Name | sangivamycin |
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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]. |
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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 |
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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
|
Symbol |
GHS06 |
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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 | |
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DownStream 1 | |