kanamienamide

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| ImageFile = Kanamienamide.svg

| ImageSize = 200px

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| PIN = (2E)-3-Methoxy-N-{(1Z)-5-[(3S,6R,8S,11S)-4,6,8-trimethyl-3-(2-methylpropyl)-2,5-dioxo-1-oxa-4-azacycloundecan-11-yl]pent-1-en-1-yl}pent-2-enamide

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| Section1 = {{Chembox Identifiers

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| PubChem = 132915918

| ChemSpiderID = 58197334

| StdInChI = 1S/C28H48N2O5/c1-9-23(34-8)19-26(31)29(6)16-12-10-11-13-24-15-14-21(4)18-22(5)27(32)30(7)25(17-20(2)3)28(33)35-24/h12,16,19-22,24-25H,9-11,13-15,17-18H2,1-8H3/b16-12-,23-19-/t21-,22+,24-,25-/m0/s1

| StdInChIKey = MTZDCZNHECVTPF-ZIXRUXROSA-N

| SMILES = CCC(=CC(=O)N(C)C=CCCCC1CCC(CC(C(=O)N(C(C(=O)O1)CC(C)C)C)C)C)OC

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| Section2 = {{Chembox Properties

| C=28|H=48|N=2|O=5

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| Section3 = {{Chembox Hazards

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Kanamienamides is a complex enol ether containing enamide that is currently undergoing research in regards to its inhibitory activity towards cancer cells. The synthesis of kanamienamide consists of several chemical techniques, including CBS asymmetric reduction, Stork-Zhao-Wittig olefination, Cu-mediated amide coupling with vinyl iodide, Evans asymmetric alkylation, and ring-closing metathesis.{{Cite journal|last=Prabhakar Reddy|first=D.|last2=Zhang|first2=Ning|last3=Yu|first3=Zhimei|last4=Wang|first4=Zhen|last5=He|first5=Yun|date=2017-10-02|title=Total Synthesis of Kanamienamide|journal=The Journal of Organic Chemistry|volume=82|issue=20|pages=11262–11268|doi=10.1021/acs.joc.7b01984|pmid=28944669|issn=0022-3263}} Kanamienamide is a natural product found in Moorea bouillonii which is a cyanobacterium.{{cite journal|last1=Sumimoto|first1=Shimpei|last2=Iwasaki|first2=Arihiro|last3=Ohno|first3=Osamu|last4=Sueyoshi|first4=Kosuke|last5=Teruya|first5=Toshiaki|last6=Suenaga|first6=Kiyotake|title=Kanamienamide, an Enamide with an Enol Ether from the Marine Cyanobacterium|journal=Organic Letters|date=13 September 2016|volume=18|issue=19|pages=4884–4887|doi=10.1021/acs.orglett.6b02364|pmid=27623268}}