| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC1085 | Bnr10s | Solvatochromic Nile Red Probe with FRET Quencher Reveal Lipid Order Heterogeneity in Living and Apoptotic Cells |
|
| DCC1086 | Bntx Maleatel | Selective delta 1 opioid receptor antagonist |
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| DCC1087 | Bo-1978 | Inhibitor of topoisomerase I/II, inducing DNA cross-linking and significantly suppressing the growth of various NSCLC cell lines with or without mutations in epidermal growth factor receptor (EGFR) |
|
| DCC1088 | Boc-phe-vinyl Ketone | Novel covalent substrate-competitive inactivator of AKT kinase |
|
| DCC1089 | bodilisant | Novel Fluorescent, Highly Affine Histamine H3 Receptor Ligand |
|
| DCC1090 | Bodipy495 | Fluorogenic dye for Live-Cell Fluorescence Microscopy |
|
| DCC1091 | Bodipy625 | Novel fluorogenic dye for Live-Cell Fluorescence Microscopy |
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| DCC1092 | Bonannione A | Natural inhibitor of protein tyrosine phosphatase 1B (PTP1B) |
|
| DCC1093 | Bont/a Lc Inhibitor 33 | Potent Botulinum Neurotoxin A Light-Chain Inhibitor |
|
| DCC1094 | Bont-in-33 | Novel potent inhibitor of Botulinum neurotoxin/A light chain (BoNT/A LC) |
|
| DCC1095 | Bop-jf549 | Novel BOP-conjufated fluorescent dual α9β1/α4β1 integrin inhibitor |
|
| DCC1096 | Bos-318 | Novel. highly potent, selective, cell-permeable furin inhibitor, rescuing key features of cystic fibrosis airway disease |
|
| DCC1097 | Bos-6-2-2-6-crbn | Proteolysis targeting chimeras (PROTAC), acting as a degrader of oncogenic BCR-ABL |
|
| DCC1098 | Bot-64 | Novel IKK-2 inhibitor, targeting the Ser177 and/or Ser181 residues in the kinase's activation loop domain. |
|
| DCC1099 | Bp1.4160 | Novel and highly potent histamine H3 receptor ligand |
|
| DCC1100 | Bp-1-108 | Potent and selective STAT5 inhibitor |
|
| DCC1101 | Bp13944 | Novel, Potential Dengue Virus NS2B/NS3 Protease Inhibitor |
|
| DCC1102 | Bp2-94 | Histamine H3 receptor agonist prodrug |
|
| DCC1103 | Bpc Hydroiodide | Novel modulator of TTD-PHD histone reader module, binding to the TTD groove, competing with linker binding and promoting open TTD-PHD conformations |
|
| DCC1104 | Bph-1218 | Novel potent SQS inhibitor |
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| DCC1105 | Bph-651 | Novel CrtM inhibitor |
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| DCC1106 | Bph-652 Potassium | Squalene synthase (SQS) inhibitor, potently inhibiting CrtM |
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| DCC1107 | bpmetap1-in-15 | The first potent inhibitor of Burkholderia pseudomallei methionine aminopeptidase |
|
| DCC1108 | Bpn-14136 Featured | Novel RBP4 antagonist with good in vitro potency and selectivity and optimal rodent pharmacokinetic (PK) and pharmacodynamic (PD) characteristics |
|
| DCC1109 | Bpr1k871 | Novel potent and selective dual FLT3/AURKA inhibitor |
|
| DCC1110 | Bpv(phen) | Potent direct PTEN inhibitor |
|
| DCC1111 | Bpv(pic)k2 | Potent and se;rctive PTEN inhibitor, activating the insulin receptor kinase, inhibiting the dephosphorylation of autophosphorylated insulin receptors and epidermal growth factor receptors of rat liver endosomes |
|
| DCC1112 | Bpyo-34 | Novel apoptosis signal-regulating kinase 1 (ASK1) inhibitor with IC50 of 0.52μM in vitro in kinase assay |
|
| DCC1113 | bractelactone | Novel potent inhibitor of human neutrophil activations |
|
| DCC1114 | BRAF PROTAC P4B | Quantity (mg or Unit) Unit Price ($/mg or $/Unit) Final Price 100 $292.50 Total: $29,250.00 50 $338.00 Total: $16,900.00 25 $396.50 Total: $9,912.50 10 $468.00 Total: $4,680.00 5 $552.50 Total: $2,762.50 |
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