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PubPharm (10)
1
Discovery of the 2,4-disubstituted quinazoline derivative as a novel neddylation inhibitor for tumor therapy
enthalten in:
Bioorganic chemistry
| 2024
von
Su, J.
|
Li, M.
|
Chang, Y.
| +7
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2
Biochemical and structural characterization of chlorhexidine as an ATP-assisted inhibitor against type 1 methionyl-tRNA synthetase from Gram-positive bacteria
enthalten in:
European journal of medicinal chemistry
| 2024
von
Lu, F.
|
Xia, K.
|
Su, J.
| +6
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3
Design, synthesis and biological evaluation of novel tubulin inhibitors targeting colchicine sites
enthalten in:
Bioorganic & medicinal chemistry letters
| 2023
von
Yuan, M.
|
Su, J.
|
Zhang, Y.
| +5
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4
Methods and compositions for treating rna virus-induced diseases
enthalten in:
Europäisches Patentamt
| 2023
von
LIU SHENG-YUNG
|
SU JINGTIAN
|
WEN WUZHE
| +1
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5
Aromatic heterocyclic compound containing 3, 4, 5-trisubstituent benzene ring, pharmaceutical composition and preparation method and application of aromatic heterocyclic compound
enthalten in:
Europäisches Patentamt
| 2022
von
DUAN YONGTAO
|
CHU YANAN
|
SU JINGTIAN
| +3
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6
Aromatic heterocyclic compound containing 3, 4, 5-trisubstituent benzene ring, pharmaceutical composition and preparation method and application of aromatic heterocyclic compound
enthalten in:
Europäisches Patentamt
| 2022
von
DUAN YONGTAO
|
CHU YANAN
|
SU JINGTIAN
| +3
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7
APJ/apelin : A promising target for the treatment of retinopathy of prematurity
enthalten in:
Drug discovery today
| 2022
von
Su, J.
|
Zhang, Y.
|
Kumar, S.
| +3
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8
The role of MOZ/KAT6A in hematological malignancies and advances in MOZ/KAT6A inhibitors
enthalten in:
Pharmacological research
| 2021
von
Su, J.
|
Wang, X.
|
Bai, Y.
| +3
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9
Antiangiogenic Therapy: Challenges and Future Directions
enthalten in:
Current topics in medicinal chemistry
| 2021
von
Su, J.
|
Zhu, H.
|
Yao, Y.
| +1
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10
NQO1-Selective Activated Prodrug of Triptolide : Synthesis and Antihepatocellular Carcinoma Activity Evaluation
enthalten in:
ACS medicinal chemistry letters
| 2018
von
Liu, M.
|
Song, W.
|
Du, X.
| +4
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1
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