TY - JOUR
T1 - Clustered patterns of species origins of nature-derived drugs and clues for future bioprospecting
AU - Zhu, Feng
AU - Qin, Chu
AU - Tao, Lin
AU - Liu, Xin
AU - Shi, Zhe
AU - Ma, Xiaohua
AU - Jia, Jia
AU - Tan, Ying
AU - Cui, Cheng
AU - Lin, Jinshun
AU - Tan, Chunyan
AU - Jiang, Yuyang
AU - Chen, Yuzong
PY - 2011/8/2
Y1 - 2011/8/2
N2 - Many drugs are nature derived. Lowdrug productivity has renewed interest in natural products as drug-discovery sources. Naturederived drugs are composed of dozens of molecular scaffolds generated by specific secondary-metabolite gene clusters in selected species. It can be hypothesized that drug-like structures probably are distributed in selective groups of species. We compared the species origins of 939 approved and 369 clinical-trial drugs with those of 119 preclinical drugs and 19,721 bioactive natural products. In contrast to the scattered distribution of bioactive natural products, these drugs are clustered into 144 of the 6,763 known species families in nature, with 80% of the approved drugs and 67% of the clinical-trial drugs concentrated in 17 and 30 drug-prolific families, respectively. Four lines of evidence from historical drug data, 13,548 marine natural products, 767medicinal plants, and19,721 bioactive natural products suggest that drugs are derived mostly from preexisting drugproductive families. Drug-productive clusters expand slowly by conventional technologies. The lack of drugs outside drug-productive families is not necessarily the result of under-exploration or late exploration by conventional technologies. New technologies that explore cryptic gene clusters, pathways, interspecies crosstalk, and high-throughput fermentation enable the discovery of novel natural products. The potential impact of these technologies on drug productivity and on the distribution patterns of drug-productive families is yet to be revealed.
AB - Many drugs are nature derived. Lowdrug productivity has renewed interest in natural products as drug-discovery sources. Naturederived drugs are composed of dozens of molecular scaffolds generated by specific secondary-metabolite gene clusters in selected species. It can be hypothesized that drug-like structures probably are distributed in selective groups of species. We compared the species origins of 939 approved and 369 clinical-trial drugs with those of 119 preclinical drugs and 19,721 bioactive natural products. In contrast to the scattered distribution of bioactive natural products, these drugs are clustered into 144 of the 6,763 known species families in nature, with 80% of the approved drugs and 67% of the clinical-trial drugs concentrated in 17 and 30 drug-prolific families, respectively. Four lines of evidence from historical drug data, 13,548 marine natural products, 767medicinal plants, and19,721 bioactive natural products suggest that drugs are derived mostly from preexisting drugproductive families. Drug-productive clusters expand slowly by conventional technologies. The lack of drugs outside drug-productive families is not necessarily the result of under-exploration or late exploration by conventional technologies. New technologies that explore cryptic gene clusters, pathways, interspecies crosstalk, and high-throughput fermentation enable the discovery of novel natural products. The potential impact of these technologies on drug productivity and on the distribution patterns of drug-productive families is yet to be revealed.
KW - Biodiversity
KW - Drug-prolific species
KW - Herb
KW - Phylogenetic tree
UR - http://www.scopus.com/inward/record.url?scp=79961223344&partnerID=8YFLogxK
U2 - 10.1073/pnas.1107336108
DO - 10.1073/pnas.1107336108
M3 - Article
C2 - 21768386
AN - SCOPUS:79961223344
SN - 0027-8424
VL - 108
SP - 12943
EP - 12948
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 31
ER -