Natural product sciences: an integrative approach to the innovations of plant natural products

The re-emergence of natural products for drug discovery in the genomics era

Harvey, A. L., Edrada‐Ebel, R., & Quinn, R. J. (2015) · Nature Reviews Drug Discovery · doi:10.1038/nrd4510 · Cited by 2,654

Coordinate Gene Activity in Response to Agents That Induce Systemic Acquired Resistance.

Ward, E. R., Uknes, S. J., Williams, S. C., Dincher, S. S., Wiederhold, D. L., Alexander, D. C., Goy, P. A., Métraux, J., & Ryals, J. A. (1991) · The Plant Cell · doi:10.1105/tpc.3.10.1085 · Cited by 1,274

Benzothiadiazole, a novel class of inducers of systemic acquired resistance, activates gene expression and disease resistance in wheat.

Görlach, J., Volrath, S., Knauf-Beiter, G., Hengy, G., Beckhove, U., Kogel, K.-H., Oostendorp, M., Staub, T. H., Ward, E., Keßmann, H., et al. (1996) · The Plant Cell · doi:10.1105/tpc.8.4.629 · Cited by 1,066

Diterpenoids from Isodon species and their biological activities

Sun, H., Huang, S., & Han, Q. (2006) · Natural Product Reports · doi:10.1039/b604174d · Cited by 552

Coordinate Gene Activity in Response to Agents That Induce Systemic Acquired Resistance

Ward, E. R., Uknes, S. J., Williams, S. C., Dincher, S. S., Wiederhold, D. L., Alexander, D. C., Goy, P. A., Métraux, J., & Ryals, J. A. (1991) · The Plant Cell · doi:10.2307/3869297 · Cited by 519

Meliaceous Limonoids: Chemistry and Biological Activities

Tan, Q., & Luo, X. (2011) · Chemical Reviews · doi:10.1021/cr9004023 · Cited by 487

Induced Disease Resistance in Plants by Chemicals

Oostendorp, M., Kunz, W., Dietrich, B., & Staub, T. (2001) · European Journal of Plant Pathology · doi:10.1023/a:1008760518772 · Cited by 469

Research Progress of Polycyclic Polyprenylated Acylphloroglucinols

Yang, X., Grossman, R. B., & Xu, G. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00551 · Cited by 377

Protein kinase C controls lysosome biogenesis independently of mTORC1

Li, Y., Xu, M., Ding, X., Chen, Y., Song, Z., Chen, L., Huang, X., Wang, X., Jian, Y., Tang, G., et al. (2016) · Nature Cell Biology · doi:10.1038/ncb3407 · Cited by 363

The saponins – polar isoprenoids with important and diverse biological activities

Osbourn, A., Goss, R. J. M., & Field, R. A. (2011) · Natural Product Reports · doi:10.1039/c1np00015b · Cited by 291

EWS-FLI-1 modulates miRNA145 and SOX2 expression to initiate mesenchymal stem cell reprogramming toward Ewing sarcoma cancer stem cellsPreprint

Riggi, N., Suvà, M.-L., Vito, C. D., Provero, P., Stehle, J., Baumer, K., Cironi, L., Janiszewska, M., Petricevic, T., Suvà, D., et al. (2010) · Genes & Development · doi:10.1101/gad.1899710 · Cited by 281

Diterpenoids from Isodon species: an update

Liu, M., Wang, W., Sun, H., & Pu, J. (2017) · Natural Product Reports · doi:10.1039/c7np00027h · Cited by 249

A small natural molecule promotes mitochondrial fusion through inhibition of the deubiquitinase USP30

Yue, W., Chen, Z., Liu, H., Chen, Y., Chen, M., Feng, D., Yan, C., Wu, H., Du, L., Wang, Y., et al. (2014) · Cell Research · doi:10.1038/cr.2014.20 · Cited by 218

X-Ray crystal structure of rocaglamide, a novel antileulemic 1H-cyclopenta[b]benzofuran from Aglaia elliptifolia

King, M., Chiang, C. M., Ling, H.-C., Fujita, E., Ochiai, M., & McPhail, A. T. (1982) · Journal of the Chemical Society Chemical Communications · doi:10.1039/c39820001150 · Cited by 187

Recent Progress in the Chemistry of Daphniphyllum Alkaloids

Chattopadhyay, A. K., & Hanessian, S. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00412 · Cited by 181

Three New Indole Alkaloids from Trigonostemon lii

Tan, C., Di, Y., Wang, Y., Zhang, Y., Si, Y., Zhang, Q., Gao, S., Hu, X., Fang, X., Li, S.-F., et al. (2010) · Organic Letters · doi:10.1021/ol100715x · Cited by 149

The Advances in the Limonoid Chemistry of the Meliaceae Family

Fang, X., T., D. Y., & J., H. X. (2011) · Current Organic Chemistry · doi:10.2174/138527211795378254 · Cited by 123

Anti-Tobacco Mosaic Virus (TMV) Quassinoids from Brucea javanica (L.) Merr.

Yan, X., Chen, J., Di, Y., Fang, X., Dong, J., Sang, P., Wang, Y., He, H. P., Zhang, Z., & Hao, X. (2010) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf903434h · Cited by 121

Lysosomes: Signaling Hubs for Metabolic Sensing and Longevity

Savini, M., Zhao, Q., & Wang, M. C. (2019) · Trends in Cell Biology · doi:10.1016/j.tcb.2019.08.008 · Cited by 116

Biosynthesis and biomimetic synthesis of alkaloids isolated from plants of the Nitraria and Myrioneuron genera: an unusual lysine-based metabolism

Gravel, E., & Poupon, E. (2009) · Natural Product Reports · doi:10.1039/b911866g · Cited by 111

Coordinate loss of a microRNA and protein-coding gene cooperate in the pathogenesis of 5q− syndrome

Kumar, M. S., Narla, A., Nonami, A., Mullally, A., Dimitrova, N., Ball, B. J., McAuley, J. R., Poveromo, L., Kutok, J. L., Galili, N., et al. (2011) · Blood · doi:10.1182/blood-2010-12-324715 · Cited by 111

Seco -pregnane steroids target the subgenomic RNA of alphavirus-like RNA viruses

Li, Y., Wang, L., Li, S., Chen, X., Shen, Y., Zhang, Z., He, H., Xu, W., Shu, Y., Liang, G., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0702398104 · Cited by 106

A diterpenoid derivative 15-oxospiramilactone inhibits Wnt/β-catenin signaling and colon cancer cell tumorigenesis

Wang, W., Liu, H., Wang, S., Hao, X., & Li, L. (2011) · Cell Research · doi:10.1038/cr.2011.30 · Cited by 103

The Limonoids and Their Antitobacco Mosaic Virus (TMV) Activities from Munronia unifoliolata Oliv.

Ge, Y., Liu, K.-X., Zhang, J.-X., Mu, S., & Hao, X. (2012) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf205362d · Cited by 102

Evolutionary Ecology of Multitrophic Interactions between Plants, Insect Herbivores and Entomopathogens

Shikano, I. (2017) · Journal of Chemical Ecology · doi:10.1007/s10886-017-0850-z · Cited by 96

The early stages of taxol biosynthesis: An interim report on the synthesis and identification of early pathway metabolites

Guerra-Bubb, J. M., Croteau, R., & Williams, R. M. (2012) · Natural Product Reports · doi:10.1039/c2np20021j · Cited by 94

Small-molecule modulation of Wnt signaling via modulating the Axin-LRP5/6 interaction

Wang, S., Yin, J., Chen, D., Nie, F., Song, X., Fei, C., Miao, H., Jing, C., Ma, W., Wang, L., et al. (2013) · Nature Chemical Biology · doi:10.1038/nchembio.1309 · Cited by 93

Benzylphenethylamine Alkaloids from Hosta plantaginea with Inhibitory Activity against Tobacco Mosaic Virus and Acetylcholinesterase

Wang, Y., Zhang, Z., Yang, F., Sun, Q., He, H., Di, Y., Mu, S., Lü, Y., Chang, Y., Zheng, Q., et al. (2007) · Journal of Natural Products · doi:10.1021/np0702077 · Cited by 89

Daphenylline, a New Alkaloid with an Unusual Skeleton, from Daphniphyllum longeracemosum

Zhang, Q., Di, Y., Li, C., Fang, X., Tan, C., Zhang, Z., Zhang, Y., He, H., Li, S., & Hao, X. (2009) · Organic Letters · doi:10.1021/ol9007958 · Cited by 81

3‐Acetonyl‐3‐hydroxyoxindole: a new inducer of systemic acquired resistance in plants

Li, Y., Zhang, Z., Jia, Y., Shen, Y., He, H., Fang, R., Chen, X., & Hao, X. (2008) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2008.00322.x · Cited by 81

Isolation and Asymmetric Total Synthesis of Perforanoid A

Lv, C., Yan, X., Tu, Q., Di, Y., Yuan, C., Fang, X., Ben‐David, Y., Xia, L., Gong, J., Shen, Y., et al. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201602783 · Cited by 78

Indole alkaloids from Ervatamia chinensis

Guo, L., He, H., Di, Y., Li, S.-F., Cheng, Y., Yang, W., Li, Y., Jian-ping, Y., Zhang, Y., & Hao, X. (2011) · Phytochemistry · doi:10.1016/j.phytochem.2011.11.002 · Cited by 74

Recently duplicated sesterterpene (C25) gene clusters in Arabidopsis thaliana modulate root microbiota

Chen, Q., Jiang, T., Liu, Y., Liu, H., Zhao, T., Liu, Z., Gan, X., Hallab, A., Wang, X., He, J., et al. (2019) · Science China Life Sciences · doi:10.1007/s11427-019-9521-2 · Cited by 74

Aphanamixoid A, a Potent Defensive Limonoid, with a New Carbon Skeleton from Aphanamixis polystachya

Cai, J., Zhang, Y., Luo, S., Chen, D., Tang, G., Yuan, C., Di, Y., Li, S., Hao, X., & He, H. (2012) · Organic Letters · doi:10.1021/ol3008149 · Cited by 68

Garmultins A–G, Biogenetically Related Polycyclic Acylphloroglucinols from Garcinia multiflora

Tian, D., Yi, P., Xia, L., Xiao, X., Fan, Y. M., Gu, W., Huang, L. J., Ben‐David, Y., Di, Y. T., Yuan, C. M., et al. (2016) · Organic Letters · doi:10.1021/acs.orglett.6b03004 · Cited by 63

Strynuxlines A and B, Alkaloids with an Unprecedented Carbon Skeleton from Strychnos nux-vomica

Fu, Y.-H., Zhang, Y., He, H., Hou, L., Di, Y., Li, S., Luo, X., & Hao, X. (2012) · Journal of Natural Products · doi:10.1021/np300339r · Cited by 60

Isolation, X-ray Crystallography, and Computational Studies of Calydaphninone, a New Alkaloid from Daphniphyllum calycillum

Di, Y., He, H., Wang, Y.-S., Li, L., Lü, Y., Gong, J.-B., Fang, X., Kong, N., Li, S., Zhu, H., et al. (2007) · Organic Letters · doi:10.1021/ol070218r · Cited by 60

Genome-wide analysis of BES1 genes in Gossypium revealed their evolutionary conserved roles in brassinosteroid signaling

Liu, Z., Qanmber, G., Lu, L., Qin, W., Liu, J., Li, J., Ma, S., Yang, Z., & Yang, Z. (2018) · Science China Life Sciences · doi:10.1007/s11427-018-9412-x · Cited by 60

Dihydroartemisinin regulates the immune system by promotion of CD8+ T lymphocytes and suppression of B cell responses

Zhang, T., Zhang, Y., Jiang, N., Xu, Z., Sang, X., Yang, N., Feng, Y., Chen, R., & Chen, Q. (2019) · Science China Life Sciences · doi:10.1007/s11427-019-9550-4 · Cited by 58

Turrapubesins A and B, First Examples of Halogenated and Maleimide-Bearing Limonoids in Nature from Turraea pubescens

Wang, X., Yin, S., Fan, C., Wang, F., Lin, L., Ding, J., & Yue, J. (2006) · Organic Letters · doi:10.1021/ol061466a · Cited by 57

Catharoseumine, a new monoterpenoid indole alkaloid possessing a peroxy bridge from Catharanthus roseus

Wang, L., He, H., Di, Y., Zhang, Y., & Hao, X. (2012) · Tetrahedron Letters · doi:10.1016/j.tetlet.2012.01.060 · Cited by 56

Cipadonoid A, a Novel Limonoid with an Unprecedented Skeleton, from Cipadessa cinerasecns

Fang, X., Di, Y., He, H., Liu, H., Zhang, Z., Ren, Y.-L., Gao, Z., Gao, S., & Hao, X. (2008) · Organic Letters · doi:10.1021/ol800415n · Cited by 54

Identification of diterpenoid compounds that interfere with Fli-1 DNA binding to suppress leukemogenesis

Liu, T., Xia, L., Yao, Y., Chen, Y., Fan, Y., Gajendran, B., Yang, J., Li, Y., Chen, J., Filmus, J., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1363-1 · Cited by 50

New phenanthrenes from Trigonostemon lii Y.T. Chang

Hu, X., Wang, Y., Kong, L., He, H., Gao, S., Liu, H., Ding, J., Xie, H., Di, Y., & Hao, X. (2009) · Tetrahedron Letters · doi:10.1016/j.tetlet.2009.03.186 · Cited by 48

Eudesmanolides from Wedelia trilobata (L.) Hitchc. as Potential Inducers of Plant Systemic Acquired Resistance

Li, Y., Hao, X., Li, S., He, H., Xiaohui, Y., Chen, Y., JiaHong, D., Zhang, Z., & 順林, 李. (2013) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf400390e · Cited by 47

Alkaloid polymorphism and ITS sequence variation in the Spiraea japonica complex (Rosaceae) in China: traces of the biological effects of the Himalaya‐Tibet Plateau uplift

Zhang, Z., Fan, L., Yang, J., Hao, X., & Zhi-Jian, G. (2006) · American Journal of Botany · doi:10.3732/ajb.93.5.762 · Cited by 45

Bioactive Limonoid Constituents of Munronia henryi

Yan, Y., Zhang, J., Huang, T., Mao, X.-Y., Gu, W., He, H., Di, Y., Li, S., Chen, D., Zhang, Y., et al. (2015) · Journal of Natural Products · doi:10.1021/np501057f · Cited by 44

Alkaloids from the Leaves of Daphniphyllum longeracemosum

Di, Y., He, H., Lü, Y., Yi, P., Li, L., Li, W., & Hao, X. (2006) · Journal of Natural Products · doi:10.1021/np060088f · Cited by 42

Natural Diterpenoid Compound Elevates Expression of Bim Protein, Which Interacts with Antiapoptotic Protein Bcl-2, Converting It to Proapoptotic Bax-like Molecule

Zhao, L., He, F., Liu, H., Zhu, Y., Tian, W., Gao, P., He, H., Yue, W., Lei, X., Ni, B., et al. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.264481 · Cited by 41

Research of Panax spp. in Kunming Institute of Botany, CAS

Qiao, Y., Shang, J.-H., Wang, D., Zhu, H., Yang, C., & Zhang, Y. (2018) · Natural Products and Bioprospecting · doi:10.1007/s13659-018-0176-8 · Cited by 40

Trichiconins A–C, Limonoids with New Carbon Skeletons from Trichilia connaroides

Liu, C., Xu, J., Han, Y.-S., Wainberg, M. A., & Yue, J. (2014) · Organic Letters · doi:10.1021/ol5027552 · Cited by 39

Cyclohexane-Fused Octahydroquinolizine Alkaloids from Myrioneuron faberi with Activity against Hepatitis C Virus

Cao, M., Zhang, Y., Li, X., Peng, Z., Jiang, J., Gu, Y., Di, Y., Li, X., Chen, D., Xia, C., et al. (2014) · The Journal of Organic Chemistry · doi:10.1021/jo501076x · Cited by 39

Lathyranone A: A Diterpenoid Possessing an Unprecedented Skeleton from Euphorbia lathyris

Gao, S., Liu, H., Wang, Y., He, H., Wang, J., Di, Y., Li, C., Fang, X., & Hao, X. (2007) · Organic Letters · doi:10.1021/ol701501p · Cited by 38

The plant sesquiterpene lactone parthenolide inhibits Wnt/β-catenin signaling by blocking synthesis of the transcriptional regulators TCF4/LEF1

Zhu, X., Yuan, C., Tian, C., Li, C., Nie, F., Song, X., Zeng, R., Wu, D., Hao, X., & Li, L. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.819300 · Cited by 38

Cipadonoids B–G, six new limonoids from Cipadessa cinerascens

Fang, X., Zhang, Q., Tan, C., Mu, S., Lü, Y., Lu, Y., Zheng, Q., Di, Y., & Hao, X. (2009) · Tetrahedron · doi:10.1016/j.tet.2009.07.023 · Cited by 37

Daphhimalenine A, a New Alkaloid with an Unprecedented Skeleton, from Daphniphyllum himalense

Zhang, Y., Di, Y., Zhang, Q., Mu, S., Tan, C., Fang, X., He, H., Li, S., & Hao, X. (2009) · Organic Letters · doi:10.1021/ol902262g · Cited by 37

Integrating transcriptome and microRNA analysis identifies genes and microRNAs for AHO-induced systemic acquired resistance in N. tabacum

Chen, Y., Dong, J., Bennetzen, J. L., Zhong, M., Yang, J., Zhang, J., Li, S., Hao, X., Zhang, Z., & Wang, X. (2017) · Scientific Reports · doi:10.1038/s41598-017-12249-y · Cited by 37

Munronoids A–J, ten new limonoids from Munronia unifoliolata Oliv

Ge, Y., Zhang, J., Mu, S.-Z., Chen, Y., Yang, F., Lü, Y., & Hao, X. (2011) · Tetrahedron · doi:10.1016/j.tet.2011.11.003 · Cited by 36

Myriberine A, a New Alkaloid with an Unprecedented Heteropentacyclic Skeleton from Myrioneuron faberi

Huang, S., Zhang, Y., Cao, M., Di, Y., Tang, G., Peng, Z., Jiang, J., He, H., & Hao, X. (2013) · Organic Letters · doi:10.1021/ol3034065 · Cited by 36

Recent advances in molecular basis for strigolactone action

Yao, R., Li, J., & Xie, D. (2017) · Science China Life Sciences · doi:10.1007/s11427-017-9195-x · Cited by 35

Identification of Ingol and Rhamnofolane Diterpenoids from Euphorbia resinifera and Their Abilities to Induce Lysosomal Biosynthesis

Zhao, N.-D., Ding, X., Song, Y. F., Yang, D., Yu, H.-L., Adelakun, T. A., Qian, W.-D., Zhang, Y., Di, Y., Gao, F., et al. (2018) · Journal of Natural Products · doi:10.1021/acs.jnatprod.7b00981 · Cited by 35

Daphlongeranines A and B, Two Novel Alkaloids Possessing Unprecedented Skeletons from Daphniphyllum longeracemosum

Li, C., Di, Y., He, H., Gao, S., Wang, Y., Lü, Y., Zhong, J., & Hao, X. (2007) · Organic Letters · doi:10.1021/ol070942+ · Cited by 34

Trichiliton A, a Novel Limonoid from Trichilia connaroides

Fang, X., Di, Y., Geng, Z., Tan, C., Guo, J. Q., Ning, J., & Hao, X. (2010) · European Journal of Organic Chemistry · doi:10.1002/ejoc.200901245 · Cited by 33

Daphmalenines A and B: Two New Alkaloids with Unusual Skeletons from Daphniphyllum himalense

Zhang, Y., Di, Y., He, H., Li, S., Lü, Y., Gong, N., & Hao, X. (2011) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201100414 · Cited by 32

Design, Synthesis, and Structural Optimization of Lycorine-Derived Phenanthridine Derivatives as Wnt/β-Catenin Signaling Pathway Agonists

Chen, D., Jing, C., Cai, J., Wu, J., Wang, S., Yin, J.-L., Li, X., Li, L., & Hao, X. (2015) · Journal of Natural Products · doi:10.1021/acs.jnatprod.5b00825 · Cited by 31

Novel flavagline‐like compounds with potent Fli‐1 inhibitory activity suppress diverse types of leukemia

Song, J., Yuan, C., Yang, J., Liu, T., Yao, Y., Xiao, X., Gajendran, B., Xu, D., Li, Y., Wang, C., et al. (2018) · FEBS Journal · doi:10.1111/febs.14690 · Cited by 31

A diterpenoid derivate compound targets selenocysteine of thioredoxin reductases and induces Bax/Bak-independent apoptosis

Liu, J., Mu, C., Yue, W., Li, J., Ma, B., Zhao, L., Liu, L., Chen, Q., Chen, Y., Liu, H., et al. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.05.038 · Cited by 30

Two New Germacranolides fromMagnolia Grandiflora

Wu, S., Luo, X., Ma, Y., Hao, X., Zhou, J., & Wu, D. (2001) · Journal of Asian Natural Products Research · doi:10.1080/10286020108041376 · Cited by 30

Kansuinone, a novel euphane-type triterpene from Euphorbia kansui

Guo, J. Q., He, H., Fang, X., Di, Y., Li, S., Zhang, Z., Leng, Y., Hua, H., & Hao, X. (2010) · Tetrahedron Letters · doi:10.1016/j.tetlet.2010.09.099 · Cited by 29

Chemical constituents from fruits of Harrisonia perforata

Yan, X., Di, Y., Fang, X., Yang, S., He, H., Li, S., Lü, Y., & Hao, X. (2011) · Phytochemistry · doi:10.1016/j.phytochem.2011.01.010 · Cited by 29

The Chemistry and Biochemistry of Spiraea japonica Complex

Hao, X., Shen, Y., Li, L. J., & He, H. (2003) · Current Medicinal Chemistry · doi:10.2174/0929867033456684 · Cited by 29

Myrifabine, the First Dimeric Myrioneuron Alkaloid from Myrioneuron faberi

Cao, M., Huang, S., Di, Y., Yuan, C., Zuo, G., Gu, Y., Zhang, Y., & Hao, X. (2013) · Organic Letters · doi:10.1021/ol403408m · Cited by 29

Daphnilongerine, an unprecedented fused pentacyclic ring system alkaloid from Daphniphyllum longeracemosum Rosenth.

Li, L., He, H., Di, Y., Gao, S., & Hao, X. (2006) · Tetrahedron Letters · doi:10.1016/j.tetlet.2006.06.144 · Cited by 28

Structure Elucidation and Biomimetic Synthesis of Hostasinine A, a New Benzylphenethylamine Alkaloid from Hosta plantaginea

Wang, Y., Gao, S., Yang, F., Sun, Q., Wang, J., Liu, H., Li, C., Di, Y., Li, S., He, H., et al. (2007) · Organic Letters · doi:10.1021/ol702438h · Cited by 27

Daphniphyllum and Diterpenoid Alkaloids from Daphniphyllum longeracemosum

Li, C., Di, Y., Mu, S., He, H., Zhang, Q., Fang, X., Zhang, Y., Li, S., Lü, Y., Gong, Y., et al. (2008) · Journal of Natural Products · doi:10.1021/np8001332 · Cited by 27

Hedychins A and B, 6,7-Dinorlabdane Diterpenoids with a Peroxide Bridge from Hedychium forrestii

Zhao, Q. X., Gao, J.-J., Qin, X., Hao, X., He, H., & Liu, H. (2018) · Organic Letters · doi:10.1021/acs.orglett.7b03836 · Cited by 27

Munronin O, a potential activator for plant resistance

Yan, Y., Tang, L., Hu, J., Wang, J., Adelakun, T. A., Yang, D., Di, Y., Zhang, Y., & Hao, X. (2018) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2018.02.001 · Cited by 27

Unprecedented Quassinoids from Eurycoma longifolia : Biogenetic Evidence and Antifeedant Effects

Yang, W.-Q., Shao, X., Deng, F., Hu, L., Xiong, Y., Huang, X., Fan, C., Jiang, R., Ye, W., & Wang, Y. (2020) · Journal of Natural Products · doi:10.1021/acs.jnatprod.0c00244 · Cited by 25

Purification and Characterization of a New Ribosome Inactivating Protein from Cinchonaglycoside C‐treated Tobacco Leaves

Li, Y., Jia, Y., Zhang, Z., Chen, X., He, H., Fang, R., & Hao, X. (2007) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2007.00476.x · Cited by 24

Daphnioldhamine A, a novel alkaloid from Daphniphyllum oldhami

Tan, C., Wang, Y., Di, Y., He, H., Mu, S., Li, S.-F., Zhang, Y., & Hao, X. (2012) · Tetrahedron Letters · doi:10.1016/j.tetlet.2012.03.021 · Cited by 24

Structural elucidation of daphniacetal A, a new oxa-cage compound isolated from Daphniphyllum macropodum Miq.

Kong, N., Zhang, Y., Gao, S., Lü, Y., Zheng, Q., Sun, Q., Yang, F., Di, Y., & Hao, X. (2008) · Tetrahedron Letters · doi:10.1016/j.tetlet.2008.12.027 · Cited by 24

3,4-seco-Diterpenoids from Trigonostemon flavidus

Tang, G., He, H., Gu, Y., Di, Y., Wang, Y., Li, S.-F., Li, S., Zhang, Y., & Hao, X. (2012) · Tetrahedron · doi:10.1016/j.tet.2012.09.052 · Cited by 24

Calycilactone A, a novel hexacyclic alkaloid from Daphniphyllum calycillum

Di, Y., He, H., Liu, H., Du, Z., Tian, J., Yang, X., Wang, Y., & Hao, X. (2006) · Tetrahedron Letters · doi:10.1016/j.tetlet.2006.05.105 · Cited by 24

Oldhamine A, a novel alkaloid from Daphniphyllum oldhami

Tan, C., Di, Y., Wang, Y., Wang, Y., Mu, S., Gao, S., Zhang, Y., Kong, N., He, H., Zhang, J., et al. (2008) · Tetrahedron Letters · doi:10.1016/j.tetlet.2008.03.126 · Cited by 24

Chemical biology reveals CARF as a positive regulator of canonical Wnt signaling by promoting TCF/β-catenin transcriptional activity

He, X., Zhang, W., Chen, Y., Nie, F., Li, C., Liu, X., Fei, C., Li, S., Song, X., Jia, Y., et al. (2017) · Cell Discovery · doi:10.1038/celldisc.2017.3 · Cited by 22

Four New Limonoids from Aphanamixis grandifolia

Tong, L., Zhang, Y., He, H., & Hao, X. (2012) · Chinese Journal of Chemistry · doi:10.1002/cjoc.201200309 · Cited by 21

Diterpene alkaloids and diterpenes from Spiraea japonica and their anti-tobacco mosaic virus activity

Ma, Y., Mao, X.-Y., Huang, L., Fan, Y., Gu, W., Chen, Y., Huang, T., Zhang, J.-X., Yuan, C., & Hao, X. (2015) · Fitoterapia · doi:10.1016/j.fitote.2015.11.019 · Cited by 20

Stemtuberolines A-G, new alkaloids from Stemona tuberosa and their anti-TMV activity

Hu, Z., An, Q., Tang, H., Yuan, C., Li, Y., Zhang, Y., & Hao, X. (2020) · Fitoterapia · doi:10.1016/j.fitote.2020.104572 · Cited by 20

Sulfur-containing and dimeric flavanols from Glycosmis montana

Wang, J., He, H., Shen, Y., & Hao, X. (2004) · Tetrahedron Letters · doi:10.1016/j.tetlet.2004.10.172 · Cited by 19

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