7-Hydroxy-4-methyl-8-nitrocoumarin Size:Contact [email protected] for quotation Smiles: CCCCNC(=O)[C@@H]1CC2=CC=CC=C2N1C(=O)[C@@H](N)CC

Smiles: CCCCNC(=O)[C@@H]1CC2=CC=CC=C2N1C(=O)[C@@H](N)CC

The metabolite identification studies with Lipid 5 indicated that hydrolysis of the primary ester is the first step in the metabolism of the lipid

InChi: InChI=1S/C21H18O14/c22-6-2-1-5(3-7(6)23)16-13(28)11(26)10-8(24)4-9(25)17(18(10)33-16)34-21-15(30)12(27)14(29)19(35-21)20(31)32/h1-4

for 24 or 48 hours) decreases the proliferation of medulloblastoma cells

Epiallopregnanolone significantly decreased response rates when compared with control condition

7-Hydroxy-4-methyl-8-nitrocoumarin Size:Contact [email protected] for quotation Smiles: CCCCNC(=O)[C@@H]1CC2=CC=CC=C2N1C(=O)[C@@H](N)CC7 Hydroxy 4 methyl 8 nitrocoumarin is a coumarin derivative. Product information CAS Number: 19037 69 5 Molecular Weight: 221. 17 Formula: C10H7NO5 Chemical Name: 7 hydroxy 4 methyl 8 nitro 2H chromen 2 one Smiles: CC1=CC(=O)OC2=C(C(O)=CC=C21)[N+]([O ])=O InChiKey: BGUBUSIGKOWDPO UHFFFAOYSA N InChi: InChI=1S C10H7NO5 c1 5 4 8(13)16 10 6(5)2 3 7(12)9(10)11(14)15 h2 4,12H,1H3 Technical Data Appearance: Solid Power Purity: 98% (or refer to the