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Others

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Cat. No. Product Name Field of Application Chemical Structure
DC43058 Teuclatriol
DC43057 Inokosterone
DC43055 2,3,24-Trihydroxyolean-12-en-28-oic acid
DC43053 Calyxamine B
DC43052 Chrysosplenol D
DC43051 3-O-Methylquercetin tetraacetate
DC43050 3,5-Dihydroxyergosta-7,22-dien-6-one
DC43049 Thioperamide maleate
Potent and selective H3 histamine receptor antagonist, crossing the blood-brain barrie
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DC43048 6-O-(3'',4''-Dimethoxycinnamoyl)catalpol
DC43046 Ginsenoside Rg6
Ginsenoside Rg6, extracted from steamed notoginseng, exhibited significantly potent inhibitory effects on IL-12 p40 production in LPSstimulated BMDCs.
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DC43045 Cylindramide
DC43044 Camaric acid
DC43042 Cycloart-23-ene-3,25-diol
DC43040 S3I-1757
Novel inhibitor of STAT3 homodimerization selectively suppresses STAT3 activity and malignant transformation
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DC43039 Eucamalol
DC43038 LLP3
A cell-permeable Survivin inhibitor. LLP-3 is an inhibitor of Survivin-Ran complex formation that induces apoptosis in tumor slice cultures, including resistant tumors.
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DC43037 Sideroxylonal A
DC43036 Dihydropinosylvin
DC43035 6-Hydroxykaempferol-3,6,7-triglucoside
DC43034 PS77
Novel allosteric Pkh inhibitor directed to the PIF-pocket, with increased selectivity for C. albicans Pkh2.
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DC43033 NU9056
Selective KAT5 (Tip60) histone acetyltransferase inhibitor (IC50 values are < 2, 60, 36, and >100 μM for KAT5, p300, pCAF and GCN5, respectively). Inhibits protein acetylation in prostate cancer cell lines and blocks DNA damage response. Decreases prolife
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DC43031 UCM53
Novel inhibitor of bacterial cell division targeting the GTP binding site of FtsZ
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DC43030 24-Methylenecycloartan-3-ol
DC43029 (+)-Lyoniresinol
DC43028 PK7242 Maleate
Novel inducer of reactivation of mutant p53 in cancer cells
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DC43027 Isomahanine
DC43026 GKL003
Novel Inhibitor of Bacterial Transcription Initiation Complex Formation
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DC43025 Murrayanol
DC43024 3-O-(E)-p-Coumaroylbetulin
DC43022 2,24-Dihydroxyursolic acid

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