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  • China
  • Product Name: Cordycepin
  • Price: ¥Inquiry/5mg
  • Purity: 98.0%
  • Stocking Period: 10 Day
  • Contact: Xueping-Zheng



73-03-0

73-03-0 structure
73-03-0 structure
  • Name: Cordycepin
  • Chemical Name: Cordycepin
  • CAS Number: 73-03-0
  • Molecular Formula: C10H13N5O3
  • Molecular Weight: 251.242
  • Catalog: Biochemical Nucleoside drugs Deoxynucleotides and their analogues
  • Create Date: 2018-03-02 08:00:00
  • Modify Date: 2024-01-02 18:58:22
  • Cordycepin, which is a nucleoside derivative isolated from Cordyceps, inhibits IL-1β-induced MMP-1 and MMP-3 expression in rheumatoid arthritis synovial fibroblasts (RASFs) in a dose-dependent manner.

Name Cordycepin
Synonyms 9H-Purin-6-amine, 9-(3-deoxy-β-D-erythro-pentofuranosyl)-
Adenine cordyceposide
EINECS 200-791-4
9H-Purine, 6-amino-9-(3-deoxy-β-D-ribofuranosyl)-
Adenosine,3-deoxy
Cordycepine
MFCD00037998
Cordycepin
Cordyceps fungus powder
cordycepin crystalline
3'-Deoxyadenosine
adenosine, 3'-deoxy-
(-)-cordycepin
3'-Deoxy-D-adenosine
Description Cordycepin, which is a nucleoside derivative isolated from Cordyceps, inhibits IL-1β-induced MMP-1 and MMP-3 expression in rheumatoid arthritis synovial fibroblasts (RASFs) in a dose-dependent manner.
Related Catalog
Target

MMP-1

MMP-3

In Vitro Cordycepin is a potent inhibitor of IL-1β-induced chemokine production and MMP expression and strongly blocks the p38/JNK/AP-1 signalling pathway in RASFs. The effect of Cordycepin on cellular toxicity of RASFs is assessed using MTT assay. Treatment of RASFs with Cordycepin (50 μM or 100 μM) for 24 h does not cause any significant change in cell viability. However, cell viability is slightly decreased when cells are incubated with 100 μM Cordycepin for 48 h[1].
Cell Assay RASFs (2×104 cells/well) are treated with various concentrations of Cordycepin (50 μM or 100 μM). After incubation for 1 h, 12 h and 24 h, cells are washed twice with PBS, MTT (0.5 mg/mL PBS) is added to each well and incubated at 37°C for 30 min. Formazan crystals formed are dissolved by adding DMSO (100 μL/well) and the absorbance is read at 570 nm using a microplate reader[1].
References

[1]. Noh EM, et al. Cordycepin inhibits IL-1beta-induced MMP-1 and MMP-3 expression in rheumatoid arthritis synovial fibroblasts. Rheumatology (Oxford). 2009 Jan;48(1):45-8.

Density 1.9±0.1 g/cm3
Boiling Point 627.2±65.0 °C at 760 mmHg
Melting Point 225-229ºC
Molecular Formula C10H13N5O3
Molecular Weight 251.242
Flash Point 333.1±34.3 °C
Exact Mass 251.101837
PSA 119.31000
LogP -0.41
Vapour Pressure 0.0±1.9 mmHg at 25°C
Index of Refraction 1.863
Storage condition −20°C

CHEMICAL IDENTIFICATION

RTECS NUMBER :
AU7358610
CHEMICAL NAME :
Adenosine, 3'-deoxy-
CAS REGISTRY NUMBER :
73-03-0
BEILSTEIN REFERENCE NO. :
0035194
LAST UPDATED :
199612
DATA ITEMS CITED :
7
MOLECULAR FORMULA :
C10-H13-N5-O3
MOLECULAR WEIGHT :
251.28
WISWESSER LINE NOTATION :
T56 BN DN FN HNJ IZ D- BT5OTJ CQ E1Q

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Intraperitoneal
DOSE :
80 mg/kg
SEX/DURATION :
female 7 day(s) after conception
TOXIC EFFECTS :
Reproductive - Fertility - other measures of fertility

MUTATION DATA

TYPE OF TEST :
DNA inhibition
TEST SYSTEM :
Human HeLa cell
DOSE/DURATION :
20 mg/L
REFERENCE :
JANTAJ Journal of Antibiotics. (Japan Antibiotics Research Assoc., 2-20-8 Kamiosaki, Shinagawa-ku, Tokyo, 141, Japan) V.2-5, 1948-52; V.21- 1968- Volume(issue)/page/year: 35,119,1982
Symbol GHS06
GHS06
Signal Word Danger
Hazard Statements H301-H315-H319-H335
Precautionary Statements P261-P301 + P310-P305 + P351 + P338
Personal Protective Equipment Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges
Hazard Codes T:Toxic
Risk Phrases R25;R36/37/38
Safety Phrases S26-S45
RIDADR UN 2811
WGK Germany 3
RTECS AU7358610
HS Code 29349990
HS Code 2934999090
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%