CDN1163   Click here for help

GtoPdb Ligand ID: 12968

Compound class: Synthetic organic
Comment: CDN1163 is an allosteric activator of the sarco/endoplasmic reticulum Ca(2+)-ATPase (SERCA) [1]. It blocks endoplasmic reticulum stress caused by dysregulated SERCA function. CDN1163 has been used to study the role of SERCA2 in intracellular Ca2+ homeostasis and endoplasmic reticulum stress, mitochondrial homeostasis and cell viability [2-4,6].
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Ligand Activity Visualisation Charts

These are box plot that provide a unique visualisation, summarising all the activity data for a ligand taken from ChEMBL and GtoPdb across multiple targets and species. Click on a plot to see the median, interquartile range, low and high data points. A value of zero indicates that no data are available. A separate chart is created for each target, and where possible the algorithm tries to merge ChEMBL and GtoPdb targets by matching them on name and UniProt accession, for each available species. However, please note that inconsistency in naming of targets may lead to data for the same target being reported across multiple charts.

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View interactive charts of activity data across species
2D Structure
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2D Structure

An image of the ligand's 2D structure. For small molecules with SMILES these are drawn using the NCI/CADD Chemical Identifier Resolver. Click on the image to access the chemical structure search tool with the ligand pre-loaded in the structure editor. For other types of ligands, e.g. longer nucleotides and peptides, a manually drawn representation of the molecule may be provided.

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Physico-chemical Properties
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Physico-chemical Properties

Calculated molecular properties are available for small molecules and natural products (not peptides). Properties were generated using the CDK toolkit. All properties were selected to enable the prediction of the Lipinski Rule-of-Five profile or ‘druglikeness’ for each ligand. For more info on each category see the help pages.

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Hydrogen bond acceptors 4
Hydrogen bond donors 1
Rotatable bonds 5
Topological polar surface area 50.69
Molecular weight 320.39
XLogP 1.98
No. Lipinski's rules broken 0
SMILES / InChI / InChIKey
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SMILES / InChI / InChIKey

SMILES (Simplified Molecular Input Line Entry Specification) A specification for unambiguously describing the structure of chemical molecules using short ASCII strings. Canonical SMILES specify a unique representation of the 2D structure without chiral or isotopic specifications. Isomeric SMILES include chiral specification and isotopes.

Standard InChI (IUPAC International Chemical Identifier) and InChIKey InChI is a non-proprietary, standard, textual identifier for chemical substances designed to facilitate linking of information and database searching. An InChIKey is a simplified version of a full InChI, designed for easier web searching.

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Canonical SMILES CC(C)OC1=CC=C(C=C1)C(=O)NC2=C3C(=CC=C2)C=CC(=N3)C
Isomeric SMILES CC(C)OC1=CC=C(C=C1)C(=O)NC2=C3N=C(C)C=CC3=CC=C2
InChI InChI=1S/C20H20N2O2/c1-13(2)24-17-11-9-16(10-12-17)20(23)22-18-6-4-5-15-8-7-14(3)21-19(15)18/h4-13H,1-3H3,(H,22,23)
InChI Key GVGVYDCVFBGALZ-UHFFFAOYSA-N
References
1. Kang S, Dahl R, Hsieh W, Shin A, Zsebo KM, Buettner C, Hajjar RJ, Lebeche D. (2016)
Small Molecular Allosteric Activator of the Sarco/Endoplasmic Reticulum Ca2+-ATPase (SERCA) Attenuates Diabetes and Metabolic Disorders.
J Biol Chem, 291 (10): 5185-98. [PMID:26702054]
2. Kimura T, Kagami K, Sato A, Osaki A, Ito K, Horii S, Toya T, Masaki N, Yasuda R, Nagatomo Y et al.. (2022)
Sarco/Endoplasmic Reticulum Ca2+ ATPase 2 Activator Ameliorates Endothelial Dysfunction; Insulin Resistance in Diabetic Mice.
Cells, 11 (9). [PMID:35563793]
3. Li K, Guo C, Ruan J, Ning B, Wong CK, Shi H, Gu J. (2023)
Cadmium Disrupted ER Ca2+ Homeostasis by Inhibiting SERCA2 Expression and Activity to Induce Apoptosis in Renal Proximal Tubular Cells.
Int J Mol Sci, 24 (6). [PMID:36983052]
4. Nguyen HT, Noriega Polo C, Wiederkehr A, Wollheim CB, Park KS. (2023)
CDN1163, an activator of sarco/endoplasmic reticulum Ca2+ ATPase, up-regulates mitochondrial functions and protects against lipotoxicity in pancreatic β-cells.
Br J Pharmacol, 180 (21): 2762-2776. [PMID:37277321]
5. Sordi G, Goti A, Young HS, Palchetti I, Tadini-Buoninsegni F. (2021)
Stimulation of Ca2+ -ATPase Transport Activity by a Small-Molecule Drug.
ChemMedChem, 16 (21): 3293-3299. [PMID:34297466]
6. Zhang W, Ye F, Pang N, Kessi M, Xiong J, Chen S, Peng J, Yang L, Yin F. (2022)
Restoration of Sarco/Endoplasmic Reticulum Ca2+-ATPase Activity Functions as a Pivotal Therapeutic Target of Anti-Glutamate-Induced Excitotoxicity to Attenuate Endoplasmic Reticulum Ca2+ Depletion.
Front Pharmacol, 13: 877175. [PMID:35517826]