Cordycepin
SIGMA/C3394 - from Cordyceps militaris
Synonym: 3′-Deoxyadenosine
CAS Number: 73-03-0
Empirical Formula (Hill Notation): C10H13N5O3
Molecular Weight: 251.24
EC Number: 200-791-4
MDL Number: MFCD00037998
Linear Formula: C10H13N5O3
Product Type: Chemical
| antibiotic activity spectrum | fungi |
| biological source | Cordyceps militaris |
| form | powder |
| InChI | 1S/C10H13N5O3/c11-8-7-9(1 |
| InChI key | OFEZSBMBBKLLBJ-BAJZRUMYSA |
| mode of action | DNA synthesis | interferes |
| enzyme | inhibits | |
| Quality Level | 200 ![]() |
| SMILES string | Nc1ncnc2n(cnc12)[C@@H]3O[ |
| storage temp. | −20°C |
| Biochem/physiol Actions: | Cordycepin is an adenosine analogue that is readily converted to cordycepin 5′-triphosphate; can be used for 3′-end labeling of RNA. |
| Features and Benefits: | This compound is a featured product for Cyclic Nucleotide and Gene Regulation research. Discover more featured Cyclic Nucleotide and Gene Regulation products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm . |
| Features and Benefits: | This compound is featured on the Adenylyl cyclases page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here . |
| General description: | Chemical structure: nucleoside |
| Packaging: | 10, 25, 100 mg in glass bottle |
| Symbol | GHS06 |
| Signal word | Danger |
| Hazard statements | H301 + H311 + H331 |
| Precautionary statements | P280 - P301 + P310 + P330 - P302 + P352 + P312 - P304 + P340 + P311 |
| Hazard Codes | T |
| Risk Statements | 25-36/37/38 |
| Safety Statements | 26-45 |
| RIDADR | UN 2811 6.1 / PGIII |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Storage Temp. | −20°C |
| UNSPSC | 12352200 |


