Ubenimex (BioDeep_00000230884)
Main id: BioDeep_00000003100
PANOMIX_OTCML-2023 Antitumor activity
代谢物信息卡片
化学式: C16H24N2O4 (308.1736)
中文名称: 乌苯美司
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC(C)CC(C(=O)O)NC(=O)C(C(CC1=CC=CC=C1)N)O
InChI: InChI=1S/C16H24N2O4/c1-10(2)8-13(16(21)22)18-15(20)14(19)12(17)9-11-6-4-3-5-7-11/h3-7,10,12-14,19H,8-9,17H2,1-2H3,(H,18,20)(H,21,22)/t12-,13+,14+/m1/s1
描述信息
Ubenimex (also known as bestatin) is a competitive protease inhibitor. It is an inhibitor of aminopeptidase B, leukotriene A4 hydrolase, aminopeptidase N. It is being studied for use in the treatment of acute myelocytic leukemia.
Ubenimex is a microbial metabolite and dipeptide with potential immunomodulatory and antitumor activities. Ubenimex competitively inhibits many aminopeptidases, including B, N and leucine aminopeptidases. Aminopeptidases has been implicated in the process of cell adhesion and invasion of tumor cells. Therefore, inhibiting aminopeptidases may partially attribute to the antitumor effect of ubenimex. This agent also activates T lymphocyte, macrophage and bone marrow stem cell as well as stimulates release of interleukin-1 and -2, thus further enhances its antitumor activity.
D000890 - Anti-Infective Agents > D000998 - Antiviral Agents > D044966 - Anti-Retroviral Agents
D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents
D004791 - Enzyme Inhibitors > D011480 - Protease Inhibitors
C308 - Immunotherapeutic Agent > C2139 - Immunostimulant
D000970 - Antineoplastic Agents
D007155 - Immunologic Factors
Bestatin is a natural, broad-spectrum, and competitive CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase inhibitor. Bestatin has anticancer effects[1][2].
同义名列表
62 个代谢物同义名
(2S)-2-[[(2S,3R)-3-amino-2-hydroxy-4-phenyl-butanoyl]amino]-4-methyl-pentanoic acid; (2S)-2-[[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanoyl]amino]-4-methylpentanoic acid; (2S)-2-[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanamido]-4-methylpentanoic acid; (S)-2-((2S,3R)-3-amino-2-hydroxy-4-phenylbutanamido)-4-methylpentanoic acid; (S)-2-((2S,3R)-3-amino-2-hydroxy-4-phenylbutanamido)-4-methylpentanoicacid; L-Leucine, N-(3-amino-2-hydroxy-1-oxo-4-phenylbutyl)-, (S-(R*,S*))-; 2-(3-AMINO-2-HYDROXY-4-PHENYL-BUTYRYLAMINO)-4-METHYL-PENTANOIC ACID; L-Leucine, N-[(2S,3R)-3-amino-2-hydroxy-1-oxo-4-phenylbutyl]-; L-LEUCINE, N-((2S,3R)-3-AMINO-2-HYDROXY-1-OXO-4-PHENYLBUTYL)-; N-[(2S,3R)-3-Amino-2-hydroxy-4-phenylbutyryl]-L-leucine, 97\\%; (S-(R*,S*))-N-(3-Amino-2-hydroxy-4-phenylbutyroyl)-L-leucine; (-)-N-((2S,3R)-3-Amino-2-hydroxy-4-phenylbutyryl)-L-leucine; N-[(2S,3R)-3-Amino-2-hydroxy-1-oxo-4-phenylbutyl]-L-leucine; N-[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanoyl]-L-leucine; N-[(2S,3R)-3-Amino-2-hydroxy-4-phenylbutyryl]-L-leucine; N-((2S,3R)-3-AMINO-2-HYDROXY-4-PHENYLBUTANOYL)-LEUCINE; ((2S,3R)-3-amino-2-hydroxy-4-phenylbutanoyl)-L-leucine; 3-(R)-Amino-2-(S)-hydroxy-4-phenylbutanoyl-(S)-leucine; bestatin, (L-Leu)-(S-(R*,S*))-isomer, hydrochloride; [(2S,3R)-3-Amino-2-hydroxy-4-phenylbutanoyl]-Leu; (3-amino-2-hydroxy-4-phenylbutanoyl)-L-leucine; 3-amino-2-hydroxy-4-phenylbutyryl-L-leucine; bestatin, (L-Leu)-(R-(R*,S*))-isomer; bestatin, (D-Leu)-(R-(R*,S*))-isomer; bestatin, (L-Leu)-(S-(R*,R*))-isomer; bestatin, (L-Leu)-(R-(R*,R*))-isomer; bestatin, (D-Leu)-(R-(R*,R*))-isomer; bestatin, (D-Leu)-(S-(R*,S*))-isomer; VGGGPCQERPFHOB-RDBSUJKOSA-N; Ubenimex (Bestatin); Ubenimex(Bestatin); Ubenimex, Bestatin; Ubenimex [INN:JAN]; Ubenimexum [Latin]; UBENIMEX [WHO-DD]; UBENIMEX [MART.]; BCBcMAP01_000178; UNII-I0J33N5627; Ubenimex- Bio-X; Ubenimex, solid; UBENIMEX [INN]; UBENIMEX [JAN]; Lopac0_000214; UBENIMEX [MI]; KBio2_002841; KBio3_000545; KBio2_005409; Ubenimex,(S); (-)-bestatin; KBio3_000546; KBio2_000273; IDI1_034023; SMP1_000030; Bio2_000753; Bio2_000273; I0J33N5627; Ubenimexum; Ubestatin; bestatin; Ubenimex; 1txr; Ubenimex
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)
0 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。
亚细胞结构定位 | 关联基因列表 |
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文献列表
- Quan Chen, Bingbing Wu, Pengfei Ge, Peng Zhang, Xia Chen. Ubenimex Combined with Pemetrexed Upregulates SOCS1 to Inhibit Lung Adenocarcinoma Progression via the JAK2-STAT3 Signaling Pathway.
Disease markers.
2022; 2022(?):5614939. doi:
10.1155/2022/5614939
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Bioorganic chemistry.
2021 11; 116(?):105343. doi:
10.1016/j.bioorg.2021.105343
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International journal of biological macromolecules.
2020 Dec; 164(?):2944-2952. doi:
10.1016/j.ijbiomac.2020.08.157
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Experimental parasitology.
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. [PMID: 33007297] - Jiangying Cao, Wei Zhao, Chunlong Zhao, Qian Liu, Shunda Li, Guozhen Zhang, C James Chou, Yingjie Zhang. Development of a Bestatin-SAHA Hybrid with Dual Inhibitory Activity against APN and HDAC.
Molecules (Basel, Switzerland).
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Drug discoveries & therapeutics.
2015 Feb; 9(1):45-52. doi:
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European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
2014 Oct; 63(?):77-86. doi:
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. [PMID: 25016073] - Yanna Zhu, Qiang Meng, Changyuan Wang, Qi Liu, Xiaokui Huo, Aijie Zhang, Pengyuan Sun, Huijun Sun, Hua Li, Kexin Liu. Methotrexate-bestatin interaction: involvement of P-glycoprotein and organic anion transporters in rats.
International journal of pharmaceutics.
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Journal of pharmaceutical sciences.
2014 Feb; 103(2):719-29. doi:
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European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
2013 Nov; 50(3-4):420-8. doi:
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Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition.
2012 Jul; 43(4):609-11, 630. doi:
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. [PMID: 22997907] - Yanna Zhu, Qiang Meng, Changyuan Wang, Qi Liu, Huijun Sun, Taiichi Kaku, Kexin Liu. Organic anion transporters involved in the excretion of bestatin in the kidney.
Peptides.
2012 Feb; 33(2):265-71. doi:
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Journal of molecular histology.
2011 Dec; 42(6):589-96. doi:
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2007 Jan; 15(1):63-76. doi:
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Plant physiology.
2006 Aug; 141(4):1400-13. doi:
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Neuropeptides.
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Gan to kagaku ryoho. Cancer & chemotherapy.
2003 Oct; 30(10):1519-22. doi:
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Gan to kagaku ryoho. Cancer & chemotherapy.
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