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InChiKey: LSVWEYNSNZJEGB-UHFFFAOYSA-N
PHT-427 inhibited the phosphorylation of both Akt and PDPK1 as well as downstream targets maximally at 8–12 h after administration corresponding to its peak plasma concentration
Solubility: DMSO : ≥ 125 mg/mL (547
Thalidomide-NH-amido-PEG3-C2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology
Ivermectin B1a-d2 676rometamol hydrochloride InChiKey: LSVWEYNSNZJEGB-UHFFFAOYSA-NProduct information Molecular Weight: 875. 09 Formula: C48H74O14 Chemical Name: 6 (butan 2 yl) 21',24' dihydroxy 12' ({5 [(5 hydroxy 4 methoxy 6 methyloxan 2 yl)oxy] 4 methoxy 6 methyloxan 2 yl}oxy) 5,11',13',22' tetramethyl 3',7',19' trioxaspiro[oxane 2,6' tetracyclo[15. 6. 1. 1,. 0,]pentacosane] 10',14',16',22' tetraen 2' one Smiles: CCC(C)C1OC2(CC3CC(CC=C(C)C(OC4CC(OC)C(OC5CC(OC)C(O)C(C)O5)C(C)O4)C(C)C=CC=C4COC5C(O)C(C)=CC(C(=O)O3)C45O)O2)CCC1C c:
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