Name | Cyclosporin H |
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Synonyms |
(3S,6S,9S,12R,15S,18S,21R,24S,30S)-30-Ethyl-33-[(1R,2R,4E)-1-hydroxy-2-methyl-4-hexen-1-yl]-6,9,18,24-tetraisobutyl-3,21-diisopropyl-1,4,7,10,12,15,19,22,25,28-decamethyl-1,4,7,10,13,16,19,22,25,28,31-undecaazacyclotritriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone
CyclosporinH 1,4,7,10,13,16,19,22,25,28,31-Undecaazacyclotritriacontane-2,5,8,11,14,17,20,23,26,29,32-undecone, 30-ethyl-33-[(1R,2R,4E)-1-hydroxy-2-methyl-4-hexen-1-yl]-1,4,7,10,12,15,19,22,25,28-decamethyl-3,21-bis(1-methylethyl)-6,9,18,24-tetrakis(2-methylpropyl)-, (3S,6S,9S,12R,15S,18S,21R,24S,30S)- cyclosiversioside H Cyclosporin Impurity 8 |
Description | Cyclosporin H, a viral transduction enhancer, increases lentiviral transduction up to 10-fold in human cord blood-derived hematopoietic stem and progenitor cells (HSPCs). Cyclosporin H displays an additive effect when combined with Rapamycin or prostaglandin E2. Cyclosporin H lacks immunosuppressant activity of cyclosporin A. |
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Related Catalog |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 1282.0±65.0 °C at 760 mmHg |
Melting Point | 162-165ºC |
Molecular Formula | C62H111N11O12 |
Molecular Weight | 1216.638 |
Flash Point | 729.1±34.3 °C |
Exact Mass | 1215.857056 |
PSA | 270.01000 |
LogP | 4.28 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.469 |