| Name | sangivamycin | 
|---|---|
| Synonyms | 7-Carboxamido-7-deazaadenosine 7-DEAZA-7-CARBAMOYLADENOSINE 7-DEAZAADENOSINE-7-CARBOXAMIDE SANGIVAMYCIN | 
| Description | Sangivamycin (NSC 65346), a nucleoside analog, is a potent inhibitor of protein kinase C (PKC) with an Ki of 10 μM. Sangivamycin has potent antiproliferative activity against a variety of human cancers[1][2]. | 
|---|---|
| Related Catalog | |
| In Vitro | Sangivamycin has differential antitumor effects in drug-sensitive MCF7/wild type (WT) cells, causing growth arrest, and in multidrug-resistant MCF7/adriamycin-resistant (ADR) human breast carcinoma cells, causing massive apoptotic cell death[2]. Sangivamycin (0.3 μM; 0-72 hours), shows almost maximal cytocidal (for MCF7/ADR) or cytostatic (for MCF7/WT) effects[2]. Sangivamycin activates caspases in MCF7/ADR cells. Upon exposure of MCF7/ADR cells to Sangivamycin (0.3 μM;), a vast amount of cleavage of lamin A to a 28-kDa fragment is detected within 48 hours[2]. | 
| References | 
| Boiling Point | 880.6ºC at 760 mmHg | 
|---|---|
| Molecular Formula | C12H15N5O5 | 
| Molecular Weight | 309.28 | 
| Flash Point | 486.4ºC | 
| Exact Mass | 327.11800 | 
| PSA | 178.97000 | 
| Vapour Pressure | 3.3E-33mmHg at 25°C | 
| CHEMICAL IDENTIFICATION
 
 
 
 
 
 
 
 HEALTH HAZARD DATAACUTE TOXICITY DATA
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 MUTATION DATA
 
 
 
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| Symbol |   GHS06 | 
|---|---|
| Signal Word | Danger | 
| Hazard Statements | H300-H310-H330 | 
| Precautionary Statements | P260-P264-P280-P284-P302 + P350-P310 | 
| Personal Protective Equipment | Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges | 
| Hazard Codes | T+ | 
| Risk Phrases | 26/27/28 | 
| RIDADR | UN 2811 6.1/PG 2 | 
| RTECS | UY9355000 | 
| Precursor 0 | |
|---|---|
| DownStream 1 | |