Omacetaxine_mepesuccinate (BioDeep_00000230419)

Main id: BioDeep_00000231164

 

PANOMIX_OTCML-2023 Chemicals and Drugs


代谢物信息卡片


(S)-1-((11bS,12S,14aR)-13-methoxy-2,3,5,6,11b,12-hexahydro-1H-[1,3]dioxolo[4,5:4,5]benzo[1,2-d]cyclopenta[b]pyrrolo[1,2-a]azepin-12-yl) 4-methyl 2-hydroxy-2-(4-hydroxy-4-methylpentyl)succinate

化学式: C29H39NO9 (545.2624684)
中文名称: 高三尖杉酯碱
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(C)(CCCC(CC(=O)OC)(C(=O)OC1C2C3=CC4=C(C=C3CCN5C2(CCC5)C=C1OC)OCO4)O)O
InChI: InChI=1S/C29H39NO9/c1-27(2,33)8-5-10-29(34,16-23(31)36-4)26(32)39-25-22(35-3)15-28-9-6-11-30(28)12-7-18-13-20-21(38-17-37-20)14-19(18)24(25)28/h13-15,24-25,33-34H,5-12,16-17H2,1-4H3/t24-,25-,28+,29-/m1/s1

描述信息

Omacetaxine mepesuccinate is a cephalotaxine-derived alkaloid ester obtained from Cephalotaxus harringtonia; used for the treatment of chronic or accelerated phase chronic myeloid leukaemia. It has a role as an antineoplastic agent, a protein synthesis inhibitor, an apoptosis inducer and an anticoronaviral agent. It is an alkaloid ester, a tertiary alcohol, an organic heteropentacyclic compound and an enol ether. It is functionally related to a cephalotaxine.
Omacetaxine mepesuccinate (formerly known as HHT or Homoharringtonine), is a cephalotaxine ester and protein synthesis inhibitor with established clinical activity as a single agent in hematological malignancies. Omacetaxine mepesuccinate is synthesized from cephalotaxine, which is an extract from the leaves of the plant, Cephalotaxus species. In October 2005, omacetaxine mepesuccinate received Orphan Drug designation from the EMEA for the treatment of chronic myeloid leukemia (CML). Then in March 2006, it received Orphan Drug status from the FDA for the treatment of CML. In November 2006, omacetaxine mepesuccinate, for the treatment of CML, was granted Fast Track designation by the FDA. Most recently, in October 2012, omacetaxine mepesuccinate was marketed under the brand name Synribo and FDA approved for patients who are intolerant and/or resistant to two or more tyrosine kinase inhibitors used to treat accelerated or chronic phase CML.
Omacetaxine mepesuccinate is a natural product found in Cephalotaxus harringtonia and Cephalotaxus fortunei with data available.
Omacetaxine Mepesuccinate is a semisynthetic formulation of the cytotoxic plant alkaloid homoharringtonine isolated from the evergreen tree Cephalotaxus with potential antineoplastic activity. Omacetaxine binds to the 80S ribosome in eukaryotic cells and inhibits protein synthesis by interfering with chain elongation. This agent also induces differentiation and apoptosis in some cancer cell types.
Semisynthetic derivative of harringtonine that acts as a protein synthesis inhibitor and induces APOPTOSIS in tumor cells. It is used in the treatment of MYELOID LEUKEMIA, CHRONIC.
See also: Omacetaxine (has active moiety).
A cephalotaxine-derived alkaloid ester obtained from Cephalotaxus harringtonia; used for the treatment of chronic or accelerated phase chronic myeloid leukaemia.
D000970 - Antineoplastic Agents > D000972 - Antineoplastic Agents, Phytogenic > D006248 - Harringtonines
C274 - Antineoplastic Agent > C2122 - Cell Differentiating Agent > C1934 - Differentiation Inducer
L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents
D004791 - Enzyme Inhibitors > D011500 - Protein Synthesis Inhibitors
C274 - Antineoplastic Agent > C1931 - Antineoplastic Plant Product
C1907 - Drug, Natural Product
Homoharringtonine (Omacetaxine mepesuccinate;HHT) is a cytotoxic alkaloid with antitumor properties which acts by inhibiting translation elongation.
Homoharringtonine (Omacetaxine mepesuccinate;HHT) is a cytotoxic alkaloid with antitumor properties which acts by inhibiting translation elongation.

同义名列表

50 个代谢物同义名

(S)-1-((11bS,12S,14aR)-13-methoxy-2,3,5,6,11b,12-hexahydro-1H-[1,3]dioxolo[4,5:4,5]benzo[1,2-d]cyclopenta[b]pyrrolo[1,2-a]azepin-12-yl) 4-methyl 2-hydroxy-2-(4-hydroxy-4-methylpentyl)succinate; 1-((1S,3aR,14bS)-2-Methoxy-1,5,6,8,9,14b-hexahydro-4H- cyclopenta(a)(1,3)dioxolo(4,5-h)pyrrolo(2,1-b)(3)benzazepin-1-yl) 4-methyl (2R)-2- hydroxy-2-(4-hydroxy-4-methylpentyl)butanedioate; 1-O-[(2S,3S,6R)-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-3-yl] 4-O-methyl (2R)-2-hydroxy-2-(4-hydroxy-4-methylpentyl)butanedioate; 1-((1S,3AR,14BS)-2-METHOXY-1,5,6,8,9,14B-HEXAHYDRO-4H-CYCLOPENTA(A)(1,3)DIOXOLO(4,5-H)PYRROLO(2,1-B)(3)BENZAZEPIN-1-YL) 4-METHYL (2R)-2-HYDROXY-2-(4-HYDROXY-4-METHYLPENTYL)BUTANEDIOATE; 1-[(1S,3aR,14bS)-2-Methoxy-1,5,6,8,9,14b-hexahydro-4H-cyclopenta[a][1,3]dioxolo[4,5-H]pyrrolo[2,1-b][3]benzazepin-1-yl] 4-methyl (2R)-2-hydroxy-2-(4-hydroxy-4-methylpentyl)butanedioate; (2S,3S,6R)-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.0^{2,6}.0^{6,10}.0^{15,19}]icosa-1(13),4,14,19-tetraen-3-yl 1-methyl (3R)-3-hydroxy-3-(4-hydroxy-4-methylpentyl)butanedioate; Cephalotaxine, 4-methyl (2R)-2-hydroxy-2-(4-hydroxy-4-methylpentyl)butanedioate (ester); Cephalotaxine 4-Methyl (2R)-2-Hydroxy-2-(4-hydroxy-4-methylpentyl)butanedioate (Ester); Cephalotaxine, O3-((2R)-2,6-dihydroxy-2-(2-methoxy-2-oxoethyl)-6-methyl-1-oxoheptyl)-; Cephalotaxine, 4-methyl-, 2-hydroxy-2-(4-hydroxy-4-methylpentyl)butanedioate (ester); Cephalotaxine, 3-[4-methyl (2R)-2-hydroxy-2-(4-hydroxy-4-methylpentyl)butanedioate]; Cephalotaxine 4-methyl (2R)-2-hydroxy-2-(4-hydroxy-4-methylpentyl)butanedioate; OMACETAXINE MEPESUCCINATE [ORANGE BOOK]; Omacetaxine mepesuccinate [USAN:INN]; (2R,3S,4S,5R)-(-)-homoharringtonine; OMACETAXINE MEPESUCCINATE [WHO-DD]; OMACETAXINE MEPESUCCINATE (MART.); OMACETAXINE MEPESUCCINATE [MART.]; OMACETAXINE MEPESUCCINATE [VANDF]; Omacetaxine mepesuccinate (USAN); Omacetaxine mepesuccinate [USAN]; Homoharringtonine, >=98\\% (HPLC); OMACETAXINE MEPESUCCINATE [INN]; Homoharringtonine (3(R))-isomer; Omacetaxine (homoharringtonine); Omacetaxine mepesuccinate;HHT; mepesuccinato de omacetaxina; HYFHYPWGAURHIV-JFIAXGOJSA-N; mepesuccinate domacetaxine; omacetaxine mepesuccinate; omacetaxini mepesuccinas; HOMOHARRINGTONINE [MI]; (-)-homoharringtonine; homoharringtonine; Homoharringtonin; UNII-6FG8041S5B; Cephalotaxine; Synribo (TN); NCI60_000917; Omacetaxine; 6FG8041S5B; Ceflatonin; Myelostat; C29H39NO9; Synribo; Tekinex; L01XX40; Omapro; ZJ-C; HHT



数据库引用编号

13 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)

3 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

  • Yuya Yoshida, Kohei Fukuoka, Miyu Sakugawa, Masayuki Kurogi, Kengo Hamamura, Keika Hamasaki, Fumiaki Tsurusaki, Kurumi Sotono, Takumi Nishi, Taiki Fukuda, Taisei Kumamoto, Kosuke Oyama, Takashi Ogino, Akito Tsuruta, Kouta Mayanagi, Tomohiro Yamashita, Hiroyuki Fuchino, Nobuo Kawahara, Kayo Yoshimatsu, Hitomi Kawakami, Satoru Koyanagi, Naoya Matsunaga, Shigehiro Ohdo. Inhibition of G protein-coupled receptor 68 using homoharringtonine attenuates chronic kidney disease-associated cardiac impairment. Translational research : the journal of laboratory and clinical medicine. 2024 Jul; 269(?):31-46. doi: 10.1016/j.trsl.2024.02.004. [PMID: 38401836]
  • Somanjana Khatua, Sudeshna Nandi, Anish Nag, Surjit Sen, Nilanjan Chakraborty, Arghya Naskar, Eda Sönmez Gürer, Daniela Calina, Krishnendu Acharya, Javad Sharifi-Rad. Homoharringtonine: updated insights into its efficacy in hematological malignancies, diverse cancers and other biomedical applications. European journal of medical research. 2024 May; 29(1):269. doi: 10.1186/s40001-024-01856-x. [PMID: 38704602]
  • Xue Zhang, Chen Mei, Zhixuan Liang, Yan Zhi, Haojun Xu, Hongjun Wang, Hong Dong. Homoharringtonine induces apoptosis of mammary carcinoma cells by inhibiting the AKT/mTOR signaling pathway. Veterinary and comparative oncology. 2024 Mar; 22(1):57-69. doi: 10.1111/vco.12948. [PMID: 38081660]
  • Francesco Pietra. Do Naturally Modified Nucleotides Contribute to Stabilizing Complexes between Ribosomes and Small Molecules? A Case Study with the Antitumor Drug Homoharringtonine. ChemMedChem. 2023 10; 18(20):e202300095. doi: 10.1002/cmdc.202300095. [PMID: 37548261]
  • Chiao-Hui Hsieh, Chen-Tsung Huang, Yi-Sheng Cheng, Chun-Hua Hsu, Wen-Ming Hsu, Yun-Hsien Chung, Yen-Lin Liu, Tsai-Shan Yang, Chia-Yu Chien, Yu-Hsuan Lee, Hsuan-Cheng Huang, Hsueh-Fen Juan. Homoharringtonine as a PHGDH inhibitor: Unraveling metabolic dependencies and developing a potent therapeutic strategy for high-risk neuroblastoma. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2023 Oct; 166(?):115429. doi: 10.1016/j.biopha.2023.115429. [PMID: 37673018]
  • Chiachen Chen, Jiande Wu, Chindo Hicks, Michael S Lan. Repurposing a plant alkaloid homoharringtonine targets insulinoma associated-1 in N-Myc-activated neuroblastoma. Cellular signalling. 2023 Jun; 109(?):110753. doi: 10.1016/j.cellsig.2023.110753. [PMID: 37301315]
  • Qi Liu, Lijun Luo, Xiaofeng Gao, Di Zhang, Xinqian Feng, Peng Yang, Hui Li, Shengjun Mao. Co-Delivery of Daunorubicin and Homoharringtonine in Folic Acid Modified-Liposomes for Enhancing Therapeutic Effect on Acute Myeloid Leukemia. Journal of pharmaceutical sciences. 2023 01; 112(1):123-131. doi: 10.1016/j.xphs.2022.04.014. [PMID: 35469834]
  • Yujian Yang, Qiuchun Yu, Lean Hu, Botao Dai, Ruxi Qi, Yu Chang, Qingwen Zhang, Zhang Zhang, Yingjun Li, Xumu Zhang. Enantioselective semisynthesis of novel cephalotaxine esters with potent antineoplastic activities against leukemia. European journal of medicinal chemistry. 2022 Dec; 244(?):114731. doi: 10.1016/j.ejmech.2022.114731. [PMID: 36242991]
  • Chun-Xue Zhao, Hui Liu, Xin Zhang, Meng-Yue Yang, Yue-Tong Wang, Yi-Jia Xing, Jun-Xin Hua, Qin Zhang, Da-Hong Li, Jiao Bai, Yong-Kui Jing, Hui-Ming Hua. Cephalotaxine-type and homoerythrina-type alkaloids with antiproliferative effects from Cephalotaxus fortunei. Organic & biomolecular chemistry. 2022 09; 20(35):7076-7084. doi: 10.1039/d2ob01242a. [PMID: 36004441]
  • Guang-Xing Yu, Yang Yu, Jing-Wu, Ling-Hui Zeng, Johann Schinnerl, Xiang-Hai Cai. Cephalotaxine homologous alkaloids from seeds of Cephalotaxus oliveri Mast. Phytochemistry. 2022 Aug; 200(?):113220. doi: 10.1016/j.phytochem.2022.113220. [PMID: 35513135]
  • Bei Zhang, Zhixin Pei, Hongxia Wang, Huimin Wu, Junjie Wang, Junjun Bai, Qinglin Song. Chidamide and Decitabine in Combination with a HAG Priming Regimen for Acute Myeloid Leukemia with TP53 Mutation. Acta medica Okayama. 2022 Feb; 76(1):63-70. doi: 10.18926/amo/63213. [PMID: 35237000]
  • Hong-Yuan Liu, Tian-Xiu Dong, Zi-Zhuo Li, Tian-Tian Li, Jian Jiang, Ming-Wei Zhu, Ting-Ting An, Yao-Dong Chen, Xiu-Hua Yang. Homoharringtonine inhibits the progression of hepatocellular carcinoma by suppressing the PI3K/AKT/GSK3β/Slug signaling pathway. Neoplasma. 2021 Sep; 68(5):924-937. doi: 10.4149/neo_2021_210113n57. [PMID: 33998239]
  • Yu Zhang, Jingjing Xiang, Ni Zhu, Hangping Ge, Xianfu Sheng, Shu Deng, Junfa Chen, Lihong Yu, Yan Zhou, Jianping Shen. Curcumin in combination with homoharringtonine suppresses lymphoma cell growth by inhibiting the TGF-β/Smad3 signaling pathway. Aging. 2021 07; 13(14):18757-18768. doi: 10.18632/aging.203319. [PMID: 34324434]
  • Yanwen Chen, Travis B Lear, John W Evankovich, Mads B Larsen, Bo Lin, Irene Alfaras, Jason R Kennerdell, Laura Salminen, Daniel P Camarco, Karina C Lockwood, Ferhan Tuncer, Jie Liu, Michael M Myerburg, John F McDyer, Yuan Liu, Toren Finkel, Bill B Chen. A high-throughput screen for TMPRSS2 expression identifies FDA-approved compounds that can limit SARS-CoV-2 entry. Nature communications. 2021 06; 12(1):3907. doi: 10.1038/s41467-021-24156-y. [PMID: 34162861]
  • Xuke Zhang, Ziteng Song, Ying Li, Huimei Wang, Shaojie Zhang, Anna-Mari Reid, Namrita Lall, Jie Zhang, Chunyan Wang, Dongho Lee, Yasushi Ohizumi, Jing Xu, Yuanqiang Guo. Cytotoxic and Antiangiogenetic Xanthones Inhibiting Tumor Proliferation and Metastasis from Garcinia xipshuanbannaensis. Journal of natural products. 2021 05; 84(5):1515-1523. doi: 10.1021/acs.jnatprod.0c01354. [PMID: 33905250]
  • Sayed S Sohrab, Mohd Suhail, Mohammad A Kamal, Esam I Azhar. Natural Products Homoharringtonine and Emetine Alkaloids as SARS-CoV-2 Treatment Options. Current pharmaceutical design. 2021; 27(32):3444-3453. doi: 10.2174/1381612826666201210121858. [PMID: 33302852]
  • Guang-Lei Ma, Nan Guo, Xi-Ling Wang, Junmin Li, Ze-Xin Jin, Yuqiao Han, Su-Zhen Dong, Juan Xiong, Jin-Feng Hu. Cytotoxic secondary metabolites from the vulnerable conifer Cephalotaxus oliveri and its associated endophytic fungus Alternaria alternate Y-4-2. Bioorganic chemistry. 2020 12; 105(?):104445. doi: 10.1016/j.bioorg.2020.104445. [PMID: 33197848]
  • Qiu-Jin Yang, Jie Zheng, Fu-Tao Dang, Yue-Meng Wan, Jing Yang. Acute pancreatitis induced by combination chemotherapy used for the treatment of acute myeloid leukemia: A case report. Medicine. 2020 Aug; 99(35):e21848. doi: 10.1097/md.0000000000021848. [PMID: 32871908]
  • Dario Cattaneo, Dario Cattaneo, Cristina Gervasoni, Mario Corbellino, Massimo Galli, Agostino Riva, Cristina Gervasoni, Emilio Clementi, Emilio Clementi. Does lopinavir really inhibit SARS-CoV-2?. Pharmacological research. 2020 08; 158(?):104898. doi: 10.1016/j.phrs.2020.104898. [PMID: 32438034]
  • Aleksandr Ianevski, Rouan Yao, Mona Høysæter Fenstad, Svetlana Biza, Eva Zusinaite, Tuuli Reisberg, Hilde Lysvand, Kirsti Løseth, Veslemøy Malm Landsem, Janne Fossum Malmring, Valentyn Oksenych, Sten Even Erlandsen, Per Arne Aas, Lars Hagen, Caroline H Pettersen, Tanel Tenson, Jan Egil Afset, Svein Arne Nordbø, Magnar Bjørås, Denis E Kainov. Potential Antiviral Options against SARS-CoV-2 Infection. Viruses. 2020 06; 12(6):. doi: 10.3390/v12060642. [PMID: 32545799]
  • Ka-Tim Choy, Alvina Yin-Lam Wong, Prathanporn Kaewpreedee, Sin Fun Sia, Dongdong Chen, Kenrie Pui Yan Hui, Daniel Ka Wing Chu, Michael Chi Wai Chan, Peter Pak-Hang Cheung, Xuhui Huang, Malik Peiris, Hui-Ling Yen. Remdesivir, lopinavir, emetine, and homoharringtonine inhibit SARS-CoV-2 replication in vitro. Antiviral research. 2020 06; 178(?):104786. doi: 10.1016/j.antiviral.2020.104786. [PMID: 32251767]
  • Zhanxia Zhang, Wei Cheng, Yongfu Pan, Lijun Jia. An anticancer agent-loaded PLGA nanomedicine with glutathione-response and targeted delivery for the treatment of lung cancer. Journal of materials chemistry. B. 2020 01; 8(4):655-665. doi: 10.1039/c9tb02284h. [PMID: 31904073]
  • Feng Liu, Jun Ma, Zhaoyu Shi, Qi Zhang, Huimei Wang, Dihua Li, Zhaohui Song, Chunyan Wang, Jin Jin, Jing Xu, Muhetaer Tuerhong, Munira Abudukeremu, Ling Shuai, Dongho Lee, Yuanqiang Guo. Clerodane Diterpenoids Isolated from the Leaves of Casearia graveolens. Journal of natural products. 2020 01; 83(1):36-44. doi: 10.1021/acs.jnatprod.9b00515. [PMID: 31916761]
  • Ioanna A Anastasiou, Ioanna Eleftheriadou, Anastasios Tentolouris, Dimitrios Tsilingiris, Nikolaos Tentolouris. In Vitro Data of Current Therapies for SARS-CoV-2. Current medicinal chemistry. 2020; 27(27):4542-4548. doi: 10.2174/0929867327666200513075430. [PMID: 32400323]
  • Chenying Li, Lei Dong, Rui Su, Ying Bi, Ying Qing, Xiaolan Deng, Yile Zhou, Chao Hu, Mengxia Yu, Hao Huang, Xi Jiang, Xia Li, Xiao He, Dongling Zou, Chao Shen, Li Han, Miao Sun, Jennifer Skibbe, Kyle Ferchen, Xi Qin, Hengyou Weng, Huilin Huang, Chunxiao Song, Jianjun Chen, Jie Jin. Homoharringtonine exhibits potent anti-tumor effect and modulates DNA epigenome in acute myeloid leukemia by targeting SP1/TET1/5hmC. Haematologica. 2020 01; 105(1):148-160. doi: 10.3324/haematol.2018.208835. [PMID: 30975912]
  • Yanyu Zhang, Ning Huang, Jie Xu, Wei Zheng, Xing Cui. Homoharringtonine Exerts an Antimyeloma Effect by Promoting Excess Parkin-Dependent Mitophagy. Drug design, development and therapy. 2020; 14(?):4749-4763. doi: 10.2147/dddt.s279054. [PMID: 33177810]
  • Ke Li, Feng Wang, Zhao-Na Yang, Bing Cui, Ping-Ping Li, Zhen-Yu Li, Zhuo-Wei Hu, Hong-Hu Zhu. PML-RARα interaction with TRIB3 impedes PPARγ/RXR function and triggers dyslipidemia in acute promyelocytic leukemia. Theranostics. 2020; 10(22):10326-10340. doi: 10.7150/thno.45924. [PMID: 32929351]
  • Petter I Andersen, Klara Krpina, Aleksandr Ianevski, Nastassia Shtaida, Eunji Jo, Jaewon Yang, Sandra Koit, Tanel Tenson, Veijo Hukkanen, Marit W Anthonsen, Magnar Bjoras, Magnus Evander, Marc P Windisch, Eva Zusinaite, Denis E Kainov. Novel Antiviral Activities of Obatoclax, Emetine, Niclosamide, Brequinar, and Homoharringtonine. Viruses. 2019 10; 11(10):. doi: 10.3390/v11100964. [PMID: 31635418]
  • Shujuan Huang, Jiajia Pan, Jing Jin, Chengying Li, Xia Li, Jiansong Huang, Xin Huang, Xiao Yan, Fengling Li, Mengxia Yu, Chao Hu, Jingrui Jin, Yu Xu, Qing Ling, Wenle Ye, Yungui Wang, Jie Jin. Abivertinib, a novel BTK inhibitor: Anti-Leukemia effects and synergistic efficacy with homoharringtonine in acute myeloid leukemia. Cancer letters. 2019 Oct; 461(?):132-143. doi: 10.1016/j.canlet.2019.07.008. [PMID: 31310800]
  • Mei-Jiao Gong, Shi-Fang Li, Yin-Li Xie, Fu-Rong Zhao, Jun-Jun Shao, Yong-Guang Zhang, Wen-Hui Wang, Hui-Yun Chang. Inhibitory effects of homoharringtonine on foot and mouth disease virus in vitro. Journal of medical virology. 2019 09; 91(9):1595-1601. doi: 10.1002/jmv.25494. [PMID: 31032977]
  • Xiaoxiao Chen, Yanjing Tang, Jing Chen, Ru Chen, Longjun Gu, Huiliang Xue, Ci Pan, Jingyan Tang, Shuhong Shen. Homoharringtonine is a safe and effective substitute for anthracyclines in children younger than 2 years old with acute myeloid leukemia. Frontiers of medicine. 2019 Jun; 13(3):378-387. doi: 10.1007/s11684-018-0658-4. [PMID: 30635781]
  • Jung-Eun Kim, Yoon-Jae Song. Anti-varicella-zoster virus activity of cephalotaxine esters in vitro. Journal of microbiology (Seoul, Korea). 2019 Jan; 57(1):74-79. doi: 10.1007/s12275-019-8514-z. [PMID: 30456755]
  • Seiichi Sakamoto, Tomofumi Miyamoto, Kazuteru Usui, Hiroyuki Tanaka, Satoshi Morimoto. Sodium-Periodate-Mediated Harringtonine Derivatives and Their Antiproliferative Activity against HL-60 Acute Leukemia Cells. Journal of natural products. 2018 01; 81(1):34-40. doi: 10.1021/acs.jnatprod.7b00541. [PMID: 29286665]
  • Dong Liu, Jing Xing, Fei Xiong, Fang Yang, Ning Gu. Preparation and in vivo safety evaluations of antileukemic homoharringtonine-loaded PEGylated liposomes. Drug development and industrial pharmacy. 2017 Apr; 43(4):652-660. doi: 10.1080/03639045.2016.1275670. [PMID: 28005445]
  • Gayoung Park, Sun Yeou Kim, Yoon-Jae Song. Ester alkaloids from Cephalotaxus interfere with the 2'3'-cGAMP-induced type I interferon pathway in vitro. PloS one. 2017; 12(8):e0182701. doi: 10.1371/journal.pone.0182701. [PMID: 28771599]
  • Sonja Krstin, Tamer Mohamed, Xiaojuan Wang, Michael Wink. How do the alkaloids emetine and homoharringtonine kill trypanosomes? An insight into their molecular modes of action. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2016 Dec; 23(14):1771-1777. doi: 10.1016/j.phymed.2016.10.008. [PMID: 27912879]
  • Cynthia M Nijenhuis, Luc Lucas, Hilde Rosing, Philmore Robertson, Edward T Hellriegel, Jan H M Schellens, And Jos H Beijnen. Metabolite profiling of 14C-omacetaxine mepesuccinate in plasma and excreta of cancer patients. Xenobiotica; the fate of foreign compounds in biological systems. 2016 Dec; 46(12):1122-1132. doi: 10.3109/00498254.2016.1152418. [PMID: 26998885]
  • Cynthia M Nijenhuis, Edward Hellriegel, Jos H Beijnen, Diane Hershock, Alwin D R Huitema, Luc Lucas, Marja Mergui-Roelvink, Mihaela Munteanu, Laura Rabinovich-Guilatt, Philmore Robertson, Hilde Rosing, Ofer Spiegelstein, Jan H M Schellens. Pharmacokinetics and excretion of (14)C-omacetaxine in patients with advanced solid tumors. Investigational new drugs. 2016 10; 34(5):565-74. doi: 10.1007/s10637-016-0360-9. [PMID: 27221729]
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