Altan (BioDeep_00000864926)
Main id: BioDeep_00000406552
PANOMIX_OTCML-2023 Volatile Flavor Compounds
代谢物信息卡片
化学式: C14H8O4 (240.0422568)
中文名称: 1,8-二羟基蒽醌
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O
InChI: InChI=1S/C14H8O4/c15-9-5-1-3-7-11(9)14(18)12-8(13(7)17)4-2-6-10(12)16/h1-6,15-16H
描述信息
A - Alimentary tract and metabolism > A06 - Drugs for constipation > A06A - Drugs for constipation > A06AB - Contact laxatives
D005765 - Gastrointestinal Agents > D002400 - Cathartics
D009676 - Noxae > D009153 - Mutagens
Danthron is a natural product extracted from the traditional Chinese medicine Salvia miltiorrhiza Bunge. Danthron functions in regulating glucose and lipid metabolism by activating AMPK.
Danthron is a natural product extracted from the traditional Chinese medicine Salvia miltiorrhiza Bunge. Danthron functions in regulating glucose and lipid metabolism by activating AMPK.
Danthron is a natural product extracted from the traditional Chinese medicine Salvia miltiorrhiza Bunge. Danthron functions in regulating glucose and lipid metabolism by activating AMPK.
同义名列表
96 个代谢物同义名
InChI=1\C14H8O4\c15-9-5-1-3-7-11(9)14(18)12-8(13(7)17)4-2-6-10(12)16\h1-6,15-16; 9,10-Anthracenedione, 1,8-dihydroxy-; 1,8-Dihydroxy-9,10-anthracenedione; 1,8-Dihydroxyanthracene-9,10-dione; 1,8-Dihydroxyanthrachinon [Czech]; 1,8-Dihydroxyanthra-9,10-quinone; 1,8-dihydroxy-9,10-anthraquinone; Anthraquinone, 1,8-dihydroxy-; 1,4,5,8-Tetroxyantraquinone; 1,8-dihydroxyanthraquinone; 1,8-Dihydroxyanthrachinon; WLN: L C666 BV IVJ DQ NQ; 1,8-Dihydroanthraquinone; component of Dorbantyl; Dantrona [INN-Spanish]; Dantronum [INN-Latin]; Dantrone [INN-French]; component of Doxidan; Dioxyanthrachinonum; component of Modane; component of Doxan; Spectrum3_000650; EINECS 204-173-5; Spectrum5_000324; Spectrum2_000603; Spectrum4_001682; NCGC00091367-02; Spectrum_001750; D108103_ALDRICH; NCGC00091367-01; Danthron [BAN]; NCIMech_000114; SPECTRUM211468; BSPBio_002259; KBioSS_002230; KBioGR_001944; MEGxp0_001693; DivK1c_000284; NCI60_041443; MLS000069608; KBio2_007366; KBio2_004798; KBio1_000284; SMR000059018; KBio3_001479; ACon1_000135; SPBio_000506; KBio2_002230; NINDS_000284; ZINC03860369; IDI1_000284; AIDS-001375; Laxanthreen; 343235-40-5; Usaf nd-59; NSC 646568; Antrapurol; EU-0099935; CHEBI:3682; Chrysazine; AIDS001375; 32073-07-7; CCRIS 3529; Neokutin S; Laxipurin; Zwitsalax; AI3-38117; chrysazin; NSC 38626; NSC646568; Scatron D; ST5330603; NSC38626; Danthron; Diaquone; Dorbanex; Pastomin; Laxanorm; 117-10-2; NSC7210; Istizin; Dantron; Laxipur; Dionone; Dorbane; Danivac; Duolax; Roydan; Bancon; C10312; Modane; Prugol; Altan; Istan; LTAN; Danthron
数据库引用编号
9 个数据库交叉引用编号
- ChEBI: CHEBI:3682
- PubChem: 2950
- DrugBank: DB04816
- ChEMBL: CHEMBL53418
- CAS: 117-10-2
- medchemexpress: HY-B0923
- KEGG: C10312
- PubChem: 12498
- KNApSAcK: 3682
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
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)
10 个相关的物种来源信息
- 49698 - Asphodelus aestivus: 10.1016/S0031-9422(00)90193-6
- 1497607 - Asphodelus fistulosus: 10.1016/S0031-9422(00)90193-6
- 1423376 - Asphodelus tenuifolius: 10.1016/S0031-9422(00)90193-6
- 38033 - Chaetomium globosum: 10.1016/J.BMC.2006.07.048
- 50278 - Cinchona pubescens: 10.1055/S-2007-969609
- 1266668 - Didemnum albopunctatum: 10.1021/NP300074Z
- 33090 - Plants: -
- 263405 - Trirhabda geminata: 10.1515/ZNC-1996-3-417
- 193294 - Watersipora subtorquata: 10.1021/NP010577+
- 53851 - 决明子: -
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
- Razieh Amini, Shadi Moradi, Rezvan Najafi, Mehrdokht Mazdeh, Amir Taherkhani. BACE1 Inhibition Utilizing Organic Compounds Holds Promise as a Potential Treatment for Alzheimer's and Parkinson's Diseases.
Oxidative medicine and cellular longevity.
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10.1155/2024/6654606
. [PMID: 38425997] - Chuanrui Ma, Zhongyan Wang, Ronglin Xia, Lingling Wei, Chao Zhang, Jing Zhang, Linna Zhao, Han Wu, Lin Kang, Shu Yang. Danthron ameliorates obesity and MAFLD through activating the interplay between PPARα/RXRα heterodimer and adiponectin receptor 2.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
2021 May; 137(?):111344. doi:
10.1016/j.biopha.2021.111344
. [PMID: 33581653] - 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] - Xiujin Shi, Yi Zhang, Baidi Lin, Yang Zhou, Wei Suo, Juanjuan Wei, Lin Zhang, Jie Lin, Fucheng Xiao, Limin Zhao, Yang Lin. Danthron attenuates experimental atherosclerosis by targeting foam cell formation.
Experimental physiology.
2021 03; 106(3):653-662. doi:
10.1113/ep089021
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Molecular pharmacology.
2019 11; 96(5):629-640. doi:
10.1124/mol.119.115964
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Journal of biomolecular structure & dynamics.
2018 Oct; 36(13):3362-3375. doi:
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Current microbiology.
2018 Mar; 75(3):343-352. doi:
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. [PMID: 21268248] - Haitao Zhang, Rong Zhou, Li Li, Jing Chen, Lili Chen, Chenjing Li, Hong Ding, Liang Yu, Lihong Hu, Hualiang Jiang, Xu Shen. Danthron functions as a retinoic X receptor antagonist by stabilizing tetramers of the receptor.
The Journal of biological chemistry.
2011 Jan; 286(3):1868-75. doi:
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Mutation research.
2009 Aug; 678(1):13-9. doi:
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Journal of bioscience and bioengineering.
2009 Mar; 107(3):296-300. doi:
10.1016/j.jbiosc.2008.10.008
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Langmuir : the ACS journal of surfaces and colloids.
2008 Apr; 24(8):4041-9. doi:
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Biomedical chromatography : BMC.
2007 Jul; 21(7):701-7. doi:
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2007 Jun; 112(2):415-6. doi:
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Biomedical chromatography : BMC.
2007 May; 21(5):502-7. doi:
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European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
2007 Apr; 66(1):135-45. doi:
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Acta biochimica Polonica.
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Fitoterapia.
2004 Jul; 75(5):505-9. doi:
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. [PMID: 15261390] - Yong-Soo Kwon, Jae-Young Koh, Dong-Keun Song, Hyoung-Chun Kim, Myung-Sang Kwon, Yeon-Sik Choi, Myung-Bok Wie. Danthron inhibits the neurotoxicity induced by various compounds causing oxidative damages including beta-amyloid (25-35) in primary cortical cultures.
Biological & pharmaceutical bulletin.
2004 May; 27(5):723-6. doi:
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Journal of ethnopharmacology.
2004 Apr; 91(2-3):351-5. doi:
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Zeitschrift fur Naturforschung. C, Journal of biosciences.
2002 Sep; 57(9-10):822-7. doi:
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Bioorganic & medicinal chemistry letters.
2001 Jul; 11(14):1839-42. doi:
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Antiviral research.
2001 Mar; 49(3):169-78. doi:
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1997 Jun; 18(6):1259-63. doi:
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