10-HCPT (BioDeep_00000000240)

 

Secondary id: BioDeep_00000398762

PANOMIX_OTCML-2023


代谢物信息卡片


(19S)-19-ethyl-7,19-dihydroxy-17-oxa-3,13-diazapentacyclo[11.8.0.0^{2,11}.0^{4,9}.0^{15,20}]henicosa-1(21),2(11),3,5,7,9,15(20)-heptaene-14,18-dione

化学式: C20H16N2O5 (364.1059)
中文名称: 10-羟基喜树碱, 羟基喜树碱, (S)-10-羟基喜树碱
谱图信息: 最多检出来源 Viridiplantae(otcml) 22.26%

分子结构信息

SMILES: CCC1(C2=C(COC1=O)C(=O)N3CC4=C(C3=C2)N=C5C=CC(=CC5=C4)O)O
InChI: InChI=1S/C20H16N2O5/c1-2-20(26)14-7-16-17-11(5-10-6-12(23)3-4-15(10)21-17)8-22(16)18(24)13(14)9-27-19(20)25/h3-7,23,26H,2,8-9H2,1H3/t20-/m0/s1

描述信息

10-Hydroxycamptothecin is a pyranoindolizinoquinoline.
10-hydroxycamptothecin is under investigation in clinical trial NCT00956787 (Study of AR-67 (DB-67) in Myelodysplastic Syndrome (MDS)).
10-Hydroxycamptothecin is a natural product found in Nothapodytes nimmoniana, Camptotheca acuminata, and Fusarium solani with data available.
D000970 - Antineoplastic Agents
(S)-10-Hydroxycamptothecin (10-HCPT;10-Hydroxycamptothecin) is a DNA topoisomerase I inhibitor of isolated from the Chinese plant Camptotheca accuminata. (S)-10-Hydroxycamptothecin exhibits a remarkable apoptosis-inducing effect. (S)-10-Hydroxycamptothecin has the potential for hepatoma, gastric carcinoma, colon cancer and leukaemia treatment[1][2][3][4].
(S)-10-Hydroxycamptothecin (10-HCPT;10-Hydroxycamptothecin) is a DNA topoisomerase I inhibitor of isolated from the Chinese plant Camptotheca accuminata. (S)-10-Hydroxycamptothecin exhibits a remarkable apoptosis-inducing effect. (S)-10-Hydroxycamptothecin has the potential for hepatoma, gastric carcinoma, colon cancer and leukaemia treatment[1][2][3][4].

同义名列表

51 个代谢物同义名

(19S)-19-ethyl-7,19-dihydroxy-17-oxa-3,13-diazapentacyclo[11.8.0.0^{2,11}.0^{4,9}.0^{15,20}]henicosa-1(21),2(11),3,5,7,9,15(20)-heptaene-14,18-dione; (S)-4-Ethyl-4,9-dihydroxy-1H-pyrano[3 inverted exclamation mark ,4 inverted exclamation mark :6,7]indolizino[1,2-b]quinoline-3,14-(4H,12H)-dione; (19S)-19-ethyl-7,19-dihydroxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2(11),3,5,7,9,15(20)-heptaene-14,18-dione; (S)-10-Hydroxycamptothecin;-;(+/-)-4-ethyl-4,9-dihydroxy-1h-pyrano[3,4:6,7]indolizino[1,2-b]quinoline-3,14(4h,12h)-dione; (S)-4-Ethyl-4,9-dihydroxy-1H-pyrano[3,4:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione ((S)-10-Hydroxycamptothecin); 4-Ethyl-4,9-dihydroxy-1,12-dihydro-4H-2-oxa-6,12a-diaza-dibenzo[b,h]fluorene-3,13-dione (10-hydroxycamptothecin); 1H-Pyrano(3,4:6,7)indolizino(1,2-b)quinoline-3,14(4H,12H)-dione, 4-ethyl-4,9-dihydroxy-, hydrate, (S)-; (S)-4-ethyl-4,9-dihydroxy-1,12-dihydro-14H-pyrano[3,4:6,7]indolizino[1,2-b]quinoline-3,14(4H)-dione; 1H-PYRANO(3,4:6,7)INDOLIZINO(1,2-B)QUINOLINE-3,14(4H,12H)-DIONE, 4-ETHYL-4,9-DIHYDROXY-, (4S)-; (20S)-4-Ethyl-4,9-dihydroxy-1,12-dihydro-4H-2-oxa-6,12a-diaza-dibenzo[b,h]fluorene-3,13-dione; 1H-Pyrano(3,4:6,7)indolizino(1,2-b)quinoline-3,14(4H,12H)-dione-,4-ethyl-4,9-dihydroxy-, (S)-; (4S)-4-Ethyl-4,9-dihydroxy-1H-pyrano[3,4:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione; (S)-4-Ethyl-4,9-dihydroxy-1H-pyrano[3,4:6,7]indolizino[1,2-b]quinoline-3,14-(4H,12H)-dione; (S)-4-Ethyl-4,9-dihydroxy-1H-pyrano[3,4:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione; 1H-Pyrano[3,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione-,4-ethyl-4,9-dihydroxy-, (S)-; 4-Ethyl-4,10-dihydroxy-1,12-dihydro-4H-2-oxa-6,12a-diaza-dibenzo[b,h]fluorene-3,13-dione; 4-Ethyl-4,9-dihydroxy-1,12-dihydro-4H-2-oxa-6,12a-diaza-dibenzo[b,h]fluorene-3,13-dione; (S)-10-Hydroxycamptothecin hydrate; 10-HYDROXYCAMPTOTHECIN [WHO-DD]; (+)-(S)-10-HYDROXYCAMPTOTHECIN; HAWSQZCWOQZXHI-FQEVSTJZSA-N; (+)-10-HYDROXYCAMPTOTHECIN; Camptothecine, 10-hydroxy-; (S)-10-Hydroxycamptothecin; Camptothecin, 10-hydroxy-; ethyl(dihydroxy)[?]dione; CAMPTOTHECIN, 10-HYDROXY; 10-hydroxycamptothecine; 10-Hydroxy camptothecin; 10-Hydroxy-Camptothecin; Camptothecin, hydroxy-; 10-Hydroxycamptothecin; Hydroxycamptothecine; Hydroxycamptothecin; Spectrum3_001621; Spectrum2_001660; Spectrum5_000549; Spectrum4_001815; UNII-9Z01632KRV; 10-Hydroxy-CPT; DivK1c_006859; KBio2_002119; NCI60_000173; KBio2_007255; KBio1_001803; KBio2_004687; KBio3_002501; 9Z01632KRV; 10-HCPT; 10-HYDROXYCAMTOTHECIN; 10-Hydroxycamptothecin



数据库引用编号

18 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)

6 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 15 ABCB1, AFP, ALB, ANXA5, BCL2, BCL2L1, BECN1, CASP3, CASP8, CASP9, CDKN1A, MAPK14, MAPK8, SGCB, VEGFA
Golgi apparatus, trans-Golgi network membrane 1 BECN1
Peripheral membrane protein 2 ANXA5, BECN1
Endosome membrane 1 BECN1
Endoplasmic reticulum membrane 2 BCL2, BECN1
Mitochondrion membrane 2 BCL2L1, BECN1
Cytoplasmic vesicle, autophagosome 1 BECN1
Nucleus 13 ALB, BCL2, BECN1, CASP3, CASP8, CASP9, CDKN1A, MAPK14, MAPK8, PARP1, PCNA, TOP1, VEGFA
autophagosome 1 BECN1
cytosol 12 ALB, ANXA5, BCL2, BCL2L1, BECN1, CASP3, CASP8, CASP9, CDKN1A, MAPK14, MAPK8, PARP1
dendrite 1 BECN1
mitochondrial membrane 1 BECN1
nuclear body 4 BECN1, CDKN1A, PARP1, PCNA
phagocytic vesicle 1 BECN1
phosphatidylinositol 3-kinase complex, class III 1 BECN1
trans-Golgi network 1 BECN1
centrosome 3 ALB, BCL2L1, PCNA
nucleoplasm 8 CASP3, CASP8, CDKN1A, MAPK14, MAPK8, PARP1, PCNA, TOP1
Cell membrane 2 ABCB1, ITGAM
Cytoplasmic side 1 BCL2L1
lamellipodium 1 CASP8
Multi-pass membrane protein 1 ABCB1
Synapse 1 MAPK8
cell surface 3 ABCB1, ITGAM, VEGFA
glutamatergic synapse 2 CASP3, MAPK14
Golgi apparatus 2 ALB, VEGFA
mitochondrial inner membrane 1 BCL2L1
neuronal cell body 1 CASP3
sarcolemma 2 ANXA5, SGCB
Cytoplasm, cytosol 2 BCL2L1, PARP1
endosome 1 BECN1
plasma membrane 3 ABCB1, ITGAM, SGCB
synaptic vesicle membrane 1 BCL2L1
Membrane 6 ABCB1, ANXA5, BCL2, ITGAM, PARP1, VEGFA
apical plasma membrane 1 ABCB1
axon 2 CCK, MAPK8
extracellular exosome 5 ABCB1, ALB, ANXA5, ITGAM, PCNA
endoplasmic reticulum 5 ALB, BCL2, BCL2L1, BECN1, VEGFA
extracellular space 5 AFP, ALB, CCK, ITGAM, VEGFA
perinuclear region of cytoplasm 1 CDKN1A
adherens junction 1 VEGFA
mitochondrion 6 BCL2, BCL2L1, CASP8, CASP9, MAPK14, PARP1
protein-containing complex 6 ALB, BCL2, CASP8, CASP9, CDKN1A, PARP1
postsynaptic density 1 CASP3
Single-pass type I membrane protein 1 ITGAM
Secreted 4 AFP, ALB, CCK, VEGFA
extracellular region 5 ALB, ANXA5, CCK, MAPK14, VEGFA
Mitochondrion outer membrane 2 BCL2, BCL2L1
Single-pass membrane protein 2 BCL2, BCL2L1
mitochondrial outer membrane 3 BCL2, BCL2L1, CASP8
Mitochondrion matrix 1 BCL2L1
mitochondrial matrix 1 BCL2L1
anchoring junction 1 ALB
transcription regulator complex 1 PARP1
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 BCL2L1
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 BCL2L1
Nucleus membrane 2 BCL2, BCL2L1
Bcl-2 family protein complex 2 BCL2, BCL2L1
nuclear membrane 2 BCL2, BCL2L1
external side of plasma membrane 2 ANXA5, ITGAM
Secreted, extracellular space, extracellular matrix 1 VEGFA
perikaryon 1 TOP1
nucleolus 3 CDKN1A, PARP1, TOP1
P-body 1 TOP1
Single-pass type II membrane protein 1 SGCB
Apical cell membrane 1 ABCB1
Cell membrane, sarcolemma 1 SGCB
Cell projection, lamellipodium 1 CASP8
Membrane raft 1 ITGAM
pore complex 1 BCL2
Cytoplasm, cytoskeleton 1 SGCB
focal adhesion 1 ANXA5
extracellular matrix 1 VEGFA
collagen-containing extracellular matrix 1 ANXA5
secretory granule 1 VEGFA
nuclear speck 1 MAPK14
Zymogen granule membrane 1 ANXA5
ciliary basal body 1 ALB
chromatin 2 PARP1, PCNA
Chromosome 2 PARP1, TOP1
cytoskeleton 2 CASP8, SGCB
centriole 1 ALB
Nucleus, nucleolus 2 PARP1, TOP1
spindle pole 2 ALB, MAPK14
nuclear replication fork 2 PARP1, PCNA
chromosome, telomeric region 2 PARP1, PCNA
blood microparticle 1 ALB
site of double-strand break 1 PARP1
fibrillar center 1 TOP1
nuclear envelope 1 PARP1
phagophore assembly site 1 BECN1
phosphatidylinositol 3-kinase complex, class III, type I 1 BECN1
phosphatidylinositol 3-kinase complex, class III, type II 1 BECN1
Nucleus, nucleoplasm 1 TOP1
specific granule membrane 1 ITGAM
tertiary granule membrane 1 ITGAM
cell body 1 CASP8
replication fork 1 PCNA
myelin sheath 1 BCL2
plasma membrane raft 1 ITGAM
ficolin-1-rich granule lumen 1 MAPK14
secretory granule lumen 1 MAPK14
endoplasmic reticulum lumen 2 AFP, ALB
male germ cell nucleus 2 PCNA, TOP1
platelet alpha granule lumen 2 ALB, VEGFA
apoptosome 1 CASP9
vesicle membrane 1 ANXA5
nuclear lamina 1 PCNA
protein-DNA complex 2 PARP1, TOP1
external side of apical plasma membrane 1 ABCB1
basal dendrite 1 MAPK8
CD95 death-inducing signaling complex 1 CASP8
death-inducing signaling complex 2 CASP3, CASP8
ripoptosome 1 CASP8
dystrophin-associated glycoprotein complex 1 SGCB
sarcoglycan complex 1 SGCB
site of DNA damage 1 PARP1
integrin complex 1 ITGAM
cyclin-dependent protein kinase holoenzyme complex 2 CDKN1A, PCNA
integrin alphaM-beta2 complex 1 ITGAM
endothelial microparticle 1 ANXA5
[Poly [ADP-ribose] polymerase 1, processed N-terminus]: Chromosome 1 PARP1
[Poly [ADP-ribose] polymerase 1, processed C-terminus]: Cytoplasm 1 PARP1
BAD-BCL-2 complex 1 BCL2
PCNA complex 1 PCNA
PCNA-p21 complex 2 CDKN1A, PCNA
replisome 1 PCNA
[N-VEGF]: Cytoplasm 1 VEGFA
[VEGFA]: Secreted 1 VEGFA
[Isoform L-VEGF189]: Endoplasmic reticulum 1 VEGFA
[Isoform VEGF121]: Secreted 1 VEGFA
[Isoform VEGF165]: Secreted 1 VEGFA
VEGF-A complex 1 VEGFA
cytoplasmic side of mitochondrial outer membrane 1 BECN1
ciliary transition fiber 1 ALB
caspase complex 1 CASP9
[Isoform Bcl-X(L)]: Mitochondrion inner membrane 1 BCL2L1
[Beclin-1-C 35 kDa]: Mitochondrion 1 BECN1
[Beclin-1-C 37 kDa]: Mitochondrion 1 BECN1


文献列表

  • Yukun Chen, Zhenzhi Wang, Xiaofan Wang, Mingliang Su, Fan Xu, Lian Yang, Lijun Jia, Zhanxia Zhang. Advances in Antitumor Nano-Drug Delivery Systems of 10-Hydroxycamptothecin. International journal of nanomedicine. 2022; 17(?):4227-4259. doi: 10.2147/ijn.s377149. [PMID: 36134205]
  • Yingjie Qi, Guangxuan Liu. Berberine-10-hydroxy camptothecine-loaded lipid microsphere for the synergistic treatment of liver cancer by inhibiting topoisomerase and HIF-1α. Drug delivery. 2021 Dec; 28(1):171-182. doi: 10.1080/10717544.2020.1870020. [PMID: 33427515]
  • Lingqiang Meng, Jianmin Dai, Shengzhong Rong, Hongmin Gao, Ze Zhang, Yingcong Zhang, Dong Chang, Hongzhi Pan. One-step electrodeposition preparation of polyaniline/f-MWCNTs as electrochemical sensors for detection of 10-hydroxycamptothecine. Biotechnology and applied biochemistry. 2021 Dec; 68(6):1192-1201. doi: 10.1002/bab.2041. [PMID: 32970340]
  • Yanni Sun, Ning Zhang, Cuiling Wang, Xiao Bai, Yahui Wei, Jianli Liu. The biosynthesis of camptothecin derivatives by Camptotheca acuminata seedlings. Natural product research. 2021 Jul; 35(14):2403-2407. doi: 10.1080/14786419.2019.1678616. [PMID: 31631694]
  • Shu Fan, Yong-Xiao Cao, Guang-Yan Li, Hao Lei, Mawusse K I Attiogbe, Jing-Chun Yao, Xue-Yan Yang, Yan-Jie Liu, Yuan-Yuan Hei, Hao Zhang, Lei Cao, Xiao-Yan Zhang, Shuai-Shuai Du, Gui-Min Zhang, San-Qi Zhang. F10, a new camptothecin derivative, was identified as a new orally-bioavailable, potent antitumor agent. European journal of medicinal chemistry. 2020 Sep; 202(?):112528. doi: 10.1016/j.ejmech.2020.112528. [PMID: 32650182]
  • Sixi Huang, Di Ren, Xinrong Wu, Ming Li, Xuesong Yu, Xiaoling Nie, Ying Wang, Yan Wang. Glycyrrhetinic Acid and TAT Peptide Modified Dual-functional Liposomes for Treatment of Hepatocellular Cancer. Current topics in medicinal chemistry. 2020; 20(27):2493-2505. doi: 10.2174/1568026620666200722110244. [PMID: 32703132]
  • Ting Zhou, Xin Tang, Wei Zhang, Jianfang Feng, Wei Wu. Preparation and in vitro and in vivo evaluations of 10-hydroxycamptothecin liposomes modified with stearyl glycyrrhetinate. Drug delivery. 2019 Dec; 26(1):673-679. doi: 10.1080/10717544.2019.1636422. [PMID: 31266376]
  • Wugang Zhang, Mulan Li, Wendi Du, Wuliang Yang, Guofeng Li, Chen Zhang, Xinli Liang, Haifang Chen. Tissue Distribution and Anti-Lung Cancer Effect of 10-Hydroxycamptothecin Combined with Platycodonis Radix and Glycyrrhizae Radix ET Rhizoma. Molecules (Basel, Switzerland). 2019 May; 24(11):. doi: 10.3390/molecules24112068. [PMID: 31151274]
  • Huai-Qiu Li, Wei-Liang Ye, Meng-Lei Huan, Ying Cheng, Dao-Zhou Liu, Han Cui, Miao Liu, Bang-le Zhang, Qi-Bing Mei, Si-Yuan Zhou. Mitochondria and nucleus delivery of active form of 10-hydroxycamptothecin with dual shell to precisely treat colorectal cancer. Nanomedicine (London, England). 2019 04; 14(8):1011-1032. doi: 10.2217/nnm-2018-0227. [PMID: 30925116]
  • Yifei Guo, Ting Wang, Hanhong Qiu, Meihua Han, Zhengqi Dong, Xiangtao Wang, Yanhong Wang. Hydroxycamptothecin nanoparticles based on poly/oligo (ethylene glycol): Architecture effects of nanocarriers on antitumor efficacy. European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V. 2019 Jan; 134(?):178-184. doi: 10.1016/j.ejpb.2018.12.003. [PMID: 30529294]
  • Yang Zhou, Tao Hong, Li Tong, Wei Liu, Xueting Yang, Jianghan Luo, Fuling Wang, Jian Li, Lijun Yan. Astragalus polysaccharide combined with 10-hydroxycamptothecin inhibits metastasis in non-small cell lung carcinoma cell lines via the MAP4K3/mTOR signaling pathway. International journal of molecular medicine. 2018 Dec; 42(6):3093-3104. doi: 10.3892/ijmm.2018.3868. [PMID: 30221690]
  • Yifei Guo, Ting Wang, Shuang Zhao, Hanhong Qiu, Meihua Han, Zhengqi Dong, Xiangtao Wang. Effect of alkyl chain on cellular uptake and antitumor activity of hydroxycamptothecin nanoparticles based on amphiphilic linear molecules. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences. 2018 Nov; 124(?):266-272. doi: 10.1016/j.ejps.2018.08.043. [PMID: 30189259]
  • Chun-Gu Wang, Wei-Na Yao, Bin Zhang, Jing Hua, Dong Liang, Heng-Shan Wang. Lung cancer and matrix metalloproteinases inhibitors of polyphenols from Selaginella tamariscina with suppression activity of migration. Bioorganic & medicinal chemistry letters. 2018 08; 28(14):2413-2417. doi: 10.1016/j.bmcl.2018.06.024. [PMID: 29921475]
  • Yifei Guo, Ting Wang, Shuang Zhao, Meihua Han, Zhengqi Dong, Xiangtao Wang, Yanhong Wang. Amphiphilic Hybrid Dendritic-Linear Molecules as Nanocarriers for Shape-Dependent Antitumor Drug Delivery. Molecular pharmaceutics. 2018 07; 15(7):2665-2673. doi: 10.1021/acs.molpharmaceut.8b00190. [PMID: 29782803]
  • Vonny Salim, A Daniel Jones, Dean DellaPenna. Camptotheca acuminata 10-hydroxycamptothecin O-methyltransferase: an alkaloid biosynthetic enzyme co-opted from flavonoid metabolism. The Plant journal : for cell and molecular biology. 2018 07; 95(1):112-125. doi: 10.1111/tpj.13936. [PMID: 29681057]
  • Haiyang Wu, Tongya Yu, Ye Tian, Yinjie Wang, Ruizhi Zhao, Shirui Mao. Enhanced liver-targeting via coadministration of 10-Hydroxycamptothecin polymeric micelles with vinegar baked Radix Bupleuri. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2018 May; 44(?):1-8. doi: 10.1016/j.phymed.2018.04.022. [PMID: 29895488]
  • Jian Zheng, Yong Ji, Changmin Shao, Lijia Jing, Yang Wang. Pharmacokinetics and tissue distribution study of 10-methoxycamptothecin in rats following intragastric administration. Journal of pharmaceutical and biomedical analysis. 2018 Feb; 149(?):564-571. doi: 10.1016/j.jpba.2017.11.062. [PMID: 29197298]
  • Xiaoshuang Ren, Lan Zhang, Yanning Zhang, Liangang Mao, Hongyun Jiang. Mitochondria response to camptothecin and hydroxycamptothecine-induced apoptosis in Spodoptera exigua cells. Pesticide biochemistry and physiology. 2017 Aug; 140(?):97-104. doi: 10.1016/j.pestbp.2017.07.003. [PMID: 28755702]
  • Minjie Sun, Jing Li, Cuiting Zhang, Ying Xie, Hongzhi Qiao, Zhigui Su, David Oupický, Qineng Ping. Arginine-Modified Nanostructured Lipid Carriers with Charge-Reversal and pH-Sensitive Membranolytic Properties for Anticancer Drug Delivery. Advanced healthcare materials. 2017 Apr; 6(8):. doi: 10.1002/adhm.201600693. [PMID: 28187243]
  • Yifei Guo, Yanna Zhao, Ting Wang, Ran Li, Meihua Han, Zhengqi Dong, Chunyan Zhu, Xiangtao Wang. Hydroxycamptothecin Nanorods Prepared by Fluorescently Labeled Oligoethylene Glycols (OEG) Codendrimer: Antitumor Efficacy in Vitro and in Vivo. Bioconjugate chemistry. 2017 02; 28(2):390-399. doi: 10.1021/acs.bioconjchem.6b00536. [PMID: 27982573]
  • Linjie Yang, Jingyi Hong, Jing Di, Yifei Guo, Meihua Han, Meifeng Liu, Xiangtao Wang. 10-Hydroxycamptothecin (HCPT) nanosuspensions stabilized by mPEG1000-HCPT conjugate: high stabilizing efficiency and improved antitumor efficacy. International journal of nanomedicine. 2017; 12(?):3681-3695. doi: 10.2147/ijn.s134005. [PMID: 28553107]
  • Zhen Liu, Hongfa Li, Yaya Fan, Yuanxue Liu, Shuli Man, Peng Yu, Wenyuan Gao. Combination treatment with Rhizoma Paridis and Rhizoma Curcuma longa extracts and 10-hydroxycamptothecin enhances the antitumor effect in H22 tumor model by increasing the plasma concentration. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2016 Oct; 83(?):627-634. doi: 10.1016/j.biopha.2016.07.026. [PMID: 27459119]
  • Chun Pan, Yan-Fen Hu, Juan Song, Hua-Shan Yi, La Wang, Yi-Ying Yang, Yong-Ping Wang, Man Zhang, Min-Hui Pan, Cheng Lu. Effects of 10-hydroxycamptothecin on intrinsic mitochondrial pathway in silkworm BmN-SWU1 cells. Pesticide biochemistry and physiology. 2016 Feb; 127(?):15-20. doi: 10.1016/j.pestbp.2015.09.001. [PMID: 26821653]
  • Min Liu, Didi Chen, Jean Felix Mukerabigwi, Sha Chen, Yuannian Zhang, Shaojun Lei, Shiying Luo, Zhili Wen, Yu Cao, Xueying Huang, Hongxuan He. Intracellular delivery of 10-hydroxycamptothecin with targeted nanostructured lipid carriers against multidrug resistance. Journal of drug targeting. 2016; 24(5):433-40. doi: 10.3109/1061186x.2015.1086358. [PMID: 26422582]
  • Yue Yuan, Jian Wen, Jie Tang, Qiming Kan, Rose Ackermann, Karl Olsen, Anna Schwendeman. Synthetic high-density lipoproteins for delivery of 10-hydroxycamptothecin. International journal of nanomedicine. 2016 ; 11(?):6229-6238. doi: 10.2147/ijn.s112835. [PMID: 27920529]
  • Xiaofeng Yang, Yingying Liu, Yanna Zhao, Meihua Han, Yifei Guo, Haixue Kuang, Xiangtao Wang. A stabilizer-free and organic solvent-free method to prepare 10-hydroxycamptothecin nanocrystals: in vitro and in vivo evaluation. International journal of nanomedicine. 2016; 11(?):2979-94. doi: 10.2147/ijn.s102726. [PMID: 27382284]
  • Yang Li, Jinyan Lin, Yu Huang, Yanxiu Li, Xiangrui Yang, Hongjie Wu, Shichao Wu, Liya Xie, Lizong Dai, Zhenqing Hou. Self-Targeted, Shape-Assisted, and Controlled-Release Self-Delivery Nanodrug for Synergistic Targeting/Anticancer Effect of Cytoplasm and Nucleus of Cancer Cells. ACS applied materials & interfaces. 2015 Nov; 7(46):25553-9. doi: 10.1021/acsami.5b07348. [PMID: 26529185]
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