Vitamin D3 (BioDeep_00000000211)

   

natural product human metabolite Endogenous blood metabolite Chemicals and Drugs


代谢物信息卡片


(1S,3Z)-3-((2E)-2-((1R,3AR,7AS)-7A-METHYL-1-((2R)-6-METHYLHEPTAN-2-YL)-2,3,3A,5,6,7-HEXAHYDRO-1H-INDEN-4-YLIDENE)ETHYLIDENE)-4-METHYLIDENE-CYCLOHEXAN-1-OL

化学式: C27H44O (384.3391974)
中文名称: 麦角钙化甾醇, 维生素D3
谱图信息: 最多检出来源 Homo sapiens(blood) 0.07%

分子结构信息

SMILES: C1C(=C)/C(=C\C=C2\[C@]3([H])CC[C@@]([H])([C@@]3(C)CCC\2)[C@]([H])(C)CCCC(C)C)/C[C@@H](O)C1
InChI: InChI=1/C27H44O/c1-19(2)8-6-9-21(4)25-15-16-26-22(10-7-17-27(25,26)5)12-13-23-18-24(28)14-11-20(23)3/h12-13,19,21,24-26,28H,3,6-11,14-18H2,1-2,4-5H3/b22-12+,23-13-/t21-,24+,25-,26+,27-/m1/s1

描述信息

Vitamin d3 appears as fine colorless crystals. Water insoluble. (NTP, 1992)
Calciol is a hydroxy seco-steroid that is (5Z,7E)-9,10-secocholesta-5,7,10(19)-triene in which the pro-S hydrogen at position 3 has been replaced by a hydroxy group. It is the inactive form of vitamin D3, being hydroxylated in the liver to calcidiol (25-hydroxyvitamin D3), which is then further hydroxylated in the kidney to give calcitriol (1,25-dihydroxyvitamin D3), the active hormone. It has a role as a human metabolite and a geroprotector. It is a seco-cholestane, a hydroxy seco-steroid, a member of D3 vitamins, a secondary alcohol and a steroid hormone.
Vitamin D, in general, is a secosteroid generated in the skin when 7-dehydrocholesterol located there interacts with ultraviolet irradiation - like that commonly found in sunlight. Both the endogenous form of vitamin D (that results from 7-dehydrocholesterol transformation), vitamin D3 (cholecalciferol), and the plant-derived form, vitamin D2 (ergocalciferol), are considered the main forms of vitamin d and are found in various types of food for daily intake. Structurally, ergocalciferol differs from cholecalciferol in that it possesses a double bond between C22 and C23 and has an additional methyl group at C24. Finally, ergocalciferol is pharmacologically less potent than cholecalciferol, which makes vitamin D3 the preferred agent for medical use. Appropriate levels of vitamin D must be upheld in the body in order to maintain calcium and phosphorus levels in a healthy physiologic range to sustain a variety of metabolic functions, transcription regulation, and bone metabolism. However, studies are also ongoing to determine whether or not cholecalciferol may also play certain roles in cancer, autoimmune disorders, cardiovascular disease, and other medical conditions that may be associated with vitamin D deficiency.
Cholecalciferol is a Vitamin D.
Cholecalciferol is a natural product found in Taiwanofungus camphoratus, Theobroma cacao, and other organisms with data available.
Cholecalciferol is a steroid hormone produced in the skin when exposed to ultraviolet light or obtained from dietary sources. The active form of cholecalciferol, 1,25-dihydroxycholecalciferol (calcitriol) plays an important role in maintaining blood calcium and phosphorus levels and mineralization of bone. The activated form of cholecalciferol binds to vitamin D receptors and modulates gene expression. This leads to an increase in serum calcium concentrations by increasing intestinal absorption of phosphorus and calcium, promoting distal renal tubular reabsorption of calcium and increasing osteoclastic resorption.
Cholecalciferol is only found in individuals that have used or taken this drug. It is a derivative of 7-dehydroxycholesterol formed by ultraviolet rays breaking of the C9-C10 bond. It differs from ergocalciferol in having a single bond between C22 and C23 and lacking a methyl group at C24. [PubChem]The first step involved in the activation of vitamin D3 is a 25-hydroxylation which is catalysed by the 25-hydroxylase in the liver and then by other enzymes. The mitochondrial sterol 27-hydroxylase catalyses the first reaction in the oxidation of the side chain of sterol intermediates. The active form of vitamin D3 (calcitriol) binds to intracellular receptors that then function as transcription factors to modulate gene expression. Like the receptors for other steroid hormones and thyroid hormones, the vitamin D receptor has hormone-binding and DNA-binding domains. The vitamin D receptor forms a complex with another intracellular receptor, the retinoid-X receptor, and that heterodimer is what binds to DNA. In most cases studied, the effect is to activate transcription, but situations are also known in which vitamin D suppresses transcription. Calcitriol increases the serum calcium concentrations by: increasing GI absorption of phosphorus and calcium, increasing osteoclastic resorption, and increasing distal renal tubula...
Vitamin D3, also called cholecalciferol, is one of the forms of vitamin D. Vitamin D3 is a steroid hormone that has long been known for its important role in regulating body levels of calcium and phosphorus, in mineralization of bone, and for the assimilation of Vitamin A. It is structurally similar to steroids such as testosterone, cholesterol, and cortisol (although vitamin D3, itself, is a secosteroid). Vitamin D3 is a derivative of 7-dehydroxycholesterol formed by ultraviolet rays breaking the C9-C10 bond. It differs from ergocalciferol in having a single bond between C22 and C23 and lacking a methyl group at C24. Vitamin D3 can also come from dietary sources, such as beef liver, cheese, egg yolks, and fatty fish (PubChem). The first step involved in the activation of vitamin D3 is a 25-hydroxylation catalyzed by 25-hydroxylase in the liver and then by other enzymes. The mitochondrial sterol 27-hydroxylase catalyzes the first reaction in the oxidation of the side chain of sterol intermediates. The active form of vitamin D3 (calcitriol) binds to intracellular receptors that then function as transcription factors to modulate gene expression. Like the receptors for other steroid hormones and thyroid hormones, the vitamin D receptor has hormone-binding and DNA-binding domains. The vitamin D receptor forms a complex with another intracellular receptor, the retinoid-X receptor, and that heterodimer is what binds to DNA. In most cases studied, the effect is to activate transcription, but situations are also known in which vitamin D suppresses transcription. Calcitriol increases the serum calcium concentrations by (1) increasing GI absorption of phosphorus and calcium, (2) increasing osteoclastic resorption, and (3) increasing distal renal tubular reabsorption of calcium. Calcitriol appears to promote intestinal absorption of calcium through binding to the vitamin D receptor in the mucosal cytoplasm of the intestine. Subsequently, calcium is absorbed through the formation of a calcium-binding protein.
Vitamin d, also known as colecalciferol or calciol, belongs to vitamin d and derivatives class of compounds. Those are compounds containing a secosteroid backbone, usually secoergostane or secocholestane. Thus, vitamin d is considered to be a secosteroid lipid molecule. Vitamin d is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Vitamin d can be found in a number of food items such as dumpling, vinegar, chocolate, and margarine, which makes vitamin d a potential biomarker for the consumption of these food products. Vitamin d can be found primarily in blood and urine. Vitamin d is a non-carcinogenic (not listed by IARC) potentially toxic compound. Vitamin d is a drug which is used for the treatment of vitamin d deficiency or insufficiency, refractory rickets (vitamin d resistant rickets), familial hypophosphatemia and hypoparathyroidism, and in the management of hypocalcemia and renal osteodystrophy in patients with chronic renal failure undergoing dialysis. also used in conjunction with calcium in the management and prevention of primary or corticosteroid-induced osteoporosis.
A - Alimentary tract and metabolism > A11 - Vitamins > A11C - Vitamin a and d, incl. combinations of the two > A11CC - Vitamin d and analogues
COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials
D000077264 - Calcium-Regulating Hormones and Agents
D018977 - Micronutrients > D014815 - Vitamins
D050071 - Bone Density Conservation Agents
Corona-virus
Coronavirus
SARS-CoV-2
COVID-19
SARS-CoV
COVID19
SARS2
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同义名列表

158 个代谢物同义名

(1S,3Z)-3-((2E)-2-((1R,3AR,7AS)-7A-METHYL-1-((2R)-6-METHYLHEPTAN-2-YL)-2,3,3A,5,6,7-HEXAHYDRO-1H-INDEN-4-YLIDENE)ETHYLIDENE)-4-METHYLIDENE-CYCLOHEXAN-1-OL; (1S,3Z)-3-[(2E)-2-[(1R,3AR,7AS)-7A-METHYL-1-[(2R)-6-METHYLHEPTAN-2-YL]-2,3,3A,5,6,7-HEXAHYDRO-1H-INDEN-4-YLIDENE]ETHYLIDENE]-4-METHYLIDENE-CYCLOHEXAN-1-OL; (1S,3Z)-3-[(2E)-2-[(1R,3aS,7aR)-7a-methyl-1-[(2R)-6-methylheptan-2-yl]-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol; (1S,3Z)-3-[(2E)-2-[(1R,3aS,7aR)-1-[(1R)-1,5-dimethylhexyl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylene-cyclohexanol; (1S,3Z)-3-{2-[(1R,3aS,4E,7aR)-7a-methyl-1-[(2R)-6-methylheptan-2-yl]-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol; Cyclohexanol, 3-[(2E)-2-[(1R,3aS,7aR)-1-[(1R)-1,5-dimethylhexyl]octahydro-7a-methyl-4H-inden-4-ylidene]ethylidene]-4-methylene-, (1S,3Z)-; Cyclohexanol, 3-((2E)-2-((1R,3aS,7aR)-1-((1R)-1,5-dimethylhexyl)octahydro-7a-methyl-4H-inden-4-ylidene)ethylidene)-4-methylene-, (1S,3Z)-; (1S,3Z)-3-[(2E)-2-[7a-Methyl-1-(6-methylheptan-2-yl)-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol; (S,Z)-3-(2-((1R,3aS,7aR,E)-7a-methyl-1-((R)-6-methylheptan-2-yl)octahydro-4H-inden-4-ylidene)ethylidene)-4-methylenecyclohexan-1-ol; Cholecalciferol (Vitamin D3), Pharmaceutical Secondary Standard; Certified Reference Material; Cholecalciferol for system suitability, European Pharmacopoeia (EP) Reference Standard; Cholecalciferol, United States Pharmacopeia (USP) Reference Standard; Cholecalciferol, European Pharmacopoeia (EP) Reference Standard; Colecalciferol, British Pharmacopoeia (BP) Reference Standard; 9,10-Secocholesta-5,7,10(19)-trien-3-ol, (3.beta.,5Z,7E)-; 9,10-Secocholestra-5,7,10(19)-trien-3-ol, (3beta,5Z,7E)-; 9,10-Secocholesta-5,7,10(19)-trien-3-ol, (3beta,5Z,7E)-; (3.beta.,5Z,7E)-9,10-secocholesta-5,7,10(19)-trien-3-ol; (3 beta,5Z,7E)-9,10-Secocholesta-5,7,10(19)-trien-3-ol; (3beta,5Z,7E)-9,10-secocholesta-5,7,10(19)-trien-3-ol; 9,10-Secocholesta-5(Z),7(E),10(19)-trien-3(.beta.)-ol; (5Z,7E)-(3S)-9,10-seco-5,7,10(19)-cholestatrien-3-ol; 9,10-Secocholesta-5,7,10(19)-trien-3-ol, (3b,5Z,7E)-; (3beta,Z,7E)-9,10-Secocholesta-5,7,10(19)-trien-3-ol; (5Z,7E)-(3S)-9,10-secocholesta-5,7,10(19)-trien-3-ol; 3-beta,Z,7E-9,10-Secocholestr-5,7,10(19)-trien-3-ol; (5E,7E)-9,10-SECOCHOLESTA-5,7,10(19)-TRIEN-3beta-OL; (3S,5Z,7E)-9,10-secocholesta-5,7,10(19)-trien-3-ol; (3b,5Z,7E)-9,10-Secocholesta-5,7,10(19)-trien-3-ol; (3Β,5Z,7E)-9,10-secocholesta-5,7,10(19)-trien-3-ol; 9,10-Seco(5Z,7E)-5,7,10(19)-cholestatrien-3beta-ol; Cholecalciferol, meets USP testing specifications; 9,10-Seco(5Z,7E)-5,7,10(19)-cholestatrien-3-ol; 9,10-Secocholesta-5,7,10(19)-trien-3-beta-ol; (5E,7E)-9,10-Secocholesta-5,7,10-trien-3-ol; VITAMIN D ASSAY SYSTEM SUITABILITY [USP-RS]; 9,10-Secocholesta-5,7,10(19)-trien-3beta-ol; CHOLECALCIFEROL COMPONENT OF FOSAMAX PLUS D; Cholecalciferol (D3), analytical standard; 9,10-Secocholesta-5,7,10(19)-trien-3?-ol; FOSAMAX PLUS D COMPONENT CHOLECALCIFEROL; CHOLECALCIFEROL IMPURITY A (EP IMPURITY); 9,10-Secocholesta-5,7,10(19)-trien-3-ol; Vitamin D3 10 microg/mL in Acetonitrile; Cholecalciferol for system suitability; Cholecalciferol, analytical standard; 9,10-secocholesta-5,7,10-trien-3-ol; Vitamin d assay system suitability; Cholecalciferol [USP:BAN:JAN:ISO]; Cholecalciferol (USP:BAN:JAN:ISO); 7-Dehydrocholesterol, irradiated; CHOLECALCIFEROL [USP MONOGRAPH]; Irradiated 7-dehydrocholesterol; COLECALCIFEROLUM [WHO-IP LATIN]; CHOLECALCIFEROL (USP MONOGRAPH); Vitamin d3 (as cholecalciferol); Activated 7-dehydrocholesterol; Cholecalciferol, >=98\\% (HPLC); CHOLECALCIFEROL (EP MONOGRAPH); CHOLECALCIFEROL [EP MONOGRAPH]; CHOLECALCIFEROL [ORANGE BOOK]; Vitamin D3 (Cholecalciferol); Colecalciferolum (INN-Latin); Colecalciferolum [INN-Latin]; GROWTH SUPPORTPATCH, HAUTUKI; Vitamin d (cholecalciferol); 5,7-CHOLESTADIEN-3-BETAL-OL; Vitamin D3; Cholecalciferol; Cholecalciferol (JP17/USP); COLECALCIFEROL [EMA EPAR]; CHOLECALCIFEROL [USP-RS]; CHOLECALCIFEROL (USP-RS); Cholecalciferol; 67-97-0; COLECALCIFEROL [WHO-IP]; Vitamin D3 emulsifiable; COLECALCIFEROL [WHO-DD]; CHOLECALCIFEROL [VANDF]; CHOLECALCIFEROL [HSDB]; COLECALCIFEROL (MART.); Colecalciferolo [DCIT]; CHOLECALCIFEROL [INCI]; COLECALCIFEROL [MART.]; CHOLECALCIFEROL [JAN]; CHOLECALCIFEROL [ISO]; Colecalciferol [INN]; 7-Dehydrocholesterol; Colecalciferol (INN); Cholecalciferol, D3; Cholecalciferol D3; Dihydrocholesterol; Colecalciferol D3; Cholecalciferolum; Duphafral D3 1000; Prestwick3_000429; Vitinc Dan-Dee-3; Cholecalciferols; VITAMIN D3 [FCC]; Vi-de-3-hydrosol; VidDe-3-hydrosol; Colecalciferolum; Colecalciferolo; Colecalcipherol; UNII-1C6V77QF41; VITAMIN D3 [MI]; NEO Dohyfral D3; Cholecalciferol; UNII-9VU1KI44GP; (+)-Vitamin D3; Oleovitamin D3; Colecalciferol; ()-Vitamin D3; BPBio1_000460; MEGxm0_000458; VIGANTOLETTEN; ACon1_001997; Delta-D (TN); vitaminum d3; Prestwick_63; D3-Vicotrat; SMP1_000068; Vitamin D 3; vitamin d-3; D3-Vigantol; DECALCITROL; Granuvit D3; 1C6V77QF41; Osteo-Vit3; 9VU1KI44GP; Vitamin D3; VITA-DESIC; Provitina; Arachitol; Micro-dee; Delsterol; ACTIVATED; Vitamin D; Trivitan; Vigantol; Vigorsan; Videkhol; Ricketon; Novel-D3; Delta-D; Quintox; FeraCol; Rampage; Devaron; Calciol; Vitamin; Deparal; A11CC05; Vi-De3; Ebivit; δ-D; CC; Vitamin D3 / Cholecalciferol (Vitamin D3) skeleton; Vitamin D3 (7-dehydrocholesterol); Vitamin D3-d7



数据库引用编号

25 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(11)

BioCyc(0)

PlantCyc(0)

代谢反应

145 个相关的代谢反应过程信息。

Reactome(96)

BioCyc(0)

WikiPathways(3)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(46)

PharmGKB(0)

18 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。



文献列表

  • Hui Guo, Bing-di Cui, Man Gong, Qing-Xia Li, Ling-Xia Zhang, Jia-Li Chen, Jun Chi, Li-Li Zhu, Er-Ping Xu, Zhi-Min Wang, Li-Ping Dai. An ethanolic extract of Arctium lappa L. leaves ameliorates experimental atherosclerosis by modulating lipid metabolism and inflammatory responses through PI3K/Akt and NF-κB singnaling pathways. Journal of ethnopharmacology. 2024 May; 325(?):117768. doi: 10.1016/j.jep.2024.117768. [PMID: 38253275]
  • Zahraa S Al-Garawi, Ahmad H Ismail Al-Qaisi, Kawthar Amer Al-Shamari, Füreya Elif Öztürkkan, Hacali Necefoğlu. The utility of Hibiscus sabdariffa L. to prepare metal oxides NPs for clinical application on osteoporosis supported by theoretical study. Bioprocess and biosystems engineering. 2024 May; 47(5):753-766. doi: 10.1007/s00449-024-03012-5. [PMID: 38573334]
  • Emilia Papakonstantinou, Nikolaos Zacharodimos, Georgios Georgiopoulos, Christina Athanasaki, Dionysia-Lydia Bothou, Sofia Tsitsou, Foteini Lympaki, Stamatia Vitsou-Anastasiou, Olga S Papadopoulou, Dimitrios Delialis, Evangelos C Alexopoulos, Eleni Petsiou, Kalliopi Keramida, Agapi I Doulgeraki, Ismini-Maria Patsopoulou, George-John E Nychas, Chrysoula C Tassou. Two-Month Consumption of Orange Juice Enriched with Vitamin D3 and Probiotics Decreases Body Weight, Insulin Resistance, Blood Lipids, and Arterial Blood Pressure in High-Cardiometabolic-Risk Patients on a Westernized Type Diet: Results from a Randomized Clinical Trial. Nutrients. 2024 Apr; 16(9):. doi: 10.3390/nu16091331. [PMID: 38732578]
  • Shubin Liu, Qiuran Yu, Jiadai Liu, Han Wang, Xiaodan Wang, Chuanjie Qin, Erchao Li, Jianguang Qin, Liqiao Chen. The interaction between lipid and vitamin D3 impacts lipid metabolism and innate immunity in Chinese mitten crabs Eriocheir sinensis. Fish & shellfish immunology. 2024 Apr; 147(?):109455. doi: 10.1016/j.fsi.2024.109455. [PMID: 38369072]
  • Rui Li, Xiaojing Han, Qiudong Wang, Chenghui Wang, Wei Jing, Haihan Zhang, Jun Wang, Weidong Pan. Network pharmacology analysis and clinical efficacy of the traditional Chinese medicine Bu-Shen-Jian-Pi. Part 3: Alleviation of hypoxia, muscle-wasting, and modulation of redox functions in amyotrophic lateral sclerosis. International journal of clinical pharmacology and therapeutics. 2024 Apr; 62(4):169-177. doi: 10.5414/cp204520. [PMID: 38431830]
  • Catarina Santos, Rui Carvalho, Ana Mafalda Fonseca, Miguel Castelo Branco, Marco Alves, Ivana Jarak. Standard Doses of Cholecalciferol Reduce Glucose and Increase Glutamine in Obesity-Related Hypertension: Results of a Randomized Trial. International journal of molecular sciences. 2024 Mar; 25(6):. doi: 10.3390/ijms25063416. [PMID: 38542390]
  • Mahesh I Sirasangi, Tamsheel Fatima Roohi, K L Krishna, Nabeel Kinattingal, Shahid Ud Din Wani, Seema Mehdi. Dietary Co-supplements attenuate the chronic unpredictable mild stress-induced depression in mice. Behavioural brain research. 2024 02; 459(?):114788. doi: 10.1016/j.bbr.2023.114788. [PMID: 38036263]
  • Francesca Uberti, Francesco Trotta, Roberta Cavalli, Rebecca Galla, Fabrizio Caldera, Sara Ferrari, Simone Mulè, Arianna Brovero, Claudio Molinari, Pasquale Pagliaro, Claudia Penna. Enhancing Vitamin D3 Efficacy: Insights from Complexation with Cyclodextrin Nanosponges and Its Impact on Gut-Brain Axes in Physiology and IBS Syndrome. International journal of molecular sciences. 2024 Feb; 25(4):. doi: 10.3390/ijms25042189. [PMID: 38396866]
  • Stephanie Gaengler, Angélique Sadlon, Caroline De Godoi Rezende Costa Molino, Walter C Willett, JoAnn E Manson, Bruno Vellas, Elisabeth Steinhagen-Thiessen, Arnold Von Eckardstein, Frank Ruschitzka, René Rizzoli, José A P da Silva, Reto W Kressig, John Kanis, E John Orav, Andreas Egli, Heike A Bischoff-Ferrari. Effects of vitamin D, omega-3 and a simple strength exercise programme in cardiovascular disease prevention: The DO-HEALTH randomized controlled trial. The journal of nutrition, health & aging. 2024 02; 28(2):100037. doi: 10.1016/j.jnha.2024.100037. [PMID: 38199870]
  • Lian Xiang, Tingwan Du, Jingjing Zhang, Yuanfan Zhang, Yanqiu Zhou, Yueying Zhao, Yong Zhou, Ling Ma. Vitamin D3 supplementation shapes the composition of gut microbiota and improves some obesity parameters induced by high-fat diet in mice. European journal of nutrition. 2024 Feb; 63(1):155-172. doi: 10.1007/s00394-023-03246-1. [PMID: 37740812]
  • Qiong Chen, Lin Liu, Yi Zhang. Vitamin D and wound healing: Assessing skin barrier function and implications for chloasma treatment. International wound journal. 2024 Jan; 21(1):e14541. doi: 10.1111/iwj.14541. [PMID: 38272820]
  • Jasim Ahmed, Bhupendra Raj Giri, Mohammed Arshad Reza, Syed S Bin Qasim, Linu Thomas, Hasan Al-Attar, Mohammed Maniruzzaman. Twin-screw extrusion of vitamin D3/iron-blend granules in corn and lentil composite flours: Stability, microstructure, and interaction of vitamin D3 with human osteoblast cells. Journal of food science. 2024 Jan; 89(1):435-449. doi: 10.1111/1750-3841.16841. [PMID: 38018266]
  • Chee Wai Ku, Angeline Jia Wen Lee, Benjarat Oh, Celeste Hong Fei Lim, Ting Yu Chang, Fabian Yap, Jerry Kok Yen Chan, See Ling Loy. The Effect of Vitamin D Supplementation in Pregnant Women with Overweight and Obesity: A Randomised Controlled Trial. Nutrients. 2023 Dec; 16(1):. doi: 10.3390/nu16010146. [PMID: 38201976]
  • Miłosz Miedziaszczyk, Adam Maciejewski, Ilona Idasiak-Piechocka, Marek Karczewski, Katarzyna Lacka. Effects of Isoflavonoid and Vitamin D Synergism on Bone Mineral Density-A Systematic and Critical Review. Nutrients. 2023 Dec; 15(24):. doi: 10.3390/nu15245014. [PMID: 38140273]
  • Xiao-Li Zhang, Qing Zhang, Xu Zhang, Qin-Wen Gu, Jin-Jing Pan, Yu-Fang Pei, Jia-Fu Li, Fei Jiang, Ling-Jing Diao, Hui-Ming Zhou, Hong-Mei Ding, Zeng-Li Zhang, Guang-Ming Zhou, Wen-Jun Wang, Bing-Yan Li. Effect of vitamin D3 supplementation in winter on physical performance of university students: a one-month randomized controlled trial. Journal of the International Society of Sports Nutrition. 2023 Dec; 20(1):2258850. doi: 10.1080/15502783.2023.2258850. [PMID: 37735799]
  • Rouba Yasser Al-Sroji, Shaza Al-Laham, Ahmad Almandili. Protective effects of vitamin D3 (cholecalciferol) on vancomycin-induced oxidative nephrotoxic damage in rats. Pharmaceutical biology. 2023 Dec; 61(1):755-766. doi: 10.1080/13880209.2023.2204916. [PMID: 37139624]
  • Maria A Azevedo, Miguel A Cerqueira, Catarina Gonçalves, Isabel R Amado, José A Teixeira, Lorenzo Pastrana. Encapsulation of vitamin D3 using rhamnolipids-based nanostructured lipid carriers. Food chemistry. 2023 Nov; 427(?):136654. doi: 10.1016/j.foodchem.2023.136654. [PMID: 37399642]
  • Aislinn F McCourt, Steven L Mulrooney, Graham J O'Neill, E Dolores O'Riordan, Aifric M O'Sullivan. Serum 25-hydroxyvitamin D response to vitamin D supplementation using different lipid delivery systems in middle-aged and older adults: a randomised controlled trial. The British journal of nutrition. 2023 11; 130(9):1548-1557. doi: 10.1017/s0007114523000636. [PMID: 36912075]
  • Esraa Habiba, Samia Ali, Yehia Ghanem, Ola Sharaki, Wafaa Hewedy. Effect of oral versus parenteral vitamin D3 supplementation on nuclear factor-κB and platelet aggregation in type 2 diabetic patients. Canadian journal of physiology and pharmacology. 2023 Nov; 101(11):610-619. doi: 10.1139/cjpp-2022-0359. [PMID: 37721213]
  • Christiano Argano, Luigi Mirarchi, Simona Amodeo, Valentina Orlando, Alessandra Torres, Salvatore Corrao. The Role of Vitamin D and Its Molecular Bases in Insulin Resistance, Diabetes, Metabolic Syndrome, and Cardiovascular Disease: State of the Art. International journal of molecular sciences. 2023 Oct; 24(20):. doi: 10.3390/ijms242015485. [PMID: 37895163]
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