enpp1 inhibitors rbs2418 (Riboscience LLC)
90
Structured Review
Riboscience LLC
enpp1 inhibitors rbs2418
Enpp1 Inhibitors Rbs2418, supplied by Riboscience LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/enpp1 inhibitors rbs2418/product/Riboscience LLC
Average 90 stars, based on 1 article reviews
Enpp1 Inhibitors Rbs2418, supplied by Riboscience LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/enpp1 inhibitors rbs2418/product/Riboscience LLC
Average 90 stars, based on 1 article reviews
enpp1 inhibitors rbs2418 - by Bioz Stars,
2026-02
90/100 stars
Images
1) Product Images from "Oral ENPP1 inhibitor designed using generative AI as next generation STING modulator for solid tumors"
Article Title: Oral ENPP1 inhibitor designed using generative AI as next generation STING modulator for solid tumors
Journal: Nature Communications
doi: 10.1038/s41467-025-59874-0
Figure Legend Snippet: A Indication prioritization tools embedded in PandaOmics to rank indications for ENPP1. B The correlation analysis of type-I IFN related immune parameters across cancer types: Correlation between ENPP1 expression in tumor cells and ISG score in conventional dendritic cells (cDC) in gastric cancer (OMIX001073, n = 10) and colorectal cancer (CRC, GSE132465 , n = 23), as well as correlation between ENPP1 expression in tumor cells and CXCL10 expression in dendritic cells (DC) and cDC percentage in triple-negative breast cancer (TNBC, GSE176078 , n = 10). Each dot represents a single patient sample. The x-axis indicates the ENPP1 expression in tumor cells and the y-axis displays the corresponding immune parameters: ISG score, CXCL10 expression or cDC percentage. The P value and correlation were performed using Pearson’s correlation coefficient, with the resulting trend line depicted in blue. The gray shaded area surrounding the trend line represents the 95% confidence intervals. Source data are provided as a Source Data file. C Spatial distribution of ENPP1, ISG score and predicted proportion of CD8 T and pro-inflammatory macrophage cells per spot in histology slide SN84_A120838_Rep2 from CRC patient (Zenodo record: 7760264). The color represents the value of ENPP1 expression, ISG score and predicted proportion of DC and NK cells per spot. Source data are provided as a Source Data file. D Spatial distribution of ENPP1, ISG score and predicted proportion of CD4 T and DC cells per spots in slide GSM6433591_094A from a TNBC patient (GEO: GSE210616 ). The color represents the value of ENPP1 expression, ISG score and predicted proportion of DC and NK cells per spot. Source data are provided as a Source Data file. E Spatial distribution of ENPP1, ISG score and predicted proportion of DC and NK cells per spot in slide 21_00734_LI_SING from a GC patient (GEO: GSE251950 ). The color represents the value of ENPP1 expression, ISG score and predicted proportion of DC and NK cells per spot. Source data are provided as a Source Data file.
Techniques Used: Expressing
Figure Legend Snippet: A Flow scheme for AI-facilitated ENPP1 inhibitor discovery. ReRSA, retrosynthesis related synthetic accessibility; SA, synthetic accessibility; PXR, pregnane xenobiotic receptor. Novelty calculated based on the dataset compiled from ChEMBL. Alchemistry, accurately estimates the relative binding free energy to prioritize molecules with efficient physics-based methods. ADMET prediction, predict physicochemical and ADMET molecular properties. B Docking pose of ISM7516 with human ENPP1. The source data are provided as a Source Data file. ENPP1 (white) is shown in ribbon and ISM7516 (cyan) is drawn in sphere, while key residues (white) and ISM7516(cyan) are shown in stick. C Docking pose of ISM5939 with human ENPP1. The source data are provided as a Source Data file. ISM5939 (yellow) was superimposed with AMP (purple, PDB ID: 6wfj) and QPS2 (green, PDB ID: 6wev). Zn atoms are shown as gray sphere and dashed lines indicate hydrogen bonds or coordination bonds. D Biochemical/cellular activity, △G cal , CYP3A4 induction, hERG inhibition and predicted hERG inhibition value of candidate inhibitors. The data are colored by profiling results. Green represents ideal profiling, orange indicates potential issues, black represents acceptable results, and red represents unacceptable outcomes. CYP3A4 induction calculated as ratio of CYP3A4 mRNA following compound treatment at 10 µM compared to rifampicin. △G cal was calculated by Alchemistry tool. hERG, human ether-a-go-go-related gene. Predicted hERG inhibition values were achieved by ADMET prediction module.
Techniques Used: Binding Assay, Activity Assay, Inhibition
Figure Legend Snippet: A Concentration response curves of ISM5939 or positive control (ENPP-1-IN-1) in ENPP1 enzymatic assay (pH 7.4, n = 2 biological replicates, 2 independent experiments). Left, 2,3- cGAMP as substrate; right, ATP as substrate. B IC 50 values for ISM5939 against human ENPP1 catalytic activity using 2’,3’ cGAMP or ATP as substrates at pH 7.4 and pH 6.5. C Concentration response curves of ISM5939 in the ENPP1 enzymatic assay at different concentrations of ATP and cGAMP ( n = 2 biological replicates). D – F The inhibitory activity of ISM5939 against the catalytic activity of (D) human ENPP2 (E) human ENPP3 and (F) table summary for IC 50 values ( n = 2 biological replicates). G The Rador map illustrating the effect of ISM5939 (10 μM) on SafetyOne44 Panel targets ( n = 2 biological replicates). H Inhibitory effects of ISM5939 on cGAMP degradation mediated by soluble ENPP1 in human plasma detected by ELISA. I Stabilization of cGAMP in vivo in murine plasma by ISM5939 ( n = 3 biological replicates). Data were analyzed by two‐tailed, unpaired Student’s t‐test. P-value < 0.05 were shown. J Potency of ISM5939 in maintaining extracellular cGAMP levels when applied to cancer cells in vitro ( n = 2 biological replicates). Data were represented as mean ± SEM. Source data are provided as a Source Data file.
Techniques Used: Concentration Assay, Positive Control, Enzymatic Assay, Activity Assay, Clinical Proteomics, Enzyme-linked Immunosorbent Assay, In Vivo, Two Tailed Test, In Vitro
Figure Legend Snippet: A Baseline ENPP1 expression levels in Paclitaxel+anti-PD1 responsive or non-responsive breast cancer patients (GEO: GSE194040 ). n = 38 for responders and n = 31 for non-responders. B Baseline ENPP1 expression levels in anti-PD-L1 responsive or non-responsive esophageal adenocarcinoma patients with high LRRC8A expression. Data were extracted from GSE165252 . n = 6 for responders and n = 3 for non-responders. For boxplots, boxes indicate 25th and 75th percentiles, the lines within boxes mark medians, whiskers extend over 1.5 times the interquartile range (IQR, the distance from 25th to 75th percentile); dots represent patient samples. C Combinational effect of ISM5939 and anti-PD-L1 therapy. MC38 tumor‐bearing C57BL/6 J mice were treated with anti‐PD‐L1 antibody (3 mg kg −1 , twice per week) alone or in combination with ISM5939 (30 mg/kg, twice a day) for indicated days ( n = 6 biological replicates per group). D Combinational effect of ISM5939 and anti-PD1 therapy. MC38 tumor‐bearing C57BL/6 J mice were treated with anti‐PD1 antibody (5 mg kg −1 , twice per week) alone or in combination with ISM5939 at the indicated doses ( n = 8 biological replicates per group). E – H Tumor infiltrating immune cells analyzed by flow cytometry. MC38 tumor‐bearing C57BL/6 J mice were treated with anti‐PD1 antibody (5 mg kg −1 , twice per week) alone or in combination with ISM5939 (20 mg kg −1 , twice a day) for 7 consecutive days ( n = 6 biological replicates). E, F The proportion of the indicated immune cells in tumor infiltrating CD45 + cells; G The ratio of CD8 + T cells (left) and CD4 + T cells (right) to Tregs. H CD69 positive ratios among the indicated immune subsets. I Tumor growth of CT26 syngeneic tumors. Tumor bearing mice ( n = 6 biological replicates per group) were treated with anti-PD1 antibody alone or in combination with ISM5939 (20 mg kg −1 , twice a day). Data are represented as mean ± SEM. For ( A , B ) and ( E – G ), data were analyzed by two‐tailed Student’s t‐test. P value < 0.05 were shown. Data were represented as mean ± SEM. Source data are provided as a Source Data file.
Techniques Used: Expressing, Flow Cytometry, Two Tailed Test
Figure Legend Snippet: A Baseline ENPP1 expression levels in chemotherapy responsive or non-responsive TNBC, HER2 positive breast cancer, ER positive breast cancer and colorectal cancer patients. Data were extracted from GSE22513 , GSE50948 , GSE22093 and GSE28702 . For TNBC, n = 8 for responders and n = 20 for non-responders; for HER2 positive breast cancer, n = 22 for responders and n = 71 for non-responders; for ER positive breast cancer, n = 10 for responders and n = 32 for non-responders; for CRC, n = 42 for responders and n = 41 for non-responders. For boxplots, boxes indicate 25th and 75th percentiles, the lines within boxes mark medians, whiskers extend over 1.5 times the interquartile range (IQR, the distance from 25th to 75th percentile); dots represent patient samples. B Maximal cGAMP release induced by combined use of cisplatin or paclitaxel with ISM5939 ( n = 2 biological replicates, two independent experiments). C – E EMT6 syngeneic tumor bearing mice treated with cisplatin and ISM5939 alone or in combination for 2 weeks to profile ( C ) differential tumor growth and ( D , E ) endpoint tumor sample bulk RNA sequencing showing ( D ) pathway enrichment (The color represents adjust P-value) and ( E ) deconvoluted immune cell populations in the tumor microenvironment post-treatment ( n = 6 biological replicates for tumor growth detection, n = 3 biological replicates for RNA sequencing). Color represents z-scores of cell population, values range from red (low population) to green (high population). F Tumor growth of 4T1 orthotopic tumor-bearing mice treated with docetaxel and ISM5939 alone or in combination. G In vitro release of cGAMP by BRCA-proficient (MDA-MB-231, ID8) or BRCA-deficient (MDA-MB-436, UWB1.289) cells treated with Olaparib or ISM5939 alone or in combination via ELISA ( n = 2 biological replicates). H Tumor growth of 4T1 orthotopic tumor-bearing mice treated with Olaparib and ISM5939 alone or in combination ( n = 7 biological replicates). Data were represented as mean ± SEM. For ( A ), ( C ), ( F ) and ( H ), data were analyzed by two‐tailed Student’s t‐test. P value < 0.05 were shown. Source data are provided as a Source Data file.
Techniques Used: Expressing, RNA Sequencing, In Vitro, Enzyme-linked Immunosorbent Assay, Two Tailed Test
Figure Legend Snippet: ISM5939 facilitates the accumulation of extracellular cGAMP by blocking ENPP1-dependent degradation, thereby triggering the cGAS-STING signaling pathway in antigen-presenting cells (APCs). This activation effectively enhances the activity of CD8 + T cells. Additionally, ISM5939 diminishes adenosine production by inhibiting ENPP1-mediated ATP hydrolysis, potentially mitigating the suppression of tumor-infiltrating T cells.
Techniques Used: Blocking Assay, Activation Assay, Activity Assay
