Paromomycin (BioDeep_00000003480)
Secondary id: BioDeep_00001868233
human metabolite blood metabolite Chemicals and Drugs Antibiotics Volatile Flavor Compounds natural product
代谢物信息卡片
化学式: C23H45N5O14 (615.296287)
中文名称: 巴龙霉素
谱图信息:
最多检出来源 Homo sapiens(blood) 0.1%
分子结构信息
SMILES: C1C(C(C(C(C1N)OC2C(C(C(C(O2)CO)O)O)N)OC3C(C(C(O3)CO)OC4C(C(C(C(O4)CN)O)O)N)O)O)N
InChI: InChI=1S/C23H45N5O14/c24-2-7-13(32)15(34)10(27)21(37-7)41-19-9(4-30)39-23(17(19)36)42-20-12(31)5(25)1-6(26)18(20)40-22-11(28)16(35)14(33)8(3-29)38-22/h5-23,29-36H,1-4,24-28H2/t5-,6+,7+,8-,9-,10-,11-,12+,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23+/m1/s1
描述信息
Paromomycin is only found in individuals that have used or taken this drug. It is an oligosaccharide antibiotic produced by various streptomyces. [PubChem]Paromomycin inhibits protein synthesis by binding to 16S ribosomal RNA. Bacterial proteins are synthesized by ribosomal RNA complexes which are composed of 2 subunits, a large subunit (50s) and small (30s) subunit, which forms a 70s ribosomal subunit. tRNA binds to the top of this ribosomal structure. Paramomycin binds to the A site, which causes defective polypeptide chains to be produced. Continuous production of defective proteins eventually leads to bacterial death.
A - Alimentary tract and metabolism > A07 - Antidiarrheals, intestinal antiinflammatory/antiinfective agents > A07A - Intestinal antiinfectives > A07AA - Antibiotics
D000890 - Anti-Infective Agents > D000977 - Antiparasitic Agents > D000981 - Antiprotozoal Agents
C784 - Protein Synthesis Inhibitor > C2363 - Aminoglycoside Antibiotic
D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents
C254 - Anti-Infective Agent > C258 - Antibiotic
KEIO_ID P126
同义名列表
44 个代谢物同义名
(2S,3S,4R,5R,6R)-5-amino-2-(aminomethyl)-6-{[(2R,3S,4R,5S)-5-{[(1R,2R,3S,5R,6S)-3,5-diamino-2-{[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-hydroxycyclohexyl]oxy}-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxy}oxane-3,4-diol; (1R,2R,3S,4R,6S)-4,6-Diamino-2-{[3-O-(2,6-diamino-2,6-dideoxy-beta-L-idopyranosyl)-beta-D-ribofuranosyl]oxy}-3-hydroxycyclohexyl 2-amino-2-deoxy-alpha-D-glucopyranoside; (1R,2R,3S,4R,6S)-4,6-Diamino-2-{[3-O-(2,6-diamino-2,6-dideoxy-β-L-idopyranosyl)-β-D-ribofuranosyl]oxy}-3-hydroxycyclohexyl 2-amino-2-deoxy-α-D-glucopyranoside; (1R,2R,3S,4R,6S)-4,6-Diamino-2-{[3-O-(2,6-diamino-2,6-dideoxy-b-L-idopyranosyl)-b-D-ribofuranosyl]oxy}-3-hydroxycyclohexyl 2-amino-2-deoxy-a-D-glucopyranoside; D-Streptamine,O-2,6-diamino-2,6-dideoxy-b-L-idopyranosyl-(1®3)-O-b-D-ribofuranosyl-(1®5)-O-[2-amino-2-deoxy-a-D-glucopyranosyl-(1®4)]-2-deoxy-; Paromomycin, beta D glucopyranosyl isomer; Paromomycin, beta-D-glucopyranosyl-isomer; beta-D-Glucopyranosyl-isomer paromomycin; Parke davis brand OF paromomycin sulfate; Cheminova brand OF paromomycin sulfate; Monarch brand OF paromomycin sulfate; Pfizer brand OF paromomycin sulfate; Paromomycin sulfate (1:1); Paromomycin sulfate (2:5); Phosphate, paromomycin; Paromomycin phosphate; Paramomycin sulphate; Sulfate, paromomycin; Paromomycin sulfate; Paramomycin sulfate; Paromomycin I; Paromomycinum; Paromomycine; Hydroxymycin; Zygomycin a1; Gabbromicina; Paucimycinum; Paromomicina; Gabbromycin; Paromomycin; Monomycin a; Paramomycin; Aminosidine; Crestomycin; Neomycin e; Aminosidin; Paucimycin; Catenulin; Estomycin; Humatin; R-400; R 400; PRM; Paromomycin
数据库引用编号
32 个数据库交叉引用编号
- ChEBI: CHEBI:7934
- KEGG: C00832
- KEGGdrug: D07467
- PubChem: 165580
- PubChem: 4689
- HMDB: HMDB0015490
- DrugBank: DB01421
- ChEMBL: CHEMBL370143
- Wikipedia: Paromomycin
- MeSH: Paromomycin
- KNApSAcK: C00018808
- chemspider: 145115
- CAS: 134235-09-9
- CAS: 7542-37-2
- MoNA: KO003896
- MoNA: KO003897
- MoNA: KO003901
- MoNA: KO003900
- MoNA: KO003893
- MoNA: KO003898
- MoNA: KO003899
- MoNA: KO003892
- MoNA: KO003894
- MoNA: KO003895
- PMhub: MS000009740
- PubChem: 4090
- PDB-CCD: PAR
- NIKKAJI: J8.952D
- RefMet: Paromomycin
- KNApSAcK: 7934
- LOTUS: LTS0142951
- LOTUS: LTS0127980
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)
16 个相关的物种来源信息
- 2 - Bacteria: LTS0127980
- 2 - Bacteria: LTS0142951
- 9606 - Homo sapiens: -
- 1883 - Streptomyces: 10.1186/S12866-019-1390-1
- 1883 - Streptomyces: 10.4014/JMB.1603.03019
- 1883 - Streptomyces: 10.7164/ANTIBIOTICS.39.1598
- 1883 - Streptomyces: LTS0127980
- 1883 - Streptomyces: LTS0142951
- 1906 - Streptomyces fradiae: 10.1039/B808734B
- 1906 - Streptomyces fradiae: LTS0142951
- 1927 - Streptomyces rimosus:
- 1927 - Streptomyces rimosus: 10.1186/S12866-019-1390-1
- 1927 - Streptomyces rimosus: 10.4014/JMB.1603.03019
- 1927 - Streptomyces rimosus: LTS0127980
- 2062 - Streptomycetaceae: LTS0127980
- 2062 - Streptomycetaceae: LTS0142951
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
- Mingxiao Liu, Di Zhang, Dongqiang Wang, Xiaodong Wu, Ying Zhang, Jigang Yin, Guan Zhu. Cost-effective In vivo and In vitro Mouse Models for Evaluating Anti-Cryptosporidial Drug Efficacy: Assessing Vorinostat, Docetaxel and Baicalein.
The Journal of infectious diseases.
2023 Jul; ?(?):. doi:
10.1093/infdis/jiad243
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Veterinary immunology and immunopathology.
2022 Jun; 248(?):110429. doi:
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Pediatric clinics of North America.
2022 02; 69(1):79-97. doi:
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Clinical pharmacokinetics.
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