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Cat. No. Product Name Field of Application Chemical Structure
DCC0980 Bibs-222
Novel nonpeptide angiotensin II receptor antagonist
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DCC0979 Bi-9740
Novel potent, highly selective, and orally bioavailable CATHEPSIN C (CTSC, CatC) inhibitor
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DCC0978 bi-83c11
Non-ATP competitive inhibitor of JNK, targeting the JNK-JIP interaction
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DCC0977 Bi-730357
Novel RORγ antagonist for the treatment of autoimmune diseases
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DCC0976 Bi-7273
Novel highly potent dual inhibitor of BRD9/BRD7
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DCC0975 Bi-5521
Novel potent and selective ATP-competitive inhibitor of glycogen synthase kinase (GSK-3), targeting both isoforms GSK-3α and GSK-3β
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DCC0974 Bi-4659
Novel potent and selective inhibitor of Alk5 (TGFßR1), blocking the phosphorylation of Smad2 and Smad3 in HaCaT cells
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DCC0973 Bi-3257
Novel inhibitor of HIV replication, preventing the formation of the capsid core structure that encapsulates the viral genome and its associated enzymes, reversing transcriptase and integrase
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DCC0972 Bi-2051
Novel highly selective, soluble and cellular permeable inhibitor of the P. falciparum protease dipeptidyl aminopeptidase 1 (DPAP1)
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DCC0971 Bi-1942
Novel potent inhibitor of human chymase with >100 fold selectivity against Cathepsin G
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DCC0969 Bi-0319
Novel PROTAC (proteolysis-targeting chimera) as a PTK2 protein degerader
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DCC0968 Bhq-o-5ht
Novel photoactivatable form of serotonin
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DCC0967 Bhq-2-succinimide Ester
Reactive dark quencher used in a variety of Fluorescence Resonance Energy Transfer (FRET) DNA detection probe.
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DCC0966 Bh3i-2
Cell-permeable apoptosis inducer, specifically preventing BH3 domain-mediated interactions between pro-apoptotic and anti-apoptotic members of the Bcl-2 family
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DCC0965 Bgt1-in-9
The first small-molecule substrate identified with high selectivity for BGT1 over the three other GAT subtypes; M1 muscarinic agonist
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DCC0964 Bg-p400-tat
Novel dual inhibitor of norepinephrine transporter (NET) function and thyrointegrin αvβ3 receptor
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DCC0963 b-glucogallin
Novel Aldose_reductase_inhibitor>aldose reductase (ALR2) inhibitor
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DCC0962 b-gf-15
Potent inhibitor of centrosomal clustering in malignant cells
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DCC0960 Bff122
Novel potent and selective inhibitor of kynurenine aminotransferase II
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DCC0959 Bf-170 Hydrochloride
Novel probe for neurofibrillary tangles (tau fibrils)
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DCC0958 Betulinic Acid Hydroxamate
Novel HIF Prolyl Hydrolase Inhibitor, preventing colonic inflammation and fibrosis in murine models of inflammatory bowel disease
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DCC0957 Bet-in-36
Novel BET inhibitor, selectively targeting BRD4-BD1 bromodomain
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DCC0956 Bet-brd7/9 Inhibitor-12
Novel Dual BET-BRD7/9 Bromodomain Inhibitor, showing a strong antiproliferative effect on various cancer cell lines that could not be observed for BD family selective inhibitors
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DCC0955 Betaxolol
Selective beta-1 adrenergic receptor antagonist with antihypertensive and anti-glaucoma activities and devoid of intrinsic sympathomimetic activity
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DCC0954 Beta-nor-lapachone
Natural antibiofilm agent and adjuvant on the antifungal therapy related to resistant infections caused by C. glabrata
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DCC0953 Beta-erythroidine Hcl
Phytoestrogen, possessing typical curare-like action
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DCC0952 Beta-cit-fp
Potent ligand of the serotonin (5-HT) and dopamine (DA) transporters used in diagonisis of Parkinson's disease as SPECT imaging precursor
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DCC0951 Beta-blocker-15
Novel negative allosteric modulator of the ß2-adrenergic receptor (ß2AR), inhibiting cAMP production through the ß2AR, but not that mediated by other Gs-coupled receptors, also inhibiting ß-arrestin recruitment to the activated ß2AR
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DCC0950 Berotralstat Hydrochloride
Novel selective inhibitor of plasma kallikrein, blocking the enzymatic activity of plasma kallikrein in releasing bradykinin, the major biologic peptide that promotes swelling and pain associated with attacks of HAE
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DCC0949 Berotralstat Analog
Novel inhibitor of plasma kallikrein
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