Cat. No. | Product name | CAS No. |
DCC4020 |
Pc407-ws
Water-soluble novel potential COX-2 inhibitor |
1242169-24-9 |
DCC4021 |
Pcb153
Non-dioxin-like (NDL) congener |
35065-27-1 |
DCC4022 |
Pcb-te2p
Novel Chelator for Cu-64 |
|
DCC4023 |
Pcc-0105002
Novel PSD95-nNOS inhibitor, disrupting the PSD95-nNOS interaction, attenuating neuropathic pain, decreasing SNL-induced spinal dorsal horn WDR neuron hyperexcitation |
|
DCC4024 |
Pcc0208018
Novel activator of effector T cells, enhancing T cell proliferation and activation to release interferon gamma (IFN-γ) and interleukin-2 (IL-2) without blocking the programmed cell death 1 (PD-1)/programmed cell death-ligand 1 (PD-L1) binding and not dire |
1673534-73-0 |
DCC4025 |
P-cf3-diepp
Novel α7 nAChR weak partial agonist, showing antinociceptive and anti-inflammatory properties |
|
DCC4026 |
p-chloro-diphenyl Diselenide
Organoselenium compound with antidepressant-like and memory enhancer actions |
20541-49-5 |
DCC4027 |
pcm126
Potent antagonist of the series disrupting EphA2-ephrinA1 interaction, blocking EphA2 phosphorylation in prostate cancer cells at low |
192876-13-4 |
DCC4028 |
p-come 102
Highly selective α1L adrenaline receptor agonist |
1354932-35-6 |
DCC4029 |
Pcpma-(1r,2r)-22e
Novel potent dopamine D3R agonist (Ki=4.1nM) |
|
DCC4030 |
Pcpma-(1r,2r)-30q
Novel potent and selective dopamine D3R partial agonist |
|
DCC4031 |
Pcpma-(1s,2s)-22e
Novel potent dopamine D3R antagonist |
|
DCC4032 |
Pcsk9 Modulator
Novel modulator of proprotein convertase subtilisin kexin like type 9 (PCSK9) |
|
DCC4033 |
Pcsk9-in-4d
Novel PCSK9 mRNA translation inhibitor |
|
DCC4034 |
Pcsk9-in-4g
Novel PCSK9 mRNA translation inhibitor |
|
DCC4035 |
Pcsk9-in-8b
Novel liver-targeted inhibitor of ribosomal synthesis of proprotein convertase subtilisin/kexin type 9 (PCSK9) |
|
DCC4036 |
Pd-1 Inhibitor 16
Novel inhibitor of PD-I/PD-L1 interaction to be used as a negative immune checkpoint regulatory and antineoplastic agent |
2005454-12-4 |
DCC4037 |
Pd-1/pd-l1 Antagonist D2
Novel potent PD-1/PD-L1 antagonist (IC50 of 16.17 nM), activating the antitumor immunity of T cells efficiently in PBMCs |
|
DCC4038 |
Pd-1/pd-l1 Inhibitor 17
Novel bifunctional inhibitor of PD-1/PD-L1 interactions, promoting dimerization, internalization, and degradation of PD-L1, suppressing tumor growth in vivo by activating antitumor immunity |
|
DCC4039 |
Pd-1/pd-l1 Inhibitor A30
Novel Potent Inhibitor of the Programmed Cell Death-1/Programmed Cell Death-Ligand 1 Interaction |
|
DCC4040 |
Pd-1/pd-l1 Inhibitor Ch1
Novel inhibitor of PD-1/PD-L1 (IC 50 value of 56.58 nM), dose-dependently promoting HepG2 cell death in a co-culture model of HepG2/hPD-L1 and Jurkat T cells, effectively inhibiting tumor growth (TGI of 76.4% at 90 mg/kg) in an immune checkpoint humanized |
|
DCC4041 |
Pd-1/pd-l1 Inhibitor P18
Novel potent programmed cell death-1 (PD-1)/programmed cell death ligand 1 (PD-L1) inhibitor (IC50 9.1 nM) |