42-(Dimethylphosphinate)rapamycin (BioDeep_00001030211)

   


代谢物信息卡片


Ridaforolimus (Deforolimus, MK-8669)

化学式: C53H84NO14P (989.5629)
中文名称: 息斯敏
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1CCC2CC(C(=CC=CC=CC(CC(C(=O)C(C(C(=CC(C(=O)CC(OC(=O)C3CCCCN3C(=O)C(=O)C1(O2)O)C(C)CC4CCC(C(C4)OC)OP(=O)(C)C)C)C)O)OC)C)C)C)OC
InChI: InChI=1S/C53H84NO14P/c1-32-18-14-13-15-19-33(2)44(63-8)30-40-23-21-38(7)53(61,67-40)50(58)51(59)54-25-17-16-20-41(54)52(60)66-45(35(4)28-39-22-24-43(46(29-39)64-9)68-69(11,12)62)31-42(55)34(3)27-37(6)48(57)49(65-10)47(56)36(5)26-32/h13-15,18-19,27,32,34-36,38-41,43-46,48-49,57,61H,16-17,20-26,28-31H2,1-12H3/b15-13+,18-14+,33-19+,37-27+/t32-,34-,35-,36-,38-,39+,40?,41+,43-,44+,45+,46-,48-,49+,53-/m1/s1

描述信息

同义名列表

3 个代谢物同义名

Ridaforolimus (Deforolimus, MK-8669); 42-(Dimethylphosphinate)rapamycin; AP 23573



数据库引用编号

6 个数据库交叉引用编号

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
Cytoplasm 11 ABCB1, AKT1, EIF4EBP1, MARK2, MTOR, PIK3C3, PIK3CA, PRKX, PTEN, RPS6KB1, TNK1
Peripheral membrane protein 3 MTOR, RDX, TNK1
Endoplasmic reticulum membrane 1 MTOR
Cytoplasmic vesicle, autophagosome 1 PIK3C3
Nucleus 6 AKT1, EIF4EBP1, MTOR, PRKX, PTEN, RPS6KB1
autophagosome 1 PIK3C3
cytosol 7 AKT1, EIF4EBP1, MTOR, PIK3C3, PIK3CA, PTEN, RPS6KB1
dendrite 2 MARK2, MTOR
phagocytic vesicle 1 MTOR
phosphatidylinositol 3-kinase complex, class III 1 PIK3C3
nucleoplasm 6 AKT1, MARK2, MTOR, PRKX, PTEN, RPS6KB1
Cell membrane 5 ABCB1, AKT1, CD48, RDX, TNF
Cytoplasmic side 2 MTOR, RDX
Cleavage furrow 1 RDX
lamellipodium 3 AKT1, PIK3CA, RDX
Multi-pass membrane protein 2 ABCB1, ABCC3
Golgi apparatus membrane 1 MTOR
cell cortex 1 AKT1
cell surface 4 ABCB1, AMELX, RPS6KB1, TNF
glutamatergic synapse 4 AKT1, GHRL, PIK3C3, RPS6KB1
Golgi membrane 2 INS, MTOR
lysosomal membrane 2 EGF, MTOR
neuronal cell body 1 TNF
postsynapse 3 AKT1, GHRL, RPS6KB1
Lysosome 1 MTOR
endosome 1 PIK3C3
plasma membrane 11 ABCB1, ABCC3, AKT1, CD48, EGF, MARK2, PIK3CA, PTEN, RDX, TNF, TNK1
Membrane 10 ABCB1, ABCC3, AKT1, CD48, EGF, MARK2, MTOR, PIK3C3, RDX, TNK1
apical plasma membrane 3 ABCB1, PTEN, RDX
axon 1 GHRL
basolateral plasma membrane 1 ABCC3
extracellular exosome 5 ABCB1, CD48, CXCL12, EGF, RDX
Lysosome membrane 1 MTOR
extracellular space 5 EGF, GHRL, INS, RDX, TNF
perinuclear region of cytoplasm 2 PIK3CA, RPS6KB1
Schaffer collateral - CA1 synapse 1 GHRL
adherens junction 1 RDX
intercalated disc 1 PIK3CA
mitochondrion 2 MARK2, RPS6KB1
protein-containing complex 1 AKT1
Microsome membrane 1 MTOR
filopodium 1 RDX
postsynaptic density 1 PTEN
TORC1 complex 1 MTOR
TORC2 complex 1 MTOR
Secreted 3 CD48, GHRL, INS
extracellular region 7 AMELX, CXCL12, EGF, GHRL, INS, PTEN, TNF
cytoplasmic side of plasma membrane 1 PTEN
Mitochondrion outer membrane 1 MTOR
mitochondrial outer membrane 2 MTOR, RPS6KB1
external side of plasma membrane 2 CXCL12, TNF
Secreted, extracellular space, extracellular matrix 1 AMELX
dendritic spine 1 PTEN
T-tubule 1 RDX
neuronal dense core vesicle lumen 1 GHRL
microtubule cytoskeleton 1 AKT1
midbody 2 PIK3C3, RDX
apical part of cell 1 RDX
cell-cell junction 1 AKT1
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 1 AKT1
Apical cell membrane 1 ABCB1
Membrane raft 2 CD48, TNF
Cytoplasm, cytoskeleton 1 RDX
focal adhesion 1 RDX
spindle 1 AKT1
GABA-ergic synapse 1 PIK3C3
Peroxisome 1 PIK3C3
Cell projection, dendritic spine 1 PTEN
Nucleus, PML body 2 MTOR, PTEN
PML body 2 MTOR, PTEN
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
collagen-containing extracellular matrix 2 AMELX, CXCL12
lateral plasma membrane 1 MARK2
axoneme 1 PIK3C3
Late endosome 1 PIK3C3
Cell projection, neuron projection 1 PTEN
neuron projection 2 PTEN, RPS6KB1
ciliary basal body 1 AKT1
cell projection 2 PTEN, RDX
phagocytic cup 1 TNF
phagocytic vesicle membrane 1 PIK3C3
cell periphery 1 RDX
cytoskeleton 1 RDX
actin filament 1 MARK2
Basolateral cell membrane 1 ABCC3
Lipid-anchor, GPI-anchor 1 CD48
nuclear envelope 1 MTOR
Endomembrane system 1 MTOR
endosome lumen 1 INS
microvillus 1 RDX
phagophore assembly site 1 PIK3C3
phosphatidylinositol 3-kinase complex, class III, type I 1 PIK3C3
phosphatidylinositol 3-kinase complex, class III, type II 1 PIK3C3
Cell projection, stereocilium 1 RDX
Cell projection, microvillus 1 RDX
Cell projection, dendrite 1 MARK2
side of membrane 1 CD48
basal plasma membrane 1 ABCC3
secretory granule lumen 2 GHRL, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 3 AMELX, GHRL, INS
cortical actin cytoskeleton 1 RDX
platelet alpha granule lumen 1 EGF
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
endocytic vesicle 1 AMELX
transport vesicle 1 INS
Schmidt-Lanterman incisure 1 PTEN
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
presynaptic endosome 1 PIK3C3
cell tip 1 RDX
clathrin-coated endocytic vesicle membrane 1 EGF
Synapse, synaptosome 1 RPS6KB1
Basal cell membrane 1 ABCC3
external side of apical plasma membrane 1 ABCB1
Cytoplasmic vesicle, phagosome 1 MTOR
postsynaptic endosome 1 PIK3C3
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
Autolysosome 1 PIK3C3
myelin sheath adaxonal region 1 PTEN
[Isoform alpha]: Secreted 1 PTEN
stereocilium base 1 RDX
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA
microtubule bundle 1 MARK2
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Samantha S Eckley, Johanna M Buschhaus, Brock A Humphries, Tanner H Robison, Kathryn E Luker, Gary D Luker. Short-Term Environmental Conditioning Enhances Tumorigenic Potential of Triple-Negative Breast Cancer Cells. Tomography (Ann Arbor, Mich.). 2019 12; 5(4):346-357. doi: 10.18383/j.tom.2019.00019. [PMID: 31893233]
  • Didier Frappaz, Sara M Federico, Andrew D J Pearson, Lia Gore, Margaret E Macy, Steven G DuBois, Isabelle Aerts, Robert Iannone, Ryan Geschwindt, Arne Van Schanke, Rui Wang, Birgit Geoerger. Phase 1 study of dalotuzumab monotherapy and ridaforolimus-dalotuzumab combination therapy in paediatric patients with advanced solid tumours. European journal of cancer (Oxford, England : 1990). 2016 07; 62(?):9-17. doi: 10.1016/j.ejca.2016.03.084. [PMID: 27185573]
  • Matthew Zibelman, Yu-Ning Wong, Karthik Devarajan, Lois Malizzia, Alycia Corrigan, Anthony J Olszanski, Crystal S Denlinger, Susan K Roethke, Colleen H Tetzlaff, Elizabeth R Plimack. Phase I study of the mTOR inhibitor ridaforolimus and the HDAC inhibitor vorinostat in advanced renal cell carcinoma and other solid tumors. Investigational new drugs. 2015 Oct; 33(5):1040-7. doi: 10.1007/s10637-015-0261-3. [PMID: 26091915]
  • Rachel M Squillace, David Miller, Scott D Wardwell, Frank Wang, Tim Clackson, Victor M Rivera. Synergistic activity of the mTOR inhibitor ridaforolimus and the antiandrogen bicalutamide in prostate cancer models. International journal of oncology. 2012 Aug; 41(2):425-32. doi: 10.3892/ijo.2012.1487. [PMID: 22614157]
  • Laetitia Coutte, Chantal Dreyer, Marie-Paule Sablin, Sandrine Faivre, Eric Raymond. [PI3K-AKT-mTOR pathway and cancer]. Bulletin du cancer. 2012 Feb; 99(2):173-80. doi: 10.1684/bdc.2011.1384. [PMID: 21742593]
  • Antonella Perotti, Alberta Locatelli, Cristiana Sessa, Dagmar Hess, Lucia Viganò, Giuseppe Capri, Michela Maur, Thomas Cerny, Sara Cresta, Federico Rojo, Joan Albanell, Silvia Marsoni, Irene Corradino, Lori Berk, Victor M Rivera, Frank Haluska, Luca Gianni. Phase IB study of the mTOR inhibitor ridaforolimus with capecitabine. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2010 Oct; 28(30):4554-61. doi: 10.1200/jco.2009.27.5867. [PMID: 20855840]
  • C Sessa, D Tosi, L Viganò, J Albanell, D Hess, M Maur, S Cresta, A Locatelli, R Angst, F Rojo, N Coceani, V M Rivera, L Berk, F Haluska, L Gianni. Phase Ib study of weekly mammalian target of rapamycin inhibitor ridaforolimus (AP23573; MK-8669) with weekly paclitaxel. Annals of oncology : official journal of the European Society for Medical Oncology. 2010 Jun; 21(6):1315-1322. doi: 10.1093/annonc/mdp504. [PMID: 19901013]
  • Jesus Rodriguez-Pascual, Elaine Cheng, Pablo Maroto, Ignacio Duran. Emergent toxicities associated with the use of mTOR inhibitors in patients with advanced renal carcinoma. Anti-cancer drugs. 2010 Jun; 21(5):478-86. doi: 10.1097/cad.0b013e32833760bf. [PMID: 20401967]
  • C Dreyer, E Raymond, S Faivre. [Targeted therapies and their indications in solid neoplasias]. La Revue de medecine interne. 2009 May; 30(5):416-24. doi: 10.1016/j.revmed.2008.12.022. [PMID: 19299048]
  • Christine M Hartford, Apurva A Desai, Linda Janisch, Theodore Karrison, Victor M Rivera, Lori Berk, John W Loewy, Hedy Kindler, Walter M Stadler, Heather L Knowles, Camille Bedrosian, Mark J Ratain. A phase I trial to determine the safety, tolerability, and maximum tolerated dose of deforolimus in patients with advanced malignancies. Clinical cancer research : an official journal of the American Association for Cancer Research. 2009 Feb; 15(4):1428-34. doi: 10.1158/1078-0432.ccr-08-2076. [PMID: 19228743]
  • Gail M Wilkes. Drug essentials mTOR inhibitors. Oncology (Williston Park, N.Y.). 2008 Apr; 22(4 Suppl Nurse Ed):43-4. doi: NULL. [PMID: 19856563]