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Cat. No.	Product Name	Field of Application
DC26034	NUC3373(Fosifloxuridine nafalbenamide) Featured	NUC-3373 is a phosphoramidate-based prodrug of the monophosphate form of 5-fluoro-2'-deoxyuridine, the active metabolite of fluorouracil,an antimetabolite fluoropyrimidine analog of the pyrimidine nucleoside, with potential antineoplastic activity.
DC26035	NUC-7738 Featured	NUC-7738 is a phosphoramidate transformation of cordycepin (3’-deoxyadenosine; 3’-dA), a derivative of adenosine that was first isolated from Cordyceps sinensis.
DC9416	Nuclear yellow	Nuclear yellow (Hoechst S769121) exhibits excitation/emission maxima ~335/495 nm when bound to DNA.
DC9486	Nucleozin Featured	Nucleozin targets influenza A nucleoprotein (NP), a multifunctional, RNA-binding protein necessary for virus replication.
DC3125	Nutlin-3 Featured	Nutlin 3 is a commercial available p53-MDM2 inhibitor, with Ki of 90 nM.
DC8454	Nutlin-3a Featured	Nutlin-3a is arbitrarily referred to as enantiomer a because it appears as the first peak from chiral purification of racemic nutlin-3 and its absolute stereocenter assignment is not known.
DC8455	Nutlin-3b	Nutlin-3b is 150-fold less potent as an inhibitor of p53-MDM2 interaction than (−)-nutlin-3, demonstrating an IC50 value of 13.6 µM.
DC21931	NV01	NV01 is a small-molecule antagonist of the H3K9me3 binding to UHRF1 tandem tudor domain (TTD) with Kd of 5 uM..
DC21932	NV03	NV03 is a small-molecule antagonist of the H3K9me3 binding to UHRF1 tandem tudor domain with Kd of 2.4 uM..
DC7988	NVP-DPP728 dihydrochloride	NVP DPP 728 is a potent and orally active inhibitor of dipeptidyl peptidase (DPP)-IV with Ki and IC50 values of 11 nM and 14 nM, respectively.
DC21430	NVP-2 Featured	NVP-2 is a potent and selective ATP-competitive cyclin dependent kinase 9 (CDK9) probe, inhibits CDK9/CycT activity with an IC50 of 0.514 nM. NVP-2 displays inhibitory effcts on CDK1/CycB, CDK2/CycA and CDK16/CycY kinases with IC50 values of 0.584 µM, 0.7
DC8312	NVP-231	NVP-231 is a potent, specific, and reversible CerK inhibitor(IC50=12±2 nM) that competitively inhibits binding of ceramide to CerK.
DC7576	NVP-AAM077 Featured	NVP-AAM077 is a potent antagonist for NMDA receptors.
DC8794	NVP-ACC-789 Featured	NVP-ACC789 is an inhibitor of VEGFR-2 (FLK-1/KDR).
DC7549	NVP-ADW742 Featured	NVP-ADW742 is an IGF-1R inhibitor with IC50 of 0.17 μM, >16-fold more potent against IGF-1R than InsR; little activity to HER2, PDGFR, VEGFR-2, Bcr-Abl and c-Kit.
DC4174	NVP-AEW541 Featured	NVP-AEW541 is a potent inhibitor of IGF-1R with IC50 of 86 nM.
DC7250	NVP-BAG956(BAG 956)	NVP-BAG956(BAG 956) is a potent, ATP-competitive and selective dual PI3K and PDK1 inhibitor in vitro and in vivo,with IC50 values to be 56, 444, 34, 117 and 240 nM for PI3K p110 alpha, beta, delta and gamma and PDK1 kinases, respectively.
DC9680	NVP-BAW2881 Featured	NVP-BAW2881 is a novel vascular endothelial growth factor (VEGF) receptor tyrosine-kinase inhibitor
DC4118	NVP-BEP800 Featured	NVP-BEP800 is a novel, fully synthetic HSP90β inhibitor with IC50 of 58 nM.
DC24053	NVP-BGJ398 phosphate Featured	NVP-BGJ398 phosphate (Infigratinib phosphate, BGJ398 phosphate) is a potent, selective pan-FGFR inhibitor with IC50 of 0.9/1.0/1.4/60 nM for FGFR1/2/3/4, also shows high potenct against mutant FGFR3-K650E with IC50 of 4.9 nM.
DC3133	NVP-BGT226 (BGT226） Featured	NVP-BGT226 is a novel dual PI3K/mTOR inhibitor with IC50 of 1 nM.
DC7473	NVP-BHG712 Featured	NVP-BHG712 is a specific EphB4 inhibitor with ED50 of 25 nM that discriminates between VEGFR and EphB4 inhibition; also shows activity against c-Raf, c-Src and c-Abl with IC50 of 0.395 μM, 1.266 μM and 1.667 μM, respectively.
DC10540	NVP-BQR695 Featured	NVP-BQR695 is a novel PI3K inhibitor.
DC7216	NVP-BSK805 dihydrochloride Featured	NVP-BSK805 is a potent and selective ATP-competitive JAK2 inhibitor with IC50 of 0.5 nM; >20-fold selectivity towards JAK1, JAK3 and TYK2.
DC8743	NVP-BVU972 Featured	NVP-BVU972 is a selective and potent Met inhibitor (IC50 = 14 nM). Antitumor agents.
DC9769	NVP-CGM097 (CGM-097) Featured	NVP-CGM097 (CGM-097) is a potent and selective MDM2 inhibitor.
DC9392	NVP-LCQ195 Featured	NVP-LCQ195 (AT9311; LCQ195) is a small molecule heterocyclic inhibitor of CDK1, CDK2, CDK3 and CDK5 with IC50 of 1-42 nM.
DC22564	NVP-MELK8a hydrochloride Featured	NVP-MELK8a hydrochloride (MELK8a hydrochloride) is a novel potent, and selective MELK inhibitor with IC50 of 2 nM.
DC7474	NVP-QAV-572	NVP-QAV-572 is a potent PI3K kianse inhibitor with IC50 of 10 nM.
DC7701	NVP-QAV680	NVP-QAV680 is a potent and selective CRTh2 receptor antagonist suitable for clinical testing in allergic diseases.

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