Paricalcitol

Synonyms: Paracalcin,19-Nor-1-25-OH2D2,19-Nor-colecalciferol

Paricalcitol is a selective vitamin D receptor agonist. Paricalcitol suppresses parathyroid hormone mRNA expression and inhibits parathyroid cell proliferation. Pariccitol is used to treat secondary hyperparathyroidism in chronic kidney disease.

Paricalcitol Chemical Structure

Paricalcitol Chemical Structure

CAS: 131918-61-1

Selleck's Paricalcitol has been cited by 3 publications

Purity & Quality Control

Batch: S668101 DMSO] 83 mg/mL] false] Ethanol] 13 mg/mL] false] Water] Insoluble] false Purity: 99.99%
99.99

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Choose Selective Vitamin Inhibitors

Biological Activity

Description Paricalcitol is a selective vitamin D receptor agonist. Paricalcitol suppresses parathyroid hormone mRNA expression and inhibits parathyroid cell proliferation. Pariccitol is used to treat secondary hyperparathyroidism in chronic kidney disease.
Targets
vitamin D receptor [1]
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05664880 Recruiting
Chronic Pancreatitis
Cedars-Sinai Medical Center|National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
June 1 2023 Early Phase 1
NCT03415854 Completed
Pancreatic Cancer|Pancreatic Ductal Adenocarcinoma|Pancreatic Adenocarcinoma|Pancreas Metastases|Adenocarcinoma
HonorHealth Research Institute|Barts Cancer Institute|Abramson Cancer Center at Penn Medicine|Salk Institute for Biological Studies|Mayo Clinic|Princeton University|Imaging Endpoints|Translational Genomics Research Institute|Stand Up To Cancer|Cancer Research UK|Lustgarten Foundation|University of California San Diego
January 31 2018 Phase 2
NCT03331562 Completed
Pancreatic Cancer|Pancreas Adenocarcinoma|Advanced Pancreatic Cancer|Metastatic Pancreatic Cancer|Metastatic Pancreatic Adenocarcinoma
Translational Genomics Research Institute|Stand Up To Cancer|Merck Sharp & Dohme LLC
December 27 2017 Phase 2
NCT02686827 Completed
Hypersensitivity
Laurian Jongejan|Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
October 2015 Phase 2
NCT01725113 Terminated
Kidney Failure|Secondary Hyperparathyroidism|Hyperphosphatemia|Hypercalcemia
Winthrop University Hospital
November 2012 Phase 4

Chemical Information & Solubility

Molecular Weight 416.64 Formula

C27H44O3

 

CAS No. 131918-61-1 SDF --
Smiles CC(C=CC(C)C(C)(C)O)C1CCC2C1(CCCC2=CC=C3CC(CC(C3)O)O)C
Storage (From the date of receipt) 3 years -20°C powder

In vitro
Batch:

DMSO : 83 mg/mL ( (199.21 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 13 mg/mL

Water : Insoluble


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In vivo
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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