ungiminorine

{{Chembox

| ImageFile = Ungiminorine.svg

| ImageSize = 200px

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| IUPACName = (1S,16R,17R,18S,19S)-17-methoxy-5,7-dioxa-12-azapentacyclo[10.6.1.0^2,10.0^4,8.0^15,19]nonadeca-2,4(8),9,14-tetraene-16,18-diol

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|Section1={{Chembox Identifiers

| CASNo = 27857-09-6

| ChEMBL = 497276

| PubChem = 10425948

| ChemSpiderID = 8601376

| SMILES = CO[C@@H]1[C@H]([C@@H]2[C@H]3C(=CCN3CC4=CC5=C(C=C24)OCO5)[C@H]1O)O

| InChI = 1/C17H19NO5/c1-21-17-15(19)9-2-3-18-6-8-4-11-12(23-7-22-11)5-10(8)13(14(9)18)16(17)20/h2,4-5,13-17,19-20H,3,6-7H2,1H3/t13-,14+,15+,16-,17-/m0/s1

| InChIKey = ZQLQBAUVRGDBJL-BIVLZKPYBI

| StdInChI = 1S/C17H19NO5/c1-21-17-15(19)9-2-3-18-6-8-4-11-12(23-7-22-11)5-10(8)13(14(9)18)16(17)20/h2,4-5,13-17,19-20H,3,6-7H2,1H3/t13-,14+,15+,16-,17-/m0/s1

| StdInChIKey = ZQLQBAUVRGDBJL-BIVLZKPYSA-N

}}

|Section2={{Chembox Properties

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|Section3={{Chembox Hazards

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Ungiminorine is an acetylcholinesterase inhibitor isolated from Narcissus.{{cite journal |last1=Ingkaninan |first1=K. |last2=Hazekamp |first2=A. |last3=de Best |first3=C. M. |last4=Irth |first4=H. |last5=Tjaden |first5=U. R. |last6=van der Heijden |first6=R. |last7=van der Greef |first7=J. |last8=Verpoorte |first8=R. |title=The application of HPLC with on-line coupled UV/MS-biochemical detection for isolation of an acetylcholinesterase inhibitor from narcissus 'Sir Winston Churchill' |journal=Journal of Natural Products |date=June 2000 |volume=63 |issue=6 |pages=803–806 |doi=10.1021/np9905719 |pmid=10869205 |url=https://www.ncbi.nlm.nih.gov/pubmed/10869205 |issn=0163-3864}}