Allantoin (BioDeep_00000400042)

natural product PANOMIX_OTCML-2023

代谢物信息卡片

(2,5-dioxoimidazolidin-4-yl)urea

化学式: C4H6N4O3 (158.0439886)
中文名称: 尿囊素
谱图信息: 最多检出来源 Homo sapiens(blood) 0.56%

分子结构信息

SMILES: C1(C(=NC(=N1)O)O)NC(=N)O
InChI: InChI=1S/C4H6N4O3/c5-3(10)6-1-2(9)8-4(11)7-1/h1H,(H3,5,6,10)(H2,7,8,9,11)

描述信息

C78284 - Agent Affecting Integumentary System > C29708 - Anti-psoriatic Agent
C78284 - Agent Affecting Integumentary System > C29700 - Astringent
D003879 - Dermatologic Agents
MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; POJWUDADGALRAB-UHFFFAOYSA-N_STSL_0150_Allantoin_8000fmol_180425_S2_LC02_MS02_50; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I.
MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I.
Allantoin is a skin conditioning agent that promotes healthy skin, stimulates new and healthy tissue growth.
Allantoin is a skin conditioning agent that promotes healthy skin, stimulates new and healthy tissue growth.

同义名列表

3 个代谢物同义名

Allantoin; (2,5-dioxoimidazolidin-4-yl)urea; 5-Ureidohydantoin

数据库引用编号

60 个数据库交叉引用编号

ChEBI: CHEBI:15676
KEGG: C01551
PubChem: 204
DrugBank: DB11100
ChEMBL: CHEMBL593429
MeSH: Allantoin
CAS: 97-59-6
CAS: 5377-33-3
MoNA: CCMSLIB00000424784
MoNA: CCMSLIB00005464137
MoNA: CCMSLIB00005464171
MoNA: CCMSLIB00005720668
MoNA: MoNA037806
MoNA: MoNA037104
MoNA: MoNA033855
MoNA: MoNA033853
MoNA: MoNA033852
MoNA: MoNA031951
MoNA: MoNA031950
MoNA: MoNA031949
MoNA: MoNA024244
MoNA: MoNA024196
MoNA: EMBL-MCF_spec34892
MoNA: MoNA010350
MoNA: MoNA010349
MoNA: MoNA010348
MoNA: MoNA010347
MoNA: MoNA010346
MoNA: MoNA010345
MoNA: VF-NPL-LTQ007732
MoNA: VF-NPL-LTQ007731
MoNA: VF-NPL-LTQ007730
MoNA: VF-NPL-QEHF028020
MoNA: VF-NPL-QEHF028019
MoNA: VF-NPL-QEHF028018
MoNA: VF-NPL-QEHF028017
MoNA: VF-NPL-QEHF028016
MoNA: VF-NPL-QEHF028015
MoNA: VF-NPL-QEHF028014
MoNA: VF-NPL-QEHF028013
MoNA: VF-NPL-QEHF028012
MoNA: VF-NPL-QEHF028011
MoNA: VF-NPL-QEHF028010
MoNA: VF-NPL-QEHF028009
MoNA: VF-NPL-QEHF028008
MoNA: VF-NPL-QEHF028007
MoNA: VF-NPL-QEHF028006
MoNA: FiehnHILIC002583
MoNA: FiehnHILIC001061
MoNA: HMDB0000462_ms_ms_672
MoNA: HMDB0000462_ms_ms_673
MoNA: HMDB0000462_ms_ms_671
MoNA: PT101693
MoNA: CCMSLIB00000578167
PubChem: 4709
KNApSAcK: C00007468
3DMET: B00317
NIKKAJI: J3.978K
RefMet: Allantoin
medchemexpress: HY-N0543

分类词条

Ureides

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

90 个相关的物种来源信息

3702 Arabidopsis thaliana:
9606 Homo sapiens:
158558 Aristolochia mollissima:
5691 Trypanosoma brucei:
7227 Drosophila melanogaster: 10.1038/S41467-019-11933-Z
29760 Vitis vinifera: 10.1016/J.DIB.2020.106469
4081 Solanum lycopersicum: 10.1038/SDATA.2014.29
158539 Aristolochia cucurbitifolia: 10.1248/CPB.48.1006
81762 Hyacinthoides non-scripta: 10.1038/S41598-019-38940-W
1569721 Blepharis linariifolia: 10.4268/CJCMM20120313
1569727 Blepharis scindica: 10.4268/CJCMM20120313
3893 Pueraria montana var. lobata:
46142 Petiveria alliacea: 10.1016/0031-9422(90)85294-P
256480 Anchusa strigosa: 10.1055/S-2003-43202
4678 Allium: 10.1016/S0031-9422(01)00216-3
158541 Aristolochia debilis:
158550 Aristolochia kaempferi: 10.1016/S0031-9422(03)00335-2
35927 Aristolochia tomentosa: 10.1016/S0031-9422(03)00335-2
266420 Aristolochia contorta:
431268 Aristolochia heterophylla: 10.1016/S0031-9422(03)00335-2
158552 Aristolochia kwangsiensis: 10.1007/S10600-011-9794-7
171878 Aristolochia zollingeriana: 10.1016/S0031-9422(00)90492-8
158551 Aristolochia kankauensis: 10.1016/S0031-9422(00)90492-8
537489 Rhinacanthus nasutus: 10.1248/CPB.46.413
141328 Rhinacanthus: 10.1016/S0031-9422(98)00425-7
314108 Aristolochia chamissonis: 10.1590/S0100-46702002000100009
158540 Aristolochia cymbifera: 10.1016/0031-9422(92)83495-K
181186 Cordia trichotoma: 10.1590/S0103-50532001000600016
353934 Tanaecium bilabiatum: 10.1076/1388-0209(200009)3841-AFT287
265763 Eleutherococcus giraldii: 10.1016/J.BSE.2012.02.004
459119 Castela tortuosa: 10.1016/0031-9422(92)80139-6
798309 Cymbastela cantharella: 10.1021/NP960562P
281732 Tethya aurantium: 10.1016/0305-0491(81)90021-3
185542 Ilex paraguariensis: 10.1016/0031-9422(93)85103-X
938085 Orthaga exvinacea: 10.1016/S0965-1748(98)00086-1
569628 Dioscorea oppositifolia:
55575 Dioscorea polystachya:
1886 Streptomyces albidoflavus: 10.1007/S00253-013-5372-1
1902 Streptomyces coelicolor: 10.1007/S00253-013-5372-1
157791 Vigna radiata: 10.1007/BF00576117
3886 Phaseolus coccineus: 10.1007/BF00576117
278672 Symphytum officinale: 10.1002/0471701343.SDP22169
12948 Aristolochia gigantea: 10.1016/S0031-9422(00)97573-3
3847 Glycine max: 10.1104/PP.77.1.129
4673 Dioscorea japonica: 10.1016/J.BMCL.2011.02.003
3702 Arabidopsis thaliana:
9606 Homo sapiens:
158558 Aristolochia mollissima:
5691 Trypanosoma brucei:
7227 Drosophila melanogaster: 10.1038/S41467-019-11933-Z
29760 Vitis vinifera: 10.1016/J.DIB.2020.106469
4081 Solanum lycopersicum: 10.1038/SDATA.2014.29
158539 Aristolochia cucurbitifolia: 10.1248/CPB.48.1006
81762 Hyacinthoides non-scripta: 10.1038/S41598-019-38940-W
1569721 Blepharis linariifolia: 10.4268/CJCMM20120313
1569727 Blepharis scindica: 10.4268/CJCMM20120313
3893 Pueraria montana var. lobata:
46142 Petiveria alliacea: 10.1016/0031-9422(90)85294-P
256480 Anchusa strigosa: 10.1055/S-2003-43202
4678 Allium: 10.1016/S0031-9422(01)00216-3
158541 Aristolochia debilis:
158550 Aristolochia kaempferi: 10.1016/S0031-9422(03)00335-2
35927 Aristolochia tomentosa: 10.1016/S0031-9422(03)00335-2
266420 Aristolochia contorta:
431268 Aristolochia heterophylla: 10.1016/S0031-9422(03)00335-2
158552 Aristolochia kwangsiensis: 10.1007/S10600-011-9794-7
171878 Aristolochia zollingeriana: 10.1016/S0031-9422(00)90492-8
158551 Aristolochia kankauensis: 10.1016/S0031-9422(00)90492-8
537489 Rhinacanthus nasutus: 10.1248/CPB.46.413
141328 Rhinacanthus: 10.1016/S0031-9422(98)00425-7
314108 Aristolochia chamissonis: 10.1590/S0100-46702002000100009
158540 Aristolochia cymbifera: 10.1016/0031-9422(92)83495-K
181186 Cordia trichotoma: 10.1590/S0103-50532001000600016
353934 Tanaecium bilabiatum: 10.1076/1388-0209(200009)3841-AFT287
265763 Eleutherococcus giraldii: 10.1016/J.BSE.2012.02.004
459119 Castela tortuosa: 10.1016/0031-9422(92)80139-6
798309 Cymbastela cantharella: 10.1021/NP960562P
281732 Tethya aurantium: 10.1016/0305-0491(81)90021-3
185542 Ilex paraguariensis: 10.1016/0031-9422(93)85103-X
938085 Orthaga exvinacea: 10.1016/S0965-1748(98)00086-1
569628 Dioscorea oppositifolia:
55575 Dioscorea polystachya:
1886 Streptomyces albidoflavus: 10.1007/S00253-013-5372-1
1902 Streptomyces coelicolor: 10.1007/S00253-013-5372-1
157791 Vigna radiata: 10.1007/BF00576117
3886 Phaseolus coccineus: 10.1007/BF00576117
278672 Symphytum officinale: 10.1002/0471701343.SDP22169
12948 Aristolochia gigantea: 10.1016/S0031-9422(00)97573-3
3847 Glycine max: 10.1104/PP.77.1.129
4673 Dioscorea japonica: 10.1016/J.BMCL.2011.02.003

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

Aigerim Soltabayeva, Assylay Kurmanbayeva, Aizat Bekturova, Dinara Oshanova, Zhadyrassyn Nurbekova, Sudhakar Srivastava, Dominic Standing, Edyta Zdunek-Zastocka, Moshe Sagi. Endogenous ureides are employed as a carbon source in Arabidopsis plants exposed to carbon starvation conditions. Plant science : an international journal of experimental plant biology. 2024 Jul; 344(?):112108. doi: 10.1016/j.plantsci.2024.112108. [PMID: 38705480]
Sorin Marian Mârza, Adela Maria Dăescu, Robert Cristian Purdoiu, Mădălina Dragomir, Mariana Tătaru, Iulia Melega, Andras-Laszlo Nagy, Adrian Gal, Flaviu Tăbăran, Sidonia Bogdan, Mirela Moldovan, Emoke Pall, Camelia Munteanu, Klara Magyari, Ionel Papuc. Healing of Skin Wounds in Rats Using Creams Based on Symphytum Officinale Extract. International journal of molecular sciences. 2024 Mar; 25(6):. doi: 10.3390/ijms25063099. [PMID: 38542069]
Xiaodan Meng, Zhiyong Zhang, Huali Wang, Furong Nai, Yihao Wei, Yongchun Li, Xinming Ma, Xiaochun Wang, Mechthild Tegeder. Multi-scale analysis provides insights into the roles of ureide permeases in wheat nitrogen use efficiency. Journal of experimental botany. 2023 Jul; ?(?):. doi: 10.1093/jxb/erad286. [PMID: 37478311]
Rizwan Alam, Rizwan Rasheed, Muhammad Arslan Ashraf, Iqbal Hussain, Shafaqat Ali. Allantoin alleviates chromium phytotoxic effects on wheat by regulating osmolyte accumulation, secondary metabolism, ROS homeostasis and nutrient acquisition. Journal of hazardous materials. 2023 Jun; 458(?):131920. doi: 10.1016/j.jhazmat.2023.131920. [PMID: 37413799]
Soni Chowrasia, Jyoti Nishad, Rekha Mahato, Kanti Kiran, Nitasana Rajkumari, Alok Kumar Panda, Hukam C Rawal, Mandira Barman, Tapan Kumar Mondal. Allantoin improves salinity tolerance in Arabidopsis and rice through synergid activation of abscisic acid and brassinosteroid biosynthesis. Plant molecular biology. 2023 May; ?(?):. doi: 10.1007/s11103-023-01350-8. [PMID: 37184674]
Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products. ACS pharmacology & translational science. 2023 May; 6(5):683-701. doi: 10.1021/acsptsci.2c00194. [PMID: 37200814]
Sławomir Dresler, Maciej Strzemski, Izabela Baczewska, Mateusz Koselski, Mohammad Bagher Hassanpouraghdam, Dariusz Szczepanek, Ireneusz Sowa, Magdalena Wójciak, Agnieszka Hanaka. Extraction of Isoflavones, Alpha-Hydroxy Acids, and Allantoin from Soybean Leaves-Optimization by a Mixture Design of the Experimental Method. Molecules (Basel, Switzerland). 2023 May; 28(9):. doi: 10.3390/molecules28093963. [PMID: 37175385]
Sławomir Dresler, Robert Zubel, Izabela Baczewska, Michał Karakuła, Jan Sawicki, Agnieszka Hanaka, Sylwia Zielińska, Bartosz J Płachno, Ireneusz Sowa, Magdalena Wójciak, Maciej Strzemski. Is there any direct link between hazardous trace metals and the allantoin content in some moss species?. The Science of the total environment. 2023 Mar; 864(?):160653. doi: 10.1016/j.scitotenv.2022.160653. [PMID: 36529391]
Gang Wang, Jiali Li, Jing Ji, Lishuang Zhang, Bowen Li, Jiaqi Zhang, Xinya Wang, Wenju Song, Chunfeng Guan. Combined application of allantoin and strain JIT1 synergistically or additively promotes the growth of rice under 2, 4-DCP stress by enhancing the phosphate solubility, improving soil enzyme activities and photosynthesis. Journal of plant physiology. 2023 Jan; 282(?):153941. doi: 10.1016/j.jplph.2023.153941. [PMID: 36739690]
Shuai Lu, Zichang Jia, Xiangfeng Meng, Yaoyu Chen, Surong Wang, Chaozhen Fu, Lei Yang, Rong Zhou, Baohua Wang, Yunying Cao. Combined Metabolomic and Transcriptomic Analysis Reveals Allantoin Enhances Drought Tolerance in Rice. International journal of molecular sciences. 2022 Nov; 23(22):. doi: 10.3390/ijms232214172. [PMID: 36430648]
Joanda P R E Silva, Laiane C O Pereira, Lucas S Abreu, Francisca S V Lins, Thalisson A de Souza, Renan F do Espírito-Santo, Renata P C Barros, Cristiane F Villarreal, José I M de Melo, Marcus T Scotti, Vicente C de O Costa, Lucas H Martorano, Fernando M Dos Santos, Raimundo Braz Filho, Marcelo S da Silva, Josean F Tavares. Targeted Isolation of Anti-inflammatory Lignans from Justicia aequilabris by Molecular Networking Approach. Journal of natural products. 2022 09; 85(9):2184-2191. doi: 10.1021/acs.jnatprod.2c00478. [PMID: 35998343]
Fengjuan Zhang, Xinxiao Sun, Xiaolin Shen, Yajun Yan, Jia Wang, Qipeng Yuan. Biosynthesis of allantoin in Escherichia coli via screening a highly effective urate oxidase. Biotechnology and bioengineering. 2022 09; 119(9):2518-2528. doi: 10.1002/bit.28126. [PMID: 35488433]
Agnieszka Hanaka, Artur Nowak, Ewa Ozimek, Sławomir Dresler, Andrzej Plak, Agnieszka Sujak, Emilia Reszczyńska, Maciej Strzemski. Effect of copper stress on Phaseolus coccineus in the presence of exogenous methyl jasmonate and/or Serratia plymuthica from the Spitsbergen soil. Journal of hazardous materials. 2022 08; 436(?):129232. doi: 10.1016/j.jhazmat.2022.129232. [PMID: 35739752]
Sławomir Dresler, Jozef Kováčik, Ireneusz Sowa, Magdalena Wójciak, Maciej Strzemski, Anna Rysiak, Peter Babula, Christopher D Todd. Allantoin overaccumulation enhances production of metabolites under excess of metals but is not tightly regulated by nitric oxide. Journal of hazardous materials. 2022 08; 436(?):129138. doi: 10.1016/j.jhazmat.2022.129138. [PMID: 35617731]
Asmin Andries, Alan Feyaerts, Djalila Mekahli, Ann Van Schepdael. Quantification of allantoin and other metabolites of the purine degradation pathway in human plasma samples using a newly developed HILIC-LC-MS/MS method. Electrophoresis. 2022 05; 43(9-10):1010-1018. doi: 10.1002/elps.202100265. [PMID: 35050532]
Charussri Leeyaphan, Supenya Varothai, Suphattra Trakanwittayarak, Pranittra Suphatsathienkul, Suthasinee Pattaravadee, Lalita Matthapan, Waranyoo Prasong, Kamonpan Lertrujiwanit, Salisa Supcharoenkul, Kanokvalai Kulthanan. A randomized controlled trial to compare the effectiveness and safety of adsorbent lotion containing tapioca starch, spent grain wax, Butyrospermum parkii extract, argania spinosa kernel oil, aloe barbadensis, rosehip oil, and allantoin with a low-potency topical corticosteroid in the treatment of intertrigo. Journal of cosmetic dermatology. 2022 Feb; 21(2):679-688. doi: 10.1111/jocd.14125. [PMID: 33811776]
Ming-Zhu Lu, Amanda M Carter, Mechthild Tegeder. Altering ureide transport in nodulated soybean results in whole-plant adjustments of metabolism, assimilate partitioning, and sink strength. Journal of plant physiology. 2022 Feb; 269(?):153613. doi: 10.1016/j.jplph.2021.153613. [PMID: 35033961]
Dmitri Svistounov, Marit D Solbu, Trond G Jenssen, Ulla Dorte Mathisen, Terkel Hansen, Katja Benedikte Prestø Elgstøen, Svetlana N Zykova. Development of quantitative assay for simultaneous measurement of purine metabolites and creatinine in biobanked urine by liquid chromatography-tandem mass spectrometry. Scandinavian journal of clinical and laboratory investigation. 2022 02; 82(1):37-49. doi: 10.1080/00365513.2021.2015799. [PMID: 35048747]
Aigerim Soltabayeva, Aizat Bekturova, Assylay Kurmanbayeva, Dinara Oshanova, Zhadyrassyn Nurbekova, Sudhakar Srivastava, Dominic Standing, Moshe Sagi. Ureides are accumulated similarly in response to UV-C irradiation and wounding in Arabidopsis leaves but are remobilized differently during recovery. Journal of experimental botany. 2022 01; 73(3):1016-1032. doi: 10.1093/jxb/erab441. [PMID: 34606608]
Lenka Hasíková, Jakub Závada, Tereza Serranová, Lenka Kotačková, Petr Kozlík, Květa Kalíková, Jiří Trnka, David Zogala, Karel Šonka, Evžen Růžička, Petr Dušek. Patients with REM sleep behavior disorder have higher serum levels of allantoin. Parkinsonism & related disorders. 2021 09; 90(?):38-43. doi: 10.1016/j.parkreldis.2021.07.031. [PMID: 34352609]
Mark J Henderson, Kathleen A Trychta, Shyh-Ming Yang, Susanne Bäck, Adam Yasgar, Emily S Wires, Carina Danchik, Xiaokang Yan, Hideaki Yano, Lei Shi, Kuo-Jen Wu, Amy Q Wang, Dingyin Tao, Gergely Zahoránszky-Kőhalmi, Xin Hu, Xin Xu, David Maloney, Alexey V Zakharov, Ganesha Rai, Fumihiko Urano, Mikko Airavaara, Oksana Gavrilova, Ajit Jadhav, Yun Wang, Anton Simeonov, Brandon K Harvey. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. Cell reports. 2021 04; 35(4):109040. doi: 10.1016/j.celrep.2021.109040. [PMID: 33910017]
Yuki Ono, Masashige Fukasawa, Kuni Sueyoshi, Norikuni Ohtake, Takashi Sato, Sayuri Tanabata, Ryo Toyota, Kyoko Higuchi, Akihiro Saito, Takuji Ohyama. Application of Nitrate, Ammonium, or Urea Changes the Concentrations of Ureides, Urea, Amino Acids and Other Metabolites in Xylem Sap and in the Organs of Soybean Plants (Glycine max (L.) Merr.). International journal of molecular sciences. 2021 Apr; 22(9):. doi: 10.3390/ijms22094573. [PMID: 33925462]
Yan-Ge Yu, Xiao-Yang Guo, Xiang-Yang Li, Dan-Dan Dai, Xin-Ran Xu, Xiao-Jin Ge, Yan-Jun Li, Tie-Gang Yang. Organ- and Age-Specific Differences of Dioscorea polystachya Compounds Measured by UPLC-QTOF/MS. Chemistry & biodiversity. 2021 Feb; 18(2):e2000856. doi: 10.1002/cbdv.202000856. [PMID: 33295037]
Anna Campanati, Gabriele Ceccarelli, Valerio Brisigotti, Elisa Molinelli, Emanuela Martina, Davide Talevi, Barbara Marconi, Melania Giannoni, Vasiliki Markantoni, Stamatios Gregoriou, George Kontochristopoulos, Annamaria Offidani. Effects of in vivo application of an overnight patch containing Allium cepa, allantoin, and pentaglycan on hypertrophic scars and keloids: Clinical, videocapillaroscopic, and ultrasonographic study. Dermatologic therapy. 2021 01; 34(1):e14665. doi: 10.1111/dth.14665. [PMID: 33314582]
Ying-Ying Teng, Ming-Li Zou, Feng-Lai Yuan, Xiao-Jin Zhou. Letter to the Editor on Objective evaluation of an occlusive overnight intensive patch containing onion extract and allantoin for hypertrophic scars. Journal of cosmetic dermatology. 2020 Dec; 19(12):3428. doi: 10.1111/jocd.13671. [PMID: 32794306]
Shuo Liu, Xuemei Yuan, Chang Ma, Jing Zhao, Zhili Xiong. 1H-NMR-based urinary metabolomic analysis for the preventive effects of gushudan on glucocorticoid-induced osteoporosis rats. Analytical biochemistry. 2020 12; 610(?):113992. doi: 10.1016/j.ab.2020.113992. [PMID: 33075315]
Kivanc Seref, Kaan Sonmez, Merve Altin Gulburun, Ozgur Ekinci, Ceren Bilkan Oge, Ozlem Gulbahar, Burak Arslan, Hasan Dagli, Ramazan Karabulut, Zafer Turkyilmaz. Protective Effects of Contractubex® on Stricture Formation after Experimental Corrosive Esophageal Burns in Rats. Archives of medical research. 2020 10; 51(7):664-669. doi: 10.1016/j.arcmed.2020.06.017. [PMID: 32654881]
Ayane Moriyama, Masutoshi Nojiri, Go Watanabe, Shinichi Enoki, Shunji Suzuki. Exogenous allantoin improves anthocyanin accumulation in grape berry skin at early stage of ripening. Journal of plant physiology. 2020 Oct; 253(?):153253. doi: 10.1016/j.jplph.2020.153253. [PMID: 32828011]
Junnan Ma, Xianglong Meng, Yi Liu, Cheng Yin, Tong Zhang, Piao Wang, Yong-Ki Park, Hyo Won Jung. Effects of a rhizome aqueous extract of Dioscorea batatas and its bioactive compound, allantoin in high fat diet and streptozotocin-induced diabetic mice and the regulation of liver, pancreas and skeletal muscle dysfunction. Journal of ethnopharmacology. 2020 Sep; 259(?):112926. doi: 10.1016/j.jep.2020.112926. [PMID: 32380247]
Ignacio Lescano, Andrés Matías Devegili, Carolina Martini, Tomás María Tessi, Claudio Alejandro González, Marcelo Desimone. Ureide metabolism in Arabidopsis thaliana is modulated by C:N balance. Journal of plant research. 2020 Sep; 133(5):739-749. doi: 10.1007/s10265-020-01215-x. [PMID: 32740857]
Lei Liu, Dan Liu, Ziyang Wang, Chunlei Zou, Bin Wang, He Zhang, Zhijia Gai, Pengfei Zhang, Yubo Wang, Caifeng Li. Exogenous allantoin improves the salt tolerance of sugar beet by increasing putrescine metabolism and antioxidant activities. Plant physiology and biochemistry : PPB. 2020 Sep; 154(?):699-713. doi: 10.1016/j.plaphy.2020.06.034. [PMID: 32750647]
Anne Guertler, Hannah Schwaiger, Julian Poetschke, Stephanie Steckmeier, Gerd Gauglitz. Objective evaluation of an occlusive overnight intensive patch containing onion extract and allantoin for hypertrophic scars. Journal of cosmetic dermatology. 2020 Sep; 19(9):2415-2420. doi: 10.1111/jocd.13561. [PMID: 32573095]
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