Desciclovir (BioDeep_00000859200)
代谢物信息卡片
化学式: C8H11N5O2 (209.0912706)
中文名称: 地昔洛韦
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1=C2C(=NC(=N1)N)N(C=N2)COCCO
InChI: InChI=1S/C8H11N5O2/c9-8-10-3-6-7(12-8)13(4-11-6)5-15-2-1-14/h3-4,14H,1-2,5H2,(H2,9,10,12)
描述信息
D000890 - Anti-Infective Agents > D000998 - Antiviral Agents
C471 - Enzyme Inhibitor > C29575 - DNA Polymerase Inhibitor
C254 - Anti-Infective Agent > C281 - Antiviral Agent
同义名列表
1 个代谢物同义名
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。
文献列表
- R A de Man, J Lindemans, S W Schalm, F J ten Kate. beta 2-Microglobulin and antiviral therapy for chronic hepatitis type B.
Antiviral research.
1989 May; 11(4):181-90. doi:
10.1016/0166-3542(89)90003-x
. [PMID: 2662897] - N A Peterslund, V Esmann, J P Geil, C M Petersen, C E Mogensen. Open study of 2-amino-9-(hydroxyethoxymethyl)-9H-purine (desciclovir) in the treatment of herpes zoster.
The Journal of antimicrobial chemotherapy.
1987 Nov; 20(5):743-51. doi:
10.1093/jac/20.5.743
. [PMID: 3429375] - B G Petty, R J Whitley, S Liao, H C Krasny, L E Rocco, L G Davis, P S Lietman. Pharmacokinetics and tolerance of desciclovir, a prodrug of acyclovir, in healthy human volunteers.
Antimicrobial agents and chemotherapy.
1987 Sep; 31(9):1317-22. doi:
10.1128/aac.31.9.1317
. [PMID: 3674844] - D B Jones, V K Rustgi, D M Kornhauser, A Woods, R Quinn, J H Hoofnagle, E A Jones. The disposition of 6-deoxyacyclovir, a xanthine oxidase-activated prodrug of acyclovir, in the isolated perfused rat liver.
Hepatology (Baltimore, Md.).
1987 Mar; 7(2):345-8. doi:
10.1002/hep.1840070222
. [PMID: 3557315] - H C Krasny, B G Petty. Metabolism of desciclovir, a prodrug of acyclovir, in humans after multiple oral dosing.
Journal of clinical pharmacology.
1987 Jan; 27(1):74-7. doi:
10.1177/009127008702700112
. [PMID: 3680558] - R P Quinn, L Gerald, S Tadepalli. Radioimmunoassay for desciclovir, 2-[(2-amino-9H-purin-9-yl)methoxy]ethanol, a prodrug for the antiviral acyclovir.
Journal of immunoassay.
1987; 8(2-3):247-65. doi:
10.1080/15321818708057025
. [PMID: 3624496] - P J Rees, P Selby, H G Prentice, P D Whiteman, D M Grant. A515U: a prodrug of acyclovir with increased oral bioavailability.
The Journal of antimicrobial chemotherapy.
1986 Oct; 18 Suppl B(?):215-22. doi:
10.1093/jac/18.supplement_b.215
. [PMID: 3793661] - I V Weller, R S Tedder, P Karayiannis, H C Thomas, A P Fiddian. A pilot study of BW A515U (6-deoxyacyclovir) in chronic hepatitis B virus infection.
Journal of hepatology.
1986; 3 Suppl 2(?):S119-22. doi:
10.1016/s0168-8278(86)80109-x
. [PMID: 3598153] - D Brigden, P Whiteman. The clinical pharmacology of acyclovir and its prodrugs.
Scandinavian journal of infectious diseases. Supplementum.
1985; 47(?):33-9. doi:
NULL
. [PMID: 3868024] - P Selby, R L Powles, S Blake, K Stolle, E K Mbidde, T J McElwain, E Hickmott, P D Whiteman. Amino (hydroxyethoxymethyl) purine: a new well-absorbed prodrug of acyclovir.
Lancet (London, England).
1984 Dec; 2(8417-8418):1428-30. doi:
10.1016/s0140-6736(84)91624-6
. [PMID: 6151046] - T A Krenitsky, W W Hall, P de Miranda, L M Beauchamp, H J Schaeffer, P D Whiteman. 6-Deoxyacyclovir: a xanthine oxidase-activated prodrug of acyclovir.
Proceedings of the National Academy of Sciences of the United States of America.
1984 May; 81(10):3209-13. doi:
10.1073/pnas.81.10.3209
. [PMID: 6587347] - P D Whiteman, A Bye, A S Fowle, S Jeal, G Land, J Posner. Tolerance and pharmacokinetics of A515U, an acyclovir analogue, in healthy volunteers.
European journal of clinical pharmacology.
1984; 27(4):471-5. doi:
10.1007/bf00549597
. [PMID: 6549167]