Fucoxanthin (BioDeep_00000000052)

human metabolite PANOMIX_OTCML-2023 Endogenous Marine Natural Products Antitumor activity

代谢物信息卡片

化学式: C42H58O6 (658.4233168000001)
中文名称: 墨角藻黄素, 岩藻黄质, 褐藻素
谱图信息: 最多检出来源 Macaca mulatta(otcml) 0.12%

分子结构信息

SMILES: C/C(=C\C=C\C=C(/C)\C=C\C=C(/C)\C(=O)C[C@]12C(C)(C)C[C@@H](C[C@@]1(C)O2)O)/C=C/C=C(\C)/C=C=C1C(C)(C)C[C@@H](C[C@@]1(C)O)OC(=O)C
InChI: InChI=1S/C42H58O6/c1-29(18-14-19-31(3)22-23-37-38(6,7)26-35(47-33(5)43)27-40(37,10)46)16-12-13-17-30(2)20-15-21-32(4)36(45)28-42-39(8,9)24-34(44)25-41(42,11)48-42/h12-22,34-35,44,46H,24-28H2,1-11H3/b13-12+,18-14+,20-15+,29-16+,30-17+,31-19+,32-21+

描述信息

Fucoxanthin is an epoxycarotenol that is found in brown seaweed and which exhibits anti-cancer, anti-diabetic, anti-oxidative and neuroprotective properties. It has a role as an algal metabolite, a CFTR potentiator, a food antioxidant, a neuroprotective agent, a hypoglycemic agent, an apoptosis inhibitor, a hepatoprotective agent, a marine metabolite and a plant metabolite. It is an epoxycarotenol, an acetate ester, a secondary alcohol, a tertiary alcohol and a member of allenes.
Fucoxanthin is a natural product found in Aequipecten opercularis, Ascidia zara, and other organisms with data available.
Fucoxanthin is a carotenoid, with formula C40H60O6. It is found as an accessory pigment in the chloroplasts of brown algae and most other heterokonts, giving them a brown or olive-green color. Fucoxanthin absorbs light primarily in the blue-green to yellow-green part of the visible spectrum, peaking at around 510-525 nm by various estimates and absorbing significantly in the range of 450 to 540 nm. -- Wikipedia [HMDB]
Fucoxanthin is a carotenoid, with formula C40H60O6. It is found as an accessory pigment in the chloroplasts of brown algae and most other heterokonts, giving them a brown or olive-green color. Fucoxanthin absorbs light primarily in the blue-green to yellow-green part of the visible spectrum, peaking at around 510-525 nm by various estimates and absorbing significantly in the range of 450 to 540 nm. -- Wikipedia.
D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids
Fucoxanthin (all-trans-Fucoxanthin) is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities[1][2][3][4][5][6][7][8][9].
Fucoxanthin is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities.
Fucoxanthin (all-trans-Fucoxanthin) is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities[1][2][3][4][5][6][7][8][9].
Fucoxanthin is a marine carotenoid and shows anti-obesity, anti-diabetic, anti-oxidant, anti-inflammatory and anticancer activities.

同义名列表

40 个代谢物同义名

InChI=1/C42H58O6/c1-29(18-14-19-31(3)22-23-37-38(6,7)26-35(47-33(5)43)27-40(37,10)46)16-12-13-17-30(2)20-15-21-32(4)36(45)28-42-39(8,9)24-34(44)25-41(42,11)48-42/h12-22,34-35,44,46H,24-28H2,1-11H3/b13-12+,18-14+,20-15+,29-16+,30-17+,31-19+,32-21+/t23?,34-; (1S,3R)-3-hydroxy-4-((3E,5E,7E,9E,11E,13E,15E)-18-((1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15-octaen-1-ylidene)-3,5,5-trimethylcyclohexyl acetate; (1S,3R)-3-hydroxy-4-((3E,5E,7E,9E,11E,13E,15E)-18-((1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15-octaenylidene)-3,5,5-trimethylcyclohexyl acetate; 3-Hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-{4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl}-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15-octaen-1-ylidene]-3,5,5-trimethylcyclohexyl acetic acid; 3-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-{4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl}-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15-octaen-1-ylidene]-3,5,5-trimethylcyclohexyl acetate; [3-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-(3-hydroxy-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-6-yl)-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15-octaenylidene]-3,5,5-trimethylcyclohexyl] acetate; beta,beta-Carotene, 3-(acetyloxy)-6,7-didehydro-5,6-epoxy-5,5,6,6,7,8-hexahydro-3,5-dihydroxy-8-oxo-, (3S,3S,5R,5R,6S,6R)-; (3S,3S,5R,5R,6S,6R,8R)-3,5-dihydroxy-8-oxo-6,7-didehydro-5,5,6,6,7,8-hexahydro-5,6-epoxy-beta,beta-caroten-3-yl acetate; (3S,3S,5R,5R,6S,6R)-3-(acetyloxy)-6,7-didehydro-5,6-epoxy-5,5,6,6,7,8-hexahydro-3,5-dihydroxy-8-oxo-beta,beta-carotene; (3S,5R,6S,3S,5R,6R)-3,5-dihydroxy-8-oxo-6,7-didehydro-5,6-epoxy-5,6,7,8,5,6-hexahydro-beta,beta-caroten-3-yl acetate; .BETA.,.BETA.-CAROTEN-8(5H)-ONE, 6,7-DIDEHYDRO-5,6-EPOXY-4,5,6,7-TETRAHYDRO-3,3,5-TRIHYDROXY-, (3S,3S,5R,5R,6S,6R)-; (3S,3S,5R,5R,6S,6R)-6,7-DIDEHYDRO-5,6-EPOXY-4,5,6,7-TETRAHYDRO-3,3,5-TRIHYDROXY-.BETA.,.BETA.-CAROTEN-8(5H)-ONE; .alpha.-Carotene, 6,7-didehydro-5,6-epoxy-4,5,5,6,7,8-hexahydro-3,3,5-trihydroxy-8-oxo-, 3-acetate, all-trans-; (3S,3S,5R,5R,6S,6R,8R)-3,5-dihydroxy-8-oxo-6,7-didehydro-5,5,6,6,7,8-hexahydro-5,6-epoxy-beta,beta-caroten-3-; (3S,5R,6R)-3-acetoxy-5,6-epoxy-3,5-dihydroxy-6,7-didehydro-5,6,7,8,5,6-hexahydro-beta,beta-caroten-8-one; 3-acetate-(7CI)-6,7-didehydro-5,6-epoxy-4,5,5,6,7,8-hexahydro-3,3,5-trihydroxy-8-oxo-α-carotene; 3-Acetate-(7ci)-6,7-didehydro-5,6-epoxy-4,5,5,6,7,8-hexahydro-3,3,5-trihydroxy-8-oxo-alpha-carotene; .ALPHA.-CAROTENE, 6,7-DIDEHYDRO-5,6-EPOXY-4,5,5,6,7,8-HEXAHYDRO-3,3,5-TRIHYDROXY-8-OXO-, 3-ACETATE; 3-Acetate-(7ci)-6,7-didehydro-5,6-epoxy-4,5,5,6,7,8-hexahydro-3,3,5-trihydroxy-8-oxo-a-carotene; 6,7-DIDEHYDRO-5,6-EPOXY-4,5,5,6,7,8-HEXAHYDRO-3,3,5-TRIHYDROXY-8-OXO-.ALPHA.-CAROTENE 3-ACETATE; Fucoxanthin (from Wakame) (Brown Seaweed) (Undaria Pinnatifida); 5-18-04-00673 (Beilstein Handbook Reference); fucoxanthin, (3S,3S,5R,5R,6S,6R,cis)-isomer; all-trans-Fucoxanthinall-trans-Fucoxanthin; ALL-E-(3S,5R,6S,3S,5R,6R)-FUCOXANTHIN; Fucoxanthin, carotenoid antioxidant; Fucoxanthin, analytical standard; fucoxanthin, (6R,13-cis)-isomer; SJWWTRQNNRNTPU-ABBNZJFMSA-; fucoxanthin, (6S)-isomer; Fucoxanthin, all-trans-; all-trans-Fucoxanthin; FUCOXANTHIN [WHO-DD]; Fucoxanthine - 50\\%; FUCOXANTHIN [INCI]; FUCOXANTHIN [MI]; UNII-06O0TC0VSM; Fucoxanthol; Fucoxanthin; 06O0TC0VSM

数据库引用编号

24 个数据库交叉引用编号

ChEBI: CHEBI:5186
KEGG: C08596
PubChem: 5364094
PubChem: 5281239
PubChem: 541529
HMDB: HMDB0002741
Metlin: METLIN3685
ChEMBL: CHEMBL1575074
Wikipedia: Fucoxanthin
MeSH: fucoxanthin
ChemIDplus: 0003351868
KNApSAcK: C00003773
foodb: FDB023058
chemspider: 4444651
chemspider: 4516336
CAS: 3351-86-8
medchemexpress: HY-N2302
PMhub: MS000008156
PubChem: 10789
LipidMAPS: LMPR01070300
PDB-CCD: A86
3DMET: B05268
NIKKAJI: J221.693K
RefMet: Fucoxanthin

分类词条

代谢反应

1 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(1)

diadinoxanthin and fucoxanthin biosynthesis: acetyl-CoA + fucoxanthinol ⟶ coenzyme A + fucoxanthin

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

71 个相关的物种来源信息

761903 - Acanthochitona defilippii: 10.1016/0305-0491(89)90393-3
761904 - Acanthochitona rubrolineata: 10.1016/0305-0491(89)90393-3
100776 - Aequipecten opercularis: 10.1016/S0021-9673(00)94508-4
322837 - Aplidium pliciferum:
107392 - Ascidia zara: 10.1016/0305-0491(85)90174-9
52969 - Ascophyllum nodosum:
30301 - Botryllus schlosseri: 10.1016/0305-0491(85)90174-9
13221 - Chrysotila carterae: 10.1016/0305-1978(77)90034-5
7719 - Ciona intestinalis: 10.1016/0305-0491(85)90174-9
35170 - Corallina officinalis: 10.1016/S0031-9422(00)98236-0
141464 - Corbicula japonica:
141464 - Corbicula japonica: 10.1021/NP058053N
141465 - Corbicula sandai: 10.1021/JF058088T
29159 - Crassostrea gigas: 10.1021/NP000476W
6655 - Cryptochiton stelleri: 10.1016/0305-0491(89)90393-3
257571 - Cystoclonium purpureum: 10.1016/S0031-9422(00)85526-0
590725 - Cystoseira barbata: 10.1016/J.FCT.2017.04.001
62298 - Desmarestia aculeata: 10.1016/S0031-9422(00)83559-1
2081491 - Diacronema lutheri: 10.1016/0305-1978(77)90034-5
2875 - Dictyota:
6511 - Dolabella auricularia: 10.2331/SUISAN.57.277
48944 - Ellisolandia elongata: 10.1016/S0031-9422(00)98236-0
94617 - Fibrocapsa japonica: 10.1016/0305-0491(84)90181-0
87148 - Fucus serratus:
49266 - Fucus vesiculosus:
87150 - Fucus virsoides: 10.1515/ZNB-1994-0923
1336858 - Gelliodes callista: 10.2331/SUISAN.53.1271
210454 - Grammatophora oceanica: 10.1016/0305-1978(88)90067-1
7729 - Halocynthia roretzi:
190923 - Hexabranchus: 10.2331/SUISAN.58.1549
74478 - Himanthalia elongata: 10.1016/J.FOODRES.2016.09.023
9606 - Homo sapiens: -
37099 - Isochrysis galbana: 10.1016/0305-1978(77)90034-5
31397 - Jania: 10.1016/S0031-9422(00)98236-0
80365 - Laminaria digitata:
142080 - Ligia exotica: 10.1016/0305-0491(90)90313-I
13599 - Liolophura japonica: 10.1016/0305-0491(89)90393-3
2171618 - Magallana gigas: 10.1021/NP000476W
311198 - Meretrix petechialis: 10.1021/JF1006243
2985 - Ochromonas: 10.1016/0305-0491(81)90110-3
1259760 - Parlibellus delognei: 10.1021/NP50035A010
35679 - Pelagococcus subviridis: 10.1016/0031-9422(89)80345-0
74467 - Pelvetia canaliculata:
33656 - Phaeocystis:
2850 - Phaeodactylum tricornutum: 10.1016/0305-1978(88)90067-1
2268599 - Placiphorella stimpsoni: 10.1016/0305-0491(89)90393-3
33090 - Plants: -
97485 - Prymnesium parvum: 10.1016/0305-1978(77)90034-5
183589 - Pseudo-nitzschia multistriata: 10.3390/MD18060313
88149 - Saccharina japonica: 10.3390/MD15020039
309358 - Saccharina latissima:
54407 - Sarcinochrysis marina: 10.1016/0305-0491(81)90110-3
3015 - Sargassum: 10.4103/0974-8490.85000
590727 - Sargassum fusiforme: 10.1271/BBB.63.605
1500693 - Sargassum incisifolium: 10.1515/ZNC-2008-11-1211
127572 - Sargassum siliquastrum: 10.1016/J.JPHOTOBIOL.2008.11.011
2843 - Skeletonema costatum: 10.1016/0305-1978(88)90067-1
216823 - Skeletonema menzelii: 10.1016/0305-1978(88)90067-1
45367 - Sporochnus comosus: 10.1021/NP1008009
7725 - Styela clava: 10.1016/0305-0491(85)90174-9
7726 - Styela plicata: 10.1016/0305-0491(85)90174-9
381694 - Stypopodium flabelliforme: 10.1021/NP050051F
52555 - Synura petersenii: 10.1016/0305-0491(81)90110-3
49261 - Thalassiosira eccentrica: 10.1016/0305-1978(88)90067-1
420259 - Thalassiosira gravida: 10.1016/0305-1978(88)90067-1
159749 - Thalassiosira oceanica: 10.1016/0305-1978(88)90067-1
35128 - Thalassiosira pseudonana: 10.1016/0305-1978(88)90067-1
49265 - Thalassiosira rotula: 10.1016/0305-1978(88)90067-1
74381 - Undaria pinnatifida: 10.1016/J.FOODCHEM.2016.05.064
29655 - Zostera marina: -
33090 - 昆布: -

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

Huiying Kuang, Xuan Peng, Yixiang Liu, Dan Li. The pro-absorptive effect of glycosylated zein-fatty acid complexes on fucoxanthin via the lipid transporter protein delivery pathway. Food chemistry. 2024 Jul; 446(?):138892. doi: 10.1016/j.foodchem.2024.138892. [PMID: 38432136]
Xueying Tian, Jiaxuan Li, Kuiyou Wang, Siyuan Fei, Xiumin Zhang, Caiyun Wu, Mingqian Tan, Wentao Su. Microfluidic fabrication of core-shell fucoxanthin nanofibers with improved environmental stability for reducing lipid accumulation in vitro. Food chemistry. 2024 Jun; 442(?):138474. doi: 10.1016/j.foodchem.2024.138474. [PMID: 38245982]
Shouxing Yang, Jinhai Li, Liping Yan, Yu Wu, Lin Zhang, Boyang Li, Haibin Tong, Xiaochun Lin. Molecular Mechanisms of Fucoxanthin in Alleviating Lipid Deposition in Metabolic Associated Fatty Liver Disease. Journal of agricultural and food chemistry. 2024 May; 72(18):10391-10405. doi: 10.1021/acs.jafc.4c00590. [PMID: 38669300]
Bingbing Guo, Weihao Zhang, Yonghui Zhou, Jingyi Zhang, Chengchu Zeng, Peipei Sun, Bin Liu. Fucoxanthin restructures the gut microbiota and metabolic functions of non-obese individuals in an in vitro fermentation model. Food & function. 2024 May; 15(9):4805-4817. doi: 10.1039/d3fo05671f. [PMID: 38563411]
Broderick Dickerson, Jonathan Maury, Victoria Jenkins, Kay Nottingham, Dante Xing, Drew E Gonzalez, Megan Leonard, Jacob Kendra, Joungbo Ko, Choongsung Yoo, Sarah Johnson, Rémi Pradelles, Martin Purpura, Ralf Jäger, Ryan Sowinski, Christopher J Rasmussen, Richard B Kreider. Effects of Supplementation with Microalgae Extract from Phaeodactylum tricornutum (Mi136) to Support Benefits from a Weight Management Intervention in Overweight Women. Nutrients. 2024 Mar; 16(7):. doi: 10.3390/nu16070990. [PMID: 38613023]
Caiyun Wu, Siyuan Xiang, Haitao Wang, Xiumin Zhang, Xueying Tian, Mingqian Tan, Wentao Su. Orally Deliverable Sequence-Targeted Fucoxanthin-Loaded Biomimetic Extracellular Vesicles for Alleviation of Nonalcoholic Fatty Liver Disease. ACS applied materials & interfaces. 2024 Feb; 16(8):9854-9867. doi: 10.1021/acsami.3c18029. [PMID: 38375789]
Milad Amerifar, Hesamoddin Arabnozari, Mohammad Shokrzadeh, Emran Habibi. Evaluation of antioxidant properties and cytotoxicity of brown algae (nizamuddinia zanardinii) in uterine (hela) and pancreatic cancer cell lines (paca-2). Human & experimental toxicology. 2024 Jan; 43(?):9603271241227228. doi: 10.1177/09603271241227228. [PMID: 38238028]
Jing Yan, Zehua Li, Yu Liang, Chaobo Yang, Wen Ou, Huaqiang Mo, Min Tang, Deshu Chen, Chongbin Zhong, Dongdong Que, Liyun Feng, Hua Xiao, Xudong Song, Pingzhen Yang. Fucoxanthin alleviated myocardial ischemia and reperfusion injury through inhibition of ferroptosis via the NRF2 signaling pathway. Food & function. 2023 Nov; 14(22):10052-10068. doi: 10.1039/d3fo02633g. [PMID: 37861458]
Ying Bai, Yihan Sun, Xiang Li, Jiaying Ren, Chenghang Sun, Xing Chen, Xiuping Dong, Hang Qi. Phycocyanin/lysozyme nanocomplexes to stabilize Pickering emulsions for fucoxanthin encapsulation. Food research international (Ottawa, Ont.). 2023 11; 173(Pt 2):113386. doi: 10.1016/j.foodres.2023.113386. [PMID: 37803725]
Junyu Hao, Jinxuan Zhang, Tao Wu. Fucoxanthin extract ameliorates obesity associated with modulation of bile acid metabolism and gut microbiota in high-fat-diet fed mice. European journal of nutrition. 2023 Oct; ?(?):. doi: 10.1007/s00394-023-03256-z. [PMID: 37831134]
Vanessa Fernandes, Bangera Sheshappa Mamatha. Fucoxanthin, a Functional Food Ingredient: Challenges in Bioavailability. Current nutrition reports. 2023 Aug; ?(?):. doi: 10.1007/s13668-023-00492-x. [PMID: 37642932]
Ching Chan. Brown is the new green: Discovery of an algal enzyme for the final step of fucoxanthin biosynthesis. The Plant cell. 2023 Aug; 35(8):2716-2717. doi: 10.1093/plcell/koad138. [PMID: 37195870]
Jia Wang, Xue Dong, Dandan Li, Zhiyao Fang, Xianyao Wan, Jing Liu. Fucoxanthin inhibits gastric cancer lymphangiogenesis and metastasis by regulating Ran expression. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2023 Jun; 118(?):154926. doi: 10.1016/j.phymed.2023.154926. [PMID: 37392675]
Jianquan Song, Hejing Zhao, Linxin Zhang, Zheng Li, Jichang Han, Chengxu Zhou, Jilin Xu, Xiaohui Li, Xiaojun Yan. The Heat Shock Transcription Factor PtHSF1 Mediates Triacylglycerol and Fucoxanthin Synthesis by Regulating the Expression of GPAT3 and DXS in Phaeodactylum tricornutum. Plant & cell physiology. 2023 Jun; 64(6):622-636. doi: 10.1093/pcp/pcad023. [PMID: 36947404]
Adrián Macías-de la Rosa, Miguel Ángel González-Cardoso, María Del Carmen Cerón-García, Lorenzo López-Rosales, Juan José Gallardo-Rodríguez, Sergio Seoane, Asterio Sánchez-Mirón, Francisco García-Camacho. Bioactives Overproduction through Operational Strategies in the Ichthyotoxic Microalga Heterosigma akashiwo Culture. Toxins. 2023 05; 15(5):. doi: 10.3390/toxins15050349. [PMID: 37235383]
Jessica Winarto, Dae-Geun Song, Cheol-Ho Pan. The Role of Fucoxanthin in Non-Alcoholic Fatty Liver Disease. International journal of molecular sciences. 2023 May; 24(9):. doi: 10.3390/ijms24098203. [PMID: 37175909]
Najmeh Oliyaei, Nader Tanideh, Marzieh Moosavi-Nasab, Amir Reza Dehghanian, Aida Iraji. Development and characterization of a fucoidan-based nanoemulsion using Nigella sativa oil for improvement of anti-obesity activity of fucoxanthin in an obese rat model. International journal of biological macromolecules. 2023 Apr; 235(?):123867. doi: 10.1016/j.ijbiomac.2023.123867. [PMID: 36870664]
Tianjun Cao, Yu Bai, Paul Buschbeck, Qiaozhu Tan, Michael B Cantrell, Yinjuan Chen, Yanyou Jiang, Run-Zhou Liu, Nana K Ries, Xiaohuo Shi, Yan Sun, Maxwell A Ware, Fenghua Yang, Huan Zhang, Jichang Han, Lihan Zhang, Jing Huang, Martin Lohr, Graham Peers, Xiaobo Li. An unexpected hydratase synthesizes the green light--absorbing pigment fucoxanthin. The Plant cell. 2023 Apr; ?(?):. doi: 10.1093/plcell/koad116. [PMID: 37100425]
Nor Hafiza Sayuti, Khairul Najmi Muhammad Nawawi, Jo Aan Goon, Norfilza Mohd Mokhtar, Suzana Makpol, Jen Kit Tan. A Review of the Effects of Fucoxanthin on NAFLD. Nutrients. 2023 Apr; 15(8):. doi: 10.3390/nu15081954. [PMID: 37111187]
Luana Calabrone, Valentina Carlini, Douglas M Noonan, Marco Festa, Cinzia Ferrario, Danilo Morelli, Debora Macis, Angelo Fontana, Luigi Pistelli, Christophe Brunet, Clementina Sansone, Adriana Albini. Skeletonema marinoi Extracts and Associated Carotenoid Fucoxanthin Downregulate Pro-Angiogenic Mediators on Prostate Cancer and Endothelial Cells. Cells. 2023 03; 12(7):. doi: 10.3390/cells12071053. [PMID: 37048126]
Yongkai Yuan, Mengjie Ma, Shuaizhong Zhang. Recent advances in delivery systems of fucoxanthin. Food chemistry. 2023 Mar; 404(Pt B):134685. doi: 10.1016/j.foodchem.2022.134685. [PMID: 36279786]
Yuxin Wang, Jia Wang, Ziqiang Gu, Shufang Yang, Yongjin He, Haijin Mou, Han Sun. Altering autotrophic carbon metabolism of Nitzschia closterium to mixotrophic mode for high-value product improvement. Bioresource technology. 2023 Mar; 371(?):128596. doi: 10.1016/j.biortech.2023.128596. [PMID: 36638896]
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