Cordycepin

Cordycepin structural formula

CAS Number73-03-0
Molecular FormulaC10H13N5O3
Molecular Weight251.247
InChI KeyOFEZSBMBBKLLBJ-BAJZRUMYSA-N
LogP-0.728
Synonyms
  • Cordycepin
  • 3'-Deoxyadenosine
  • Adenosine, 3'-deoxy-
  • 73-03-0
  • 3'-deoxyadenosine
  • 4-26-00-03594
  • ADENOSINE, 3'-DEOXY-
  • BRN 0035194
  • 9-(beta-D-3'-Deoxyribofuranosyl)adenine
  • EINECS 200-791-4
  • NSC 401022
  • beta-D-erythro-Pentofuranoside, adenine-9 3-deoxy-
  • 9H-Purin-6-amine, 9-(3-deoxy-beta-D-erythro-pentofuranosyl)-
  • UNII-GZ8VF4M2J8
  • 9-Cordyceposidoadenine
  • 9H-Purine, 6-amino-9-(3-deoxy-beta-D-ribofuranosyl)-
  • Cordycepine

Applications:

HPLC Method for Analysis of 3′-Deoxyadenosine and 2′-Deoxyadenosine on BIST B+ Column

December 1, 2022

HPLC Method for Cordycepin, Deoxyadenosine on BIST B+ by SIELC Technologies

Cordycepin is an adenosine analogue with the chemical formula C10H13N5O3. It is reported to prevent cell reproduction in various cancer cells. It also might possess antioxidant and anti-inflammatory properties, when considered in addition with it’s ability to cross the blood-brain barrier, it may become widely used in pharmaceuticals.

Deoxyadenosine is a deoxyribonucleoside with the chemical formula C10H13N5O3. It is a derivative of adenosine. High presence of it can kill T lymphocytes and kill those cells, leading to adenosine deaminase severe combined immunodeficiency disease, also known as ADA-SCID.

Cordycepin, Deoxyadenosine can be retained and analyzed using the BIST B+ stationary phase column. The analysis utilizes an isocratic method with a simple mobile phase consisting of water and acetonitrile (MeCN) with a Phosphoric Acid buffer. Detection is performed using UV.

Condition

ColumnBIST B+, 4.6 x 150 mm, 5 µm, 100 A, dual ended
Mobile PhaseMeCN – 85%
BufferH3PO4 – 0.2%
Flow Rate1.0 ml/min
DetectionUV 260 nm
Peak Retention Time8.2, 9.8 min

Description

Class of CompoundsNucleosides
Analyzing CompoundsCordycepin, Deoxyadenosine

Application Column

BIST B+

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A
Column options: dual ended

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Application Analytes:
Cordycepin
Deoxyadenosine

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Separation of Adenosine, Cordycepin and Adenine on Newcrom AH Column

April 8, 2020

HPLC Method for Adenosine, Cordycepin, Adenine on Newcrom AH by SIELC Technologies

 

 

High Performance Liquid Chromatography (HPLC) Method for Analysis of Adenosine, Cordycepin, Adenine.

Adenosine is a key building block of energy-carrying molecules with the chemical formula C10H13N5O4. It has a variety of other uses, including being a inhibitory neurotransmitter which helps with sleep and acting as a blood flow regulator. Medicinally, it is used as treatment for supraventricular tachycardia (SVT). You can find detailed UV spectra of Adenosine and information about its various lambda maxima by visiting the following link.

Cordycepin is an adenosine analogue with the chemical formula C10H13N5O3. It is reported to prevent cell reproduction in various cancer cells. It also might possess antioxidant and anti-inflammatory properties, when considered in addition with it’s ability to cross the blood-brain barrier, it may become widely used in pharmaceuticals.

Due to cordycepin having a very similar structure to adenosine, it has shown to have inhibitive properties on the COVID-19 coronavirus. However, due to their similar structures, the separation of the two sugars can be challenging. Both sugars can be separated isocratically in about six minutes on the Newcrom AH mixed-mode column, which has both hydrophobic and cationic exchange properties. The mobile phase consists of acetonitrile (ACN, MeCN) and water with ammonium formate as a buffer which makes it mass-spec (MS) compatible. It can also be UV detected at 260nm.

 

Condition

Column Newcrom AH, 4.6 x 150 mm, 5 µm, 100 A, dual ended
Mobile Phase MeCN/H2O – 10/90%
Buffer AmFm pH 3.0- 20 mM
Flow Rate 1.0 ml/min
Detection UV 260 nm,  MS-compatible mobile phase

Description

Class of Compounds Hydrophilic, Drug, Xanthine, Nucleobase
Analyzing Compounds Adenosine, Cordycepin, Adenine

Application Column

Newcrom AH

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A
Column options: dual ended

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Application Analytes:
Adenine
Adenosine
Cordycepin

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

Separation of Cordycepin on Newcrom R1 HPLC column

February 16, 2018
Separation of Cordycepin on Newcrom C18 HPLC column

Cordycepin can be analyzed by this reverse phase (RP) HPLC method with simple conditions. The mobile phase contains an acetonitrile (MeCN), water, and phosphoric acid. For Mass-Spec (MS) compatible applications the phosphoric acid needs to be replaced with formic acid. Smaller 3 µm particles columns available for fast UPLC applications. This liquid chromatography method is scalable and can be used for isolation impurities in preparative separation. It also suitable for pharmacokinetics.

Application Column

Newcrom R1

The Newcrom columns are a family of reverse-phase-based columns. Newcrom A, AH, B, and BH are all mixed-mode columns with either positive or negative ion-pairing groups attached to either short (25 Å) or long (100 Å) ligand chains. Newcrom R1 is a special reverse-phase column with low silanol activity.

Select options
Application Analytes:
Cordycepin
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.