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suggesting that inhibition of the CBP bromodomain may provide a novel small molecule therapeutic approach for cancer immunotherapy
24)25)28-20(29)27-14-2-1-3-17(10-14)30-16-7-4-13(12-26)5-8-16/h1-11H
IC50≈8 nM)
is a potent and selective inhibitor of histone deacetylase 8 (HDAC8) with an IC50 ~10 nM
InChi: InChI=1S/C34H28N6O14S4
(R)-Sulforaphane Size:2mg solid suggesting that inhibition of the(R) Sulforaphane (L Sulforaphane) is a highly potent inducer of the Keap1 Nrf2 ARE pathway. (R) Sulforaphane is a far more potent inducer of the carcinogen detoxifying enzyme systems in rat liver and lung than the S isomer. Product information CAS Number: 142825 10 3 Molecular Weight: 177. 29 Formula: C6H11NOS2 Synonym: L Sulforaphane Chemical Name: 1 isothiocyanato 4 [(R) methanesulfinyl]butane Smiles: C[S@@](=O)CCCCN=C=S InChiKey: SUVMJBTUFCVSAD
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