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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| 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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