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

CAS: 73-03-0 Cat. No.: C110081 Peso molecular: 251.24 Beilstein Registry Number: 35194 Número EC: 200-791-4
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥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
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25mg
C110081-25mg
3
9,90US$
100mg
C110081-100mg
7
16,90US$
500mg
C110081-500mg
1
39,90US$
1g
C110081-1g
1
59,90US$
5g
C110081-5g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

164,90US$

247,90US$
Guardar 83,00 US$ (33.48%)
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

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

📋

Quality documents

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

📚

Literature proof

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

Descripción general

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
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-(
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
Nucleoside antagonist, able to interfere with RNA synthesis. Inhibits NF-κB signaling. Anti-inflammatory and antitumor effects in vitro and in vivo .
Fuente
from Cordyceps militaris
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
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%
Nombres e identificadores
Pubchem Sid488180045
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180045
Sonrisas canónicasC1C(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
InChIKeyOFEZSBMBBKLLBJ-BAJZRUMYSA-N
INCHI1S/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
Isómeros SMILES C1[C@H](O[C@H]([C@@H]1O)N2C=NC3=C(N=CN=C32)N)CO
WGK Alemania 3
RTECS AU7358610
Número ONU 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

KingdomOrganic compounds
SuperclassNucleosides, nucleotides, and analogues
ClasePurine nucleosides
SubclassPurine 3'-deoxyribonucleosides
Intermediate Tree Nodes Not available
Direct ParentPurine 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 FrameworkAromatic 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
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ADA Tclin Adenosine deaminase (129 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
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BXPC-3 (2997 Activities)
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CCRF-CEM (65223 Activities)
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HL-60 (67320 Activities)
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HT-29 (80576 Activities)
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K562 (73714 Activities)
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MCF7 (126967 Activities)
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MOLT-4 (49676 Activities)
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MT4 (17854 Activities)
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RPMI-8226 (44974 Activities)
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THP-1 (11052 Activities)
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MIA PaCa-2 (5949 Activities)
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HepG2 (196354 Activities)
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KG-1 (867 Activities)
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SW-620 (52400 Activities)
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MV4-11 (7307 Activities)
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TLR4 Tchem Toll-like receptor 4 (970 Activities)
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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
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RL (305 Activities)
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NCI-H929 (451 Activities)
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HEL 92.1.7 (74 Activities)
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Hdac6 Histone deacetylase 6 (222 Activities)
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NS5B Hepatitis C virus NS5B RNA-dependent RNA polymerase (3026 Activities)
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Trypanosoma cruzi (99888 Activities)
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Trichomonas vaginalis (2376 Activities)
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Human alphaherpesvirus 2 (4932 Activities)
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Human respirovirus 3 (1674 Activities)
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Human alphaherpesvirus 1 (11089 Activities)
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Human immunodeficiency virus 1 (70413 Activities)
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Vesicular stomatitis virus (4460 Activities)
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Vero (26788 Activities)
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NIH3T3 (5395 Activities)
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L929 (3802 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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Rela Transcription factor p65 (175 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mammalian orthoreovirus 1 (1523 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP51 Sterol 14-alpha demethylase (857 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATP-dependent molecular chaperone HSP82 (2186 Activities)
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TIM23 Mitochondrial import inner membrane translocase subunit TIM23 (781 Activities)
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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

30 results found

Lot NumberCertificate TypeFechaArticulo
A2615270Certificate of AnalysisJan 05, 2026 C110081
A2615271Certificate of AnalysisJan 05, 2026 C110081
A2615272Certificate of AnalysisJan 05, 2026 C110081
B2225372Certificate of AnalysisDec 12, 2025 C110081
G2530195Certificate of AnalysisJul 18, 2025 C110081
G2530194Certificate of AnalysisJul 18, 2025 C110081
G2530193Certificate of AnalysisJul 18, 2025 C110081
G2530192Certificate of AnalysisJul 18, 2025 C110081
G2530190Certificate of AnalysisJul 18, 2025 C110081
A2605070Certificate of AnalysisJul 18, 2025 C110081
E2526627Certificate of AnalysisMar 15, 2025 C110081
E2514222Certificate of AnalysisMar 15, 2025 C110081
E2514221Certificate of AnalysisMar 15, 2025 C110081
G2315439Certificate of AnalysisJul 21, 2023 C110081
G2315441Certificate of AnalysisJul 21, 2023 C110081
G2315524Certificate of AnalysisJul 21, 2023 C110081
G2315527Certificate of AnalysisJul 21, 2023 C110081
K2422321Certificate of AnalysisJul 06, 2023 C110081
I2321107Certificate of AnalysisJul 06, 2023 C110081
F2415067Certificate of AnalysisJul 06, 2023 C110081
I2321092Certificate of AnalysisJul 06, 2023 C110081
I2321091Certificate of AnalysisJul 06, 2023 C110081
B2328530Certificate of AnalysisFeb 04, 2023 C110081
B2328526Certificate of AnalysisFeb 04, 2023 C110081
B2328543Certificate of AnalysisFeb 04, 2023 C110081
B2328537Certificate of AnalysisFeb 04, 2023 C110081
B2328538Certificate of AnalysisFeb 04, 2023 C110081
B2225371Certificate of AnalysisDec 15, 2021 C110081
B2225370Certificate of AnalysisDec 15, 2021 C110081
B2225352Certificate of AnalysisDec 15, 2021 C110081

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Propiedades químicas y físicas
SolubilidadSoluble in DMSO (100 mM), methanol, and water
Sensibilidadheat sensitive;Moisture sensitive
Rotación específica [α]-46° (C=1,H2O)
Punto de fusión (°C)224-228°C
Peso molecular251.240 g/mol
XLogP3-1.200
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count7
Rotatable Bond Count2
Exact Mass251.102 Da
Monoisotopic Mass251.102 Da
Topological Polar Surface Area119.000 Ų
Heavy Atom Count18
Formal Charge0
Complexity307.000
Isotope Atom Count0
Defined Atom Stereocenter Count3
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Baiyi Yan, Yanchun Gong, Wei Meng, Huizhen Sun, Wenxi Li, Kaizhi Ding, Caixia Dang, Xiaofei Gao, Wei Sun, Chunhua Yuan, Songhua Wang, Li-Hua Yao.  (2023)  Cordycepin protects islet β-cells against glucotoxicity and lipotoxicity via modulating related proteins of ROS/JNK signaling pathway.  BIOMEDICINE & PHARMACOTHERAPY,      [PMID:37100012] [10.1016/j.biopha.2023.114776]
2. Xinyue Li, Yuanyuan Fan, Zhengbao Zha, Deyan Gong, Jiajia Yu, Qianhui Li, Ruoyao Li, Hua Wang, Fei Wang.  (2023)  Cordycepin-Loaded Macrophage Vesicles for Targeted Nonalcoholic Steatohepatitis Attenuation.  ADVANCED FUNCTIONAL MATERIALS,  33  (18): (2214059).  [PMID:] [10.1002/adfm.202214059]
3. Ya Chen, Yuan Jiang, Xinyu Huang, Lin Chen, Hao Yang, Jian Zhao, Beibei Liang.  (2022)  Cordycepin Inhibits the Growth of Hepatocellular Carcinoma by Regulating the Pathway of Aerobic Glycolysis.  Evidence-based Complementary and Alternative Medicine,      [PMID:36467556] [10.1155/2022/6454482]
4. Yu Wang, Zejun Pei, Zaixiang Lou, Hongxin Wang.  (2022)  Evaluation of Anti-Biofilm Capability of Cordycepin Against Candida albicans.  Infection and Drug Resistance,      [PMID:33574683] [10.2147/IDR.S285690]
5. Weng Chunyue, Mi Zheyan, Li Meijing, Qin Haibin, Hu Zhongce, Liu Zhiqiang, Zheng Yuguo, Wang Yuanshan.  (2022)  Improvement of S-adenosyl-L-methionine production in Saccharomyces cerevisiae by atmospheric and room temperature plasma-ultraviolet compound mutagenesis and droplet microfluidic adaptive evolution.  3 Biotech,  12  (9): (1-15).  [PMID:35975026] [10.1007/s13205-022-03297-x]
6. Huizhen Sun, Anyong Zhang, Yanchun Gong, Wei Sun, Baiyi Yan, Shuihong Lei, Li-Hua Yao.  (2022)  Improving effect of cordycepin on insulin synthesis and secretion in normal and oxidative-damaged INS-1 cells.  EUROPEAN JOURNAL OF PHARMACOLOGY,      [PMID:35196519] [10.1016/j.ejphar.2022.174843]
7. Jing Yang, Yiwen Zhou, Jinsong Shi.  (2020)  Cordycepin protects against acute pancreatitis by modulating NF-κB and NLRP3 inflammasome activation via AMPK.  LIFE SCIENCES,      [PMID:32268154] [10.1016/j.lfs.2020.117645]
8. Hao Song, Li-Ping Huang, Yuping Li, Chao Liu, Songhua Wang, Wei Meng, Shanshan Wei, Xin-Ping Liu, Yanchun Gong, Li-Hua Yao.  (2018)  Neuroprotective effects of cordycepin inhibit Aβ-induced apoptosis in hippocampal neurons.  NEUROTOXICOLOGY,      [PMID:30031108] [10.1016/j.neuro.2018.07.008]
9. Qi Yize, Zhou Yao, Li Jiyang, Zhu Fangyuan, Guo Gengni, Wang Can, Yu Man, Wang Yijie, Ma Tengfei, Feng Shanwu, Zhou Li.  (2024)  3′-Deoxyadenosin alleviates methamphetamine-induced aberrant synaptic plasticity and seeking behavior by inhibiting the NLRP3 inflammasome.  Neural Regeneration Research,  19  (10): (2270).  [PMID:38488561] [10.4103/1673-5374.392887]
10. Yanhong Bi, Ruiping Fu, Weiliang Hua, Xinyu Xiong, Chun Zhu, Xiaobao Nie, Zhaoyu Wang.  (2025)  An empirical exploration of the capacity of choline chloride/lactic acid eutectics to extract and stabilize natural polyhydroxy compounds.  FOOD CHEMISTRY,      [PMID:40120314] [10.1016/j.foodchem.2025.143873]
11. Zhu Liang, Keyan Zhang, Hongli Guo, Xujiao Tang, Mingzhu Chen, Jinsong Shi, Jing Yang.  (2024)  Cordycepin alleviates hepatic fibrosis in association with the inhibition of glutaminolysis to promote hepatic stellate cell senescence.  INTERNATIONAL IMMUNOPHARMACOLOGY,      [PMID:38565039] [10.1016/j.intimp.2024.111981]
12. Chen Ya, Zhu Congcong, Tai Zongguang, Lian Tianyan, Zhu Quangang, Chen Zhongjian.  (2024)  Cordycepin Ameliorates Psoriasis-Like Skin Lesion by Regulating p53/MDM2 Feedback Loop.  MOLECULAR BIOTECHNOLOGY,      [PMID:38914920] [10.1007/s12033-024-01211-9]
13. Huizhen Sun, Shanshan Wei, Yanchun Gong, Kaizhi Ding, Shan Tang, Wei Sun, Chunhua Yuan, Liping Huang, Zhibing Liu, Chong Chen, Lihua Yao.  (2024)  Neuroprotective effects of cordycepin inhibit glutamate-induced apoptosis in hippocampal neurons.  CELL STRESS & CHAPERONES,      [PMID:38219840] [10.1016/j.cstres.2024.01.001]
14. Wanying Song, Xinyue Zhang, Huiyi Yang, Hanyu Liu, Baodong Wei.  (2025)  Soy Sauce Fermentation with Cordyceps militaris: Process Optimization and Functional Profiling.  Foods,  14  (15): (2711).  [PMID:40807648] [10.3390/foods14152711]
15. Mengjiao Li, Fuqiang Liu, Lulu Guo, Wu Fan, Jiazhong Wang, Binbin Lu, Guangfeng Hong, Wenjuan Zhang, Shu Tian, Jian Mao, Jianping Xie.  (2025)  Distribution and Pharmacokinetic Characteristics of Cordycepin in Rat: Investigated by UHPLC-HRMS/MS and Blood–Brain Synchronous Microdialysis.  BIOMEDICAL CHROMATOGRAPHY,  39  (4): (e70038).  [PMID:40071940] [10.1002/bmc.70038]
16. Yiheng Chen, Wenzhen Zhang, Lian Lin, Tingting Wang, Qinxin Xu, Xijie Zhou, Zhipeng Wu.  (2025)  Cordycepin promotes the survival of random-pattern skin flaps via autophagy in a rat model.  CELLULAR SIGNALLING,      [PMID:40480432] [10.1016/j.cellsig.2025.111890]
17. Wang Yu, Pei Zejun, Lou Zaixiang, Bandić Luna Maslov, Wang Hongxin.  (2025)  Cordycepin is an effective antifungal agent and targets multiple pathways and structures in yeasts.  JOURNAL OF APPLIED MICROBIOLOGY,      [PMID:40471709] [10.1093/jambio/lxaf141]
18. Wenbo Li, Shushu Li, Qingshi Wen, Xiaohan Zhang, Ke Zhang, Chenglun Tang, Fengxia Zou, Keke Zhang, Pengfei Jiao, Pengpeng Yang.  (2025)  Comparative Analysis of Physicochemical Properties for Three Crystal Forms of Cordycepin and Their Interconversion Relationship.  Crystals,  15  (12): (1043).  [PMID:] [10.3390/cryst15121043]
19. Fang Yixiao, Li Ning, Fan Youhong, Zhang Zhenye, Cai Yuchen, Guo Mengwei, Yang Lin, Jiang Shipeng, Zheng Binglian, Mei Jun, Ren Guodong.  (2026)  Characterization of the miRNA turnover landscape and its regulation in Arabidopsis.  PLANT CELL,  38  (3):   [PMID:] [10.1093/plcell/koag052]
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