Avatrombopag

Synonyms: AKR-501,E5501,YM477

Avatrombopag (AKR-501,E5501,YM477) is an orally administered, small-molecule thrombopoietin receptor (c-Mpl) agonist which increases platelet number, but not platelet activation.

Avatrombopag Chemical Structure

Avatrombopag Chemical Structure

CAS: 570406-98-3

Purity & Quality Control

Batch: Purity: 99.96%
99.96

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Biological Activity

Description Avatrombopag (AKR-501,E5501,YM477) is an orally administered, small-molecule thrombopoietin receptor (c-Mpl) agonist which increases platelet number, but not platelet activation.
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05772546 Not yet recruiting
Gastrointestinal Cancer|Gastrointestinal Neoplasms|Chemotherapy-Induced Thrombocytopenia
Hanny Al-Samkari MD|Swedish Orphan Biovitrum|Massachusetts General Hospital
September 2023 Phase 2
NCT04312789 Withdrawn
Platelet Disorder
Ayman Saad|Sobi Inc.|Ohio State University Comprehensive Cancer Center
December 2022 Phase 2
NCT05518331 Recruiting
Refractory Aplastic Anemia
Institute of Hematology & Blood Diseases Hospital China|Peking University People''s Hospital|Xiyuan Hospital of China Academy of Chinese Medical Sciences|Second Hospital of Shanxi Medical University|First Affiliated Hospital of Harbin Medical University|The First Hospital of Hebei Medical University
June 1 2022 Not Applicable
NCT05218226 Recruiting
Chemotherapy-induced Thrombocytopenia|Avatrombopag
Institute of Hematology & Blood Diseases Hospital China|Tianjin Medical University Cancer Institute and Hospital|Tianjin Medical University Second Hospital|Tianjin Third Central Hospital|Tianjin People''s Hospital|Henan Cancer Hospital|The Second Affiliated Hospital of Kunming Medical University
February 10 2022 Phase 2
NCT04949009 Unknown status
Primary Immune Thrombocytopenia
Shandong University
March 1 2021 --
NCT04609891 Completed
Thrombocytopenia
Anhui Provincial Cancer Hospital
May 26 2020 Not Applicable

Chemical Information & Solubility

Molecular Weight 649.65 Formula

C29H34Cl2N6O3S2

CAS No. 570406-98-3 SDF --
Smiles C1CCC(CC1)N2CCN(CC2)C3=C(N=C(S3)NC(=O)C4=CC(=C(N=C4)N5CCC(CC5)C(=O)O)Cl)C6=CC(=CS6)Cl
Storage (From the date of receipt) 3 years -20°C powder

In vitro
Batch:

DMSO : 20 mg/mL ( (30.78 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : Insoluble

Ethanol : Insoluble


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In vivo
Batch:

Add solvents to the product individually and in order.


In vivo Formulation Calculator

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In vivo Formulation Calculator (Clear solution)

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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.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

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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