sordarin (BioDeep_00000301983)
代谢物信息卡片
化学式: C27H40O8 (492.272304)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC1CCC2C1CC3(C4CC2(C3(C(=C4)C(C)C)C(=O)O)C=O)COC5C(C(C(C(O5)C)OC)O)O
InChI: InChI=1S/C27H40O8/c1-13(2)19-8-16-9-25(11-28)18-7-6-14(3)17(18)10-26(16,27(19,25)24(31)32)12-34-23-21(30)20(29)22(33-5)15(4)35-23/h8,11,13-18,20-23,29-30H,6-7,9-10,12H2,1-5H3,(H,31,32)/t14-,15-,16+,17-,18-,20+,21+,22-,23-,25+,26+,27+/m1/s1
相关代谢途径
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代谢反应
0 个相关的代谢反应过程信息。
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INOH(0)
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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。
文献列表
- Thomas P Tully, James S Bergum, Steven R Schwarz, Susan C Durand, Jeffrey M Howell, Ramesh N Patel, Paul M Cino. Improvement of sordarin production through process optimization: combining traditional approaches with DOE.
Journal of industrial microbiology & biotechnology.
2007 Mar; 34(3):193-202. doi:
10.1007/s10295-006-0186-0. [PMID: 17131104] - P Aviles, C Falcoz, M J Guillén, R San Roman, F Gómez De Las Heras, D Gargallo-Viola. Correlation between in vitro and in vivo activities of GM 237354, a new sordarin derivative, against Candida albicans in an in vitro pharmacokinetic-pharmacodynamic model and influence of protein binding.
Antimicrobial agents and chemotherapy.
2001 Oct; 45(10):2746-54. doi:
10.1128/aac.45.10.2746-2754.2001. [PMID: 11557464] - P Aviles, A Pateman, R San Roman, M J Guillén, F Gómez De Las Heras, D Gargallo-Viola. Animal pharmacokinetics and interspecies scaling of sordarin derivatives following intravenous administration.
Antimicrobial agents and chemotherapy.
2001 Oct; 45(10):2787-92. doi:
10.1128/aac.45.10.2787-2792.2001. [PMID: 11557470] - A Martinez, P Aviles, E Jimenez, J Caballero, D Gargallo-Viola. Activities of sordarins in experimental models of candidiasis, aspergillosis, and pneumocystosis.
Antimicrobial agents and chemotherapy.
2000 Dec; 44(12):3389-94. doi:
10.1128/aac.44.12.3389-3394.2000. [PMID: 11083645] - P Aviles, C Falcoz, R San Roman, D Gargallo-Viola. Pharmacokinetics-pharmacodynamics of a sordarin derivative (GM 237354) in a murine model of lethal candidiasis.
Antimicrobial agents and chemotherapy.
2000 Sep; 44(9):2333-40. doi:
10.1128/aac.44.9.2333-2340.2000. [PMID: 10952576] - K V Clemons, D A Stevens. Efficacies of sordarin derivatives GM193663, GM211676, and GM237354 in a murine model of systemic coccidioidomycosis. p6.
Antimicrobial agents and chemotherapy.
2000 Jul; 44(7):1874-7. doi:
10.1128/aac.44.7.1874-1877.2000. [PMID: 10858347] - Fostel, Lartey. Emerging novel antifungal agents.
Drug discovery today.
2000 Jan; 5(1):25-32. doi:
10.1016/s1359-6446(99)01430-0. [PMID: 10637546] - J R Graybill, L Najvar, A Fothergill, R Bocanegra, F G de las Heras. Activities of sordarins in murine histoplasmosis.
Antimicrobial agents and chemotherapy.
1999 Jul; 43(7):1716-8. doi:
10.1128/aac.43.7.1716. [PMID: 10390228] - M C Justice, M J Hsu, B Tse, T Ku, J Balkovec, D Schmatz, J Nielsen. Elongation factor 2 as a novel target for selective inhibition of fungal protein synthesis.
The Journal of biological chemistry.
1998 Feb; 273(6):3148-51. doi:
10.1074/jbc.273.6.3148. [PMID: 9452424]