Costatolide (BioDeep_00000843796)
代谢物信息卡片
化学式: C22H26O5 (370.17801460000004)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CCCC1=CC(=O)OC2=C1C3=C(C=CC(O3)(C)C)C4=C2C(C(C(O4)C)C)O
InChI: InChI=1S/C22H26O5/c1-6-7-13-10-15(23)26-21-16(13)20-14(8-9-22(4,5)27-20)19-17(21)18(24)11(2)12(3)25-19/h8-12,18,24H,6-7H2,1-5H3/t11-,12-,18-/m0/s1
描述信息
D000890 - Anti-Infective Agents > D000998 - Antiviral Agents > D044966 - Anti-Retroviral Agents
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
- Irena Kostova. Coumarins as inhibitors of HIV reverse transcriptase.
Current HIV research.
2006 Jul; 4(3):347-63. doi:
10.2174/157016206777709393. [PMID: 16842086] - Maira Huerta-Reyes, Maria Del Carmen Basualdo, Fumiko Abe, Manuel Jimenez-Estrada, Carmen Soler, Ricardo Reyes-Chilpa. HIV-1 inhibitory compounds from Calophyllum brasiliense leaves.
Biological & pharmaceutical bulletin.
2004 Sep; 27(9):1471-5. doi:
10.1248/bpb.27.1471. [PMID: 15340243] - Donglei Yu, Madoka Suzuki, Lan Xie, Susan L Morris-Natschke, Kuo-Hsiung Lee. Recent progress in the development of coumarin derivatives as potent anti-HIV agents.
Medicinal research reviews.
2003 May; 23(3):322-45. doi:
10.1002/med.10034. [PMID: 12647313] - David A Eiznhamer, Terri Creagh, Jon L Ruckle, Dwain T Tolbert, Jeremy Giltner, Bipul Dutta, Michael T Flavin, Tuah Jenta, Ze-Qi Xu. Safety and pharmacokinetic profile of multiple escalating doses of (+)-calanolide A, a naturally occurring nonnucleoside reverse transcriptase inhibitor, in healthy HIV-negative volunteers.
HIV clinical trials.
2002 Nov; 3(6):435-50. doi:
10.1310/9gde-f2r1-w2rl-e9fj. [PMID: 12501127] - T Creagh, J L Ruckle, D T Tolbert, J Giltner, D A Eiznhamer, B Dutta, M T Flavin, Z Q Xu. Safety and pharmacokinetics of single doses of (+)-calanolide a, a novel, naturally occurring nonnucleoside reverse transcriptase inhibitor, in healthy, human immunodeficiency virus-negative human subjects.
Antimicrobial agents and chemotherapy.
2001 May; 45(5):1379-86. doi:
10.1128/aac.45.5.1379-1386.2001. [PMID: 11302799] - Z Q Xu, K J Norris, D S Weinberg, J Kardatzke, P Wertz, P Frank, M T Flavin. Quantification of (+)-calanolide A, a novel and naturally occurring anti-HIV agent, by high-performance liquid chromatography in plasma from rat, dog and human.
Journal of chromatography. B, Biomedical sciences and applications.
2000 Jun; 742(2):267-75. doi:
10.1016/s0378-4347(00)00170-5. [PMID: 10901131] - Z Q Xu, E R Kern, L Westbrook, L B Allen, R W Buckheit, C K Tseng, T Jenta, M T Flavin. Plant-derived and semi-synthetic calanolide compounds with in vitro activity against both human immunodeficiency virus type 1 and human cytomegalovirus.
Antiviral chemistry & chemotherapy.
2000 Jan; 11(1):23-9. doi:
10.1177/095632020001100102. [PMID: 10693651] - L Hanna. Calanolide A: a natural non-nucleoside reverse transcriptase inhibitor.
BETA : bulletin of experimental treatments for AIDS : a publication of the San Francisco AIDS Foundation.
1999 Apr; 12(2):8-9. doi:
. [PMID: 11366704] - R A Newman, W Chen, T L Madden. Pharmaceutical properties of related calanolide compounds with activity against human immunodeficiency virus.
Journal of pharmaceutical sciences.
1998 Sep; 87(9):1077-80. doi:
10.1021/js980122d. [PMID: 9724557] - ". Natural compound shows anti-HIV activity.
AIDS patient care and STDs.
1998 May; 12(5):410. doi:
". [PMID: 11361986] - T C McKee, R W Fuller, C D Covington, J H Cardellina, R J Gulakowski, B L Krepps, J B McMahon, M R Boyd. New pyranocoumarins isolated from Calophyllum lanigerum and Calophyllum teysmannii.
Journal of natural products.
1996 Aug; 59(8):754-8. doi:
10.1021/np9603784. [PMID: 8792623]