Name | SGD-1882 |
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Synonyms |
5H-Pyrrolo[2,1-c][1,4]benzodiazepin-5-one, 2-(4-aminophenyl)-8-[3-[[(11aS)-5,11a-dihydro-7-methoxy-2-(4-methoxyphenyl)-5-oxo-1H-pyrrolo[2,1-c][1,4]benzodiazepin-8-yl]oxy]propoxy]-1,11a-dihydro-7-methoxy-, (11aS)-
(11aS)-2-(4-Aminophenyl)-7-methoxy-8-(3-{[(11aS)-7-methoxy-2-(4-methoxyphenyl)-5-oxo-5,11a-dihydro-1H-pyrrolo[2,1-c][1,4]benzodiazepin-8-yl]oxy}propoxy)-1,11a-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one SGD-1882 IRE1I9FE08 |
Description | SGD-1882 is a cytotoxic, DNA minor-groove crosslinking agent pyrrolobenzodiazepine (PBD) dimer, acting as the payload for ADCs. |
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Related Catalog | |
In Vitro | SGD-1882 is the cytotoxic payload undergoing clinical evaluation for anti-CD33 and anti-CD70 conjugates[1]. SGD-1882 is not an MDR1 substrate, and SGN-CD33A is conjugated to the SGD-1882. SGN-CD33A can kill MDR1 expressing CD33 positive AML patient samples and is currently in Phase I[2]. |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 977.7±65.0 °C at 760 mmHg |
Molecular Formula | C42H39N5O7 |
Molecular Weight | 725.788 |
Flash Point | 545.1±34.3 °C |
Exact Mass | 725.284973 |
LogP | 2.87 |
Vapour Pressure | 0.0±0.3 mmHg at 25°C |
Index of Refraction | 1.676 |