasia patients (BPH). In the present paper, 20 urine samples from BPH patients and 20 from PCa patients were investigated to develop a metabolomics strategy useful to distinguish malignancy from benign hyperplasia.

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