Cordycepin - Moligand™, ≥98% , CAS No.73-03-0

Name: Cordycepin - Moligand™, ≥98% , CAS No.73-03-0
SKU: C110081
Availability: InStock

CAS: 73-03-0 Cat. No.: C110081 Fórmula: C₁₀H₁₃N₅O₃ Peso molecular: 251.24 Beilstein Registry Number: 35194 Número CE: 200-791-4

19 Citations COA

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Cordycepin - Moligand™, ≥98% CAS No(73-03-0) C110081 by Aladdin Scientific

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Disponível para encomenda

GRADE & PURITY Moligand™ ? ≥98%

Synonyms

Cordycepin, from Cordyceps militaris | CORDYCEPIN [MI] | 9-(3-Deoxy-b-D-erythro-pentofuranosyl)-9H-purin-6-amine | Cordycepin, >=98.0% (HPLC) | UNII-GZ8VF4M2J8 | AC-22613 | MFCD00037998 | NSC-63984 | Q2256677 | Z3041517973 | AKOS015854875 | (2R,3R,5S)-2-(

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Visão geral Specifications Nomes e identificadores Documentation Advanced Data Taxonomic Classification Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas FAQs e artigos Citations of This Product Calculadoras de soluções Revisões

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Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 19 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Visão geral

Cordycepin is a nucleoside analog that acts as an anticancer and antifungal agent. Cordycepin inhibits growth of various tumor cells in vitro. It can be converted to 3'-deoxyadenosine triphosphate (3'-dATP), which inhibits ATP-dependent DNA synthesis. Cordycepin is also useful for the study of messenger RNA transcription.
An anticancer, antifungal nucleoside analog.

Specifications

Sinónimos

Especificações e pureza

Moligand™, ≥98%

Mecanismos bioquímicos e fisiológicos

Nucleoside antagonist, able to interfere with RNA synthesis. Inhibits NF-κB signaling. Anti-inflammatory and antitumor effects in vitro and in vivo .

Fonte

from Cordyceps militaris

Condições de armazenamento de armazenamento

Store at 2-8°C,Argon charged

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Grau

Moligand™

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureza

≥98%

Nomes e identificadores

Pubchem Sid

488180045

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488180045

Sorrisos canónicos

C1C(OC(C1O)N2C=NC3=C(N=CN=C32)N)CO

IUPAC Name

(2R,3R,5S)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolan-3-ol

InChIKey

OFEZSBMBBKLLBJ-BAJZRUMYSA-N

INCHI

1S/C10H13N5O3/c11-8-7-9(13-3-12-8)15(4-14-7)10-6(17)1-5(2-16)18-10/h3-6,10,16-17H,1-2H2,(H2,11,12,13)/t5-,6+,10+/m0/s1

SMILES isoméricas

C1[C@H](O[C@H]([C@@H]1O)N2C=NC3=C(N=CN=C32)N)CO

WGK Alemanha

RTECS

AU7358610

Número UN

2811

Peso molecular

251.24

Beilstein

35194

Reaxy-Rn

7169449

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7169449&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Classe Purine nucleosides
    - Subclass Purine 3'-deoxyribonucleosides

Kingdom	Organic compounds
Superclass	Nucleosides, nucleotides, and analogues
Classe	Purine nucleosides
Subclass	Purine 3'-deoxyribonucleosides
Intermediate Tree Nodes	Not available
Direct Parent	Purine 3'-deoxyribonucleosides
Alternative Parents	6-aminopurines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Purine 3'-deoxyribonucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Tetrahydrofuran - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Alcohol - Organic nitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Descrição	This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.
External Descriptors	adenosines - 3'-deoxyribonucleoside
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Estrutura 3D

Alvos associados (humanos)

ADA Tclin Adenosine deaminase (129 Activities)

Discover Target: ADA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

Discover Target: ADORA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

BXPC-3 (2997 Activities)

Lot Number	Certificate Type	Data	Item
H2624175	Certificate of Analysis	Jul 29, 2026	C110081
H2624174	Certificate of Analysis	Jul 29, 2026	C110081
H2624173	Certificate of Analysis	Jul 29, 2026	C110081
H2624172	Certificate of Analysis	Jul 29, 2026	C110081
A2615270	Certificate of Analysis	Jan 05, 2026	C110081
F2608106	Certificate of Analysis	Jan 05, 2026	C110081
A2615271	Certificate of Analysis	Jan 05, 2026	C110081
A2615272	Certificate of Analysis	Jan 05, 2026	C110081
B2225372	Certificate of Analysis	Dec 12, 2025	C110081
A2605070	Certificate of Analysis	Jul 18, 2025	C110081
G2530195	Certificate of Analysis	Jul 18, 2025	C110081
G2530194	Certificate of Analysis	Jul 18, 2025	C110081
G2530193	Certificate of Analysis	Jul 18, 2025	C110081
G2530192	Certificate of Analysis	Jul 18, 2025	C110081
G2530190	Certificate of Analysis	Jul 18, 2025	C110081
E2514221	Certificate of Analysis	Mar 15, 2025	C110081
E2514222	Certificate of Analysis	Mar 15, 2025	C110081
E2526627	Certificate of Analysis	Mar 15, 2025	C110081
G2315524	Certificate of Analysis	Jul 21, 2023	C110081
G2315527	Certificate of Analysis	Jul 21, 2023	C110081
G2315441	Certificate of Analysis	Jul 21, 2023	C110081
G2315439	Certificate of Analysis	Jul 21, 2023	C110081
F2415067	Certificate of Analysis	Jul 06, 2023	C110081
I2321091	Certificate of Analysis	Jul 06, 2023	C110081
I2321092	Certificate of Analysis	Jul 06, 2023	C110081
I2321107	Certificate of Analysis	Jul 06, 2023	C110081
K2422321	Certificate of Analysis	Jul 06, 2023	C110081
B2328543	Certificate of Analysis	Feb 04, 2023	C110081
B2328538	Certificate of Analysis	Feb 04, 2023	C110081
B2328537	Certificate of Analysis	Feb 04, 2023	C110081
B2328530	Certificate of Analysis	Feb 04, 2023	C110081
B2328526	Certificate of Analysis	Feb 04, 2023	C110081
B2225371	Certificate of Analysis	Dec 15, 2021	C110081
B2225370	Certificate of Analysis	Dec 15, 2021	C110081
B2225352	Certificate of Analysis	Dec 15, 2021	C110081

Solubilidade	Soluble in DMSO (100 mM), methanol, and water
Sensibilidade	heat sensitive;Moisture sensitive
Rotação específica [α]	-46° (C=1,H2O)
Ponto de fusão (°C)	224-228°C
Peso molecular	251.240 g/mol
XLogP3	-1.200
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	7
Rotatable Bond Count	2
Exact Mass	251.102 Da
Monoisotopic Mass	251.102 Da
Topological Polar Surface Area	119.000 Å²
Heavy Atom Count	18
Formal Charge	0
Complexity	307.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	3
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Cordycepin - Moligand™, ≥98% , CAS No.73-03-0

Storage & shipping

Quality documents

Literature proof

Visão geral

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Avaliações dos Clientes

📚 Citations by Application

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