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Inhibitor Report for: IsovanihuperzineA

General
Type Derivative of Huperzine
Chemical_Nomenclature (13E)-13-ethylidene-1-[(3-hydroxy-4-methoxyphenyl)methylideneamino]-11-methyl-6-azatricyclo[7.3.1.02,7]trideca-2(7),3,10-trien-5-one
Canonical SMILES CC=C1C2CC3=C(C1(CC(=C2)C)N=CC4=CC(=C(C=C4)OC)O)C=CC(=O)N3
InChI InChI=1S/C23H24N2O3/c1-4-17-16-9-14(2)12-23(17,18-6-8-22(27)25-19(18)11-16)24-13-15-5-7-21(28-3)20(26)10-15/h4-10,13,16,26H,11-12H2,1-3H3,(H,25,27)/b17-4+,24-13? InChI=1S/C23H24N2O3/c1-4-17-16-9-14(2)12-23(17,18-6-8-22(27)25-19(18)11-16)24-13-15-5-7-21(28-3)20(26)10-15/h4-10,13,16,26H,11-12H2,1-3H3,(H,25,27)/b17-4+,24-13?/t16-,23+/m0/s1
InChIKey LRSQBNHUUIRBHN-WXOLMZBGSA-N LRSQBNHUUIRBHN-GQSJKZJISA-N
Other name(s) IVHA
________________________________________________________________________________________________
MW|376.45
Formula|C23H24N2O3
CAS_number|
PubChem|44612534, 129628155
UniChem|LRSQBNHUUIRBHN-WXOLMZBGSA-N, LRSQBNHUUIRBHN-GQSJKZJISA-N
IUPHAR|
Wikipedia|

Target
Families | IsovanihuperzineA ligand of proteins in family: ACHE

References:
Search PubMed for references concerning: IsovanihuperzineA
    Title: Effects of isovanihuperzine A on cholinesterase and scopolamine-induced memory impairment
    Xiong ZQ, Tang XC, Lin JL, Zhu DY
    Ref: Acta Pharmacol Sin, 16:21, 1995 : PubMed